Dolphin
Senior Member (Voting Rights)
https://www.gastrojournal.org/article/S0016-5085(18)34766-8/abstract
Article in Press
Rome Foundation Working Team Report on Post-Infection Irritable Bowel Syndrome
DOI: https://doi.org/10.1053/j.gastro.2018.07.011
Abstract
Background & Aims
The existence of post-infection 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 was to summarize the available evidence on the pathophysiology of PI-IBS and provide guidance for diagnosis and treatment, based upon 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 prior to 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 is 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 upon team consensus. We also propose areas for investigations.
Key words:
gastrointestinal infection, microbiome, Campylobacter, serotonin, barrier function
Key words:
gastrointestinal infection, microbiome, Campylobacter, serotonin
Abbreviations:
IBS (irritable bowel syndrome), PI-IBS (post-infection irritable bowel syndrome), FGIDs (functional gastrointestinal disorders), SNPs (single nucleotide polymorphisms), 5HT (serotonin), EC (enterochromaffin), ICC (interstitial cells of Cajal), PCR (polymerase chain reaction), IBS-C (IBS with constipation), IBS-D (IBS with diarrhea), IBS-M (IBS mixed), IBD (inflammatory bowel disease), PI-FD (post-infection functional dyspepsia), HADS (hospital anxiety and depression scale), Tsp (Trichinella spiralis), Np (Nippostrogylus brasiliensis), Cp (Cryptosporidium parvum), Gd (Giardia duodenalis), Cj (Campylobacter jejuni), Cr (Citrobacter rodentium), MCC (migrating myoelectrical complexes), DRG (dorsal root ganglia), FODMAPs (fermentable oligo-), di- (monosaccharides and polyols), FMT (fecal microbial transplantation), SERT (serotonin reuptake transporter)
Article Info
Article in Press
Rome Foundation Working Team Report on Post-Infection Irritable Bowel Syndrome
DOI: https://doi.org/10.1053/j.gastro.2018.07.011
Abstract
Background & Aims
The existence of post-infection 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 was to summarize the available evidence on the pathophysiology of PI-IBS and provide guidance for diagnosis and treatment, based upon 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 prior to 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 is 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 upon team consensus. We also propose areas for investigations.
Key words:
gastrointestinal infection, microbiome, Campylobacter, serotonin, barrier function
Key words:
gastrointestinal infection, microbiome, Campylobacter, serotonin
Abbreviations:
IBS (irritable bowel syndrome), PI-IBS (post-infection irritable bowel syndrome), FGIDs (functional gastrointestinal disorders), SNPs (single nucleotide polymorphisms), 5HT (serotonin), EC (enterochromaffin), ICC (interstitial cells of Cajal), PCR (polymerase chain reaction), IBS-C (IBS with constipation), IBS-D (IBS with diarrhea), IBS-M (IBS mixed), IBD (inflammatory bowel disease), PI-FD (post-infection functional dyspepsia), HADS (hospital anxiety and depression scale), Tsp (Trichinella spiralis), Np (Nippostrogylus brasiliensis), Cp (Cryptosporidium parvum), Gd (Giardia duodenalis), Cj (Campylobacter jejuni), Cr (Citrobacter rodentium), MCC (migrating myoelectrical complexes), DRG (dorsal root ganglia), FODMAPs (fermentable oligo-), di- (monosaccharides and polyols), FMT (fecal microbial transplantation), SERT (serotonin reuptake transporter)
Article Info