Evidence map›Paper›PMID 42598726›Full record

ArticleCrohn's & colitis 3602026

Continued concomitant antibiotic or immunosuppression therapies reduce the risk of pouchitis among patients with ileal pouch-anal anastomosis and primary sclerosing cholangitis.

John P Haydek, Priscila Santiago, Joseph Carter Powers, Latchmin Ruplall, Hoang Anh Richardson, Erin Causey, Mohamed Elhawary, Taylor Karl, Rami Tfayli, Jana G Hashash and 7 more

Abstract read
In one paragraph

Article in Crohn's & colitis 360, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

17 authors.

John P HaydekDivision of Gastroenterology and Hepatology, University of North Carolina, Chapel Hill, NC, United States.ORCID https://orcid.org/0000-0003-2094-7181
Priscila SantiagoDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, United States.ORCID https://orcid.org/0000-0003-2231-2884
Joseph Carter PowersDivision of Gastroenterology, Cleveland Clinic, Cleveland, OH, United States.
Latchmin RuplallDivision of Gastroenterology and Hepatology, NYU Langone Health, New York, NY, United States.
Hoang Anh RichardsonDivision of Gastroenterology, Hepatology, and Nutrition, Vanderbilt University, Nashville, TN, United States.
Erin CauseyDivision of Gastroenterology, Hepatology, and Nutrition, Vanderbilt University, Nashville, TN, United States.
Mohamed ElhawaryDivision of Gastroenterology and Hepatology, NYU Langone Health, New York, NY, United States.
Taylor KarlDivision of Gastroenterology and Hepatology, University of Colorado School of Medicine, Aurora, CO, United States.ORCID https://orcid.org/0009-0000-5737-1302
Rami TfayliDivision of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, FL, United States.
Jana G HashashDivision of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, FL, United States.ORCID https://orcid.org/0000-0001-8305-9742
Taha QaziDivision of Gastroenterology, Cleveland Clinic, Cleveland, OH, United States.ORCID https://orcid.org/0000-0001-6770-9055
Shannon ChangDivision of Gastroenterology and Hepatology, NYU Langone Health, New York, NY, United States.ORCID https://orcid.org/0000-0001-6195-5386
Sara HorstDivision of Gastroenterology, Hepatology, and Nutrition, Vanderbilt University, Nashville, TN, United States.ORCID https://orcid.org/0000-0003-3585-9643
Frank I ScottDivision of Gastroenterology and Hepatology, University of Colorado School of Medicine, Aurora, CO, United States.ORCID https://orcid.org/0000-0002-6021-0419
Millie D LongDivision of Gastroenterology and Hepatology, University of North Carolina, Chapel Hill, NC, United States.ORCID https://orcid.org/0000-0001-5983-2758
Laura RaffalsDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, United States.ORCID https://orcid.org/0000-0002-5267-2592
Edward L BarnesDivision of Gastroenterology and Hepatology, University of North Carolina, Chapel Hill, NC, United States.ORCID https://orcid.org/0000-0001-9894-8796

Funding

Treatment Approaches and Outcomes in Pouch-related Disorders after Colectomy for Ulcerative ColitisK23DK127157 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BARNES, EDWARD · 2021 to 2025
$1.0M
NIDDK NIH HHS K23 DK127157
6 · The paper itself

Abstract

Background: Complications such as intermittent pouchitis (IP) and chronic inflammatory disorders of the pouch (CP) are common after ileal pouch-anal anastomosis (IPAA), particularly among patients with both ulcerative colitis and primary sclerosing cholangitis (PSC). There are no standardized approaches for prophylaxis against these complications for patients with PSC undergoing IPAA. We compared outcomes among patients with PSC and IPAA who received antibiotic or immunosuppressive therapies to those who did not. Methods: We designed a retrospective cohort study that included patients with ulcerative colitis and PSC from 7 tertiary care centers that underwent IPAA between 1994 and 2023. Patients were categorized on whether they received medications following IPAA that may provide primary prophylactic benefit, such as antibiotics, probiotics, immunomodulators, or biologic medications; and the proportion of patients developing IP and CP was evaluated. Results: A total of 172 patients were included in the cohort, and 13 (7.6%) patients received antibiotics or immunosuppressant medications. Antibiotics and probiotics were the most common therapy (5 patients, 2.9%), followed by biologics, small-molecule inhibitors, immunomodulators, or mesalamine (all 1 patient, 0.6%). Compared to patients not receiving antibiotics or immunosuppression, patients receiving antibiotics or immunosuppression were significantly less likely to develop IP (69.2% vs 91.2%; Conclusions: In this retrospective cohort of patients with ulcerative colitis and PSC undergoing IPAA, usage of concomitant antibiotics or immunosuppression was low. However, use of concomitant antibiotics or immunosuppression may decrease the burden of inflammatory conditions of the pouch in these high-risk patients.

Indexed as

chronic antibiotic–dependent pouchitischronic antibiotic refractory pouchitisCrohn’s-like disease of the pouchpouchitisprimary sclerosing cholangitis

Identifiers

PMID42598726
PMCPMC13472676

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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.