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      Deconstructing the Minimum Clinically Important Difference (MCID)

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          Abstract

          Purpose

          The minimal clinically important difference (MCID) is a way of dichotomizing data for assessment of success or failure based on clinically meaningful changes. The magnitude of the MCID is often misunderstood to be a singular quantity applicable across studies. However, substantial differences have been reported among MCIDs for the same outcome measures usually based upon differences extrinsic to the calculation. This study explores the effects of variabilities intrinsic to the calculation of the MCID.

          Methods

          The MCIDs for two knee replacement patient-reported outcomes measures of pain and function were calculated at 1 year postoperative with an integrative anchor and distribution-based method using external anchor questions and receiver operator characteristic (ROC) curves. The effects upon the magnitude and precision of the MCIDs of varying the anchor questions, the thresholds for success/failure, and the sample sizes were examined.

          Results

          Wide variabilities were observed in both the magnitudes and precision of the MCIDs. The threshold for success had the largest effect on magnitude of pain scores, while the sample size had the largest effect on precision. For function scores, the sample size had the largest effect on magnitude, and the anchor question had the largest effect on precision.

          Conclusion

          Comparisons among MCIDs are difficult to interpret if elements of the calculations are different and influence the results. While factors extrinsic to the calculations, e.g., study population, trial design, methods of calculation, etc., are known to produce differences in the magnitude of MCIDs, this study shows that more subtle and less obvious factors intrinsic to the calculations have profound effects on both the magnitude and precision of MCIDs. Comparisons among MCIDs should be made with caution and call for greater transparency in reporting intrinsic methods. It is probably advisable for individual studies to calculate their own MCIDs and not rely on published values.

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          Most cited references22

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          Index for rating diagnostic tests

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            Measurement of health status. Ascertaining the minimal clinically important difference.

            In recent years quality of life instruments have been featured as primary outcomes in many randomized trials. One of the challenges facing the investigator using such measures is determining the significance of any differences observed, and communicating that significance to clinicians who will be applying the trial results. We have developed an approach to elucidating the significance of changes in score in quality of life instruments by comparing them to global ratings of change. Using this approach we have established a plausible range within which the minimal clinically important difference (MCID) falls. In three studies in which instruments measuring dyspnea, fatigue, and emotional function in patients with chronic heart and lung disease were applied the MCID was represented by mean change in score of approximately 0.5 per item, when responses were presented on a seven point Likert scale. Furthermore, we have established ranges for changes in questionnaire scores that correspond to moderate and large changes in the domains of interest. This information will be useful in interpreting questionnaire scores, both in individuals and in groups of patients participating in controlled trials, and in the planning of new trials.
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              Clinical importance of changes in chronic pain intensity measured on an 11-point numerical pain rating scale.

              Pain intensity is frequently measured on an 11-point pain intensity numerical rating scale (PI-NRS), where 0=no pain and 10=worst possible pain. However, it is difficult to interpret the clinical importance of changes from baseline on this scale (such as a 1- or 2-point change). To date, there are no data driven estimates for clinically important differences in pain intensity scales used for chronic pain studies. We have estimated a clinically important difference on this scale by relating it to global assessments of change in multiple studies of chronic pain. Data on 2724 subjects from 10 recently completed placebo-controlled clinical trials of pregabalin in diabetic neuropathy, postherpetic neuralgia, chronic low back pain, fibromyalgia, and osteoarthritis were used. The studies had similar designs and measurement instruments, including the PI-NRS, collected in a daily diary, and the standard seven-point patient global impression of change (PGIC), collected at the endpoint. The changes in the PI-NRS from baseline to the endpoint were compared to the PGIC for each subject. Categories of "much improved" and "very much improved" were used as determinants of a clinically important difference and the relationship to the PI-NRS was explored using graphs, box plots, and sensitivity/specificity analyses. A consistent relationship between the change in PI-NRS and the PGIC was demonstrated regardless of study, disease type, age, sex, study result, or treatment group. On average, a reduction of approximately two points or a reduction of approximately 30% in the PI-NRS represented a clinically important difference. The relationship between percent change and the PGIC was also consistent regardless of baseline pain, while higher baseline scores required larger raw changes to represent a clinically important difference. The application of these results to future studies may provide a standard definition of clinically important improvement in clinical trials of chronic pain therapies. Use of a standard outcome across chronic pain studies would greatly enhance the comparability, validity, and clinical applicability of these studies.
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                Author and article information

                Journal
                Orthop Res Rev
                Orthop Res Rev
                orr
                Orthopedic Research and Reviews
                Dove
                1179-1462
                17 February 2022
                2022
                : 14
                : 35-42
                Affiliations
                [1 ]Lifespan Biostatistics Core, Rhode Island Hospital , Providence, RI, USA
                [2 ]Department of Orthopedic Surgery, Warren Alpert Medical School of Brown University , Providence, RI, USA
                Author notes
                Correspondence: Roy Aaron, Email Roy_Aaron@Brown.edu
                Author information
                http://orcid.org/0000-0002-0745-2267
                Article
                349268
                10.2147/ORR.S349268
                8860454
                35210873
                a907b1d2-3355-4d97-9a8c-91fc43e8dabf
                © 2022 Molino et al.

                This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License ( http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms ( https://www.dovepress.com/terms.php).

                History
                : 13 November 2021
                : 27 January 2022
                Page count
                Figures: 2, Tables: 4, References: 22, Pages: 8
                Funding
                Funded by: the Miriam Hospital to Roy Aaron;
                This work is supported by a grant from The Miriam Hospital to Roy Aaron.
                Categories
                Original Research

                outcome assessment,categorical measure,clinical improvement

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