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本文引用的文献

1
Prophylactic therapy with Fibrogammin P is associated with a decreased incidence of bleeding episodes: a retrospective study.预防性使用 Fibrogammin P 可降低出血事件发生率:一项回顾性研究。
Haemophilia. 2010 Mar;16(2):316-21. doi: 10.1111/j.1365-2516.2009.02123.x. Epub 2009 Dec 15.
2
Paediatric haemophilia with inhibitors: existing management options, treatment gaps and unmet needs.小儿血友病伴抑制物:现有管理选择、治疗差距和未满足的需求。
Haemophilia. 2009 Sep;15(5):983-9. doi: 10.1111/j.1365-2516.2009.01999.x.
3
Clinical prediction models for inhibitor development in severe hemophilia A.
J Thromb Haemost. 2009 Jul;7 Suppl 1:98-102. doi: 10.1111/j.1538-7836.2009.03437.x.
4
Prophylaxis in 10 patients with severe haemophilia A and inhibitor: different approaches for different clinical situations.10例重度甲型血友病伴抑制物患者的预防治疗:针对不同临床情况的不同方法。
Haemophilia. 2009 Jan;15(1):203-9. doi: 10.1111/j.1365-2516.2008.01915.x.
5
Break-through bleeding in relation to predicted factor VIII levels in patients receiving prophylactic treatment for severe hemophilia A.接受重度甲型血友病预防性治疗的患者中突破性出血与预测的因子VIII水平的关系
J Thromb Haemost. 2009 Mar;7(3):413-20. doi: 10.1111/j.1538-7836.2008.03270.x. Epub 2008 Dec 20.
6
Evaluation of liposomal dose in recombinant factor VIII reconstituted with pegylated liposomes for the treatment of patients with severe haemophilia A.聚乙二醇化脂质体重构重组凝血因子VIII治疗重度甲型血友病患者时脂质体剂量的评估。
Thromb Haemost. 2008 Sep;100(3):429-34.
7
Back to the future: a recent history of haemophilia treatment.回到未来:血友病治疗的近期历史
Haemophilia. 2008 Jul;14 Suppl 3:10-8. doi: 10.1111/j.1365-2516.2008.01708.x.
8
Establishment of embryonic stem cells secreting human factor VIII for cell-based treatment of hemophilia A.建立分泌人凝血因子VIII的胚胎干细胞用于A型血友病的细胞治疗
J Thromb Haemost. 2008 Aug;6(8):1352-9. doi: 10.1111/j.1538-7836.2008.03022.x. Epub 2008 May 15.
9
The phenotypic heterogeneity of severe hemophilia.重度血友病的表型异质性。
Semin Thromb Hemost. 2008 Feb;34(1):128-41. doi: 10.1055/s-2008-1066024.
10
Implantable central venous access device procedures in haemophilia patients without an inhibitor: systematic review of the literature and institutional experience.无抑制物血友病患者的可植入式中心静脉通路装置操作:文献系统综述及机构经验
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重新审视急性医学中的血友病管理。

Revisiting hemophilia management in acute medicine.

作者信息

Sahu Sandeep, Lata Indu, Singh Surendra, Kumar Mukesh

机构信息

Department of Anaesthesiology, Lucknow, UP, India.

出版信息

J Emerg Trauma Shock. 2011 Apr;4(2):292-8. doi: 10.4103/0974-2700.82225.

DOI:10.4103/0974-2700.82225
PMID:21769217
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3132370/
Abstract

The World Federation of Hemophilia estimates that more than 350,000 people globally have a form of the disease. Hemophilia A is a bleeding disorder that has a spectrum of manifestations ranging from persistent bleeding after minor trauma to spontaneous hemorrhage. We report a case of a male patient with hemophilia A who received general anesthesia for removal of foreign body from the nose. There was no excessive blood loss during surgery. Perioperatively, the patient received recombinant factor VIII coverage. Rest of the postoperative course was uneventful. Literature on the clinical management of patient with hemophilia A are reviewed and considerations for perioperative preparation and management of hemophilic patient are presented.

摘要

世界血友病联盟估计,全球有超过35万人患有某种形式的血友病。甲型血友病是一种出血性疾病,其表现范围从轻微创伤后持续出血到自发性出血。我们报告一例甲型血友病男性患者,因鼻腔异物取出接受全身麻醉。手术期间无过多失血。围手术期,患者接受了重组凝血因子VIII替代治疗。术后其余过程顺利。本文回顾了甲型血友病患者临床管理的相关文献,并提出了血友病患者围手术期准备和管理的注意事项。