Systematic Review of Motor Function Scales and Patient-Reported Outcomes in Spinal Muscular Atrophy

6 June 2022, 9:56 EDT

Summary

Fifteen motor function scales and patient-reported outcomes were identified to be commonly used (≥5 studies), of which 11 had available validation assessments. Each instrument has its strengths and limitations. It is imperative that the patient population (e.g., age, mobility), goals of treatment, and outcomes or endpoints of interest be considered when selecting the appropriate motor function scales and patient-reported outcomes for clinical studies.


Original Article

Systematic Review of Motor Function Scales and Patient-Reported Outcomes in Spinal Muscular Atrophy

American Journal of Physical Medicine & Rehabilitation

Wu, Jennifer W. PhD; Pepler, Laura PhD; Maturi, Bridget MSc; Afonso, Alexandria C. F. PhD; Sarmiento, Janice PhD; Haldenby, Renee MSc


Abstract

Spinal muscular atrophy is a heterogeneous disease that results in loss of motor function. In an evolving treatment landscape, establishing the suitability and limitations of existing motor function scales and patient-reported outcomes used to monitor patients with this disease is important. A systematic review was conducted to examine utility of motor function scales and patient-reported outcomes in evaluating patients with spinal muscular atrophy. Published literature was reviewed up to June 2021 with no start date restriction. Of the reports screened, 122 were deemed appropriate for inclusion and are discussed in this review (including 24 validation studies for motor function scales or patient-reported outcomes). Fifteen motor function scales and patient-reported outcomes were identified to be commonly used (≥5 studies), of which 11 had available validation assessments. Each instrument has its strengths and limitations. It is imperative that the patient population (e.g., age, mobility), goals of treatment, and outcomes or endpoints of interest be considered when selecting the appropriate motor function scales and patient-reported outcomes for clinical studies.


ACKNOWLEDGMENTS

The authors thank Synapse Medical Communications, Inc., Oakville, Ontario, Canada, for providing Medical writing assistance.

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