Evidence map›Paper›PMID 41132863›Full record

ArticleFrontline gastroenterology2024

Optimising triage of urgent referrals for suspected IBD: results from the Birmingham IBD inception study.

Peter Rimmer, Jonathan Cheesbrough, Jane Harris, Melanie Love, Samantha Tull, Asif Iqbal, Daniel Regan-Komito, Rachel Cooney, Karl Hazel, Naveen Sharma and 4 more

Abstract read
In one paragraph

Article in Frontline gastroenterology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

14 authors.

Peter RimmerBirmingham NIHR Biomedical Research Centre in Inflammation, University of Birmingham, Birmingham, UK.ORCID 0000-0002-0528-6154
Jonathan CheesbroughBirmingham NIHR Biomedical Research Centre in Inflammation, University of Birmingham, Birmingham, UK.
Jane HarrisGastroenterology Department, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Melanie LoveGastroenterology Department, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Samantha TullInstitute of Cardiovascular Sciences, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.
Asif IqbalBirmingham NIHR Biomedical Research Centre in Inflammation, University of Birmingham, Birmingham, UK.
Daniel Regan-KomitoImmunology, Infectious Diseases and Ophthalmology (I2O), Roche Pharma Research & Early Development, F Hoffman La Roche, Basel, Switzerland.
Rachel CooneyBirmingham NIHR Biomedical Research Centre in Inflammation, University of Birmingham, Birmingham, UK.ORCID 0000-0003-3710-157X
Karl HazelBirmingham NIHR Biomedical Research Centre in Inflammation, University of Birmingham, Birmingham, UK.
Naveen SharmaGastroenterology Department, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Thomas DietrichBirmingham NIHR Biomedical Research Centre in Inflammation, University of Birmingham, Birmingham, UK.
Iain ChappleBirmingham NIHR Biomedical Research Centre in Inflammation, University of Birmingham, Birmingham, UK.
Mohammad Nabil QuraishiBirmingham NIHR Biomedical Research Centre in Inflammation, University of Birmingham, Birmingham, UK.
Tariq H IqbalBirmingham NIHR Biomedical Research Centre in Inflammation, University of Birmingham, Birmingham, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Diagnostic delays in inflammatory bowel disease (IBD) result in adverse outcomes. We report a bespoke diagnostic pathway to assess how best to combine clinical history and faecal calprotectin (FCP) for early diagnosis and efficient resource utilisation. Methods: A rapid-access pathway was implemented for suspected IBD patients referred outside urgent 'two-week wait' criteria. Patients were triaged using symptoms and FCP. A 13-point symptom history was taken prediagnosis and clinical indices, including repeat FCP, collected prospectively. Results: Of 767 patients (January 2021-August 2023), 423 were diagnosed with IBD (208 Crohn's disease (CD), 215 ulcerative colitis (UC)). Most common symptoms in CD were abdominal pain (84%), looser stools (84%) and fatigue (79%) and in UC per-rectal bleeding (94%), urgency (82%) and looser stools (81%). Strongest IBD predictors were blood mixed with stools (CD OR 4.38; 95% CI 2.40-7.98, UC OR 33.68; 15.47-73.33) and weight loss (CD OR 3.39; 2.14-5.38, UC OR 2.33; 1.37-4.00). Repeat FCP testing showed reduction from baseline in non-IBD. Both measurements >100 µg/g (area under the curve (AUC) 0.800) and >200 µg/g (AUC 0.834) collectively predicted IBD. However, a second value ≥220 µg/g considered alone, regardless of the first result, was more accurate (Youden's index 0.735, AUC 0.923). Modelling symptoms with FCP increased AUC to 0.947. Conclusion: Serial FCP measurement prevents unnecessary colonoscopy. Two FCPs >200 µg/g could stream patients direct to colonoscopy, with two >100 µg/g prompting clinic review. A second result ≥220 µg/g was more accurate than dual-result thresholds. Coupling home FCP testing with key symptoms may form the basis of effective self-referral pathways.

Indexed as

CROHN'S DISEASEIBD CLINICALINFLAMMATORY BOWEL DISEASEULCERATIVE COLITIS

Identifiers

PMID41132863
PMCPMC12542818

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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.