Evidence map›Paper›PMID 39963249›Full record

ArticleTherapeutic advances in gastroenterology2025

Higher disease activity of inflammatory bowel disease predisposes to

Krista Vitikainen, Merit Kase, Leo Meriranta, Pauliina Molander, Clas-Göran Af Björkesten, Veli-Jukka Anttila, Perttu Arkkila

Abstract read
In one paragraph

Article in Therapeutic advances in gastroenterology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Biomedicines · 2025
    Review
  3. 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

7 authors.

Krista VitikainenHUS Helsinki University Hospital, Haartmaninkatu 4, P.O. Box 340, Helsinki 00029, Finland.ORCID https://orcid.org/0009-0006-1609-383X
Merit KaseHUS Helsinki University Hospital, Helsinki, Finland.
Leo MerirantaHUS Helsinki University Hospital, Helsinki, Finland.
Pauliina MolanderAbdominal Center, Gastroenterology, HUS Helsinki University Hospital and Helsinki University, Helsinki, Finland.ORCID https://orcid.org/0000-0002-9494-3573
Clas-Göran Af BjörkestenAbdominal Center, Gastroenterology, HUS Helsinki University Hospital and Helsinki University, Helsinki, Finland.
Veli-Jukka AnttilaDepartment of Infectious Diseases, Helsinki University Hospital and Helsinki University, Helsinki, Finland.
Perttu ArkkilaAbdominal Center, Gastroenterology, HUS Helsinki University Hospital and Helsinki University, Helsinki, Finland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Objectives: To identify clinical risk factors for CDI and its recurrence among patients with IBD. Design: Case-control cohort study of IBD patients with and without episodes of CDI. Methods: A case-control study of 279 IBD patients with CDI. Medical history and IBD-related symptoms 3 months preceding a toxin-positive CDI were recorded and compared with age- and sex-matched IBD patients without CDI. Outcomes of CDI in IBD patients were recorded 2-6 months after CDI. Results: Based on clinical symptoms and fecal calprotectin levels, IBD is active before CDI. Recently diagnosed IBD seemed to increase the risk for CDI. Corticosteroid usage frequently preceded CDI episodes. Advanced therapies were not associated with CDI. Antibiotic intake was not registered before CDI in 30% of the episodes. Recurrent CDI (rCDI) occurred in 30% (84/279) of IBD-CDI patients and 67% (90/135) of those episodes were registered within 90 days from the preceding episode. Most (79%) rCDI patients had ulcerative colitis (UC). CDI could complicate underlying IBD by increasing the need for escalation in IBD-related medical therapy and leading to hospitalization but it did not seem to increase the risk of colectomy. Conclusion: The major risk factors associated with CDI in IBD patients were IBD activity before infection, UC and colonic Crohn's disease, short duration of IBD, corticosteroid usage, and hospitalization. Patients with active IBD and a shorter disease duration may benefit from more frequent follow-ups in the early stages, as they appear to be at higher risk of developing CDI.

Indexed as

Clostridioides difficilegastrointestinal infectionsinflammatory bowel disease

Identifiers

PMID39963249
PMCPMC11831662

What OpenQuestion holds

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Registered trials

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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.