Evidence map›Paper›PMID 39403112›Full record

ArticleJGH open : an open access journal of gastroenterology and hepatology2024

Ten-year outcomes of a prospective population-based incidence cohort of inflammatory bowel disease patients from Canterbury, New Zealand.

Angela J Forbes, Chris M A Frampton, Andrew S Day, Millie DeVries, Nina McVicar, Heidi Su, Richard B Gearry

Abstract read
In one paragraph

Article in JGH open : an open access journal of gastroenterology and hepatology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

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

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

  1. Pooled it
  2. 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.

Angela J ForbesDepartment of Medicine University of Otago Christchurch Christchurch New Zealand.ORCID https://orcid.org/0000-0003-0186-5877
Chris M A FramptonDepartment of Medicine University of Otago Christchurch Christchurch New Zealand.ORCID https://orcid.org/0000-0003-0603-5661
Andrew S DayDepartment of Paediatrics University of Otago Christchurch Christchurch New Zealand.ORCID https://orcid.org/0000-0003-2290-7386
Millie DeVriesGastroenterology Department Te Whatu Ora, Health New Zealand, Waitaha Canterbury Christchurch New Zealand.
Nina McVicarGastroenterology Department Te Whatu Ora, Health New Zealand, Waitaha Canterbury Christchurch New Zealand.
Heidi SuGastroenterology Department Te Whatu Ora, Health New Zealand, Waitaha Canterbury Christchurch New Zealand.ORCID https://orcid.org/0009-0007-0620-1160
Richard B GearryDepartment of Medicine University of Otago Christchurch Christchurch New Zealand.ORCID https://orcid.org/0000-0002-2298-5141

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aim: Inflammatory bowel disease (IBD) is a progressive condition where ongoing inflammation in the gastrointestinal tract can lead to complications such as strictures, and fistulae. The long-term outcomes of newly diagnosed patients under current medical therapy can be used to plan health service provision and guide patients. Methods: Prospective population-based data on all incident patients diagnosed with IBD in Canterbury was gathered in 2014 ( Results: Medical records of 184 IBD patients were able to be retrieved. Immunomodulators were used by 62% and biologics by 35%; hospitalization occurred for 42% and surgery for 15%. Montreal phenotype progression occurred for 21 and 7% of the cohort died. Younger age at diagnosis hazard ratio (HR) 2.1 (95% confidence interval [CI] 1.1-4.0) and Crohn's disease HR 1.7 (95% CI 1.1-2.6) was associated with immunomodulator use. Younger age was also associated with biologic use HR 2.9 (95% CI 1.2-6.9). Male gender was associated with surgery HR 2.8 (95% CI 1.2-6.4). Perianal disease at diagnosis (14.7%) was associated with immunomodulator use HR 2.58 (95% CI 1.44-4.59) and Montreal phenotype progression HR 2.93 (95% CI 1.10-7.77). Conclusion: In the 10 years since diagnosis disease progression and treatment escalation occurred for most of this population-based cohort. Earlier intervention for patients with higher-risk characteristics may improve long-term outcomes reducing the burden on health systems.

Indexed as

Crohn's diseasedisease progressioninflammatory bowel diseaseNew Zealandoutcomesulcerative colitis

Identifiers

PMID39403112
PMCPMC11472240

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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.