Title | Risk factors and outcomes of infections caused by extremely drug-resistant gram-negative bacilli in patients hospitalized in intensive care units. |
Publication Type | Journal Article |
Year of Publication | 2014 |
Authors | Patel SJ, Oliveira AP, Zhou JJulia, Alba L, E Furuya Y, Weisenberg SA, Jia H, Clock SA, Kubin CJ, Jenkins SG, Schuetz AN, Behta M, Della-Latta P, Whittier S, Rhee K, Saiman L |
Journal | Am J Infect Control |
Volume | 42 |
Issue | 6 |
Pagination | 626-31 |
Date Published | 2014 Jun |
ISSN | 1527-3296 |
Keywords | Acinetobacter Infections, Adolescent, Age Factors, Aged, Amikacin, Anti-Bacterial Agents, Case-Control Studies, Cross Infection, Drug Resistance, Multiple, Bacterial, Female, Gram-Negative Bacterial Infections, Hospital Mortality, Humans, Immunocompromised Host, Intensive Care Units, Klebsiella Infections, Klebsiella pneumoniae, Levofloxacin, Liver Diseases, Male, Middle Aged, Pseudomonas aeruginosa, Pseudomonas Infections, Risk Factors, Time Factors |
Abstract | BACKGROUND: Extremely drug-resistant gram-negative bacilli (XDR-GNB) increasingly cause health care-associated infections (HAIs) in intensive care units (ICUs). METHODS: A matched case-control (1:2) study was conducted from February 2007 to January 2010 in 16 ICUs. Case and control subjects had HAIs caused by GNB susceptible to ≤1 antibiotic versus ≥2 antibiotics, respectively. Logistic and Cox proportional hazards regression assessed risk factors for HAIs and predictors of mortality, respectively. RESULTS: Overall, 103 case and 195 control subjects were enrolled. An immunocompromised state (odds ratio [OR], 1.55; P = .047) and exposure to amikacin (OR, 13.81; P < .001), levofloxacin (OR, 2.05; P = .005), or trimethoprim-sulfamethoxazole (OR, 3.42; P = .009) were factors associated with XDR-GNB HAIs. Multiple factors in both case and control subjects significantly predicted increased mortality at different time intervals after HAI diagnosis. At 7 days, liver disease (hazard ratio [HR], 5.52), immunocompromised state (HR, 3.41), and bloodstream infection (HR, 2.55) predicted mortality; at 15 days, age (HR, 1.02 per year increase), liver disease (HR, 3.34), and immunocompromised state (HR, 2.03) predicted mortality; and, at 30 days, age (HR, 1.02 per 1-year increase), liver disease (HR, 3.34), immunocompromised state (HR, 2.03), and hospitalization in a medical ICU (HR, 1.85) predicted mortality. CONCLUSION: HAIs caused by XDR-GNB were associated with potentially modifiable factors. Age, liver disease, and immunocompromised state, but not XDR-GNB HAIs, were associated with mortality. |
DOI | 10.1016/j.ajic.2014.01.027 |
Alternate Journal | Am J Infect Control |
PubMed ID | 24725516 |
PubMed Central ID | PMC4083852 |
Grant List | KL2 RR024997 / RR / NCRR NIH HHS / United States KL2RR024997 / RR / NCRR NIH HHS / United States T90 NR010824 / NR / NINR NIH HHS / United States R01 CI000537 / CI / NCPDCID CDC HHS / United States UL1 TR000457 / TR / NCATS NIH HHS / United States |