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

详细信息    查看全文

• 作者：Sameer J. Patel ; MD ; MPH^a ; ^{sameer.patel@northwestern.edu" class="auth_mail} ; André ; P. Oliveira ; MPH^a ; Juyan Julia Zhou ; MS ; MPH^a ; Luis Alba ; BS^a ; E. Yoko Furuya ; MD ; MS^b ; ^c ; Scott A. Weisenberg ; MD ; MSc^d ; Haomiao Jia ; PhD^e ; ^f ; Sarah A. Clock ; PhD ; MPH^a ; Christine J. Kubin ; PharmD^b ; ^g ; Stephen G. Jenkins ; PhD^h ; Audrey N. Schuetz ; MD ; MPH^h ; ⁱ ; Maryam Behta ; PharmD^j ; Phyllis Della-Latta ; PhD^k ; Susan Whittier ; PhD^k ; Kyu Rhee ; MD ; PhD^l ; Lisa Saiman ; MD ; MPH^a ; ^c
• 关键词：Antibiotic resistance ; Gram-negative bacteria ; Health care-associated infection ; Mortality
• 刊名：American Journal of Infection Control
• 出版年：June 2014
• 年：2014
• 卷：42
• 期：6
• 页码：626-631
• 全文大小：251 K

文摘

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.