| Literature DB >> 34463169 |
Mousumi Bose1, Jean-Baptiste Roullet2, K Michael Gibson2, William B Rizzo3, Hana M Mansur1, Alice McConnell4, Carolyn A Hoffman5, Melissa L DiBacco6, Phillip L Pearl6.
Abstract
Succinic semialdehyde dehydrogenase deficiency (SSADHD), a rare disorder of GABA metabolism, presents with significant neurodevelopmental morbidity. Although there is a growing interest in the concept of quality of life through patient reports as a meaningful outcome in rare disease clinical trials, little is known about the overall impact of SSADHD from the patient/family perspective. The purpose of this study was to determine issues related to quality of life and patient/family experience through a focus group discussion with family caregivers of patients with SSADHD. The discussion included the input of 5 family caregivers, and highlighted concerns related to physical function, cognitive and intellectual function, psychological and behavioral function, social function, and family impact. These themes represent appropriate starting points in the development of a quality-of-life survey that may serve as a meaningful clinical tool in future studies of SSADHD.Entities:
Keywords: behavior; inborn errors of metabolism; intellectual disability; outcome; quality of life
Mesh:
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Year: 2021 PMID: 34463169 PMCID: PMC8664972 DOI: 10.1177/08830738211028388
Source DB: PubMed Journal: J Child Neurol ISSN: 0883-0738 Impact factor: 1.987