Predictors of Placebo Response to Local (Intra‐Articular) Therapy In Osteoarthritis: An Individual Participant Data Meta‐Analysis

Author:

Yu Shirley P.1ORCID,van Middelkoop Marienke2,Deveza Leticia A.1ORCID,Ferreira Manuela L.3,Bierma‐Zeinstra Sita2,Zhang Weiya4,Atchia Ismaël5,Birrell Fraser6,Bhagavath Venkatsha7,Hunter David J.1ORCID

Affiliation:

1. Sydney Musculoskeletal Health, The Kolling Institute, School of Medicine, Faculty of Medicine and Health, University of Sydney, Sydney, and Royal North Shore Hospital St. Leonards New South Wales Australia

2. Erasmus MC, University Medical Centre Rotterdam Rotterdam The Netherlands

3. Sydney Musculoskeletal Health, The Kolling Institute, School of Health Sciences, Faculty of Medicine and Health University of Sydney Sydney New South Wales Australia

4. Academic Rheumatology, Injury, Inflammation and Recovery Sciences, University of Nottingham and City Hospital and Pain Centre Versus Arthritis University of Nottingham Nottingham UK

5. Northumbria Healthcare NHS Foundation Trust Newcastle upon Tyne UK

6. Northumbria Healthcare NHS Foundation Trust and Medical Research Council‐Versus Arthritis Centre for Integrated Research into Musculoskeletal Ageing Newcastle University Newcastle upon Tyne UK

7. Sydney Musculoskeletal Health, The Kolling Institute, School of Medicine, Faculty of Medicine and Health, University of Sydney, Sydney, and Northern Sydney Local Health District, Royal North Shore Hospital St. Leonards New South Wales Australia

Abstract

ObjectiveWe undertook this study to evaluate potential predictors of placebo response with intra‐articular (IA) injections for knee/hip osteoarthritis (OA) using individual participant data (IPD) from existing trials.MethodsRandomized placebo‐controlled trials evaluating IA glucocorticoid or hyaluronic acid published to September 2018 were selected. IPD for disease characteristics and outcome measures were acquired. Potential predictors of placebo response included participant characteristics, pain severity, intervention, and trial design. Placebo response was defined as at least a 20% reduction in baseline pain. Logistic regression models and odds ratios were computed as effect measures to evaluate patient and pain mechanisms and then pooled using a random effects model. Generalized mixed‐effect models were applied to intervention and trial characteristics.ResultsOf 56 eligible trials, 6 shared data, and these were combined with the existing 4 OA Trial Bank studies, yielding 10 studies with IPD of 621 placebo participants for analysis. In the total placebo population, at short‐term follow‐up, the use of local anesthetic and ultrasound guidance were associated with reduced odds of placebo response. At midterm follow‐up, mid‐ to long‐term trial duration was associated with increased odds of placebo response, and worse baseline function scores were associated with reduced odds of a placebo response.ConclusionThe administration of local anesthetics or ultrasound guidance may reduce IA placebo response at short‐term follow‐up. At midterm follow‐up, participants with worse baseline function scores may be less likely to respond to IA placebo, and mid‐ to long‐term trial duration may enhance the placebo response. Further studies are required to corroborate these potential predictors of IA placebo response.

Funder

Dutch Arthritis Association

European Commission

Foundation for Research in Rheumatology

National Health and Medical Research Council

Versus Arthritis

ZonMw

Publisher

Wiley

Subject

Rheumatology

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