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AMR
is a free and open-source R package to simplify the analysis and prediction of Antimicrobial Resistance (AMR) and to work with microbial and antimicrobial properties by using evidence-based methods. It supports any data format, including WHONET/EARS-Net data.
After installing this package, R knows ~65,000 microorganisms and ~500 antibiotics by name and code, and knows all about valid RSI and MIC values.
Used to SPSS? Read our tutorial on how to import data from SPSS, SAS or Stata and learn in which ways R outclasses any of these statistical packages.
We created this package for both academic research and routine analysis at the Faculty of Medical Sciences of the University of Groningen, the Netherlands, and the Medical Microbiology & Infection Prevention (MMBI) department of the University Medical Center Groningen (UMCG). This R package is actively maintained and is free software; you can freely use and distribute it for both personal and commercial (but not patent) purposes under the terms of the GNU General Public License version 2.0 (GPL-2), as published by the Free Software Foundation. Read the full license here.
This package can be used for:
This package is ready-to-use for a professional environment by specialists in the following fields:
Medical Microbiology
Veterinary Microbiology
Microbial Ecology
Developers
This package is available on the official R network (CRAN), which has a peer-reviewed submission process. Install this package in R with:
It will be downloaded and installed automatically. For RStudio, click on the menu Tools > Install Packages… and then type in “AMR” and press Install.
Note: Not all functions on this website may be available in this latest release. To use all functions and data sets mentioned on this website, install the latest development version.
To find out how to conduct AMR analysis, please continue reading here to get started or click the links in the ‘How to’ menu.
This package contains the complete taxonomic tree of almost all microorganisms from the authoritative and comprehensive Catalogue of Life (www.catalogueoflife.org).
Included are:
All ~55,000 (sub)species from the kingdoms of Archaea, Bacteria and Protozoa
All ~3,500 (sub)species from these orders of the kingdom of Fungi: Eurotiales, Onygenales, Pneumocystales, Saccharomycetales, Schizosaccharomycetales and Tremellales.
The kingdom of Fungi is a very large taxon with almost 300,000 different (sub)species, of which most are not microbial (but rather macroscopic, like mushrooms). Because of this, not all fungi fit the scope of this package and including everything would tremendously slow down our algorithms too. By only including the aforementioned taxonomic orders, the most relevant fungi are covered (like all species of Aspergillus, Candida, Cryptococcus, Histoplasma, Pneumocystis, Saccharomyces and Trichophyton).
All ~2,000 (sub)species from ~100 other relevant genera, from the kingdoms of Animalia and Plantae (like Strongyloides and Taenia)
All ~21,000 previously accepted names of included (sub)species that have been taxonomically renamed
The responsible author(s) and year of scientific publication
This data is updated annually - check the included version with catalogue_of_life_version()
.
About the Catalogue of Life
The Catalogue of Life is the most comprehensive and authoritative global index of species currently available. It holds essential information on the names, relationships and distributions of over 1.6 million species. The Catalogue of Life is used to support the major biodiversity and conservation information services such as the Global Biodiversity Information Facility (GBIF), Encyclopedia of Life (EoL) and the International Union for Conservation of Nature Red List. It is recognised by the Convention on Biological Diversity as a significant component of the Global Taxonomy Initiative and a contribution to Target 1 of the Global Strategy for Plant Conservation.
Read more about the data from the Catalogue of Life in our manual.
WHO Collaborating Centre for Drug Statistics Methodology
This package contains all ~500 antimicrobial drugs and their Anatomical Therapeutic Chemical (ATC) codes, ATC groups and Defined Daily Dose (DDD) from the World Health Organization Collaborating Centre for Drug Statistics Methodology (WHOCC, https://www.whocc.no) and the Pharmaceuticals Community Register of the European Commission.
Read more about the data from WHOCC in our manual.
We support WHONET and EARS-Net data. Exported files from WHONET can be imported into R and can be analysed easily using this package. For education purposes, we created an example data set WHONET
with the exact same structure as a WHONET export file. Furthermore, this package also contains a data set antibiotics
with all EARS-Net antibiotic abbreviations, and knows almost all WHONET abbreviations for microorganisms. When using WHONET data as input for analysis, all input parameters will be set automatically.
Read our tutorial about how to work with WHONET data here.
The AMR
package basically does four important things:
It cleanses existing data by providing new classes for microoganisms, antibiotics and antimicrobial results (both S/I/R and MIC). By installing this package, you teach R everything about microbiology that is needed for analysis. These functions all use intelligent rules to guess results that you would expect:
as.mo()
to get an ID of a microorganism. The IDs are human readable for the trained eye - the ID of Klebsiella pneumoniae is “B_KLBSL_PNE” (B stands for Bacteria) and the ID of S. aureus is “B_STPHY_AUR”. The function takes almost any text as input that looks like the name or code of a microorganism like “E. coli”, “esco” or “esccol” and tries to find expected results using intelligent rules combined with the included Catalogue of Life data set. It only takes milliseconds to find results, please see our benchmarks. Moreover, it can group Staphylococci into coagulase negative and positive (CoNS and CoPS, see source) and can categorise Streptococci into Lancefield groups (like beta-haemolytic Streptococcus Group B, source).as.rsi()
to transform values to valid antimicrobial results. It produces just S, I or R based on your input and warns about invalid values. Even values like “<=0.002; S” (combined MIC/RSI) will result in “S”.as.mic()
to cleanse your MIC values. It produces a so-called factor (called ordinal in SPSS) with valid MIC values as levels. A value like “<=0.002; S” (combined MIC/RSI) will result in “<=0.002”.as.atc()
to get the ATC code of an antibiotic as defined by the WHO. This package contains a database with most LIS codes, official names, DDDs and even trade names of antibiotics. For example, the values “Furabid”, “Furadantin”, “nitro” all return the ATC code of Nitrofurantoine.It enhances existing data and adds new data from data sets included in this package.
eucast_rules()
to apply EUCAST expert rules to isolates (not the translation from MIC to RSI values).first_isolate()
to identify the first isolates of every patient using guidelines from the CLSI (Clinical and Laboratory Standards Institute).
mdro()
(abbreviation of Multi Drug Resistant Organisms) to check your isolates for exceptional resistance with country-specific guidelines or EUCAST rules. Currently, national guidelines for Germany and the Netherlands are supported.microorganisms
contains the complete taxonomic tree of ~65,000 microorganisms. Furthermore, some colloquial names and all Gram stains are available, which enables resistance analysis of e.g. different antibiotics per Gram stain. The package also contains functions to look up values in this data set like mo_genus()
, mo_family()
, mo_gramstain()
or even mo_phylum()
. As they use as.mo()
internally, they also use the same intelligent rules for determination. For example, mo_genus("MRSA")
and mo_genus("S. aureus")
will both return "Staphylococcus"
. They also come with support for German, Dutch, Spanish, Italian, French and Portuguese. These functions can be used to add new variables to your data.antibiotics
contains almost 500 antimicrobial drugs with their ATC code, EARS-Net code, common LIS codes, official name, trivial name and DDD of both oral and parenteral administration. It also contains hundreds of trade names. Use functions like atc_name()
and atc_tradenames()
to look up values. The atc_*
functions use as.atc()
internally so they support the same intelligent rules to guess the most probable result. For example, atc_name("Fluclox")
, atc_name("Floxapen")
and atc_name("J01CF05")
will all return "Flucloxacillin"
. These functions can again be used to add new variables to your data.It analyses the data with convenient functions that use well-known methods.
portion_R()
, portion_IR()
, portion_I()
, portion_SI()
and portion_S()
functions. Similarly, the number of isolates can be determined with the count_R()
, count_IR()
, count_I()
, count_SI()
and count_S()
functions. All these functions can be used with the dplyr
package (e.g. in conjunction with summarise()
)geom_rsi()
, a function made for the ggplot2
packageresistance_predict()
functionkurtosis()
, skewness()
and create frequency tables with freq()
It teaches the user how to use all the above actions.
septic_patients
data set. This data set contains:
WHONET
data set. This data set only contains fake data, but with the exact same structure as files exported by WHONET. Read more about WHONET on its tutorial page.