as.rsi.Rd
Interpret 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
. Invalid antimicrobial interpretations will be translated as NA
with a warning.
as.rsi(x, ...) # S3 method for mic as.rsi( x, mo, ab = deparse(substitute(x)), guideline = "EUCAST", uti = FALSE, ... ) # S3 method for disk as.rsi( x, mo, ab = deparse(substitute(x)), guideline = "EUCAST", uti = FALSE, ... ) # S3 method for data.frame as.rsi(x, col_mo = NULL, guideline = "EUCAST", uti = NULL, ...) is.rsi(x) is.rsi.eligible(x, threshold = 0.05)
x | vector of values (for class |
---|---|
... | parameters passed on to methods |
mo | any (vector of) text that can be coerced to a valid microorganism code with |
ab | any (vector of) text that can be coerced to a valid antimicrobial code with |
guideline | defaults to the latest included EUCAST guideline, run |
uti | (Urinary Tract Infection) A vector with logicals ( |
col_mo | column name of the IDs of the microorganisms (see |
threshold | maximum fraction of invalid antimicrobial interpretations of |
Ordered factor with new class rsi
Run unique(rsi_translation$guideline)
for a list of all supported guidelines. The repository of this package contains this machine readable version of these guidelines.
These guidelines are machine readable, since .
After using as.rsi()
, you can use eucast_rules()
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 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
parameter.
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 (http://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 = Increased exposure, but still susceptible
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, we are largely happy with the unlying code, and major changes are unlikely. This means that the unlying code will generally evolve by adding new arguments; we will avoid removing arguments or changing the meaning of existing arguments.
If the unlying code needs breaking changes, they will occur gradually. To begin with, the function or argument will be deprecated; it will 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.
On our website https://msberends.gitlab.io/AMR you can find a comprehensive tutorial about how to conduct AMR analysis, the complete documentation of all functions (which reads a lot easier than here in R) and an example analysis using WHONET data.
# For INTERPRETING disk diffusion and MIC values ----------------------- # a whole data set, even with combined MIC values and disk zones df <- data.frame(microorganism = "E. coli", AMP = as.mic(8), CIP = as.mic(0.256), GEN = as.disk(18), TOB = as.disk(16), NIT = as.mic(32)) as.rsi(df) # the dplyr way library(dplyr) df %>% mutate_at(vars(AMP:TOB), as.rsi, mo = "E. coli") 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:TOB), as.rsi, mo = "E. coli", uti = TRUE) # 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") # 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 freq(rsi_data) # frequency table with informative header library(dplyr) example_isolates %>% mutate_at(vars(PEN:RIF), as.rsi) # 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(is.rsi.eligible, as.rsi)) # default threshold of `is.rsi.eligible` is 5%. is.rsi.eligible(WHONET$`First name`) # fails, >80% is invalid is.rsi.eligible(WHONET$`First name`, threshold = 0.99) # succeeds