Understanding characteristics, conditions and treatment patterns among males diagnosed with Rett syndrome: an analysis of commercial health insurance claims

Author:

Davis Tigwa1,Parab Purva1,May Damian M12,Ruetsch Charles1

Affiliation:

1. Health Analytics, LLC, Columbia, MD 21045, USA

2. Senior Director, Health Economics & Outcomes Research, Acadia Pharmaceuticals, San Diego, CA 92130, USA

Abstract

Background: Though rarely diagnosed with Rett syndrome, males account for 3–5% of all cases in the USA. Nevertheless, few studies have examined characteristics of males with Rett syndrome and their healthcare service utilization using commercially available healthcare claims data. Objective: Improve understanding of healthcare service utilization and cost associated with the population of males with Rett syndrome. Methods: Data were integrated medical and pharmacy claims. Male individuals with more than two claims with a primary diagnosis of Rett syndrome were stratified into age groups (<5 years; ≥5 and <10 years; and ≥10 years). Patient descriptions, comorbidities, service utilization and cost were measured. Results: Mean age was 20.4 years and most patients had Medicaid. Epilepsy, incontinence, dyspnea and dysphagia were common comorbidities during follow-up. Individuals averaged 6.7 office visits, 4.1 outpatient visits, 2.2 emergency admissions and 4.5 inpatient admissions per year. Occupational therapy was used more than physical and speech therapy. Conclusion: The study improves understanding of males with Rett syndrome within a commercially available dataset.

Funder

ACADIA Pharmaceuticals

Publisher

Future Medicine Ltd

Subject

General Medicine

Reference30 articles.

1. National Institute of Neurological Disorders and Stroke. Rett syndrome (2023). www.ninds.nih.gov/health-information/disorders/rett-syndrome

2. Genetic and Rare Diseases Information Center. Rett syndrome – about the disease (2023). https://rarediseases.info.nih.gov/diseases/5696/rett-syndrome

3. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

4. Towards a better diagnosis and treatment of Rett syndrome: a model synaptic disorder

5. Parental origin of de novo MECP2 mutations in Rett syndrome

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