1. Analysis of nationwide hemophilia care: A cohort study using two Japanese healthcare claims databases
- Author
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Ei Kinai, Midori Ono, Akinori Oh, Mihoko Ota, Yasuo Myaguchi, and Hitoshi Ueda
- Subjects
cohort study ,disease management ,factor VIII ,hemophilia A ,Medicine - Abstract
Abstract Background and aims In many developed countries, hemophilia care is provided by specialized centers which can offer standardized high‐quality care for patients and collect data for patient registries. However, in countries with less centralized provision of hemophilia care, registry data lacks accuracy and medical care is inconsistent among providers. Claims databases can be an alternative for obtaining nationwide data on hemophilia care, and we applied this approach to evaluate inequalities in hemophilia care in Japan. Methods Medical records of hemophilia A patients were collected by a combination of ICD‐10 code (D66) and prescribed coagulation factors from two major Japanese claims databases (JMDC and Medical Data Vision [MDV]). Patient records with an anti‐inhibitor coagulant complex were excluded. Based on the annual number of hemophilia A patients, medical facilities were categorized into specialized facilities (SP, ≥5 patients) and nonspecialized facilities (N‐SP,
- Published
- 2022
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