Sun-Hong Kwon, Ji Kyoung Park, Hee Jo Baek, Jin Hyun Nam, Serim Min, Ae-Ryeo Cho, Aeran Jung, Young-Shil Park
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We observed joint procedures, life-threatening haemorrhages and comorbidities between 2008 and 2021.</p><p><strong>Results: </strong>The number of identified PwHAs was 1193 in 2008 and 1517 in 2021. The proportion of older adult patients has increased over the past 14 years. The joint procedure rates per 1000 patients were 61.2 (95% CI 48.0‒76.9) in 2008 and 17.1 (11.2‒25.1) in 2021. The rate was highest in patients with a severe phenotype. Annually, less than 2% of patients experienced life-threatening haemorrhages, with approximately 90% of the cases attributed to central nervous system and gastrointestinal bleeding. The prevalence of hypertension and diabetes increased over the years (6% in 2008 and 15% in 2021, and 6% in 2008 and 9% in 2021, respectively).</p><p><strong>Conclusion: </strong>This study revealed previously unreported long-term trends in haemophilia-related outcomes and comorbidities in Korean PwHA. 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引用次数: 0
摘要
背景:在过去的十年中,因子VIII (FVIII)的总体使用和预防性使用在韩国有所增加。然而,没有全国性的结果数据证明其影响。本研究旨在识别血友病A (PwHA)患者,并使用国家索赔数据观察关节相关结局和危及生命的出血的趋势。方法:本系列横断面研究分析了来自韩国健康保险和审查评估的索赔数据。在2007年至2022年期间,至少两次用FVIII治疗的PwHA被确定。我们观察了2008年至2021年间的联合手术、危及生命的出血和合并症。结果:2008年鉴定PwHAs为1193个,2021年鉴定PwHAs为1517个。在过去14年中,老年患者的比例有所增加。2008年每1000名患者的关节手术率为61.2 (95% CI 48.0-76.9), 2021年为17.1(11.2-25.1)。在表型严重的患者中发病率最高。每年,不到2%的患者出现危及生命的出血,其中约90%的病例归因于中枢神经系统和胃肠道出血。高血压和糖尿病患病率逐年上升(2008年为6%,2021年为15%,2008年为6%,2021年为9%)。结论:这项研究揭示了韩国PwHA血友病相关结果和合并症的长期趋势。尽管老年患者的数量有所增加,但随着时间的推移,关节相关并发症有所减少。14年来观察到的趋势为加强PwHA的治疗提供了宝贵的见解。
Burden of Haemophilia A in South Korea: A Serial Cross-Sectional Study From 2008 to 2021.
Background: Overall use of factor VIII (FVIII) and prophylactic use have increased in South Korea over the past decade. However, there are no nationwide outcome data demonstrating its impact. This study aimed to identify patients with haemophilia A (PwHA) and observe trends in joint-related outcomes and life-threatening haemorrhages using national claims data.
Methods: This serial cross-sectional study analysed claims data from the Health Insurance and Review Assessment in South Korea. PwHA treated with FVIII at least twice between 2007 and 2022 were identified. We observed joint procedures, life-threatening haemorrhages and comorbidities between 2008 and 2021.
Results: The number of identified PwHAs was 1193 in 2008 and 1517 in 2021. The proportion of older adult patients has increased over the past 14 years. The joint procedure rates per 1000 patients were 61.2 (95% CI 48.0‒76.9) in 2008 and 17.1 (11.2‒25.1) in 2021. The rate was highest in patients with a severe phenotype. Annually, less than 2% of patients experienced life-threatening haemorrhages, with approximately 90% of the cases attributed to central nervous system and gastrointestinal bleeding. The prevalence of hypertension and diabetes increased over the years (6% in 2008 and 15% in 2021, and 6% in 2008 and 9% in 2021, respectively).
Conclusion: This study revealed previously unreported long-term trends in haemophilia-related outcomes and comorbidities in Korean PwHA. Although the number of older adult patients has increased, joint-related complications have decreased over time. The trends, observed over 14 years, provide valuable insights for enhancing the treatment of PwHA.
期刊介绍:
Haemophilia is an international journal dedicated to the exchange of information regarding the comprehensive care of haemophilia. The Journal contains review articles, original scientific papers and case reports related to haemophilia care, with frequent supplements. Subjects covered include:
clotting factor deficiencies, both inherited and acquired: haemophilia A, B, von Willebrand''s disease, deficiencies of factor V, VII, X and XI
replacement therapy for clotting factor deficiencies
component therapy in the developing world
transfusion transmitted disease
haemophilia care and paediatrics, orthopaedics, gynaecology and obstetrics
nursing
laboratory diagnosis
carrier detection
psycho-social concerns
economic issues
audit
inherited platelet disorders.