portion.Rd
These functions can be used to calculate the (co-)resistance of microbial isolates (i.e. percentage of S, SI, I, IR or R). All functions support quasiquotation with pipes, can be used in dplyr
s summarise
and support grouped variables, see Examples.
portion_R
and portion_IR
can be used to calculate resistance, portion_S
and portion_SI
can be used to calculate susceptibility.
portion_R(..., minimum = 30, as_percent = FALSE, also_single_tested = FALSE) portion_IR(..., minimum = 30, as_percent = FALSE, also_single_tested = FALSE) portion_I(..., minimum = 30, as_percent = FALSE, also_single_tested = FALSE) portion_SI(..., minimum = 30, as_percent = FALSE, also_single_tested = FALSE) portion_S(..., minimum = 30, as_percent = FALSE, also_single_tested = FALSE) portion_df(data, translate_ab = "name", language = get_locale(), minimum = 30, as_percent = FALSE, combine_IR = FALSE)
... | one or more vectors (or columns) with antibiotic interpretations. They will be transformed internally with |
---|---|
minimum | the minimum allowed number of available (tested) isolates. Any isolate count lower than |
as_percent | a logical to indicate whether the output must be returned as a hundred fold with % sign (a character). A value of |
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_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. IR (susceptible vs. non-susceptible) |
M39 Analysis and Presentation of Cumulative Antimicrobial Susceptibility Test Data, 4th Edition, 2014, Clinical and Laboratory Standards Institute (CLSI). https://clsi.org/standards/products/microbiology/documents/m39/.
Wickham H. Tidy Data. The Journal of Statistical Software, vol. 59, 2014. http://vita.had.co.nz/papers/tidy-data.html
Double or, when as_percent = TRUE
, a character.
Remember that you should filter your table to let it contain only first isolates! Use first_isolate
to determine them in your data set.
These functions are not meant to count isolates, but to calculate the portion of resistance/susceptibility. Use the count
functions to count isolates. Low counts can infuence the outcome - these portion
functions may camouflage this, since they only return the portion albeit being dependent on the minimum
parameter.
portion_df
takes any variable from data
that has an "rsi"
class (created with as.rsi
) and calculates the portions 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"
.
To calculate the probability (p) of susceptibility of one antibiotic, we use this formula:
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.
count_*
to count resistant and susceptible isolates.
# NOT RUN { # septic_patients is a data set available in the AMR package. It is true, genuine data. ?septic_patients # Calculate resistance portion_R(septic_patients$AMX) portion_IR(septic_patients$AMX) # Or susceptibility portion_S(septic_patients$AMX) portion_SI(septic_patients$AMX) # Do the above with pipes: library(dplyr) septic_patients %>% portion_R(AMX) septic_patients %>% portion_IR(AMX) septic_patients %>% portion_S(AMX) septic_patients %>% portion_SI(AMX) septic_patients %>% group_by(hospital_id) %>% summarise(p = portion_S(CIP), n = n_rsi(CIP)) # n_rsi works like n_distinct in dplyr septic_patients %>% group_by(hospital_id) %>% summarise(R = portion_R(CIP, as_percent = TRUE), I = portion_I(CIP, as_percent = TRUE), S = portion_S(CIP, as_percent = TRUE), 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! # Calculate co-resistance between amoxicillin/clav acid and gentamicin, # so we can see that combination therapy does a lot more than mono therapy: septic_patients %>% portion_S(AMC) # S = 71.4% septic_patients %>% count_all(AMC) # n = 1879 septic_patients %>% portion_S(GEN) # S = 74.0% septic_patients %>% count_all(GEN) # n = 1855 septic_patients %>% portion_S(AMC, GEN) # S = 92.3% septic_patients %>% count_all(AMC, GEN) # n = 1798 septic_patients %>% group_by(hospital_id) %>% summarise(cipro_p = portion_S(CIP, as_percent = TRUE), cipro_n = count_all(CIP), genta_p = portion_S(GEN, as_percent = TRUE), genta_n = count_all(GEN), combination_p = portion_S(CIP, GEN, as_percent = TRUE), combination_n = count_all(CIP, GEN)) # Get portions S/I/R immediately of all rsi columns septic_patients %>% select(AMX, CIP) %>% portion_df(translate = FALSE) # It also supports grouping variables septic_patients %>% select(hospital_id, AMX, CIP) %>% group_by(hospital_id) %>% portion_df(translate = FALSE) # }# NOT RUN { # calculate current empiric combination therapy of Helicobacter gastritis: my_table %>% filter(first_isolate == TRUE, genus == "Helicobacter") %>% summarise(p = portion_S(AMX, MTR), # amoxicillin with metronidazole n = count_all(AMX, MTR)) # }