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异基因造血干细胞移植受者中与艰难梭菌相关的疾病:风险关联、保护关联和结局。

Clostridium difficile-associated disease in allogeneic hematopoietic stem-cell transplant recipients: risk associations, protective associations, and outcomes.

机构信息

Department of Medicine, Washington University School of Medicine, St. Louis, MO, USA.

出版信息

Clin Transplant. 2010 Mar-Apr;24(2):192-8. doi: 10.1111/j.1399-0012.2009.01035.x. Epub 2009 Jul 13.

Abstract

The purpose of this study was to evaluate risk factors, protective factors, and outcomes associated with Clostridium difficile-associated disease (CDAD) in allogeneic hematopoietic stem-cell transplant (HSCT) recipients. A case-control study was performed with 37 CDAD cases and 67 controls. In the multivariable logistic regression analysis, receipt of a third or fourth generation cephalosporin was associated with increased risk of CDAD (OR = 4.6, 95% CI 1.6-13.1). Receipt of growth factors was associated with decreased risk of CDAD (OR=0.1, 95% CI 0.02-0.3). Cases were more likely to develop a blood stream infection after CDAD than were controls at any point before discharge (p < 0.001). CDAD cases were more likely than controls to develop new onset graft-vs.-host disease (GVHD) (p < 0.001), new onset severe GVHD (p < 0.001), or new onset gut GVHD (p = 0.007) after CDAD/discharge. Severe CDAD was a risk factor for death at 180 d in multivariable Cox proportional hazards regression (HR=2.6, 95% CI 1.1-6.2). CDAD is a significant cause of morbidity and mortality in allogeneic HSCT patients, but modifiable risk factors exist. Further study is needed to determine the best methods of decreasing patients' risk of CDAD.

摘要

本研究旨在评估异基因造血干细胞移植(HSCT)受者中与艰难梭状芽孢杆菌相关性疾病(CDAD)相关的风险因素、保护因素和结局。采用病例对照研究,共纳入 37 例 CDAD 病例和 67 例对照。多变量逻辑回归分析显示,第三代或第四代头孢菌素的使用与 CDAD 风险增加相关(OR=4.6,95%CI 1.6-13.1)。生长因子的使用与 CDAD 风险降低相关(OR=0.1,95%CI 0.02-0.3)。与对照组相比,CDAD 病例在出院前任何时间发生血流感染的可能性更高(p<0.001)。与对照组相比,CDAD 病例更有可能在发生 CDAD/出院后出现新发移植物抗宿主病(GVHD)(p<0.001)、新发严重 GVHD(p<0.001)或新发肠道 GVHD(p=0.007)。多变量 Cox 比例风险回归分析显示,严重 CDAD 是 180 天死亡的危险因素(HR=2.6,95%CI 1.1-6.2)。CDAD 是异基因 HSCT 患者发病率和死亡率的重要原因,但存在可改变的风险因素。需要进一步研究以确定降低患者 CDAD 风险的最佳方法。

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