• 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

产后因子VIII抑制剂。文献综述,特别提及类固醇和免疫抑制治疗的价值。

Post-partum factor VIII inhibitors. A review of the literature with special reference to the value of steroid and immunosuppressive treatment.

作者信息

Hauser I, Schneider B, Lechner K

机构信息

First Dept. of Internal Medicine, University of Vienna, Austria.

出版信息

Thromb Haemost. 1995 Jan;73(1):1-5.

PMID:7740477
Abstract

In a retrospective study 51 published cases of post-partum factor VIII inhibitors were analyzed with regard to the outcome according to treatment. The overall outcome was favorable with 97% survival at two years. The probability of complete remission (CR, absence of the inhibitor and normalization of factor VIII activity) was almost 100% at 30 months. Steroid treatment appears to be not superior to no treatment, but patients treated with immunosuppressive drugs (cyclophosphamide, azathioprine, 6-mercaptopurine) had a significantly shorter time to CR. In the absence of a randomized trial this analysis may be helpful for decision-making in women with factor VIII post-partum inhibitors. Because of the retrospective study design, conclusions have to be regarded with caution.

摘要

在一项回顾性研究中,根据治疗情况对已发表的51例产后因子VIII抑制剂病例的结果进行了分析。总体结果良好,两年生存率为97%。30个月时完全缓解(CR,抑制剂消失且因子VIII活性正常化)的概率几乎为100%。类固醇治疗似乎并不优于不治疗,但接受免疫抑制药物(环磷酰胺、硫唑嘌呤、6-巯基嘌呤)治疗的患者达到CR的时间明显更短。在缺乏随机试验的情况下,该分析可能有助于产后因子VIII抑制剂女性患者的决策。由于采用回顾性研究设计,结论必须谨慎看待。

相似文献

1
Post-partum factor VIII inhibitors. A review of the literature with special reference to the value of steroid and immunosuppressive treatment.产后因子VIII抑制剂。文献综述,特别提及类固醇和免疫抑制治疗的价值。
Thromb Haemost. 1995 Jan;73(1):1-5.
2
[Macrohaematuria post-partum: an unusual case of acquired haemophilia after pregnancy].产后肉眼血尿:一例妊娠后获得性血友病的罕见病例
G Ital Nefrol. 2002 Mar-Apr;19(2):204-8.
3
Postpartum factor VIII inhibitors. Report of two cases with special reference to the efficacy of various treatments.
Wien Klin Wochenschr. 1993;105(12):355-8.
4
Experience with factor VIII: C inhibitors and acquired von Willebrand's disease in an adult at Ramathibodi Hospital.拉玛蒂博迪医院一名成年患者的VIII因子:C抑制剂与获得性血管性血友病的诊疗经验
Southeast Asian J Trop Med Public Health. 1993;24 Suppl 1:152-8.
5
Acquired hemophilia: a case report of 2 patients with acquired factor VIII inhibitor treated with rituximab plus a short course of steroid and review of the literature.获得性血友病:2例接受利妥昔单抗联合短期类固醇治疗的获得性凝血因子VIII抑制物患者的病例报告及文献复习
Clin Appl Thromb Hemost. 2007 Oct;13(4):443-8. doi: 10.1177/1076029607303777.
6
A survey of 215 non-hemophilic patients with inhibitors to Factor VIII.一项针对215名非血友病性VIII因子抑制物患者的调查。
Thromb Haemost. 1981 Jun 30;45(3):200-3.
7
Acquired factor VIII inhibitors in non-haemophilic patients: clinical experience of 15 cases.非血友病患者获得性凝血因子 VIII 抑制剂:15 例临床经验
Haemophilia. 2004 Nov;10(6):713-21. doi: 10.1111/j.1365-2516.2004.01031.x.
8
[Immunosuppressive treatment of a spontaneous inhibitor hemophilia A using cyclophosphamide, vincristine and prednisone following prior Factor VIII stimulation].[在先前使用凝血因子 VIII 刺激后,使用环磷酰胺、长春新碱和泼尼松对自发性抑制性血友病 A 进行免疫抑制治疗]
Schweiz Med Wochenschr. 1996 Nov 23;126(47):2026-31.
9
[Long-term response to rituximab in a patient with acquired hemophilia].[利妥昔单抗对一名获得性血友病患者的长期疗效]
Rev Invest Clin. 2011 Mar-Apr;63(2):210-2.
10
[Combined treatment with factor VIII and immunosuppressive agents in a young woman with acquired factor VIII inhibitor].[一名获得性因子 VIII 抑制剂年轻女性患者采用因子 VIII 与免疫抑制剂联合治疗]
Sangre (Barc). 1996 Apr;41(2):147-50.

引用本文的文献

1
Acquired Hemophilia-A Case Series and Review.获得性血友病——病例系列及综述
J Clin Med. 2025 Feb 26;14(5):1597. doi: 10.3390/jcm14051597.
2
Acquired Hemophilia A In Adults: A Multicenter Study from Turkey.成人获得性血友病A:来自土耳其的多中心研究。
Indian J Hematol Blood Transfus. 2023 Jan;39(1):107-115. doi: 10.1007/s12288-022-01556-8. Epub 2022 Jul 31.
3
Acquired Haemophilia A: A Review of What We Know.获得性血友病A:我们所了解的综述。
J Blood Med. 2022 Nov 23;13:691-710. doi: 10.2147/JBM.S342077. eCollection 2022.
4
Immune complications and their management in inherited and acquired bleeding disorders.遗传性和获得性出血性疾病的免疫并发症及其处理。
Blood. 2022 Sep 8;140(10):1075-1085. doi: 10.1182/blood.2022016530.
5
Acquired Haemophilia A: An Intriguing Disease.获得性血友病A:一种引人入胜的疾病。
Mediterr J Hematol Infect Dis. 2020 Jul 1;12(1):e2020045. doi: 10.4084/MJHID.2020.045. eCollection 2020.
6
Identification of people with acquired hemophilia in a large electronic health record database.在大型电子健康记录数据库中识别获得性血友病患者。
J Blood Med. 2017 Jul 19;8:89-97. doi: 10.2147/JBM.S136060. eCollection 2017.
7
A Hematological Menace: Multiple Venous Thrombosis Complicated by Acquired Factor VIII Deficiency.一种血液学威胁:多发性静脉血栓形成合并获得性因子 VIII 缺乏症。
Am J Case Rep. 2016 Apr 4;17:214-8. doi: 10.12659/ajcr.895316.
8
A rare and life-threatening cause of epistaxis.鼻出血一种罕见且危及生命的病因。
BMJ Case Rep. 2015 Dec 23;2015:bcr2015213528. doi: 10.1136/bcr-2015-213528.
9
Role of rituximab in the treatment of postpartum acquired haemophilia A: a systematic review of the literature.利妥昔单抗在产后获得性甲型血友病治疗中的作用:文献系统评价
Blood Transfus. 2015 Jul;13(3):396-400. doi: 10.2450/2014.0242-14. Epub 2014 Dec 17.
10
Second case of postpartum acquired hemophilia A in a Korean female.
Blood Res. 2014 Sep;49(3):205-7. doi: 10.5045/br.2014.49.3.205. Epub 2014 Sep 25.