Act Fast as Time Is Less: High Faecal Carriage of Carbapenem-Resistant in Critical Care Patients.

J Clin Diagn Res

Research Scholar in Critical Microbiology, Department of Microbiology, S.L. Raheja Hospital (A Fortis Associate), Mumbai, Maharashtra, India .

Published: September 2016

Introduction: Carbapenem-resistant (CRE) are drug-resistant Gram-negative bacteria that are present in the community as well as in hospitals. Their infection and colonisation puts critically ill patients at high risk due to the drug-resistant nature of the strains and possible spreading of these organisms, even in a hospital environment.

Aim: To examine the presence and types of species in patients admitted directly from the community.

Materials And Methods: The present study was a one-month pilot conducted in the ICU of a tertiary care hospital in Mumbai, India in 2015. Faecal samples of patients admitted from the community directly to the ICU were analysed using tests like MHT (Modified Hodge) and EDTA for the presence of IMP (action on Imipenem) and KPC ( Test Pneumoniae Carbapenemase) producing strains of . Polymerase Chain Reaction (PCR) was performed to look for , , 1, , and KPC genes. Antibiotic Sensitivity Test was carried out as per CLSI guidelines.

Results: The results showed an alarming level of faecal carriage rates in adult ICU patients. was the most common carbapenem-resistant isolate, closely followed by . PCR results revealed nine strains were positive for (KPC) gene, from which 7 were and one each of and was observed. Antibiotic Sensitivity Test results showed that the isolates had maximum sensitivity to Colistin (100%) and Tigecycline (95%).

Conclusion: These levels indicate that in the absence of CRE screenings, proper isolation of carrier patients is not possible, leading to possible spreading of these resistant bacteria strains in ICUs. A longer period of study is required to obtain more substantial data to validate the results of this pilot.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5071929PMC
http://dx.doi.org/10.7860/JCDR/2016/17638.8400DOI Listing

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