Litcius/Paper detail

The Spinal Muscular Atrophy Health Index: A novel outcome for measuring how a patient feels and functions

Christine Zizzi, Elizabeth Luebbe, Phillip Mongiovi, Michael Hunter, Nuran Dilek, Connie Garland, Emma Ciafaloni, Craig M. Zaidman, John T. Kissel, Michael McDermott, Nicholas E. Johnson, Valeria Sansone, Chad Heatwole

2021Muscle & Nerve38 citationsDOI

Abstract

INTRODUCTION: The Spinal Muscular Atrophy Health Index (SMA-HI) is a multifaceted, disease-specific, patient-reported outcome to measure an SMA patient's perception of their disease burden. In preparation for upcoming therapeutic trials, we examine the validity, reliability, and usability of the SMA-HI in adults, teenagers, and children with SMA. METHODS: Using data from a cross-sectional study of 359 international adult patients with SMA, we identified the most relevant symptoms to include in the SMA-HI. We utilized factor analysis, patient interviews with adults and minors (age 8-15 years), known-group validity testing, and test-retest reliability assessments to evaluate and refine the SMA-HI. RESULTS: The SMA-HI measures overall disease burden and 15 areas of SMA health. Fifteen adult patients and five patients, age 8 to 15 years, participated in semistructured qualitative interviews and found the SMA-HI to be comprehensive, easily completed, and to have clear meaning. The final SMA-HI and its subscales demonstrated good internal consistency (Cronbach α = 0.77-0.96), high test-retest reliability (intraclass correlation coefficient = 0.60-0.96), and an ability to differentiate between SMA groups with different disease severities affecting areas such as employment and ambulation (P < .0001 for both). DISCUSSION: This research provides evidence that the SMA-HI is a valid, relevant, and reliable outcome measure to assess multifaceted patient-reported disease burden in older children, teenagers, and adults with SMA. The SMA-HI provides an opportunity for researchers and clinicians to measure a SMA patient's perception of their health and determine relevant changes in response to therapeutic intervention or disease progression.

Topics & Concepts

SMA*Cronbach's alphaSpinal muscular atrophyIntraclass correlationMedicinePhysical therapyPatient-reported outcomePhysical medicine and rehabilitationDiseasePsychologyGerontologyQuality of life (healthcare)Clinical psychologyPsychometricsInternal medicineMathematicsNursingCombinatoricsNeurogenetic and Muscular Disorders ResearchMuscle Physiology and DisordersAmyotrophic Lateral Sclerosis Research