Evidence map›Paper›PMID 40512051›Full record

ReviewInflammatory bowel diseases2025

A Guide to the Patient-Centric Use of Vedolizumab for Crohn's Disease.

David T Rubin, Ailsa L Hart

Abstract readReview
In one paragraph

Review in Inflammatory bowel diseases, 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. Article
  2. Review
  3. Review
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

2 authors.

David T RubinUniversity of Chicago Medicine Inflammatory Bowel Disease Center, Chicago, IL, USA.ORCID 0000-0001-5647-1723
Ailsa L HartSt Mark's National Bowel Hospital, London, UK.ORCID 0000-0002-7141-6076

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Crohn's disease (CD) is a chronic, progressive, and debilitating disease characterized by inflammation of the gastrointestinal tract. It can have a significant impact on quality of life if not adequately controlled by appropriate treatment. In recent years, disease management strategies for CD have evolved from a focus on treating symptoms toward the additional goal of early treatment to modify disease progression and prevent bowel damage. Advanced therapies, including biologics, are a key part of the modern medical treatment paradigm for CD, but their introduction has made the treatment landscape more complex. Knowing which advanced therapy to use, when, and for which patient is challenging for health care providers. The α4β7 integrin inhibitor vedolizumab has demonstrated effectiveness, tolerability, and an acceptable long-term safety profile in patients with CD. In this review, we discuss the use of vedolizumab in the management of CD to help clinicians make evidence-based treatment decisions and maximize benefits for their patients. We summarize the medical management of CD, the unique gut-selective mechanism of action of vedolizumab, and the current clinical guidelines for using vedolizumab in patients with CD. We detail the ability of vedolizumab to achieve mucosal healing and alter disease progression and present the evidence that supports the use of vedolizumab as a first-line biologic early in the disease course in patients with CD. Finally, we address some of the perceived drawbacks of using vedolizumab in CD, including concerns about slow onset of action, impact of disease location, and exacerbation of extraintestinal manifestations.

Indexed as

Antibodies, Monoclonal, HumanizedCrohn DiseaseGastrointestinal AgentsPatient-Centered CarePractice Guidelines as TopicHumansQuality of LifeAntibodies, Monoclonal, HumanizedGastrointestinal Agentsvedolizumabbiologicsclinical guidelinesCrohn’s diseasevedolizumab

Identifiers

PMID40512051
PMCPMC12342800

What OpenQuestion holds

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LicenceCC BY
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.