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A comparison of vancomycin and metronidazole for the treatment of Clostridium difficile-associated diarrhea, stratified by disease severity.万古霉素与甲硝唑治疗艰难梭菌相关性腹泻的比较,按疾病严重程度分层
Clin Infect Dis. 2007 Aug 1;45(3):302-7. doi: 10.1086/519265. Epub 2007 Jun 19.
2
Severity of Clostridium difficile-associated disease (CDAD) in allogeneic stem cell transplant recipients: evaluation of a CDAD severity grading system.异基因造血干细胞移植受者艰难梭菌相关疾病(CDAD)的严重程度:CDAD严重程度分级系统的评估
Infect Control Hosp Epidemiol. 2007 Feb;28(2):208-11. doi: 10.1086/511792. Epub 2007 Jan 26.
3
Surveillance of nosocomial infections in adult recipients of allogeneic and autologous bone marrow and peripheral blood stem-cell transplantation.对同种异体和自体骨髓及外周血干细胞移植成年受者医院感染的监测。
Bone Marrow Transplant. 2003 May;31(9):795-801. doi: 10.1038/sj.bmt.1703920.
4
Outbreak of Clostridium difficile-related diarrhoea in an adult oncology unit: risk factors and microbiological characteristics.成人肿瘤科艰难梭菌相关性腹泻的暴发:危险因素及微生物学特征
J Hosp Infect. 2003 Mar;53(3):187-92. doi: 10.1053/jhin.2002.1356.
5
Rarity of toxigenic Clostridium difficile infections after hematopoietic stem cell transplantation: implications for symptomatic management of diarrhea.造血干细胞移植后产毒艰难梭菌感染的罕见性:对腹泻症状管理的启示
Bone Marrow Transplant. 2002 Oct;30(8):517-9. doi: 10.1038/sj.bmt.1703703.
6
Clostridium difficile infection in patients with neutropenia.中性粒细胞减少患者的艰难梭菌感染
Clin Infect Dis. 2002 Mar 1;34(5):723. doi: 10.1086/338721.
7
Clostridium difficile.艰难梭菌
Gastroenterol Clin North Am. 2001 Sep;30(3):753-77, ix-x. doi: 10.1016/s0889-8553(05)70209-0.
8
Clostridium difficile infection in patients with neutropenia.中性粒细胞减少患者的艰难梭菌感染
Clin Infect Dis. 2001 Sep 15;33(6):786-91. doi: 10.1086/322616. Epub 2001 Aug 10.
9
Clostridium difficile infection in allogeneic stem cell transplant recipients is associated with severe graft-versus-host disease and non-relapse mortality.异基因造血干细胞移植受者的艰难梭菌感染与严重移植物抗宿主病及非复发死亡率相关。
Bone Marrow Transplant. 2000 Oct;26(8):871-6. doi: 10.1038/sj.bmt.1702627.
10
Infectious gastro-enteritis: an uncommon cause of diarrhoea in adult allogeneic and autologous stem cell transplant recipients.感染性肠胃炎:成年异体和自体干细胞移植受者腹泻的罕见病因。
Bone Marrow Transplant. 2000 Aug;26(3):299-303. doi: 10.1038/sj.bmt.1702484.

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.

DOI:10.1111/j.1399-0012.2009.01035.x
PMID:19624693
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3390201/
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。