Guideline for the Management of Clostridium Difficile Infection in Children and Adolescents With Cancer and Pediatric Hematopoietic Stem-Cell Transplantation Recipients
AuthorDiorio, C; Robinson, PD; Ammann, RA; Castagnola, E; Erickson, K; Esbenshade, A; Fisher, BT; Haeusler, GM; Kuczynski, S; Lehrnbecher, T; ...
Source TitleJournal of Clinical Oncology
PublisherAMER SOC CLINICAL ONCOLOGY
University of Melbourne Author/sHaeusler, Gabrielle
AffiliationSir Peter MacCallum Department of Oncology
Document TypeJournal Article
CitationsDiorio, C., Robinson, P. D., Ammann, R. A., Castagnola, E., Erickson, K., Esbenshade, A., Fisher, B. T., Haeusler, G. M., Kuczynski, S., Lehrnbecher, T., Phillips, R., Cabral, S., Dupuis, L. L. & Sung, L. (2018). Guideline for the Management of Clostridium Difficile Infection in Children and Adolescents With Cancer and Pediatric Hematopoietic Stem-Cell Transplantation Recipients. JOURNAL OF CLINICAL ONCOLOGY, 36 (31), pp.3162-+. https://doi.org/10.1200/JCO.18.00407.
Access StatusOpen Access
PURPOSE: The aim of this work was to develop a clinical practice guideline for the prevention and treatment of Clostridium difficile infection (CDI) in children and adolescents with cancer and pediatric hematopoietic stem-cell transplantation (HSCT) patients. METHODS: An international multidisciplinary panel of experts in pediatric oncology and infectious diseases with patient advocate representation was convened. We performed systematic reviews of randomized controlled trials for the prevention or treatment of CDI in any population and considered the directness of the evidence to children with cancer and pediatric HSCT patients. We used the Grading of Recommendations Assessment, Development, and Evaluation approach to generate recommendations. RESULTS: The panel made strong recommendations to administer either oral metronidazole or oral vancomycin for the initial treatment of nonsevere CDI and oral vancomycin for the initial treatment of severe CDI. Fidaxomicin may be considered in the setting of recurrent CDI. The panel suggested that probiotics not be routinely used for the prevention of CDI, and that monoclonal antibodies and probiotics not be routinely used for the treatment of CDI. A strong recommendation to not use fecal microbiota transplantation was made in this population. We identified key knowledge gaps and suggested directions for future research. CONCLUSION: We present a guideline for the prevention and treatment of CDI in children and adolescents with cancer and pediatric HSCT patients. Future research should include randomized controlled trials that involve children with cancer and pediatric HSCT patients to improve the management of CDI in this population.
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