An observational study of pediatric healthcare burden in Angelman syndrome: Results from a real-world study

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Abstract

Background: The objective of this study is to describe variations in the healthcare resource utilization (HRU) among individuals with Angelman syndrome (AS) over the first 12 years of life. Data for this study were drawn from the AS Natural History study (ASNHS), which is an observational study on the developmental progress, behavior, and medical morbidity of individuals with AS conducted over eight years. Caregiver-reported information on hospitalization, surgery, and medication utilization was used to assess HRU. Repeated measures mixed effect models were used to assess the relationship between age and probability of hospitalization, surgery, and prescription medication utilization. Results: Mean age at study enrollment was 6 years of age and both sexes were equally represented. The mean number of visits per participant was three. Results from this study suggest that individuals with AS have a high HRU burden. Hospitalization and surgery burden were highest in the first year of life. Use of medications for seizures and sleep disturbance increased over time. Conclusions: The study highlights the significant healthcare burden among individuals with AS. Future studies that estimate cost and caregiver burden associated with AS are needed to assess the lifelong economic impact of AS on families and healthcare system.

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Khan, N., Cabo, R., Tan, W. H., Tayag, R., & Bird, L. M. (2019). An observational study of pediatric healthcare burden in Angelman syndrome: Results from a real-world study. Orphanet Journal of Rare Diseases, 14(1). https://doi.org/10.1186/s13023-019-1210-6

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