count.Rd
These functions can be used to count resistant/susceptible microbial isolates. All functions support quasiquotation with pipes, can be used in dplyr
s summarise
and support grouped variables, see Examples.
count_R
and count_IR
can be used to count resistant isolates, count_S
and count_SI
can be used to count susceptible isolates.
count_R(..., also_single_tested = FALSE) count_IR(..., also_single_tested = FALSE) count_I(..., also_single_tested = FALSE) count_SI(..., also_single_tested = FALSE) count_S(..., also_single_tested = FALSE) count_all(...) n_rsi(...) count_df(data, translate_ab = "name", language = get_locale(), combine_SI = TRUE, combine_IR = FALSE)
... | one or more vectors (or columns) with antibiotic interpretations. They will be transformed internally with |
---|---|
also_single_tested | a logical to indicate whether (in combination therapies) also observations should be included where not all antibiotics were tested, but at least one of the tested antibiotics contains a target interpretation (e.g. S in case of |
data | a |
translate_ab | a column name of the |
language | language of the returned text, defaults to system language (see |
combine_SI | a logical to indicate whether all values of S and I must be merged into one, so the output only consists of S+I vs. R (susceptible vs. resistant). This used to be the parameter |
combine_IR | a logical to indicate whether all values of I and R must be merged into one, so the output only consists of S vs. I+R (susceptible vs. non-susceptible). This is outdated, see parameter |
Wickham H. Tidy Data. The Journal of Statistical Software, vol. 59, 2014. http://vita.had.co.nz/papers/tidy-data.html
Integer
These functions are meant to count isolates. Use the portion_*
functions to calculate microbial resistance.
n_rsi
is an alias of count_all
. They can be used to count all available isolates, i.e. where all input antibiotics have an available result (S, I or R). Their use is equal to n_distinct
. Their function is equal to count_S(...) + count_IR(...)
.
count_df
takes any variable from data
that has an "rsi"
class (created with as.rsi
) and counts the amounts of R, I and S. The resulting tidy data (see Source) data.frame
will have three rows (S/I/R) and a column for each variable with class "rsi"
.
In 2019, EUCAST has decided to change the definitions of susceptibility testing categories S, I and R as shown below. Results of several consultations on the new definitions are available on the EUCAST website under "Consultations".
SSusceptible, standard dosing regimen: 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.
ISusceptible, 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.
RResistant: 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.
Source: http://www.eucast.org/newsiandr/.
This AMR package honours this new insight.
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.
portion_*
to calculate microbial resistance and susceptibility.
# NOT RUN { # septic_patients is a data set available in the AMR package. It is true, genuine data. ?septic_patients # Count resistant isolates count_R(septic_patients$AMX) count_IR(septic_patients$AMX) # Or susceptible isolates count_S(septic_patients$AMX) count_SI(septic_patients$AMX) # Count all available isolates count_all(septic_patients$AMX) n_rsi(septic_patients$AMX) # Since n_rsi counts available isolates, you can # calculate back to count e.g. non-susceptible isolates. # This results in the same: count_IR(septic_patients$AMX) portion_IR(septic_patients$AMX) * n_rsi(septic_patients$AMX) library(dplyr) septic_patients %>% group_by(hospital_id) %>% summarise(R = count_R(CIP), I = count_I(CIP), S = count_S(CIP), n1 = count_all(CIP), # the actual total; sum of all three n2 = n_rsi(CIP), # same - analogous to n_distinct total = n()) # NOT the number of tested isolates! # Count co-resistance between amoxicillin/clav acid and gentamicin, # so we can see that combination therapy does a lot more than mono therapy. # Please mind that `portion_S` calculates percentages right away instead. count_S(septic_patients$AMC) # S = 1342 (71.4%) count_all(septic_patients$AMC) # n = 1879 count_S(septic_patients$GEN) # S = 1372 (74.0%) count_all(septic_patients$GEN) # n = 1855 with(septic_patients, count_S(AMC, GEN)) # S = 1660 (92.3%) with(septic_patients, # n = 1798 n_rsi(AMC, GEN)) # Get portions S/I/R immediately of all rsi columns septic_patients %>% select(AMX, CIP) %>% count_df(translate = FALSE) # It also supports grouping variables septic_patients %>% select(hospital_id, AMX, CIP) %>% group_by(hospital_id) %>% count_df(translate = FALSE) # }