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重度凝血因子VII缺乏症的长期预防

Long-term prophylaxis in severe factor VII deficiency.

作者信息

Siboni S M, Biguzzi E, Mistretta C, Garagiola I, Peyvandi F

机构信息

Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, Dipartimento delle Units Multispecialistiche e dei Trapianti, Unità Operativa Complessa di Ematologia non Tumorale e Coagulopatie, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico and University of Milan, Milan, Italy.

出版信息

Haemophilia. 2015 Nov;21(6):812-9. doi: 10.1111/hae.12702. Epub 2015 May 8.

Abstract

INTRODUCTION

The spectrum of bleeding problems in FVII deficiency is highly variable and FVII levels and causative genetic mutations correlate poorly with the bleeding risk. Long-term prophylaxis is generally initiated in order to prevent subsequent CNS bleeding after a first event or in patients with other major/ life threatening/ frequent bleeding symptoms as gastrointestinal bleeding or hemarthrosis. However few data are available in the literature regarding FVII prophylaxis and clinical decisions cannot be based on evidence.

AIMS

We report the data available in the literature on FVII prophylaxis and our personal experience regarding three patients affected by severe FVII deficiency.

METHODS

Specific papers on long-term prophylaxis in severe FVII deficiency were identified using the database, PUBMED.

RESULTS

The most frequent indications for long-term prophylaxis were CNS bleeding (58%), hemartrosis (15%) and GI bleeding (9%). Patients were treated with various dosages and frequency. Prophylactic treatment with 10-30U/kg (pdFVII) or 20-30mcg/kg (rFVIIa) twice or three times/weeks was described to be effective.

CONCLUSIONS

In the literature and in our experience, prophylaxis can be considered in patients with severe FVII deficiency and severe bleeding phenotype. A dose of 10-30U/kg (pdFVII) or 20-30 microg/kg (rFVIIa) twice or three times/week is usually administrated, but dose and frequency can be tailored based on the clinical follow-up of the patients. Since hemarthrosis is a frequent manifestation, a suggestion to improve the outcomes of patients with severe FVII deficiency is to monitor joint condition in order to identify early arthropathy that could be another indication to start secondary prophylaxis.

摘要

引言

FVII缺乏症患者的出血问题范围差异很大,FVII水平和致病基因突变与出血风险的相关性较差。长期预防通常是为了防止首次事件后发生中枢神经系统出血,或用于患有其他严重/危及生命/频繁出血症状(如胃肠道出血或关节积血)的患者。然而,关于FVII预防的文献资料很少,临床决策无法基于证据。

目的

我们报告文献中关于FVII预防的可用数据以及我们对三名严重FVII缺乏症患者的个人经验。

方法

使用数据库PUBMED识别有关严重FVII缺乏症长期预防的特定论文。

结果

长期预防最常见的适应症是中枢神经系统出血(58%)、关节积血(15%)和胃肠道出血(9%)。患者接受了不同剂量和频率的治疗。据描述,每周两次或三次给予10 - 30U/kg(重组凝血因子VII)或20 - 30mcg/kg(重组活化凝血因子VII)的预防性治疗是有效的。

结论

根据文献和我们的经验,对于严重FVII缺乏症和严重出血表型的患者可以考虑进行预防。通常给予10 - 30U/kg(重组凝血因子VII)或20 - 30μg/kg(重组活化凝血因子VII),每周两次或三次,但剂量和频率可根据患者的临床随访情况进行调整。由于关节积血是常见表现,对于改善严重FVII缺乏症患者的治疗效果的一个建议是监测关节状况,以便识别可能是开始二级预防的另一个指征的早期关节病。

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