Analysis of nationwide hemophilia care: A cohort study using two Japanese healthcare claims databases

Analysis of nationwide hemophilia care: A cohort study using two Japanese healthcare claims databases

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 la...

Full description

Bibliographic Details
Main Authors: Ei Kinai, Midori Ono, Akinori Oh, Mihoko Ota, Yasuo Myaguchi, Hitoshi Ueda
Format: Article
Language:English
Published: Wiley 2022-01-01
Series:Health Science Reports
Subjects:
cohort study
disease management
factor VIII
hemophilia A
Online Access:https://doi.org/10.1002/hsr2.498

Similar Items

Similar Items