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Demographics and medical burden of osteogenesis imperfecta: a nationwide database analysis.
Shih, Chien-An; Li, Chia-Chun; Chang, Yin-Fan; Hwang, Jawl-Shan; Tsai, Meng-Che; Chou, Yen-Yin; Lin, Chii-Jeng; Huang, Ming-Tung; Hong, Chih-Kai; Tai, Ta-Wei; Wu, Chih-Hsing.
Afiliação
  • Shih CA; Department of Orthopedics, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
  • Li CC; Medical Device R & D Core Laboratory, National Cheng Kung University Hospital, Tainan, Taiwan.
  • Chang YF; Department of Orthopedics, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
  • Hwang JS; Institute of Allied Health Sciences, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
  • Tsai MC; Department of Family Medicine, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
  • Chou YY; Department of Family Medicine, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
  • Lin CJ; Institute of Gerontology, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
  • Huang MT; Department of Family Medicine, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
  • Hong CK; Division of Endocrinology and Metabolism, Department of Internal Medicine, Chang Gung Memorial Hospital, Chang Gung University, Taoyuan, Taiwan.
  • Tai TW; Department of Pediatrics, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
  • Wu CH; Department of Pediatrics, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Osteoporos Int ; 35(7): 1185-1193, 2024 Jul.
Article em En | MEDLINE | ID: mdl-38563961
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteogênese Imperfeita / Bases de Dados Factuais Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged / Newborn País/Região como assunto: Asia Idioma: En Revista: Osteoporos Int Assunto da revista: METABOLISMO / ORTOPEDIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Taiwan

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteogênese Imperfeita / Bases de Dados Factuais Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged / Newborn País/Região como assunto: Asia Idioma: En Revista: Osteoporos Int Assunto da revista: METABOLISMO / ORTOPEDIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Taiwan