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Rome Foundation Working Team Report on Post-Infection Irritable Bowel Syndrome

Barbara, G. (författare)
Grover, M. (författare)
Bercik, P. (författare)
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Corsetti, M. (författare)
Ghoshal, U. C. (författare)
Öhman, Lena, 1967 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för mikrobiologi och immunologi,Institute of Biomedicine, Department of Microbiology and Immunology
Rajilic-Stojanovic, M. (författare)
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 (creator_code:org_t)
Elsevier BV, 2019
2019
Engelska.
Ingår i: Gastroenterology. - : Elsevier BV. - 0016-5085. ; 156:1
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • BACKGROUND & AIMS: The existence of postinfection irritable bowel syndrome (PI-IBS) has been substantiated by epidemiology studies conducted in diverse geographic and clinical settings. However, the available evidence has not been well summarized, and there is little guidance for diagnosis and treatment of PI-IBS. The ROME Foundation has produced a working team report to summarize the available evidence on the pathophysiology of PI-IBS and provide guidance for diagnosis and treatment, based on findings reported in the literature and clinical experience. METHODS: The working team conducted an evidence-based review of publication databases for articles describing the clinical features (diagnosis), pathophysiology (intestinal sensorimotor function, microbiota, immune dysregulation, barrier dysfunction, enteroendocrine pathways, and genetics), and animal models of PI-IBS. We used a Delphi-based consensus system to create guidelines for management of PI-IBS and a developed treatment algorithm based on published findings and experiences of team members. RESULTS: PI-IBS develops in about 10% of patients with infectious enteritis. Risk factors include female sex, younger age, psychological distress during or before acute gastroenteritis, and severity of the acute episode. The pathogenesis of PI-PBS appears to involve changes in the intestinal microbiome as well as epithelial, serotonergic, and immune system factors. However, these mechanisms are incompletely understood. There are no evidence-based, effective pharmacologic strategies for treatment of PI-IBS. We provide a consensus-based treatment algorithm, based on clinical presentation and potential disease mechanisms. CONCLUSIONS: Based on a systematic review of the literature and team experience, we summarize the clinical features, pathophysiology (from animal models and human studies), and progression of PI-IBS. Based on these findings, we present an algorithm for diagnosis and treatment of PI-IBS based on team consensus. We also propose areas for future investigation.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Gastroenterologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Gastroenterology and Hepatology (hsv//eng)

Nyckelord

Gastrointestinal Infection
Microbiome
Campylobacter
Serotonin
Barrier Function
bile-acid malabsorption
functional gastrointestinal disorders
enterochromaffin cell hyperplasia
placebo-controlled trial
low fodmap
diet
follow-up
bacterial gastroenteritis
mouse model
interstitial-cells
double-blind
Gastroenterology & Hepatology
ewart gt
1950
bmj-british medical journal
v1
p405
audhary na
1962
quarterly journal of medicine
v31
p307

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