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Demographics and medical burden of osteogenesis imperfecta: a nationwide database analysis.
- Source :
-
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA [Osteoporos Int] 2024 Jul; Vol. 35 (7), pp. 1185-1193. Date of Electronic Publication: 2024 Apr 02. - Publication Year :
- 2024
-
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.<br />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.<br />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.<br />Results: 319 OI patients (M/Fâ=â153/166) 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.<br />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.<br /> (© 2024. International Osteoporosis Foundation and Bone Health and Osteoporosis Foundation.)
- Subjects :
- Humans
Male
Female
Child
Adolescent
Child, Preschool
Taiwan epidemiology
Young Adult
Infant
Adult
Prevalence
Incidence
Cost of Illness
Middle Aged
Hospitalization statistics & numerical data
Comorbidity
Age Distribution
Registries
Infant, Newborn
Sex Distribution
Length of Stay statistics & numerical data
Osteogenesis Imperfecta epidemiology
Osteogenesis Imperfecta complications
Databases, Factual
Subjects
Details
- Language :
- English
- ISSN :
- 1433-2965
- Volume :
- 35
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA
- Publication Type :
- Academic Journal
- Accession number :
- 38563961
- Full Text :
- https://doi.org/10.1007/s00198-024-07051-2