ArticleThe Journal of pediatrics2016
Patient-Reported Outcomes Measurement Information System in Children with Crohn's Disease.
Article in The Journal of pediatrics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.
What it found
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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.
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.
Who cites it
14 citing papers in PubMed.
- Use of Patient-Reported Outcomes Measurement Information System Pediatric Measures as Clinical Trial Endpoints: Experience from a Multicenter Pragmatic Trial in Children with Crohn's Disease.The Journal of pediatrics · 2022Trial
- Patient-Reported Outcomes from a Randomized, Active-Controlled, Open-Label, Phase 3 Trial of Burosumab Versus Conventional Therapy in Children with X-Linked Hypophosphatemia.Calcified tissue international · 2021Trial
- Discrepancies in perceptions of well-being: comparing parental and pediatric PROMIS-patient-reported outcomes in Crohn's disease.Journal of patient-reported outcomes · 2025Article
- Clinical usefulness of patient-reported-outcome-measurement information system in Pediatric Crohn's Disease: a cross-sectional study.Health and quality of life outcomes · 2024Article
- Patient-Reported Outcomes Measurement Information System as a Clinical Tool for Capturing the Patient Perspective in Pediatric Inflammatory Bowel Disease: A Narrative Review.Children (Basel, Switzerland) · 2024Review
- Computerized-adaptive testing versus short forms for pediatric inflammatory bowel disease patient-reported outcome assessment.Journal of clinical and translational science · 2023Article
- Anxiety and Depressive Symptoms Are Not Associated With Future Pediatric Crohn's Disease Activity.Inflammatory bowel diseases · 2022Article
- A Study Protocol for the Management of Children With Juvenile Idiopathic Arthritis Based on ePROs.Frontiers in pediatrics · 2022Article
- Responsiveness of the Patient-reported Outcomes Measurement Information System (PROMIS) Pediatric Measures to Changes in Disease Status and Quality of Life Among Children and Adolescents With Crohn's Disease.Inflammatory bowel diseases · 2021Article
- Transition Readiness Not Associated With Measures of Health in Youth With IBD.Inflammatory bowel diseases · 2021Article
- The lived experience of anxiety and the many facets of pain: A qualitative, arts-based approach.Canadian journal of pain = Revue canadienne de la douleur · 2020Article
- Improving Quality in the Care of Patients with Inflammatory Bowel Diseases.Inflammatory bowel diseases · 2018Review
- Assessing responsiveness over time of the PROMISQuality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation · 2018Article
- Parent Experience of Neonatal Encephalopathy.Journal of child neurology · 2017Article
Corrections and comments
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Authors and funding
8 authors.
Funding
Abstract
objectivesTo assess the criterion validity and responsiveness of Patient-Reported Outcomes Measurement Information System (PROMIS) in a web-based cohort of children with Crohn's disease. STUDY
designWe recruited children with Crohn's disease (ages 9-17 years) and their parents from the web-based Crohn's and Colitis Foundation of America Kids and Teens Study cohort. Upon entry into the cohort and 6 months later, children self-reported Crohn's disease activity, health-related quality of life, and PROMIS domains of pain interference, anxiety, depression, fatigue, and peer relationships.
resultsMean PROMIS scores for the 276 participating patients were worse among those with worse self-reported Crohn's disease activity (per Short Crohn's Disease Activity Index, P < .005 for all), Crohn's disease activity in the prior 6 months (per Manitoba Index, P < .01 for all), and health-related quality of life (per IMPACT-35, P < .001 for all). One hundred forty-three patients and their parents completed follow-up questionnaires, 75% of whom reported stable disease activity. Those with improved Crohn's disease activity reported improved PROMIS scores, and those with worsened Crohn's disease activity reported worse PROMIS scores for all domains except anxiety. All participants reported improved anxiety from baseline, but those with stable or worsened Crohn's disease activity reported less improvement (P = .07).
conclusionsPROMIS scores were significantly associated with Crohn's disease activity in a linear and clinically meaningful manner, and responded to change in Crohn's disease activity over a 6-month period. This supports the criterion validity and responsiveness of pediatric PROMIS.
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