Performance of Quantification of Modified Hodge Test : An Evaluation with Klebsiella pneumoniae Carbapenemase-Producing Enterobacteriaceae Isolates

Modified Hodge Test (MHT) has been suggested as screening tests for carbapenemases, but concerns regarding its difficult interpretation and common false-positive results obtained in the presence of other β-lactamases have been noted. This study aimed to quantify the enhanced growth formed by the ind...

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Veröffentlicht in:BioMed research international 2014-01, Vol.2014 (2014), p.1-6
Hauptverfasser: Barth, Afonso Luis, Zavascki, Alexandre P., Linhares, Adriano Rostirolla, Ribeiro, Vanessa Bley
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Linhares, Adriano Rostirolla
Ribeiro, Vanessa Bley
description Modified Hodge Test (MHT) has been suggested as screening tests for carbapenemases, but concerns regarding its difficult interpretation and common false-positive results obtained in the presence of other β-lactamases have been noted. This study aimed to quantify the enhanced growth formed by the indicator strain and thus evaluate the performance of a quantitative interpretation of MHT for KPC screening. MHT was performed in 50 KPC-producing isolates and 334 non-carbapenemase-producing isolates, using ertapenem (ETP) and meropenem (MEM) as substrates. The size of enhanced growth of indicator strain was measured for each isolate tested and for the positive control used, and a ratio was calculated. Our results revealed 17 different ETP and MEM ratios, with distinct sensitivity (SN) and specificity (SP). Higher SN combined to higher SP was achieved when ETP and MEM ratios were 0.45, with a SN value of 96% for both substrates and SP values of 99.4% and 100% for ETP and MEM, respectively. The quantification with both substrates increased SP of the test for KPC detection. Considering that MHT is the unique phenotypic test that is referred to by CLSI, a more accurate approach for its interpretation could be applied to make it a more useful tool.
doi_str_mv 10.1155/2014/139305
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This study aimed to quantify the enhanced growth formed by the indicator strain and thus evaluate the performance of a quantitative interpretation of MHT for KPC screening. MHT was performed in 50 KPC-producing isolates and 334 non-carbapenemase-producing isolates, using ertapenem (ETP) and meropenem (MEM) as substrates. The size of enhanced growth of indicator strain was measured for each isolate tested and for the positive control used, and a ratio was calculated. Our results revealed 17 different ETP and MEM ratios, with distinct sensitivity (SN) and specificity (SP). Higher SN combined to higher SP was achieved when ETP and MEM ratios were 0.45, with a SN value of 96% for both substrates and SP values of 99.4% and 100% for ETP and MEM, respectively. The quantification with both substrates increased SP of the test for KPC detection. Considering that MHT is the unique phenotypic test that is referred to by CLSI, a more accurate approach for its interpretation could be applied to make it a more useful tool.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Puplishing Corporation</pub><pmid>24790988</pmid><doi>10.1155/2014/139305</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; PubMed Central Open Access; Wiley Online Library Open Access; PubMed Central; Alma/SFX Local Collection
subjects Bacterial Proteins - analysis
Bacteriological Techniques - methods
Bacteriology
Beta lactamases
beta-Lactamases - analysis
Biosynthesis
E coli
Enterobacter
Enterobacteriaceae
Enzymes
Genetic aspects
Humans
Klebsiella pneumoniae
Klebsiella pneumoniae - enzymology
Klebsiella pneumoniae - isolation & purification
Low income groups
Methods
Microbiological research
Properties
Ratios
Reproducibility of Results
Sensitivity and Specificity
Studies
title Performance of Quantification of Modified Hodge Test : An Evaluation with Klebsiella pneumoniae Carbapenemase-Producing Enterobacteriaceae Isolates
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