Real-DMD: Caregiver Baseline Characteristics From an Electronic Survey of Long-Term Real-World Experiences of Patients With Duchenne Muscular Dystrophy (DMD)

Author(s)

Filipovic Audhya I1, Patel S1, Yang M2, Tuttle E3, Martins B2, Yang F4, Lan JJ2, Gooch KL1
1Sarepta Therapeutics, Inc., Cambridge, MA, USA, 2Analysis Group, Inc., Boston, MA, USA, 3Analysis Group, Inc., Menlo Park, CA, USA, 4Analysis Group, Inc., London, UK

OBJECTIVES: DMD is a rare, progressive neuromuscular disorder primarily affecting young males, leading to muscle weakness and functional decline. Caring for patients with DMD can impact caregivers’ physical and psychological well-being and ability to work. REAL-DMD is a real-world, observational, prospective, longitudinal cohort study surveying caregivers of DMD patients on caregiving experience and patient function. Caregiver characteristics and experiences at baseline are reported.

METHODS: Adult caregivers of ambulatory DMD patients recruited from US patient advocacy groups (Parent Project Muscular Dystrophy; The Akari Foundation) completed a web-based survey reporting their socio-demographics, employment status, ability to work, and daily hours spent caregiving. Patient-Reported Outcome Measurement Information (PROMIS®) Global Health was also collected.

RESULTS: In total, 123 caregivers in REAL-DMD completed the baseline survey (mean±SD age: 40.6±7.3 years). Most participants were female (91.9%) and White (86.2%) and cared for 1 child with DMD (1 child: 82.1%; 2+ children: 17.9%). Mean age of care recipient was 9.6±4.7 years. 57.7% of caregivers reported having anxiety or depression, with 35.8% undergoing treatment. Most caregivers were employed full- (43.1%) or part-time (20.3%). 65.0% reported experiencing impact on their ability to work due to caregiving responsibilities, including lower productivity (22.8%), switching jobs (20.3%), or reducing hours (19.5%). 28.5% temporarily stopped working, went on leave, or permanently left the workforce. Caregivers reported spending a mean±SD of 8.8±7.0 hours daily caring for the patient. Physical health of caregivers (PROMIS T-score: 49.1±7.9) was comparable to the US general population (50±10), while mental health was one-half SD lower (44.7±8.3).

CONCLUSIONS: REAL-DMD baseline caregiver findings provide insights into the characteristics of caregivers of ambulatory DMD patients in a real-world setting. Findings indicate impact on mental health and ability to work, along with substantial time commitments. Longitudinal data from REAL-DMD will characterize changes in caregiver impact over time as the care recipients’ disease progresses.

Conference/Value in Health Info

2024-11, ISPOR Europe 2024, Barcelona, Spain

Value in Health, Volume 27, Issue 12, S2 (December 2024)

Code

PCR284

Topic

Patient-Centered Research

Topic Subcategory

Patient-reported Outcomes & Quality of Life Outcomes

Disease

Musculoskeletal Disorders (Arthritis, Bone Disorders, Osteoporosis, Other Musculoskeletal), Rare & Orphan Diseases

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