Patel Sameer J, Oliveira André P, Zhou Juyan Julia, Alba Luis, Furuya E Yoko, Weisenberg Scott A, Jia Haomiao, Clock Sarah A, Kubin Christine J, Jenkins Stephen G, Schuetz Audrey N, Behta Maryam, Della-Latta Phyllis, Whittier Susan, Rhee Kyu, Saiman Lisa
Department of Pediatrics, Columbia University Medical Center, New York, NY.
Department of Pediatrics, Columbia University Medical Center, New York, NY.
Am J Infect Control. 2014 Jun;42(6):626-31. doi: 10.1016/j.ajic.2014.01.027. Epub 2014 Apr 13.
Extremely drug-resistant gram-negative bacilli (XDR-GNB) increasingly cause health care-associated infections (HAIs) in intensive care units (ICUs).
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.
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.
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.
耐多药革兰阴性杆菌(XDR-GNB)日益导致重症监护病房(ICU)中的医疗保健相关感染(HAI)。
2007年2月至2010年1月在16个ICU中进行了一项匹配病例对照(1:2)研究。病例组和对照组的HAI分别由对≤1种抗生素敏感的革兰阴性杆菌和对≥2种抗生素敏感的革兰阴性杆菌引起。逻辑回归和Cox比例风险回归分别评估了HAI的危险因素和死亡率的预测因素。
总体而言,纳入了103例病例和195例对照。免疫功能低下状态(比值比[OR],1.55;P = 0.047)以及使用阿米卡星(OR,13.81;P < 0.001)、左氧氟沙星(OR,2.05;P = 0.005)或甲氧苄啶-磺胺甲恶唑(OR,3.42;P = 0.009)是与XDR-GNB HAI相关的因素。病例组和对照组中的多种因素在HAI诊断后的不同时间间隔显著预测了死亡率增加。在7天时,肝病(风险比[HR],5.52)、免疫功能低下状态(HR,3.41)和血流感染(HR,2.55)预测死亡率;在15天时,年龄(HR,每年增加1.02)、肝病(HR,3.34)和免疫功能低下状态(HR,2.03)预测死亡率;在30天时,年龄(HR,每增加1岁1.02)、肝病(HR,3.34)、免疫功能低下状态(HR,2.03)以及在医疗ICU住院(HR,1.85)预测死亡率。
XDR-GNB引起的HAI与潜在可改变的因素相关。年龄、肝病和免疫功能低下状态而非XDR-GNB HAI与死亡率相关。