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My Treatment Approach to Clostridioides difficile Infection
Institution:1. Division of Gastroenterology and Hepatology, Department of Medicine, Rochester, Minnesota;2. Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Rochester, Minnesota;3. Department of Surgery, Rochester, Minnesota;5. Department of Health Sciences Research, Rochester, Minnesota;7. Division of Infectious Diseases, Department of Medicine, Rochester, Minnesota;8. Department of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, Minnesota;4. Department of Veterinary Pathobiology, Texas A&M College of Veterinary Medicine and Biomedical Sciences, College Station, Texas;6. Department of Microbiology and Immunology, University of Minnesota Medical School, Minneapolis, Minnesota;1. Department of Molecular and Cell Biology, University of Cape Town, Cape Town, South Africa;2. Medical, Molecular and Forensic Sciences, Murdoch University, Murdoch, Western Australia WA, Australia;3. School of Medical and Health Sciences, Edith Cowan University, Joondalup, WA, Australia;4. Department of Microbiology, PathWest Laboratory Medicine, Nedlands, WA, Australia;5. School of Biomedical Sciences, The University of Western Australia, Crawley, WA, Australia;1. Division of Gastroenterology, Indiana University School of Medicine, Indianapolis, Indiana;3. Department of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota;4. Department of Biostatistics, The Richard M. Fairbanks School of Public Health and School of Medicine, Indiana University, Indianapolis, Indiana;6. Division of Gastroenterology, Hepatology, and Nutrition, University of Minnesota, Minneapolis, Minnesota;5. Division of Gastroenterology, Department of Medicine, University of Alberta, Edmonton, Alberta, Canada;7. Division of Digestive Diseases, Department of Medicine;12. Division of Infectious Diseases, Department of Medicine;8. Department of Pathology, Emory University, Atlanta, Georgia;10. Division of Gastroenterology, Hepatology, and Endoscopy, Department of Medicine, Brigham and Women’s Hospital, Boston, Massachusetts;9. Division of Gastroenterology, Department of Medicine, University of California San Francisco, San Francisco, California;1. Division of Gastroenterology and Hepatology, The Brooklyn Hospital Center, Academic Affiliate of the Icahn School of Medicine at Mount Sinai, Clinical Affiliate of the Mount Sinai Hospital, Brooklyn, NY, USA;2. School of Medicine, St. George''s University, True Blue, Grenada, The West Indies;3. Department of Medicine, The Brooklyn Hospital Center, Academic Affiliate of the Icahn School of Medicine at Mount Sinai, Clinical Affiliate of the Mount Sinai Hospital, Brooklyn, NY, USA;1. Division of Protective Immunity, Department of Pathology and Laboratory Medicine, Children''s Hospital of Philadelphia, Philadelphia, PA, 19104, USA;2. Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, 19104, USA;1. Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota;2. Division of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, Minnesota
Abstract:Clostridioides difficile infection is the most common cause of infectious diarrhea in hospitals with an increasing incidence in the community. Clinical presentation of C difficile infection ranges from diarrhea manageable in the outpatient setting to fulminant infection requiring intensive care admission. There have been significant advances in the management of primary and recurrent C difficile infection including diagnostics, newer antibiotics, antibody treatments, and microbiome restoration therapies. Because of the risk of clinical false-positive results with the polymerase chain reaction test, a two-step assay combining an enzyme immune assay for glutamate dehydrogenase and the C difficile toxin is being used. Cost permitting, I treat a first episode of C difficile infection preferably with fidaxomicin over vancomycin but not metronidazole. The most common complication after C difficile infection is recurrence. I manage a first recurrence with a vancomycin taper and pulse or fidaxomicin and recommend a single dose of intravenous bezlotoxumab (a monoclonal antibody against the toxin B) to reduce recurrence rates for those patients at high risk. Patients with multiply recurrent C difficile infection are managed with a course of antibiotics such as vancomycin or fidaxomicin followed by microbiota restoration. The success of fecal microbiota transplantation is greater than 85%, compared with the 40% to 50% success rate of antibiotics in this situation. Fecal microbiota transplantation is heterogeneous and has rare but serious risks such as transmission of infections. Standardized microbiota restoration therapies are in clinical development and have completed phase III clinical trials. This review answers common clinical questions in the management of C difficile infection.
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