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@@ -31,7 +31,7 @@
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<a class="navbar-brand me-2" href="https://amr-for-r.org/index.html">AMR (for R)</a>
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<small class="nav-text text-muted me-auto" data-bs-toggle="tooltip" data-bs-placement="bottom" title="">3.0.1.9057</small>
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<!-- Generated by pkgdown: do not edit by hand --><html lang="en"><head><meta http-equiv="Content-Type" content="text/html; charset=UTF-8"><meta charset="utf-8"><meta http-equiv="X-UA-Compatible" content="IE=edge"><meta name="viewport" content="width=device-width, initial-scale=1, shrink-to-fit=no"><title>CLAUDE.md — AMR R Package • AMR (for R)</title><!-- favicons --><link rel="icon" type="image/png" sizes="96x96" href="favicon-96x96.png"><link rel="icon" type="”image/svg+xml”" href="favicon.svg"><link rel="apple-touch-icon" sizes="180x180" href="apple-touch-icon.png"><link rel="icon" sizes="any" href="favicon.ico"><link rel="manifest" href="site.webmanifest"><script src="deps/jquery-3.6.0/jquery-3.6.0.min.js"></script><meta name="viewport" content="width=device-width, initial-scale=1, shrink-to-fit=no"><link href="deps/bootstrap-5.3.1/bootstrap.min.css" rel="stylesheet"><script src="deps/bootstrap-5.3.1/bootstrap.bundle.min.js"></script><link href="deps/Lato-0.4.10/font.css" rel="stylesheet"><link href="deps/Fira_Code-0.4.10/font.css" rel="stylesheet"><link href="deps/font-awesome-6.5.2/css/all.min.css" rel="stylesheet"><link href="deps/font-awesome-6.5.2/css/v4-shims.min.css" rel="stylesheet"><script src="deps/headroom-0.11.0/headroom.min.js"></script><script src="deps/headroom-0.11.0/jQuery.headroom.min.js"></script><script src="deps/bootstrap-toc-1.0.1/bootstrap-toc.min.js"></script><script src="deps/clipboard.js-2.0.11/clipboard.min.js"></script><script src="deps/search-1.0.0/autocomplete.jquery.min.js"></script><script src="deps/search-1.0.0/fuse.min.js"></script><script src="deps/search-1.0.0/mark.min.js"></script><!-- pkgdown --><script src="pkgdown.js"></script><link href="extra.css" rel="stylesheet"><script src="extra.js"></script><meta property="og:title" content="CLAUDE.md — AMR R Package"><meta property="og:image" content="https://amr-for-r.org/logo.svg"><link rel="stylesheet" href="https://cdn.jsdelivr.net/npm/katex@0.16.11/dist/katex.min.css" integrity="sha384-nB0miv6/jRmo5UMMR1wu3Gz6NLsoTkbqJghGIsx//Rlm+ZU03BU6SQNC66uf4l5+" crossorigin="anonymous"><script defer src="https://cdn.jsdelivr.net/npm/katex@0.16.11/dist/katex.min.js" integrity="sha384-7zkQWkzuo3B5mTepMUcHkMB5jZaolc2xDwL6VFqjFALcbeS9Ggm/Yr2r3Dy4lfFg" crossorigin="anonymous"></script><script defer src="https://cdn.jsdelivr.net/npm/katex@0.16.11/dist/contrib/auto-render.min.js" integrity="sha384-43gviWU0YVjaDtb/GhzOouOXtZMP/7XUzwPTstBeZFe/+rCMvRwr4yROQP43s0Xk" crossorigin="anonymous" onload="renderMathInElement(document.body);"></script></head><body>
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<!-- Generated by pkgdown: do not edit by hand --><html lang="en"><head><meta http-equiv="Content-Type" content="text/html; charset=UTF-8"><meta charset="utf-8"><meta http-equiv="X-UA-Compatible" content="IE=edge"><meta name="viewport" content="width=device-width, initial-scale=1, shrink-to-fit=no"><title>CLAUDE.md — AMR R Package • AMR (for R)</title><!-- favicons --><link rel="icon" type="image/png" sizes="96x96" href="favicon-96x96.png"><link rel="icon" type="”image/svg+xml”" href="favicon.svg"><link rel="apple-touch-icon" sizes="180x180" href="apple-touch-icon.png"><link rel="icon" sizes="any" href="favicon.ico"><link rel="manifest" href="site.webmanifest"><script src="deps/jquery-3.6.0/jquery-3.6.0.min.js"></script><meta name="viewport" content="width=device-width, initial-scale=1, shrink-to-fit=no"><link href="deps/bootstrap-5.3.8/bootstrap.min.css" rel="stylesheet"><script src="deps/bootstrap-5.3.8/bootstrap.bundle.min.js"></script><link href="deps/Lato-0.4.10/font.css" rel="stylesheet"><link href="deps/Fira_Code-0.4.10/font.css" rel="stylesheet"><link href="deps/font-awesome-6.5.2/css/all.min.css" rel="stylesheet"><link href="deps/font-awesome-6.5.2/css/v4-shims.min.css" rel="stylesheet"><script src="deps/headroom-0.11.0/headroom.min.js"></script><script src="deps/headroom-0.11.0/jQuery.headroom.min.js"></script><script src="deps/bootstrap-toc-1.0.1/bootstrap-toc.min.js"></script><script src="deps/clipboard.js-2.0.11/clipboard.min.js"></script><script src="deps/search-1.0.0/autocomplete.jquery.min.js"></script><script src="deps/search-1.0.0/fuse.min.js"></script><script src="deps/search-1.0.0/mark.min.js"></script><!-- pkgdown --><script src="pkgdown.js"></script><link href="extra.css" rel="stylesheet"><script src="extra.js"></script><meta property="og:title" content="CLAUDE.md — AMR R Package"><meta property="og:image" content="https://amr-for-r.org/logo.svg"><link rel="stylesheet" href="https://cdn.jsdelivr.net/npm/katex@0.16.11/dist/katex.min.css" integrity="sha384-nB0miv6/jRmo5UMMR1wu3Gz6NLsoTkbqJghGIsx//Rlm+ZU03BU6SQNC66uf4l5+" crossorigin="anonymous"><script defer src="https://cdn.jsdelivr.net/npm/katex@0.16.11/dist/katex.min.js" integrity="sha384-7zkQWkzuo3B5mTepMUcHkMB5jZaolc2xDwL6VFqjFALcbeS9Ggm/Yr2r3Dy4lfFg" crossorigin="anonymous"></script><script defer src="https://cdn.jsdelivr.net/npm/katex@0.16.11/dist/contrib/auto-render.min.js" integrity="sha384-43gviWU0YVjaDtb/GhzOouOXtZMP/7XUzwPTstBeZFe/+rCMvRwr4yROQP43s0Xk" crossorigin="anonymous" onload="renderMathInElement(document.body);"></script></head><body>
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<!-- Generated by pkgdown: do not edit by hand --><html lang="en"><head><meta http-equiv="Content-Type" content="text/html; charset=UTF-8"><meta charset="utf-8"><meta http-equiv="X-UA-Compatible" content="IE=edge"><meta name="viewport" content="width=device-width, initial-scale=1, shrink-to-fit=no"><title>License • AMR (for R)</title><!-- favicons --><link rel="icon" type="image/png" sizes="96x96" href="favicon-96x96.png"><link rel="icon" type="”image/svg+xml”" href="favicon.svg"><link rel="apple-touch-icon" sizes="180x180" href="apple-touch-icon.png"><link rel="icon" sizes="any" href="favicon.ico"><link rel="manifest" href="site.webmanifest"><script src="deps/jquery-3.6.0/jquery-3.6.0.min.js"></script><meta name="viewport" content="width=device-width, initial-scale=1, shrink-to-fit=no"><link href="deps/bootstrap-5.3.8/bootstrap.min.css" rel="stylesheet"><script src="deps/bootstrap-5.3.8/bootstrap.bundle.min.js"></script><link href="deps/Lato-0.4.10/font.css" rel="stylesheet"><link href="deps/Fira_Code-0.4.10/font.css" rel="stylesheet"><link href="deps/font-awesome-6.5.2/css/all.min.css" rel="stylesheet"><link href="deps/font-awesome-6.5.2/css/v4-shims.min.css" rel="stylesheet"><script src="deps/headroom-0.11.0/headroom.min.js"></script><script src="deps/headroom-0.11.0/jQuery.headroom.min.js"></script><script src="deps/bootstrap-toc-1.0.1/bootstrap-toc.min.js"></script><script src="deps/clipboard.js-2.0.11/clipboard.min.js"></script><script src="deps/search-1.0.0/autocomplete.jquery.min.js"></script><script src="deps/search-1.0.0/fuse.min.js"></script><script src="deps/search-1.0.0/mark.min.js"></script><!-- pkgdown --><script src="pkgdown.js"></script><link href="extra.css" rel="stylesheet"><script src="extra.js"></script><meta property="og:title" content="License"><meta property="og:image" content="https://amr-for-r.org/logo.svg"><link rel="stylesheet" href="https://cdn.jsdelivr.net/npm/katex@0.16.11/dist/katex.min.css" integrity="sha384-nB0miv6/jRmo5UMMR1wu3Gz6NLsoTkbqJghGIsx//Rlm+ZU03BU6SQNC66uf4l5+" crossorigin="anonymous"><script defer src="https://cdn.jsdelivr.net/npm/katex@0.16.11/dist/katex.min.js" integrity="sha384-7zkQWkzuo3B5mTepMUcHkMB5jZaolc2xDwL6VFqjFALcbeS9Ggm/Yr2r3Dy4lfFg" crossorigin="anonymous"></script><script defer src="https://cdn.jsdelivr.net/npm/katex@0.16.11/dist/contrib/auto-render.min.js" integrity="sha384-43gviWU0YVjaDtb/GhzOouOXtZMP/7XUzwPTstBeZFe/+rCMvRwr4yROQP43s0Xk" crossorigin="anonymous" onload="renderMathInElement(document.body);"></script></head><body>
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<a class="navbar-brand me-2" href="index.html">AMR (for R)</a>
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<small class="nav-text text-muted me-auto" data-bs-toggle="tooltip" data-bs-placement="bottom" title="">3.0.1.9057</small>
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@@ -30,7 +30,7 @@
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<a class="navbar-brand me-2" href="../index.html">AMR (for R)</a>
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<small class="nav-text text-muted me-auto" data-bs-toggle="tooltip" data-bs-placement="bottom" title="">3.0.1.9057</small>
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<small class="nav-text text-muted me-auto" data-bs-toggle="tooltip" data-bs-placement="bottom" title="">3.0.1.9061</small>
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@@ -91,7 +91,7 @@
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website update since they are based on randomly created values and the
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page was written in <a href="https://rmarkdown.rstudio.com/" class="external-link">R
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Markdown</a>. However, the methodology remains unchanged. This page was
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generated on 02 May 2026.</p>
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generated on 23 June 2026.</p>
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<div class="section level2">
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<h2 id="introduction">Introduction<a class="anchor" aria-label="anchor" href="#introduction"></a>
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</h2>
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@@ -147,21 +147,21 @@ make the structure of your data generally look like this:</p>
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</tr></thead>
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<tbody>
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<tr class="odd">
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<td align="center">2026-05-02</td>
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<td align="center">2026-06-23</td>
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<td align="center">abcd</td>
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<td align="center">Escherichia coli</td>
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<td align="center">S</td>
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<td align="center">S</td>
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</tr>
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<tr class="even">
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<td align="center">2026-05-02</td>
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<td align="center">2026-06-23</td>
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<td align="center">abcd</td>
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<td align="center">Escherichia coli</td>
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<td align="center">S</td>
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<td align="center">R</td>
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</tr>
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<tr class="odd">
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<td align="center">2026-05-02</td>
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<td align="center">2026-06-23</td>
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<td align="center">efgh</td>
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<td align="center">Escherichia coli</td>
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<td align="center">R</td>
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@@ -218,7 +218,7 @@ cleaned as SIR values as well.</p>
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<p>With <code><a href="../reference/as.mo.html">as.mo()</a></code>, users can transform arbitrary
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microorganism names or codes to current taxonomy. The <code>AMR</code>
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package contains up-to-date taxonomic data. To be specific, currently
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included data were retrieved on 24 Jun 2024.</p>
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included data were retrieved on 07 May 2026.</p>
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<p>The codes of the AMR packages that come from <code><a href="../reference/as.mo.html">as.mo()</a></code> are
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short, but still human readable. More importantly, <code><a href="../reference/as.mo.html">as.mo()</a></code>
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supports all kinds of input:</p>
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@@ -287,24 +287,23 @@ taxonomic codes. Let’s check this:</p>
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<span><span class="co">#> Also matched: <span style="font-style: italic;">Klebsiella pneumoniae</span> complex<span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FFFF87;">0.707</span>), <span style="font-style: italic;">Klebsiella pneumoniae</span></span></span>
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<span><span class="co">#> <span style="font-style: italic;">ozaenae</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FFFF87;">0.707</span>), <span style="font-style: italic;">Klebsiella pneumoniae pneumoniae</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FFFF87;">0.688</span>), <span style="font-style: italic;">Klebsiella</span></span></span>
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<span><span class="co">#> <span style="font-style: italic;">pneumoniae rhinoscleromatis</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FFFF87;">0.658</span>), <span style="font-style: italic;">Klebsiella pasteurii</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FF5F5F;">0.500</span>), <span style="font-style: italic;">Klebsiella</span></span></span>
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<span><span class="co">#> <span style="font-style: italic;">planticola</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FF5F5F;">0.500</span>), <span style="font-style: italic;">Kingella potus</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FF5F5F;">0.400</span>), <span style="font-style: italic;">Kluyveromyces pseudotropicale</span></span></span>
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<span><span class="co">#> <span style="color: #0000BB;">(</span><span style="color: #080808; background-color: #FF5F5F;">0.386</span>), <span style="font-style: italic;">Kluyveromyces pseudotropicalis</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FF5F5F;">0.363</span>), and <span style="font-style: italic;">Kosakonia pseudosacchari</span></span></span>
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<span><span class="co">#> <span style="color: #0000BB;">(</span><span style="color: #080808; background-color: #FF5F5F;">0.361</span>)</span></span>
|
||||
<span><span class="co">#> <span style="font-style: italic;">planticola</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FF5F5F;">0.500</span>), <span style="font-style: italic;">Kosakonia pseudosacchari</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FF5F5F;">0.471</span>), <span style="font-style: italic;">Kaistella palustris</span></span></span>
|
||||
<span><span class="co">#> <span style="color: #0000BB;">(</span><span style="color: #080808; background-color: #FF5F5F;">0.435</span>), <span style="font-style: italic;">Kingella potus</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FF5F5F;">0.435</span>), and <span style="font-style: italic;">Kocuria palustris</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FF5F5F;">0.435</span>)</span></span>
|
||||
<span><span class="co">#> <span style="color: #B2B2B2;">-------------------------------------------------------------------------------</span></span></span>
|
||||
<span><span class="co">#> <span style="color: #0000BB;">"S. aureus"</span> -> <span style="font-weight: bold; font-style: italic;">Staphylococcus aureus</span> (B_STPHY_AURS, <span style="color: #080808; background-color: #FFFF87;">0.690</span>)</span></span>
|
||||
<span><span class="co">#> Also matched: <span style="font-style: italic;">Staphylococcus aureus aureus</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FFD787;">0.643</span>), <span style="font-style: italic;">Staphylococcus argenteus</span></span></span>
|
||||
<span><span class="co">#> <span style="color: #0000BB;">(</span><span style="color: #080808; background-color: #FFD787;">0.625</span>), <span style="font-style: italic;">Staphylococcus aureus anaerobius</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FFD787;">0.625</span>), <span style="font-style: italic;">Staphylococcus auricularis</span></span></span>
|
||||
<span><span class="co">#> <span style="color: #0000BB;">(</span><span style="color: #080808; background-color: #FFD787;">0.615</span>), <span style="font-style: italic;">Salmonella</span> Aurelianis<span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FFD787;">0.595</span>), <span style="font-style: italic;">Salmonella</span> Aarhus<span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FFD787;">0.588</span>), <span style="font-style: italic;">Salmonella</span></span></span>
|
||||
<span><span class="co">#> Amounderness<span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FFD787;">0.587</span>), <span style="font-style: italic;">Staphylococcus argensis</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FFD787;">0.587</span>), <span style="font-style: italic;">Streptococcus australis</span></span></span>
|
||||
<span><span class="co">#> <span style="color: #0000BB;">(</span><span style="color: #080808; background-color: #FFD787;">0.587</span>), and <span style="font-style: italic;">Salmonella choleraesuis arizonae</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FFD787;">0.562</span>)</span></span>
|
||||
<span><span class="co">#> <span style="color: #0000BB;">(</span><span style="color: #080808; background-color: #FFD787;">0.625</span>), <span style="font-style: italic;">Staphylococcus aureus anaerobius</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FFD787;">0.625</span>), <span style="font-style: italic;">Streptomyces aureus</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FFD787;">0.618</span>),</span></span>
|
||||
<span><span class="co">#> <span style="font-style: italic;">Staphylococcus auricularis</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FFD787;">0.615</span>), <span style="font-style: italic;">Streptomyces azureus</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FFD787;">0.609</span>), <span style="font-style: italic;">Salmonella</span></span></span>
|
||||
<span><span class="co">#> Aurelianis<span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FFD787;">0.595</span>), <span style="font-style: italic;">Salmonella</span> Aarhus<span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FFD787;">0.588</span>), <span style="font-style: italic;">Salmonella</span> Amounderness<span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FFD787;">0.587</span>),</span></span>
|
||||
<span><span class="co">#> and <span style="font-style: italic;">Staphylococcus argensis</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FFD787;">0.587</span>)</span></span>
|
||||
<span><span class="co">#> <span style="color: #B2B2B2;">-------------------------------------------------------------------------------</span></span></span>
|
||||
<span><span class="co">#> <span style="color: #0000BB;">"S. pneumoniae"</span> -> <span style="font-weight: bold; font-style: italic;">Streptococcus pneumoniae</span> (B_STRPT_PNMN, <span style="color: #080808; background-color: #5FD7AF;">0.750</span>)</span></span>
|
||||
<span><span class="co">#> Also matched: <span style="font-style: italic;">Streptococcus pseudopneumoniae</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FFFF87;">0.700</span>), <span style="font-style: italic;">Streptococcus phocae</span></span></span>
|
||||
<span><span class="co">#> <span style="font-style: italic;">salmonis</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FFD787;">0.552</span>), <span style="font-style: italic;">Serratia proteamaculans quinovora</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FF5F5F;">0.545</span>), <span style="font-style: italic;">Streptococcus</span></span></span>
|
||||
<span><span class="co">#> <span style="font-style: italic;">pseudoporcinus</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FF5F5F;">0.536</span>), <span style="font-style: italic;">Staphylococcus piscifermentans</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FF5F5F;">0.533</span>), <span style="font-style: italic;">Staphylococcus</span></span></span>
|
||||
<span><span class="co">#> <span style="font-style: italic;">pseudintermedius</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FF5F5F;">0.532</span>), <span style="font-style: italic;">Serratia proteamaculans proteamaculans</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FF5F5F;">0.526</span>),</span></span>
|
||||
<span><span class="co">#> <span style="font-style: italic;">Streptococcus gallolyticus pasteurianus</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FF5F5F;">0.526</span>), <span style="font-style: italic;">Salmonella</span> Portanigra<span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FF5F5F;">0.524</span>),</span></span>
|
||||
<span><span class="co">#> and <span style="font-style: italic;">Streptococcus periodonticum</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FF5F5F;">0.519</span>)</span></span>
|
||||
<span><span class="co">#> Also matched: <span style="font-style: italic;">Streptococcus parapneumoniae</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FFFF87;">0.714</span>), <span style="font-style: italic;">Streptococcus</span></span></span>
|
||||
<span><span class="co">#> <span style="font-style: italic;">pseudopneumoniae</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FFFF87;">0.700</span>), <span style="font-style: italic;">Serratia proteamaculans quinivorans</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FFD787;">0.557</span>),</span></span>
|
||||
<span><span class="co">#> <span style="font-style: italic;">Streptococcus phocae salmonis</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FFD787;">0.552</span>), <span style="font-style: italic;">Serratia proteamaculans quinovora</span></span></span>
|
||||
<span><span class="co">#> <span style="color: #0000BB;">(</span><span style="color: #080808; background-color: #FF5F5F;">0.545</span>), <span style="font-style: italic;">Sphingomonas piscinae</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FF5F5F;">0.538</span>), <span style="font-style: italic;">Streptococcus pseudoporcinus</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FF5F5F;">0.536</span>),</span></span>
|
||||
<span><span class="co">#> <span style="font-style: italic;">Staphylococcus piscifermentans</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FF5F5F;">0.533</span>), <span style="font-style: italic;">Staphylococcus pseudintermedius</span></span></span>
|
||||
<span><span class="co">#> <span style="color: #0000BB;">(</span><span style="color: #080808; background-color: #FF5F5F;">0.532</span>), and <span style="font-style: italic;">Serratia proteamaculans proteamaculans</span><span style="color: #0000BB;"> (</span><span style="color: #080808; background-color: #FF5F5F;">0.526</span>)</span></span>
|
||||
<span><span class="co">#> <span style="color: #00BBBB;">ℹ</span> Only the first 10 other matches of each record are shown. Run ``</span></span>
|
||||
<span><span class="co">#> `print(mo_uncertainties(), n = ...)` `` to view more entries, or save</span></span>
|
||||
<span><span class="co">#> `mo_uncertainties()` to an object.</span></span></code></pre></div>
|
||||
@@ -633,36 +632,46 @@ in:</p>
|
||||
<div class="section level3">
|
||||
<h3 id="generate-antibiograms">Generate antibiograms<a class="anchor" aria-label="anchor" href="#generate-antibiograms"></a>
|
||||
</h3>
|
||||
<p>Since AMR v2.0 (March 2023), it is very easy to create different
|
||||
types of antibiograms, with support for 20 different languages.</p>
|
||||
<p>There are four antibiogram types, as proposed by Klinker <em>et
|
||||
<p>The <code>AMR</code> package supports 28 different languages for
|
||||
antibiograms and provides four types, as proposed by Klinker <em>et
|
||||
al.</em> (2021, <a href="https://doi.org/10.1177/20499361211011373" class="external-link">DOI
|
||||
10.1177/20499361211011373</a>), and they are all supported by the new
|
||||
<code><a href="../reference/antibiogram.html">antibiogram()</a></code> function:</p>
|
||||
10.1177/20499361211011373</a>):</p>
|
||||
<ol style="list-style-type: decimal">
|
||||
<li>
|
||||
<strong>Traditional Antibiogram (TA)</strong> e.g, for the
|
||||
susceptibility of <em>Pseudomonas aeruginosa</em> to
|
||||
piperacillin/tazobactam (TZP)</li>
|
||||
<strong>Traditional Antibiogram (TA)</strong> – susceptibility of a
|
||||
species to individual antibiotics</li>
|
||||
<li>
|
||||
<strong>Combination Antibiogram (CA)</strong> e.g, for the
|
||||
sdditional susceptibility of <em>Pseudomonas aeruginosa</em> to TZP +
|
||||
tobramycin versus TZP alone</li>
|
||||
<strong>Combination Antibiogram (CA)</strong> – susceptibility of a
|
||||
species to combination regimens</li>
|
||||
<li>
|
||||
<strong>Syndromic Antibiogram (SA)</strong> e.g, for the
|
||||
susceptibility of <em>Pseudomonas aeruginosa</em> to TZP among
|
||||
respiratory specimens (obtained among ICU patients only)</li>
|
||||
<strong>Syndromic Antibiogram (SA)</strong> – susceptibility of a
|
||||
species, stratified by clinical syndrome or setting</li>
|
||||
<li>
|
||||
<strong>Weighted-Incidence Syndromic Combination Antibiogram
|
||||
(WISCA)</strong> e.g, for the susceptibility of <em>Pseudomonas
|
||||
aeruginosa</em> to TZP among respiratory specimens (obtained among ICU
|
||||
patients only) for male patients age >=65 years with heart
|
||||
failure</li>
|
||||
(WISCA)</strong> – estimated empirical coverage of a <em>regimen</em>
|
||||
for a <em>syndrome</em>, weighted by pathogen incidence and with
|
||||
quantified uncertainty</li>
|
||||
</ol>
|
||||
<p>In this section, we show how to use the <code><a href="../reference/antibiogram.html">antibiogram()</a></code>
|
||||
function to create any of the above antibiogram types. For starters,
|
||||
this is what the included <code>example_isolates</code> data set looks
|
||||
like:</p>
|
||||
<p><strong>If your goal is to guide empirical therapy, WISCA should be
|
||||
your default.</strong> The reason is simple: when you start empirical
|
||||
treatment, you do not know which pathogen is causing the infection. Your
|
||||
next patient will not present with a species label attached to them.
|
||||
What matters is the probability that the <em>regimen</em> you choose
|
||||
will cover <em>whatever pathogen turns out to be the cause</em>, given
|
||||
the local epidemiology of the syndrome. Traditional antibiograms do not
|
||||
answer that question. They fragment information by species, ignore how
|
||||
frequently each species causes the syndrome, do not evaluate combination
|
||||
regimens, and provide no measure of uncertainty. WISCA addresses all of
|
||||
these limitations using a Bayesian framework (Hebert <em>et al.</em>,
|
||||
2012; Bielicki <em>et al.</em>, 2016). See the <a href="https://amr-for-r.org/articles/WISCA.html">WISCA vignette</a> for
|
||||
the full explanation.</p>
|
||||
<p>Traditional, combination, and syndromic antibiograms remain useful
|
||||
for <strong>surveillance</strong> purposes, i.e., tracking resistance
|
||||
trends per species over time. But if you care about clinical impact,
|
||||
about choosing the right empirical regimen for your patient, use
|
||||
WISCA.</p>
|
||||
<p>For starters, this is what the included <code>example_isolates</code>
|
||||
data set looks like:</p>
|
||||
<div class="sourceCode" id="cb15"><pre class="downlit sourceCode r">
|
||||
<code class="sourceCode R"><span><span class="va">example_isolates</span></span>
|
||||
<span><span class="co">#> <span style="color: #949494;"># A tibble: 2,000 × 46</span></span></span>
|
||||
@@ -686,13 +695,162 @@ like:</p>
|
||||
<span><span class="co">#> <span style="color: #949494;"># TCY <sir>, TGC <sir>, DOX <sir>, ERY <sir>, CLI <sir>, AZM <sir>,</span></span></span>
|
||||
<span><span class="co">#> <span style="color: #949494;"># IPM <sir>, MEM <sir>, MTR <sir>, CHL <sir>, COL <sir>, MUP <sir>, …</span></span></span></code></pre></div>
|
||||
<div class="section level4">
|
||||
<h4 id="wisca-recommended-for-empirical-therapy-guidance">WISCA (recommended for empirical therapy guidance)<a class="anchor" aria-label="anchor" href="#wisca-recommended-for-empirical-therapy-guidance"></a>
|
||||
</h4>
|
||||
<p>Use the <code><a href="../reference/antibiogram.html">wisca()</a></code> function, or equivalently
|
||||
<code>antibiogram(..., wisca = TRUE)</code>. WISCA produces a single
|
||||
coverage estimate per regimen for the entire syndrome, weighted by
|
||||
pathogen incidence, with a 95% credible interval from Bayesian Monte
|
||||
Carlo simulation:</p>
|
||||
<div class="sourceCode" id="cb16"><pre class="downlit sourceCode r">
|
||||
<code class="sourceCode R"><span><span class="va">wisca_result</span> <span class="op"><-</span> <span class="va">example_isolates</span> <span class="op"><a href="https://magrittr.tidyverse.org/reference/pipe.html" class="external-link">%>%</a></span></span>
|
||||
<span> <span class="fu"><a href="../reference/antibiogram.html">wisca</a></span><span class="op">(</span></span>
|
||||
<span> antimicrobials <span class="op">=</span> <span class="fu"><a href="https://rdrr.io/r/base/c.html" class="external-link">c</a></span><span class="op">(</span><span class="st">"TZP"</span>, <span class="st">"TZP+TOB"</span>, <span class="st">"TZP+GEN"</span><span class="op">)</span>,</span>
|
||||
<span> minimum <span class="op">=</span> <span class="fl">10</span></span>
|
||||
<span> <span class="op">)</span> <span class="co"># Recommended threshold: ≥30</span></span>
|
||||
<span><span class="va">wisca_result</span></span></code></pre></div>
|
||||
<table style="width:100%;" class="table">
|
||||
<colgroup>
|
||||
<col width="24%">
|
||||
<col width="37%">
|
||||
<col width="37%">
|
||||
</colgroup>
|
||||
<thead><tr class="header">
|
||||
<th align="left">Piperacillin/tazobactam</th>
|
||||
<th align="left">Piperacillin/tazobactam + Gentamicin</th>
|
||||
<th align="left">Piperacillin/tazobactam + Tobramycin</th>
|
||||
</tr></thead>
|
||||
<tbody><tr class="odd">
|
||||
<td align="left">70.2% (64.8-75.2%)</td>
|
||||
<td align="left">93.6% (92.2-95%)</td>
|
||||
<td align="left">89.9% (87-92.3%)</td>
|
||||
</tr></tbody>
|
||||
</table>
|
||||
<p>The output tells you: <em>“given the species distribution in your
|
||||
data, there is an estimated X% probability that this regimen covers the
|
||||
infection, with 95% credible interval [lower, upper]”</em>. That is the
|
||||
clinically relevant question.</p>
|
||||
<p>For <strong>syndrome-specific</strong> or <strong>patient-specific
|
||||
WISCA</strong>, use the <code>syndromic_group</code> argument or group
|
||||
your data first. You can stratify by anything: ward, age group, risk
|
||||
profile, acquisition type. The <code>syndromic_group</code> argument
|
||||
accepts any column or expression:</p>
|
||||
<div class="sourceCode" id="cb17"><pre class="downlit sourceCode r">
|
||||
<code class="sourceCode R"><span><span class="va">wisca_out</span> <span class="op"><-</span> <span class="va">example_isolates</span> <span class="op"><a href="https://magrittr.tidyverse.org/reference/pipe.html" class="external-link">%>%</a></span></span>
|
||||
<span> <span class="fu"><a href="../reference/top_n_microorganisms.html">top_n_microorganisms</a></span><span class="op">(</span>n <span class="op">=</span> <span class="fl">10</span><span class="op">)</span> <span class="op"><a href="https://magrittr.tidyverse.org/reference/pipe.html" class="external-link">%>%</a></span></span>
|
||||
<span> <span class="fu"><a href="https://dplyr.tidyverse.org/reference/group_by.html" class="external-link">group_by</a></span><span class="op">(</span></span>
|
||||
<span> age_group <span class="op">=</span> <span class="fu"><a href="../reference/age_groups.html">age_groups</a></span><span class="op">(</span><span class="va">age</span>, <span class="fu"><a href="https://rdrr.io/r/base/c.html" class="external-link">c</a></span><span class="op">(</span><span class="fl">25</span>, <span class="fl">50</span>, <span class="fl">75</span><span class="op">)</span><span class="op">)</span>,</span>
|
||||
<span> <span class="va">gender</span></span>
|
||||
<span> <span class="op">)</span> <span class="op"><a href="https://magrittr.tidyverse.org/reference/pipe.html" class="external-link">%>%</a></span></span>
|
||||
<span> <span class="fu"><a href="../reference/antibiogram.html">wisca</a></span><span class="op">(</span>antimicrobials <span class="op">=</span> <span class="fu"><a href="https://rdrr.io/r/base/c.html" class="external-link">c</a></span><span class="op">(</span><span class="st">"TZP"</span>, <span class="st">"TZP+TOB"</span>, <span class="st">"TZP+GEN"</span><span class="op">)</span><span class="op">)</span></span>
|
||||
<span></span>
|
||||
<span><span class="va">wisca_out</span></span></code></pre></div>
|
||||
<table class="table">
|
||||
<colgroup>
|
||||
<col width="8%">
|
||||
<col width="6%">
|
||||
<col width="20%">
|
||||
<col width="32%">
|
||||
<col width="32%">
|
||||
</colgroup>
|
||||
<thead><tr class="header">
|
||||
<th align="left">age_group</th>
|
||||
<th align="left">gender</th>
|
||||
<th align="left">Piperacillin/tazobactam</th>
|
||||
<th align="left">Piperacillin/tazobactam + Gentamicin</th>
|
||||
<th align="left">Piperacillin/tazobactam + Tobramycin</th>
|
||||
</tr></thead>
|
||||
<tbody>
|
||||
<tr class="odd">
|
||||
<td align="left">0-24</td>
|
||||
<td align="left">F</td>
|
||||
<td align="left">56.8% (29.9-81.3%)</td>
|
||||
<td align="left">70.7% (45.2-89%)</td>
|
||||
<td align="left">65.9% (42.3-86.6%)</td>
|
||||
</tr>
|
||||
<tr class="even">
|
||||
<td align="left">0-24</td>
|
||||
<td align="left">M</td>
|
||||
<td align="left">59.5% (31.2-85.5%)</td>
|
||||
<td align="left">76.1% (56.5-92%)</td>
|
||||
<td align="left">59.6% (31.7-85.1%)</td>
|
||||
</tr>
|
||||
<tr class="odd">
|
||||
<td align="left">25-49</td>
|
||||
<td align="left">F</td>
|
||||
<td align="left">67.7% (43.9-89.7%)</td>
|
||||
<td align="left">93.8% (87.4-98.1%)</td>
|
||||
<td align="left">87% (70.1-97%)</td>
|
||||
</tr>
|
||||
<tr class="even">
|
||||
<td align="left">25-49</td>
|
||||
<td align="left">M</td>
|
||||
<td align="left">56.9% (26.6-86.2%)</td>
|
||||
<td align="left">91% (82-97.2%)</td>
|
||||
<td align="left">76.6% (51.4-93.5%)</td>
|
||||
</tr>
|
||||
<tr class="odd">
|
||||
<td align="left">50-74</td>
|
||||
<td align="left">F</td>
|
||||
<td align="left">68% (54.1-81.8%)</td>
|
||||
<td align="left">96.9% (94.6-98.5%)</td>
|
||||
<td align="left">90.2% (82-96.2%)</td>
|
||||
</tr>
|
||||
<tr class="even">
|
||||
<td align="left">50-74</td>
|
||||
<td align="left">M</td>
|
||||
<td align="left">67% (56-78.5%)</td>
|
||||
<td align="left">96.7% (94.1-98.5%)</td>
|
||||
<td align="left">86.7% (77.3-94.4%)</td>
|
||||
</tr>
|
||||
<tr class="odd">
|
||||
<td align="left">75+</td>
|
||||
<td align="left">F</td>
|
||||
<td align="left">73.1% (61.8-84.1%)</td>
|
||||
<td align="left">97.7% (95.9-99%)</td>
|
||||
<td align="left">92.8% (85.7-97.2%)</td>
|
||||
</tr>
|
||||
<tr class="even">
|
||||
<td align="left">75+</td>
|
||||
<td align="left">M</td>
|
||||
<td align="left">74% (63.6-82.6%)</td>
|
||||
<td align="left">97.9% (96-99%)</td>
|
||||
<td align="left">94.7% (89.3-97.9%)</td>
|
||||
</tr>
|
||||
</tbody>
|
||||
</table>
|
||||
<p>Keep in mind that more granular stratification produces more relevant
|
||||
estimates for each subgroup, but with wider credible intervals due to
|
||||
smaller sample sizes. There is always a trade-off between granularity
|
||||
and precision. If local numbers are small, consider pooling data from
|
||||
multiple sites (Bielicki <em>et al.</em>, 2016).</p>
|
||||
<p>For reliable WISCA results, ensure your data includes <strong>only
|
||||
first isolates</strong> (use <code><a href="../reference/first_isolate.html">first_isolate()</a></code>) and consider
|
||||
filtering for <strong>the top <em>n</em> species</strong> (use
|
||||
<code><a href="../reference/top_n_microorganisms.html">top_n_microorganisms()</a></code>), since rare contaminants can
|
||||
distort coverage estimates.</p>
|
||||
<p>After creating the WISCA model, assessments can be done on the
|
||||
distributions of the Monte Carlo simulations that WISCA carried out:</p>
|
||||
<div class="sourceCode" id="cb18"><pre class="downlit sourceCode r">
|
||||
<code class="sourceCode R"><span><span class="fu"><a href="../reference/antibiogram.html">wisca_plot</a></span><span class="op">(</span><span class="va">wisca_out</span><span class="op">)</span></span></code></pre></div>
|
||||
<p><img src="AMR_files/figure-html/wisca_plots-1.png" class="r-plt" alt="" width="720"></p>
|
||||
<div class="sourceCode" id="cb19"><pre class="downlit sourceCode r">
|
||||
<code class="sourceCode R"><span><span class="fu"><a href="../reference/antibiogram.html">wisca_plot</a></span><span class="op">(</span><span class="va">wisca_out</span>, wisca_plot_type <span class="op">=</span> <span class="st">"posterior_coverage"</span><span class="op">)</span></span></code></pre></div>
|
||||
<p><img src="AMR_files/figure-html/wisca_plots-2.png" class="r-plt" alt="" width="720"></p>
|
||||
<div class="sourceCode" id="cb20"><pre class="downlit sourceCode r">
|
||||
<code class="sourceCode R"><span></span>
|
||||
<span><span class="co"># a ggplot2 extension for WISCAs and other antibiograms:</span></span>
|
||||
<span><span class="fu">ggplot2</span><span class="fu">::</span><span class="fu"><a href="https://ggplot2.tidyverse.org/reference/autoplot.html" class="external-link">autoplot</a></span><span class="op">(</span><span class="va">wisca_out</span><span class="op">)</span></span></code></pre></div>
|
||||
<p><img src="AMR_files/figure-html/wisca_plots-3.png" class="r-plt" alt="" width="720"></p>
|
||||
</div>
|
||||
<div class="section level4">
|
||||
<h4 id="traditional-antibiogram">Traditional Antibiogram<a class="anchor" aria-label="anchor" href="#traditional-antibiogram"></a>
|
||||
</h4>
|
||||
<p>To create a traditional antibiogram, simply state which antibiotics
|
||||
should be used. The <code>antibiotics</code> argument in the
|
||||
<code><a href="../reference/antibiogram.html">antibiogram()</a></code> function supports any (combination) of the
|
||||
previously mentioned antibiotic class selectors:</p>
|
||||
<div class="sourceCode" id="cb16"><pre class="downlit sourceCode r">
|
||||
<p>If you need per-species susceptibility rates, e.g., for AMR
|
||||
surveillance reports, the traditional antibiogram remains the right
|
||||
tool. It reports the proportion of susceptible isolates per species per
|
||||
antibiotic:</p>
|
||||
<div class="sourceCode" id="cb21"><pre class="downlit sourceCode r">
|
||||
<code class="sourceCode R"><span><span class="fu"><a href="../reference/antibiogram.html">antibiogram</a></span><span class="op">(</span><span class="va">example_isolates</span>,</span>
|
||||
<span> antibiotics <span class="op">=</span> <span class="fu"><a href="https://rdrr.io/r/base/c.html" class="external-link">c</a></span><span class="op">(</span><span class="fu"><a href="../reference/antimicrobial_selectors.html">aminoglycosides</a></span><span class="op">(</span><span class="op">)</span>, <span class="fu"><a href="../reference/antimicrobial_selectors.html">carbapenems</a></span><span class="op">(</span><span class="op">)</span><span class="op">)</span></span>
|
||||
<span><span class="op">)</span></span>
|
||||
@@ -821,7 +979,7 @@ Greek, Hindi, Indonesian, Italian, Japanese, Korean, Norwegian, Polish,
|
||||
Portuguese, Romanian, Russian, Spanish, Swahili, Swedish, Turkish,
|
||||
Ukrainian, Urdu, or Vietnamese. In this next example, we force the
|
||||
language to be Spanish using the <code>language</code> argument:</p>
|
||||
<div class="sourceCode" id="cb17"><pre class="downlit sourceCode r">
|
||||
<div class="sourceCode" id="cb22"><pre class="downlit sourceCode r">
|
||||
<code class="sourceCode R"><span><span class="fu"><a href="../reference/antibiogram.html">antibiogram</a></span><span class="op">(</span><span class="va">example_isolates</span>,</span>
|
||||
<span> mo_transform <span class="op">=</span> <span class="st">"gramstain"</span>,</span>
|
||||
<span> antibiotics <span class="op">=</span> <span class="fu"><a href="../reference/antimicrobial_selectors.html">aminoglycosides</a></span><span class="op">(</span><span class="op">)</span>,</span>
|
||||
@@ -864,11 +1022,13 @@ language to be Spanish using the <code>language</code> argument:</p>
|
||||
</table>
|
||||
</div>
|
||||
<div class="section level4">
|
||||
<h4 id="combined-antibiogram">Combined Antibiogram<a class="anchor" aria-label="anchor" href="#combined-antibiogram"></a>
|
||||
<h4 id="combination-antibiogram">Combination Antibiogram<a class="anchor" aria-label="anchor" href="#combination-antibiogram"></a>
|
||||
</h4>
|
||||
<p>To create a combined antibiogram, use antibiotic codes or names with
|
||||
a plus <code>+</code> character like this:</p>
|
||||
<div class="sourceCode" id="cb18"><pre class="downlit sourceCode r">
|
||||
<p>A combination antibiogram shows how much additional susceptibility a
|
||||
second agent adds for a given species. This is useful for surveillance
|
||||
of combination regimens, but note that it is still species-stratified
|
||||
and does not account for pathogen incidence in the syndrome:</p>
|
||||
<div class="sourceCode" id="cb23"><pre class="downlit sourceCode r">
|
||||
<code class="sourceCode R"><span><span class="va">combined_ab</span> <span class="op"><-</span> <span class="fu"><a href="../reference/antibiogram.html">antibiogram</a></span><span class="op">(</span><span class="va">example_isolates</span>,</span>
|
||||
<span> antibiotics <span class="op">=</span> <span class="fu"><a href="https://rdrr.io/r/base/c.html" class="external-link">c</a></span><span class="op">(</span><span class="st">"TZP"</span>, <span class="st">"TZP+TOB"</span>, <span class="st">"TZP+GEN"</span><span class="op">)</span>,</span>
|
||||
<span> ab_transform <span class="op">=</span> <span class="cn">NULL</span></span>
|
||||
@@ -948,10 +1108,13 @@ a plus <code>+</code> character like this:</p>
|
||||
<div class="section level4">
|
||||
<h4 id="syndromic-antibiogram">Syndromic Antibiogram<a class="anchor" aria-label="anchor" href="#syndromic-antibiogram"></a>
|
||||
</h4>
|
||||
<p>To create a syndromic antibiogram, the <code>syndromic_group</code>
|
||||
argument must be used. This can be any column in the data, or e.g. an
|
||||
<code><a href="https://rdrr.io/r/base/ifelse.html" class="external-link">ifelse()</a></code> with calculations based on certain columns:</p>
|
||||
<div class="sourceCode" id="cb19"><pre class="downlit sourceCode r">
|
||||
<p>A syndromic antibiogram stratifies per-species susceptibility by
|
||||
clinical context (ward, specimen type, etc.). It adds clinical context
|
||||
to the traditional antibiogram but is still species-level, without
|
||||
incidence weighting or uncertainty quantification. For surveillance by
|
||||
setting this is fine; for empirical therapy guidance, WISCA is
|
||||
preferred:</p>
|
||||
<div class="sourceCode" id="cb24"><pre class="downlit sourceCode r">
|
||||
<code class="sourceCode R"><span><span class="fu"><a href="../reference/antibiogram.html">antibiogram</a></span><span class="op">(</span><span class="va">example_isolates</span>,</span>
|
||||
<span> antibiotics <span class="op">=</span> <span class="fu"><a href="https://rdrr.io/r/base/c.html" class="external-link">c</a></span><span class="op">(</span><span class="fu"><a href="../reference/antimicrobial_selectors.html">aminoglycosides</a></span><span class="op">(</span><span class="op">)</span>, <span class="fu"><a href="../reference/antimicrobial_selectors.html">carbapenems</a></span><span class="op">(</span><span class="op">)</span><span class="op">)</span>,</span>
|
||||
<span> syndromic_group <span class="op">=</span> <span class="st">"ward"</span></span>
|
||||
@@ -1125,511 +1288,14 @@ argument must be used. This can be any column in the data, or e.g. an
|
||||
</table>
|
||||
</div>
|
||||
<div class="section level4">
|
||||
<h4 id="weighted-incidence-syndromic-combination-antibiogram-wisca">Weighted-Incidence Syndromic Combination Antibiogram (WISCA)<a class="anchor" aria-label="anchor" href="#weighted-incidence-syndromic-combination-antibiogram-wisca"></a>
|
||||
</h4>
|
||||
<p>To create a <strong>Weighted-Incidence Syndromic Combination
|
||||
Antibiogram (WISCA)</strong>, simply set <code>wisca = TRUE</code> in
|
||||
the <code><a href="../reference/antibiogram.html">antibiogram()</a></code> function, or use the dedicated
|
||||
<code><a href="../reference/antibiogram.html">wisca()</a></code> function. Unlike traditional antibiograms, WISCA
|
||||
provides syndrome-based susceptibility estimates, weighted by pathogen
|
||||
incidence and antimicrobial susceptibility patterns.</p>
|
||||
<div class="sourceCode" id="cb20"><pre class="downlit sourceCode r">
|
||||
<code class="sourceCode R"><span><span class="va">example_isolates</span> <span class="op"><a href="https://magrittr.tidyverse.org/reference/pipe.html" class="external-link">%>%</a></span></span>
|
||||
<span> <span class="fu"><a href="../reference/antibiogram.html">wisca</a></span><span class="op">(</span></span>
|
||||
<span> antibiotics <span class="op">=</span> <span class="fu"><a href="https://rdrr.io/r/base/c.html" class="external-link">c</a></span><span class="op">(</span><span class="st">"TZP"</span>, <span class="st">"TZP+TOB"</span>, <span class="st">"TZP+GEN"</span><span class="op">)</span>,</span>
|
||||
<span> minimum <span class="op">=</span> <span class="fl">10</span></span>
|
||||
<span> <span class="op">)</span> <span class="co"># Recommended threshold: ≥30</span></span></code></pre></div>
|
||||
<table style="width:100%;" class="table">
|
||||
<colgroup>
|
||||
<col width="24%">
|
||||
<col width="37%">
|
||||
<col width="37%">
|
||||
</colgroup>
|
||||
<thead><tr class="header">
|
||||
<th align="left">Piperacillin/tazobactam</th>
|
||||
<th align="left">Piperacillin/tazobactam + Gentamicin</th>
|
||||
<th align="left">Piperacillin/tazobactam + Tobramycin</th>
|
||||
</tr></thead>
|
||||
<tbody><tr class="odd">
|
||||
<td align="left">69.4% (64.3-74.3%)</td>
|
||||
<td align="left">92.6% (91.1-93.9%)</td>
|
||||
<td align="left">88.7% (85.8-91.2%)</td>
|
||||
</tr></tbody>
|
||||
</table>
|
||||
<p>WISCA uses a <strong>Bayesian decision model</strong> to integrate
|
||||
data from multiple pathogens, improving empirical therapy guidance,
|
||||
especially for low-incidence infections. It is
|
||||
<strong>pathogen-agnostic</strong>, meaning results are syndrome-based
|
||||
rather than stratified by microorganism.</p>
|
||||
<p>For reliable results, ensure your data includes <strong>only first
|
||||
isolates</strong> (use <code><a href="../reference/first_isolate.html">first_isolate()</a></code>) and consider
|
||||
filtering for <strong>the top <em>n</em> species</strong> (use
|
||||
<code><a href="../reference/top_n_microorganisms.html">top_n_microorganisms()</a></code>), as WISCA outcomes are most
|
||||
meaningful when based on robust incidence estimates.</p>
|
||||
<p>For <strong>patient- or syndrome-specific WISCA</strong>, run the
|
||||
function on a grouped <code>tibble</code>, i.e., using
|
||||
<code><a href="https://dplyr.tidyverse.org/reference/group_by.html" class="external-link">group_by()</a></code> first:</p>
|
||||
<div class="sourceCode" id="cb21"><pre class="downlit sourceCode r">
|
||||
<code class="sourceCode R"><span><span class="va">example_isolates</span> <span class="op"><a href="https://magrittr.tidyverse.org/reference/pipe.html" class="external-link">%>%</a></span></span>
|
||||
<span> <span class="fu"><a href="../reference/top_n_microorganisms.html">top_n_microorganisms</a></span><span class="op">(</span>n <span class="op">=</span> <span class="fl">10</span><span class="op">)</span> <span class="op"><a href="https://magrittr.tidyverse.org/reference/pipe.html" class="external-link">%>%</a></span></span>
|
||||
<span> <span class="fu"><a href="https://dplyr.tidyverse.org/reference/group_by.html" class="external-link">group_by</a></span><span class="op">(</span></span>
|
||||
<span> age_group <span class="op">=</span> <span class="fu"><a href="../reference/age_groups.html">age_groups</a></span><span class="op">(</span><span class="va">age</span>, <span class="fu"><a href="https://rdrr.io/r/base/c.html" class="external-link">c</a></span><span class="op">(</span><span class="fl">25</span>, <span class="fl">50</span>, <span class="fl">75</span><span class="op">)</span><span class="op">)</span>,</span>
|
||||
<span> <span class="va">gender</span></span>
|
||||
<span> <span class="op">)</span> <span class="op"><a href="https://magrittr.tidyverse.org/reference/pipe.html" class="external-link">%>%</a></span></span>
|
||||
<span> <span class="fu"><a href="../reference/antibiogram.html">wisca</a></span><span class="op">(</span>antibiotics <span class="op">=</span> <span class="fu"><a href="https://rdrr.io/r/base/c.html" class="external-link">c</a></span><span class="op">(</span><span class="st">"TZP"</span>, <span class="st">"TZP+TOB"</span>, <span class="st">"TZP+GEN"</span><span class="op">)</span><span class="op">)</span></span></code></pre></div>
|
||||
<table style="width:100%;" class="table">
|
||||
<colgroup>
|
||||
<col width="1%">
|
||||
<col width="0%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="3%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="3%">
|
||||
<col width="2%">
|
||||
</colgroup>
|
||||
<thead><tr class="header">
|
||||
<th align="left">age_group</th>
|
||||
<th align="left">gender</th>
|
||||
<th align="left">Amikacin</th>
|
||||
<th align="left">Amoxicillin</th>
|
||||
<th align="left">Amoxicillin/clavulanic acid</th>
|
||||
<th align="left">Ampicillin</th>
|
||||
<th align="left">Azithromycin</th>
|
||||
<th align="left">Benzylpenicillin</th>
|
||||
<th align="left">Cefazolin</th>
|
||||
<th align="left">Cefepime</th>
|
||||
<th align="left">Cefotaxime</th>
|
||||
<th align="left">Cefoxitin</th>
|
||||
<th align="left">Ceftazidime</th>
|
||||
<th align="left">Ceftriaxone</th>
|
||||
<th align="left">Cefuroxime</th>
|
||||
<th align="left">Chloramphenicol</th>
|
||||
<th align="left">Ciprofloxacin</th>
|
||||
<th align="left">Clindamycin</th>
|
||||
<th align="left">Colistin</th>
|
||||
<th align="left">Doxycycline</th>
|
||||
<th align="left">Erythromycin</th>
|
||||
<th align="left">Flucloxacillin</th>
|
||||
<th align="left">Fosfomycin</th>
|
||||
<th align="left">Gentamicin</th>
|
||||
<th align="left">Imipenem</th>
|
||||
<th align="left">Kanamycin</th>
|
||||
<th align="left">Linezolid</th>
|
||||
<th align="left">Meropenem</th>
|
||||
<th align="left">Metronidazole</th>
|
||||
<th align="left">Moxifloxacin</th>
|
||||
<th align="left">Mupirocin</th>
|
||||
<th align="left">Nitrofurantoin</th>
|
||||
<th align="left">Oxacillin</th>
|
||||
<th align="left">Piperacillin/tazobactam</th>
|
||||
<th align="left">Rifampicin</th>
|
||||
<th align="left">Teicoplanin</th>
|
||||
<th align="left">Tetracycline</th>
|
||||
<th align="left">Tigecycline</th>
|
||||
<th align="left">Tobramycin</th>
|
||||
<th align="left">Trimethoprim</th>
|
||||
<th align="left">Trimethoprim/sulfamethoxazole</th>
|
||||
<th align="left">Vancomycin</th>
|
||||
</tr></thead>
|
||||
<tbody>
|
||||
<tr class="odd">
|
||||
<td align="left">0-24</td>
|
||||
<td align="left">F</td>
|
||||
<td align="left">45.4% (15.4-79%)</td>
|
||||
<td align="left">50.1% (20.5-77.6%)</td>
|
||||
<td align="left">69% (44.5-88.5%)</td>
|
||||
<td align="left">50.4% (20.6-77.3%)</td>
|
||||
<td align="left">41.9% (18.1-65.6%)</td>
|
||||
<td align="left">36.1% (12.3-64.3%)</td>
|
||||
<td align="left">NA</td>
|
||||
<td align="left">NA</td>
|
||||
<td align="left">63.9% (34.6-87.6%)</td>
|
||||
<td align="left">56.7% (25.9-85.8%)</td>
|
||||
<td align="left">51.5% (25.6-74.4%)</td>
|
||||
<td align="left">63.4% (32-88.1%)</td>
|
||||
<td align="left">70.4% (45.4-89.1%)</td>
|
||||
<td align="left">54% (22.3-85.3%)</td>
|
||||
<td align="left">69.8% (45.9-88.9%)</td>
|
||||
<td align="left">39.3% (17.7-64.6%)</td>
|
||||
<td align="left">45.3% (18.1-75.9%)</td>
|
||||
<td align="left">50.1% (21.5-80.5%)</td>
|
||||
<td align="left">41.7% (19.1-67.6%)</td>
|
||||
<td align="left">55.8% (23.7-83.3%)</td>
|
||||
<td align="left">63.5% (32.6-89.4%)</td>
|
||||
<td align="left">69.3% (44.6-88.3%)</td>
|
||||
<td align="left">63.6% (36.1-88.2%)</td>
|
||||
<td align="left">45.5% (15.7-77.7%)</td>
|
||||
<td align="left">43.3% (17.8-71.2%)</td>
|
||||
<td align="left">55.9% (24.3-82.2%)</td>
|
||||
<td align="left">NA</td>
|
||||
<td align="left">NA</td>
|
||||
<td align="left">56.5% (24.3-85%)</td>
|
||||
<td align="left">56.8% (30.9-82.3%)</td>
|
||||
<td align="left">50.5% (19.4-80.8%)</td>
|
||||
<td align="left">56.9% (26.7-85%)</td>
|
||||
<td align="left">42.3% (18.3-68.8%)</td>
|
||||
<td align="left">40.2% (17.6-67.7%)</td>
|
||||
<td align="left">49.8% (20-79.3%)</td>
|
||||
<td align="left">56.1% (22-85.4%)</td>
|
||||
<td align="left">64.5% (39.6-85.5%)</td>
|
||||
<td align="left">69.7% (42.3-90.4%)</td>
|
||||
<td align="left">75.4% (52.1-91.7%)</td>
|
||||
<td align="left">48.5% (24.3-72.6%)</td>
|
||||
</tr>
|
||||
<tr class="even">
|
||||
<td align="left">0-24</td>
|
||||
<td align="left">M</td>
|
||||
<td align="left">41.9% (15.2-72.5%)</td>
|
||||
<td align="left">49.4% (23.3-75.5%)</td>
|
||||
<td align="left">73.8% (51.8-90.1%)</td>
|
||||
<td align="left">49.3% (22.7-76%)</td>
|
||||
<td align="left">63.4% (40.7-83.5%)</td>
|
||||
<td align="left">41.8% (20.4-64.8%)</td>
|
||||
<td align="left">56.8% (25.2-83.5%)</td>
|
||||
<td align="left">58.2% (29.1-85.8%)</td>
|
||||
<td align="left">59.7% (29.1-87.4%)</td>
|
||||
<td align="left">59.3% (29.1-86.6%)</td>
|
||||
<td align="left">24.9% (8.9-47.3%)</td>
|
||||
<td align="left">58.5% (28-86.5%)</td>
|
||||
<td align="left">72.1% (47.9-90.5%)</td>
|
||||
<td align="left">NA</td>
|
||||
<td align="left">77.2% (53-93.2%)</td>
|
||||
<td align="left">61.6% (36.2-83.6%)</td>
|
||||
<td align="left">25.5% (8.7-46.1%)</td>
|
||||
<td align="left">69.4% (44.6-89.4%)</td>
|
||||
<td align="left">63.4% (41.8-82.7%)</td>
|
||||
<td align="left">64% (37.6-85.6%)</td>
|
||||
<td align="left">NA</td>
|
||||
<td align="left">63.5% (40.9-83.1%)</td>
|
||||
<td align="left">58.7% (27.6-86.5%)</td>
|
||||
<td align="left">41.8% (13.6-71.2%)</td>
|
||||
<td align="left">48.3% (17.9-78%)</td>
|
||||
<td align="left">59.2% (27.4-86.4%)</td>
|
||||
<td align="left">NA</td>
|
||||
<td align="left">NA</td>
|
||||
<td align="left">NA</td>
|
||||
<td align="left">53% (21.3-83.7%)</td>
|
||||
<td align="left">57.2% (24.6-84.6%)</td>
|
||||
<td align="left">59.9% (29.7-85.6%)</td>
|
||||
<td align="left">48.2% (16.1-80.4%)</td>
|
||||
<td align="left">48.4% (17.4-79.8%)</td>
|
||||
<td align="left">68% (43.5-87.3%)</td>
|
||||
<td align="left">65.7% (36-89.2%)</td>
|
||||
<td align="left">44.3% (17.2-73.4%)</td>
|
||||
<td align="left">69.4% (46.9-87.8%)</td>
|
||||
<td align="left">74% (50.8-90.9%)</td>
|
||||
<td align="left">75.3% (52.4-92.2%)</td>
|
||||
</tr>
|
||||
<tr class="odd">
|
||||
<td align="left">25-49</td>
|
||||
<td align="left">F</td>
|
||||
<td align="left">46.8% (26.7-65.6%)</td>
|
||||
<td align="left">39% (26.3-52.9%)</td>
|
||||
<td align="left">73.8% (63.5-82.6%)</td>
|
||||
<td align="left">39.3% (27.2-54.4%)</td>
|
||||
<td align="left">54.8% (44.9-64.8%)</td>
|
||||
<td align="left">36.5% (26.3-47.1%)</td>
|
||||
<td align="left">66.4% (46.1-85%)</td>
|
||||
<td align="left">69.2% (49.1-86.2%)</td>
|
||||
<td align="left">70.2% (50.5-86.2%)</td>
|
||||
<td align="left">68.1% (48.6-85.4%)</td>
|
||||
<td align="left">27.9% (19.2-37.9%)</td>
|
||||
<td align="left">70.1% (50.5-87.1%)</td>
|
||||
<td align="left">71.4% (61.7-80.4%)</td>
|
||||
<td align="left">58.2% (35.3-79.9%)</td>
|
||||
<td align="left">85.5% (74.1-94.2%)</td>
|
||||
<td align="left">67.1% (55.8-77.4%)</td>
|
||||
<td align="left">25.8% (17-36%)</td>
|
||||
<td align="left">75.5% (61.2-88.2%)</td>
|
||||
<td align="left">54.9% (44.8-65.6%)</td>
|
||||
<td align="left">55.2% (37.8-72.5%)</td>
|
||||
<td align="left">60.9% (38.3-81.8%)</td>
|
||||
<td align="left">75.2% (65.7-83.5%)</td>
|
||||
<td align="left">69.9% (50.1-86.6%)</td>
|
||||
<td align="left">37.5% (17.7-57.9%)</td>
|
||||
<td align="left">50.7% (30.8-68.7%)</td>
|
||||
<td align="left">69.4% (48.6-86.7%)</td>
|
||||
<td align="left">NA</td>
|
||||
<td align="left">56.9% (36.2-77.7%)</td>
|
||||
<td align="left">53.3% (30.9-75.6%)</td>
|
||||
<td align="left">60.1% (38.1-81.8%)</td>
|
||||
<td align="left">64.3% (43.2-83.6%)</td>
|
||||
<td align="left">66% (45.7-85.2%)</td>
|
||||
<td align="left">50.1% (30-69.6%)</td>
|
||||
<td align="left">38.8% (19.6-58.9%)</td>
|
||||
<td align="left">75.8% (61.6-88.1%)</td>
|
||||
<td align="left">73.3% (56.6-89.5%)</td>
|
||||
<td align="left">62.7% (47.6-77.1%)</td>
|
||||
<td align="left">70.4% (58.7-80.2%)</td>
|
||||
<td align="left">90% (82.9-95.4%)</td>
|
||||
<td align="left">71.6% (61.7-80.4%)</td>
|
||||
</tr>
|
||||
<tr class="even">
|
||||
<td align="left">25-49</td>
|
||||
<td align="left">M</td>
|
||||
<td align="left">49.8% (24.2-75.8%)</td>
|
||||
<td align="left">16.5% (8.1-27.4%)</td>
|
||||
<td align="left">72.4% (60.5-83.5%)</td>
|
||||
<td align="left">16.6% (7.7-28.2%)</td>
|
||||
<td align="left">55.9% (43.6-67.9%)</td>
|
||||
<td align="left">24.9% (14.7-37.6%)</td>
|
||||
<td align="left">60.3% (33.2-82.4%)</td>
|
||||
<td align="left">55.3% (27.6-81.8%)</td>
|
||||
<td align="left">55.9% (29.7-81.1%)</td>
|
||||
<td align="left">56.2% (27.7-82.1%)</td>
|
||||
<td align="left">22.2% (12.7-33.9%)</td>
|
||||
<td align="left">55.6% (29.1-81.8%)</td>
|
||||
<td align="left">73.7% (62.6-83.8%)</td>
|
||||
<td align="left">52.9% (25.2-79.6%)</td>
|
||||
<td align="left">67.1% (53-79.8%)</td>
|
||||
<td align="left">57.8% (43.5-71.8%)</td>
|
||||
<td align="left">22.3% (12.6-33.6%)</td>
|
||||
<td align="left">73% (57.8-85.5%)</td>
|
||||
<td align="left">55.8% (43-68.2%)</td>
|
||||
<td align="left">66.5% (51.6-79.4%)</td>
|
||||
<td align="left">63.1% (40.3-84.5%)</td>
|
||||
<td align="left">83.9% (74.5-91.7%)</td>
|
||||
<td align="left">56.4% (28.4-84%)</td>
|
||||
<td align="left">45.4% (18.9-73.8%)</td>
|
||||
<td align="left">59.4% (37.6-77.9%)</td>
|
||||
<td align="left">56.3% (28.8-81.1%)</td>
|
||||
<td align="left">NA</td>
|
||||
<td align="left">52.8% (24.7-78.7%)</td>
|
||||
<td align="left">64.2% (40.2-84.5%)</td>
|
||||
<td align="left">62.9% (37.7-85.1%)</td>
|
||||
<td align="left">60.5% (37.1-80.7%)</td>
|
||||
<td align="left">55.8% (29.4-82.9%)</td>
|
||||
<td align="left">65.4% (48.7-80.8%)</td>
|
||||
<td align="left">54.5% (31.7-73.7%)</td>
|
||||
<td align="left">72.8% (58.7-84.8%)</td>
|
||||
<td align="left">84.8% (72.4-93.6%)</td>
|
||||
<td align="left">66.7% (44.5-84.1%)</td>
|
||||
<td align="left">71.4% (58.9-82.6%)</td>
|
||||
<td align="left">86.6% (77.9-93.7%)</td>
|
||||
<td align="left">77.1% (65.5-87.1%)</td>
|
||||
</tr>
|
||||
<tr class="odd">
|
||||
<td align="left">50-74</td>
|
||||
<td align="left">F</td>
|
||||
<td align="left">44.8% (35.8-54.1%)</td>
|
||||
<td align="left">30.1% (24.9-35.3%)</td>
|
||||
<td align="left">74.1% (69.2-78.7%)</td>
|
||||
<td align="left">30% (24.6-35.4%)</td>
|
||||
<td align="left">41.9% (36.5-47.3%)</td>
|
||||
<td align="left">23.5% (18.6-29%)</td>
|
||||
<td align="left">73.1% (62-82.9%)</td>
|
||||
<td align="left">76.6% (66.1-86%)</td>
|
||||
<td align="left">74.8% (64.9-84.5%)</td>
|
||||
<td align="left">74.6% (64.2-83.3%)</td>
|
||||
<td align="left">37.5% (32.3-43.4%)</td>
|
||||
<td align="left">74.8% (64.4-83.8%)</td>
|
||||
<td align="left">74.5% (69.7-78.9%)</td>
|
||||
<td align="left">61.2% (40.3-82.4%)</td>
|
||||
<td align="left">79.4% (73-85%)</td>
|
||||
<td align="left">44.9% (38.7-51%)</td>
|
||||
<td align="left">37.8% (32.7-43.3%)</td>
|
||||
<td align="left">63.8% (47.6-80.1%)</td>
|
||||
<td align="left">41.7% (36.6-46.9%)</td>
|
||||
<td align="left">58.1% (40-75.1%)</td>
|
||||
<td align="left">65.2% (53.5-76.6%)</td>
|
||||
<td align="left">78.7% (73.8-83.2%)</td>
|
||||
<td align="left">80.6% (70.3-90%)</td>
|
||||
<td align="left">28.1% (10.1-46.6%)</td>
|
||||
<td align="left">53.2% (42.9-62.4%)</td>
|
||||
<td align="left">79.3% (68.7-88.6%)</td>
|
||||
<td align="left">NA</td>
|
||||
<td align="left">49.5% (37.5-61.8%)</td>
|
||||
<td align="left">67.8% (48.5-86%)</td>
|
||||
<td align="left">75.1% (63.3-86.3%)</td>
|
||||
<td align="left">56.6% (37.8-74.2%)</td>
|
||||
<td align="left">67.7% (56.4-79.6%)</td>
|
||||
<td align="left">50.6% (40.9-59.1%)</td>
|
||||
<td align="left">41.3% (31.5-50.4%)</td>
|
||||
<td align="left">59% (48.3-74.5%)</td>
|
||||
<td align="left">87.7% (80.4-94.1%)</td>
|
||||
<td align="left">62.2% (55.4-68.4%)</td>
|
||||
<td align="left">55.5% (49.8-61.1%)</td>
|
||||
<td align="left">68% (62.7-73.3%)</td>
|
||||
<td align="left">60.9% (55.8-66.1%)</td>
|
||||
</tr>
|
||||
<tr class="even">
|
||||
<td align="left">50-74</td>
|
||||
<td align="left">M</td>
|
||||
<td align="left">38.8% (30.6-48.6%)</td>
|
||||
<td align="left">34.6% (29.1-40.3%)</td>
|
||||
<td align="left">75% (70-79.5%)</td>
|
||||
<td align="left">34.7% (29.2-40.5%)</td>
|
||||
<td align="left">43.4% (37.8-48.5%)</td>
|
||||
<td align="left">21% (16.5-26.4%)</td>
|
||||
<td align="left">64.3% (54.1-74.1%)</td>
|
||||
<td align="left">65.9% (56.5-75.4%)</td>
|
||||
<td align="left">67.3% (58.3-77%)</td>
|
||||
<td align="left">65.9% (56.1-75.9%)</td>
|
||||
<td align="left">32.9% (27.6-38%)</td>
|
||||
<td align="left">67.3% (57.4-76.8%)</td>
|
||||
<td align="left">74.1% (69.2-78.8%)</td>
|
||||
<td align="left">63.5% (42.4-83%)</td>
|
||||
<td align="left">76.9% (71.6-81.9%)</td>
|
||||
<td align="left">47.3% (40.9-53.8%)</td>
|
||||
<td align="left">30.8% (26.1-36.1%)</td>
|
||||
<td align="left">68.5% (53.5-81.9%)</td>
|
||||
<td align="left">43.4% (37.7-48.8%)</td>
|
||||
<td align="left">58.1% (42.4-73.2%)</td>
|
||||
<td align="left">68.1% (53.5-82.2%)</td>
|
||||
<td align="left">79.1% (74.4-83.1%)</td>
|
||||
<td align="left">69% (59.7-78.3%)</td>
|
||||
<td align="left">24.8% (9.5-40.5%)</td>
|
||||
<td align="left">49.7% (35-63.2%)</td>
|
||||
<td align="left">68.1% (58.1-77.6%)</td>
|
||||
<td align="left">53.8% (32-75%)</td>
|
||||
<td align="left">51.7% (36.1-67.3%)</td>
|
||||
<td align="left">68.8% (51.1-85.7%)</td>
|
||||
<td align="left">70.2% (54.7-85.3%)</td>
|
||||
<td align="left">53.2% (37.5-68.7%)</td>
|
||||
<td align="left">66.5% (55-76.8%)</td>
|
||||
<td align="left">56.2% (45.8-65.4%)</td>
|
||||
<td align="left">44% (30.3-57.5%)</td>
|
||||
<td align="left">71.9% (58.2-82.2%)</td>
|
||||
<td align="left">86.8% (77.3-93.6%)</td>
|
||||
<td align="left">54.1% (46.9-61.4%)</td>
|
||||
<td align="left">67.1% (61.5-72.5%)</td>
|
||||
<td align="left">81% (76.4-85.2%)</td>
|
||||
<td align="left">66.3% (61-71.2%)</td>
|
||||
</tr>
|
||||
<tr class="odd">
|
||||
<td align="left">75+</td>
|
||||
<td align="left">F</td>
|
||||
<td align="left">51.4% (41.7-62%)</td>
|
||||
<td align="left">30.9% (26.2-36.5%)</td>
|
||||
<td align="left">74.4% (70.3-78.6%)</td>
|
||||
<td align="left">30.9% (25.7-36.1%)</td>
|
||||
<td align="left">36.6% (32-41.6%)</td>
|
||||
<td align="left">20.7% (16.2-25.4%)</td>
|
||||
<td align="left">73.6% (63.6-82.5%)</td>
|
||||
<td align="left">79.1% (70.6-86.8%)</td>
|
||||
<td align="left">78.6% (69.9-86.3%)</td>
|
||||
<td align="left">76% (67.5-83.7%)</td>
|
||||
<td align="left">43.1% (38.6-48%)</td>
|
||||
<td align="left">78.9% (70.5-86.4%)</td>
|
||||
<td align="left">77% (72.6-81.3%)</td>
|
||||
<td align="left">63.2% (43.2-84.1%)</td>
|
||||
<td align="left">77.7% (72.1-83.2%)</td>
|
||||
<td align="left">41.2% (36-46.4%)</td>
|
||||
<td align="left">39.1% (34.2-44.4%)</td>
|
||||
<td align="left">63.7% (46.3-80.6%)</td>
|
||||
<td align="left">36.5% (31.9-41.2%)</td>
|
||||
<td align="left">57.1% (39.8-76%)</td>
|
||||
<td align="left">65.8% (57.2-73.5%)</td>
|
||||
<td align="left">84.6% (80.6-88%)</td>
|
||||
<td align="left">81.9% (73.7-89.5%)</td>
|
||||
<td align="left">33.3% (13.7-53%)</td>
|
||||
<td align="left">49.6% (42.3-56.1%)</td>
|
||||
<td align="left">81.3% (73.2-88.9%)</td>
|
||||
<td align="left">55.9% (33.5-76.5%)</td>
|
||||
<td align="left">41% (31.4-51.8%)</td>
|
||||
<td align="left">63.7% (43.8-82.3%)</td>
|
||||
<td align="left">77.8% (66-87.4%)</td>
|
||||
<td align="left">56.3% (37.3-75.1%)</td>
|
||||
<td align="left">71.8% (62-82.2%)</td>
|
||||
<td align="left">48.3% (41.5-54.9%)</td>
|
||||
<td align="left">43.3% (36.2-50.7%)</td>
|
||||
<td align="left">63% (45.3-80.3%)</td>
|
||||
<td align="left">85.9% (79.9-90.9%)</td>
|
||||
<td align="left">70.4% (64.1-76.8%)</td>
|
||||
<td align="left">60.4% (55.1-65.8%)</td>
|
||||
<td align="left">77.6% (73.4-82.1%)</td>
|
||||
<td align="left">55.3% (50.4-60.1%)</td>
|
||||
</tr>
|
||||
<tr class="even">
|
||||
<td align="left">75+</td>
|
||||
<td align="left">M</td>
|
||||
<td align="left">52.6% (43.3-62.6%)</td>
|
||||
<td align="left">33% (28.1-38%)</td>
|
||||
<td align="left">77.4% (73.3-81.5%)</td>
|
||||
<td align="left">33% (28.2-38.2%)</td>
|
||||
<td align="left">36.8% (32.3-41.8%)</td>
|
||||
<td align="left">17.9% (12.6-23.2%)</td>
|
||||
<td align="left">64.4% (55.4-73.3%)</td>
|
||||
<td align="left">71.2% (63.1-79.1%)</td>
|
||||
<td align="left">67.9% (59.5-75.8%)</td>
|
||||
<td align="left">65.3% (56.3-73.6%)</td>
|
||||
<td align="left">42.6% (37.8-47.4%)</td>
|
||||
<td align="left">68.2% (59.7-76.4%)</td>
|
||||
<td align="left">75.1% (70.9-79.2%)</td>
|
||||
<td align="left">64.1% (45.8-81.8%)</td>
|
||||
<td align="left">77.6% (72-82.6%)</td>
|
||||
<td align="left">41% (36-46.4%)</td>
|
||||
<td align="left">39.9% (35.1-44.5%)</td>
|
||||
<td align="left">62.1% (46-78.8%)</td>
|
||||
<td align="left">36.9% (32.4-41.4%)</td>
|
||||
<td align="left">59.7% (43.4-76.6%)</td>
|
||||
<td align="left">64.7% (56.6-73.6%)</td>
|
||||
<td align="left">83% (79.4-86.7%)</td>
|
||||
<td align="left">75.7% (66.6-83%)</td>
|
||||
<td align="left">31.6% (12.1-51.7%)</td>
|
||||
<td align="left">51.8% (44.9-58%)</td>
|
||||
<td align="left">74.2% (65.8-82.7%)</td>
|
||||
<td align="left">NA</td>
|
||||
<td align="left">52.2% (41.5-60.8%)</td>
|
||||
<td align="left">69.3% (50.5-86.4%)</td>
|
||||
<td align="left">72.2% (58.7-83.4%)</td>
|
||||
<td align="left">59.3% (41.6-76.7%)</td>
|
||||
<td align="left">73.1% (64.3-81.4%)</td>
|
||||
<td align="left">49.9% (42.4-56.9%)</td>
|
||||
<td align="left">46.3% (38.2-53.1%)</td>
|
||||
<td align="left">59.7% (44.2-75.7%)</td>
|
||||
<td align="left">86.8% (81.4-91.3%)</td>
|
||||
<td align="left">72% (66.3-77.6%)</td>
|
||||
<td align="left">55.8% (50.3-61.1%)</td>
|
||||
<td align="left">73.3% (68.9-77.6%)</td>
|
||||
<td align="left">57% (52.2-61.6%)</td>
|
||||
</tr>
|
||||
</tbody>
|
||||
</table>
|
||||
</div>
|
||||
<div class="section level4">
|
||||
<h4 id="plotting-antibiograms">Plotting antibiograms<a class="anchor" aria-label="anchor" href="#plotting-antibiograms"></a>
|
||||
</h4>
|
||||
<p>Antibiograms can be plotted using <code><a href="https://ggplot2.tidyverse.org/reference/autoplot.html" class="external-link">autoplot()</a></code> from the
|
||||
<code>ggplot2</code> packages, since this <code>AMR</code> package
|
||||
provides an extension to that function:</p>
|
||||
<div class="sourceCode" id="cb22"><pre class="downlit sourceCode r">
|
||||
<code class="sourceCode R"><span><span class="fu"><a href="https://ggplot2.tidyverse.org/reference/autoplot.html" class="external-link">autoplot</a></span><span class="op">(</span><span class="va">combined_ab</span><span class="op">)</span></span></code></pre></div>
|
||||
<p>All antibiogram types, including WISCA, can be plotted using
|
||||
<code><a href="https://ggplot2.tidyverse.org/reference/autoplot.html" class="external-link">autoplot()</a></code> from the <code>ggplot2</code> package, since
|
||||
this <code>AMR</code> package provides an extension to that
|
||||
function:</p>
|
||||
<div class="sourceCode" id="cb25"><pre class="downlit sourceCode r">
|
||||
<code class="sourceCode R"><span><span class="fu"><a href="https://ggplot2.tidyverse.org/reference/autoplot.html" class="external-link">autoplot</a></span><span class="op">(</span><span class="va">wisca_result</span><span class="op">)</span></span></code></pre></div>
|
||||
<p><img src="AMR_files/figure-html/unnamed-chunk-10-1.png" class="r-plt" alt="" width="720"></p>
|
||||
<p>To calculate antimicrobial resistance in a more sensible way, also by
|
||||
correcting for too few results, we use the <code><a href="../reference/proportion.html">resistance()</a></code> and
|
||||
@@ -1657,7 +1323,7 @@ proportion of R (<code><a href="../reference/proportion.html">proportion_R()</a>
|
||||
I (<code><a href="../reference/proportion.html">proportion_SI()</a></code>, equal to
|
||||
<code><a href="../reference/proportion.html">susceptibility()</a></code>). These functions can be used on their
|
||||
own:</p>
|
||||
<div class="sourceCode" id="cb23"><pre class="downlit sourceCode r">
|
||||
<div class="sourceCode" id="cb26"><pre class="downlit sourceCode r">
|
||||
<code class="sourceCode R"><span><span class="va">our_data_1st</span> <span class="op"><a href="https://magrittr.tidyverse.org/reference/pipe.html" class="external-link">%>%</a></span> <span class="fu"><a href="../reference/proportion.html">resistance</a></span><span class="op">(</span><span class="va">AMX</span><span class="op">)</span></span>
|
||||
<span><span class="co">#> <span style="color: #00BBBB;">ℹ</span> `resistance()` assumes the EUCAST guideline and thus considers the 'I'</span></span>
|
||||
<span><span class="co">#> category susceptible. Set the `guideline` argument or the `AMR_guideline`</span></span>
|
||||
@@ -1666,7 +1332,7 @@ own:</p>
|
||||
<span><span class="co">#> [1] 0.4203377</span></span></code></pre></div>
|
||||
<p>Or can be used in conjunction with <code><a href="https://dplyr.tidyverse.org/reference/group_by.html" class="external-link">group_by()</a></code> and
|
||||
<code><a href="https://dplyr.tidyverse.org/reference/summarise.html" class="external-link">summarise()</a></code>, both from the <code>dplyr</code> package:</p>
|
||||
<div class="sourceCode" id="cb24"><pre class="downlit sourceCode r">
|
||||
<div class="sourceCode" id="cb27"><pre class="downlit sourceCode r">
|
||||
<code class="sourceCode R"><span><span class="va">our_data_1st</span> <span class="op"><a href="https://magrittr.tidyverse.org/reference/pipe.html" class="external-link">%>%</a></span></span>
|
||||
<span> <span class="fu"><a href="https://dplyr.tidyverse.org/reference/group_by.html" class="external-link">group_by</a></span><span class="op">(</span><span class="va">hospital</span><span class="op">)</span> <span class="op"><a href="https://magrittr.tidyverse.org/reference/pipe.html" class="external-link">%>%</a></span></span>
|
||||
<span> <span class="fu"><a href="https://dplyr.tidyverse.org/reference/summarise.html" class="external-link">summarise</a></span><span class="op">(</span>amoxicillin <span class="op">=</span> <span class="fu"><a href="../reference/proportion.html">resistance</a></span><span class="op">(</span><span class="va">AMX</span><span class="op">)</span><span class="op">)</span></span>
|
||||
@@ -1684,7 +1350,7 @@ own:</p>
|
||||
diameters can be interpreted into clinical breakpoints (SIR) using
|
||||
<code><a href="../reference/as.sir.html">as.sir()</a></code>. Here’s an example with randomly generated MIC
|
||||
values for <em>Klebsiella pneumoniae</em> and ciprofloxacin:</p>
|
||||
<div class="sourceCode" id="cb25"><pre class="downlit sourceCode r">
|
||||
<div class="sourceCode" id="cb28"><pre class="downlit sourceCode r">
|
||||
<code class="sourceCode R"><span><span class="fu"><a href="https://rdrr.io/r/base/Random.html" class="external-link">set.seed</a></span><span class="op">(</span><span class="fl">123</span><span class="op">)</span></span>
|
||||
<span><span class="va">mic_values</span> <span class="op"><-</span> <span class="fu"><a href="../reference/random.html">random_mic</a></span><span class="op">(</span><span class="fl">100</span><span class="op">)</span></span>
|
||||
<span><span class="va">sir_values</span> <span class="op"><-</span> <span class="fu"><a href="../reference/as.sir.html">as.sir</a></span><span class="op">(</span><span class="va">mic_values</span>, mo <span class="op">=</span> <span class="st">"K. pneumoniae"</span>, ab <span class="op">=</span> <span class="st">"cipro"</span>, guideline <span class="op">=</span> <span class="st">"EUCAST 2024"</span><span class="op">)</span></span>
|
||||
@@ -1715,7 +1381,7 @@ breakpoints, facilitating automated AMR data processing.</p>
|
||||
using <code>ggplot2</code>, using the new <code><a href="../reference/plot.html">scale_y_mic()</a></code> for
|
||||
the y-axis and <code><a href="../reference/plot.html">scale_colour_sir()</a></code> to colour-code SIR
|
||||
categories.</p>
|
||||
<div class="sourceCode" id="cb26"><pre class="downlit sourceCode r">
|
||||
<div class="sourceCode" id="cb29"><pre class="downlit sourceCode r">
|
||||
<code class="sourceCode R"><span><span class="co"># add a group</span></span>
|
||||
<span><span class="va">my_data</span><span class="op">$</span><span class="va">group</span> <span class="op"><-</span> <span class="fu"><a href="https://rdrr.io/r/base/rep.html" class="external-link">rep</a></span><span class="op">(</span><span class="fu"><a href="https://rdrr.io/r/base/c.html" class="external-link">c</a></span><span class="op">(</span><span class="st">"A"</span>, <span class="st">"B"</span>, <span class="st">"C"</span>, <span class="st">"D"</span><span class="op">)</span>, each <span class="op">=</span> <span class="fl">25</span><span class="op">)</span></span>
|
||||
<span></span>
|
||||
@@ -1739,16 +1405,16 @@ across different groups while incorporating clinical breakpoints.</p>
|
||||
<code>ggplot2</code>’s function <code><a href="https://ggplot2.tidyverse.org/reference/autoplot.html" class="external-link">autoplot()</a></code> has been
|
||||
extended by this package to directly plot MIC and disk diffusion
|
||||
values:</p>
|
||||
<div class="sourceCode" id="cb27"><pre class="downlit sourceCode r">
|
||||
<div class="sourceCode" id="cb30"><pre class="downlit sourceCode r">
|
||||
<code class="sourceCode R"><span><span class="fu"><a href="https://ggplot2.tidyverse.org/reference/autoplot.html" class="external-link">autoplot</a></span><span class="op">(</span><span class="va">mic_values</span><span class="op">)</span></span></code></pre></div>
|
||||
<p><img src="AMR_files/figure-html/autoplot-1.png" class="r-plt" alt="" width="720"></p>
|
||||
<div class="sourceCode" id="cb28"><pre class="downlit sourceCode r">
|
||||
<div class="sourceCode" id="cb31"><pre class="downlit sourceCode r">
|
||||
<code class="sourceCode R"><span></span>
|
||||
<span><span class="co"># by providing `mo` and `ab`, colours will indicate the SIR interpretation:</span></span>
|
||||
<span><span class="fu"><a href="https://ggplot2.tidyverse.org/reference/autoplot.html" class="external-link">autoplot</a></span><span class="op">(</span><span class="va">mic_values</span>, mo <span class="op">=</span> <span class="st">"K. pneumoniae"</span>, ab <span class="op">=</span> <span class="st">"cipro"</span>, guideline <span class="op">=</span> <span class="st">"EUCAST 2024"</span><span class="op">)</span></span></code></pre></div>
|
||||
<p><img src="AMR_files/figure-html/autoplot-2.png" class="r-plt" alt="" width="720"></p>
|
||||
<hr>
|
||||
<p><em>Author: Dr. Matthijs Berends, 23rd Feb 2025</em></p>
|
||||
<p><em>Author: Dr. Matthijs Berends, 23rd June 2026</em></p>
|
||||
</div>
|
||||
</div>
|
||||
</main><aside class="col-md-3"><nav id="toc" aria-label="Table of contents"><h2>On this page</h2>
|
||||
|
||||
285
articles/AMR.md
285
articles/AMR.md
@@ -3,7 +3,7 @@
|
||||
**Note:** values on this page will change with every website update
|
||||
since they are based on randomly created values and the page was written
|
||||
in [R Markdown](https://rmarkdown.rstudio.com/). However, the
|
||||
methodology remains unchanged. This page was generated on 02 May 2026.
|
||||
methodology remains unchanged. This page was generated on 23 June 2026.
|
||||
|
||||
## Introduction
|
||||
|
||||
@@ -51,9 +51,9 @@ structure of your data generally look like this:
|
||||
|
||||
| date | patient_id | mo | AMX | CIP |
|
||||
|:----------:|:----------:|:----------------:|:---:|:---:|
|
||||
| 2026-05-02 | abcd | Escherichia coli | S | S |
|
||||
| 2026-05-02 | abcd | Escherichia coli | S | R |
|
||||
| 2026-05-02 | efgh | Escherichia coli | R | S |
|
||||
| 2026-06-23 | abcd | Escherichia coli | S | S |
|
||||
| 2026-06-23 | abcd | Escherichia coli | S | R |
|
||||
| 2026-06-23 | efgh | Escherichia coli | R | S |
|
||||
|
||||
### Needed R packages
|
||||
|
||||
@@ -112,7 +112,7 @@ SIR values as well.
|
||||
With [`as.mo()`](https://amr-for-r.org/reference/as.mo.md), users can
|
||||
transform arbitrary microorganism names or codes to current taxonomy.
|
||||
The `AMR` package contains up-to-date taxonomic data. To be specific,
|
||||
currently included data were retrieved on 24 Jun 2024.
|
||||
currently included data were retrieved on 07 May 2026.
|
||||
|
||||
The codes of the AMR packages that come from
|
||||
[`as.mo()`](https://amr-for-r.org/reference/as.mo.md) are short, but
|
||||
@@ -199,24 +199,23 @@ mo_uncertainties()
|
||||
#> Also matched: Klebsiella pneumoniae complex (0.707), Klebsiella pneumoniae
|
||||
#> ozaenae (0.707), Klebsiella pneumoniae pneumoniae (0.688), Klebsiella
|
||||
#> pneumoniae rhinoscleromatis (0.658), Klebsiella pasteurii (0.500), Klebsiella
|
||||
#> planticola (0.500), Kingella potus (0.400), Kluyveromyces pseudotropicale
|
||||
#> (0.386), Kluyveromyces pseudotropicalis (0.363), and Kosakonia pseudosacchari
|
||||
#> (0.361)
|
||||
#> planticola (0.500), Kosakonia pseudosacchari (0.471), Kaistella palustris
|
||||
#> (0.435), Kingella potus (0.435), and Kocuria palustris (0.435)
|
||||
#> -------------------------------------------------------------------------------
|
||||
#> "S. aureus" -> Staphylococcus aureus (B_STPHY_AURS, 0.690)
|
||||
#> Also matched: Staphylococcus aureus aureus (0.643), Staphylococcus argenteus
|
||||
#> (0.625), Staphylococcus aureus anaerobius (0.625), Staphylococcus auricularis
|
||||
#> (0.615), Salmonella Aurelianis (0.595), Salmonella Aarhus (0.588), Salmonella
|
||||
#> Amounderness (0.587), Staphylococcus argensis (0.587), Streptococcus australis
|
||||
#> (0.587), and Salmonella choleraesuis arizonae (0.562)
|
||||
#> (0.625), Staphylococcus aureus anaerobius (0.625), Streptomyces aureus (0.618),
|
||||
#> Staphylococcus auricularis (0.615), Streptomyces azureus (0.609), Salmonella
|
||||
#> Aurelianis (0.595), Salmonella Aarhus (0.588), Salmonella Amounderness (0.587),
|
||||
#> and Staphylococcus argensis (0.587)
|
||||
#> -------------------------------------------------------------------------------
|
||||
#> "S. pneumoniae" -> Streptococcus pneumoniae (B_STRPT_PNMN, 0.750)
|
||||
#> Also matched: Streptococcus pseudopneumoniae (0.700), Streptococcus phocae
|
||||
#> salmonis (0.552), Serratia proteamaculans quinovora (0.545), Streptococcus
|
||||
#> pseudoporcinus (0.536), Staphylococcus piscifermentans (0.533), Staphylococcus
|
||||
#> pseudintermedius (0.532), Serratia proteamaculans proteamaculans (0.526),
|
||||
#> Streptococcus gallolyticus pasteurianus (0.526), Salmonella Portanigra (0.524),
|
||||
#> and Streptococcus periodonticum (0.519)
|
||||
#> Also matched: Streptococcus parapneumoniae (0.714), Streptococcus
|
||||
#> pseudopneumoniae (0.700), Serratia proteamaculans quinivorans (0.557),
|
||||
#> Streptococcus phocae salmonis (0.552), Serratia proteamaculans quinovora
|
||||
#> (0.545), Sphingomonas piscinae (0.538), Streptococcus pseudoporcinus (0.536),
|
||||
#> Staphylococcus piscifermentans (0.533), Staphylococcus pseudintermedius
|
||||
#> (0.532), and Serratia proteamaculans proteamaculans (0.526)
|
||||
#> ℹ Only the first 10 other matches of each record are shown. Run ``
|
||||
#> `print(mo_uncertainties(), n = ...)` `` to view more entries, or save
|
||||
#> `mo_uncertainties()` to an object.
|
||||
@@ -575,33 +574,42 @@ our_data_1st[all(betalactams() == "R"), ]
|
||||
|
||||
### Generate antibiograms
|
||||
|
||||
Since AMR v2.0 (March 2023), it is very easy to create different types
|
||||
of antibiograms, with support for 20 different languages.
|
||||
The `AMR` package supports 28 different languages for antibiograms and
|
||||
provides four types, as proposed by Klinker *et al.* (2021, [DOI
|
||||
10.1177/20499361211011373](https://doi.org/10.1177/20499361211011373)):
|
||||
|
||||
There are four antibiogram types, as proposed by Klinker *et al.* (2021,
|
||||
[DOI
|
||||
10.1177/20499361211011373](https://doi.org/10.1177/20499361211011373)),
|
||||
and they are all supported by the new
|
||||
[`antibiogram()`](https://amr-for-r.org/reference/antibiogram.md)
|
||||
function:
|
||||
1. **Traditional Antibiogram (TA)** – susceptibility of a species to
|
||||
individual antibiotics
|
||||
2. **Combination Antibiogram (CA)** – susceptibility of a species to
|
||||
combination regimens
|
||||
3. **Syndromic Antibiogram (SA)** – susceptibility of a species,
|
||||
stratified by clinical syndrome or setting
|
||||
4. **Weighted-Incidence Syndromic Combination Antibiogram (WISCA)** –
|
||||
estimated empirical coverage of a *regimen* for a *syndrome*,
|
||||
weighted by pathogen incidence and with quantified uncertainty
|
||||
|
||||
1. **Traditional Antibiogram (TA)** e.g, for the susceptibility of
|
||||
*Pseudomonas aeruginosa* to piperacillin/tazobactam (TZP)
|
||||
2. **Combination Antibiogram (CA)** e.g, for the sdditional
|
||||
susceptibility of *Pseudomonas aeruginosa* to TZP + tobramycin
|
||||
versus TZP alone
|
||||
3. **Syndromic Antibiogram (SA)** e.g, for the susceptibility of
|
||||
*Pseudomonas aeruginosa* to TZP among respiratory specimens
|
||||
(obtained among ICU patients only)
|
||||
4. **Weighted-Incidence Syndromic Combination Antibiogram (WISCA)**
|
||||
e.g, for the susceptibility of *Pseudomonas aeruginosa* to TZP among
|
||||
respiratory specimens (obtained among ICU patients only) for male
|
||||
patients age \>=65 years with heart failure
|
||||
**If your goal is to guide empirical therapy, WISCA should be your
|
||||
default.** The reason is simple: when you start empirical treatment, you
|
||||
do not know which pathogen is causing the infection. Your next patient
|
||||
will not present with a species label attached to them. What matters is
|
||||
the probability that the *regimen* you choose will cover *whatever
|
||||
pathogen turns out to be the cause*, given the local epidemiology of the
|
||||
syndrome. Traditional antibiograms do not answer that question. They
|
||||
fragment information by species, ignore how frequently each species
|
||||
causes the syndrome, do not evaluate combination regimens, and provide
|
||||
no measure of uncertainty. WISCA addresses all of these limitations
|
||||
using a Bayesian framework (Hebert *et al.*, 2012; Bielicki *et al.*,
|
||||
2016). See the [WISCA
|
||||
vignette](https://amr-for-r.org/articles/WISCA.html) for the full
|
||||
explanation.
|
||||
|
||||
In this section, we show how to use the
|
||||
[`antibiogram()`](https://amr-for-r.org/reference/antibiogram.md)
|
||||
function to create any of the above antibiogram types. For starters,
|
||||
this is what the included `example_isolates` data set looks like:
|
||||
Traditional, combination, and syndromic antibiograms remain useful for
|
||||
**surveillance** purposes, i.e., tracking resistance trends per species
|
||||
over time. But if you care about clinical impact, about choosing the
|
||||
right empirical regimen for your patient, use WISCA.
|
||||
|
||||
For starters, this is what the included `example_isolates` data set
|
||||
looks like:
|
||||
|
||||
``` r
|
||||
|
||||
@@ -628,13 +636,106 @@ example_isolates
|
||||
#> # IPM <sir>, MEM <sir>, MTR <sir>, CHL <sir>, COL <sir>, MUP <sir>, …
|
||||
```
|
||||
|
||||
#### WISCA (recommended for empirical therapy guidance)
|
||||
|
||||
Use the [`wisca()`](https://amr-for-r.org/reference/antibiogram.md)
|
||||
function, or equivalently `antibiogram(..., wisca = TRUE)`. WISCA
|
||||
produces a single coverage estimate per regimen for the entire syndrome,
|
||||
weighted by pathogen incidence, with a 95% credible interval from
|
||||
Bayesian Monte Carlo simulation:
|
||||
|
||||
``` r
|
||||
|
||||
wisca_result <- example_isolates %>%
|
||||
wisca(
|
||||
antimicrobials = c("TZP", "TZP+TOB", "TZP+GEN"),
|
||||
minimum = 10
|
||||
) # Recommended threshold: ≥30
|
||||
wisca_result
|
||||
```
|
||||
|
||||
| Piperacillin/tazobactam | Piperacillin/tazobactam + Gentamicin | Piperacillin/tazobactam + Tobramycin |
|
||||
|:---|:---|:---|
|
||||
| 70.2% (64.8-75.2%) | 93.6% (92.2-95%) | 89.9% (87-92.3%) |
|
||||
|
||||
The output tells you: *“given the species distribution in your data,
|
||||
there is an estimated X% probability that this regimen covers the
|
||||
infection, with 95% credible interval \[lower, upper\]”*. That is the
|
||||
clinically relevant question.
|
||||
|
||||
For **syndrome-specific** or **patient-specific WISCA**, use the
|
||||
`syndromic_group` argument or group your data first. You can stratify by
|
||||
anything: ward, age group, risk profile, acquisition type. The
|
||||
`syndromic_group` argument accepts any column or expression:
|
||||
|
||||
``` r
|
||||
|
||||
wisca_out <- example_isolates %>%
|
||||
top_n_microorganisms(n = 10) %>%
|
||||
group_by(
|
||||
age_group = age_groups(age, c(25, 50, 75)),
|
||||
gender
|
||||
) %>%
|
||||
wisca(antimicrobials = c("TZP", "TZP+TOB", "TZP+GEN"))
|
||||
|
||||
wisca_out
|
||||
```
|
||||
|
||||
| age_group | gender | Piperacillin/tazobactam | Piperacillin/tazobactam + Gentamicin | Piperacillin/tazobactam + Tobramycin |
|
||||
|:---|:---|:---|:---|:---|
|
||||
| 0-24 | F | 56.8% (29.9-81.3%) | 70.7% (45.2-89%) | 65.9% (42.3-86.6%) |
|
||||
| 0-24 | M | 59.5% (31.2-85.5%) | 76.1% (56.5-92%) | 59.6% (31.7-85.1%) |
|
||||
| 25-49 | F | 67.7% (43.9-89.7%) | 93.8% (87.4-98.1%) | 87% (70.1-97%) |
|
||||
| 25-49 | M | 56.9% (26.6-86.2%) | 91% (82-97.2%) | 76.6% (51.4-93.5%) |
|
||||
| 50-74 | F | 68% (54.1-81.8%) | 96.9% (94.6-98.5%) | 90.2% (82-96.2%) |
|
||||
| 50-74 | M | 67% (56-78.5%) | 96.7% (94.1-98.5%) | 86.7% (77.3-94.4%) |
|
||||
| 75+ | F | 73.1% (61.8-84.1%) | 97.7% (95.9-99%) | 92.8% (85.7-97.2%) |
|
||||
| 75+ | M | 74% (63.6-82.6%) | 97.9% (96-99%) | 94.7% (89.3-97.9%) |
|
||||
|
||||
Keep in mind that more granular stratification produces more relevant
|
||||
estimates for each subgroup, but with wider credible intervals due to
|
||||
smaller sample sizes. There is always a trade-off between granularity
|
||||
and precision. If local numbers are small, consider pooling data from
|
||||
multiple sites (Bielicki *et al.*, 2016).
|
||||
|
||||
For reliable WISCA results, ensure your data includes **only first
|
||||
isolates** (use
|
||||
[`first_isolate()`](https://amr-for-r.org/reference/first_isolate.md))
|
||||
and consider filtering for **the top *n* species** (use
|
||||
[`top_n_microorganisms()`](https://amr-for-r.org/reference/top_n_microorganisms.md)),
|
||||
since rare contaminants can distort coverage estimates.
|
||||
|
||||
After creating the WISCA model, assessments can be done on the
|
||||
distributions of the Monte Carlo simulations that WISCA carried out:
|
||||
|
||||
``` r
|
||||
|
||||
wisca_plot(wisca_out)
|
||||
```
|
||||
|
||||

|
||||
|
||||
``` r
|
||||
|
||||
wisca_plot(wisca_out, wisca_plot_type = "posterior_coverage")
|
||||
```
|
||||
|
||||

|
||||
|
||||
``` r
|
||||
|
||||
|
||||
# a ggplot2 extension for WISCAs and other antibiograms:
|
||||
ggplot2::autoplot(wisca_out)
|
||||
```
|
||||
|
||||

|
||||
|
||||
#### Traditional Antibiogram
|
||||
|
||||
To create a traditional antibiogram, simply state which antibiotics
|
||||
should be used. The `antibiotics` argument in the
|
||||
[`antibiogram()`](https://amr-for-r.org/reference/antibiogram.md)
|
||||
function supports any (combination) of the previously mentioned
|
||||
antibiotic class selectors:
|
||||
If you need per-species susceptibility rates, e.g., for AMR surveillance
|
||||
reports, the traditional antibiogram remains the right tool. It reports
|
||||
the proportion of susceptible isolates per species per antibiotic:
|
||||
|
||||
``` r
|
||||
|
||||
@@ -691,10 +792,12 @@ antibiogram(example_isolates,
|
||||
| Gram negativo | 98% (96-99%,N=256) | 96% (95-98%,N=684) | 0% (0-10%,N=35) | 96% (94-97%,N=686) |
|
||||
| Gram positivo | 0% (0-1%,N=436) | 63% (60-66%,N=1170) | 0% (0-1%,N=436) | 34% (31-38%,N=665) |
|
||||
|
||||
#### Combined Antibiogram
|
||||
#### Combination Antibiogram
|
||||
|
||||
To create a combined antibiogram, use antibiotic codes or names with a
|
||||
plus `+` character like this:
|
||||
A combination antibiogram shows how much additional susceptibility a
|
||||
second agent adds for a given species. This is useful for surveillance
|
||||
of combination regimens, but note that it is still species-stratified
|
||||
and does not account for pathogen incidence in the syndrome:
|
||||
|
||||
``` r
|
||||
|
||||
@@ -719,10 +822,12 @@ combined_ab
|
||||
|
||||
#### Syndromic Antibiogram
|
||||
|
||||
To create a syndromic antibiogram, the `syndromic_group` argument must
|
||||
be used. This can be any column in the data, or e.g. an
|
||||
[`ifelse()`](https://rdrr.io/r/base/ifelse.html) with calculations based
|
||||
on certain columns:
|
||||
A syndromic antibiogram stratifies per-species susceptibility by
|
||||
clinical context (ward, specimen type, etc.). It adds clinical context
|
||||
to the traditional antibiogram but is still species-level, without
|
||||
incidence weighting or uncertainty quantification. For surveillance by
|
||||
setting this is fine; for empirical therapy guidance, WISCA is
|
||||
preferred:
|
||||
|
||||
``` r
|
||||
|
||||
@@ -752,80 +857,16 @@ antibiogram(example_isolates,
|
||||
| Clinical | *S. pneumoniae* | 0% (0-5%,N=78) | 0% (0-5%,N=78) | NA | 0% (0-5%,N=78) | NA | 0% (0-5%,N=78) |
|
||||
| ICU | *S. pneumoniae* | 0% (0-12%,N=30) | 0% (0-12%,N=30) | NA | 0% (0-12%,N=30) | NA | 0% (0-12%,N=30) |
|
||||
|
||||
#### Weighted-Incidence Syndromic Combination Antibiogram (WISCA)
|
||||
|
||||
To create a **Weighted-Incidence Syndromic Combination Antibiogram
|
||||
(WISCA)**, simply set `wisca = TRUE` in the
|
||||
[`antibiogram()`](https://amr-for-r.org/reference/antibiogram.md)
|
||||
function, or use the dedicated
|
||||
[`wisca()`](https://amr-for-r.org/reference/antibiogram.md) function.
|
||||
Unlike traditional antibiograms, WISCA provides syndrome-based
|
||||
susceptibility estimates, weighted by pathogen incidence and
|
||||
antimicrobial susceptibility patterns.
|
||||
|
||||
``` r
|
||||
|
||||
example_isolates %>%
|
||||
wisca(
|
||||
antibiotics = c("TZP", "TZP+TOB", "TZP+GEN"),
|
||||
minimum = 10
|
||||
) # Recommended threshold: ≥30
|
||||
```
|
||||
|
||||
| Piperacillin/tazobactam | Piperacillin/tazobactam + Gentamicin | Piperacillin/tazobactam + Tobramycin |
|
||||
|:---|:---|:---|
|
||||
| 69.4% (64.3-74.3%) | 92.6% (91.1-93.9%) | 88.7% (85.8-91.2%) |
|
||||
|
||||
WISCA uses a **Bayesian decision model** to integrate data from multiple
|
||||
pathogens, improving empirical therapy guidance, especially for
|
||||
low-incidence infections. It is **pathogen-agnostic**, meaning results
|
||||
are syndrome-based rather than stratified by microorganism.
|
||||
|
||||
For reliable results, ensure your data includes **only first isolates**
|
||||
(use
|
||||
[`first_isolate()`](https://amr-for-r.org/reference/first_isolate.md))
|
||||
and consider filtering for **the top *n* species** (use
|
||||
[`top_n_microorganisms()`](https://amr-for-r.org/reference/top_n_microorganisms.md)),
|
||||
as WISCA outcomes are most meaningful when based on robust incidence
|
||||
estimates.
|
||||
|
||||
For **patient- or syndrome-specific WISCA**, run the function on a
|
||||
grouped `tibble`, i.e., using
|
||||
[`group_by()`](https://dplyr.tidyverse.org/reference/group_by.html)
|
||||
first:
|
||||
|
||||
``` r
|
||||
|
||||
example_isolates %>%
|
||||
top_n_microorganisms(n = 10) %>%
|
||||
group_by(
|
||||
age_group = age_groups(age, c(25, 50, 75)),
|
||||
gender
|
||||
) %>%
|
||||
wisca(antibiotics = c("TZP", "TZP+TOB", "TZP+GEN"))
|
||||
```
|
||||
|
||||
| age_group | gender | Amikacin | Amoxicillin | Amoxicillin/clavulanic acid | Ampicillin | Azithromycin | Benzylpenicillin | Cefazolin | Cefepime | Cefotaxime | Cefoxitin | Ceftazidime | Ceftriaxone | Cefuroxime | Chloramphenicol | Ciprofloxacin | Clindamycin | Colistin | Doxycycline | Erythromycin | Flucloxacillin | Fosfomycin | Gentamicin | Imipenem | Kanamycin | Linezolid | Meropenem | Metronidazole | Moxifloxacin | Mupirocin | Nitrofurantoin | Oxacillin | Piperacillin/tazobactam | Rifampicin | Teicoplanin | Tetracycline | Tigecycline | Tobramycin | Trimethoprim | Trimethoprim/sulfamethoxazole | Vancomycin |
|
||||
|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|:---|
|
||||
| 0-24 | F | 45.4% (15.4-79%) | 50.1% (20.5-77.6%) | 69% (44.5-88.5%) | 50.4% (20.6-77.3%) | 41.9% (18.1-65.6%) | 36.1% (12.3-64.3%) | NA | NA | 63.9% (34.6-87.6%) | 56.7% (25.9-85.8%) | 51.5% (25.6-74.4%) | 63.4% (32-88.1%) | 70.4% (45.4-89.1%) | 54% (22.3-85.3%) | 69.8% (45.9-88.9%) | 39.3% (17.7-64.6%) | 45.3% (18.1-75.9%) | 50.1% (21.5-80.5%) | 41.7% (19.1-67.6%) | 55.8% (23.7-83.3%) | 63.5% (32.6-89.4%) | 69.3% (44.6-88.3%) | 63.6% (36.1-88.2%) | 45.5% (15.7-77.7%) | 43.3% (17.8-71.2%) | 55.9% (24.3-82.2%) | NA | NA | 56.5% (24.3-85%) | 56.8% (30.9-82.3%) | 50.5% (19.4-80.8%) | 56.9% (26.7-85%) | 42.3% (18.3-68.8%) | 40.2% (17.6-67.7%) | 49.8% (20-79.3%) | 56.1% (22-85.4%) | 64.5% (39.6-85.5%) | 69.7% (42.3-90.4%) | 75.4% (52.1-91.7%) | 48.5% (24.3-72.6%) |
|
||||
| 0-24 | M | 41.9% (15.2-72.5%) | 49.4% (23.3-75.5%) | 73.8% (51.8-90.1%) | 49.3% (22.7-76%) | 63.4% (40.7-83.5%) | 41.8% (20.4-64.8%) | 56.8% (25.2-83.5%) | 58.2% (29.1-85.8%) | 59.7% (29.1-87.4%) | 59.3% (29.1-86.6%) | 24.9% (8.9-47.3%) | 58.5% (28-86.5%) | 72.1% (47.9-90.5%) | NA | 77.2% (53-93.2%) | 61.6% (36.2-83.6%) | 25.5% (8.7-46.1%) | 69.4% (44.6-89.4%) | 63.4% (41.8-82.7%) | 64% (37.6-85.6%) | NA | 63.5% (40.9-83.1%) | 58.7% (27.6-86.5%) | 41.8% (13.6-71.2%) | 48.3% (17.9-78%) | 59.2% (27.4-86.4%) | NA | NA | NA | 53% (21.3-83.7%) | 57.2% (24.6-84.6%) | 59.9% (29.7-85.6%) | 48.2% (16.1-80.4%) | 48.4% (17.4-79.8%) | 68% (43.5-87.3%) | 65.7% (36-89.2%) | 44.3% (17.2-73.4%) | 69.4% (46.9-87.8%) | 74% (50.8-90.9%) | 75.3% (52.4-92.2%) |
|
||||
| 25-49 | F | 46.8% (26.7-65.6%) | 39% (26.3-52.9%) | 73.8% (63.5-82.6%) | 39.3% (27.2-54.4%) | 54.8% (44.9-64.8%) | 36.5% (26.3-47.1%) | 66.4% (46.1-85%) | 69.2% (49.1-86.2%) | 70.2% (50.5-86.2%) | 68.1% (48.6-85.4%) | 27.9% (19.2-37.9%) | 70.1% (50.5-87.1%) | 71.4% (61.7-80.4%) | 58.2% (35.3-79.9%) | 85.5% (74.1-94.2%) | 67.1% (55.8-77.4%) | 25.8% (17-36%) | 75.5% (61.2-88.2%) | 54.9% (44.8-65.6%) | 55.2% (37.8-72.5%) | 60.9% (38.3-81.8%) | 75.2% (65.7-83.5%) | 69.9% (50.1-86.6%) | 37.5% (17.7-57.9%) | 50.7% (30.8-68.7%) | 69.4% (48.6-86.7%) | NA | 56.9% (36.2-77.7%) | 53.3% (30.9-75.6%) | 60.1% (38.1-81.8%) | 64.3% (43.2-83.6%) | 66% (45.7-85.2%) | 50.1% (30-69.6%) | 38.8% (19.6-58.9%) | 75.8% (61.6-88.1%) | 73.3% (56.6-89.5%) | 62.7% (47.6-77.1%) | 70.4% (58.7-80.2%) | 90% (82.9-95.4%) | 71.6% (61.7-80.4%) |
|
||||
| 25-49 | M | 49.8% (24.2-75.8%) | 16.5% (8.1-27.4%) | 72.4% (60.5-83.5%) | 16.6% (7.7-28.2%) | 55.9% (43.6-67.9%) | 24.9% (14.7-37.6%) | 60.3% (33.2-82.4%) | 55.3% (27.6-81.8%) | 55.9% (29.7-81.1%) | 56.2% (27.7-82.1%) | 22.2% (12.7-33.9%) | 55.6% (29.1-81.8%) | 73.7% (62.6-83.8%) | 52.9% (25.2-79.6%) | 67.1% (53-79.8%) | 57.8% (43.5-71.8%) | 22.3% (12.6-33.6%) | 73% (57.8-85.5%) | 55.8% (43-68.2%) | 66.5% (51.6-79.4%) | 63.1% (40.3-84.5%) | 83.9% (74.5-91.7%) | 56.4% (28.4-84%) | 45.4% (18.9-73.8%) | 59.4% (37.6-77.9%) | 56.3% (28.8-81.1%) | NA | 52.8% (24.7-78.7%) | 64.2% (40.2-84.5%) | 62.9% (37.7-85.1%) | 60.5% (37.1-80.7%) | 55.8% (29.4-82.9%) | 65.4% (48.7-80.8%) | 54.5% (31.7-73.7%) | 72.8% (58.7-84.8%) | 84.8% (72.4-93.6%) | 66.7% (44.5-84.1%) | 71.4% (58.9-82.6%) | 86.6% (77.9-93.7%) | 77.1% (65.5-87.1%) |
|
||||
| 50-74 | F | 44.8% (35.8-54.1%) | 30.1% (24.9-35.3%) | 74.1% (69.2-78.7%) | 30% (24.6-35.4%) | 41.9% (36.5-47.3%) | 23.5% (18.6-29%) | 73.1% (62-82.9%) | 76.6% (66.1-86%) | 74.8% (64.9-84.5%) | 74.6% (64.2-83.3%) | 37.5% (32.3-43.4%) | 74.8% (64.4-83.8%) | 74.5% (69.7-78.9%) | 61.2% (40.3-82.4%) | 79.4% (73-85%) | 44.9% (38.7-51%) | 37.8% (32.7-43.3%) | 63.8% (47.6-80.1%) | 41.7% (36.6-46.9%) | 58.1% (40-75.1%) | 65.2% (53.5-76.6%) | 78.7% (73.8-83.2%) | 80.6% (70.3-90%) | 28.1% (10.1-46.6%) | 53.2% (42.9-62.4%) | 79.3% (68.7-88.6%) | NA | 49.5% (37.5-61.8%) | 67.8% (48.5-86%) | 75.1% (63.3-86.3%) | 56.6% (37.8-74.2%) | 67.7% (56.4-79.6%) | 50.6% (40.9-59.1%) | 41.3% (31.5-50.4%) | 59% (48.3-74.5%) | 87.7% (80.4-94.1%) | 62.2% (55.4-68.4%) | 55.5% (49.8-61.1%) | 68% (62.7-73.3%) | 60.9% (55.8-66.1%) |
|
||||
| 50-74 | M | 38.8% (30.6-48.6%) | 34.6% (29.1-40.3%) | 75% (70-79.5%) | 34.7% (29.2-40.5%) | 43.4% (37.8-48.5%) | 21% (16.5-26.4%) | 64.3% (54.1-74.1%) | 65.9% (56.5-75.4%) | 67.3% (58.3-77%) | 65.9% (56.1-75.9%) | 32.9% (27.6-38%) | 67.3% (57.4-76.8%) | 74.1% (69.2-78.8%) | 63.5% (42.4-83%) | 76.9% (71.6-81.9%) | 47.3% (40.9-53.8%) | 30.8% (26.1-36.1%) | 68.5% (53.5-81.9%) | 43.4% (37.7-48.8%) | 58.1% (42.4-73.2%) | 68.1% (53.5-82.2%) | 79.1% (74.4-83.1%) | 69% (59.7-78.3%) | 24.8% (9.5-40.5%) | 49.7% (35-63.2%) | 68.1% (58.1-77.6%) | 53.8% (32-75%) | 51.7% (36.1-67.3%) | 68.8% (51.1-85.7%) | 70.2% (54.7-85.3%) | 53.2% (37.5-68.7%) | 66.5% (55-76.8%) | 56.2% (45.8-65.4%) | 44% (30.3-57.5%) | 71.9% (58.2-82.2%) | 86.8% (77.3-93.6%) | 54.1% (46.9-61.4%) | 67.1% (61.5-72.5%) | 81% (76.4-85.2%) | 66.3% (61-71.2%) |
|
||||
| 75+ | F | 51.4% (41.7-62%) | 30.9% (26.2-36.5%) | 74.4% (70.3-78.6%) | 30.9% (25.7-36.1%) | 36.6% (32-41.6%) | 20.7% (16.2-25.4%) | 73.6% (63.6-82.5%) | 79.1% (70.6-86.8%) | 78.6% (69.9-86.3%) | 76% (67.5-83.7%) | 43.1% (38.6-48%) | 78.9% (70.5-86.4%) | 77% (72.6-81.3%) | 63.2% (43.2-84.1%) | 77.7% (72.1-83.2%) | 41.2% (36-46.4%) | 39.1% (34.2-44.4%) | 63.7% (46.3-80.6%) | 36.5% (31.9-41.2%) | 57.1% (39.8-76%) | 65.8% (57.2-73.5%) | 84.6% (80.6-88%) | 81.9% (73.7-89.5%) | 33.3% (13.7-53%) | 49.6% (42.3-56.1%) | 81.3% (73.2-88.9%) | 55.9% (33.5-76.5%) | 41% (31.4-51.8%) | 63.7% (43.8-82.3%) | 77.8% (66-87.4%) | 56.3% (37.3-75.1%) | 71.8% (62-82.2%) | 48.3% (41.5-54.9%) | 43.3% (36.2-50.7%) | 63% (45.3-80.3%) | 85.9% (79.9-90.9%) | 70.4% (64.1-76.8%) | 60.4% (55.1-65.8%) | 77.6% (73.4-82.1%) | 55.3% (50.4-60.1%) |
|
||||
| 75+ | M | 52.6% (43.3-62.6%) | 33% (28.1-38%) | 77.4% (73.3-81.5%) | 33% (28.2-38.2%) | 36.8% (32.3-41.8%) | 17.9% (12.6-23.2%) | 64.4% (55.4-73.3%) | 71.2% (63.1-79.1%) | 67.9% (59.5-75.8%) | 65.3% (56.3-73.6%) | 42.6% (37.8-47.4%) | 68.2% (59.7-76.4%) | 75.1% (70.9-79.2%) | 64.1% (45.8-81.8%) | 77.6% (72-82.6%) | 41% (36-46.4%) | 39.9% (35.1-44.5%) | 62.1% (46-78.8%) | 36.9% (32.4-41.4%) | 59.7% (43.4-76.6%) | 64.7% (56.6-73.6%) | 83% (79.4-86.7%) | 75.7% (66.6-83%) | 31.6% (12.1-51.7%) | 51.8% (44.9-58%) | 74.2% (65.8-82.7%) | NA | 52.2% (41.5-60.8%) | 69.3% (50.5-86.4%) | 72.2% (58.7-83.4%) | 59.3% (41.6-76.7%) | 73.1% (64.3-81.4%) | 49.9% (42.4-56.9%) | 46.3% (38.2-53.1%) | 59.7% (44.2-75.7%) | 86.8% (81.4-91.3%) | 72% (66.3-77.6%) | 55.8% (50.3-61.1%) | 73.3% (68.9-77.6%) | 57% (52.2-61.6%) |
|
||||
|
||||
#### Plotting antibiograms
|
||||
|
||||
Antibiograms can be plotted using
|
||||
All antibiogram types, including WISCA, can be plotted using
|
||||
[`autoplot()`](https://ggplot2.tidyverse.org/reference/autoplot.html)
|
||||
from the `ggplot2` packages, since this `AMR` package provides an
|
||||
from the `ggplot2` package, since this `AMR` package provides an
|
||||
extension to that function:
|
||||
|
||||
``` r
|
||||
|
||||
autoplot(combined_ab)
|
||||
autoplot(wisca_result)
|
||||
```
|
||||
|
||||

|
||||
@@ -989,4 +1030,4 @@ autoplot(mic_values, mo = "K. pneumoniae", ab = "cipro", guideline = "EUCAST 202
|
||||
|
||||
------------------------------------------------------------------------
|
||||
|
||||
*Author: Dr. Matthijs Berends, 23rd Feb 2025*
|
||||
*Author: Dr. Matthijs Berends, 23rd June 2026*
|
||||
|
||||
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|
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@@ -30,7 +30,7 @@
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@@ -30,7 +30,7 @@
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<link href="../deps/font-awesome-6.5.2/css/v4-shims.min.css" rel="stylesheet">
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@@ -30,7 +30,7 @@
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<a class="navbar-brand me-2" href="../index.html">AMR (for R)</a>
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<small class="nav-text text-muted me-auto" data-bs-toggle="tooltip" data-bs-placement="bottom" title="">3.0.1.9057</small>
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<button class="navbar-toggler" type="button" data-bs-toggle="collapse" data-bs-target="#navbar" aria-controls="navbar" aria-expanded="false" aria-label="Toggle navigation">
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@@ -200,7 +200,7 @@ function:</p>
|
||||
<span><span class="co">#> [1] "Caryophanales" "Enterobacterales" "Lactobacillales" "Pseudomonadales"</span></span>
|
||||
<span><span class="co">#> Importance of components:</span></span>
|
||||
<span><span class="co">#> PC1 PC2 PC3 PC4 PC5 PC6 PC7</span></span>
|
||||
<span><span class="co">#> Standard deviation 2.1539 1.6807 0.6138 0.33879 0.20808 0.03140 9.577e-17</span></span>
|
||||
<span><span class="co">#> Standard deviation 2.1539 1.6807 0.6138 0.33879 0.20808 0.03140 1.232e-16</span></span>
|
||||
<span><span class="co">#> Proportion of Variance 0.5799 0.3531 0.0471 0.01435 0.00541 0.00012 0.000e+00</span></span>
|
||||
<span><span class="co">#> Cumulative Proportion 0.5799 0.9330 0.9801 0.99446 0.99988 1.00000 1.000e+00</span></span></code></pre></div>
|
||||
<pre><code><span><span class="co">#> Groups (n=4, named as 'order'):</span></span>
|
||||
|
||||
@@ -123,7 +123,7 @@ summary(pca_result)
|
||||
#> [1] "Caryophanales" "Enterobacterales" "Lactobacillales" "Pseudomonadales"
|
||||
#> Importance of components:
|
||||
#> PC1 PC2 PC3 PC4 PC5 PC6 PC7
|
||||
#> Standard deviation 2.1539 1.6807 0.6138 0.33879 0.20808 0.03140 9.577e-17
|
||||
#> Standard deviation 2.1539 1.6807 0.6138 0.33879 0.20808 0.03140 1.232e-16
|
||||
#> Proportion of Variance 0.5799 0.3531 0.0471 0.01435 0.00541 0.00012 0.000e+00
|
||||
#> Cumulative Proportion 0.5799 0.9330 0.9801 0.99446 0.99988 1.00000 1.000e+00
|
||||
```
|
||||
|
||||
@@ -12,8 +12,8 @@
|
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<link rel="icon" sizes="any" href="../favicon.ico">
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<link rel="manifest" href="../site.webmanifest">
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@@ -30,7 +30,7 @@
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<a class="navbar-brand me-2" href="../index.html">AMR (for R)</a>
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@@ -30,7 +30,7 @@
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<a class="navbar-brand me-2" href="../index.html">AMR (for R)</a>
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<button class="navbar-toggler" type="button" data-bs-toggle="collapse" data-bs-target="#navbar" aria-controls="navbar" aria-expanded="false" aria-label="Toggle navigation">
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@@ -87,89 +87,98 @@
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|
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|
||||
|
||||
<blockquote>
|
||||
<p>This explainer was largely written by our <a href="https://chat.amr-for-r.org" class="external-link">AMR for R Assistant</a>, a ChatGPT
|
||||
manually-trained model able to answer any question about the
|
||||
<code>AMR</code> package.</p>
|
||||
</blockquote>
|
||||
<div class="section level2">
|
||||
<h2 id="introduction">Introduction<a class="anchor" aria-label="anchor" href="#introduction"></a>
|
||||
<h2 id="why-wisca">Why WISCA?<a class="anchor" aria-label="anchor" href="#why-wisca"></a>
|
||||
</h2>
|
||||
<p>Clinical guidelines for empirical antimicrobial therapy require
|
||||
<em>probabilistic reasoning</em>: what is the chance that a regimen will
|
||||
cover the likely infecting organisms, before culture results are
|
||||
available?</p>
|
||||
<p>This is the purpose of <strong>WISCA</strong>, or
|
||||
<strong>Weighted-Incidence Syndromic Combination
|
||||
Antibiogram</strong>.</p>
|
||||
<p>WISCA is a Bayesian approach that integrates:</p>
|
||||
<p>When a clinician starts empirical antimicrobial therapy, the
|
||||
causative pathogen is unknown. The question they need answered is not
|
||||
<em>“what proportion of</em> E. coli <em>is susceptible to
|
||||
ciprofloxacin?“</em> but rather <em>“what is the probability that this
|
||||
regimen will adequately cover whatever pathogen turns out to be causing
|
||||
my patient’s infection?”</em></p>
|
||||
<p>The traditional cumulative antibiogram, as standardised by CLSI M39,
|
||||
cannot answer that question. It presents susceptibility percentages per
|
||||
species per antibiotic, but:</p>
|
||||
<ul>
|
||||
<li>
|
||||
<strong>Pathogen prevalence</strong> (how often each species causes
|
||||
the syndrome),</li>
|
||||
<strong>It fragments information by organism.</strong> The clinician
|
||||
must mentally combine susceptibility rates across multiple species,
|
||||
weighting by how often each species causes the syndrome, a calculation
|
||||
nobody does at the bedside.</li>
|
||||
<li>
|
||||
<strong>Regimen susceptibility</strong> (how often a regimen works
|
||||
<em>if</em> the pathogen is known),</li>
|
||||
<strong>It ignores pathogen incidence.</strong> A species that
|
||||
causes 2% of infections is given the same visual weight as one that
|
||||
causes 60%.</li>
|
||||
<li>
|
||||
<strong>It does not evaluate combination regimens.</strong> Much
|
||||
empirical therapy consists of two or more agents, but the traditional
|
||||
antibiogram only shows monotherapy per organism.</li>
|
||||
<li>
|
||||
<strong>It provides no measure of uncertainty.</strong> A reported
|
||||
“90% susceptible” based on 50 isolates has a 95% confidence interval of
|
||||
roughly 78-97% (Clopper-Pearson), yet the antibiogram presents it as a
|
||||
point estimate without context.</li>
|
||||
</ul>
|
||||
<p>to estimate the <strong>overall empirical coverage</strong> of
|
||||
antimicrobial regimens, with quantified uncertainty.</p>
|
||||
<p>This vignette explains how WISCA works, why it is useful, and how to
|
||||
apply it using the <code>AMR</code> package.</p>
|
||||
<p><strong>WISCA</strong> (Weighted-Incidence Syndromic Combination
|
||||
Antibiogram) resolves all four limitations. It estimates the probability
|
||||
that a regimen will provide adequate empirical coverage for a given
|
||||
infection syndrome, weighted by local pathogen incidence, with full
|
||||
uncertainty quantification via Bayesian inference.</p>
|
||||
<p>The concept was introduced by Hebert <em>et al.</em> (2012), who
|
||||
demonstrated that traditional antibiogram susceptibility rates could be
|
||||
misleading: ciprofloxacin appeared 84% effective against <em>E.
|
||||
coli</em> in the traditional antibiogram, but WISCA revealed only 62%
|
||||
coverage for UTI and 37% for abdominal infections, because enterococci
|
||||
(intrinsically resistant) and other species contribute substantially to
|
||||
these syndromes. Randhawa <em>et al.</em> (2014) showed that
|
||||
WISCA-guided regimen selection could improve time-to-adequate-coverage
|
||||
on the ICU by over 40%. Bielicki <em>et al.</em> (2016) introduced the
|
||||
Bayesian framework now used in this package, enabling credible intervals
|
||||
and multi-centre pooling. Cook <em>et al.</em> (2022) applied it
|
||||
globally across 52 hospitals in 23 countries.</p>
|
||||
</div>
|
||||
<div class="section level2">
|
||||
<h2 id="why-traditional-antibiograms-fall-short">Why traditional antibiograms fall short<a class="anchor" aria-label="anchor" href="#why-traditional-antibiograms-fall-short"></a>
|
||||
</h2>
|
||||
<p>A standard antibiogram gives you:</p>
|
||||
<pre><code>Species → Antibiotic → Susceptibility %</code></pre>
|
||||
<p>But clinicians don’t know the species <em>a priori</em>. They need to
|
||||
choose a regimen that covers the <strong>likely pathogens</strong>,
|
||||
without knowing which one is present.</p>
|
||||
<p>Traditional antibiograms calculate the susceptibility % as just the
|
||||
number of resistant isolates divided by the total number of tested
|
||||
isolates. Therefore, traditional antibiograms:</p>
|
||||
<ul>
|
||||
<li>Fragment information by organism,</li>
|
||||
<li>Do not weight by real-world prevalence,</li>
|
||||
<li>Do not account for combination therapy or sample size,</li>
|
||||
<li>Do not provide uncertainty.</li>
|
||||
</ul>
|
||||
</div>
|
||||
<div class="section level2">
|
||||
<h2 id="the-idea-of-wisca">The idea of WISCA<a class="anchor" aria-label="anchor" href="#the-idea-of-wisca"></a>
|
||||
<h2 id="the-idea">The idea<a class="anchor" aria-label="anchor" href="#the-idea"></a>
|
||||
</h2>
|
||||
<p>WISCA asks:</p>
|
||||
<blockquote>
|
||||
<p>“What is the <strong>probability</strong> that this regimen
|
||||
<strong>will cover</strong> the pathogen, given the syndrome?”</p>
|
||||
</blockquote>
|
||||
<p>This means combining two things:</p>
|
||||
<p>This means combining two quantities:</p>
|
||||
<ul>
|
||||
<li>
|
||||
<strong>Incidence</strong> of each pathogen in the syndrome,</li>
|
||||
<strong>Pathogen incidence</strong> in the syndrome (how often each
|
||||
species causes it),</li>
|
||||
<li>
|
||||
<strong>Susceptibility</strong> of each pathogen to the
|
||||
regimen.</li>
|
||||
</ul>
|
||||
<p>We can write this as:</p>
|
||||
<p><math display="block" xmlns="http://www.w3.org/1998/Math/MathML"><semantics><mrow><mtext mathvariant="normal">Coverage</mtext><mo>=</mo><munder><mo>∑</mo><mi>i</mi></munder><mo stretchy="false" form="prefix">(</mo><msub><mtext mathvariant="normal">Incidence</mtext><mi>i</mi></msub><mo>×</mo><msub><mtext mathvariant="normal">Susceptibility</mtext><mi>i</mi></msub><mo stretchy="false" form="postfix">)</mo></mrow><annotation encoding="application/x-tex">\text{Coverage} = \sum_i (\text{Incidence}_i \times \text{Susceptibility}_i)</annotation></semantics></math></p>
|
||||
<p>For example, suppose:</p>
|
||||
<p>For example, suppose in your hospital:</p>
|
||||
<ul>
|
||||
<li>
|
||||
<em>E. coli</em> causes 60% of cases, and 90% of <em>E. coli</em>
|
||||
are susceptible to a drug.</li>
|
||||
<em>E. coli</em> causes 60% of UTIs, and 90% of <em>E. coli</em> are
|
||||
susceptible to a drug.</li>
|
||||
<li>
|
||||
<em>Klebsiella</em> causes 40% of cases, and 70% of
|
||||
<em>Klebsiella</em> causes 40% of UTIs, and 70% of
|
||||
<em>Klebsiella</em> are susceptible.</li>
|
||||
</ul>
|
||||
<p>Then:</p>
|
||||
<p><math display="block" xmlns="http://www.w3.org/1998/Math/MathML"><semantics><mrow><mtext mathvariant="normal">Coverage</mtext><mo>=</mo><mo stretchy="false" form="prefix">(</mo><mn>0.6</mn><mo>×</mo><mn>0.9</mn><mo stretchy="false" form="postfix">)</mo><mo>+</mo><mo stretchy="false" form="prefix">(</mo><mn>0.4</mn><mo>×</mo><mn>0.7</mn><mo stretchy="false" form="postfix">)</mo><mo>=</mo><mn>0.82</mn></mrow><annotation encoding="application/x-tex">\text{Coverage} = (0.6 \times 0.9) + (0.4 \times 0.7) = 0.82</annotation></semantics></math></p>
|
||||
<p>But in real data, incidence and susceptibility are <strong>estimated
|
||||
from samples</strong>, so they carry uncertainty. WISCA models this
|
||||
<strong>probabilistically</strong>, using conjugate Bayesian
|
||||
<p>That 82% is a far more clinically meaningful number than the
|
||||
species-level “90% of <em>E. coli</em>” and “70% of <em>Klebsiella</em>”
|
||||
reported separately in a traditional antibiogram, because it directly
|
||||
answers the question the clinician actually faces.</p>
|
||||
<p>But in real data, both incidence and susceptibility are
|
||||
<strong>estimated from finite samples</strong>, so they carry
|
||||
uncertainty. A sample of 50 isolates is not a census. WISCA models this
|
||||
uncertainty <strong>probabilistically</strong>, using conjugate Bayesian
|
||||
distributions.</p>
|
||||
</div>
|
||||
<div class="section level2">
|
||||
<h2 id="the-bayesian-engine-behind-wisca">The Bayesian engine behind WISCA<a class="anchor" aria-label="anchor" href="#the-bayesian-engine-behind-wisca"></a>
|
||||
<h2 id="the-bayesian-engine">The Bayesian engine<a class="anchor" aria-label="anchor" href="#the-bayesian-engine"></a>
|
||||
</h2>
|
||||
<div class="section level3">
|
||||
<h3 id="pathogen-incidence">Pathogen incidence<a class="anchor" aria-label="anchor" href="#pathogen-incidence"></a>
|
||||
@@ -180,27 +189,38 @@ distributions.</p>
|
||||
<math display="inline" xmlns="http://www.w3.org/1998/Math/MathML"><semantics><mi>K</mi><annotation encoding="application/x-tex">K</annotation></semantics></math>
|
||||
be the number of pathogens,</li>
|
||||
<li>
|
||||
<math display="inline" xmlns="http://www.w3.org/1998/Math/MathML"><semantics><mrow><mi>α</mi><mo>=</mo><mo stretchy="false" form="prefix">(</mo><mn>1</mn><mo>,</mo><mn>1</mn><mo>,</mo><mi>…</mi><mo>,</mo><mn>1</mn><mo stretchy="false" form="postfix">)</mo></mrow><annotation encoding="application/x-tex">\alpha = (1, 1, \ldots, 1)</annotation></semantics></math>
|
||||
be a <strong>Dirichlet</strong> prior (uniform),</li>
|
||||
<math display="inline" xmlns="http://www.w3.org/1998/Math/MathML"><semantics><mrow><mi>𝛂</mi><mo>=</mo><mo stretchy="false" form="prefix">(</mo><mn>1</mn><mo>,</mo><mn>1</mn><mo>,</mo><mi>…</mi><mo>,</mo><mn>1</mn><mo stretchy="false" form="postfix">)</mo></mrow><annotation encoding="application/x-tex">\boldsymbol{\alpha} = (1, 1, \ldots, 1)</annotation></semantics></math>
|
||||
be a
|
||||
<math display="inline" xmlns="http://www.w3.org/1998/Math/MathML"><semantics><mtext mathvariant="normal">Dirichlet</mtext><annotation encoding="application/x-tex">\text{Dirichlet}</annotation></semantics></math>
|
||||
prior (uniform, non-informative),</li>
|
||||
<li>
|
||||
<math display="inline" xmlns="http://www.w3.org/1998/Math/MathML"><semantics><mrow><mi>n</mi><mo>=</mo><mo stretchy="false" form="prefix">(</mo><msub><mi>n</mi><mn>1</mn></msub><mo>,</mo><mi>…</mi><mo>,</mo><msub><mi>n</mi><mi>K</mi></msub><mo stretchy="false" form="postfix">)</mo></mrow><annotation encoding="application/x-tex">n = (n_1, \ldots, n_K)</annotation></semantics></math>
|
||||
be the observed counts per species.</li>
|
||||
<math display="inline" xmlns="http://www.w3.org/1998/Math/MathML"><semantics><mrow><mi>𝐧</mi><mo>=</mo><mo stretchy="false" form="prefix">(</mo><msub><mi>n</mi><mn>1</mn></msub><mo>,</mo><mi>…</mi><mo>,</mo><msub><mi>n</mi><mi>K</mi></msub><mo stretchy="false" form="postfix">)</mo></mrow><annotation encoding="application/x-tex">\boldsymbol{n} = (n_1, \ldots, n_K)</annotation></semantics></math>
|
||||
be the observed isolate counts per species.</li>
|
||||
</ul>
|
||||
<p>Then the posterior incidence is:</p>
|
||||
<p><math display="block" xmlns="http://www.w3.org/1998/Math/MathML"><semantics><mrow><mi>p</mi><mo>∼</mo><mtext mathvariant="normal">Dirichlet</mtext><mo stretchy="false" form="prefix">(</mo><msub><mi>α</mi><mn>1</mn></msub><mo>+</mo><msub><mi>n</mi><mn>1</mn></msub><mo>,</mo><mi>…</mi><mo>,</mo><msub><mi>α</mi><mi>K</mi></msub><mo>+</mo><msub><mi>n</mi><mi>K</mi></msub><mo stretchy="false" form="postfix">)</mo></mrow><annotation encoding="application/x-tex">p \sim \text{Dirichlet}(\alpha_1 + n_1, \ldots, \alpha_K + n_K)</annotation></semantics></math></p>
|
||||
<p><math display="block" xmlns="http://www.w3.org/1998/Math/MathML"><semantics><mrow><mi>𝐩</mi><mo>∼</mo><mtext mathvariant="normal">Dirichlet</mtext><mo stretchy="false" form="prefix">(</mo><msub><mi>α</mi><mn>1</mn></msub><mo>+</mo><msub><mi>n</mi><mn>1</mn></msub><mo>,</mo><mi>…</mi><mo>,</mo><msub><mi>α</mi><mi>K</mi></msub><mo>+</mo><msub><mi>n</mi><mi>K</mi></msub><mo stretchy="false" form="postfix">)</mo></mrow><annotation encoding="application/x-tex">\boldsymbol{p} \sim \text{Dirichlet}(\alpha_1 + n_1, \ldots, \alpha_K + n_K)</annotation></semantics></math></p>
|
||||
<p>To simulate from this, we use:</p>
|
||||
<p><math display="block" xmlns="http://www.w3.org/1998/Math/MathML"><semantics><mrow><msub><mi>x</mi><mi>i</mi></msub><mo>∼</mo><mtext mathvariant="normal">Gamma</mtext><mo stretchy="false" form="prefix">(</mo><msub><mi>α</mi><mi>i</mi></msub><mo>+</mo><msub><mi>n</mi><mi>i</mi></msub><mo>,</mo><mspace width="0.222em"></mspace><mn>1</mn><mo stretchy="false" form="postfix">)</mo><mo>,</mo><mspace width="1.0em"></mspace><msub><mi>p</mi><mi>i</mi></msub><mo>=</mo><mfrac><msub><mi>x</mi><mi>i</mi></msub><mrow><munderover><mo>∑</mo><mrow><mi>j</mi><mo>=</mo><mn>1</mn></mrow><mi>K</mi></munderover><msub><mi>x</mi><mi>j</mi></msub></mrow></mfrac></mrow><annotation encoding="application/x-tex">x_i \sim \text{Gamma}(\alpha_i + n_i,\ 1), \quad p_i = \frac{x_i}{\sum_{j=1}^{K} x_j}</annotation></semantics></math></p>
|
||||
<p>The Dirichlet is the conjugate prior for multinomial data. With the
|
||||
non-informative prior
|
||||
<math display="inline" xmlns="http://www.w3.org/1998/Math/MathML"><semantics><mrow><mtext mathvariant="normal">Dirichlet</mtext><mo stretchy="false" form="prefix">(</mo><mn>1</mn><mo>,</mo><mn>1</mn><mo>,</mo><mi>…</mi><mo>,</mo><mn>1</mn><mo stretchy="false" form="postfix">)</mo></mrow><annotation encoding="application/x-tex">\text{Dirichlet}(1, 1, \ldots, 1)</annotation></semantics></math>,
|
||||
the posterior is dominated by the data once sample sizes are reasonable.
|
||||
With small samples, the posterior is appropriately more diffuse,
|
||||
reflecting genuine uncertainty, and the resulting credible intervals
|
||||
will be wider.</p>
|
||||
</div>
|
||||
<div class="section level3">
|
||||
<h3 id="susceptibility">Susceptibility<a class="anchor" aria-label="anchor" href="#susceptibility"></a>
|
||||
</h3>
|
||||
<p>Each pathogen–regimen pair has a prior and data:</p>
|
||||
<p>Each pathogen-regimen pair has a prior and observed data:</p>
|
||||
<ul>
|
||||
<li>Prior:
|
||||
<math display="inline" xmlns="http://www.w3.org/1998/Math/MathML"><semantics><mrow><mtext mathvariant="normal">Beta</mtext><mo stretchy="false" form="prefix">(</mo><msub><mi>α</mi><mn>0</mn></msub><mo>,</mo><msub><mi>β</mi><mn>0</mn></msub><mo stretchy="false" form="postfix">)</mo></mrow><annotation encoding="application/x-tex">\text{Beta}(\alpha_0, \beta_0)</annotation></semantics></math>,
|
||||
with default
|
||||
<math display="inline" xmlns="http://www.w3.org/1998/Math/MathML"><semantics><mrow><msub><mi>α</mi><mn>0</mn></msub><mo>=</mo><msub><mi>β</mi><mn>0</mn></msub><mo>=</mo><mn>1</mn></mrow><annotation encoding="application/x-tex">\alpha_0 = \beta_0 = 1</annotation></semantics></math>
|
||||
</li>
|
||||
<li>Default prior:
|
||||
<math display="inline" xmlns="http://www.w3.org/1998/Math/MathML"><semantics><mrow><mtext mathvariant="normal">Beta</mtext><mo stretchy="false" form="prefix">(</mo><mn>0.5</mn><mo>,</mo><mn>0.5</mn><mo stretchy="false" form="postfix">)</mo></mrow><annotation encoding="application/x-tex">\text{Beta}(0.5, 0.5)</annotation></semantics></math>
|
||||
(Jeffreys prior)</li>
|
||||
<li>Intrinsically resistant pairs:
|
||||
<math display="inline" xmlns="http://www.w3.org/1998/Math/MathML"><semantics><mrow><mtext mathvariant="normal">Beta</mtext><mo stretchy="false" form="prefix">(</mo><mn>1</mn><mo>,</mo><mn>9999</mn><mo stretchy="false" form="postfix">)</mo></mrow><annotation encoding="application/x-tex">\text{Beta}(1, 9999)</annotation></semantics></math>,
|
||||
forcing near-zero susceptibility regardless of observed data (based on
|
||||
EUCAST Expected Resistant Phenotypes)</li>
|
||||
<li>Data:
|
||||
<math display="inline" xmlns="http://www.w3.org/1998/Math/MathML"><semantics><mi>S</mi><annotation encoding="application/x-tex">S</annotation></semantics></math>
|
||||
susceptible out of
|
||||
@@ -224,27 +244,76 @@ I (intermediate [CLSI], or susceptible, increased exposure
|
||||
<math display="inline" xmlns="http://www.w3.org/1998/Math/MathML"><semantics><mrow><mi>𝐩</mi><mo>∼</mo><mtext mathvariant="normal">Dirichlet</mtext></mrow><annotation encoding="application/x-tex">\boldsymbol{p} \sim \text{Dirichlet}</annotation></semantics></math>
|
||||
</li>
|
||||
<li>Simulate susceptibility:
|
||||
<math display="inline" xmlns="http://www.w3.org/1998/Math/MathML"><semantics><mrow><msub><mi>θ</mi><mi>i</mi></msub><mo>∼</mo><mtext mathvariant="normal">Beta</mtext><mo stretchy="false" form="prefix">(</mo><mn>1</mn><mo>+</mo><msub><mi>S</mi><mi>i</mi></msub><mo>,</mo><mspace width="0.222em"></mspace><mn>1</mn><mo>+</mo><msub><mi>R</mi><mi>i</mi></msub><mo stretchy="false" form="postfix">)</mo></mrow><annotation encoding="application/x-tex">\theta_i \sim \text{Beta}(1 + S_i,\ 1 + R_i)</annotation></semantics></math>
|
||||
<math display="inline" xmlns="http://www.w3.org/1998/Math/MathML"><semantics><mrow><msub><mi>θ</mi><mi>i</mi></msub><mo>∼</mo><mtext mathvariant="normal">Beta</mtext><mo stretchy="false" form="prefix">(</mo><msub><mi>α</mi><mn>0</mn></msub><mo>+</mo><msub><mi>S</mi><mi>i</mi></msub><mo>,</mo><mspace width="0.222em"></mspace><msub><mi>β</mi><mn>0</mn></msub><mo>+</mo><msub><mi>N</mi><mi>i</mi></msub><mo>−</mo><msub><mi>S</mi><mi>i</mi></msub><mo stretchy="false" form="postfix">)</mo></mrow><annotation encoding="application/x-tex">\theta_i \sim \text{Beta}(\alpha_0 + S_i,\ \beta_0 + N_i - S_i)</annotation></semantics></math>
|
||||
</li>
|
||||
<li>Combine:</li>
|
||||
</ol>
|
||||
<p><math display="block" xmlns="http://www.w3.org/1998/Math/MathML"><semantics><mrow><mtext mathvariant="normal">Coverage</mtext><mo>=</mo><munderover><mo>∑</mo><mrow><mi>i</mi><mo>=</mo><mn>1</mn></mrow><mi>K</mi></munderover><msub><mi>p</mi><mi>i</mi></msub><mo>⋅</mo><msub><mi>θ</mi><mi>i</mi></msub></mrow><annotation encoding="application/x-tex">\text{Coverage} = \sum_{i=1}^{K} p_i \cdot \theta_i</annotation></semantics></math></p>
|
||||
<p>Repeat this simulation (e.g. 1000×) and summarise:</p>
|
||||
<p>Repeat this simulation (e.g., 1000 times) and summarise:</p>
|
||||
<ul>
|
||||
<li>
|
||||
<strong>Mean</strong> = expected coverage</li>
|
||||
<li>
|
||||
<strong>Quantiles</strong> = credible interval</li>
|
||||
<strong>Quantiles</strong> = credible interval (95% by default)</li>
|
||||
</ul>
|
||||
<p>Because each simulation draws from the full posterior, the resulting
|
||||
distribution of coverage estimates naturally captures the joint
|
||||
uncertainty in both pathogen incidence and susceptibility. The credible
|
||||
interval tells you how confident you can be in the coverage estimate,
|
||||
something a traditional antibiogram never provides.</p>
|
||||
</div>
|
||||
</div>
|
||||
<div class="section level2">
|
||||
<h2 id="when-to-use-wisca-vs--traditional-antibiograms">When to use WISCA vs. traditional antibiograms<a class="anchor" aria-label="anchor" href="#when-to-use-wisca-vs--traditional-antibiograms"></a>
|
||||
</h2>
|
||||
<table class="table">
|
||||
<thead><tr class="header">
|
||||
<th>Goal</th>
|
||||
<th>Recommended approach</th>
|
||||
</tr></thead>
|
||||
<tbody>
|
||||
<tr class="odd">
|
||||
<td>Guide empirical therapy decisions</td>
|
||||
<td><strong>WISCA</strong></td>
|
||||
</tr>
|
||||
<tr class="even">
|
||||
<td>Compare regimens for a syndrome</td>
|
||||
<td><strong>WISCA</strong></td>
|
||||
</tr>
|
||||
<tr class="odd">
|
||||
<td>Evaluate combination regimens</td>
|
||||
<td><strong>WISCA</strong></td>
|
||||
</tr>
|
||||
<tr class="even">
|
||||
<td>Antimicrobial stewardship (A-team)</td>
|
||||
<td><strong>WISCA</strong></td>
|
||||
</tr>
|
||||
<tr class="odd">
|
||||
<td>Track resistance trends per species</td>
|
||||
<td>Traditional / Combination</td>
|
||||
</tr>
|
||||
<tr class="even">
|
||||
<td>AMR surveillance reporting</td>
|
||||
<td>Traditional / Syndromic</td>
|
||||
</tr>
|
||||
<tr class="odd">
|
||||
<td>Understand species-level epidemiology</td>
|
||||
<td>Traditional</td>
|
||||
</tr>
|
||||
</tbody>
|
||||
</table>
|
||||
<p>In short: if the end goal involves a <em>patient</em> who does not
|
||||
yet have a culture result, WISCA is the appropriate tool. If the end
|
||||
goal is <em>surveillance</em> of resistance at the species level, the
|
||||
traditional antibiogram remains fit for purpose.</p>
|
||||
</div>
|
||||
<div class="section level2">
|
||||
<h2 id="practical-use-in-the-amr-package">Practical use in the <code>AMR</code> package<a class="anchor" aria-label="anchor" href="#practical-use-in-the-amr-package"></a>
|
||||
</h2>
|
||||
<div class="section level3">
|
||||
<h3 id="prepare-data-and-simulate-synthetic-syndrome">Prepare data and simulate synthetic syndrome<a class="anchor" aria-label="anchor" href="#prepare-data-and-simulate-synthetic-syndrome"></a>
|
||||
<h3 id="prepare-data">Prepare data<a class="anchor" aria-label="anchor" href="#prepare-data"></a>
|
||||
</h3>
|
||||
<div class="sourceCode" id="cb2"><pre class="downlit sourceCode r">
|
||||
<div class="sourceCode" id="cb1"><pre class="downlit sourceCode r">
|
||||
<code class="sourceCode R"><span><span class="kw"><a href="https://rdrr.io/r/base/library.html" class="external-link">library</a></span><span class="op">(</span><span class="va"><a href="https://amr-for-r.org">AMR</a></span><span class="op">)</span></span>
|
||||
<span><span class="va">data</span> <span class="op"><-</span> <span class="va">example_isolates</span></span>
|
||||
<span></span>
|
||||
@@ -271,13 +340,13 @@ I (intermediate [CLSI], or susceptible, increased exposure
|
||||
<span><span class="co">#> <span style="color: #949494;"># TCY <sir>, TGC <sir>, DOX <sir>, ERY <sir>, CLI <sir>, AZM <sir>,</span></span></span>
|
||||
<span><span class="co">#> <span style="color: #949494;"># IPM <sir>, MEM <sir>, MTR <sir>, CHL <sir>, COL <sir>, MUP <sir>, …</span></span></span>
|
||||
<span></span>
|
||||
<span><span class="co"># Add a fake syndrome column</span></span>
|
||||
<span><span class="va">data</span><span class="op">$</span><span class="va">syndrome</span> <span class="op"><-</span> <span class="fu"><a href="https://rdrr.io/r/base/ifelse.html" class="external-link">ifelse</a></span><span class="op">(</span><span class="va">data</span><span class="op">$</span><span class="va">mo</span> <span class="op"><a href="../reference/like.html">%like%</a></span> <span class="st">"coli"</span>, <span class="st">"UTI"</span>, <span class="st">"No UTI"</span><span class="op">)</span></span></code></pre></div>
|
||||
<span><span class="co"># Add a synthetic syndrome column for demonstration</span></span>
|
||||
<span><span class="va">data</span><span class="op">$</span><span class="va">syndrome</span> <span class="op"><-</span> <span class="fu"><a href="https://rdrr.io/r/base/ifelse.html" class="external-link">ifelse</a></span><span class="op">(</span><span class="va">data</span><span class="op">$</span><span class="va">mo</span> <span class="op"><a href="../reference/like.html">%like%</a></span> <span class="st">"coli"</span>, <span class="st">"UTI"</span>, <span class="st">"Non-UTI"</span><span class="op">)</span></span></code></pre></div>
|
||||
</div>
|
||||
<div class="section level3">
|
||||
<h3 id="basic-wisca-antibiogram">Basic WISCA antibiogram<a class="anchor" aria-label="anchor" href="#basic-wisca-antibiogram"></a>
|
||||
<h3 id="basic-wisca">Basic WISCA<a class="anchor" aria-label="anchor" href="#basic-wisca"></a>
|
||||
</h3>
|
||||
<div class="sourceCode" id="cb3"><pre class="downlit sourceCode r">
|
||||
<div class="sourceCode" id="cb2"><pre class="downlit sourceCode r">
|
||||
<code class="sourceCode R"><span><span class="fu"><a href="../reference/antibiogram.html">wisca</a></span><span class="op">(</span><span class="va">data</span>,</span>
|
||||
<span> antimicrobials <span class="op">=</span> <span class="fu"><a href="https://rdrr.io/r/base/c.html" class="external-link">c</a></span><span class="op">(</span><span class="st">"AMC"</span>, <span class="st">"CIP"</span>, <span class="st">"GEN"</span><span class="op">)</span></span>
|
||||
<span><span class="op">)</span></span></code></pre></div>
|
||||
@@ -288,16 +357,19 @@ I (intermediate [CLSI], or susceptible, increased exposure
|
||||
<th align="left">Gentamicin</th>
|
||||
</tr></thead>
|
||||
<tbody><tr class="odd">
|
||||
<td align="left">73.7% (71.7-75.8%)</td>
|
||||
<td align="left">77% (74.3-79.4%)</td>
|
||||
<td align="left">72.8% (70.7-74.8%)</td>
|
||||
<td align="left">74.2% (72.1-76.1%)</td>
|
||||
<td align="left">78.4% (75.6-81.1%)</td>
|
||||
<td align="left">72.5% (70.4-74.6%)</td>
|
||||
</tr></tbody>
|
||||
</table>
|
||||
</div>
|
||||
<div class="section level3">
|
||||
<h3 id="use-combination-regimens">Use combination regimens<a class="anchor" aria-label="anchor" href="#use-combination-regimens"></a>
|
||||
</h3>
|
||||
<div class="sourceCode" id="cb4"><pre class="downlit sourceCode r">
|
||||
<p>Combination regimens are specified with a <code>+</code> separator.
|
||||
WISCA evaluates whether <em>at least one</em> agent in the combination
|
||||
covers the pathogen:</p>
|
||||
<div class="sourceCode" id="cb3"><pre class="downlit sourceCode r">
|
||||
<code class="sourceCode R"><span><span class="fu"><a href="../reference/antibiogram.html">wisca</a></span><span class="op">(</span><span class="va">data</span>,</span>
|
||||
<span> antimicrobials <span class="op">=</span> <span class="fu"><a href="https://rdrr.io/r/base/c.html" class="external-link">c</a></span><span class="op">(</span><span class="st">"AMC"</span>, <span class="st">"AMC + CIP"</span>, <span class="st">"AMC + GEN"</span><span class="op">)</span></span>
|
||||
<span><span class="op">)</span></span></code></pre></div>
|
||||
@@ -313,16 +385,18 @@ I (intermediate [CLSI], or susceptible, increased exposure
|
||||
<th align="left">Amoxicillin/clavulanic acid + Gentamicin</th>
|
||||
</tr></thead>
|
||||
<tbody><tr class="odd">
|
||||
<td align="left">73.8% (71.8-75.7%)</td>
|
||||
<td align="left">87.5% (85.9-89%)</td>
|
||||
<td align="left">89.7% (88.2-91.1%)</td>
|
||||
<td align="left">74.2% (72.2-76.1%)</td>
|
||||
<td align="left">88.8% (87.2-90.4%)</td>
|
||||
<td align="left">90.8% (89.4-92.2%)</td>
|
||||
</tr></tbody>
|
||||
</table>
|
||||
</div>
|
||||
<div class="section level3">
|
||||
<h3 id="stratify-by-syndrome">Stratify by syndrome<a class="anchor" aria-label="anchor" href="#stratify-by-syndrome"></a>
|
||||
</h3>
|
||||
<div class="sourceCode" id="cb5"><pre class="downlit sourceCode r">
|
||||
<p>Use <code>syndromic_group</code> to produce separate WISCA estimates
|
||||
per clinical stratum. You can pass a column name or any expression:</p>
|
||||
<div class="sourceCode" id="cb4"><pre class="downlit sourceCode r">
|
||||
<code class="sourceCode R"><span><span class="fu"><a href="../reference/antibiogram.html">wisca</a></span><span class="op">(</span><span class="va">data</span>,</span>
|
||||
<span> antimicrobials <span class="op">=</span> <span class="fu"><a href="https://rdrr.io/r/base/c.html" class="external-link">c</a></span><span class="op">(</span><span class="st">"AMC"</span>, <span class="st">"AMC + CIP"</span>, <span class="st">"AMC + GEN"</span><span class="op">)</span>,</span>
|
||||
<span> syndromic_group <span class="op">=</span> <span class="st">"syndrome"</span></span>
|
||||
@@ -342,22 +416,22 @@ I (intermediate [CLSI], or susceptible, increased exposure
|
||||
</tr></thead>
|
||||
<tbody>
|
||||
<tr class="odd">
|
||||
<td align="left">No UTI</td>
|
||||
<td align="left">70.1% (67.8-72.3%)</td>
|
||||
<td align="left">85.2% (83.1-87.2%)</td>
|
||||
<td align="left">87.1% (85.3-88.7%)</td>
|
||||
<td align="left">Non-UTI</td>
|
||||
<td align="left">70.3% (67.9-72.7%)</td>
|
||||
<td align="left">86.8% (84.9-88.7%)</td>
|
||||
<td align="left">88.4% (86.4-90.2%)</td>
|
||||
</tr>
|
||||
<tr class="even">
|
||||
<td align="left">UTI</td>
|
||||
<td align="left">80.9% (77.7-83.8%)</td>
|
||||
<td align="left">88.2% (85.7-90.5%)</td>
|
||||
<td align="left">90.9% (88.7-93%)</td>
|
||||
<td align="left">80.3% (77-83.3%)</td>
|
||||
<td align="left">88.4% (85.7-90.8%)</td>
|
||||
<td align="left">91% (88.3-93.3%)</td>
|
||||
</tr>
|
||||
</tbody>
|
||||
</table>
|
||||
<p>The <code>AMR</code> package is available in 28 languages, which can
|
||||
all be used for the <code><a href="../reference/antibiogram.html">wisca()</a></code> function too:</p>
|
||||
<div class="sourceCode" id="cb6"><pre class="downlit sourceCode r">
|
||||
<div class="sourceCode" id="cb5"><pre class="downlit sourceCode r">
|
||||
<code class="sourceCode R"><span><span class="fu"><a href="../reference/antibiogram.html">wisca</a></span><span class="op">(</span><span class="va">data</span>,</span>
|
||||
<span> antimicrobials <span class="op">=</span> <span class="fu"><a href="https://rdrr.io/r/base/c.html" class="external-link">c</a></span><span class="op">(</span><span class="st">"AMC"</span>, <span class="st">"AMC + CIP"</span>, <span class="st">"AMC + GEN"</span><span class="op">)</span>,</span>
|
||||
<span> syndromic_group <span class="op">=</span> <span class="fu"><a href="https://rdrr.io/r/base/grep.html" class="external-link">gsub</a></span><span class="op">(</span><span class="st">"UTI"</span>, <span class="st">"UCI"</span>, <span class="va">data</span><span class="op">$</span><span class="va">syndrome</span><span class="op">)</span>,</span>
|
||||
@@ -378,20 +452,36 @@ all be used for the <code><a href="../reference/antibiogram.html">wisca()</a></c
|
||||
</tr></thead>
|
||||
<tbody>
|
||||
<tr class="odd">
|
||||
<td align="left">No UCI</td>
|
||||
<td align="left">70% (67.8-72.4%)</td>
|
||||
<td align="left">85.3% (83.3-87.2%)</td>
|
||||
<td align="left">87% (85.3-88.8%)</td>
|
||||
<td align="left">Non-UCI</td>
|
||||
<td align="left">70.4% (68-72.8%)</td>
|
||||
<td align="left">86.7% (84.6-88.7%)</td>
|
||||
<td align="left">88.5% (86.5-90.2%)</td>
|
||||
</tr>
|
||||
<tr class="even">
|
||||
<td align="left">UCI</td>
|
||||
<td align="left">80.9% (77.7-83.9%)</td>
|
||||
<td align="left">88.2% (85.5-90.6%)</td>
|
||||
<td align="left">90.9% (88.7-93%)</td>
|
||||
<td align="left">80.3% (77.2-83.5%)</td>
|
||||
<td align="left">88.4% (85.5-90.8%)</td>
|
||||
<td align="left">91% (88.4-93.1%)</td>
|
||||
</tr>
|
||||
</tbody>
|
||||
</table>
|
||||
</div>
|
||||
<div class="section level3">
|
||||
<h3 id="interpreting-the-output">Interpreting the output<a class="anchor" aria-label="anchor" href="#interpreting-the-output"></a>
|
||||
</h3>
|
||||
<p>Each row shows the estimated empirical coverage for a regimen, with a
|
||||
95% credible interval. When comparing regimens:</p>
|
||||
<ul>
|
||||
<li>
|
||||
<strong>Overlapping credible intervals</strong> mean there is no
|
||||
statistically significant difference in coverage. If a narrower-spectrum
|
||||
regimen overlaps with a broader one, the narrower-spectrum option can be
|
||||
preferred on stewardship grounds.</li>
|
||||
<li>
|
||||
<strong>Non-overlapping credible intervals</strong> indicate a
|
||||
clinically meaningful difference in coverage.</li>
|
||||
</ul>
|
||||
</div>
|
||||
</div>
|
||||
<div class="section level2">
|
||||
<h2 id="sensible-defaults-which-can-be-customised">Sensible defaults, which can be customised<a class="anchor" aria-label="anchor" href="#sensible-defaults-which-can-be-customised"></a>
|
||||
@@ -407,14 +497,43 @@ susceptible</li>
|
||||
</ul>
|
||||
</div>
|
||||
<div class="section level2">
|
||||
<h2 id="practical-considerations">Practical considerations<a class="anchor" aria-label="anchor" href="#practical-considerations"></a>
|
||||
</h2>
|
||||
<ul>
|
||||
<li>
|
||||
<strong>First isolates only</strong>: always deduplicate using
|
||||
<code><a href="../reference/first_isolate.html">first_isolate()</a></code> before running WISCA. Repeat isolates
|
||||
introduce bias.</li>
|
||||
<li>
|
||||
<strong>Pathogen selection</strong>: consider filtering with
|
||||
<code><a href="../reference/top_n_microorganisms.html">top_n_microorganisms()</a></code>. Including rare contaminants
|
||||
(e.g. CoNS without clinical context) can distort estimates and may
|
||||
artificially lower coverage (Cook <em>et al.</em>, 2022).</li>
|
||||
<li>
|
||||
<strong>Sample size</strong>: coverage estimates become reliable
|
||||
with approximately 100+ isolates. For smaller datasets, consider pooling
|
||||
data from multiple sites, but only after verifying that pathogen
|
||||
distributions are sufficiently similar (Bielicki <em>et al.</em>,
|
||||
2016).</li>
|
||||
<li>
|
||||
<strong>Culture request bias</strong>: WISCA is only as good as the
|
||||
data it is based on. If cultures are selectively requested (e.g. only
|
||||
after treatment failure), the dataset will be biased towards resistant
|
||||
isolates. A robust culture policy is essential for reliable
|
||||
estimates.</li>
|
||||
</ul>
|
||||
</div>
|
||||
<div class="section level2">
|
||||
<h2 id="limitations">Limitations<a class="anchor" aria-label="anchor" href="#limitations"></a>
|
||||
</h2>
|
||||
<ul>
|
||||
<li>It assumes your data are representative</li>
|
||||
<li>No adjustment for patient-level covariates, although these could be
|
||||
passed onto the <code>syndromic_group</code> argument</li>
|
||||
<li>WISCA does not model resistance over time, you might want to use
|
||||
<code>tidymodels</code> for that, for which we <a href="https://amr-for-r.org/articles/AMR_with_tidymodels.html">wrote a
|
||||
<li>It assumes your data are representative of the patient population
|
||||
you are treating</li>
|
||||
<li>No direct adjustment for patient-level covariates, although these
|
||||
can be passed onto the <code>syndromic_group</code> argument for
|
||||
stratification</li>
|
||||
<li>WISCA does not model resistance trends over time; for that, you
|
||||
might want to use <code>tidymodels</code>, for which we <a href="https://amr-for-r.org/articles/AMR_with_tidymodels.html">wrote a
|
||||
basic introduction</a>
|
||||
</li>
|
||||
</ul>
|
||||
@@ -424,24 +543,48 @@ basic introduction</a>
|
||||
</h2>
|
||||
<p>WISCA enables:</p>
|
||||
<ul>
|
||||
<li>Empirical regimen comparison,</li>
|
||||
<li>Syndrome-specific coverage estimation,</li>
|
||||
<li>Fully probabilistic interpretation.</li>
|
||||
<li>
|
||||
<strong>Empirical regimen comparison</strong>, answering the
|
||||
clinician’s actual question</li>
|
||||
<li>
|
||||
<strong>Syndrome-specific coverage estimation</strong>, stratifiable
|
||||
by any clinical variable</li>
|
||||
<li>
|
||||
<strong>Fully probabilistic interpretation</strong>, with credible
|
||||
intervals that honestly communicate uncertainty</li>
|
||||
</ul>
|
||||
<p>It is available in the <code>AMR</code> package via either:</p>
|
||||
<div class="sourceCode" id="cb7"><pre class="downlit sourceCode r">
|
||||
<div class="sourceCode" id="cb6"><pre class="downlit sourceCode r">
|
||||
<code class="sourceCode R"><span><span class="fu"><a href="../reference/antibiogram.html">wisca</a></span><span class="op">(</span><span class="va">...</span><span class="op">)</span></span>
|
||||
<span></span>
|
||||
<span><span class="fu"><a href="../reference/antibiogram.html">antibiogram</a></span><span class="op">(</span><span class="va">...</span>, wisca <span class="op">=</span> <span class="cn">TRUE</span><span class="op">)</span></span></code></pre></div>
|
||||
</div>
|
||||
<div class="section level2">
|
||||
<h2 id="reference">Reference<a class="anchor" aria-label="anchor" href="#reference"></a>
|
||||
<h2 id="references">References<a class="anchor" aria-label="anchor" href="#references"></a>
|
||||
</h2>
|
||||
<p>Bielicki, JA, et al. (2016). <em>Selecting appropriate empirical
|
||||
antibiotic regimens for paediatric bloodstream infections: application
|
||||
of a Bayesian decision model to local and pooled antimicrobial
|
||||
resistance surveillance data.</em> <strong>J Antimicrob
|
||||
Chemother</strong>. 71(3):794-802. <a href="https://doi.org/10.1093/jac/dkv397" class="external-link uri">https://doi.org/10.1093/jac/dkv397</a></p>
|
||||
<ol style="list-style-type: decimal">
|
||||
<li>Hebert C, Ridgway J, Vekhter B, Brown EC, Weber SG, Robicsek A.
|
||||
Demonstration of the weighted-incidence syndromic combination
|
||||
antibiogram: an empiric prescribing decision aid. <em>Infect Control
|
||||
Hosp Epidemiol.</em> 2012;33(4):381-388. <a href="https://doi.org/10.1086/664768" class="external-link uri">https://doi.org/10.1086/664768</a>
|
||||
</li>
|
||||
<li>Randhawa V, Sarwar S, Walker S, Elligsen M, Palmay L, Daneman N.
|
||||
Weighted-incidence syndromic combination antibiograms to guide empiric
|
||||
treatment of critical care infections: a retrospective cohort study.
|
||||
<em>Crit Care.</em> 2014;18(3):R112. <a href="https://doi.org/10.1186/cc13901" class="external-link uri">https://doi.org/10.1186/cc13901</a>
|
||||
</li>
|
||||
<li>Bielicki JA, Sharland M, Johnson AP, Henderson KL, Cromwell DA.
|
||||
Selecting appropriate empirical antibiotic regimens for paediatric
|
||||
bloodstream infections: application of a Bayesian decision model to
|
||||
local and pooled antimicrobial resistance surveillance data. <em>J
|
||||
Antimicrob Chemother.</em> 2016;71(3):794-802. <a href="https://doi.org/10.1093/jac/dkv397" class="external-link uri">https://doi.org/10.1093/jac/dkv397</a>
|
||||
</li>
|
||||
<li>Cook A, Sharland M, Yau Y, Bielicki J. Improving empiric antibiotic
|
||||
prescribing in pediatric bloodstream infections: a potential application
|
||||
of weighted-incidence syndromic combination antibiograms (WISCA).
|
||||
<em>Expert Rev Anti Infect Ther.</em> 2022;20(3):445-456. <a href="https://doi.org/10.1080/14787210.2021.1967145" class="external-link uri">https://doi.org/10.1080/14787210.2021.1967145</a>
|
||||
</li>
|
||||
</ol>
|
||||
</div>
|
||||
</main><aside class="col-md-3"><nav id="toc" aria-label="Table of contents"><h2>On this page</h2>
|
||||
</nav></aside>
|
||||
|
||||
@@ -1,59 +1,61 @@
|
||||
# Estimating Empirical Coverage with WISCA
|
||||
|
||||
> This explainer was largely written by our [AMR for R
|
||||
> Assistant](https://chat.amr-for-r.org), a ChatGPT manually-trained
|
||||
> model able to answer any question about the `AMR` package.
|
||||
## Why WISCA?
|
||||
|
||||
## Introduction
|
||||
When a clinician starts empirical antimicrobial therapy, the causative
|
||||
pathogen is unknown. The question they need answered is not *“what
|
||||
proportion of* E. coli *is susceptible to ciprofloxacin?“* but rather
|
||||
*“what is the probability that this regimen will adequately cover
|
||||
whatever pathogen turns out to be causing my patient’s infection?”*
|
||||
|
||||
Clinical guidelines for empirical antimicrobial therapy require
|
||||
*probabilistic reasoning*: what is the chance that a regimen will cover
|
||||
the likely infecting organisms, before culture results are available?
|
||||
The traditional cumulative antibiogram, as standardised by CLSI M39,
|
||||
cannot answer that question. It presents susceptibility percentages per
|
||||
species per antibiotic, but:
|
||||
|
||||
This is the purpose of **WISCA**, or **Weighted-Incidence Syndromic
|
||||
Combination Antibiogram**.
|
||||
- **It fragments information by organism.** The clinician must mentally
|
||||
combine susceptibility rates across multiple species, weighting by how
|
||||
often each species causes the syndrome, a calculation nobody does at
|
||||
the bedside.
|
||||
- **It ignores pathogen incidence.** A species that causes 2% of
|
||||
infections is given the same visual weight as one that causes 60%.
|
||||
- **It does not evaluate combination regimens.** Much empirical therapy
|
||||
consists of two or more agents, but the traditional antibiogram only
|
||||
shows monotherapy per organism.
|
||||
- **It provides no measure of uncertainty.** A reported “90%
|
||||
susceptible” based on 50 isolates has a 95% confidence interval of
|
||||
roughly 78-97% (Clopper-Pearson), yet the antibiogram presents it as a
|
||||
point estimate without context.
|
||||
|
||||
WISCA is a Bayesian approach that integrates:
|
||||
**WISCA** (Weighted-Incidence Syndromic Combination Antibiogram)
|
||||
resolves all four limitations. It estimates the probability that a
|
||||
regimen will provide adequate empirical coverage for a given infection
|
||||
syndrome, weighted by local pathogen incidence, with full uncertainty
|
||||
quantification via Bayesian inference.
|
||||
|
||||
- **Pathogen prevalence** (how often each species causes the syndrome),
|
||||
- **Regimen susceptibility** (how often a regimen works *if* the
|
||||
pathogen is known),
|
||||
The concept was introduced by Hebert *et al.* (2012), who demonstrated
|
||||
that traditional antibiogram susceptibility rates could be misleading:
|
||||
ciprofloxacin appeared 84% effective against *E. coli* in the
|
||||
traditional antibiogram, but WISCA revealed only 62% coverage for UTI
|
||||
and 37% for abdominal infections, because enterococci (intrinsically
|
||||
resistant) and other species contribute substantially to these
|
||||
syndromes. Randhawa *et al.* (2014) showed that WISCA-guided regimen
|
||||
selection could improve time-to-adequate-coverage on the ICU by over
|
||||
40%. Bielicki *et al.* (2016) introduced the Bayesian framework now used
|
||||
in this package, enabling credible intervals and multi-centre pooling.
|
||||
Cook *et al.* (2022) applied it globally across 52 hospitals in 23
|
||||
countries.
|
||||
|
||||
to estimate the **overall empirical coverage** of antimicrobial
|
||||
regimens, with quantified uncertainty.
|
||||
|
||||
This vignette explains how WISCA works, why it is useful, and how to
|
||||
apply it using the `AMR` package.
|
||||
|
||||
## Why traditional antibiograms fall short
|
||||
|
||||
A standard antibiogram gives you:
|
||||
|
||||
Species → Antibiotic → Susceptibility %
|
||||
|
||||
But clinicians don’t know the species *a priori*. They need to choose a
|
||||
regimen that covers the **likely pathogens**, without knowing which one
|
||||
is present.
|
||||
|
||||
Traditional antibiograms calculate the susceptibility % as just the
|
||||
number of resistant isolates divided by the total number of tested
|
||||
isolates. Therefore, traditional antibiograms:
|
||||
|
||||
- Fragment information by organism,
|
||||
- Do not weight by real-world prevalence,
|
||||
- Do not account for combination therapy or sample size,
|
||||
- Do not provide uncertainty.
|
||||
|
||||
## The idea of WISCA
|
||||
## The idea
|
||||
|
||||
WISCA asks:
|
||||
|
||||
> “What is the **probability** that this regimen **will cover** the
|
||||
> pathogen, given the syndrome?”
|
||||
|
||||
This means combining two things:
|
||||
This means combining two quantities:
|
||||
|
||||
- **Incidence** of each pathogen in the syndrome,
|
||||
- **Pathogen incidence** in the syndrome (how often each species causes
|
||||
it),
|
||||
- **Susceptibility** of each pathogen to the regimen.
|
||||
|
||||
We can write this as:
|
||||
@@ -62,11 +64,11 @@ We can write this as:
|
||||
\text{Coverage} = \sum_i (\text{Incidence}_i \times \text{Susceptibility}_i)
|
||||
```
|
||||
|
||||
For example, suppose:
|
||||
For example, suppose in your hospital:
|
||||
|
||||
- *E. coli* causes 60% of cases, and 90% of *E. coli* are susceptible to
|
||||
- *E. coli* causes 60% of UTIs, and 90% of *E. coli* are susceptible to
|
||||
a drug.
|
||||
- *Klebsiella* causes 40% of cases, and 70% of *Klebsiella* are
|
||||
- *Klebsiella* causes 40% of UTIs, and 70% of *Klebsiella* are
|
||||
susceptible.
|
||||
|
||||
Then:
|
||||
@@ -75,24 +77,32 @@ Then:
|
||||
\text{Coverage} = (0.6 \times 0.9) + (0.4 \times 0.7) = 0.82
|
||||
```
|
||||
|
||||
But in real data, incidence and susceptibility are **estimated from
|
||||
samples**, so they carry uncertainty. WISCA models this
|
||||
**probabilistically**, using conjugate Bayesian distributions.
|
||||
That 82% is a far more clinically meaningful number than the
|
||||
species-level “90% of *E. coli*” and “70% of *Klebsiella*” reported
|
||||
separately in a traditional antibiogram, because it directly answers the
|
||||
question the clinician actually faces.
|
||||
|
||||
## The Bayesian engine behind WISCA
|
||||
But in real data, both incidence and susceptibility are **estimated from
|
||||
finite samples**, so they carry uncertainty. A sample of 50 isolates is
|
||||
not a census. WISCA models this uncertainty **probabilistically**, using
|
||||
conjugate Bayesian distributions.
|
||||
|
||||
## The Bayesian engine
|
||||
|
||||
### Pathogen incidence
|
||||
|
||||
Let:
|
||||
|
||||
- $`K`$ be the number of pathogens,
|
||||
- $`\alpha = (1, 1, \ldots, 1)`$ be a **Dirichlet** prior (uniform),
|
||||
- $`n = (n_1, \ldots, n_K)`$ be the observed counts per species.
|
||||
- $`\boldsymbol{\alpha} = (1, 1, \ldots, 1)`$ be a $`\text{Dirichlet}`$
|
||||
prior (uniform, non-informative),
|
||||
- $`\boldsymbol{n} = (n_1, \ldots, n_K)`$ be the observed isolate counts
|
||||
per species.
|
||||
|
||||
Then the posterior incidence is:
|
||||
|
||||
``` math
|
||||
p \sim \text{Dirichlet}(\alpha_1 + n_1, \ldots, \alpha_K + n_K)
|
||||
\boldsymbol{p} \sim \text{Dirichlet}(\alpha_1 + n_1, \ldots, \alpha_K + n_K)
|
||||
```
|
||||
|
||||
To simulate from this, we use:
|
||||
@@ -101,12 +111,21 @@ To simulate from this, we use:
|
||||
x_i \sim \text{Gamma}(\alpha_i + n_i,\ 1), \quad p_i = \frac{x_i}{\sum_{j=1}^{K} x_j}
|
||||
```
|
||||
|
||||
The Dirichlet is the conjugate prior for multinomial data. With the
|
||||
non-informative prior $`\text{Dirichlet}(1, 1, \ldots, 1)`$, the
|
||||
posterior is dominated by the data once sample sizes are reasonable.
|
||||
With small samples, the posterior is appropriately more diffuse,
|
||||
reflecting genuine uncertainty, and the resulting credible intervals
|
||||
will be wider.
|
||||
|
||||
### Susceptibility
|
||||
|
||||
Each pathogen–regimen pair has a prior and data:
|
||||
Each pathogen-regimen pair has a prior and observed data:
|
||||
|
||||
- Prior: $`\text{Beta}(\alpha_0, \beta_0)`$, with default
|
||||
$`\alpha_0 = \beta_0 = 1`$
|
||||
- Default prior: $`\text{Beta}(0.5, 0.5)`$ (Jeffreys prior)
|
||||
- Intrinsically resistant pairs: $`\text{Beta}(1, 9999)`$, forcing
|
||||
near-zero susceptibility regardless of observed data (based on EUCAST
|
||||
Expected Resistant Phenotypes)
|
||||
- Data: $`S`$ susceptible out of $`N`$ tested
|
||||
|
||||
The $`S`$ category could also include values SDD (susceptible,
|
||||
@@ -126,21 +145,44 @@ Putting it together:
|
||||
1. Simulate pathogen incidence:
|
||||
$`\boldsymbol{p} \sim \text{Dirichlet}`$
|
||||
2. Simulate susceptibility:
|
||||
$`\theta_i \sim \text{Beta}(1 + S_i,\ 1 + R_i)`$
|
||||
$`\theta_i \sim \text{Beta}(\alpha_0 + S_i,\ \beta_0 + N_i - S_i)`$
|
||||
3. Combine:
|
||||
|
||||
``` math
|
||||
\text{Coverage} = \sum_{i=1}^{K} p_i \cdot \theta_i
|
||||
```
|
||||
|
||||
Repeat this simulation (e.g. 1000×) and summarise:
|
||||
Repeat this simulation (e.g., 1000 times) and summarise:
|
||||
|
||||
- **Mean** = expected coverage
|
||||
- **Quantiles** = credible interval
|
||||
- **Quantiles** = credible interval (95% by default)
|
||||
|
||||
Because each simulation draws from the full posterior, the resulting
|
||||
distribution of coverage estimates naturally captures the joint
|
||||
uncertainty in both pathogen incidence and susceptibility. The credible
|
||||
interval tells you how confident you can be in the coverage estimate,
|
||||
something a traditional antibiogram never provides.
|
||||
|
||||
## When to use WISCA vs. traditional antibiograms
|
||||
|
||||
| Goal | Recommended approach |
|
||||
|---------------------------------------|---------------------------|
|
||||
| Guide empirical therapy decisions | **WISCA** |
|
||||
| Compare regimens for a syndrome | **WISCA** |
|
||||
| Evaluate combination regimens | **WISCA** |
|
||||
| Antimicrobial stewardship (A-team) | **WISCA** |
|
||||
| Track resistance trends per species | Traditional / Combination |
|
||||
| AMR surveillance reporting | Traditional / Syndromic |
|
||||
| Understand species-level epidemiology | Traditional |
|
||||
|
||||
In short: if the end goal involves a *patient* who does not yet have a
|
||||
culture result, WISCA is the appropriate tool. If the end goal is
|
||||
*surveillance* of resistance at the species level, the traditional
|
||||
antibiogram remains fit for purpose.
|
||||
|
||||
## Practical use in the `AMR` package
|
||||
|
||||
### Prepare data and simulate synthetic syndrome
|
||||
### Prepare data
|
||||
|
||||
``` r
|
||||
|
||||
@@ -170,11 +212,11 @@ data
|
||||
#> # TCY <sir>, TGC <sir>, DOX <sir>, ERY <sir>, CLI <sir>, AZM <sir>,
|
||||
#> # IPM <sir>, MEM <sir>, MTR <sir>, CHL <sir>, COL <sir>, MUP <sir>, …
|
||||
|
||||
# Add a fake syndrome column
|
||||
data$syndrome <- ifelse(data$mo %like% "coli", "UTI", "No UTI")
|
||||
# Add a synthetic syndrome column for demonstration
|
||||
data$syndrome <- ifelse(data$mo %like% "coli", "UTI", "Non-UTI")
|
||||
```
|
||||
|
||||
### Basic WISCA antibiogram
|
||||
### Basic WISCA
|
||||
|
||||
``` r
|
||||
|
||||
@@ -183,12 +225,15 @@ wisca(data,
|
||||
)
|
||||
```
|
||||
|
||||
| Amoxicillin/clavulanic acid | Ciprofloxacin | Gentamicin |
|
||||
|:----------------------------|:-----------------|:-------------------|
|
||||
| 73.7% (71.7-75.8%) | 77% (74.3-79.4%) | 72.8% (70.7-74.8%) |
|
||||
| Amoxicillin/clavulanic acid | Ciprofloxacin | Gentamicin |
|
||||
|:----------------------------|:-------------------|:-------------------|
|
||||
| 74.2% (72.1-76.1%) | 78.4% (75.6-81.1%) | 72.5% (70.4-74.6%) |
|
||||
|
||||
### Use combination regimens
|
||||
|
||||
Combination regimens are specified with a `+` separator. WISCA evaluates
|
||||
whether *at least one* agent in the combination covers the pathogen:
|
||||
|
||||
``` r
|
||||
|
||||
wisca(data,
|
||||
@@ -198,10 +243,13 @@ wisca(data,
|
||||
|
||||
| Amoxicillin/clavulanic acid | Amoxicillin/clavulanic acid + Ciprofloxacin | Amoxicillin/clavulanic acid + Gentamicin |
|
||||
|:---|:---|:---|
|
||||
| 73.8% (71.8-75.7%) | 87.5% (85.9-89%) | 89.7% (88.2-91.1%) |
|
||||
| 74.2% (72.2-76.1%) | 88.8% (87.2-90.4%) | 90.8% (89.4-92.2%) |
|
||||
|
||||
### Stratify by syndrome
|
||||
|
||||
Use `syndromic_group` to produce separate WISCA estimates per clinical
|
||||
stratum. You can pass a column name or any expression:
|
||||
|
||||
``` r
|
||||
|
||||
wisca(data,
|
||||
@@ -212,8 +260,8 @@ wisca(data,
|
||||
|
||||
| Syndromic Group | Amoxicillin/clavulanic acid | Amoxicillin/clavulanic acid + Ciprofloxacin | Amoxicillin/clavulanic acid + Gentamicin |
|
||||
|:---|:---|:---|:---|
|
||||
| No UTI | 70.1% (67.8-72.3%) | 85.2% (83.1-87.2%) | 87.1% (85.3-88.7%) |
|
||||
| UTI | 80.9% (77.7-83.8%) | 88.2% (85.7-90.5%) | 90.9% (88.7-93%) |
|
||||
| Non-UTI | 70.3% (67.9-72.7%) | 86.8% (84.9-88.7%) | 88.4% (86.4-90.2%) |
|
||||
| UTI | 80.3% (77-83.3%) | 88.4% (85.7-90.8%) | 91% (88.3-93.3%) |
|
||||
|
||||
The `AMR` package is available in 28 languages, which can all be used
|
||||
for the [`wisca()`](https://amr-for-r.org/reference/antibiogram.md)
|
||||
@@ -230,8 +278,20 @@ wisca(data,
|
||||
|
||||
| Grupo sindrómico | Amoxicilina/ácido clavulánico | Amoxicilina/ácido clavulánico + Ciprofloxacina | Amoxicilina/ácido clavulánico + Gentamicina |
|
||||
|:---|:---|:---|:---|
|
||||
| No UCI | 70% (67.8-72.4%) | 85.3% (83.3-87.2%) | 87% (85.3-88.8%) |
|
||||
| UCI | 80.9% (77.7-83.9%) | 88.2% (85.5-90.6%) | 90.9% (88.7-93%) |
|
||||
| Non-UCI | 70.4% (68-72.8%) | 86.7% (84.6-88.7%) | 88.5% (86.5-90.2%) |
|
||||
| UCI | 80.3% (77.2-83.5%) | 88.4% (85.5-90.8%) | 91% (88.4-93.1%) |
|
||||
|
||||
### Interpreting the output
|
||||
|
||||
Each row shows the estimated empirical coverage for a regimen, with a
|
||||
95% credible interval. When comparing regimens:
|
||||
|
||||
- **Overlapping credible intervals** mean there is no statistically
|
||||
significant difference in coverage. If a narrower-spectrum regimen
|
||||
overlaps with a broader one, the narrower-spectrum option can be
|
||||
preferred on stewardship grounds.
|
||||
- **Non-overlapping credible intervals** indicate a clinically
|
||||
meaningful difference in coverage.
|
||||
|
||||
## Sensible defaults, which can be customised
|
||||
|
||||
@@ -239,22 +299,45 @@ wisca(data,
|
||||
- `conf_interval = 0.95`: coverage interval width
|
||||
- `combine_SI = TRUE`: count “I” and “SDD” as susceptible
|
||||
|
||||
## Practical considerations
|
||||
|
||||
- **First isolates only**: always deduplicate using
|
||||
[`first_isolate()`](https://amr-for-r.org/reference/first_isolate.md)
|
||||
before running WISCA. Repeat isolates introduce bias.
|
||||
- **Pathogen selection**: consider filtering with
|
||||
[`top_n_microorganisms()`](https://amr-for-r.org/reference/top_n_microorganisms.md).
|
||||
Including rare contaminants (e.g. CoNS without clinical context) can
|
||||
distort estimates and may artificially lower coverage (Cook *et al.*,
|
||||
2022).
|
||||
- **Sample size**: coverage estimates become reliable with approximately
|
||||
100+ isolates. For smaller datasets, consider pooling data from
|
||||
multiple sites, but only after verifying that pathogen distributions
|
||||
are sufficiently similar (Bielicki *et al.*, 2016).
|
||||
- **Culture request bias**: WISCA is only as good as the data it is
|
||||
based on. If cultures are selectively requested (e.g. only after
|
||||
treatment failure), the dataset will be biased towards resistant
|
||||
isolates. A robust culture policy is essential for reliable estimates.
|
||||
|
||||
## Limitations
|
||||
|
||||
- It assumes your data are representative
|
||||
- No adjustment for patient-level covariates, although these could be
|
||||
passed onto the `syndromic_group` argument
|
||||
- WISCA does not model resistance over time, you might want to use
|
||||
`tidymodels` for that, for which we [wrote a basic
|
||||
- It assumes your data are representative of the patient population you
|
||||
are treating
|
||||
- No direct adjustment for patient-level covariates, although these can
|
||||
be passed onto the `syndromic_group` argument for stratification
|
||||
- WISCA does not model resistance trends over time; for that, you might
|
||||
want to use `tidymodels`, for which we [wrote a basic
|
||||
introduction](https://amr-for-r.org/articles/AMR_with_tidymodels.html)
|
||||
|
||||
## Summary
|
||||
|
||||
WISCA enables:
|
||||
|
||||
- Empirical regimen comparison,
|
||||
- Syndrome-specific coverage estimation,
|
||||
- Fully probabilistic interpretation.
|
||||
- **Empirical regimen comparison**, answering the clinician’s actual
|
||||
question
|
||||
- **Syndrome-specific coverage estimation**, stratifiable by any
|
||||
clinical variable
|
||||
- **Fully probabilistic interpretation**, with credible intervals that
|
||||
honestly communicate uncertainty
|
||||
|
||||
It is available in the `AMR` package via either:
|
||||
|
||||
@@ -265,10 +348,26 @@ wisca(...)
|
||||
antibiogram(..., wisca = TRUE)
|
||||
```
|
||||
|
||||
## Reference
|
||||
## References
|
||||
|
||||
Bielicki, JA, et al. (2016). *Selecting appropriate empirical antibiotic
|
||||
regimens for paediatric bloodstream infections: application of a
|
||||
Bayesian decision model to local and pooled antimicrobial resistance
|
||||
surveillance data.* **J Antimicrob Chemother**. 71(3):794-802.
|
||||
<https://doi.org/10.1093/jac/dkv397>
|
||||
1. Hebert C, Ridgway J, Vekhter B, Brown EC, Weber SG, Robicsek A.
|
||||
Demonstration of the weighted-incidence syndromic combination
|
||||
antibiogram: an empiric prescribing decision aid. *Infect Control
|
||||
Hosp Epidemiol.* 2012;33(4):381-388.
|
||||
<https://doi.org/10.1086/664768>
|
||||
2. Randhawa V, Sarwar S, Walker S, Elligsen M, Palmay L, Daneman N.
|
||||
Weighted-incidence syndromic combination antibiograms to guide
|
||||
empiric treatment of critical care infections: a retrospective
|
||||
cohort study. *Crit Care.* 2014;18(3):R112.
|
||||
<https://doi.org/10.1186/cc13901>
|
||||
3. Bielicki JA, Sharland M, Johnson AP, Henderson KL, Cromwell DA.
|
||||
Selecting appropriate empirical antibiotic regimens for paediatric
|
||||
bloodstream infections: application of a Bayesian decision model to
|
||||
local and pooled antimicrobial resistance surveillance data. *J
|
||||
Antimicrob Chemother.* 2016;71(3):794-802.
|
||||
<https://doi.org/10.1093/jac/dkv397>
|
||||
4. Cook A, Sharland M, Yau Y, Bielicki J. Improving empiric antibiotic
|
||||
prescribing in pediatric bloodstream infections: a potential
|
||||
application of weighted-incidence syndromic combination antibiograms
|
||||
(WISCA). *Expert Rev Anti Infect Ther.* 2022;20(3):445-456.
|
||||
<https://doi.org/10.1080/14787210.2021.1967145>
|
||||
|
||||
@@ -12,8 +12,8 @@
|
||||
<link rel="icon" sizes="any" href="../favicon.ico">
|
||||
<link rel="manifest" href="../site.webmanifest">
|
||||
<script src="../deps/jquery-3.6.0/jquery-3.6.0.min.js"></script><meta name="viewport" content="width=device-width, initial-scale=1, shrink-to-fit=no">
|
||||
<link href="../deps/bootstrap-5.3.1/bootstrap.min.css" rel="stylesheet">
|
||||
<script src="../deps/bootstrap-5.3.1/bootstrap.bundle.min.js"></script><link href="../deps/Lato-0.4.10/font.css" rel="stylesheet">
|
||||
<link href="../deps/bootstrap-5.3.8/bootstrap.min.css" rel="stylesheet">
|
||||
<script src="../deps/bootstrap-5.3.8/bootstrap.bundle.min.js"></script><link href="../deps/Lato-0.4.10/font.css" rel="stylesheet">
|
||||
<link href="../deps/Fira_Code-0.4.10/font.css" rel="stylesheet">
|
||||
<link href="../deps/font-awesome-6.5.2/css/all.min.css" rel="stylesheet">
|
||||
<link href="../deps/font-awesome-6.5.2/css/v4-shims.min.css" rel="stylesheet">
|
||||
@@ -30,7 +30,7 @@
|
||||
|
||||
<a class="navbar-brand me-2" href="../index.html">AMR (for R)</a>
|
||||
|
||||
<small class="nav-text text-muted me-auto" data-bs-toggle="tooltip" data-bs-placement="bottom" title="">3.0.1.9057</small>
|
||||
<small class="nav-text text-muted me-auto" data-bs-toggle="tooltip" data-bs-placement="bottom" title="">3.0.1.9061</small>
|
||||
|
||||
|
||||
<button class="navbar-toggler" type="button" data-bs-toggle="collapse" data-bs-target="#navbar" aria-controls="navbar" aria-expanded="false" aria-label="Toggle navigation">
|
||||
@@ -80,7 +80,7 @@
|
||||
<main id="main" class="col-md-9"><div class="page-header">
|
||||
<img src="../logo.svg" class="logo" alt=""><h1>Download data sets for download / own use</h1>
|
||||
|
||||
<h4 data-toc-skip class="date">02 May 2026</h4>
|
||||
<h4 data-toc-skip class="date">23 June 2026</h4>
|
||||
|
||||
<small class="dont-index">Source: <a href="https://github.com/msberends/AMR/blob/main/vignettes/datasets.Rmd" class="external-link"><code>vignettes/datasets.Rmd</code></a></small>
|
||||
<div class="d-none name"><code>datasets.Rmd</code></div>
|
||||
@@ -104,42 +104,43 @@ available in Python.</p>
|
||||
<h2 id="microorganisms-full-microbial-taxonomy">
|
||||
<code>microorganisms</code>: Full Microbial Taxonomy<a class="anchor" aria-label="anchor" href="#microorganisms-full-microbial-taxonomy"></a>
|
||||
</h2>
|
||||
<p>A data set with 78 679 rows and 26 columns, containing the following
|
||||
column names:<br><em>mo</em>, <em>fullname</em>, <em>status</em>, <em>kingdom</em>,
|
||||
<em>phylum</em>, <em>class</em>, <em>order</em>, <em>family</em>,
|
||||
<em>genus</em>, <em>species</em>, <em>subspecies</em>, <em>rank</em>,
|
||||
<em>ref</em>, <em>oxygen_tolerance</em>, <em>source</em>, <em>lpsn</em>,
|
||||
<p>A data set with 96 982 rows and 28 columns, containing the following
|
||||
column names:<br><em>mo</em>, <em>fullname</em>, <em>status</em>, <em>domain</em>,
|
||||
<em>kingdom</em>, <em>phylum</em>, <em>class</em>, <em>order</em>,
|
||||
<em>family</em>, <em>genus</em>, <em>species</em>, <em>subspecies</em>,
|
||||
<em>rank</em>, <em>ref</em>, <em>oxygen_tolerance</em>,
|
||||
<em>morphology</em>, <em>source</em>, <em>lpsn</em>,
|
||||
<em>lpsn_parent</em>, <em>lpsn_renamed_to</em>, <em>mycobank</em>,
|
||||
<em>mycobank_parent</em>, <em>mycobank_renamed_to</em>, <em>gbif</em>,
|
||||
<em>gbif_parent</em>, <em>gbif_renamed_to</em>, <em>prevalence</em>, and
|
||||
<em>snomed</em>.</p>
|
||||
<p>This data set is in R available as <code>microorganisms</code>, after
|
||||
you load the <code>AMR</code> package.</p>
|
||||
<p>It was last updated on 18 September 2025 12:58:34 UTC. Find more info
|
||||
<p>It was last updated on 22 June 2026 23:38:13 UTC. Find more info
|
||||
about the contents, (scientific) source, and structure of this <a href="https://amr-for-r.org/reference/microorganisms.html">data set
|
||||
here</a>.</p>
|
||||
<p><strong>Direct download links:</strong></p>
|
||||
<ul>
|
||||
<li>Download as <a href="https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.rds" class="external-link">original
|
||||
R Data Structure (RDS) file</a> (1.8 MB)<br>
|
||||
R Data Structure (RDS) file</a> (2.2 MB)<br>
|
||||
</li>
|
||||
<li>Download as <a href="https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.txt" class="external-link">tab-separated
|
||||
text file</a> (17.7 MB)<br>
|
||||
text file</a> (23.1 MB)<br>
|
||||
</li>
|
||||
<li>Download as <a href="https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.xlsx" class="external-link">Microsoft
|
||||
Excel workbook</a> (8.8 MB)<br>
|
||||
Excel workbook</a> (11.4 MB)<br>
|
||||
</li>
|
||||
<li>Download as <a href="https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.feather" class="external-link">Apache
|
||||
Feather file</a> (8.4 MB)<br>
|
||||
Feather file</a> (11 MB)<br>
|
||||
</li>
|
||||
<li>Download as <a href="https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.parquet" class="external-link">Apache
|
||||
Parquet file</a> (3.8 MB)<br>
|
||||
Parquet file</a> (4.6 MB)<br>
|
||||
</li>
|
||||
<li>Download as <a href="https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.sav" class="external-link">IBM
|
||||
SPSS Statistics data file</a> (28.4 MB)<br>
|
||||
SPSS Statistics data file</a> (35.2 MB)<br>
|
||||
</li>
|
||||
<li>Download as <a href="https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.dta" class="external-link">Stata
|
||||
DTA file</a> (89.5 MB)</li>
|
||||
DTA file</a> (96.6 MB)</li>
|
||||
</ul>
|
||||
<p><strong>NOTE: The exported files for SPSS and Stata contain only the
|
||||
first 50 SNOMED codes per record, as their file size would otherwise
|
||||
@@ -157,41 +158,42 @@ all SNOMED codes as comma separated values.</p>
|
||||
</tr></thead>
|
||||
<tbody>
|
||||
<tr class="odd">
|
||||
<td align="center">(unknown kingdom)</td>
|
||||
<td align="center">1</td>
|
||||
<td align="center"></td>
|
||||
<td align="center">20</td>
|
||||
</tr>
|
||||
<tr class="even">
|
||||
<td align="center">Animalia</td>
|
||||
<td align="center">1 628</td>
|
||||
<td align="center">(unknown kingdom)</td>
|
||||
<td align="center">8</td>
|
||||
</tr>
|
||||
<tr class="odd">
|
||||
<td align="center">Animalia</td>
|
||||
<td align="center">2 015</td>
|
||||
</tr>
|
||||
<tr class="even">
|
||||
<td align="center">Archaea</td>
|
||||
<td align="center">1 419</td>
|
||||
<td align="center">150</td>
|
||||
</tr>
|
||||
<tr class="odd">
|
||||
<td align="center">Bacillati</td>
|
||||
<td align="center">24 200</td>
|
||||
</tr>
|
||||
<tr class="even">
|
||||
<td align="center">Bacteria</td>
|
||||
<td align="center">39 249</td>
|
||||
</tr>
|
||||
<tr class="odd">
|
||||
<td align="center">Chromista</td>
|
||||
<td align="center">178</td>
|
||||
</tr>
|
||||
<tr class="even">
|
||||
<td align="center">Fungi</td>
|
||||
<td align="center">28 137</td>
|
||||
<td align="center">2</td>
|
||||
</tr>
|
||||
</tbody>
|
||||
</table>
|
||||
<p>First 6 rows when filtering on genus <em>Escherichia</em>:</p>
|
||||
<table style="width:100%;" class="table">
|
||||
<table class="table">
|
||||
<colgroup>
|
||||
<col width="4%">
|
||||
<col width="6%">
|
||||
<col width="5%">
|
||||
<col width="2%">
|
||||
<col width="2%">
|
||||
<col width="3%">
|
||||
<col width="3%">
|
||||
<col width="4%">
|
||||
<col width="4%">
|
||||
<col width="3%">
|
||||
<col width="4%">
|
||||
<col width="2%">
|
||||
<col width="3%">
|
||||
@@ -199,6 +201,7 @@ all SNOMED codes as comma separated values.</p>
|
||||
<col width="2%">
|
||||
<col width="5%">
|
||||
<col width="6%">
|
||||
<col width="2%">
|
||||
<col width="1%">
|
||||
<col width="1%">
|
||||
<col width="2%">
|
||||
@@ -210,12 +213,13 @@ all SNOMED codes as comma separated values.</p>
|
||||
<col width="2%">
|
||||
<col width="3%">
|
||||
<col width="2%">
|
||||
<col width="10%">
|
||||
<col width="9%">
|
||||
</colgroup>
|
||||
<thead><tr class="header">
|
||||
<th align="center">mo</th>
|
||||
<th align="center">fullname</th>
|
||||
<th align="center">status</th>
|
||||
<th align="center">domain</th>
|
||||
<th align="center">kingdom</th>
|
||||
<th align="center">phylum</th>
|
||||
<th align="center">class</th>
|
||||
@@ -227,6 +231,7 @@ all SNOMED codes as comma separated values.</p>
|
||||
<th align="center">rank</th>
|
||||
<th align="center">ref</th>
|
||||
<th align="center">oxygen_tolerance</th>
|
||||
<th align="center">morphology</th>
|
||||
<th align="center">source</th>
|
||||
<th align="center">lpsn</th>
|
||||
<th align="center">lpsn_parent</th>
|
||||
@@ -246,6 +251,7 @@ all SNOMED codes as comma separated values.</p>
|
||||
<td align="center">Escherichia</td>
|
||||
<td align="center">accepted</td>
|
||||
<td align="center">Bacteria</td>
|
||||
<td align="center">Pseudomonadati</td>
|
||||
<td align="center">Pseudomonadota</td>
|
||||
<td align="center">Gammaproteobacteria</td>
|
||||
<td align="center">Enterobacterales</td>
|
||||
@@ -256,6 +262,7 @@ all SNOMED codes as comma separated values.</p>
|
||||
<td align="center">genus</td>
|
||||
<td align="center">Castellani et al., 1919</td>
|
||||
<td align="center">facultative anaerobe</td>
|
||||
<td align="center">rods</td>
|
||||
<td align="center">LPSN</td>
|
||||
<td align="center">515602</td>
|
||||
<td align="center">482</td>
|
||||
@@ -263,8 +270,8 @@ all SNOMED codes as comma separated values.</p>
|
||||
<td align="center"></td>
|
||||
<td align="center"></td>
|
||||
<td align="center"></td>
|
||||
<td align="center"></td>
|
||||
<td align="center">11158430</td>
|
||||
<td align="center">CS33H</td>
|
||||
<td align="center">CRYWR</td>
|
||||
<td align="center"></td>
|
||||
<td align="center">1</td>
|
||||
<td align="center">407310004, 407251000, 407281008, …</td>
|
||||
@@ -274,6 +281,7 @@ all SNOMED codes as comma separated values.</p>
|
||||
<td align="center">Escherichia adecarboxylata</td>
|
||||
<td align="center">synonym</td>
|
||||
<td align="center">Bacteria</td>
|
||||
<td align="center">Pseudomonadati</td>
|
||||
<td align="center">Pseudomonadota</td>
|
||||
<td align="center">Gammaproteobacteria</td>
|
||||
<td align="center">Enterobacterales</td>
|
||||
@@ -284,6 +292,7 @@ all SNOMED codes as comma separated values.</p>
|
||||
<td align="center">species</td>
|
||||
<td align="center">Leclerc, 1962</td>
|
||||
<td align="center">likely facultative anaerobe</td>
|
||||
<td align="center">rods</td>
|
||||
<td align="center">LPSN</td>
|
||||
<td align="center">776052</td>
|
||||
<td align="center">515602</td>
|
||||
@@ -291,9 +300,9 @@ all SNOMED codes as comma separated values.</p>
|
||||
<td align="center"></td>
|
||||
<td align="center"></td>
|
||||
<td align="center"></td>
|
||||
<td align="center"></td>
|
||||
<td align="center"></td>
|
||||
<td align="center"></td>
|
||||
<td align="center">CS33J</td>
|
||||
<td align="center">CS33H</td>
|
||||
<td align="center">3SVX6</td>
|
||||
<td align="center">1</td>
|
||||
<td align="center"></td>
|
||||
</tr>
|
||||
@@ -302,6 +311,7 @@ all SNOMED codes as comma separated values.</p>
|
||||
<td align="center">Escherichia albertii</td>
|
||||
<td align="center">accepted</td>
|
||||
<td align="center">Bacteria</td>
|
||||
<td align="center">Pseudomonadati</td>
|
||||
<td align="center">Pseudomonadota</td>
|
||||
<td align="center">Gammaproteobacteria</td>
|
||||
<td align="center">Enterobacterales</td>
|
||||
@@ -312,6 +322,7 @@ all SNOMED codes as comma separated values.</p>
|
||||
<td align="center">species</td>
|
||||
<td align="center">Huys et al., 2003</td>
|
||||
<td align="center">facultative anaerobe</td>
|
||||
<td align="center">rods</td>
|
||||
<td align="center">LPSN</td>
|
||||
<td align="center">776053</td>
|
||||
<td align="center">515602</td>
|
||||
@@ -319,8 +330,8 @@ all SNOMED codes as comma separated values.</p>
|
||||
<td align="center"></td>
|
||||
<td align="center"></td>
|
||||
<td align="center"></td>
|
||||
<td align="center">5427575</td>
|
||||
<td align="center"></td>
|
||||
<td align="center">3BGTB</td>
|
||||
<td align="center">CS33H</td>
|
||||
<td align="center"></td>
|
||||
<td align="center">1</td>
|
||||
<td align="center">419388003</td>
|
||||
@@ -330,6 +341,7 @@ all SNOMED codes as comma separated values.</p>
|
||||
<td align="center">Escherichia blattae</td>
|
||||
<td align="center">synonym</td>
|
||||
<td align="center">Bacteria</td>
|
||||
<td align="center">Pseudomonadati</td>
|
||||
<td align="center">Pseudomonadota</td>
|
||||
<td align="center">Gammaproteobacteria</td>
|
||||
<td align="center">Enterobacterales</td>
|
||||
@@ -340,6 +352,7 @@ all SNOMED codes as comma separated values.</p>
|
||||
<td align="center">species</td>
|
||||
<td align="center">Burgess et al., 1973</td>
|
||||
<td align="center">likely facultative anaerobe</td>
|
||||
<td align="center">rods</td>
|
||||
<td align="center">LPSN</td>
|
||||
<td align="center">776056</td>
|
||||
<td align="center">515602</td>
|
||||
@@ -347,9 +360,9 @@ all SNOMED codes as comma separated values.</p>
|
||||
<td align="center"></td>
|
||||
<td align="center"></td>
|
||||
<td align="center"></td>
|
||||
<td align="center"></td>
|
||||
<td align="center"></td>
|
||||
<td align="center"></td>
|
||||
<td align="center">CS33K</td>
|
||||
<td align="center">CS33H</td>
|
||||
<td align="center">4X4P7</td>
|
||||
<td align="center">1</td>
|
||||
<td align="center"></td>
|
||||
</tr>
|
||||
@@ -358,6 +371,7 @@ all SNOMED codes as comma separated values.</p>
|
||||
<td align="center">Escherichia coli</td>
|
||||
<td align="center">accepted</td>
|
||||
<td align="center">Bacteria</td>
|
||||
<td align="center">Pseudomonadati</td>
|
||||
<td align="center">Pseudomonadota</td>
|
||||
<td align="center">Gammaproteobacteria</td>
|
||||
<td align="center">Enterobacterales</td>
|
||||
@@ -368,6 +382,7 @@ all SNOMED codes as comma separated values.</p>
|
||||
<td align="center">species</td>
|
||||
<td align="center">Castellani et al., 1919</td>
|
||||
<td align="center">facultative anaerobe</td>
|
||||
<td align="center">rods</td>
|
||||
<td align="center">LPSN</td>
|
||||
<td align="center">776057</td>
|
||||
<td align="center">515602</td>
|
||||
@@ -375,8 +390,8 @@ all SNOMED codes as comma separated values.</p>
|
||||
<td align="center"></td>
|
||||
<td align="center"></td>
|
||||
<td align="center"></td>
|
||||
<td align="center">11286021</td>
|
||||
<td align="center"></td>
|
||||
<td align="center">NT3L7</td>
|
||||
<td align="center">CS33H</td>
|
||||
<td align="center"></td>
|
||||
<td align="center">1</td>
|
||||
<td align="center">1095001000112106, 715307006, 737528008, …</td>
|
||||
@@ -386,6 +401,7 @@ all SNOMED codes as comma separated values.</p>
|
||||
<td align="center">Escherichia coli coli</td>
|
||||
<td align="center">accepted</td>
|
||||
<td align="center">Bacteria</td>
|
||||
<td align="center">Pseudomonadati</td>
|
||||
<td align="center">Pseudomonadota</td>
|
||||
<td align="center">Gammaproteobacteria</td>
|
||||
<td align="center">Enterobacterales</td>
|
||||
@@ -396,6 +412,7 @@ all SNOMED codes as comma separated values.</p>
|
||||
<td align="center">subspecies</td>
|
||||
<td align="center"></td>
|
||||
<td align="center"></td>
|
||||
<td align="center"></td>
|
||||
<td align="center">GBIF</td>
|
||||
<td align="center"></td>
|
||||
<td align="center">776057</td>
|
||||
@@ -404,7 +421,7 @@ all SNOMED codes as comma separated values.</p>
|
||||
<td align="center"></td>
|
||||
<td align="center"></td>
|
||||
<td align="center">12233256</td>
|
||||
<td align="center">11286021</td>
|
||||
<td align="center">NT3L7</td>
|
||||
<td align="center"></td>
|
||||
<td align="center">1</td>
|
||||
<td align="center"></td>
|
||||
@@ -424,8 +441,8 @@ column names:<br><em>ab</em>, <em>cid</em>, <em>name</em>, <em>group</em>, <em>a
|
||||
<em>iv_ddd</em>, <em>iv_units</em>, and <em>loinc</em>.</p>
|
||||
<p>This data set is in R available as <code>antimicrobials</code>, after
|
||||
you load the <code>AMR</code> package.</p>
|
||||
<p>It was last updated on 2 May 2026 12:56:26 UTC. Find more info about
|
||||
the contents, (scientific) source, and structure of this <a href="https://amr-for-r.org/reference/antimicrobials.html">data set
|
||||
<p>It was last updated on 23 June 2026 12:38:59 UTC. Find more info
|
||||
about the contents, (scientific) source, and structure of this <a href="https://amr-for-r.org/reference/antimicrobials.html">data set
|
||||
here</a>.</p>
|
||||
<p><strong>Direct download links:</strong></p>
|
||||
<ul>
|
||||
@@ -595,14 +612,14 @@ inhibitors</td>
|
||||
<code>clinical_breakpoints</code>: Interpretation from MIC values
|
||||
& disk diameters to SIR<a class="anchor" aria-label="anchor" href="#clinical_breakpoints-interpretation-from-mic-values-disk-diameters-to-sir"></a>
|
||||
</h2>
|
||||
<p>A data set with 45 730 rows and 14 columns, containing the following
|
||||
<p>A data set with 45 555 rows and 14 columns, containing the following
|
||||
column names:<br><em>guideline</em>, <em>type</em>, <em>host</em>, <em>method</em>,
|
||||
<em>site</em>, <em>mo</em>, <em>rank_index</em>, <em>ab</em>,
|
||||
<em>ref_tbl</em>, <em>disk_dose</em>, <em>breakpoint_S</em>,
|
||||
<em>breakpoint_R</em>, <em>uti</em>, and <em>is_SDD</em>.</p>
|
||||
<p>This data set is in R available as <code>clinical_breakpoints</code>,
|
||||
after you load the <code>AMR</code> package.</p>
|
||||
<p>It was last updated on 2 April 2026 09:42:19 UTC. Find more info
|
||||
<p>It was last updated on 22 June 2026 23:38:13 UTC. Find more info
|
||||
about the contents, (scientific) source, and structure of this <a href="https://amr-for-r.org/reference/clinical_breakpoints.html">data
|
||||
set here</a>.</p>
|
||||
<p><strong>Direct download links:</strong></p>
|
||||
@@ -620,7 +637,7 @@ Excel workbook</a> (2.7 MB)<br>
|
||||
Feather file</a> (2 MB)<br>
|
||||
</li>
|
||||
<li>Download as <a href="https://github.com/msberends/AMR/raw/main/data-raw/datasets/clinical_breakpoints.parquet" class="external-link">Apache
|
||||
Parquet file</a> (0.2 MB)<br>
|
||||
Parquet file</a> (0.1 MB)<br>
|
||||
</li>
|
||||
<li>Download as <a href="https://github.com/msberends/AMR/raw/main/data-raw/datasets/clinical_breakpoints.sav" class="external-link">IBM
|
||||
SPSS Statistics data file</a> (7.5 MB)<br>
|
||||
@@ -784,13 +801,13 @@ DTA file</a> (12.6 MB)</li>
|
||||
<code>microorganisms.groups</code>: Species Groups and
|
||||
Microbiological Complexes<a class="anchor" aria-label="anchor" href="#microorganisms-groups-species-groups-and-microbiological-complexes"></a>
|
||||
</h2>
|
||||
<p>A data set with 534 rows and 4 columns, containing the following
|
||||
<p>A data set with 530 rows and 4 columns, containing the following
|
||||
column names:<br><em>mo_group</em>, <em>mo</em>, <em>mo_group_name</em>, and
|
||||
<em>mo_name</em>.</p>
|
||||
<p>This data set is in R available as
|
||||
<code>microorganisms.groups</code>, after you load the <code>AMR</code>
|
||||
package.</p>
|
||||
<p>It was last updated on 26 March 2025 16:19:17 UTC. Find more info
|
||||
<p>It was last updated on 22 June 2026 23:38:13 UTC. Find more info
|
||||
about the contents, (scientific) source, and structure of this <a href="https://amr-for-r.org/reference/microorganisms.groups.html">data
|
||||
set here</a>.</p>
|
||||
<p><strong>Direct download links:</strong></p>
|
||||
@@ -802,7 +819,7 @@ R Data Structure (RDS) file</a> (6 kB)<br>
|
||||
text file</a> (50 kB)<br>
|
||||
</li>
|
||||
<li>Download as <a href="https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.groups.xlsx" class="external-link">Microsoft
|
||||
Excel workbook</a> (20 kB)<br>
|
||||
Excel workbook</a> (19 kB)<br>
|
||||
</li>
|
||||
<li>Download as <a href="https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.groups.feather" class="external-link">Apache
|
||||
Feather file</a> (19 kB)<br>
|
||||
@@ -811,10 +828,10 @@ Feather file</a> (19 kB)<br>
|
||||
Parquet file</a> (13 kB)<br>
|
||||
</li>
|
||||
<li>Download as <a href="https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.groups.sav" class="external-link">IBM
|
||||
SPSS Statistics data file</a> (65 kB)<br>
|
||||
SPSS Statistics data file</a> (64 kB)<br>
|
||||
</li>
|
||||
<li>Download as <a href="https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.groups.dta" class="external-link">Stata
|
||||
DTA file</a> (83 kB)</li>
|
||||
DTA file</a> (82 kB)</li>
|
||||
</ul>
|
||||
<p><strong>Example content</strong></p>
|
||||
<table class="table">
|
||||
@@ -876,11 +893,11 @@ DTA file</a> (83 kB)</li>
|
||||
<code>intrinsic_resistant</code>: Intrinsic Bacterial
|
||||
Resistance<a class="anchor" aria-label="anchor" href="#intrinsic_resistant-intrinsic-bacterial-resistance"></a>
|
||||
</h2>
|
||||
<p>A data set with 285 928 rows and 2 columns, containing the following
|
||||
<p>A data set with 294 079 rows and 2 columns, containing the following
|
||||
column names:<br><em>mo</em> and <em>ab</em>.</p>
|
||||
<p>This data set is in R available as <code>intrinsic_resistant</code>,
|
||||
after you load the <code>AMR</code> package.</p>
|
||||
<p>It was last updated on 22 April 2026 06:16:44 UTC. Find more info
|
||||
<p>It was last updated on 22 June 2026 23:38:13 UTC. Find more info
|
||||
about the contents, (scientific) source, and structure of this <a href="https://amr-for-r.org/reference/intrinsic_resistant.html">data set
|
||||
here</a>.</p>
|
||||
<p><strong>Direct download links:</strong></p>
|
||||
@@ -889,10 +906,10 @@ here</a>.</p>
|
||||
R Data Structure (RDS) file</a> (0.1 MB)<br>
|
||||
</li>
|
||||
<li>Download as <a href="https://github.com/msberends/AMR/raw/main/data-raw/datasets/intrinsic_resistant.txt" class="external-link">tab-separated
|
||||
text file</a> (10.6 MB)<br>
|
||||
text file</a> (10.9 MB)<br>
|
||||
</li>
|
||||
<li>Download as <a href="https://github.com/msberends/AMR/raw/main/data-raw/datasets/intrinsic_resistant.xlsx" class="external-link">Microsoft
|
||||
Excel workbook</a> (3.3 MB)<br>
|
||||
Excel workbook</a> (3.1 MB)<br>
|
||||
</li>
|
||||
<li>Download as <a href="https://github.com/msberends/AMR/raw/main/data-raw/datasets/intrinsic_resistant.feather" class="external-link">Apache
|
||||
Feather file</a> (2.5 MB)<br>
|
||||
@@ -901,10 +918,10 @@ Feather file</a> (2.5 MB)<br>
|
||||
Parquet file</a> (0.3 MB)<br>
|
||||
</li>
|
||||
<li>Download as <a href="https://github.com/msberends/AMR/raw/main/data-raw/datasets/intrinsic_resistant.sav" class="external-link">IBM
|
||||
SPSS Statistics data file</a> (15.5 MB)<br>
|
||||
SPSS Statistics data file</a> (16 MB)<br>
|
||||
</li>
|
||||
<li>Download as <a href="https://github.com/msberends/AMR/raw/main/data-raw/datasets/intrinsic_resistant.dta" class="external-link">Stata
|
||||
DTA file</a> (27.5 MB)</li>
|
||||
DTA file</a> (28.6 MB)</li>
|
||||
</ul>
|
||||
<p><strong>Example content</strong></p>
|
||||
<p>Example rows when filtering on <em>Enterobacter cloacae</em>:</p>
|
||||
@@ -1810,17 +1827,17 @@ set here</a>.</p>
|
||||
<h2 id="microorganisms-codes-common-laboratory-codes">
|
||||
<code>microorganisms.codes</code>: Common Laboratory Codes<a class="anchor" aria-label="anchor" href="#microorganisms-codes-common-laboratory-codes"></a>
|
||||
</h2>
|
||||
<p>A data set with 6 050 rows and 2 columns, containing the following
|
||||
<p>A data set with 6 029 rows and 2 columns, containing the following
|
||||
column names:<br><em>code</em> and <em>mo</em>.</p>
|
||||
<p>This data set is in R available as <code>microorganisms.codes</code>,
|
||||
after you load the <code>AMR</code> package.</p>
|
||||
<p>It was last updated on 30 March 2026 08:01:49 UTC. Find more info
|
||||
<p>It was last updated on 22 June 2026 23:38:13 UTC. Find more info
|
||||
about the contents, (scientific) source, and structure of this <a href="https://amr-for-r.org/reference/microorganisms.codes.html">data
|
||||
set here</a>.</p>
|
||||
<p><strong>Direct download links:</strong></p>
|
||||
<ul>
|
||||
<li>Download as <a href="https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.codes.rds" class="external-link">original
|
||||
R Data Structure (RDS) file</a> (28 kB)<br>
|
||||
R Data Structure (RDS) file</a> (27 kB)<br>
|
||||
</li>
|
||||
<li>Download as <a href="https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.codes.txt" class="external-link">tab-separated
|
||||
text file</a> (0.1 MB)<br>
|
||||
@@ -1832,7 +1849,7 @@ Excel workbook</a> (98 kB)<br>
|
||||
Feather file</a> (0.1 MB)<br>
|
||||
</li>
|
||||
<li>Download as <a href="https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.codes.parquet" class="external-link">Apache
|
||||
Parquet file</a> (69 kB)<br>
|
||||
Parquet file</a> (68 kB)<br>
|
||||
</li>
|
||||
<li>Download as <a href="https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.codes.sav" class="external-link">IBM
|
||||
SPSS Statistics data file</a> (0.2 MB)<br>
|
||||
|
||||
@@ -15,44 +15,44 @@ laboratory information systems.
|
||||
|
||||
## `microorganisms`: Full Microbial Taxonomy
|
||||
|
||||
A data set with 78 679 rows and 26 columns, containing the following
|
||||
A data set with 96 982 rows and 28 columns, containing the following
|
||||
column names:
|
||||
*mo*, *fullname*, *status*, *kingdom*, *phylum*, *class*, *order*,
|
||||
*family*, *genus*, *species*, *subspecies*, *rank*, *ref*,
|
||||
*oxygen_tolerance*, *source*, *lpsn*, *lpsn_parent*, *lpsn_renamed_to*,
|
||||
*mycobank*, *mycobank_parent*, *mycobank_renamed_to*, *gbif*,
|
||||
*gbif_parent*, *gbif_renamed_to*, *prevalence*, and *snomed*.
|
||||
*mo*, *fullname*, *status*, *domain*, *kingdom*, *phylum*, *class*,
|
||||
*order*, *family*, *genus*, *species*, *subspecies*, *rank*, *ref*,
|
||||
*oxygen_tolerance*, *morphology*, *source*, *lpsn*, *lpsn_parent*,
|
||||
*lpsn_renamed_to*, *mycobank*, *mycobank_parent*, *mycobank_renamed_to*,
|
||||
*gbif*, *gbif_parent*, *gbif_renamed_to*, *prevalence*, and *snomed*.
|
||||
|
||||
This data set is in R available as `microorganisms`, after you load the
|
||||
`AMR` package.
|
||||
|
||||
It was last updated on 18 September 2025 12:58:34 UTC. Find more info
|
||||
about the contents, (scientific) source, and structure of this [data set
|
||||
It was last updated on 22 June 2026 23:38:13 UTC. Find more info about
|
||||
the contents, (scientific) source, and structure of this [data set
|
||||
here](https://amr-for-r.org/reference/microorganisms.html).
|
||||
|
||||
**Direct download links:**
|
||||
|
||||
- Download as [original R Data Structure (RDS)
|
||||
file](https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.rds)
|
||||
(1.8 MB)
|
||||
(2.2 MB)
|
||||
- Download as [tab-separated text
|
||||
file](https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.txt)
|
||||
(17.7 MB)
|
||||
(23.1 MB)
|
||||
- Download as [Microsoft Excel
|
||||
workbook](https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.xlsx)
|
||||
(8.8 MB)
|
||||
(11.4 MB)
|
||||
- Download as [Apache Feather
|
||||
file](https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.feather)
|
||||
(8.4 MB)
|
||||
(11 MB)
|
||||
- Download as [Apache Parquet
|
||||
file](https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.parquet)
|
||||
(3.8 MB)
|
||||
(4.6 MB)
|
||||
- Download as [IBM SPSS Statistics data
|
||||
file](https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.sav)
|
||||
(28.4 MB)
|
||||
(35.2 MB)
|
||||
- Download as [Stata DTA
|
||||
file](https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.dta)
|
||||
(89.5 MB)
|
||||
(96.6 MB)
|
||||
|
||||
**NOTE: The exported files for SPSS and Stata contain only the first 50
|
||||
SNOMED codes per record, as their file size would otherwise exceed 100
|
||||
@@ -69,23 +69,23 @@ Included (sub)species per taxonomic kingdom:
|
||||
|
||||
| Kingdom | Number of (sub)species |
|
||||
|:-----------------:|:----------------------:|
|
||||
| (unknown kingdom) | 1 |
|
||||
| Animalia | 1 628 |
|
||||
| Archaea | 1 419 |
|
||||
| Bacteria | 39 249 |
|
||||
| Chromista | 178 |
|
||||
| Fungi | 28 137 |
|
||||
| | 20 |
|
||||
| (unknown kingdom) | 8 |
|
||||
| Animalia | 2 015 |
|
||||
| Archaea | 150 |
|
||||
| Bacillati | 24 200 |
|
||||
| Bacteria | 2 |
|
||||
|
||||
First 6 rows when filtering on genus *Escherichia*:
|
||||
|
||||
| mo | fullname | status | kingdom | phylum | class | order | family | genus | species | subspecies | rank | ref | oxygen_tolerance | source | lpsn | lpsn_parent | lpsn_renamed_to | mycobank | mycobank_parent | mycobank_renamed_to | gbif | gbif_parent | gbif_renamed_to | prevalence | snomed |
|
||||
|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|
|
||||
| B_ESCHR | Escherichia | accepted | Bacteria | Pseudomonadota | Gammaproteobacteria | Enterobacterales | Enterobacteriaceae | Escherichia | | | genus | Castellani et al., 1919 | facultative anaerobe | LPSN | 515602 | 482 | | | | | | 11158430 | | 1 | 407310004, 407251000, 407281008, … |
|
||||
| B_ESCHR_ADCR | Escherichia adecarboxylata | synonym | Bacteria | Pseudomonadota | Gammaproteobacteria | Enterobacterales | Enterobacteriaceae | Escherichia | adecarboxylata | | species | Leclerc, 1962 | likely facultative anaerobe | LPSN | 776052 | 515602 | 777447 | | | | | | | 1 | |
|
||||
| B_ESCHR_ALBR | Escherichia albertii | accepted | Bacteria | Pseudomonadota | Gammaproteobacteria | Enterobacterales | Enterobacteriaceae | Escherichia | albertii | | species | Huys et al., 2003 | facultative anaerobe | LPSN | 776053 | 515602 | | | | | 5427575 | | | 1 | 419388003 |
|
||||
| B_ESCHR_BLTT | Escherichia blattae | synonym | Bacteria | Pseudomonadota | Gammaproteobacteria | Enterobacterales | Enterobacteriaceae | Escherichia | blattae | | species | Burgess et al., 1973 | likely facultative anaerobe | LPSN | 776056 | 515602 | 788468 | | | | | | | 1 | |
|
||||
| B_ESCHR_COLI | Escherichia coli | accepted | Bacteria | Pseudomonadota | Gammaproteobacteria | Enterobacterales | Enterobacteriaceae | Escherichia | coli | | species | Castellani et al., 1919 | facultative anaerobe | LPSN | 776057 | 515602 | | | | | 11286021 | | | 1 | 1095001000112106, 715307006, 737528008, … |
|
||||
| B_ESCHR_COLI_COLI | Escherichia coli coli | accepted | Bacteria | Pseudomonadota | Gammaproteobacteria | Enterobacterales | Enterobacteriaceae | Escherichia | coli | coli | subspecies | | | GBIF | | 776057 | | | | | 12233256 | 11286021 | | 1 | |
|
||||
| mo | fullname | status | domain | kingdom | phylum | class | order | family | genus | species | subspecies | rank | ref | oxygen_tolerance | morphology | source | lpsn | lpsn_parent | lpsn_renamed_to | mycobank | mycobank_parent | mycobank_renamed_to | gbif | gbif_parent | gbif_renamed_to | prevalence | snomed |
|
||||
|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|:--:|
|
||||
| B_ESCHR | Escherichia | accepted | Bacteria | Pseudomonadati | Pseudomonadota | Gammaproteobacteria | Enterobacterales | Enterobacteriaceae | Escherichia | | | genus | Castellani et al., 1919 | facultative anaerobe | rods | LPSN | 515602 | 482 | | | | | CS33H | CRYWR | | 1 | 407310004, 407251000, 407281008, … |
|
||||
| B_ESCHR_ADCR | Escherichia adecarboxylata | synonym | Bacteria | Pseudomonadati | Pseudomonadota | Gammaproteobacteria | Enterobacterales | Enterobacteriaceae | Escherichia | adecarboxylata | | species | Leclerc, 1962 | likely facultative anaerobe | rods | LPSN | 776052 | 515602 | 777447 | | | | CS33J | CS33H | 3SVX6 | 1 | |
|
||||
| B_ESCHR_ALBR | Escherichia albertii | accepted | Bacteria | Pseudomonadati | Pseudomonadota | Gammaproteobacteria | Enterobacterales | Enterobacteriaceae | Escherichia | albertii | | species | Huys et al., 2003 | facultative anaerobe | rods | LPSN | 776053 | 515602 | | | | | 3BGTB | CS33H | | 1 | 419388003 |
|
||||
| B_ESCHR_BLTT | Escherichia blattae | synonym | Bacteria | Pseudomonadati | Pseudomonadota | Gammaproteobacteria | Enterobacterales | Enterobacteriaceae | Escherichia | blattae | | species | Burgess et al., 1973 | likely facultative anaerobe | rods | LPSN | 776056 | 515602 | 788468 | | | | CS33K | CS33H | 4X4P7 | 1 | |
|
||||
| B_ESCHR_COLI | Escherichia coli | accepted | Bacteria | Pseudomonadati | Pseudomonadota | Gammaproteobacteria | Enterobacterales | Enterobacteriaceae | Escherichia | coli | | species | Castellani et al., 1919 | facultative anaerobe | rods | LPSN | 776057 | 515602 | | | | | NT3L7 | CS33H | | 1 | 1095001000112106, 715307006, 737528008, … |
|
||||
| B_ESCHR_COLI_COLI | Escherichia coli coli | accepted | Bacteria | Pseudomonadati | Pseudomonadota | Gammaproteobacteria | Enterobacterales | Enterobacteriaceae | Escherichia | coli | coli | subspecies | | | | GBIF | | 776057 | | | | | 12233256 | NT3L7 | | 1 | |
|
||||
|
||||
------------------------------------------------------------------------
|
||||
|
||||
@@ -100,8 +100,8 @@ names:
|
||||
This data set is in R available as `antimicrobials`, after you load the
|
||||
`AMR` package.
|
||||
|
||||
It was last updated on 2 May 2026 12:56:26 UTC. Find more info about the
|
||||
contents, (scientific) source, and structure of this [data set
|
||||
It was last updated on 23 June 2026 12:38:59 UTC. Find more info about
|
||||
the contents, (scientific) source, and structure of this [data set
|
||||
here](https://amr-for-r.org/reference/antimicrobials.html).
|
||||
|
||||
**Direct download links:**
|
||||
@@ -147,7 +147,7 @@ as comma separated values.
|
||||
|
||||
## `clinical_breakpoints`: Interpretation from MIC values & disk diameters to SIR
|
||||
|
||||
A data set with 45 730 rows and 14 columns, containing the following
|
||||
A data set with 45 555 rows and 14 columns, containing the following
|
||||
column names:
|
||||
*guideline*, *type*, *host*, *method*, *site*, *mo*, *rank_index*, *ab*,
|
||||
*ref_tbl*, *disk_dose*, *breakpoint_S*, *breakpoint_R*, *uti*, and
|
||||
@@ -156,7 +156,7 @@ column names:
|
||||
This data set is in R available as `clinical_breakpoints`, after you
|
||||
load the `AMR` package.
|
||||
|
||||
It was last updated on 2 April 2026 09:42:19 UTC. Find more info about
|
||||
It was last updated on 22 June 2026 23:38:13 UTC. Find more info about
|
||||
the contents, (scientific) source, and structure of this [data set
|
||||
here](https://amr-for-r.org/reference/clinical_breakpoints.html).
|
||||
|
||||
@@ -176,7 +176,7 @@ here](https://amr-for-r.org/reference/clinical_breakpoints.html).
|
||||
(2 MB)
|
||||
- Download as [Apache Parquet
|
||||
file](https://github.com/msberends/AMR/raw/main/data-raw/datasets/clinical_breakpoints.parquet)
|
||||
(0.2 MB)
|
||||
(0.1 MB)
|
||||
- Download as [IBM SPSS Statistics data
|
||||
file](https://github.com/msberends/AMR/raw/main/data-raw/datasets/clinical_breakpoints.sav)
|
||||
(7.5 MB)
|
||||
@@ -199,14 +199,14 @@ here](https://amr-for-r.org/reference/clinical_breakpoints.html).
|
||||
|
||||
## `microorganisms.groups`: Species Groups and Microbiological Complexes
|
||||
|
||||
A data set with 534 rows and 4 columns, containing the following column
|
||||
A data set with 530 rows and 4 columns, containing the following column
|
||||
names:
|
||||
*mo_group*, *mo*, *mo_group_name*, and *mo_name*.
|
||||
|
||||
This data set is in R available as `microorganisms.groups`, after you
|
||||
load the `AMR` package.
|
||||
|
||||
It was last updated on 26 March 2025 16:19:17 UTC. Find more info about
|
||||
It was last updated on 22 June 2026 23:38:13 UTC. Find more info about
|
||||
the contents, (scientific) source, and structure of this [data set
|
||||
here](https://amr-for-r.org/reference/microorganisms.groups.html).
|
||||
|
||||
@@ -220,7 +220,7 @@ here](https://amr-for-r.org/reference/microorganisms.groups.html).
|
||||
(50 kB)
|
||||
- Download as [Microsoft Excel
|
||||
workbook](https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.groups.xlsx)
|
||||
(20 kB)
|
||||
(19 kB)
|
||||
- Download as [Apache Feather
|
||||
file](https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.groups.feather)
|
||||
(19 kB)
|
||||
@@ -229,10 +229,10 @@ here](https://amr-for-r.org/reference/microorganisms.groups.html).
|
||||
(13 kB)
|
||||
- Download as [IBM SPSS Statistics data
|
||||
file](https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.groups.sav)
|
||||
(65 kB)
|
||||
(64 kB)
|
||||
- Download as [Stata DTA
|
||||
file](https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.groups.dta)
|
||||
(83 kB)
|
||||
(82 kB)
|
||||
|
||||
**Example content**
|
||||
|
||||
@@ -249,14 +249,14 @@ here](https://amr-for-r.org/reference/microorganisms.groups.html).
|
||||
|
||||
## `intrinsic_resistant`: Intrinsic Bacterial Resistance
|
||||
|
||||
A data set with 285 928 rows and 2 columns, containing the following
|
||||
A data set with 294 079 rows and 2 columns, containing the following
|
||||
column names:
|
||||
*mo* and *ab*.
|
||||
|
||||
This data set is in R available as `intrinsic_resistant`, after you load
|
||||
the `AMR` package.
|
||||
|
||||
It was last updated on 22 April 2026 06:16:44 UTC. Find more info about
|
||||
It was last updated on 22 June 2026 23:38:13 UTC. Find more info about
|
||||
the contents, (scientific) source, and structure of this [data set
|
||||
here](https://amr-for-r.org/reference/intrinsic_resistant.html).
|
||||
|
||||
@@ -267,10 +267,10 @@ here](https://amr-for-r.org/reference/intrinsic_resistant.html).
|
||||
(0.1 MB)
|
||||
- Download as [tab-separated text
|
||||
file](https://github.com/msberends/AMR/raw/main/data-raw/datasets/intrinsic_resistant.txt)
|
||||
(10.6 MB)
|
||||
(10.9 MB)
|
||||
- Download as [Microsoft Excel
|
||||
workbook](https://github.com/msberends/AMR/raw/main/data-raw/datasets/intrinsic_resistant.xlsx)
|
||||
(3.3 MB)
|
||||
(3.1 MB)
|
||||
- Download as [Apache Feather
|
||||
file](https://github.com/msberends/AMR/raw/main/data-raw/datasets/intrinsic_resistant.feather)
|
||||
(2.5 MB)
|
||||
@@ -279,10 +279,10 @@ here](https://amr-for-r.org/reference/intrinsic_resistant.html).
|
||||
(0.3 MB)
|
||||
- Download as [IBM SPSS Statistics data
|
||||
file](https://github.com/msberends/AMR/raw/main/data-raw/datasets/intrinsic_resistant.sav)
|
||||
(15.5 MB)
|
||||
(16 MB)
|
||||
- Download as [Stata DTA
|
||||
file](https://github.com/msberends/AMR/raw/main/data-raw/datasets/intrinsic_resistant.dta)
|
||||
(27.5 MB)
|
||||
(28.6 MB)
|
||||
|
||||
**Example content**
|
||||
|
||||
@@ -464,14 +464,14 @@ here](https://amr-for-r.org/reference/example_isolates_unclean.html).
|
||||
|
||||
## `microorganisms.codes`: Common Laboratory Codes
|
||||
|
||||
A data set with 6 050 rows and 2 columns, containing the following
|
||||
A data set with 6 029 rows and 2 columns, containing the following
|
||||
column names:
|
||||
*code* and *mo*.
|
||||
|
||||
This data set is in R available as `microorganisms.codes`, after you
|
||||
load the `AMR` package.
|
||||
|
||||
It was last updated on 30 March 2026 08:01:49 UTC. Find more info about
|
||||
It was last updated on 22 June 2026 23:38:13 UTC. Find more info about
|
||||
the contents, (scientific) source, and structure of this [data set
|
||||
here](https://amr-for-r.org/reference/microorganisms.codes.html).
|
||||
|
||||
@@ -479,7 +479,7 @@ here](https://amr-for-r.org/reference/microorganisms.codes.html).
|
||||
|
||||
- Download as [original R Data Structure (RDS)
|
||||
file](https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.codes.rds)
|
||||
(28 kB)
|
||||
(27 kB)
|
||||
- Download as [tab-separated text
|
||||
file](https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.codes.txt)
|
||||
(0.1 MB)
|
||||
@@ -491,7 +491,7 @@ here](https://amr-for-r.org/reference/microorganisms.codes.html).
|
||||
(0.1 MB)
|
||||
- Download as [Apache Parquet
|
||||
file](https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.codes.parquet)
|
||||
(69 kB)
|
||||
(68 kB)
|
||||
- Download as [IBM SPSS Statistics data
|
||||
file](https://github.com/msberends/AMR/raw/main/data-raw/datasets/microorganisms.codes.sav)
|
||||
(0.2 MB)
|
||||
|
||||
@@ -1,5 +1,5 @@
|
||||
<!DOCTYPE html>
|
||||
<!-- Generated by pkgdown: do not edit by hand --><html lang="en"><head><meta http-equiv="Content-Type" content="text/html; charset=UTF-8"><meta charset="utf-8"><meta http-equiv="X-UA-Compatible" content="IE=edge"><meta name="viewport" content="width=device-width, initial-scale=1, shrink-to-fit=no"><title>Articles • AMR (for R)</title><!-- favicons --><link rel="icon" type="image/png" sizes="96x96" href="../favicon-96x96.png"><link rel="icon" type="”image/svg+xml”" href="../favicon.svg"><link rel="apple-touch-icon" sizes="180x180" href="../apple-touch-icon.png"><link rel="icon" sizes="any" href="../favicon.ico"><link rel="manifest" href="../site.webmanifest"><script src="../deps/jquery-3.6.0/jquery-3.6.0.min.js"></script><meta name="viewport" content="width=device-width, initial-scale=1, shrink-to-fit=no"><link href="../deps/bootstrap-5.3.1/bootstrap.min.css" rel="stylesheet"><script src="../deps/bootstrap-5.3.1/bootstrap.bundle.min.js"></script><link href="../deps/Lato-0.4.10/font.css" rel="stylesheet"><link href="../deps/Fira_Code-0.4.10/font.css" rel="stylesheet"><link href="../deps/font-awesome-6.5.2/css/all.min.css" rel="stylesheet"><link href="../deps/font-awesome-6.5.2/css/v4-shims.min.css" rel="stylesheet"><script src="../deps/headroom-0.11.0/headroom.min.js"></script><script src="../deps/headroom-0.11.0/jQuery.headroom.min.js"></script><script src="../deps/bootstrap-toc-1.0.1/bootstrap-toc.min.js"></script><script src="../deps/clipboard.js-2.0.11/clipboard.min.js"></script><script src="../deps/search-1.0.0/autocomplete.jquery.min.js"></script><script src="../deps/search-1.0.0/fuse.min.js"></script><script src="../deps/search-1.0.0/mark.min.js"></script><!-- pkgdown --><script src="../pkgdown.js"></script><link href="../extra.css" rel="stylesheet"><script src="../extra.js"></script><meta property="og:title" content="Articles"><meta property="og:image" content="https://amr-for-r.org/logo.svg"><link rel="stylesheet" href="https://cdn.jsdelivr.net/npm/katex@0.16.11/dist/katex.min.css" integrity="sha384-nB0miv6/jRmo5UMMR1wu3Gz6NLsoTkbqJghGIsx//Rlm+ZU03BU6SQNC66uf4l5+" crossorigin="anonymous"><script defer src="https://cdn.jsdelivr.net/npm/katex@0.16.11/dist/katex.min.js" integrity="sha384-7zkQWkzuo3B5mTepMUcHkMB5jZaolc2xDwL6VFqjFALcbeS9Ggm/Yr2r3Dy4lfFg" crossorigin="anonymous"></script><script defer src="https://cdn.jsdelivr.net/npm/katex@0.16.11/dist/contrib/auto-render.min.js" integrity="sha384-43gviWU0YVjaDtb/GhzOouOXtZMP/7XUzwPTstBeZFe/+rCMvRwr4yROQP43s0Xk" crossorigin="anonymous" onload="renderMathInElement(document.body);"></script></head><body>
|
||||
<!-- Generated by pkgdown: do not edit by hand --><html lang="en"><head><meta http-equiv="Content-Type" content="text/html; charset=UTF-8"><meta charset="utf-8"><meta http-equiv="X-UA-Compatible" content="IE=edge"><meta name="viewport" content="width=device-width, initial-scale=1, shrink-to-fit=no"><title>Articles • AMR (for R)</title><!-- favicons --><link rel="icon" type="image/png" sizes="96x96" href="../favicon-96x96.png"><link rel="icon" type="”image/svg+xml”" href="../favicon.svg"><link rel="apple-touch-icon" sizes="180x180" href="../apple-touch-icon.png"><link rel="icon" sizes="any" href="../favicon.ico"><link rel="manifest" href="../site.webmanifest"><script src="../deps/jquery-3.6.0/jquery-3.6.0.min.js"></script><meta name="viewport" content="width=device-width, initial-scale=1, shrink-to-fit=no"><link href="../deps/bootstrap-5.3.8/bootstrap.min.css" rel="stylesheet"><script src="../deps/bootstrap-5.3.8/bootstrap.bundle.min.js"></script><link href="../deps/Lato-0.4.10/font.css" rel="stylesheet"><link href="../deps/Fira_Code-0.4.10/font.css" rel="stylesheet"><link href="../deps/font-awesome-6.5.2/css/all.min.css" rel="stylesheet"><link href="../deps/font-awesome-6.5.2/css/v4-shims.min.css" rel="stylesheet"><script src="../deps/headroom-0.11.0/headroom.min.js"></script><script src="../deps/headroom-0.11.0/jQuery.headroom.min.js"></script><script src="../deps/bootstrap-toc-1.0.1/bootstrap-toc.min.js"></script><script src="../deps/clipboard.js-2.0.11/clipboard.min.js"></script><script src="../deps/search-1.0.0/autocomplete.jquery.min.js"></script><script src="../deps/search-1.0.0/fuse.min.js"></script><script src="../deps/search-1.0.0/mark.min.js"></script><!-- pkgdown --><script src="../pkgdown.js"></script><link href="../extra.css" rel="stylesheet"><script src="../extra.js"></script><meta property="og:title" content="Articles"><meta property="og:image" content="https://amr-for-r.org/logo.svg"><link rel="stylesheet" href="https://cdn.jsdelivr.net/npm/katex@0.16.11/dist/katex.min.css" integrity="sha384-nB0miv6/jRmo5UMMR1wu3Gz6NLsoTkbqJghGIsx//Rlm+ZU03BU6SQNC66uf4l5+" crossorigin="anonymous"><script defer src="https://cdn.jsdelivr.net/npm/katex@0.16.11/dist/katex.min.js" integrity="sha384-7zkQWkzuo3B5mTepMUcHkMB5jZaolc2xDwL6VFqjFALcbeS9Ggm/Yr2r3Dy4lfFg" crossorigin="anonymous"></script><script defer src="https://cdn.jsdelivr.net/npm/katex@0.16.11/dist/contrib/auto-render.min.js" integrity="sha384-43gviWU0YVjaDtb/GhzOouOXtZMP/7XUzwPTstBeZFe/+rCMvRwr4yROQP43s0Xk" crossorigin="anonymous" onload="renderMathInElement(document.body);"></script></head><body>
|
||||
<a href="#main" class="visually-hidden-focusable">Skip to contents</a>
|
||||
|
||||
|
||||
@@ -7,7 +7,7 @@
|
||||
|
||||
<a class="navbar-brand me-2" href="../index.html">AMR (for R)</a>
|
||||
|
||||
<small class="nav-text text-muted me-auto" data-bs-toggle="tooltip" data-bs-placement="bottom" title="">3.0.1.9057</small>
|
||||
<small class="nav-text text-muted me-auto" data-bs-toggle="tooltip" data-bs-placement="bottom" title="">3.0.1.9061</small>
|
||||
|
||||
|
||||
<button class="navbar-toggler" type="button" data-bs-toggle="collapse" data-bs-target="#navbar" aria-controls="navbar" aria-expanded="false" aria-label="Toggle navigation">
|
||||
|
||||
@@ -1,5 +1,5 @@
|
||||
<!DOCTYPE html>
|
||||
<!-- Generated by pkgdown: do not edit by hand --><html lang="en"><head><meta http-equiv="Content-Type" content="text/html; charset=UTF-8"><meta charset="utf-8"><meta http-equiv="X-UA-Compatible" content="IE=edge"><meta name="viewport" content="width=device-width, initial-scale=1, shrink-to-fit=no"><title>Authors and Citation • AMR (for R)</title><!-- favicons --><link rel="icon" type="image/png" sizes="96x96" href="favicon-96x96.png"><link rel="icon" type="”image/svg+xml”" href="favicon.svg"><link rel="apple-touch-icon" sizes="180x180" href="apple-touch-icon.png"><link rel="icon" sizes="any" href="favicon.ico"><link rel="manifest" href="site.webmanifest"><script src="deps/jquery-3.6.0/jquery-3.6.0.min.js"></script><meta name="viewport" content="width=device-width, initial-scale=1, shrink-to-fit=no"><link href="deps/bootstrap-5.3.1/bootstrap.min.css" rel="stylesheet"><script src="deps/bootstrap-5.3.1/bootstrap.bundle.min.js"></script><link href="deps/Lato-0.4.10/font.css" rel="stylesheet"><link href="deps/Fira_Code-0.4.10/font.css" rel="stylesheet"><link href="deps/font-awesome-6.5.2/css/all.min.css" rel="stylesheet"><link href="deps/font-awesome-6.5.2/css/v4-shims.min.css" rel="stylesheet"><script src="deps/headroom-0.11.0/headroom.min.js"></script><script src="deps/headroom-0.11.0/jQuery.headroom.min.js"></script><script src="deps/bootstrap-toc-1.0.1/bootstrap-toc.min.js"></script><script src="deps/clipboard.js-2.0.11/clipboard.min.js"></script><script src="deps/search-1.0.0/autocomplete.jquery.min.js"></script><script src="deps/search-1.0.0/fuse.min.js"></script><script src="deps/search-1.0.0/mark.min.js"></script><!-- pkgdown --><script src="pkgdown.js"></script><link href="extra.css" rel="stylesheet"><script src="extra.js"></script><meta property="og:title" content="Authors and Citation"><meta property="og:image" content="https://amr-for-r.org/logo.svg"><link rel="stylesheet" href="https://cdn.jsdelivr.net/npm/katex@0.16.11/dist/katex.min.css" integrity="sha384-nB0miv6/jRmo5UMMR1wu3Gz6NLsoTkbqJghGIsx//Rlm+ZU03BU6SQNC66uf4l5+" crossorigin="anonymous"><script defer src="https://cdn.jsdelivr.net/npm/katex@0.16.11/dist/katex.min.js" integrity="sha384-7zkQWkzuo3B5mTepMUcHkMB5jZaolc2xDwL6VFqjFALcbeS9Ggm/Yr2r3Dy4lfFg" crossorigin="anonymous"></script><script defer src="https://cdn.jsdelivr.net/npm/katex@0.16.11/dist/contrib/auto-render.min.js" integrity="sha384-43gviWU0YVjaDtb/GhzOouOXtZMP/7XUzwPTstBeZFe/+rCMvRwr4yROQP43s0Xk" crossorigin="anonymous" onload="renderMathInElement(document.body);"></script></head><body>
|
||||
<!-- Generated by pkgdown: do not edit by hand --><html lang="en"><head><meta http-equiv="Content-Type" content="text/html; charset=UTF-8"><meta charset="utf-8"><meta http-equiv="X-UA-Compatible" content="IE=edge"><meta name="viewport" content="width=device-width, initial-scale=1, shrink-to-fit=no"><title>Authors and Citation • AMR (for R)</title><!-- favicons --><link rel="icon" type="image/png" sizes="96x96" href="favicon-96x96.png"><link rel="icon" type="”image/svg+xml”" href="favicon.svg"><link rel="apple-touch-icon" sizes="180x180" href="apple-touch-icon.png"><link rel="icon" sizes="any" href="favicon.ico"><link rel="manifest" href="site.webmanifest"><script src="deps/jquery-3.6.0/jquery-3.6.0.min.js"></script><meta name="viewport" content="width=device-width, initial-scale=1, shrink-to-fit=no"><link href="deps/bootstrap-5.3.8/bootstrap.min.css" rel="stylesheet"><script src="deps/bootstrap-5.3.8/bootstrap.bundle.min.js"></script><link href="deps/Lato-0.4.10/font.css" rel="stylesheet"><link href="deps/Fira_Code-0.4.10/font.css" rel="stylesheet"><link href="deps/font-awesome-6.5.2/css/all.min.css" rel="stylesheet"><link href="deps/font-awesome-6.5.2/css/v4-shims.min.css" rel="stylesheet"><script src="deps/headroom-0.11.0/headroom.min.js"></script><script src="deps/headroom-0.11.0/jQuery.headroom.min.js"></script><script src="deps/bootstrap-toc-1.0.1/bootstrap-toc.min.js"></script><script src="deps/clipboard.js-2.0.11/clipboard.min.js"></script><script src="deps/search-1.0.0/autocomplete.jquery.min.js"></script><script src="deps/search-1.0.0/fuse.min.js"></script><script src="deps/search-1.0.0/mark.min.js"></script><!-- pkgdown --><script src="pkgdown.js"></script><link href="extra.css" rel="stylesheet"><script src="extra.js"></script><meta property="og:title" content="Authors and Citation"><meta property="og:image" content="https://amr-for-r.org/logo.svg"><link rel="stylesheet" href="https://cdn.jsdelivr.net/npm/katex@0.16.11/dist/katex.min.css" integrity="sha384-nB0miv6/jRmo5UMMR1wu3Gz6NLsoTkbqJghGIsx//Rlm+ZU03BU6SQNC66uf4l5+" crossorigin="anonymous"><script defer src="https://cdn.jsdelivr.net/npm/katex@0.16.11/dist/katex.min.js" integrity="sha384-7zkQWkzuo3B5mTepMUcHkMB5jZaolc2xDwL6VFqjFALcbeS9Ggm/Yr2r3Dy4lfFg" crossorigin="anonymous"></script><script defer src="https://cdn.jsdelivr.net/npm/katex@0.16.11/dist/contrib/auto-render.min.js" integrity="sha384-43gviWU0YVjaDtb/GhzOouOXtZMP/7XUzwPTstBeZFe/+rCMvRwr4yROQP43s0Xk" crossorigin="anonymous" onload="renderMathInElement(document.body);"></script></head><body>
|
||||
<a href="#main" class="visually-hidden-focusable">Skip to contents</a>
|
||||
|
||||
|
||||
@@ -7,7 +7,7 @@
|
||||
|
||||
<a class="navbar-brand me-2" href="index.html">AMR (for R)</a>
|
||||
|
||||
<small class="nav-text text-muted me-auto" data-bs-toggle="tooltip" data-bs-placement="bottom" title="">3.0.1.9057</small>
|
||||
<small class="nav-text text-muted me-auto" data-bs-toggle="tooltip" data-bs-placement="bottom" title="">3.0.1.9061</small>
|
||||
|
||||
|
||||
<button class="navbar-toggler" type="button" data-bs-toggle="collapse" data-bs-target="#navbar" aria-controls="navbar" aria-expanded="false" aria-label="Toggle navigation">
|
||||
|
||||
7
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Reference in New Issue
Block a user