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Types of interpretive errors in susceptibility testing
Author(s) -
BJÖRKLIND ANDERS,
RINGERTZ SIGNE,
KRONVALL GÖRAN
Publication year - 1989
Publication title -
apmis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.909
H-Index - 88
eISSN - 1600-0463
pISSN - 0903-4641
DOI - 10.1111/j.1699-0463.1989.tb00502.x
Subject(s) - microbiology and biotechnology , nalidixic acid , pseudomonas aeruginosa , biology , norfloxacin , staphylococcus saprophyticus , antibiotics , ciprofloxacin , bacteria , staphylococcus aureus , staphylococcus , genetics
A total of 548 strains of the eleven most common urinary tract pathogens were investigated for possible errors in norfloxacin susceptibility tests comparing MIC determinations with disk diffusion assays. Most strains were found to be sensitive with MIC‐90 values below 1.0 for the Enterobacteriaceae while the classical nalidixic acid resistant species, the gram‐positive bacteria and Pseudomonas aeruginosa , were less susceptible to norfloxacin with MIC‐90 above 1.0 mg/l. MIC‐values close to interpretive MIC‐limits were recorded for S. faecalis and S. agalactiae using the recommendations of the national Committee for Clinical Laboratory Standards (NCCLS) (susceptible, S ≤ 4.0) and for P. aeruginosa and S. aureus using the Swedish Reference Group for Antibiotics (SRGA) standards (S ≤ 1.0). Susceptibility interpretations for these species showed a lack of accuracy consistent with methodological problems of reproducibility, an error called type I. The changes in the MIC‐limits required for these strains to correct the error would be S ≤ 4 for P. aeruginosa and S. aureus , S ≤ 8 for S. agalactiae and S ≤ 0.5 for S. faecalis. A type II error, occurring when a bacterial species shows a regression line different from the regular line, was also identified for S. saprophyticus. The use of breakpoints derived from single strains regression analysis corrected this error and also reduced the frequency of similar misinterpretations in other species. The term “species‐specific MIC‐limits” should be introduced along with the established concept of “species‐specific interpretive zone breakpoints” to allow for the correction of type I interpretive errors. Type II errors can be corrected by using species‐specific interpretive breakpoints, either issued by reference laboratories or derived by calculations from single‐strain regression analysis in the individual laboratory.

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