The validity, responsiveness, and score interpretation of the PROMISnq Physical Function - Multiple Sclerosis 15a short form in multiple sclerosis.


Journal

Multiple sclerosis and related disorders
ISSN: 2211-0356
Titre abrégé: Mult Scler Relat Disord
Pays: Netherlands
ID NLM: 101580247

Informations de publication

Date de publication:
Jun 2022
Historique:
received: 15 11 2021
revised: 16 02 2022
accepted: 18 03 2022
pubmed: 23 5 2022
medline: 15 6 2022
entrez: 22 5 2022
Statut: ppublish

Résumé

A valid, sensitive patient-reported outcome (PRO) measure of physical function (PF) for people with multiple sclerosis (MS) would have substantial value in routine care and clinical research. We now describe development of the PROMISnq Short Form v2.0 PF - Multiple Sclerosis 15a [PROMISnq PF(MS)15a] for assessing PF in relapsing and progressive MS. Also, the validity, reliability, and responsiveness of the PROMISnq PF(MS)15a is evaluated, minimal important difference (MID) thresholds for score change estimated and a score interpretation guide developed. A mixed-methods sequential design was employed. Relevant PF concepts were elicited through semi-structured interviews with people with relapsing MS, and then mapped to the PROMIS PF item bank. Measurement experts integrated results from interviews with people with MS and input from a panel of neurologists to generate a draft short form. Relevance and comprehensiveness of the draft short form were assessed in cognitive debriefing interviews with people with relapsing or progressive MS. Subsequently, item reduction and evaluation of psychometric properties were performed in two observational studies: a cross-sectional study in the US (n = 296), and a 96-week longitudinal study in the UK MS Register cohort (n = 558). The main outcomes and measures are estimates of: known-groups validity, convergent validity, reliability, responsiveness; MID for worsening. Factor analyses supported the unidimensionality of the newly derived 15-item short form. Cronbach's alpha (≥ 0.97) and intraclass correlation coefficient (≥ 0.97) of test-retest scores (5-27 days) indicated strong reliability. Convergent validity was demonstrated by moderate-to-strong correlations with scores on related PRO measures. Scores discriminated among patient groups classified by levels of physical health and other criteria. Score changes of 2.3-2.7 points are proposed as MID criteria for minimal worsening in PF. PROMISnq PF(MS)15a demonstrated reliability, validity and sensitivity to change. Input from patients and clinicians ensured the content is comprehensive and relevant for people with MS.

Sections du résumé

BACKGROUND BACKGROUND
A valid, sensitive patient-reported outcome (PRO) measure of physical function (PF) for people with multiple sclerosis (MS) would have substantial value in routine care and clinical research. We now describe development of the PROMISnq Short Form v2.0 PF - Multiple Sclerosis 15a [PROMISnq PF(MS)15a] for assessing PF in relapsing and progressive MS. Also, the validity, reliability, and responsiveness of the PROMISnq PF(MS)15a is evaluated, minimal important difference (MID) thresholds for score change estimated and a score interpretation guide developed.
METHODS METHODS
A mixed-methods sequential design was employed. Relevant PF concepts were elicited through semi-structured interviews with people with relapsing MS, and then mapped to the PROMIS PF item bank. Measurement experts integrated results from interviews with people with MS and input from a panel of neurologists to generate a draft short form. Relevance and comprehensiveness of the draft short form were assessed in cognitive debriefing interviews with people with relapsing or progressive MS. Subsequently, item reduction and evaluation of psychometric properties were performed in two observational studies: a cross-sectional study in the US (n = 296), and a 96-week longitudinal study in the UK MS Register cohort (n = 558). The main outcomes and measures are estimates of: known-groups validity, convergent validity, reliability, responsiveness; MID for worsening.
RESULTS RESULTS
Factor analyses supported the unidimensionality of the newly derived 15-item short form. Cronbach's alpha (≥ 0.97) and intraclass correlation coefficient (≥ 0.97) of test-retest scores (5-27 days) indicated strong reliability. Convergent validity was demonstrated by moderate-to-strong correlations with scores on related PRO measures. Scores discriminated among patient groups classified by levels of physical health and other criteria. Score changes of 2.3-2.7 points are proposed as MID criteria for minimal worsening in PF.
CONCLUSION CONCLUSIONS
PROMISnq PF(MS)15a demonstrated reliability, validity and sensitivity to change. Input from patients and clinicians ensured the content is comprehensive and relevant for people with MS.

Identifiants

pubmed: 35598408
pii: S2211-0348(22)00268-1
doi: 10.1016/j.msard.2022.103753
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

103753

Informations de copyright

Copyright © 2022. Published by Elsevier B.V.

Auteurs

Paul Kamudoni (P)

Global Evidence and Value Development - R&D, Merck Healthcare KGaA, Darmstadt, Germany. Electronic address: paul.kamudoni@merckgroup.com.

Dagmar Amtmann (D)

Department of Rehabilitation Medicine, University of Washington, Seattle, WA, USA.

Jeffrey Johns (J)

Institute of Medicines Development, Cardiff, United Kingdom.

Karon F Cook (KF)

Feral Scholars, Broaddus, Texas, USA.

Rana Salem (R)

Department of Rehabilitation Medicine, University of Washington, Seattle, WA, USA.

Sam Salek (S)

School of Life and Medical Sciences, University of Hertfordshire, Hatfield, United Kingdom.

Jana Raab (J)

Global Evidence and Value Development - R&D, Merck Healthcare KGaA, Darmstadt, Germany.

Rod Middleton (R)

UK MS Register, Swansea University Medical School, Swansea, United Kingdom.

Pavle Repovic (P)

Swedish Medical Center, Seattle, WA, USA.

Kevin N Alschuler (KN)

Department of Rehabilitation Medicine, University of Washington, Seattle, WA, USA; Department of Neurology, University of Washington, Seattle, WA, USA.

Gloria von Geldern (G)

Department of Neurology, University of Washington, Seattle, WA, USA.

Annette Wundes (A)

Department of Rehabilitation Medicine, University of Washington, Seattle, WA, USA; Department of Neurology, University of Washington, Seattle, WA, USA.

Amy Barrett (A)

Patient-Centered Outcomes Assessment, RTI Health Solutions, Research Triangle Park, NC, USA.

Oyebimpe Olayinka-Amao (O)

Patient-Centered Outcomes Assessment, RTI Health Solutions, Research Triangle Park, NC, USA.

Christian Henke (C)

Global Evidence and Value Development - R&D, Merck Healthcare KGaA, Darmstadt, Germany.

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Classifications MeSH