Demographics and medical burden of osteogenesis imperfecta: a nationwide database analysis
Journal
Osteoporosis International
Journal Volume
35
Journal Issue
7
Start Page
1185-1193
ISSN
0937-941X
1433-2965
Date Issued
2024-04-02
Author(s)
Shih, Chien-An
Li, Chia-Chun
Chang, Yin-Fan
Hwang, Jawl-Shan
Tsai, Meng-Che
Chou, Yen-Yin
Lin, Chii-Jeng
Huang, Ming-Tung
Tai, Ta-Wei
Wu, Chih-Hsing
Abstract
The epidemiological data on osteogenesis imperfecta (OI) in Asia is limited. This study, representing the first comprehensive epidemiological investigation on OI in Taiwan, reveals high medical resource utilization and underscores the importance of early diagnosis to enhance care quality.
Introduction: This study examines osteogenesis imperfecta, a hereditary connective tissue disorder causing pediatric fractures and limb deformities, using a nationwide database from Taiwan to analyze clinical features and medical burden.
Methods: The study identified validated OI patients from the Catastrophic Illness Registry in the National Health Insurance Research Database from 2008 to 2019. Demographic data and medical resource utilization were analyzed. A multivariate Cox model assessed the influence of sex, validation age, and comorbidities.
Results: 319 OI patients (M/F = 153/166) were identified, with 58% validated before age 20. Prevalence and incidence were 0.8-1.3/100,000 and 0.02-0.09/100,000, respectively, with higher rates in the pediatric demographic. In the study period, 69.6% of the patients had admission history, primarily to pediatric and orthopedic wards. The median admission number was 3, with a median length of stay of 12 days and a median inpatient cost of approximately 3,163 USD during the period. Lower limb fractures were the main reason for hospitalization. 57% of OI patients received bisphosphonate treatment. The leading causes of mortality were OI-related deaths, neurovascular disease, and cardiovascular disease. The median age of validation in the non-survival group was significantly higher compared to the survival group (33 vs. 14 years), and patients validated during childhood required more inpatient fracture surgeries than those validated during adulthood.
Conclusion: This study provides comprehensive real-world evidence on the clinical characteristics and high medical resource utilization of OI patients in a low prevalence region like Taiwan. Early diagnosis is crucial for improving care quality and enhancing health outcomes.
Subjects
Epidemiology
Fracture
Mortality
Osteogenesis imperfecta
Real-world evidence
Publisher
Springer Science and Business Media LLC
Type
journal article