mirror of https://github.com/msberends/AMR.git
306 lines
11 KiB
R
306 lines
11 KiB
R
# ==================================================================== #
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# TITLE #
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# AMR: An R Package for Working with Antimicrobial Resistance Data #
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# #
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# SOURCE #
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# https://github.com/msberends/AMR #
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# #
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# CITE AS #
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# Berends MS, Luz CF, Friedrich AW, Sinha BNM, Albers CJ, Glasner C #
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# (2022). AMR: An R Package for Working with Antimicrobial Resistance #
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# Data. Journal of Statistical Software, 104(3), 1-31. #
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# doi:10.18637/jss.v104.i03 #
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# #
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# Developed at the University of Groningen and the University Medical #
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# Center Groningen in The Netherlands, in collaboration with many #
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# colleagues from around the world, see our website. #
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# #
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# This R package is free software; you can freely use and distribute #
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# it for both personal and commercial purposes under the terms of the #
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# GNU General Public License version 2.0 (GNU GPL-2), as published by #
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# the Free Software Foundation. #
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# We created this package for both routine data analysis and academic #
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# research and it was publicly released in the hope that it will be #
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# useful, but it comes WITHOUT ANY WARRANTY OR LIABILITY. #
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# #
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# Visit our website for the full manual and a complete tutorial about #
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# how to conduct AMR data analysis: https://msberends.github.io/AMR/ #
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# ==================================================================== #
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library(openxlsx)
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library(dplyr)
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library(tidyr)
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library(cleaner)
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library(AMR)
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# USE THIS FUNCTION TO READ THE EUCAST EXCEL FILE THAT CONTAINS THE BREAKPOINT TABLES
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read_EUCAST <- function(sheet, file, guideline_name) {
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message("\nGetting sheet: ", sheet)
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sheet.bak <- sheet
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uncertainties <- NULL
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add_uncertainties <- function(old, new) {
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if (is.null(old)) {
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new
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} else {
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bind_rows(old, new)
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}
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}
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raw_data <- read.xlsx(
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xlsxFile = file,
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sheet = sheet,
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colNames = FALSE,
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skipEmptyRows = FALSE,
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skipEmptyCols = FALSE,
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fillMergedCells = TRUE,
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na.strings = c("", "-", "NA", "IE", "IP")
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)
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probable_rows <- suppressWarnings(raw_data %>% mutate_all(as.double) %>% summarise_all(~ sum(!is.na(.))) %>% unlist() %>% max())
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if (probable_rows == 0) {
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message("NO ROWS FOUND")
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message("------------------------")
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return(NULL)
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}
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# in the info header in the Excel file, EUCAST mentions which genera are targeted
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if (sheet %like% "anaerob.*Gram.*posi") {
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sheet <- paste0(c(
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"Actinomyces", "Bifidobacterium", "Clostridioides",
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"Clostridium", "Cutibacterium", "Eggerthella",
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"Eubacterium", "Lactobacillus", "Propionibacterium",
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"Staphylococcus saccharolyticus"
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),
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collapse = "_"
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)
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} else if (sheet %like% "anaerob.*Gram.*nega") {
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sheet <- paste0(c(
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"Bacteroides",
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"Bilophila",
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"Fusobacterium",
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"Mobiluncus",
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"Parabacteroides",
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"Porphyromonas",
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"Prevotella"
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),
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collapse = "_"
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)
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} else if (sheet == "Streptococcus A,B,C,G") {
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sheet <- paste0(microorganisms %>%
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filter(genus == "Streptococcus") %>%
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mutate(lancefield = mo_name(mo, Lancefield = TRUE)) %>%
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filter(lancefield %like% "^Streptococcus group") %>%
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pull(fullname),
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collapse = "_"
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)
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} else if (sheet %like% "PK.*PD") {
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sheet <- "UNKNOWN"
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}
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mo_sheet <- paste0(suppressMessages(as.mo(unlist(strsplit(sheet, "_")))), collapse = "|")
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if (!is.null(mo_uncertainties())) uncertainties <- add_uncertainties(uncertainties, mo_uncertainties())
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set_columns_names <- function(x, cols) {
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colnames(x) <- cols[1:length(colnames(x))]
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x
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}
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get_mo <- function(x) {
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for (i in seq_len(length(x))) {
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y <- trimws2(unlist(strsplit(x[i], "(,|and)")))
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y <- trimws2(gsub("[(].*[)]", "", y))
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y <- suppressWarnings(suppressMessages(as.mo(y)))
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if (!is.null(mo_uncertainties())) uncertainties <<- add_uncertainties(uncertainties, mo_uncertainties())
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y <- y[!is.na(y) & y != "UNKNOWN"]
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x[i] <- paste(y, collapse = "|")
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}
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x
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}
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MICs_with_trailing_superscript <- c(
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seq(from = 0.0011, to = 0.0019, by = 0.0001),
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seq(from = 0.031, to = 0.039, by = 0.001),
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seq(from = 0.061, to = 0.069, by = 0.001),
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seq(from = 0.1251, to = 0.1259, by = 0.0001),
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seq(from = 0.251, to = 0.259, by = 0.001),
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seq(from = 0.51, to = 0.59, by = 0.01),
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seq(from = 11, to = 19, by = 1),
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seq(from = 161, to = 169, by = 01),
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seq(from = 21, to = 29, by = 1),
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seq(from = 321, to = 329, by = 1),
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seq(from = 41, to = 49, by = 1),
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seq(from = 81, to = 89, by = 1)
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)
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has_superscript <- function(x) {
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# because due to floating point error, 0.1252 is not in:
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# seq(from = 0.1251, to = 0.1259, by = 0.0001)
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sapply(x, function(x) any(near(x, MICs_with_trailing_superscript)))
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}
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has_zone_diameters <- rep(any(unlist(raw_data) %like% "zone diameter"), nrow(raw_data))
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cleaned <- raw_data %>%
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as_tibble() %>%
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set_columns_names(LETTERS) %>%
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transmute(
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drug = A,
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MIC_S = B,
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MIC_R = C,
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disk_dose = ifelse(has_zone_diameters, E, NA_character_),
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disk_S = ifelse(has_zone_diameters, `F`, NA_character_),
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disk_R = ifelse(has_zone_diameters, G, NA_character_)
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) %>%
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filter(
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!is.na(drug),
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!(is.na(MIC_S) & is.na(MIC_R) & is.na(disk_S) & is.na(disk_R)),
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MIC_S %unlike% "(MIC|S ≤|note)",
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MIC_S %unlike% "^[-]",
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drug != MIC_S,
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) %>%
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mutate(
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administration = case_when(
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drug %like% "[( ]oral" ~ "oral",
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drug %like% "[( ]iv" ~ "iv",
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TRUE ~ NA_character_
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),
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uti = ifelse(drug %like% "(UTI|urinary|urine)", TRUE, FALSE),
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systemic = ifelse(drug %like% "(systemic|septic)", TRUE, FALSE),
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mo = ifelse(drug %like% "([.]|spp)", get_mo(drug), mo_sheet)
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) %>%
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# clean disk doses
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mutate(disk_dose = clean_character(disk_dose, remove = "[^0-9.-]")) %>%
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# clean MIC and disk values
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mutate(
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MIC_S = gsub(".,.", "", MIC_S), # remove superscript notes with comma, like 0.5^2,3
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MIC_R = gsub(".,.", "", MIC_R),
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disk_S = gsub(".,.", "", disk_S),
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disk_R = gsub(".,.", "", disk_R),
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MIC_S = clean_double(MIC_S), # make them valid numeric values
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MIC_R = clean_double(MIC_R),
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disk_S = clean_integer(disk_S),
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disk_R = clean_integer(disk_R),
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# invalid MIC values have a superscript text, delete those
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MIC_S = ifelse(has_superscript(MIC_S),
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substr(MIC_S, 1, nchar(MIC_S) - 1),
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MIC_S
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),
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MIC_R = ifelse(has_superscript(MIC_R),
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substr(MIC_R, 1, nchar(MIC_R) - 1),
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MIC_R
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),
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# and some are just awful
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MIC_S = ifelse(MIC_S == 43.4, 4, MIC_S),
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MIC_R = ifelse(MIC_R == 43.4, 4, MIC_R),
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) %>%
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# clean drug names
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mutate(
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drug = gsub(" ?[(, ].*$", "", drug),
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drug = gsub("[1-9]+$", "", drug),
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ab = as.ab(drug)
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) %>%
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select(ab, mo, everything(), -drug) %>%
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as.data.frame(stringsAsFactors = FALSE)
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# new row for every different MO mentioned
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for (i in 1:nrow(cleaned)) {
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mo <- cleaned[i, "mo", drop = TRUE]
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if (grepl(pattern = "|", mo, fixed = TRUE)) {
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mo_vect <- unlist(strsplit(mo, "|", fixed = TRUE))
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cleaned[i, "mo"] <- mo_vect[1]
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for (j in seq_len(length(mo_vect))) {
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cleaned <- bind_rows(cleaned, cleaned[i, , drop = FALSE])
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cleaned[nrow(cleaned), "mo"] <- mo_vect[j]
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}
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}
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}
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cleaned <- cleaned %>%
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distinct(ab, mo, administration, uti, systemic, .keep_all = TRUE) %>%
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arrange(ab, mo) %>%
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mutate_at(c("MIC_S", "MIC_R", "disk_S", "disk_R"), as.double) %>%
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pivot_longer(c("MIC_S", "MIC_R", "disk_S", "disk_R"), "type") %>%
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mutate(
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method = ifelse(type %like% "MIC", "MIC", "DISK"),
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type = gsub("^.*_", "breakpoint_", type)
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) %>%
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pivot_wider(names_from = type, values_from = value) %>%
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mutate(
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guideline = guideline_name,
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disk_dose = ifelse(method == "DISK", disk_dose, NA_character_),
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mo = ifelse(mo == "", mo_sheet, mo)
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) %>%
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filter(!(is.na(breakpoint_S) & is.na(breakpoint_R))) %>%
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# comply with clinical_breakpoints for now
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transmute(guideline,
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method,
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site = case_when(
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uti ~ "UTI",
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systemic ~ "Systemic",
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TRUE ~ administration
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),
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mo, ab,
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ref_tbl = sheet.bak,
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disk_dose = ifelse(!is.na(disk_dose), paste0(disk_dose, "ug"), NA_character_),
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breakpoint_S,
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breakpoint_R
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) %>%
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as.data.frame(stringsAsFactors = FALSE)
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if (!is.null(uncertainties)) {
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print(uncertainties %>% distinct(input, mo, .keep_all = TRUE))
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}
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message("Estimated: ", probable_rows, ", gained: ", cleaned %>% count(ab) %>% nrow())
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message("------------------------")
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cleaned
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}
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# Actual import -----------------------------------------------------------
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file <- "data-raw/v_11.0_Breakpoint_Tables.xlsx"
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sheets <- readxl::excel_sheets(file)
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guideline_name <- "EUCAST 2021"
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sheets_to_analyse <- sheets[!sheets %in% c("Content", "Changes", "Notes", "Guidance", "Dosages", "Technical uncertainty", "Topical agents")]
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# takes the longest time:
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new_EUCAST <- read_EUCAST(
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sheet = sheets_to_analyse[1],
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file = file,
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guideline_name = guideline_name
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)
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for (i in 2:length(sheets_to_analyse)) {
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tryCatch(
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new_EUCAST <<- bind_rows(
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new_EUCAST,
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read_EUCAST(
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sheet = sheets_to_analyse[i],
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file = file,
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guideline_name = guideline_name
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)
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),
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error = function(e) message(e$message)
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)
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}
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# 2021-07-12 fix for Morganellaceae (check other lines too next time)
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morg <- clinical_breakpoints %>%
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as_tibble() %>%
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filter(
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ab == "IPM",
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guideline == "EUCAST 2021",
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mo == as.mo("Enterobacterales")
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) %>%
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mutate(mo = as.mo("Morganellaceae"))
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morg[which(morg$method == "MIC"), "breakpoint_S"] <- 0.001
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morg[which(morg$method == "MIC"), "breakpoint_R"] <- 4
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morg[which(morg$method == "DISK"), "breakpoint_S"] <- 50
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morg[which(morg$method == "DISK"), "breakpoint_R"] <- 19
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clinical_breakpoints <- clinical_breakpoints %>%
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bind_rows(morg) %>%
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bind_rows(morg %>%
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mutate(guideline = "EUCAST 2020")) %>%
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arrange(desc(guideline), ab, mo, method)
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