Epidemiology and Outcomes of Clostridium difficile Infections in Hematopoietic Stem Cell Transplant Recipients

被引:164
作者
Alonso, Carolyn D. [1 ,2 ]
Treadway, Suzanne B. [1 ]
Hanna, David B. [3 ]
Huff, Carol Ann [4 ]
Neofytos, Dionissios [1 ]
Carroll, Karen C. [5 ]
Marr, Kieren A. [1 ,4 ]
机构
[1] Johns Hopkins Univ Hosp, Dept Med, Baltimore, MD 21287 USA
[2] Beth Israel Deaconess Med Ctr, Dept Med, Boston, MA 02215 USA
[3] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD USA
[4] Johns Hopkins Univ Hosp, Dept Oncol, Baltimore, MD 21287 USA
[5] Johns Hopkins Univ Hosp, Dept Pathol, Baltimore, MD 21287 USA
关键词
VERSUS-HOST-DISEASE; PROTON PUMP INHIBITORS; MARROW-TRANSPLANTATION; DIARRHEA; VANCOMYCIN; MORTALITY; RISK; POPULATION; TOXIN;
D O I
10.1093/cid/cir1035
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:1053 / 1063
页数:11
相关论文
共 37 条
[1]   CLOSTRIDIUM-DIFFICILE INFECTION ASSOCIATED WITH ANTINEOPLASTIC CHEMOTHERAPY - A REVIEW [J].
ANAND, A ;
GLATT, AE .
CLINICAL INFECTIOUS DISEASES, 1993, 17 (01) :109-113
[2]  
[Anonymous], 2006, COMMON TERMINOLOGY C
[3]   Incidence of Clostridium difficile-associated diarrhea before and after autologous peripheral blood stem cell transplantation for lymphoma and multiple myeloma [J].
Arango, JI ;
Restrepo, A ;
Schneider, DL ;
Callander, NS ;
Ochoa-Bayona, JL ;
Restrepo, MI ;
Bradshaw, P ;
Patterson, J ;
Freytes, CO .
BONE MARROW TRANSPLANTATION, 2006, 37 (05) :517-521
[4]   High prevalence of diarrhea but infrequency of documented Clostridium difficile in autologous peripheral blood progenitor cell transplant recipients [J].
Avery, R ;
Pohlman, B ;
Adal, K ;
Bolwell, B ;
Goldman, M ;
Kalaycio, M ;
Hall, G ;
Andresen, S ;
Mossad, S ;
Schmitt, S ;
Mason, P ;
Longworth, D .
BONE MARROW TRANSPLANTATION, 2000, 25 (01) :67-69
[5]   Clostridium difficile: progress and challenges [J].
Bartlett, John G. .
ANTIMICROBIAL THERAPEUTICS REVIEWS, 2010, 1213 :62-69
[6]   Incidence and outcome of Clostridium difficile infection following autologous peripheral blood stem cell transplantation [J].
Bilgrami, S ;
Feingold, JM ;
Dorsky, D ;
Edwards, RL ;
Bona, RD ;
Khan, AM ;
Rodriguez-Pinero, F ;
Clive, J ;
Tutschka, PJ .
BONE MARROW TRANSPLANTATION, 1999, 23 (10) :1039-1042
[7]   Clostridium difficile-associated disease in human stem cell transplant recipients: coming epidemic or false alarm? [J].
Bobak, D. ;
Arfons, L. M. ;
Creger, R. J. ;
Lazarus, H. M. .
BONE MARROW TRANSPLANTATION, 2008, 42 (11) :705-713
[8]   Frequency of sample submission for optimal utilization of the cell culture cytotoxicity assay for detection of Clostridium difficile toxin [J].
Borek, AP ;
Aird, DZ ;
Carroll, KC .
JOURNAL OF CLINICAL MICROBIOLOGY, 2005, 43 (06) :2994-2995
[9]   Antimicrobial therapy of Clostridium difficile-associated diarrhea [J].
Bouza, Emilio ;
Burillo, Almudena ;
Munoz, Patricia .
MEDICAL CLINICS OF NORTH AMERICA, 2006, 90 (06) :1141-+
[10]   High-dose cyclophosphamide for severe aplastic anemia: long-term follow-up [J].
Brodsky, Robert A. ;
Chen, Allen R. ;
Dorr, Donna ;
Fuchs, Ephraim J. ;
Huff, Carol Ann ;
Luznik, Leo ;
Smith, B. Douglas ;
Matsui, William H. ;
Goodman, Steven N. ;
Ambinder, Richard F. ;
Jones, Richard J. .
BLOOD, 2010, 115 (11) :2136-2141