Division of Infectious Diseases, Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Clin Infect Dis. 2021 Mar 15;72(6):953-960. doi: 10.1093/cid/ciaa190.
Approximately 40% of all Enterobacterales (EB) bloodstream infections (BSIs) among solid organ transplant recipients (SOTRs) are due to extended-spectrum β-lactamase (ESBL)-producing organisms, but risk factors for such infections remain ill defined in this population. We sought to determine the risk factors for ESBL-EB BSIs among SOTRs.
A multicenter case-control study was performed. All SOTRs with an EB BSI at the Hospital of the University of Pennsylvania and University of Maryland Medical Center between 1 January 2007 and 30 June 2018 and at The Johns Hopkins Hospital between 1 January 2005 and 31 December 2015 were included. Cases were those with an ESBL-EB BSI. Controls were those with a non-ESBL-EB BSI. Multivariable logistic regression was performed to determine risk factors for ESBL-EB BSI.
There were 988 episodes of EB BSI, of which 395 (40%) were due to an ESBL-EB. On multivariable analysis, the independent risk factors for ESBL-EB BSI included: ESBL-EB on prior culture (aOR, 12.75; 95% CI, 3.23-50.33; P < .001), a corticosteroid-containing immunosuppression regimen (aOR 1.30; 95% CI 1.03-1.65; P = .030), acute rejection treated with corticosteroids (aOR 1.18; 95% CI 1.16-1.19; P < .001), and exposure to third-generation cephalosporins (aOR 1.95; 95% CI 1.48-2.57; P < .001), echinocandins (aOR 1.61; 95% CI 1.08-2.40; P = .020), and trimethoprim-sulfamethoxazole (aOR 1.35; 95% CI 1.10-1.64; P = .003).
We identified several novel risk factors that are uniquely important to the SOTR population, including exposure to trimethoprim-sulfamethoxazole and corticosteroid-containing immunosuppressive regimens. Further studies exploring these associations and testing interventions aimed at these modifiable risk factors among SOTRs are needed.
在实体器官移植受者(SOTR)中,约 40%的肠杆菌科(EB)血流感染(BSI)是由产超广谱β-内酰胺酶(ESBL)的生物体引起的,但此类感染的危险因素在该人群中仍未明确界定。我们旨在确定 SOTR 中 ESBL-EB BSI 的危险因素。
进行了一项多中心病例对照研究。2007 年 1 月 1 日至 2018 年 6 月 30 日期间,宾夕法尼亚大学医院和马里兰大学医学中心以及 2005 年 1 月 1 日至 2015 年 12 月 31 日期间约翰霍普金斯医院的所有发生 EB BSI 的 SOTR 均被纳入研究。病例是指发生 ESBL-EB BSI 的患者。对照组为非 ESBL-EB BSI 患者。采用多变量逻辑回归分析确定 ESBL-EB BSI 的危险因素。
共发生 988 例 EB BSI,其中 395 例(40%)由 ESBL-EB 引起。多变量分析显示,ESBL-EB BSI 的独立危险因素包括:先前培养出 ESBL-EB(比值比,12.75;95%置信区间,3.23-50.33;P<0.001)、含皮质类固醇的免疫抑制方案(比值比,1.30;95%置信区间,1.03-1.65;P=0.030)、皮质类固醇治疗的急性排斥反应(比值比,1.18;95%置信区间,1.16-1.19;P<0.001)和三代头孢菌素(比值比,1.95;95%置信区间,1.48-2.57;P<0.001)、棘白菌素类(比值比,1.61;95%置信区间,1.08-2.40;P=0.020)和复方磺胺甲噁唑(比值比,1.35;95%置信区间,1.10-1.64;P=0.003)。
我们确定了一些新的危险因素,这些危险因素对 SOTR 人群尤为重要,包括接触复方磺胺甲噁唑和含皮质类固醇的免疫抑制方案。需要进一步研究这些关联,并测试针对 SOTR 中这些可改变危险因素的干预措施。