• Young Bae Choi, Ye Jee Shim, Soon Gu Kim, Won Kee Lee, and Benign Hematology Committee of the Korean Pediatric Hematology-Oncology Group (KPHOG).
• Department of Pediatrics, Ajou University Hospital, Ajou University School of Medicine, Suwon, Korea.
• J. Korean Med. Sci. 2023 Jul 31; 38 (30): e235e235.

BackgroundThere has been remarkable progress in hemophilia A (HA) treatment in Korea. Viral inactivation products were developed in 1989, use of recombinant factor VIII (FVIII) concentrates started in 2002, and prophylaxis expanded thereafter. This study was conducted to identify the changes in complications in HA before and after 1989 or 2002.MethodsThe study was performed using the 2007-2019 Healthcare Big Data Hub of the Health Insurance Review and Assessment Service.ResultsAmong 2,557 patients, 1,084 had ≥ 1 complication; 829 had joint problems, 328 had viral infections, 146 had neurologic sequelae, and 87 underwent 113 surgeries or procedures due to complications. Patients born after 1989 had a significantly lower risk of viral infections than those born before 1989; 27.1% vs. 1.4% (P < 0.001, odds ratio [OR], 0.037). Patients born after 2002 had a significantly lower risk of joint problems than those born before 2002; 36.8% vs. 24.7% (P < 0.001, OR, 0.538). Patients born after 2002 had a higher incidence of neurologic sequelae than those born before 2002; 3.7% vs. 11.1% (P < 0.001, OR, 3.210). Medical expenses for complication-associated surgeries or procedures were ₩2,957,557,005.ConclusionViral infections have significantly decreased in Korean patients with HA. The degree of reduction of joint problems was lower than we expected, because it took > 10 years to expand prophylaxis widely. Neurologic sequelae have not decreased; thus, additional efforts to decrease intracranial hemorrhage are needed. We suggest personalized dosing of FVIII and more meticulous care during childbirth to further reduce the complications.© 2023 The Korean Academy of Medical Sciences.

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