Evidence map›Paper›PMID 28806445›Full record

SynthesisJAMA pediatrics2017

Use of Laboratory Markers in Addition to Symptoms for Diagnosis of Inflammatory Bowel Disease in Children: A Meta-analysis of Individual Patient Data.

Gea A Holtman, Yvonne Lisman-van Leeuwen, Andrew S Day, Ulrika L Fagerberg, Paul Henderson, Stevan T Leach, Gøri Perminow, David Mack, Patrick F van Rheenen, Els van de Vijver and 3 more

Open access · bronzeAbstract readMeta-Analysis
In one paragraph

Synthesis in JAMA pediatrics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 2 pooled it
3.7field-weighted citation impact, top 7% of its field
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

21 citing papers in PubMed, 2 syntheses or guidelines pooled it, 46 citations in OpenAlex.

  1. Pooled it
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  7. Inflammatory Bowel Disease in Jordanian Children: A Tertiary Center Experience.Pediatric gastroenterology, hepatology & nutrition · 2025
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  16. [Role of NLRP1 and NLRP3 inflammasome signaling pathways in the immune mechanism of inflammatory bowel disease in children].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2020
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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

13 authors at 11 institutions in 8 countries.

Gea A HoltmanDepartment of General Practice, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Yvonne Lisman-van LeeuwenDepartment of General Practice, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Andrew S DayDepartment of Paediatric Gastroenterology, Sydney Children's Hospital, Randwick, Australia.
Ulrika L FagerbergCentre for Clinical Research, Department of Paediatrics, Västmanlands Hospital, Västerås, Sweden.
Paul HendersonDepartment of Paediatric Gastroenterology and Nutrition, Royal Hospital for Sick Children, Edinburgh, Scotland.
Stevan T LeachSchool of Women's and Children's Health, Sydney Children's Hospital, Randwick, Australia.
Gøri PerminowDepartment of Paediatrics, Oslo University Hospital, Oslo, Norway.
David MackDeparment of Pediatrics, Children's Hospital of Eastern Ontario, University of Ottawa, Ottawa, Canada.
Patrick F van RheenenDepartment of Paediatric Gastroenterology, University Medical Centre Groningen, University of Groningen, Groningen, the Netherlands.
Els van de VijverDepartment of Paediatric Gastroenterology, Antwerp University Hospital, Edegem, Belgium.
David C WilsonDepartment of Paediatric Gastroenterology and Nutrition, Royal Hospital for Sick Children, Edinburgh, Scotland.
Johannes B ReitsmaJulius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, the Netherlands.
Marjolein Y BergerDepartment of General Practice, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
University Medical Center Groningen · NLAntwerp University Hospital · BEChildren's Hospital of Eastern Ontario · CAKarolinska Institutet · SEOslo University Hospital · NORoyal Hospital for Sick Children · GBSydney Children's Hospital · AUUniversity Medical Center Utrecht · NLUniversity of Edinburgh · GBUniversity of Groningen · NLUniversity of Otago · NZ

Funding

Medical Research Council G0800675MRF_ C0482
6 · The paper itself

Abstract

Importance: Blood markers and fecal calprotectin are used in the diagnostic workup for inflammatory bowel disease (IBD) in pediatric patients. Any added diagnostic value of these laboratory markers remains unclear. Objective: To determine whether adding laboratory markers to evaluation of signs and symptoms improves accuracy when diagnosing pediatric IBD. Data Sources: A literature search of MEDLINE and EMBASE from inception through September 26, 2016. Studies were identified using indexing terms and free-text words related to child, target condition IBD, and diagnostic accuracy. Study Selection: Two reviewers independently selected studies evaluating the diagnostic accuracy of more than 1 blood marker or fecal calprotectin for IBD, confirmed by endoscopy and histopathology or clinical follow-up, in pediatric patients with chronic gastrointestinal symptoms. Studies that included healthy controls and/or patients with known IBD were excluded. Data Extraction and Synthesis: Individual patient data from each eligible study were requested from the authors. In addition, 2 reviewers independently assessed quality with Quality Assessment of Diagnostic Accuracy Studies-2. Mean Outcomes and Measures: Laboratory markers were added as a single test to a basic prediction model based on symptoms. Outcome measures were improvement of discrimination by adding markers as a single test and improvement of risk classification of pediatric patients by adding the best marker. Results: Of the 16 eligible studies, authors of 8 studies (n = 1120 patients) provided their data sets. All blood markers and fecal calprotectin individually significantly improved the discrimination between pediatric patients with and those without IBD, when added to evaluation of symptoms. The best marker-fecal calprotectin-improved the area under the curve of symptoms by 0.26 (95% CI, 0.21-0.31). The second best marker-erythrocyte sedimentation rate-improved the area under the curve of symptoms by 0.16 (95% CI, 0.11-0.21). When fecal calprotectin was added to the model, the proportion of patients without IBD correctly classified as low risk of IBD increased from 33% to 91%. The proportion of patients with IBD incorrectly classified as low risk of IBD decreased from 16% to 9%. The proportion of the total number of patients assigned to the intermediate-risk category decreased from 55% to 6%. Conclusions and Relevance: In a hospital setting, fecal calprotectin added the most diagnostic value to symptoms compared with blood markers. Adding fecal calprotectin to the diagnostic workup of pediatric patients with symptoms suggestive of IBD considerably decreased the number of patients in the group in whom challenges in clinical decision making are most prevalent.

Indexed as

BiomarkersChildDiagnosis, DifferentialFecesFemaleHumansInflammatory Bowel DiseasesLeukocyte L1 Antigen ComplexMaleSensitivity and SpecificityBiomarkersLeukocyte L1 Antigen Complex

Identifiers

PMID28806445
PMCPMC5710621
OpenAlexW2750180480

What OpenQuestion holds

Textmetadata
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.