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(v1.7.1.9063) not_intrinsic_resistant
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@@ -194,7 +194,7 @@ check_dataset_integrity <- function() {
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data_in_globalenv <- ls(envir = globalenv())
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overwritten <- data_in_pkg[data_in_pkg %in% data_in_globalenv]
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# exception for example_isolates
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overwritten <- overwritten[overwritten != "example_isolates"]
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overwritten <- overwritten[overwritten %unlike% "example_isolates"]
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if (length(overwritten) > 0) {
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if (length(overwritten) > 1) {
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plural <- c("s are", "", "s")
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@@ -38,11 +38,6 @@
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#' All columns in the data in which these functions are called will be searched for known antibiotic names, abbreviations, brand names, and codes (ATC, EARS-Net, WHO, etc.) according to the [antibiotics] data set. This means that a selector such as [aminoglycosides()] will pick up column names like 'gen', 'genta', 'J01GB03', 'tobra', 'Tobracin', etc.
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#'
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#' The [ab_class()] function can be used to filter/select on a manually defined antibiotic class. It searches for results in the [antibiotics] data set within the columns `group`, `atc_group1` and `atc_group2`.
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#'
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#' The [ab_selector()] function can be used to internally filter the [antibiotics] data set on any results, see *Examples*. It allows for filtering on a (part of) a certain name, and/or a group name or even a minimum of DDDs for oral treatment. This function yields the highest flexibility, but is also the least user-friendly, since it requires a hard-coded filter to set.
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#'
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#' The [administrable_per_os()] and [administrable_iv()] functions also rely on the [antibiotics] data set - antibiotic columns will be matched where a DDD (defined daily dose) for resp. oral and IV treatment is available in the [antibiotics] data set.
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#'
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#' @section Full list of supported (antibiotic) classes:
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#'
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#' `r paste0(" * ", na.omit(sapply(DEFINED_AB_GROUPS, function(ab) ifelse(tolower(gsub("^AB_", "", ab)) %in% ls(envir = asNamespace("AMR")), paste0("[", tolower(gsub("^AB_", "", ab)), "()] can select: \\cr ", vector_and(paste0(ab_name(eval(parse(text = ab), envir = asNamespace("AMR")), language = NULL, tolower = TRUE), " (", eval(parse(text = ab), envir = asNamespace("AMR")), ")"), quotes = FALSE, sort = TRUE)), character(0)), USE.NAMES = FALSE)), "\n", collapse = "")`
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@@ -105,6 +100,12 @@
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#' # You can combine selectors with '&' to be more specific:
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#' example_isolates %>%
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#' select(penicillins() & administrable_per_os())
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#'
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#' # get AMR for only drugs that matter - no intrinsic resistance:
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#' example_isolates %>%
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#' filter(mo_genus() %in% c("Escherichia", "Klebsiella")) %>%
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#' group_by(hospital_id) %>%
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#' summarise(across(not_intrinsic_resistant(), resistance))
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#'
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#' # get susceptibility for antibiotics whose name contains "trim":
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#' example_isolates %>%
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@@ -167,6 +168,7 @@ ab_class <- function(ab_class,
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}
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#' @rdname antibiotic_class_selectors
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#' @details The [ab_selector()] function can be used to internally filter the [antibiotics] data set on any results, see *Examples*. It allows for filtering on a (part of) a certain name, and/or a group name or even a minimum of DDDs for oral treatment. This function yields the highest flexibility, but is also the least user-friendly, since it requires a hard-coded filter to set.
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#' @export
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ab_selector <- function(filter,
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only_rsi_columns = FALSE,
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@@ -193,90 +195,6 @@ ab_selector <- function(filter,
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class = c("ab_selector", "character"))
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}
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#' @rdname antibiotic_class_selectors
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#' @export
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administrable_per_os <- function(only_rsi_columns = FALSE, ...) {
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meet_criteria(only_rsi_columns, allow_class = "logical", has_length = 1)
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# get_current_data() has to run each time, for cases where e.g., filter() and select() are used in same call
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# but it only takes a couple of milliseconds
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vars_df <- get_current_data(arg_name = NA, call = -2)
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# to improve speed, get_column_abx() will only run once when e.g. in a select or group call
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ab_in_data <- get_column_abx(vars_df, info = FALSE, only_rsi_columns = only_rsi_columns, sort = FALSE)
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agents_all <- antibiotics[which(!is.na(antibiotics$oral_ddd)), "ab", drop = TRUE]
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agents <- antibiotics[which(antibiotics$ab %in% ab_in_data & !is.na(antibiotics$oral_ddd)), "ab", drop = TRUE]
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agents <- ab_in_data[ab_in_data %in% agents]
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message_agent_names(function_name = "administrable_per_os",
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agents = agents,
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ab_group = "administrable_per_os",
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examples = paste0(" (such as ",
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vector_or(ab_name(sample(agents_all,
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size = min(5, length(agents_all)),
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replace = FALSE),
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tolower = TRUE,
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language = NULL),
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quotes = FALSE),
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")"))
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structure(unname(agents),
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class = c("ab_selector", "character"))
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}
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#' @rdname antibiotic_class_selectors
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#' @export
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administrable_iv <- function(only_rsi_columns = FALSE, ...) {
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meet_criteria(only_rsi_columns, allow_class = "logical", has_length = 1)
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# get_current_data() has to run each time, for cases where e.g., filter() and select() are used in same call
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# but it only takes a couple of milliseconds
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vars_df <- get_current_data(arg_name = NA, call = -2)
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# to improve speed, get_column_abx() will only run once when e.g. in a select or group call
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ab_in_data <- get_column_abx(vars_df, info = FALSE, only_rsi_columns = only_rsi_columns, sort = FALSE)
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agents_all <- antibiotics[which(!is.na(antibiotics$iv_ddd)), "ab", drop = TRUE]
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agents <- antibiotics[which(antibiotics$ab %in% ab_in_data & !is.na(antibiotics$iv_ddd)), "ab", drop = TRUE]
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agents <- ab_in_data[ab_in_data %in% agents]
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message_agent_names(function_name = "administrable_iv",
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agents = agents,
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ab_group = "administrable_iv",
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examples = "")
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structure(unname(agents),
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class = c("ab_selector", "character"))
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}
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# nolint start
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# #' @rdname antibiotic_class_selectors
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# #' @export
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# not_intrinsic_resistant <- function(mo, ..., only_rsi_columns = FALSE, ...) {
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# meet_criteria(mo, allow_class = c("mo", "data.frame", "list", "character", "numeric", "integer", "factor"), has_length = 1, allow_NA = FALSE)
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# meet_criteria(only_rsi_columns, allow_class = "logical", has_length = 1)
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#
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# x <- as.mo(mo, ...)
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# wont_work <- intrinsic_resistant[which(intrinsic_resistant$microorganism == mo_name(x, language = NULL)),
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# "antibiotic",
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# drop = TRUE]
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#
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# # get_current_data() has to run each time, for cases where e.g., filter() and select() are used in same call
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# # but it only takes a couple of milliseconds
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# vars_df <- get_current_data(arg_name = NA, call = -2)
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# # to improve speed, get_column_abx() will only run once when e.g. in a select or group call
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# ab_in_data <- get_column_abx(vars_df, info = FALSE, only_rsi_columns = only_rsi_columns, sort = FALSE)
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#
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# agents <- ab_in_data[!names(ab_in_data) %in% as.character(as.ab(wont_work))]
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#
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# # show used version number once per session (pkg_env will reload every session)
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# if (message_not_thrown_before("intrinsic_resistant_version.ab", entire_session = TRUE)) {
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# message_("Determining intrinsic resistance based on ",
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# format_eucast_version_nr(3.2, markdown = FALSE), ". ",
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# font_red("This note will be shown once per session."))
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# }
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#
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# message_agent_names(function_name = "not_intrinsic_resistant",
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# agents = ab_in_data,
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# ab_group = NULL,
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# examples = "",
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# call = mo_name(x, language = NULL))
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#
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# agents
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# }
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# nolint end
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#' @rdname antibiotic_class_selectors
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#' @export
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aminoglycosides <- function(only_rsi_columns = FALSE, only_treatable = TRUE, ...) {
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@@ -456,6 +374,94 @@ ureidopenicillins <- function(only_rsi_columns = FALSE, ...) {
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ab_select_exec("ureidopenicillins", only_rsi_columns = only_rsi_columns)
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}
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#' @rdname antibiotic_class_selectors
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#' @details The [administrable_per_os()] and [administrable_iv()] functions also rely on the [antibiotics] data set - antibiotic columns will be matched where a DDD (defined daily dose) for resp. oral and IV treatment is available in the [antibiotics] data set.
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#' @export
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administrable_per_os <- function(only_rsi_columns = FALSE, ...) {
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meet_criteria(only_rsi_columns, allow_class = "logical", has_length = 1)
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# get_current_data() has to run each time, for cases where e.g., filter() and select() are used in same call
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# but it only takes a couple of milliseconds
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vars_df <- get_current_data(arg_name = NA, call = -2)
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# to improve speed, get_column_abx() will only run once when e.g. in a select or group call
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ab_in_data <- get_column_abx(vars_df, info = FALSE, only_rsi_columns = only_rsi_columns, sort = FALSE)
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agents_all <- antibiotics[which(!is.na(antibiotics$oral_ddd)), "ab", drop = TRUE]
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agents <- antibiotics[which(antibiotics$ab %in% ab_in_data & !is.na(antibiotics$oral_ddd)), "ab", drop = TRUE]
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agents <- ab_in_data[ab_in_data %in% agents]
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message_agent_names(function_name = "administrable_per_os",
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agents = agents,
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ab_group = "administrable_per_os",
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examples = paste0(" (such as ",
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vector_or(ab_name(sample(agents_all,
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size = min(5, length(agents_all)),
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replace = FALSE),
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tolower = TRUE,
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language = NULL),
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quotes = FALSE),
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")"))
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structure(unname(agents),
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class = c("ab_selector", "character"))
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}
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#' @rdname antibiotic_class_selectors
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#' @export
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administrable_iv <- function(only_rsi_columns = FALSE, ...) {
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meet_criteria(only_rsi_columns, allow_class = "logical", has_length = 1)
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# get_current_data() has to run each time, for cases where e.g., filter() and select() are used in same call
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# but it only takes a couple of milliseconds
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vars_df <- get_current_data(arg_name = NA, call = -2)
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# to improve speed, get_column_abx() will only run once when e.g. in a select or group call
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ab_in_data <- get_column_abx(vars_df, info = FALSE, only_rsi_columns = only_rsi_columns, sort = FALSE)
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agents_all <- antibiotics[which(!is.na(antibiotics$iv_ddd)), "ab", drop = TRUE]
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agents <- antibiotics[which(antibiotics$ab %in% ab_in_data & !is.na(antibiotics$iv_ddd)), "ab", drop = TRUE]
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agents <- ab_in_data[ab_in_data %in% agents]
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message_agent_names(function_name = "administrable_iv",
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agents = agents,
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ab_group = "administrable_iv",
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examples = "")
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structure(unname(agents),
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class = c("ab_selector", "character"))
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}
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#' @rdname antibiotic_class_selectors
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#' @inheritParams eucast_rules
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#' @details The [not_intrinsic_resistant()] function can be used to only select antibiotic columns that pose no intrinsic resistance for the microorganisms in the data set. For example, if a data set contains only microorganism codes or names of *E. coli* and *K. pneumoniae* and contains a column "vancomycin", this column will be removed (or rather, unselected) using this function. It currently applies `r format_eucast_version_nr(names(EUCAST_VERSION_EXPERT_RULES[length(EUCAST_VERSION_EXPERT_RULES)]))` to determine intrinsic resistance, using the [eucast_rules()] function internally. Because of this determination, this function is quite slow in terms of performance.
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#' @export
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not_intrinsic_resistant <- function(only_rsi_columns = FALSE, col_mo = NULL, version_expertrules = 3.3, ...) {
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meet_criteria(only_rsi_columns, allow_class = "logical", has_length = 1)
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# get_current_data() has to run each time, for cases where e.g., filter() and select() are used in same call
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# but it only takes a couple of milliseconds
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vars_df <- get_current_data(arg_name = NA, call = -2)
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# to improve speed, get_column_abx() will only run once when e.g. in a select or group call
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ab_in_data <- get_column_abx(vars_df, info = FALSE, only_rsi_columns = only_rsi_columns, sort = FALSE)
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# intrinsic vars
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vars_df_R <- tryCatch(sapply(eucast_rules(vars_df,
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col_mo = col_mo,
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version_expertrules = version_expertrules,
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rules = "expert",
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info = FALSE),
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function(col) tryCatch(!any(is.na(col)) && all(col == "R"),
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error = function(e) FALSE)),
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error = function(e) stop_("in not_intrinsic_resistant(): ", e$message, call = FALSE))
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agents <- ab_in_data[ab_in_data %in% names(vars_df_R[which(vars_df_R)])]
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if (length(agents) > 0 &&
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message_not_thrown_before(paste0("not_intrinsic_resistant.", paste(sort(agents), collapse = "|")))) {
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agents_formatted <- paste0("'", font_bold(agents, collapse = NULL), "'")
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agents_names <- ab_name(names(agents), tolower = TRUE, language = NULL)
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need_name <- generalise_antibiotic_name(agents) != generalise_antibiotic_name(agents_names)
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agents_formatted[need_name] <- paste0(agents_formatted[need_name], " (", agents_names[need_name], ")")
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message_("For `not_intrinsic_resistant()` removing ",
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ifelse(length(agents) == 1, "column ", "columns "),
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vector_and(agents_formatted, quotes = FALSE, sort = FALSE))
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}
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vars_df_R <- names(vars_df_R)[which(!vars_df_R)]
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# find columns that are abx, but also intrinsic R
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out <- unname(intersect(ab_in_data, vars_df_R))
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structure(out,
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class = c("ab_selector", "character"))
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}
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ab_select_exec <- function(function_name,
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only_rsi_columns = FALSE,
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only_treatable = FALSE,
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@@ -465,7 +471,6 @@ ab_select_exec <- function(function_name,
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vars_df <- get_current_data(arg_name = NA, call = -3)
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# to improve speed, get_column_abx() will only run once when e.g. in a select or group call
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ab_in_data <- get_column_abx(vars_df, info = FALSE, only_rsi_columns = only_rsi_columns, sort = FALSE)
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# untreatable drugs
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untreatable <- antibiotics[which(antibiotics$name %like% "-high|EDTA|polysorbate"), "ab", drop = TRUE]
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if (only_treatable == TRUE & any(untreatable %in% names(ab_in_data))) {
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+1
-1
@@ -59,7 +59,7 @@ format_eucast_version_nr <- function(version, markdown = TRUE) {
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#' @param verbose a [logical] to turn Verbose mode on and off (default is off). In Verbose mode, the function does not apply rules to the data, but instead returns a data set in logbook form with extensive info about which rows and columns would be effected and in which way. Using Verbose mode takes a lot more time.
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#' @param version_breakpoints the version number to use for the EUCAST Clinical Breakpoints guideline. Can be either `r vector_or(names(EUCAST_VERSION_BREAKPOINTS), reverse = TRUE)`.
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#' @param version_expertrules the version number to use for the EUCAST Expert Rules and Intrinsic Resistance guideline. Can be either `r vector_or(names(EUCAST_VERSION_EXPERT_RULES), reverse = TRUE)`.
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#' @param ampc_cephalosporin_resistance a [character] value that should be applied to cefotaxime, ceftriaxone and ceftazidime for AmpC de-repressed cephalosporin-resistant mutants, defaults to `NA`. Currently only works when `version_expertrules` is `3.2`; '*EUCAST Expert Rules v3.2 on Enterobacterales*' states that results of cefotaxime, ceftriaxone and ceftazidime should be reported with a note, or results should be suppressed (emptied) for these three agents. A value of `NA` (the default) for this argument will remove results for these three agents, while e.g. a value of `"R"` will make the results for these agents resistant. Use `NULL` or `FALSE` to not alter results for these three agents of AmpC de-repressed cephalosporin-resistant mutants. Using `TRUE` is equal to using `"R"`. \cr For *EUCAST Expert Rules* v3.2, this rule applies to: `r vector_and(gsub("[^a-zA-Z ]+", "", unlist(strsplit(EUCAST_RULES_DF[which(EUCAST_RULES_DF$reference.version == 3.2 & EUCAST_RULES_DF$reference.rule %like% "ampc"), "this_value"][1], "|", fixed = TRUE))), quotes = "*")`.
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#' @param ampc_cephalosporin_resistance a [character] value that should be applied to cefotaxime, ceftriaxone and ceftazidime for AmpC de-repressed cephalosporin-resistant mutants, defaults to `NA`. Currently only works when `version_expertrules` is `3.2` and higher; these version of '*EUCAST Expert Rules on Enterobacterales*' state that results of cefotaxime, ceftriaxone and ceftazidime should be reported with a note, or results should be suppressed (emptied) for these three agents. A value of `NA` (the default) for this argument will remove results for these three agents, while e.g. a value of `"R"` will make the results for these agents resistant. Use `NULL` or `FALSE` to not alter results for these three agents of AmpC de-repressed cephalosporin-resistant mutants. Using `TRUE` is equal to using `"R"`. \cr For *EUCAST Expert Rules* v3.2, this rule applies to: `r vector_and(gsub("[^a-zA-Z ]+", "", unlist(strsplit(EUCAST_RULES_DF[which(EUCAST_RULES_DF$reference.version %in% c(3.2, 3.3) & EUCAST_RULES_DF$reference.rule %like% "ampc"), "this_value"][1], "|", fixed = TRUE))), quotes = "*")`.
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#' @param ... column name of an antibiotic, see section *Antibiotics* below
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#' @param ab any (vector of) text that can be coerced to a valid antibiotic code with [as.ab()]
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#' @param administration route of administration, either `r vector_or(dosage$administration)`
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+4
-3
@@ -238,9 +238,10 @@ get_column_abx <- function(x,
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if (sort == TRUE) {
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out <- out[order(names(out), out)]
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}
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duplicates <- c(out[duplicated(out)], out[duplicated(names(out))])
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duplicates <- duplicates[unique(names(duplicates))]
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out <- c(out[!names(out) %in% names(duplicates)], duplicates)
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# only keep the first hits, no duplicates
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duplicates <- c(out[duplicated(names(out))], out[duplicated(unname(out))])
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out <- out[!duplicated(names(out))]
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out <- out[!duplicated(unname(out))]
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if (sort == TRUE) {
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out <- out[order(names(out), out)]
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}
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@@ -27,7 +27,7 @@
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#'
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#' This algorithm is used by [as.mo()] and all the [`mo_*`][mo_property()] functions to determine the most probable match of taxonomic records based on user input.
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#' @inheritSection lifecycle Stable Lifecycle
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#' @author Matthijs S. Berends
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#' @author Dr. Matthijs Berends
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#' @param x Any user input value(s)
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#' @param n A full taxonomic name, that exists in [`microorganisms$fullname`][microorganisms]
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#' @section Matching Score for Microorganisms:
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@@ -96,6 +96,7 @@
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#' mo_ref("E. coli") # "Castellani et al., 1919"
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#' mo_authors("E. coli") # "Castellani et al."
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#' mo_year("E. coli") # 1919
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#' mo_lpsn("E. coli") # 776057 (LPSN record ID)
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#'
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#' # abbreviations known in the field -----------------------------------------
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#' mo_genus("MRSA") # "Staphylococcus"
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@@ -538,6 +539,19 @@ mo_year <- function(x, language = get_locale(), ...) {
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suppressWarnings(as.integer(x))
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}
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#' @rdname mo_property
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#' @export
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mo_lpsn <- function(x, language = get_locale(), ...) {
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if (missing(x)) {
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# this tries to find the data and an <mo> column
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x <- find_mo_col(fn = "mo_rank")
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}
|
||||
meet_criteria(x, allow_NA = TRUE)
|
||||
meet_criteria(language, has_length = 1, is_in = c(LANGUAGES_SUPPORTED, ""), allow_NULL = TRUE, allow_NA = TRUE)
|
||||
|
||||
mo_validate(x = x, property = "species_id", language = language, ...)
|
||||
}
|
||||
|
||||
#' @rdname mo_property
|
||||
#' @export
|
||||
mo_rank <- function(x, language = get_locale(), ...) {
|
||||
@@ -724,6 +738,8 @@ mo_validate <- function(x, property, language, ...) {
|
||||
|
||||
if (property == "mo") {
|
||||
return(set_clean_class(x, new_class = c("mo", "character")))
|
||||
} else if (property == "species_id") {
|
||||
return(as.double(x))
|
||||
} else if (property == "snomed") {
|
||||
return(as.double(eval(parse(text = x))))
|
||||
} else {
|
||||
|
||||
Reference in new issue
Block a user