Faecal microbiota transplant for recurrent Clostridium difficile infection - guidance (IPG485)

Source:
National Institute for Health and Care Excellence - NICE
Publication date:
27 March 2014

Abstract

The National Institute for Health and Care Excellence (NICE) has issued full guidance to the NHS in England, Wales, Scotland and Northern Ireland on Faecal microbiota transplant for recurrent clostridium difficile infection, in March 2014.

November 2019: The US Food and Drug Administration has advised that stool donors for faecal microbiota transplantation should be screened with questions that specifically address risk factors for colonization with Multi Drug Resistant Organisms (MDROs), and individuals at higher risk of colonization with MDROs should be excluded as donors. In addition donor stool should be specifically tested for MDROs and not used if positive.
NICE is currently seeking advice from professional experts on whether to update this guidance.

Description

Clostridium difficile (C. difficile) is a commensal bacterium that lives harmlessly in the gut of approximately 5% of healthy people. The use of broad-spectrum antibiotics and immunosuppressive agents can alter the balance of bacterial species in the gut, resulting in an overgrowth of C. difficile. Symptoms of mild C. difficile infections (CDIs) include purulent watery diarrhoea, abdominal cramps, nausea and dehydration. In more severe cases the infection can cause bloody diarrhoea and fever. In a few people CDIs can lead to pseudomembranous colitis, sepsis, toxic megacolon, colonic rupture, and death. The risk of death increases in patients with multiple comorbidities.

First-line treatment involves rehydration and antibiotic therapy. Clinical responses are generally favourable but some patients have recurrent or refractory CDIs. For these people, further courses of antibiotics are used. An example of management algorithms can be found in Public Health England’s Updated guidance on the management and treatment of Clostridium difficile infection (June, 2013).

Coding and clinical classification codes for this guidance