Use of the Assessment of Caregiver Experience with Neuromuscular Disease (ACEND) in Spinal Muscular Atrophy

Author:

Brown Laurey12ORCID,Hoffman Katie12,Corbo-Galli Chiara3,Dong Siyuan4ORCID,Zumpf Katelyn4,Weigel Christa1,Blomgren Colleen1,Munson Hannah2,Bidwell Jessa2,Rao Vamshi25,Kuntz Nancy L.25ORCID,Schwaede Abigail2,Krosschell Kristin J.56ORCID

Affiliation:

1. Department of Rehabilitation Services, Ann & Robert H. Lurie Children’s Hospital of Chicago, Chicago, IL 60611, USA

2. Division of Neurology, Ann & Robert H. Lurie Children’s Hospital of Chicago, Chicago, IL 60611, USA

3. Weinberg College of Arts and Sciences, Northwestern University, Evanston, IL 60208, USA

4. Department of Preventive Medicine, Division of Biostatistics, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA

5. Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA

6. Department of Physical Therapy and Human Movement Sciences, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA

Abstract

Background: Spinal muscular atrophy (SMA) has a remarkable impact on function and participation. Subsequently, the caregivers of individuals with SMA are impacted as well. Providers and the SMA community should be aware of the presence of and likely expectations for the existence of caregiver burden. Methods: The Assessment of Caregiver Experience with Neuromuscular Disease (ACEND) quantifies caregivers’ perceptions of function and quality of life pertaining to time, finance and emotion. Analyses were conducted among SMA types and ambulatory and ventilatory status. Participants with SMA had varying ranges of function and were on pharmaceutical treatment. Total ACEND score, longitudinal change in total ACEND score, total quality of life (QOL) score, change in total QOL score and subdomains for QOL, including time, emotion and finance, were all explored. Results: Overall, the ACEND demonstrated discriminant validity and some observed trends. Total ACEND scores improved for caregivers of those with SMA 2, remained stable longitudinally for caregivers of those with SMA 1 and 3 and were not influenced by ventilation status. The caregivers of individuals with SMA 1 had the lowest total quality of life (QOL) score, as did the caregivers of non-ambulatory individuals and those requiring assisted ventilation. Longitudinally, there were no changes in total QOL between caregivers of individuals with different SMA types or ambulatory or ventilation status. There were some differences in emotional needs, but no differences in financial impact between the caregivers of individuals with different types of SMA or ambulatory and ventilatory status. Conclusions: With this information enlightening the presence of caregiver burden and expected changes in burden with pharmaceutical treatment, providers, third party payors and the SMA community at large can better assist, equip and empower those providing the necessary assistance to enable the lives of those with SMA.

Funder

National Institutes of Health’s National Center for Advancing Translational Sciences

Publisher

MDPI AG

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