诊断学理论与实践 ›› 2023, Vol. 22 ›› Issue (02): 89-115.doi: 10.16150/j.1671-2870.2023.02.001
薛峰1, 戴菁2, 陈丽霞3a, 刘葳1, 张厚强3a, 吴润晖4, 孙竞5, 张心声6, 吴竞生7, 赵永强3b, 王学锋2(), 杨仁池1()
收稿日期:
2023-02-12
出版日期:
2023-04-25
发布日期:
2023-08-31
通讯作者:
杨仁池 E-mail: rcyang65@163.com; 王学锋 E-mail: wxf63@shumu.edu.cn
XUE Feng1, DAI Jing2, CHEN Lixia3a, LIU Wei1, ZHANG Houqiang3a, WU Runhui4, SUN Jing5, ZHANG Xinsheng6, WU Jingsheng7, ZHAO Yongqiang3b, WANG Xuefeng2(), YANG Renchi1()
Received:
2023-02-12
Online:
2023-04-25
Published:
2023-08-31
摘要:
近年来,我国高度重视罕见病的防治。作为罕见病的代表疾病之一,我国的血友病防治取得了较大进步。1986年至1989年,全国血友病研究协作组按统一的方法及标准开展了我国的血友病流行病学调查,结果显示我国的血友病患病率为2.73/10万人口,国内各地区间患病率差异无统计学意义。2014年,荟萃分析显示我国的血友病患病率为2.8/10万。2018年,基于天津城市人口的数据,推算天津当地的血友病患病率为3.09/10万。随着血友病分级诊疗体系建设的全面推进,我国要求申请血友病综合管理中心和诊疗中心的医院必须能独立开展血友病诊断相关筛查试验和确诊试验。血友病诊断中,对于凝血因子活性测定,我国多数实验室通常采用基于活化部分凝血活酶时间(activated partial thromboplastin time, APTT)检测的一期法(凝固法)。但需注意,对于某些特殊类型的血友病需采用2种以上的活性检测方法。我国患者F8基因的各突变类型与国际数据报道类似;我国患者F9基因突变以单个碱基点突变为主,未发现突变热点。截至2023年6月,我国共有261家中心通过全国血友病登记系统,登记包括血友病在内的遗传性出血性疾病共计4万余例。我国的血友病治疗史经过不充分按需治疗、小剂量预防治疗探索等,目前已经往更高疗效的较高剂量预防及个体化预防治疗迈进。本报告基于登记数据及文献,全面总结我国血友病领域临床研究以及医疗保障方面的进展,分析不足之处,以期为进一步提高我国血友病诊疗水平指明方向。
中图分类号:
薛峰, 戴菁, 陈丽霞, 刘葳, 张厚强, 吴润晖, 孙竞, 张心声, 吴竞生, 赵永强, 王学锋, 杨仁池. 中国血友病诊治报告2023[J]. 诊断学理论与实践, 2023, 22(02): 89-115.
XUE Feng, DAI Jing, CHEN Lixia, LIU Wei, ZHANG Houqiang, WU Runhui, SUN Jing, ZHANG Xinsheng, WU Jingsheng, ZHAO Yongqiang, WANG Xuefeng, YANG Renchi. Report on diagnosis and treatment of hemophilia in China 2023[J]. Journal of Diagnostics Concepts & Practice, 2023, 22(02): 89-115.
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