Interpret minimum inhibitory concentration (MIC) values and disk diffusion diameters according to EUCAST or CLSI, or clean up existing R/SI values. This transforms the input to a new class rsi
, which is an ordered factor with levels S < I < R
.
as.rsi(x, ...)
NA_rsi_
is.rsi(x)
is.rsi.eligible(x, threshold = 0.05)
# S3 method for mic
as.rsi(
x,
mo = NULL,
ab = deparse(substitute(x)),
guideline = "EUCAST",
uti = FALSE,
conserve_capped_values = FALSE,
add_intrinsic_resistance = FALSE,
reference_data = AMR::rsi_translation,
...
)
# S3 method for disk
as.rsi(
x,
mo = NULL,
ab = deparse(substitute(x)),
guideline = "EUCAST",
uti = FALSE,
add_intrinsic_resistance = FALSE,
reference_data = AMR::rsi_translation,
...
)
# S3 method for data.frame
as.rsi(
x,
...,
col_mo = NULL,
guideline = "EUCAST",
uti = NULL,
conserve_capped_values = FALSE,
add_intrinsic_resistance = FALSE,
reference_data = AMR::rsi_translation
)
An object of class rsi
(inherits from ordered
, factor
) of length 1.
vector of values (for class mic
: MIC values in mg/L, for class disk
: a disk diffusion radius in millimetres)
for using on a data.frame: names of columns to apply as.rsi()
on (supports tidy selection like AMX:VAN
). Otherwise: arguments passed on to methods.
maximum fraction of invalid antimicrobial interpretations of x
, see Examples
any (vector of) text that can be coerced to valid microorganism codes with as.mo()
, can be left empty to determine it automatically
any (vector of) text that can be coerced to a valid antimicrobial code with as.ab()
defaults to the latest included EUCAST guideline, see Details for all options
(Urinary Tract Infection) A vector with logicals (TRUE
or FALSE
) to specify whether a UTI specific interpretation from the guideline should be chosen. For using as.rsi()
on a data.frame, this can also be a column containing logicals or when left blank, the data set will be searched for a column 'specimen', and rows within this column containing 'urin' (such as 'urine', 'urina') will be regarded isolates from a UTI. See Examples.
a logical to indicate that MIC values starting with ">"
(but not ">="
) must always return "R" , and that MIC values starting with "<"
(but not "<="
) must always return "S"
(only useful when using a EUCAST guideline) a logical to indicate whether intrinsic antibiotic resistance must also be considered for applicable bug-drug combinations, meaning that e.g. ampicillin will always return "R" in Klebsiella species. Determination is based on the intrinsic_resistant data set, that itself is based on 'EUCAST Expert Rules' and 'EUCAST Intrinsic Resistance and Unusual Phenotypes' v3.2 (2020).
a data.frame to be used for interpretation, which defaults to the rsi_translation data set. Changing this argument allows for using own interpretation guidelines. This argument must contain a data set that is equal in structure to the rsi_translation data set (same column names and column types). Please note that the guideline
argument will be ignored when reference_data
is manually set.
column name of the IDs of the microorganisms (see as.mo()
), defaults to the first column of class mo
. Values will be coerced using as.mo()
.
Ordered factor with new class <rsi>
The as.rsi()
function works in four ways:
For cleaning raw / untransformed data. The data will be cleaned to only contain values S, I and R and will try its best to determine this with some intelligence. For example, mixed values with R/SI interpretations and MIC values such as "<0.25; S"
will be coerced to "S"
. Combined interpretations for multiple test methods (as seen in laboratory records) such as "S; S"
will be coerced to "S"
, but a value like "S; I"
will return NA
with a warning that the input is unclear.
For interpreting minimum inhibitory concentration (MIC) values according to EUCAST or CLSI. You must clean your MIC values first using as.mic()
, that also gives your columns the new data class mic
. Also, be sure to have a column with microorganism names or codes. It will be found automatically, but can be set manually using the mo
argument.
Using dplyr
, R/SI interpretation can be done very easily with either:
Operators like "<=" will be stripped before interpretation. When using conserve_capped_values = TRUE
, an MIC value of e.g. ">2" will always return "R", even if the breakpoint according to the chosen guideline is ">=4". This is to prevent that capped values from raw laboratory data would not be treated conservatively. The default behaviour (conserve_capped_values = FALSE
) considers ">2" to be lower than ">=4" and might in this case return "S" or "I".
For interpreting disk diffusion diameters according to EUCAST or CLSI. You must clean your disk zones first using as.disk()
, that also gives your columns the new data class disk
. Also, be sure to have a column with microorganism names or codes. It will be found automatically, but can be set manually using the mo
argument.
Using dplyr
, R/SI interpretation can be done very easily with either:
For interpreting a complete data set, with automatic determination of MIC values, disk diffusion diameters, microorganism names or codes, and antimicrobial test results. This is done very simply by running as.rsi(data)
.
For interpreting MIC values as well as disk diffusion diameters, currently implemented guidelines are EUCAST (2011-2021) and CLSI (2010-2020).
Thus, the guideline
argument must be set to e.g., "EUCAST 2021"
or "CLSI 2020"
. By simply using "EUCAST"
(the default) or "CLSI"
as input, the latest version of that guideline will automatically be selected. You can set your own data set using the reference_data
argument. The guideline
argument will then be ignored.
After using as.rsi()
, you can use the eucast_rules()
defined by EUCAST to (1) apply inferred susceptibility and resistance based on results of other antimicrobials and (2) apply intrinsic resistance based on taxonomic properties of a microorganism.
The repository of this package contains a machine-readable version of all guidelines. This is a CSV file consisting of 22,000 rows and 10 columns. This file is machine-readable, since it contains one row for every unique combination of the test method (MIC or disk diffusion), the antimicrobial agent and the microorganism. This allows for easy implementation of these rules in laboratory information systems (LIS). Note that it only contains interpretation guidelines for humans - interpretation guidelines from CLSI for animals were removed.
The function is.rsi()
detects if the input contains class <rsi>
. If the input is a data.frame, it iterates over all columns and returns a logical vector.
The function is.rsi.eligible()
returns TRUE
when a columns contains at most 5% invalid antimicrobial interpretations (not S and/or I and/or R), and FALSE
otherwise. The threshold of 5% can be set with the threshold
argument. If the input is a data.frame, it iterates over all columns and returns a logical vector.
NA_rsi_
is a missing value of the new <rsi>
class.
In 2019, the European Committee on Antimicrobial Susceptibility Testing (EUCAST) has decided to change the definitions of susceptibility testing categories R and S/I as shown below (https://www.eucast.org/newsiandr/).
R = Resistant
A microorganism is categorised as Resistant when there is a high likelihood of therapeutic failure even when there is increased exposure. Exposure is a function of how the mode of administration, dose, dosing interval, infusion time, as well as distribution and excretion of the antimicrobial agent will influence the infecting organism at the site of infection.
S = Susceptible
A microorganism is categorised as Susceptible, standard dosing regimen, when there is a high likelihood of therapeutic success using a standard dosing regimen of the agent.
I = Susceptible, Increased exposure
A microorganism is categorised as Susceptible, Increased exposure when there is a high likelihood of therapeutic success because exposure to the agent is increased by adjusting the dosing regimen or by its concentration at the site of infection.
This AMR package honours this (new) insight. Use susceptibility()
(equal to proportion_SI()
) to determine antimicrobial susceptibility and count_susceptible()
(equal to count_SI()
) to count susceptible isolates.
The lifecycle of this function is stable. In a stable function, major changes are unlikely. This means that the unlying code will generally evolve by adding new arguments; removing arguments or changing the meaning of existing arguments will be avoided.
If the unlying code needs breaking changes, they will occur gradually. For example, an argument will be deprecated and first continue to work, but will emit an message informing you of the change. Next, typically after at least one newly released version on CRAN, the message will be transformed to an error.
All reference data sets (about microorganisms, antibiotics, R/SI interpretation, EUCAST rules, etc.) in this AMR
package are publicly and freely available. We continually export our data sets to formats for use in R, SPSS, SAS, Stata and Excel. We also supply flat files that are machine-readable and suitable for input in any software program, such as laboratory information systems. Please find all download links on our website, which is automatically updated with every code change.
On our website https://msberends.github.io/AMR/ you can find a comprehensive tutorial about how to conduct AMR data analysis, the complete documentation of all functions and an example analysis using WHONET data.
summary(example_isolates) # see all R/SI results at a glance
# \donttest{
if (require("skimr")) {
# class <rsi> supported in skim() too:
skim(example_isolates)
}
# }
# For INTERPRETING disk diffusion and MIC values -----------------------
# a whole data set, even with combined MIC values and disk zones
df <- data.frame(microorganism = "Escherichia coli",
AMP = as.mic(8),
CIP = as.mic(0.256),
GEN = as.disk(18),
TOB = as.disk(16),
NIT = as.mic(32),
ERY = "R")
as.rsi(df)
# for single values
as.rsi(x = as.mic(2),
mo = as.mo("S. pneumoniae"),
ab = "AMP",
guideline = "EUCAST")
as.rsi(x = as.disk(18),
mo = "Strep pneu", # `mo` will be coerced with as.mo()
ab = "ampicillin", # and `ab` with as.ab()
guideline = "EUCAST")
# \donttest{
# the dplyr way
if (require("dplyr")) {
df %>% mutate_if(is.mic, as.rsi)
df %>% mutate_if(function(x) is.mic(x) | is.disk(x), as.rsi)
df %>% mutate(across(where(is.mic), as.rsi))
df %>% mutate_at(vars(AMP:TOB), as.rsi)
df %>% mutate(across(AMP:TOB, as.rsi))
df %>%
mutate_at(vars(AMP:TOB), as.rsi, mo = .$microorganism)
# to include information about urinary tract infections (UTI)
data.frame(mo = "E. coli",
NIT = c("<= 2", 32),
from_the_bladder = c(TRUE, FALSE)) %>%
as.rsi(uti = "from_the_bladder")
data.frame(mo = "E. coli",
NIT = c("<= 2", 32),
specimen = c("urine", "blood")) %>%
as.rsi() # automatically determines urine isolates
df %>%
mutate_at(vars(AMP:NIT), as.rsi, mo = "E. coli", uti = TRUE)
}
# For CLEANING existing R/SI values ------------------------------------
as.rsi(c("S", "I", "R", "A", "B", "C"))
as.rsi("<= 0.002; S") # will return "S"
rsi_data <- as.rsi(c(rep("S", 474), rep("I", 36), rep("R", 370)))
is.rsi(rsi_data)
plot(rsi_data) # for percentages
barplot(rsi_data) # for frequencies
# the dplyr way
if (require("dplyr")) {
example_isolates %>%
mutate_at(vars(PEN:RIF), as.rsi)
# same:
example_isolates %>%
as.rsi(PEN:RIF)
# fastest way to transform all columns with already valid AMR results to class `rsi`:
example_isolates %>%
mutate_if(is.rsi.eligible, as.rsi)
# note: from dplyr 1.0.0 on, this will be:
# example_isolates %>%
# mutate(across(where(is.rsi.eligible), as.rsi))
}
# }