Song Kyoung-Ho, Kim Moonsuk, Kim Chung Jong, Cho Jeong Eun, Choi Yun Jung, Park Jeong Su, Ahn Soyeon, Jang Hee-Chang, Park Kyung-Hwa, Jung Sook-In, Yoon Nara, Kim Dong-Min, Hwang Jeong-Hwan, Lee Chang Seop, Lee Jae Hoon, Kwak Yee Gyung, Kim Eu Suk, Park Seong Yeon, Park Yoonseon, Lee Kkot Sil, Lee Yeong-Seon, Kim Hong Bin
Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, South Korea.
Department of Laboratory Medicine, Seoul National University Bundang Hospital, Seongnam, South Korea.
Antimicrob Agents Chemother. 2017 Feb 23;61(3). doi: 10.1128/AAC.01845-16. Print 2017 Mar.
There are conflicting data on the association of vancomycin MIC (VAN-MIC) with treatment outcomes in 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 (ISA) infections, defined as the isolation of 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 (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.
关于万古霉素最低抑菌浓度(VAN - MIC)与感染治疗结局之间的关联,存在相互矛盾的数据。我们调查了高VAN - MIC与30天死亡率之间的关系,并在一大群侵袭性(ISA)感染患者中确定了死亡的风险因素,侵袭性感染定义为从通常无菌的部位分离出(某种病原体)。在两年期间,1027名患有ISA感染的成年患者被纳入10家医院,其中包括673名(66%)耐甲氧西林(MRSA)感染患者。通过Etest检测有200株(19.5%)分离株VAN - MIC高(≥1.5毫克/升),通过肉汤微量稀释法(BMD)检测有87株(8.5%)。全因30天死亡率为27.4%。两种方法检测出的高VAN - MIC均与全因30天死亡率无关,这一发现对于不同的MIC检测方法和甲氧西林敏感性而言都是一致的。我们得出结论,在ISA感染中,高VAN - MIC与全因30天死亡率增加无关。我们的数据支持这样一种观点,即仅VAN - MIC不足以作为改变当前临床实践的依据。