Treatment of Clostridioides (Clostridium) difficile infection
- PMID: 31801387
- PMCID: PMC7877971
- DOI: 10.1080/07853890.2019.1701703
Treatment of Clostridioides (Clostridium) difficile infection
Abstract
Clostridioides (formerly: Clostridium) difficile infection (CDI) is a major cause of diarrhoea for inpatients as well as outpatients. Usually, CDI is healthcare-associated but the number of community-acquired infections is increasing. CDI is generally associated with changes in the normal intestinal microbiota caused by administration of antibiotics. Elderly and immunocompromised patients are at greater risk for CDI and CDI recurrence. Recently, the treatment options of CDI have undergone major changes: current recommendations speak against using metronidazole for primary CDI, fidaxomicin and bezlotoxumab have been added to the treatment armamentarium and microbial replacement therapies have emerged. Several other therapies are undergoing clinical trials. In this article, we review current treatment guidelines, present the most recent data on the options to treat CDI and glance towards future developments.KEY MESSAGESThe cornerstones for the treatment of CDI are vancomycin and fidaxomicin. Metronidazole should be used only in mild-to-moderate disease in younger patients who have no or only few risk factors for recurrence.In recurrent CDI, bezlotoxumab infusion (a monoclonal antibody against C. difficile toxin B) may be considered as an adjunctive therapeutic strategy in addition to the standard care provided to patients with several risk factors for recurrence.Faecal microbiota transplantation (FMT) should be offered to patients with frequently recurring CDI.
Keywords: C. difficile diarrhoea; Clostridioides difficile; Clostridium difficile; faecal microbiota transplantation.
Conflict of interest statement
J.O. has been a scientific advisor (review panel or advisory committee) to Astellas, Gilead Sciences Finland, GlaxoSmithKline, MSD Finland, and Unimedic Pharma AB, received lecture honoraria from Gilead Sciences Finland, GlaxoSmithKline, MSD Finland and Pfizer, and received coverage for congress travel/accommodation expenses from Gilead, Grifols, Janssen, MSD and Pfizer. V-J.A. has received lecture honoraria from MSD, Astellas, Roche, Pfizer, BristolMyersSquibb and Unimedic Pharma AB. E.M. has been a scientific advisor (review panel or advisory committee) and received lecture honoraria from MSD Finland.
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