| Literature DB >> 27956430 |
Kyoung-Ho Song1, Moonsuk Kim1, Chung Jong Kim1, Jeong Eun Cho1, Yun Jung Choi1, Jeong Su Park2, Soyeon Ahn3, Hee-Chang Jang4, Kyung-Hwa Park4, Sook-In Jung4, Nara Yoon5, Dong-Min Kim5, Jeong-Hwan Hwang6, Chang Seop Lee6, Jae Hoon Lee7, Yee Gyung Kwak8, Eu Suk Kim1, Seong Yeon Park9, Yoonseon Park10, Kkot Sil Lee11, Yeong-Seon Lee12, Hong Bin Kim13.
Abstract
There are conflicting data on the association of vancomycin MIC (VAN-MIC) with treatment outcomes in Staphylococcus aureus infections. We investigated the relationship between high VAN-MIC and 30-day mortality and identified the risk factors for mortality in a large cohort of patients with invasive S. aureus (ISA) infections, defined as the isolation of S. aureus from a normally sterile site. Over a 2-year period, 1,027 adult patients with ISA infections were enrolled in 10 hospitals, including 673 (66%) patients with methicillin-resistant S. aureus (MRSA) infections. There were 200 (19.5%) isolates with high VAN-MIC (≥1.5 mg/liter) by Etest and 87 (8.5%) by broth microdilution (BMD). The all-cause 30-day mortality rate was 27.4%. High VAN-MIC by either method was not associated with all-cause 30-day mortality, and this finding was consistent across MIC methodologies and methicillin susceptibilities. We conclude that high VAN-MIC is not associated with increased risk of all-cause 30-day mortality in ISA infections. Our data support the view that VAN-MIC alone is not sufficient evidence to change current clinical practice.Entities:
Keywords: MIC; Staphylococcus aureus; bacteremia; methicillin resistant; methicillin susceptible; vancomycin
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Year: 2017 PMID: 27956430 PMCID: PMC5328555 DOI: 10.1128/AAC.01845-16
Source DB: PubMed Journal: Antimicrob Agents Chemother ISSN: 0066-4804 Impact factor: 5.191