Literature DB >> 27280328

Pediatric-Collaborative Health Outcomes Information Registry (Peds-CHOIR): a learning health system to guide pediatric pain research and treatment.

Rashmi P Bhandari1, Amanda B Feinstein1, Samantha E Huestis1, Elliot J Krane1, Ashley L Dunn1, Lindsey L Cohen2, Ming C Kao1, Beth D Darnall1, Sean C Mackey1.   

Abstract

The pediatric adaptation of the Collaborative Health Outcomes Information Registry (Peds-CHOIR) is a free, open-source, flexible learning health care system (LHS) that meets the call by the Institute of Medicine for the development of national registries to guide research and precision pain medicine. This report is a technical account of the first application of Peds-CHOIR with 3 aims: (1) to describe the design and implementation process of the LHS; (2) to highlight how the clinical system concurrently cultivates a research platform rich in breadth (eg, clinic characteristics) and depth (eg, unique patient- and caregiver-reporting patterns); and (3) to demonstrate the utility of capturing patient-caregiver dyad data in real time, with dynamic outcomes tracking that informs clinical decisions and delivery of treatments. Technical, financial, and systems-based considerations of Peds-CHOIR are discussed. Cross-sectional retrospective data from patients with chronic pain (N = 352; range, 8-17 years; mean, 13.9 years) and their caregivers are reported, including National Institutes of Health Patient-Reported Outcomes Measurement Information System (PROMIS) domains (mobility, pain interference, fatigue, peer relations, anxiety, and depression) and the Pain Catastrophizing Scale. Consistent with the literature, analyses of initial visits revealed impairments across physical, psychological, and social domains. Patients and caregivers evidenced agreement in observable variables (mobility); however, caregivers consistently endorsed greater impairment regarding internal experiences (pain interference, fatigue, peer relations, anxiety, and depression) than patients' self-report. A platform like Peds-CHOIR highlights predictors of chronic pain outcomes on a group level and facilitates individually tailored treatment(s). Challenges of implementation and future directions are discussed.

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Year:  2016        PMID: 27280328      PMCID: PMC4988911          DOI: 10.1097/j.pain.0000000000000609

Source DB:  PubMed          Journal:  Pain        ISSN: 0304-3959            Impact factor:   7.926


  63 in total

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Journal:  J Pediatr Psychol       Date:  2011-07-10

2.  Development and psychometric properties of the PROMIS(®) pediatric fatigue item banks.

Authors:  Jin-Shei Lai; Brian D Stucky; David Thissen; James W Varni; Esi Morgan DeWitt; Debra E Irwin; Karin B Yeatts; Darren A DeWalt
Journal:  Qual Life Res       Date:  2013-02-02       Impact factor: 4.147

3.  Cognitive behavioral therapy for the treatment of juvenile fibromyalgia: a multisite, single-blind, randomized, controlled clinical trial.

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Journal:  Arthritis Rheum       Date:  2012-01

4.  Clinical utility and validity of the Functional Disability Inventory among a multicenter sample of youth with chronic pain.

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Journal:  Pain       Date:  2011-03-31       Impact factor: 6.961

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Authors:  P Fearon; M Hotopf
Journal:  BMJ       Date:  2001-05-12

7.  Temporal daily associations between pain and sleep in adolescents with chronic pain versus healthy adolescents.

Authors:  Amy S Lewandowski; Tonya M Palermo; Stacy De la Motte; Rochelle Fu
Journal:  Pain       Date:  2010-08-16       Impact factor: 6.961

Review 8.  Interdisciplinary chronic pain management: past, present, and future.

Authors:  Robert J Gatchel; Donald D McGeary; Cindy A McGeary; Ben Lippe
Journal:  Am Psychol       Date:  2014 Feb-Mar

9.  PROMIS Pediatric Peer Relationships Scale: development of a peer relationships item bank as part of social health measurement.

Authors:  Darren A Dewalt; David Thissen; Brian D Stucky; Michelle M Langer; Esi Morgan Dewitt; Debra E Irwin; Jin-Shei Lai; Karin B Yeatts; Heather E Gross; Olivia Taylor; James W Varni
Journal:  Health Psychol       Date:  2013-06-17       Impact factor: 4.267

10.  Disease experience and psychosocial adjustment in children with juvenile rheumatoid arthritis: children's versus mothers' reports.

Authors:  S T Ennett; B M DeVellis; J A Earp; D Kredich; R W Warren; C L Wilhelm
Journal:  J Pediatr Psychol       Date:  1991-10
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  23 in total

1.  The Effect of Pain Catastrophizing on Outcomes: A Developmental Perspective Across Children, Adolescents, and Young Adults With Chronic Pain.

Authors:  Amanda B Feinstein; John A Sturgeon; Beth D Darnall; Ashley L Dunn; Tom Rico; Ming C Kao; Rashmi P Bhandari
Journal:  J Pain       Date:  2016-11-05       Impact factor: 5.820

Review 2.  What is the future of patient-reported outcomes in sickle-cell disease?

Authors:  Sharon A Singh; Nitya Bakshi; Prashant Mahajan; Claudia R Morris
Journal:  Expert Rev Hematol       Date:  2020-10-15       Impact factor: 2.929

3.  Risk and Resilience in Pediatric Pain: The Roles of Parent and Adolescent Catastrophizing and Acceptance.

Authors:  Amanda B Feinstein; John A Sturgeon; Rashmi P Bhandari; Isabel A Yoon; Alexandra C Ross; Samantha E Huestis; Anya T Griffin; Laura E Simons
Journal:  Clin J Pain       Date:  2018-12       Impact factor: 3.442

4.  The SHOnet learning health system: Infrastructure for continuous learning in pediatric rehabilitation.

Authors:  Nikolas Koscielniak; Diane Jenkins; Sahar Hassani; Cathleen Buckon; Joshua S Tucker; Susan Sienko; Carole A Tucker
Journal:  Learn Health Syst       Date:  2022-02-15

5.  Signature for Pain Recovery IN Teens (SPRINT): protocol for a multisite prospective signature study in chronic musculoskeletal pain.

Authors:  Laura Simons; Massieh Moayedi; Robert C Coghill; Jennifer Stinson; Martin S Angst; Nima Aghaeepour; Brice Gaudilliere; Christopher D King; Marina López-Solà; Marie-Eve Hoeppli; Emma Biggs; Ed Ganio; Sara E Williams; Kenneth R Goldschneider; Fiona Campbell; Danielle Ruskin; Elliot J Krane; Suellen Walker; Gillian Rush; Marissa Heirich
Journal:  BMJ Open       Date:  2022-06-08       Impact factor: 3.006

6.  Comparison of pain and psychosocial correlates among Hispanic and Non-Hispanic White youth with chronic pain.

Authors:  Ana B Goya Arce; Patricia A Richardson; Susan T Tran; Rashmi P Bhandari
Journal:  Pain Rep       Date:  2022-07-18

7.  Assessing a child or adolescent with low back pain is different to assessing an adult with low back pain.

Authors:  Joshua W Pate; Rhiannon Joslin; Karen Hurtubise; David B Anderson
Journal:  J Paediatr Child Health       Date:  2022-02-26       Impact factor: 1.929

Review 8.  Best practices for virtual care to support youth with chronic pain and their families: a rapid systematic review to inform health care and policy during COVID-19 and beyond.

Authors:  Kathryn A Birnie; Tieghan Killackey; Jennifer Stinson; Melanie Noel; Diane L Lorenzetti; Justina Marianayagam; Isabel Jordan; Evie Jordan; Alexandra Neville; Maria Pavlova; Fiona Campbell; Chitra Lalloo
Journal:  Pain Rep       Date:  2021-06-03

9.  Baseline Characteristics of a Dyadic Cohort of Mothers With Chronic Pain and Their Children.

Authors:  Anna C Wilson; Amanda L Stone; Katrina M Poppert Cordts; Amy L Holley; Sean Mackey; Beth D Darnall; Tonya M Palermo
Journal:  Clin J Pain       Date:  2020-10       Impact factor: 3.423

Review 10.  Catastrophizing, pain, and functional outcomes for children with chronic pain: a meta-analytic review.

Authors:  Megan M Miller; Samantha M Meints; Adam T Hirsh
Journal:  Pain       Date:  2018-12       Impact factor: 7.926

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