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Delphi study to define core clinical outcomes for inclusion in a complex regional pain syndrome international research registry and data bank

Llewellyn, Alison; Buckle, Lisa; Grieve, Sharon; Birklein, Frank; Brunner, Florian; Goebel, Andreas; Harden, R. Norman; Bruehl, Stephen; Vaughan-Spickers, Nicole; Connett, Robyn; McCabe, Candida

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Authors

Profile image of Alison Llewellyn

Alison Llewellyn Alison.Llewellyn@uwe.ac.uk
Associate Professor in Clinical Research

Lisa Buckle

Frank Birklein

Florian Brunner

Andreas Goebel

R. Norman Harden

Stephen Bruehl

Nicole Vaughan-Spickers

Robyn Connett

Candy McCabe Candy.Mccabe@uwe.ac.uk
Professor of Clinical Research and Practice



Abstract

ABSTRACT: Complex regional pain syndrome (CRPS) clinical trials have historically captured a diverse range of outcomes. A minimum set of CRPS patient-reported outcomes has been agreed for inclusion in a future CRPS international clinical research registry and data bank. This study aimed to identify a complementary set of core clinical outcomes. Clinicians and researchers from the international CRPS community informed the content of a 2-round electronic Delphi study. Participation was invited from members of the International Association for the Study of Pain CRPS Special Interest Group and the International Research Consortium for CRPS. In round 1, participants rated the relevance of 59 clinical outcomes in relation to the question "What is the clinical presentation and course of CRPS, and what factors influence it?" (1 = not relevant and 9 = highly relevant). In round 2, participants rerated each outcome in the light of the round 1 median scores. The criterion for consensus was median score ≥7, agreed by 75% of respondents. The core study team considered the feasibility of data collection of each identified outcome in agreeing final selections. Sixty respondents completed both survey rounds, with responses broadly consistent across professions. Nine outcomes met the consensus criterion. Final outcomes recommended for inclusion in the core clinical set were record of medications, presence of posttraumatic stress disorder, extent of allodynia, and skin temperature difference between limbs. Study findings provide robust recommendations for core clinical outcome data fields in the future CPRS international clinical research registry. Alongside patient-reported outcomes, these data will enable a better understanding of CRPS.

Journal Article Type Article
Acceptance Date Jun 27, 2022
Online Publication Date Jul 4, 2022
Publication Date Mar 1, 2023
Deposit Date Jul 8, 2022
Publicly Available Date Jul 5, 2023
Journal Pain
Print ISSN 0304-3959
Electronic ISSN 1872-6623
Publisher Lippincott, Williams & Wilkins
Peer Reviewed Peer Reviewed
Volume 164
Issue 3
Pages 543-554
DOI https://doi.org/10.1097/j.pain.0000000000002729
Keywords Delphi; clinical outcomes; complex regional pain syndrome; international research registry
Public URL https://uwe-repository.worktribe.com/output/9680851
Publisher URL https://journals.lww.com/pain/Abstract/9900/A_Delphi_study_to_define_core_clinical_outcomes.123.aspx

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A Delphi study to define core clinical outcomes for inclusion in a complex regional pain syndrome international research registry and data bank (577 Kb)
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Licence
http://creativecommons.org/licenses/by-nc/4.0/

Publisher Licence URL
http://creativecommons.org/licenses/by-nc/4.0/

Copyright Statement
This is the author’s accepted manuscript of the article 'Llewellyn, A., Buckle, L., Grieve, S., Birklein, F., Brunner, F., Goebel, A., …McCabe, C. (2023). Delphi study to define core clinical outcomes for inclusion in a complex regional pain syndrome international research registry and data bank. PAIN, 164(3), 543-554'.

DOI: https://doi.org/10.1097/j.pain.0000000000002729


The final published version is available here: https://journals.lww.com/pain/Abstract/9900/A_Delphi_study_to_define_core_clinical_outcomes.123.aspx






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