Department of Medicine, The Johns Hopkins Hospital, Baltimore, MD 21205, USA.
Clin Infect Dis. 2012 Apr;54(8):1053-63. doi: 10.1093/cid/cir1035. Epub 2012 Mar 12.
Background. Clostridium difficile is the leading cause of infectious diarrhea among hospitalized patients and is a major concern for patients undergoing hematopoietic stem cell transplantation (HSCT). Risk factors and the natural history of C. difficile infection (CDI) are poorly understood in this population. Methods. We performed a retrospective nested case-control study to describe the epidemiology, timing, and risk factors for CDI among adult patients who received HSCTs at our center from January 2003 through December 2008. Results. The overall 1-year incidence of CDI was 9.2% among HSCTs performed (n = 999). The median time to diagnosis of CDI was short among both autologous and allogeneic HSCT recipients (6.5 days and 33 days, respectively). Risk factors for CDI in allogeneic HSCT recipients included receipt of chemotherapy prior to conditioning for HSCT, broad-spectrum antimicrobial use, and acute graft-versus-host disease (GVHD; adjusted odds ratio [AOR], 4.45; 95% confidence interval [CI], 1.54-12.84; P = .006). There was a strong relationship between early CDI and subsequent development of gastrointestinal tract GVHD in the year following allogeneic HSCT (P < .001). Gastrointestinal GVHD was also strongly associated with an increased risk for recurrent CDI (AOR, 4.23 [95% CI, 1.20-14.86]; P = .02). Conclusions. These results highlight the high incidence and early timing of CDI after HSCT. Early timing, coupled with the noted risk of pretransplant chemotherapy, suggests that the natural history of disease in some patients may involve colonization prior to HSCT. A potentially important interplay between CDI and GVHD involving the gastrointestinal tract was observed.
艰难梭菌是住院患者感染性腹泻的主要原因,也是接受造血干细胞移植(HSCT)患者的主要关注点。在该人群中,艰难梭菌感染(CDI)的危险因素和自然史了解甚少。
我们进行了一项回顾性巢式病例对照研究,以描述 2003 年 1 月至 2008 年 12 月在我们中心接受 HSCT 的成年患者中 CDI 的流行病学、时间和危险因素。
HSCT 后 1 年内 CDI 的总发生率为 9.2%(n=999)。无论是自体 HSCT 还是异基因 HSCT 受者,CDI 的中位诊断时间都很短(分别为 6.5 天和 33 天)。异基因 HSCT 受者 CDI 的危险因素包括在 HSCT 预处理前接受化疗、广谱抗菌药物使用和急性移植物抗宿主病(GVHD;调整后的优势比 [OR],4.45;95%置信区间 [CI],1.54-12.84;P=0.006)。异基因 HSCT 后早期 CDI 与随后一年内胃肠道 GVHD 的发生密切相关(P<0.001)。胃肠道 GVHD 也与复发性 CDI的风险增加密切相关(OR,4.23[95%CI,1.20-14.86];P=0.02)。
这些结果强调了 HSCT 后 CDI 的高发生率和早期发病时间。早期发病时间,加上移植前化疗的风险,表明某些患者疾病的自然史可能涉及 HSCT 前的定植。观察到 CDI 和涉及胃肠道的 GVHD 之间存在潜在的重要相互作用。