Colistin-based treatment for extensively drug-resistant Acinetobacter baumannii pneumonia |
| |
Affiliation: | 1. Center for Biotechnology and Law, University of Houston Law Center, Houston, Texas, USA;2. Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, Washington, USA;3. Department of Pathology, University of Washington, Seattle, Washington, USA;4. Department of Bioethics and Humanities, University of Washington, Seattle, Washington, USA;5. Department of Medicine/Medical Genetics, University of Washington, Seattle, Washington, USA;6. Department of Genome Sciences, University of Washington, Seattle, Washington, USA |
| |
Abstract: | 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; P < 0.001 for each point increase], duration from infection onset to receipt of active regimen (aOR = 1.01; P = 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. |
| |
Keywords: | Extensively drug-resistant Pneumonia Outcomes Treatment Colistin |
本文献已被 ScienceDirect 等数据库收录! |
|