Risk factors and outcomes of infections caused by extremely drug-resistant gram-negative bacilli in patients hospitalized in intensive care units.

TitleRisk factors and outcomes of infections caused by extremely drug-resistant gram-negative bacilli in patients hospitalized in intensive care units.
Publication TypeJournal Article
Year of Publication2014
AuthorsPatel 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
JournalAm J Infect Control
Volume42
Issue6
Pagination626-31
Date Published2014 Jun
ISSN1527-3296
KeywordsAcinetobacter 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.

DOI10.1016/j.ajic.2014.01.027
Alternate JournalAm J Infect Control
PubMed ID24725516
PubMed Central IDPMC4083852
Grant ListKL2 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