• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

韩国甲型血友病负担:2008年至2021年的系列横断面研究

Burden of Haemophilia A in South Korea: A Serial Cross-Sectional Study From 2008 to 2021.

作者信息

Kwon Sun-Hong, Park Ji Kyoung, Baek Hee Jo, Nam Jin Hyun, Min Serim, Cho Ae-Ryeo, Jung Aeran, Park Young-Shil

机构信息

School of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea.

Department of Pediatrics, Inje University College of Medicine, Busan Paik Hospital, Busan, Republic of Korea.

出版信息

Haemophilia. 2025 Jul;31(4):687-695. doi: 10.1111/hae.70064. Epub 2025 May 30.

DOI:10.1111/hae.70064
PMID:40444601
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12306853/
Abstract

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.

摘要

背景

在过去十年中,韩国的凝血因子VIII(FVIII)总体使用量和预防性使用量均有所增加。然而,尚无全国性的结果数据证明其影响。本研究旨在通过全国性索赔数据识别甲型血友病患者(PwHA),并观察关节相关结局和危及生命的出血情况的趋势。

方法

这项系列横断面研究分析了韩国健康保险审查评估机构的索赔数据。确定了2007年至2022年间至少接受过两次FVIII治疗的PwHA。我们观察了2008年至2021年间的关节手术、危及生命的出血情况和合并症。

结果

2008年确定的PwHA数量为1193例,2021年为1517例。在过去14年中,老年患者的比例有所增加。每1000例患者的关节手术率在2008年为61.2(95%CI 48.0‒76.9),2021年为17.1(11.2‒25.1)。该比率在重型表型患者中最高。每年,不到2%的患者发生危及生命的出血,其中约90%的病例归因于中枢神经系统和胃肠道出血。高血压和糖尿病的患病率多年来有所增加(分别从2008年的6%和2021年的15%,以及2008年的6%和2021年的9%)。

结论

本研究揭示了韩国PwHA中此前未报告的血友病相关结局和合并症的长期趋势。尽管老年患者数量有所增加,但随着时间的推移,关节相关并发症有所减少。在14年中观察到的这些趋势为加强PwHA的治疗提供了有价值的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6be/12306853/676927da2e64/HAE-31-687-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6be/12306853/6c0d9fd18bdd/HAE-31-687-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6be/12306853/aa06766bb7ff/HAE-31-687-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6be/12306853/82b7e74d590c/HAE-31-687-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6be/12306853/676927da2e64/HAE-31-687-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6be/12306853/6c0d9fd18bdd/HAE-31-687-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6be/12306853/aa06766bb7ff/HAE-31-687-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6be/12306853/82b7e74d590c/HAE-31-687-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6be/12306853/676927da2e64/HAE-31-687-g004.jpg

相似文献

1
Burden of Haemophilia A in South Korea: A Serial Cross-Sectional Study From 2008 to 2021.韩国甲型血友病负担:2008年至2021年的系列横断面研究
Haemophilia. 2025 Jul;31(4):687-695. doi: 10.1111/hae.70064. Epub 2025 May 30.
2
Efanesoctocog Alfa versus Standard and Extended Half-Life Factor VIII Prophylaxis in Adolescent and Adult Patients with Haemophilia A without Inhibitors.依费奈索托考格阿尔法与标准及延长半衰期因子VIII预防治疗对无抑制物的青少年和成年甲型血友病患者的疗效比较
Adv Ther. 2025 Jan;42(1):427-441. doi: 10.1007/s12325-024-03032-3. Epub 2024 Nov 22.
3
Clotting factor concentrates for preventing bleeding and bleeding-related complications in previously treated individuals with haemophilia A or B.用于预防既往接受过治疗的 A 型或 B 型血友病患者出血和出血相关并发症的凝血因子浓缩物。
Cochrane Database Syst Rev. 2021 Aug 18;8(8):CD014201. doi: 10.1002/14651858.CD014201.
4
Antifibrinolytic therapy for preventing oral bleeding in patients with haemophilia or Von Willebrand disease undergoing minor oral surgery or dental extractions.抗纤维蛋白溶解疗法用于预防血友病或血管性血友病患者在接受小型口腔手术或拔牙时的口腔出血。
Cochrane Database Syst Rev. 2015 Dec 24(12):CD011385. doi: 10.1002/14651858.CD011385.pub2.
5
Different doses of prophylactic platelet transfusion for preventing bleeding in people with haematological disorders after myelosuppressive chemotherapy or stem cell transplantation.不同剂量预防性血小板输注对预防血液系统疾病患者在骨髓抑制性化疗或干细胞移植后出血的作用
Cochrane Database Syst Rev. 2015 Oct 27;2015(10):CD010984. doi: 10.1002/14651858.CD010984.pub2.
6
Comparison of different platelet count thresholds to guide administration of prophylactic platelet transfusion for preventing bleeding in people with haematological disorders after myelosuppressive chemotherapy or stem cell transplantation.比较不同血小板计数阈值,以指导预防性血小板输注的应用,从而预防血液系统疾病患者在骨髓抑制性化疗或干细胞移植后发生出血。
Cochrane Database Syst Rev. 2015 Nov 18;2015(11):CD010983. doi: 10.1002/14651858.CD010983.pub2.
7
[Translated article] Pharmacokinetic-guided switching from standard half-life factor VIII to extended half-life pegylated factor VIII in haemophilia A therapy in clinical practice.[翻译文章] 在临床实践中,血友病A治疗中基于药代动力学指导从标准半衰期的凝血因子VIII转换为延长半衰期的聚乙二醇化凝血因子VIII 。
Farm Hosp. 2025 Jul-Aug;49(4):T205-T211. doi: 10.1016/j.farma.2024.12.007. Epub 2025 Feb 14.
8
What Are the Complications, Function, and Survival of Tumor-devitalized Autografts Used in Patients With Limb-sparing Surgery for Bone and Soft Tissue Tumors? A Japanese Musculoskeletal Oncology Group Multi-institutional Study.肿瘤灭活自体移植物用于保肢手术治疗骨和软组织肿瘤患者的并发症、功能和生存情况如何?日本肌肉骨骼肿瘤学组多机构研究。
Clin Orthop Relat Res. 2023 Nov 1;481(11):2110-2124. doi: 10.1097/CORR.0000000000002720. Epub 2023 Jun 14.
9
Anti-vascular endothelial growth factor biosimilars for neovascular age-related macular degeneration.抗血管内皮生长因子生物类似药治疗新生血管性年龄相关性黄斑变性。
Cochrane Database Syst Rev. 2024 Jun 3;6(6):CD015804. doi: 10.1002/14651858.CD015804.pub2.
10
TSUBASA Study: Evaluating Association of Physical Activity and Bleeding Events in People With Haemophilia A Without Factor VIII Inhibitors Receiving Emicizumab.翼(TSUBASA)研究:评估接受艾美赛珠单抗治疗的无因子VIII抑制剂的A型血友病患者身体活动与出血事件之间的关联。
Haemophilia. 2025 Jul;31(4):703-712. doi: 10.1111/hae.70070. Epub 2025 Jun 18.

本文引用的文献

1
Complication Analysis in Korean Patients With Hemophilia A From 2007 to 2019: A Nationwide Study by the Health Insurance Review and Assessment Service Database.2007 年至 2019 年韩国血友病 A 患者的并发症分析:一项由健康保险审查和评估服务数据库进行的全国性研究。
J Korean Med Sci. 2023 Jul 31;38(30):e235. doi: 10.3346/jkms.2023.38.e235.
2
Long-term impact of primary prophylaxis on joint status in patients with severe hemophilia A.一级预防对重度甲型血友病患者关节状态的长期影响。
Res Pract Thromb Haemost. 2023 Jan 12;7(1):100005. doi: 10.1016/j.rpth.2022.100005. eCollection 2023 Jan.
3
Prevalence of comorbid conditions among older males with haemophilia receiving care in haemophilia treatment centers in the United States.
美国血友病治疗中心接受治疗的老年男性血友病患者合并症的患病率。
Haemophilia. 2022 Nov;28(6):986-995. doi: 10.1111/hae.14647. Epub 2022 Aug 4.
4
Reduced cardiovascular morbidity in patients with hemophilia: results of a 5-year multinational prospective study.血友病患者心血管发病率降低:一项为期 5 年的多国前瞻性研究结果。
Blood Adv. 2022 Feb 8;6(3):902-908. doi: 10.1182/bloodadvances.2021005260.
5
Recent Advances in the Treatment of Hemophilia: A Review.血友病治疗的最新进展:综述
Biologics. 2021 Jun 15;15:221-235. doi: 10.2147/BTT.S252580. eCollection 2021.
6
Cardiovascular risk factors among adult patients with haemophilia.成年血友病患者的心血管危险因素。
Int J Hematol. 2021 Jun;113(6):884-892. doi: 10.1007/s12185-021-03104-y. Epub 2021 Mar 7.
7
Health care resource utilization and costs among adult patients with hemophilia A on factor VIII prophylaxis: an administrative claims analysis.血友病 A 成年患者接受因子 VIII 预防治疗的卫生保健资源利用和成本:一项行政索赔分析。
J Manag Care Spec Pharm. 2021 Mar;27(3):316-326. doi: 10.18553/jmcp.2021.27.3.316.
8
Mortality, life expectancy, and causes of death of persons with hemophilia in the Netherlands 2001-2018.2001 - 2018年荷兰血友病患者的死亡率、预期寿命及死因
J Thromb Haemost. 2021 Mar;19(3):645-653. doi: 10.1111/jth.15182. Epub 2020 Dec 18.
9
WFH Guidelines for the Management of Hemophilia, 3rd edition.《血友病管理的居家指南》第三版
Haemophilia. 2020 Aug;26 Suppl 6:1-158. doi: 10.1111/hae.14046. Epub 2020 Aug 3.
10
Hemophilia therapy: the future has begun.血友病治疗:未来已来。
Haematologica. 2020 Mar;105(3):545-553. doi: 10.3324/haematol.2019.232132. Epub 2020 Feb 14.