Clostridium difficile Infection after Adult Autologous Stem Cell Transplantation: A Multicenter Study of Epidemiology and Risk Factors

被引:36
作者
Alonso, Carolyn D. [1 ]
Dufresne, Simon F. [2 ,3 ]
Hanna, David B. [4 ]
Labbe, Annie-Claude [2 ,3 ]
Treadway, Suzanne B. [5 ]
Neofytos, Dionissios [6 ]
Belanger, Sylvie [2 ,3 ]
Huff, Carol Ann [7 ]
Laverdiere, Michel [2 ,3 ]
Marr, Kieren A. [6 ]
机构
[1] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Div Infect Dis,Dept Med, Boston, MA 02215 USA
[2] Hop Maisonneuve Rosemont Montreal, Dept Microbiol, Quebec City, PQ, Canada
[3] Hop Maisonneuve Rosemont Montreal, Dept Infect Dis, Quebec City, PQ, Canada
[4] Albert Einstein Coll Med Bronx, Dept Epidemiol & Populat Hlth, New York, NY USA
[5] Penn State Milton S Hershey Med Ctr, Four Diamonds Div Pediat Hematol & Oncol, Hershey, PA USA
[6] Johns Hopkins Univ, Sch Med, Dept Med, Div Infect Dis, Baltimore, MD 21205 USA
[7] Johns Hopkins Univ, Sch Med, Dept Oncol, Div Hematol Malignancies, Baltimore, MD 21205 USA
关键词
Clostridium difficile; Stem cell transplantation; Mucositis; Antibiotics; NAP-1; DISEASE; DIARRHEA; RECIPIENTS; ANTIBODY; OUTCOMES;
D O I
10.1016/j.bbmt.2013.07.022
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We sought to describe the epidemiology of Clostridium difficile infection (CDI) among adult recipients of autologous hematopoietic stem cell transplantation (auto-HSCT) within the first year after HSCT in centers with variable epidemiology of hypertoxigenic strains. A multicenter, retrospective nested case-control study was conducted among 873 auto-HSCT recipients at Johns Hopkins Hospital (JHH) and Hopital Maisonneuve-Rosemont (HMR) between January 2003 and December 2008. Despite center differences in the prevalence of NAP-1 strains during the study period (21% to 43% at JHH versus 80% to 84% in HMR), the 1-year incidence of CDI was similar in the 2 hospitals (6.2% at JHH versus 5.7% at HMR). The median time to infection was 11 days (interquartile range, 1 to 27 days). In case-control analyses, grade >= 2 mucositis (odds ratio [OR], 3.00; P = .02) and receipt of a fourth-generation cephalosporin (OR, 2.76; P = .04) were identified as predictors for CDI. Mucositis was the strongest predictor of risk for CDI in multivariate analysis (adjusted OR, 2.77; P = .03). CDI is a common and early complication of auto-HSCT. Treatment-related gastrointestinal mucosal damage, along with the potentially modifiable risk of antimicrobial exposure, influence the risk for CDI early after auto-HSCT. (C) 2013 American Society for Blood and Marrow Transplantation.
引用
收藏
页码:1502 / 1508
页数:7
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