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Meta-Analysis
. 2019 Aug;7(8):e5.
doi: 10.2106/JBJS.RVW.18.00150.

A Comparison of Treatment Effects for Nonsurgical Therapies and the Minimum Clinically Important Difference in Knee Osteoarthritis: A Systematic Review

Affiliations
Meta-Analysis

A Comparison of Treatment Effects for Nonsurgical Therapies and the Minimum Clinically Important Difference in Knee Osteoarthritis: A Systematic Review

Andrew Concoff et al. JBJS Rev. 2019 Aug.

Abstract

Background: The minimum clinically important difference (MCID) was developed to ascertain the smallest change in an outcome that patients perceive as beneficial. The objectives of the present review were (1) to compare the MCIDs for pain assessments used among guidelines and meta-analyses investigating different nonsurgical therapies for knee osteoarthritis and (2) to compare the effect estimates of different nonsurgical interventions against a single commonly-utilized MCID threshold.

Methods: Systematic and manual searches were conducted to identify guidelines and meta-analyses evaluating pain outcomes for nonsurgical knee osteoarthritis interventions. Individual treatment effects for pain were presented on a common scale (the standardized mean difference [SMD]). To evaluate the perception of the relative benefit of each nonsurgical treatment, the variation in MCIDs selected from the published MCID literature was assessed.

Results: Thirty-seven guidelines and meta-analyses were included. MCIDs were often presented as an SMD or a mean difference (MD) on a validated scale and varied in magnitude across sources. This analysis demonstrated that intra-articular hyaluronic acid, intra-articular corticosteroids, and acetaminophen all had relatively larger effect sizes than topical nonsteroidal anti-inflammatory drugs (NSAIDs). Higher-molecular-weight intra-articular hyaluronic acid had a greater relative effect compared with both non-selective and cyclooxygenase-2-selective oral NSAIDs. Evaluating the treatment effect estimates against a commonly utilized MCID revealed similarities in which observations attained clinical significance among treatments; however, this observation varied across the range of reported MCIDs.

Conclusions: The present review confirmed the variability in the MCIDs for pain assessments that are used across guidelines and meta-analyses evaluating nonsurgical interventions for knee osteoarthritis. This variability may yield conflicting treatment recommendations, ranging from rejecting treatments that are indeed efficacious to accepting treatments that may not be beneficial. Additional research is required to determine why some nonsurgical therapies are more consistently recommended in knee osteoarthritis guidelines than others as these findings suggest similarities in their effect estimates for pain. Relevant stakeholders need to reach a consensus on a standard approach to determining the MCIDs for these therapies to ensure that appropriate and effective treatment options are available to patients prior to invasive surgical intervention.

Level of evidence: Therapeutic Level IV. See Instructions for Authors for a complete description of levels of evidence.

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Figures

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Flow diagram of search results.
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Fig. 5
Fig. 5
Comparison of treatment effect estimates for topical and oral NSAIDs, acetaminophen, and intra-articular corticosteroids and hyaluronic acid from recent meta-analyses,,. The blue line indicates the AAOS MCID for WOMAC pain (0.39), and the red line indicates the range of other reported MCIDs (0.20 to 0.50). IA = intra-articular, MW = molecular weight, NSAID = nonsteroidal anti-inflammatory drug, SMD = standardized mean difference.
Fig. 6
Fig. 6
Ratios of the point estimates for topical NSAIDs (top panel), COX-2-selective NSAIDs (middle panel), and non-selective NSAIDs (bottom panel) relative to other nonsurgical therapies. Values of <1.0 indicate that the effect estimate for the respective NSAID was larger than the comparison treatment. *Ratio = 1.0. HA = hyaluronic acid, IA = intra-articular, MW = molecular weight, NSAID = nonsteroidal anti-inflammatory drug.

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