Colistin-based treatment for extensively drug-resistant Acinetobacter baumannii pneumonia

被引:78
作者
Khawcharoenporn, Thana [1 ]
Pruetpongpun, Nattapol [1 ]
Tiamsak, Pimsiri [2 ]
Rutchanawech, Sasinuch [1 ]
Mundy, Linda M. [3 ]
Apisarnthanarak, Anucha [1 ]
机构
[1] Thammasat Univ, Fac Med, Div Infect Dis, Pathum Thani, Thailand
[2] Thammasat Univ, Pathum Thani, Thailand
[3] GlaxoSmithKline, Collegeville, PA USA
关键词
Extensively drug resistant; Acinetobacter baumannii; Pneumonia; Outcomes; Treatment; Colist in; VENTILATOR-ASSOCIATED PNEUMONIA; MULTICENTER; COMBINATIONS; INFECTIONS; EFFICACY; IMIPENEM;
D O I
10.1016/j.ijantimicag.2014.01.016
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Data for treatment and outcomes of extensively drug-resistant Acinetobacter baumannii (XDR-AB) pneumonia are limited. A retrospective cohort study of 236 adult patients with XDR-AB pneumonia was conducted between January 2009 and December 2012. The median age of subjects was 70 years (range 17-95 years), 53% were male, 55% had ventilator-associated pneumonia and 42% had been admitted to the intensive care unit. All XDR-AB isolates were susceptible only to tigecycline and colistin; 52 (22%) of the 236 subjects did not receive an agent active against XDR-AB, with an associated 28-day survival of 0%. Colistin-based two-drug combination treatment was prescribed to 166 subjects (70%); regimens included (i) colistin and high-dose sulbactam (n = 93); (ii) colistin and tigecycline (n=43); and (iii) colistin and high-dose prolonged infusion of a carbapenem (n = 30). The 28-day survival rate and mean length of hospital stay were not statistically different between these three regimens (65%, 53% and 60% and 39, 39 and 38 days, respectively). Predictors of mortality included Acute Physiology and Chronic Health Evaluation (APACHE) II score [adjusted odds ratio (aOR) = 1.11; 13<0.001 for each point increase], duration from infection onset to receipt of active regimen (aOR = 1.01; 13=0.002 for each hour delay), underlying malignancy (aOR = 3.46; P=0.01) and chronic kidney disease (aOR = 2.85; P=0.03). These findings suggest that the three colistin-based two-drug combination regimens may be treatment options for XDR-AB pneumonia. Crown Copyright (C) 2014 Published by Elsevier B.V. on behalf of International Society of Chemotherapy. All rights reserved.
引用
收藏
页码:378 / 382
页数:5
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