Lavallée Christian, Labbé Annie-Claude, Talbot Jean-Daniel, Alonso Carolyn D, Marr Kieren A, Cohen Sandra, Laverdière Michel, Dufresne Simon Frédéric
Department of Infectious Diseases and Medical Microbiology, Hôpital Maisonneuve-Rosemont, Université de Montréal, Montréal, QC, Canada.
Division of Infectious Diseases, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
Transpl Infect Dis. 2017 Feb;19(1). doi: 10.1111/tid.12648. Epub 2017 Jan 11.
Clostridium difficile infection (CDI) is a significant complication of allogeneic hematopoietic stem cell transplantation (allo-HSCT). Our primary objective was to determine risk factors for the development of CDI during the first year following allo-HSCT.
A matched case-control study nested in a cohort of allo-HSCT at a single hospital in Montréal, Québec, Canada, was conducted from 2002 through 2011.
Sixty-five of 760 patients who underwent allo-HSCT between 2002 and 2011 developed CDI, representing an incidence of 8.6%. We selected 123 controls matched for year of transplant for risk factor analyses. In the multivariable analysis, receipt of trimethoprim-sulfamethoxazole (TMP-SMX) prior to transplantation (adjusted odds ratio [aOR] 0.07, 95% confidence interval [CI] 0.02-0.27), mucositis (aOR 5.90, 95% CI 2.08-16.72), and reactivation of cytomegalovirus (CMV) (aOR 6.17, 95% CI 2.17-17.57) and of other Herpesviridae viruses (aOR 3.04, 95% CI 1.13-8.16) were the variables that remained statistically associated with CDI. High-risk antibiotic use in the late post-transplant period (aOR 7.63, 95% CI 2.14-27.22) was associated with development of late CDI.
This study revealed reactivation of CMV and other Herpesviridae viruses as novel risk factors for CDI. Administration of TMP-SMX prior to transplantation was independently associated with a decreased risk of CDI. Early and late CDI after HSCT may have distinct risk factors.
艰难梭菌感染(CDI)是异基因造血干细胞移植(allo-HSCT)的一种重要并发症。我们的主要目标是确定allo-HSCT后第一年发生CDI的危险因素。
2002年至2011年在加拿大魁北克省蒙特利尔市一家医院进行了一项巢式病例对照研究,该研究嵌套于allo-HSCT队列中。
2002年至2011年间接受allo-HSCT的760例患者中有65例发生了CDI,发病率为8.6%。我们选择了123例与移植年份匹配的对照进行危险因素分析。在多变量分析中,移植前接受甲氧苄啶-磺胺甲恶唑(TMP-SMX)治疗(调整优势比[aOR]0.07,95%置信区间[CI]0.02-0.27)、发生黏膜炎(aOR 5.90,95%CI 2.08-16.72)以及巨细胞病毒(CMV)再激活(aOR 6.17,95%CI 2.17-17.57)和其他疱疹病毒科病毒再激活(aOR 3.04,95%CI 1.13-8.16)是与CDI仍存在统计学关联的变量。移植后期使用高风险抗生素(aOR 7.63,95%CI 2.14-27.22)与迟发性CDI的发生相关。
本研究揭示CMV和其他疱疹病毒科病毒再激活是CDI的新危险因素。移植前给予TMP-SMX与CDI风险降低独立相关。HSCT后的早期和晚期CDI可能有不同的危险因素。