Literature DB >> 36125521

Selecting patient-reported outcome measures of health-related quality of life in adult rheumatology: quality and breadth of coverage.

Erin Knight1,2, Karen E Schifferdecker3,4, Guy S Eakin5, Bryce B Reeve6.   

Abstract

Patient-centered research should assess outcomes important to patients and include patient-reported outcome measures (PROMs) to assess health-related quality of life (HRQOL) domains. Using a well-known HRQOL framework (World Health Organization QOL, or WHOQOL), we reviewed established PROMs used with adults with different types of arthritis to evaluate their HRQOL domain coverage and psychometric evidence to help PROM users select measures and determine whether other measures should be validated and/or developed. Nineteen PROMs and 92 corresponding articles were reviewed to determine which HRQOL domains were assessed. To support a streamlined but rigorous review, we used a rating system based on criteria established in part through existing rubrics (e.g., OMERACT COSMIN). Psychometric properties were rated on a scale from 1 to 18, where 18 was strongest. We examined the intersection between level of domain coverage and extent of psychometric support. Measures most commonly assessed physical health and level of independence, while fewer assessed social relations, environment, and psychological health. No measures assessed spirituality and religion, which may be relevant depending on intended use. PROMs with higher psychometric evidence tended to assess a broader range of HRQOL domains. Rubric scores ranged from 3 to 16, with an average of 9.3. Prominent and psychometrically sound PROMs are available that cover many of the WHOQOL domains. While gaps exist in the domain of spirituality, future work should focus on refining optimal use of existing PROMs relevant for arthritis versus developing new measures. We provide guidance on selecting PROMs, to that end.
© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  Health-related quality of life; Patient-reported outcomes; Psychometrics; Quality of life; Review

Year:  2022        PMID: 36125521     DOI: 10.1007/s00296-022-05200-6

Source DB:  PubMed          Journal:  Rheumatol Int        ISSN: 0172-8172            Impact factor:   3.580


  32 in total

1.  Rheumatology outcomes: the patient's perspective.

Authors:  Alison Carr; Sarah Hewlett; Rod Hughes; Helene Mitchell; Sarah Ryan; Maggie Carr; John Kirwan
Journal:  J Rheumatol       Date:  2003-04       Impact factor: 4.666

Review 2.  Impact of patient-reported outcome measures on routine practice: a structured review.

Authors:  Susan Marshall; Kirstie Haywood; Ray Fitzpatrick
Journal:  J Eval Clin Pract       Date:  2006-10       Impact factor: 2.431

3.  Framework to assess the effects of using patient-reported outcome measures in chronic care management.

Authors:  Maria-Jose Santana; David Feeny
Journal:  Qual Life Res       Date:  2013-12-07       Impact factor: 4.147

4.  Patient perspective: fatigue as a recommended patient centered outcome measure in rheumatoid arthritis.

Authors:  John R Kirwan; Patricia Minnock; Ade Adebajo; Barry Bresnihan; Ernest Choy; Maarten de Wit; Mieke Hazes; Pam Richards; Kenneth Saag; Maria Suarez-Almazor; George Wells; Sarah Hewlett
Journal:  J Rheumatol       Date:  2007-05       Impact factor: 4.666

5.  Rheumatology outcomes: the patient's perspective. A multicentre focus group interview study of Swedish rheumatoid arthritis patients.

Authors:  M Ahlmén; U Nordenskiöld; B Archenholtz; I Thyberg; R Rönnqvist; L Lindén; A-K Andersson; K Mannerkorpi
Journal:  Rheumatology (Oxford)       Date:  2004-09-20       Impact factor: 7.580

6.  The applications of PROs in clinical practice: what are they, do they work, and why?

Authors:  Joanne Greenhalgh
Journal:  Qual Life Res       Date:  2008-12-23       Impact factor: 4.147

7.  Successful Stepwise Development of Patient Research Partnership: 14 Years' Experience of Actions and Consequences in Outcome Measures in Rheumatology (OMERACT).

Authors:  Maarten de Wit; John R Kirwan; Peter Tugwell; Dorcas Beaton; Maarten Boers; Peter Brooks; Sarah Collins; Philip G Conaghan; Maria-Antonietta D'Agostino; Cathie Hofstetter; Rod Hughes; Amye Leong; Ann Lyddiatt; Lyn March; James May; Pamela Montie; Pamela Richards; Lee S Simon; Jasvinder A Singh; Vibeke Strand; Marieke Voshaar; Clifton O Bingham; Laure Gossec
Journal:  Patient       Date:  2017-04       Impact factor: 3.883

Review 8.  Call for action: how to improve use of patient-reported outcomes to guide clinical decision making in rheumatoid arthritis.

Authors:  Bruno Fautrel; Rieke Alten; Bruce Kirkham; Inmaculada de la Torre; Frederick Durand; Jane Barry; Thorsten Holzkaemper; Walid Fakhouri; Peter C Taylor
Journal:  Rheumatol Int       Date:  2018-03-21       Impact factor: 2.631

9.  Stakeholder Development of an Online Program to Track Arthritis-Related Patient-Reported Outcomes Longitudinally: Live Yes! INSIGHTS.

Authors:  Karen E Schifferdecker; Rebecca L Butcher; Erin Knight; Emily Creek; M Suzanne Schrandt; Laura Marrow; Marie Jaffe; Arlene Vinci; Guy Eakin
Journal:  ACR Open Rheumatol       Date:  2020-11-25

10.  Domains of quality of life: results of a three-stage Delphi consensus procedure among patients, family of patients, clinicians, scientists and the general public.

Authors:  Suzanne Pietersma; Marieke de Vries; M Elske van den Akker-van Marle
Journal:  Qual Life Res       Date:  2013-11-17       Impact factor: 4.147

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