Evidence map›Paper›PMID 41101763›Full record

ArticleInflammatory bowel diseases2026

Comparative Risk of Serious Infections Associated With Treatment of Inflammatory Bowel Disease.

Nabeel Khan, Ramaswamy Sundararajan, Dhruvan Patel, Manthankumar Patel, Janak Bahirwani, Nadim Mahmud

Abstract readComparative Study
In one paragraph

Article in Inflammatory bowel diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. 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

6 authors.

Nabeel KhanDepartment of Gastroenterology, Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA, United States.ORCID 0000-0002-5368-7518
Ramaswamy SundararajanDepartment of Gastroenterology, Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA, United States.ORCID 0000-0002-9169-6036
Dhruvan PatelDepartment of Gastroenterology, Mercy Fitzgerald Hospital, Darby, PA, United States.
Manthankumar PatelDepartment of Gastroenterology, Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA, United States.ORCID 0000-0001-6133-8660
Janak BahirwaniDepartment of Gastroenterology, Kadlec Regional Medical Center, Richland, WA, United States.ORCID 0000-0002-9150-521X
Nadim MahmudDepartment of Gastroenterology, Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA, United States.ORCID 0000-0003-1889-3954

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThere is paucity of data on the risk of infection-related hospitalization among inflammatory bowel disease (IBD) patients exposed to newer biologics. Our aim was to assess the overall and comparative risk of infection-related hospitalization, among IBD patients exposed to different IBD medication classes.

methodsThis was a retrospective cohort study of adult IBD patients in the Veterans Health Administration. New initiators of different IBD medication classes were identified, and the primary outcome was infection requiring hospitalization. Survival analysis methods were used to evaluate the association between time-updated IBD medications and these outcomes, adjusted for key confounders.

resultsThe cohort included 14 554 IBD patients. There were 3131 infection hospitalizations over a median follow-up of 49.5 months (interquartile range, 21.2-60.0 months). No other class of medication was associated with a statistically significant difference in the risk of acquiring an infection-related hospitalization compared with patients exposed to a combination therapy of anti-tumor necrosis factor (TNF) inhibitors and thiopurines (TPs). There was a significantly increased risk of gastrointestinal infections with vedolizumab (hazard ration, 1.42; 95% confidence interval, 1.13-1.80; P = .003) relative to anti-TNF inhibitors + TPs. Anti-TNF inhibitor monotherapy had a lower risk when compared with vedolizumab.

conclusionsIn this nationwide IBD cohort, there was not an increased risk of infection-related hospitalization among patients exposed to vedolizumab, ustekinumab, and tofacitinib as compared with patients on anti-TNF inhibitor and TP combination therapy and rates of infection-related hospitalization were low overall. These findings should guide clinical decision making and patient-physician discussions when selecting a therapeutic agent with the primary emphasis on efficacy.

Indexed as

Biological ProductsGastrointestinal AgentsHospitalizationInfectionsInflammatory Bowel DiseasesAdultAntibodies, Monoclonal, HumanizedFemaleFollow-Up StudiesHumansMaleMiddle AgedPiperidinesPyrimidinesRetrospective StudiesRisk FactorsAntibodies, Monoclonal, HumanizedBiological ProductsGastrointestinal AgentsPiperidinesPyrimidinestofacitinibTumor Necrosis Factor InhibitorsvedolizumabCrohn’s diseaseinfectious diseaseinflammatory bowel diseaseulcerative colitis

Identifiers

PMID41101763
PMCPMC12857427

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.