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
. Values that cannot be interpreted will be returned as NA
with a warning.
as.rsi(x, ...) 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 )
x | vector of values (for class |
---|---|
... | for using on a data.frame: names of columns to apply |
threshold | maximum fraction of invalid antimicrobial interpretations of |
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, see Details for all options |
uti | (Urinary Tract Infection) A vector with logicals ( |
conserve_capped_values | a logical to indicate that MIC values starting with |
add_intrinsic_resistance | (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). |
reference_data | 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 |
col_mo | column name of the IDs of the microorganisms (see |
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:
your_data %>% mutate_if(is.mic, as.rsi) # until dplyr 1.0.0 your_data %>% mutate(across((is.mic), as.rsi)) # since dplyr 1.0.0
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.
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, supported guidelines to be used as input for the guideline
argument are: "CLSI 2010", "CLSI 2011", "CLSI 2012", "CLSI 2013", "CLSI 2014", "CLSI 2015", "CLSI 2016", "CLSI 2017", "CLSI 2018", "CLSI 2019", "EUCAST 2011", "EUCAST 2012", "EUCAST 2013", "EUCAST 2014", "EUCAST 2015", "EUCAST 2016", "EUCAST 2017", "EUCAST 2018", "EUCAST 2019", "EUCAST 2020", "EUCAST 2021".
Simply using "CLSI"
or "EUCAST"
as input will automatically select the latest version of that guideline. 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 20,486 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 returns a vector in which all columns are checked for this class.
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.
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 = 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, 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, a 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. As we would like to better understand the backgrounds and needs of our users, please participate in our survey!
summary(example_isolates) # see all R/SI results at a glance 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((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((is.rsi.eligible), as.rsi)) } # }