Evidence map›Paper›PMID 27444134›Full record

ArticleAlimentary pharmacology & therapeutics2016

High risk of post-infectious irritable bowel syndrome in patients with Clostridium difficile infection.

A Wadhwa, M F Al Nahhas, R A Dierkhising, R Patel, P Kashyap, D S Pardi, S Khanna, M Grover

Open access · bronzeAbstract read
In one paragraph

Article in Alimentary pharmacology & therapeutics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 2 pooled it
9.1field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

56 citing papers in PubMed, 2 syntheses or guidelines pooled it, 96 citations in OpenAlex.

  1. Guideline
  2. Guideline
  3. Five-Day Treatment withNutrients · 2025
    Trial
  4. SER-109, an Investigational Microbiome Drug to Reduce Recurrence After Clostridioides difficile Infection: Lessons Learned From a Phase 2 Trial.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2021
    Trial
  5. Article
  6. Review
  7. Open forum infectious diseases · 2026
    Article
  8. Review
  9. Irritable bowel syndrome afterMedicine and pharmacy reports · 2025
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Recurrent Clostridioides difficile Infection: Current Clinical Management and Microbiome-Based Therapies.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2023
    Review
  16. The Prevalence, Humanistic Burden, and Health Care Impact of Irritable Bowel Syndrome Among United States Veterans.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2023
    Article
  17. Biofilms and Benign Colonic Diseases.International journal of molecular sciences · 2022
    Review
  18. Article
  19. Review
  20. TcdB ofInternational journal of molecular sciences · 2022
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

A WadhwaDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
M F Al NahhasDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
R A DierkhisingDivision of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, MN, USA.
R PatelDivision of Clinical Microbiology, Mayo Clinic, Rochester, MN, USA.
P KashyapDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
D S PardiDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
S KhannaDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
M GroverDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
Mayo Clinic in Arizona · USMayo Clinic · USMayo Clinic in Florida · US

Funding

Mayo Clinic Center for Translational Science ActivitiesUL1TR000135 · NCATS · MAYO CLINIC ROCHESTER · PI KHOSLA, SUNDEEP · 2012 to 2015
$41.2M
PILOT AND FEASIBILTY PROGRAMP30DK084567 · NIDDK · MAYO CLINIC ROCHESTER · PI Samar Ibrahim · 2009 to 2026
$22.2M
"Barrier function alterations in post-infectious irritable bowel syndrome"K23DK103911 · NIDDK · MAYO CLINIC ROCHESTER · PI GROVER, MADHUSUDAN · 2015 to 2019
$804k
MECHANISMS OF ALTERATION OF GASTROINTESTINAL MOTILITY BY GUT MICROBIOTAK08DK100638 · NIDDK · MAYO CLINIC ROCHESTER · PI KASHYAP, PURNA C · 2014 to 2017
$610k
NCATS NIH HHS UL1 TR000135NIDDK NIH HHS K08 DK100638NIDDK NIH HHS K23 DK103911NIDDK NIH HHS P30 DK084567
6 · The paper itself

Abstract

backgroundInfectious enteritis is a commonly identified risk factor for irritable bowel syndrome (IBS). The incidence of Clostridium difficile infection (CDI) is on the rise. However, there is limited information on post-infectious IBS (PI-IBS) development following CDI and the host- and infection-related risk factors are not known.

aimTo determine the incidence and risk factors for PI-IBS following CDI.

methodsA total of 684 cases of CDI identified from September 2012 to November 2013 were surveyed. Participants completed the Rome III IBS questionnaire and details on the CDI episode. Predictive modelling was done using logistic regression to evaluate risk factors for PI-IBS development.

resultsA total of 315 CDI cases responded (46% response rate) and 205 were at-risk (no pre-CDI IBS) for PI-IBS development. A total of 52/205 (25%) met the Rome III criteria for IBS ≥6 months following CDI. IBS-mixed was most common followed by IBS-diarrhoea. In comparison to those without subsequent PI-IBS, greater percentage of PI-IBS patients had CDI symptoms >7 days, nausea, vomiting, abdominal pain during CDI, anxiety and a higher BMI. Using logistic regression, CDI symptoms >7 days [Odds ratio (OR): 2.96, P = 0.01], current anxiety (OR: 1.33, P < 0.0001) and a higher BMI (OR: 1.08, P = 0.004) were independently associated with PI-IBS development; blood in the stool during CDI was protective (OR: 0.44, P = 0.06).

conclusionsIn this cohort study, new-onset IBS is common after CDI. Longer CDI duration, current anxiety and higher BMI are associated with the diagnosis of C. difficile PI-IBS. This chronic sequela should be considered during active management and follow-up of patients with CDI.

Indexed as

Abdominal PainAdultClostridioides difficileClostridium InfectionsCohort StudiesDiarrheaFemaleHumansIncidenceIrritable Bowel SyndromeLogistic ModelsMaleMiddle AgedRisk Factors

Identifiers

PMID27444134
PMCPMC4982831
OpenAlexW2480405806

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.