Diagnostic Accuracy of the Simplified Carbapenem Inactivation Method versus the Modified Hodge Test in Carbapenem-Resistant Pseudomonas aeruginosa: A Cross-Sectional Study
Aug 2026· Open Access Indonesian Journal of Medical Reviews· Vol 6, pp. 281-296· 0 citations
Abstract
Background: Carbapenem-resistant Pseudomonas aeruginosa (CRPA) is among the pathogens contributing most to the global burden of antimicrobial resistance, and its pooled prevalence in Indonesia reaches 43%. Carbapenem resistance and carbapenemase production are not equivalent, and only the enzymatic route is transmissible and therapeutically decisive. Molecular confirmation is unavailable in most Indonesian laboratories, so an accurate low-cost phenotypic assay is needed.
Objective: To compare the simplified carbapenem inactivation method (sCIM) with the Modified Hodge Test (MHT) for detecting carbapenemase production in carbapenem-resistant P. aeruginosa.
Methods: This cross-sectional diagnostic-accuracy study evaluated 30 meropenem- and imipenem-resistant clinical isolates archived at Dr. Soetomo General Academic Hospital, Surabaya, using PCR for blaIMP, blaGES, blaOXA, blaNDM, blaKPC and blaVIM as the reference standard.
Result: A carbapenemase gene was detected in 13/30 isolates (43.3%): blaIMP in 9, blaGES in 3 and blaOXA in 1. sCIM achieved 92.31% sensitivity (95% confidence interval 64.0-99.8), 100.00% specificity (80.5-100.0), 96.7% accuracy and near-perfect agreement with PCR (kappa 0.932). MHT achieved 46.15% sensitivity (19.2-74.9), 88.24% specificity (63.6-98.5) and fair agreement (kappa 0.360). The paired exact McNemar test confirmed the sensitivity advantage of sCIM (p = 0.031), and bootstrapping showed a 26.6-percentage-point difference in overall accuracy (95% confidence interval 10.0-43.3). MHT detected no blaGES-positive isolate and only 6/9 blaIMP-positive isolates; sCIM detected all of both, while neither assay detected the single poorly expressed blaOXA isolate.
Conclusion: sCIM is an accurate, rapid and inexpensive assay that should replace MHT in Indonesian laboratories and feed directly into stewardship and infection-control decisions.
The mCIM → D73C → simplex PCR workflow demonstrated practical value for carbapenemase detection in clinical microbiology laboratories and described antimicrobial susceptibility profiles and analyze associations between resistance genotype and phenotype.
T. Nguyen, D. Tran, V. Ngo· Tạp chí Y Dược Huế· 0 citations
ABSTRACT The detection of carbapenemases in Pseudomonas aeruginosa remains challenging due to a great variety of other resistance mechanisms, and most laboratories, therefore, do not test for them. This study aimed to comparatively evaluate seven phenotypic carbapenemase detection assays across three epidemiological se...
Lukas Schaffarczyk, Rebekka Laufenberg, Timo J. B. van Eldijk et al.· Journal of Clinical Microbio...· 0 citations
The sequential workflow of mCIM screening, D73C classification, and PCR confirmation demonstrated practical value for carbapenemase detection in clinical microbiology laboratories.
T. Nguyen, Be Hai¹˒², Bình Đình Trần et al.· 0 citations
BACKGROUND
Rapid and accurate detection of carbapenemase-producing Klebsiella pneumoniae is essential for effective antimicrobial therapy and infection control, yet molecular methods remain costly and technically demanding. This two-center study, representing two different geographic regions of Turkey, compared the per...
BACKGROUND
Carbapenem-resistant Klebsiella pneumoniae (CRKp) strains are a major public health threat.
AIM
This study aimed to compare multiplex lateral flow immunochromatographic testing (LFT) and polymerase chain reaction (PCR) for detecting carbapenemase genes in carbapenem-resistant K. pneumoniae (CRKp). A second...
O. Yapıcı, E. Dalmanoğlu, A. Şener et al.· Nigerian Journal of Clinical...· 0 citations
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