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564. A Five-Year Evolutionary Study of the Minimum Inhibitory Concentrations of Methicillin-resistant Staphylococcus aureus to Mupirocin, Chlorhexidine, and Octenidine in a Singaporean Tertiary Institution
Author(s) -
Shuwei Zheng,
Shimin Jasmine Chung,
Heng Chiak James Sim,
Xiaoyi Zhu,
Si Xuan Tan,
Tara M Chlebicka,
Yiong Huak Chan,
Tze Peng Lim,
Lay Hoon Andrea Kwa,
Maciej Piotr Chlebicki
Publication year - 2019
Publication title -
open forum infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.546
H-Index - 35
ISSN - 2328-8957
DOI - 10.1093/ofid/ofz360.633
Subject(s) - medicine , broth microdilution , mupirocin , methicillin resistant staphylococcus aureus , staphylococcus aureus , minimum inhibitory concentration , microbiology and biotechnology , chlorhexidine , bioburden , carriage , staphylococcal infections , antibiotics , surgery , biology , pathology , bacteria , dentistry , genetics
Background Methicillin-resistant Staphylococcus aureus (MRSA) is a common cause of healthcare-associated infection. Eradication of MRSA carriage reduces clinical infection and prevents transmission. In Singapore General Hospital, a series of hospital-wide measures were instituted over three years (Figure 1) to reduce mupirocin (MUP) resistance, and to decrease the bioburden of MRSA colonization amongst inpatients using octenidine (OCT)-based products. Methods A prevalence study was conducted at three time points (TPs) on consecutive MRSA screening isolates to evaluate for their minimum inhibitory concentrations (MICs) to CHG, OCT and MUP using broth microdilution sensitive plates and the presence of the ileS-2 gene, in 2013 (pre-intervention TP, TP1; n = 160), 2016 (early post-intervention TP, TP2; n = 99) and 2017 (late post-intervention TP, TP3; n = 76). Statistical analyses were performed using the Chi-square test with reference from TP1. Results A significant improvement in MUP susceptibility by MIC (256 µg/mL) and ileS-2 testing reduced from 25.0% (TP1) to 12.1% (TP2; P = 0.014) to 5.3% (TP3; P = 0.001) and 30.0% (TP1) to 18.2% (TP2; P = 0.036) to 9.2% (TP3; P = 0.001), respectively. OCT MIC range remained stable at 0.5 to 1 across all three TPs. The number of isolates with reduced CHG susceptibility (MIC ≥4 mg/L) increased over the three TPs from 23.1% to 27.2% (P = 0.45) to 42.1% (P = 0.003), despite decreasing CHG prescription. Conclusion A restrictive MUP usage policy can improve MUP susceptibility amongst MRSA isolates over time. Widespread OCT use did not appear to result in a rise of OCT MIC over the intervention period. Although the clinical significance of reduced susceptibility to CHG remains uncertain, this worrying trend in our institution deserves further studies to better understand mechanisms of CHG resistance. Disclosures All authors: No reported disclosures.

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