Multidrug Resistant Acinetobacter baumannii: Risk Factors for Appearance of Imipenem Resistant Strains on Patients Formerly with Susceptible Strains

被引:51
作者
Ye, Jung-Jr [1 ]
Huang, Ching-Tai [1 ]
Shie, Shian-Sen [1 ]
Huang, Po-Yen [1 ]
Su, Lin-Hui [2 ]
Chiu, Cheng-Hsun [3 ]
Leu, Hsieh-Shong [1 ]
Chiang, Ping-Cherng [1 ]
机构
[1] Chang Gung Mem Hosp, Dept Internal Med, Div Infect Dis, Tao Yuan, Taiwan
[2] Chang Gung Mem Hosp, Linkou Med Ctr, Dept Pathol, Div Clin Pathol, Tao Yuan, Taiwan
[3] Chang Gung Childrens Hosp, Dept Pediat, Div Pediat Infect Dis, Tao Yuan, Taiwan
来源
PLOS ONE | 2010年 / 5卷 / 03期
关键词
INTENSIVE-CARE-UNIT; ANTIMICROBIAL RESISTANCE; CARBAPENEM RESISTANCE; ANTIBIOTIC-RESISTANCE; HOSPITAL OUTBREAK; IN-VITRO; ACQUISITION; INFECTIONS; EPIDEMIOLOGY; SULBACTAM;
D O I
10.1371/journal.pone.0009947
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Multidrug resistant Acinetobacter baumannii (MDRAB) is an important nosocomial pathogen usually susceptible to carbapenems; however, growing number of imipenem resistant MDRAB (IR-MDRAB) poses further clinical challenge. The study was designed to identify the risk factors for appearance of IR-MDRAB on patients formerly with imipenem susceptible MDRAB (IS-MDRAB) and the impact on clinical outcomes. Methodology/Principal Findings: A retrospective case control study was carried out for 209 consecutive episodes of IS-MDRAB infection or colonization from August 2001 to March 2005. Forty-nine (23.4%) episodes with succeeding clinical isolates of IR-MDRAB were defined as the cases and 160 (76.6%) with all subsequent clinical isolates of IS-MDRAB were defined as the controls. Quantified antimicrobial selective pressure, "time at risk'', severity of illness, comorbidity, and demographic data were incorporated for multivariate analysis, which revealed imipenem or meropenem as the only significant independent risk factor for the appearance of IR-MDRAB (adjusted OR, 1.18; 95% CI, 1.09 to 1.27). With selected cases and controls matched to exclude exogenous source of IR-MDRAB, multivariate analysis still identified carbapenem as the only independent risk factor (adjusted OR, 1.48; 95% CI, 1.14 to 1.92). Case patients had a higher crude mortality rate compared to control patients (57.1% vs. 31.3%, p = 0.001), and the mortality of case patients was associated with shorter duration of "time at risk'', i.e., faster appearance of IR-MDRAB (adjusted OR, 0.9; 95% CI, 0.83 to 0.98). Conclusions/Significance: Judicious use of carbapenem with deployment of antibiotics stewardship measures is critical for reducing IR-MDRAB and the associated unfavorable outcome.
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页数:6
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