Literature DB >> 34798944

Assessing Patient-Reported Outcomes in Pediatric Rheumatic Diseases: Considerations and Future Directions.

Christina K Zigler1, Rachel L Randell2, Bryce B Reeve3.   

Abstract

For children with pediatric rheumatic diseases (PRDs), the inclusion of patient-reported outcomes (PROs) is critical to inform decision making in health care delivery and research settings. PROs are direct reports from a child on their health status, without interpretation by anyone else. PROs improve understanding of the patient experience, allow clinicians to provide patient-centered care, and add value to clinical trials. When PROs cannot be collected directly from the patient, caregiver-proxy reports can provide important information on the child's more observable symptoms and functioning. In this article, we describe the current use of PROs in specific PRDs, align current research with best practice recommendations for both clinical care and research settings, highlight exciting new developments, and identify areas for future research.
Copyright © 2021 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Clinical care; Clinical trials; Future directions; Patient-reported outcome measures; Patient-reported outcomes; Pediatric rheumatic diseases

Mesh:

Year:  2022        PMID: 34798944      PMCID: PMC9311483          DOI: 10.1016/j.rdc.2021.09.008

Source DB:  PubMed          Journal:  Rheum Dis Clin North Am        ISSN: 0889-857X            Impact factor:   2.032


  73 in total

Review 1.  Assessing health status and quality-of-life instruments: attributes and review criteria.

Authors:  Neil Aaronson; Jordi Alonso; Audrey Burnam; Kathleen N Lohr; Donald L Patrick; Edward Perrin; Ruth E Stein
Journal:  Qual Life Res       Date:  2002-05       Impact factor: 4.147

2.  Comparing patient, parent, and staff descriptions of fatigue in pediatric oncology patients.

Authors:  P S Hinds; M Hockenberry-Eaton; E Gilger; N Kline; C Burleson; S Bottomley; A Quargnenti
Journal:  Cancer Nurs       Date:  1999-08       Impact factor: 2.592

3.  Evidence for Updating the Core Domain Set of Outcome Measures for Juvenile Idiopathic Arthritis: Report from a Special Interest Group at OMERACT 2016.

Authors:  Esi M Morgan; Meredith P Riebschleger; Jennifer Horonjeff; Alessandro Consolaro; Jane E Munro; Susan Thornhill; Timothy Beukelman; Hermine I Brunner; Emily L Creek; Julia G Harris; Daniel B Horton; Daniel J Lovell; Melissa L Mannion; Judyann C Olson; Homaira Rahimi; Maria Chiara Gallo; Serena Calandra; Angelo Ravelli; Sarah Ringold; Susan Shenoi; Jennifer Stinson; Karine Toupin-April; Vibeke Strand; Clifton O Bingham
Journal:  J Rheumatol       Date:  2017-08-15       Impact factor: 4.666

4.  PROMIS(®) pediatric self-report scales distinguish subgroups of children within and across six common pediatric chronic health conditions.

Authors:  Darren A DeWalt; Heather E Gross; Debbie S Gipson; David T Selewski; Esi Morgan DeWitt; Carlton D Dampier; Pamela S Hinds; I-Chan Huang; David Thissen; James W Varni
Journal:  Qual Life Res       Date:  2015-02-26       Impact factor: 4.147

Review 5.  International guidance on the selection of patient-reported outcome measures in clinical trials: a review.

Authors:  Norah L Crossnohere; Michael Brundage; Melanie J Calvert; Madeleine King; Bryce B Reeve; Elissa Thorner; Albert W Wu; Claire Snyder
Journal:  Qual Life Res       Date:  2020-09-14       Impact factor: 4.147

6.  Multicenter validation of a new quality of life measure in pediatric lupus.

Authors:  L Nandini Moorthy; Margaret G E Peterson; Maria Baratelli; Melanie J Harrison; Karen B Onel; Elizabeth C Chalom; Kathleen Haines; Philip J Hashkes; Thomas J A Lehman
Journal:  Arthritis Rheum       Date:  2007-10-15

7.  Development of six PROMIS pediatrics proxy-report item banks.

Authors:  Debra E Irwin; Heather E Gross; Brian D Stucky; David Thissen; Esi Morgan DeWitt; Jin Shei Lai; Dagmar Amtmann; Leyla Khastou; James W Varni; Darren A DeWalt
Journal:  Health Qual Life Outcomes       Date:  2012-02-22       Impact factor: 3.186

Review 8.  Is there a difference between child self-ratings and parent proxy-ratings of the quality of life of children with a diagnosis of attention-deficit hyperactivity disorder (ADHD)? A systematic review of the literature.

Authors:  Helen Galloway; Emily Newman
Journal:  Atten Defic Hyperact Disord       Date:  2016-12-22

9.  Development of a consensus core dataset in juvenile dermatomyositis for clinical use to inform research.

Authors:  Liza J McCann; Clarissa A Pilkington; Adam M Huber; Angelo Ravelli; Duncan Appelbe; Jamie J Kirkham; Paula R Williamson; Amita Aggarwal; Lisa Christopher-Stine; Tamas Constantin; Brian M Feldman; Ingrid Lundberg; Sue Maillard; Pernille Mathiesen; Ruth Murphy; Lauren M Pachman; Ann M Reed; Lisa G Rider; Annet van Royen-Kerkof; Ricardo Russo; Stefan Spinty; Lucy R Wedderburn; Michael W Beresford
Journal:  Ann Rheum Dis       Date:  2017-10-30       Impact factor: 19.103

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