Literature DB >> 32618660

Fecal Bile Acid Testing in Assessing Patients With Chronic Unexplained Diarrhea: Implications for Healthcare Utilization.

Priya Vijayvargiya1, Daniel Gonzalez Izundegui1, Gerardo Calderon2, Sarah Tawfic3, Sarah Batbold3, Michael Camilleri1.   

Abstract

INTRODUCTION: Bile acid (BA) diarrhea is the cause in ∼26% of chronic unexplained (nonbloody) diarrhea (CUD) based on SeHCAT testing. To assess fecal BA excretion and healthcare utilization in patients with CUD.
METHODS: In a retrospective review of 1,071 consecutive patients with CUD who completed 48-hour fecal BA testing, we analyzed the symptoms, diagnostic tests performed, and final diagnoses.
RESULTS: After 135 patients were excluded because of mucosal diseases, increased BA excretion was identified in 476 (51%) of the 936 patients with CUD: 29% with selective increase in primary BA and 22% with increased total BA excretion (35% with normal primary BA excretion). There were no differences in demographics, clinical symptoms, or history of cholecystectomy in patients with elevated total or selective primary fecal BA excretion compared with patients with normal excretion. Before the 48-hour fecal BA excretion test was performed, patients completed on average 1.2 transaxial imaging, 2.6 endoscopic procedures, and 1.6 miscellaneous tests/person. Less than 10% of these tests identified the etiology of CUD. Total fecal BAs >3,033 µmol/48 hour or primary BAs >25% had a 93% negative predictive value to exclude mucosal disease. Among patients with increased fecal BA excretion, >70% reported diarrhea improved with BA sequestrant compared with 26% with normal fecal BA excretion. Patients with selective elevation in primary fecal BAs were 3.1 times (95% confidence interval, 1.5-6.63) more likely to respond to BA sequestrant therapy compared with those with elevated total fecal BAs. DISCUSSION: Increased fecal BA excretion is frequent (51%) in patients with CUD. Early 48-hour fecal BA evaluation has the potential to decrease healthcare utilization in CUD.

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Year:  2020        PMID: 32618660      PMCID: PMC7680261          DOI: 10.14309/ajg.0000000000000637

Source DB:  PubMed          Journal:  Am J Gastroenterol        ISSN: 0002-9270            Impact factor:   10.864


  28 in total

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2.  AGA Clinical Practice Guidelines on the Laboratory Evaluation of Functional Diarrhea and Diarrhea-Predominant Irritable Bowel Syndrome in Adults (IBS-D).

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3.  Curbing Unnecessary and Wasted Diagnostic Imaging.

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Review 4.  Diagnosis and Management of Microscopic Colitis.

Authors:  Darrell S Pardi
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5.  Bile acid malabsorption in microscopic colitis and in previously unexplained functional chronic diarrhea.

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6.  Performance characteristics of serum C4 and FGF19 measurements to exclude the diagnosis of bile acid diarrhoea in IBS-diarrhoea and functional diarrhoea.

Authors:  P Vijayvargiya; M Camilleri; P Carlson; A Lueke; J O'Neill; D Burton; I Busciglio; L Donato
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7.  The response of patients with bile acid diarrhoea to the farnesoid X receptor agonist obeticholic acid.

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Review 8.  Systematic review: the prevalence of idiopathic bile acid malabsorption as diagnosed by SeHCAT scanning in patients with diarrhoea-predominant irritable bowel syndrome.

Authors:  L Wedlake; R A'Hern; D Russell; K Thomas; J R F Walters; H J N Andreyev
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Review 9.  Biomarkers for bile acid diarrhoea in functional bowel disorder with diarrhoea: a systematic review and meta-analysis.

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Journal:  Neurogastroenterol Motil       Date:  2021-11-09       Impact factor: 3.598

3.  High prevalence of primary bile acid diarrhoea in patients with functional diarrhoea and irritable bowel syndrome-diarrhoea, based on Rome III and Rome IV criteria.

Authors:  Mohamed G Shiha; Zohaib Ashgar; Ellen M Fraser; Matthew Kurien; Imran Aziz
Journal:  EClinicalMedicine       Date:  2020-07-15

Review 4.  Pathophysiology and Clinical Management of Bile Acid Diarrhea.

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Review 5.  The Role of Bile Acids in Chronic Diarrhea.

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6.  Impact of Bile Acid Diarrhea in Patients With Diarrhea-Predominant Irritable Bowel Syndrome on Symptoms and Quality of Life.

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Journal:  Clin Gastroenterol Hepatol       Date:  2021-12-04       Impact factor: 13.576

  6 in total

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