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1 型血管性血友病患者出血倾向和抗出血治疗效果与血管性血友病因子清除率增加。

Bleeding tendency and efficacy of anti-haemorrhagic treatments in patients with type 1 von Willebrand disease and increased von Willebrand factor clearance.

机构信息

Department of Hematology and Hemophilia and Thrombosis Center, San Bortolo Hospital, Vicenza, Italy.

出版信息

Thromb Haemost. 2011 Apr;105(4):647-54. doi: 10.1160/TH10-11-0697. Epub 2011 Jan 25.

DOI:10.1160/TH10-11-0697
PMID:21264446
Abstract

Accelerated clearance of von Willebrand factor (VWF) has been recently identified as a major pathophysiologic mechanism inducing low VWF in some patients with von Willebrand disease (VWD). The frequency of bleeding and the best treatment of these patients have never been evaluated prospectively in large series of patients. It was the aim of the present study to prospectively evaluate clinical events of 60 heterozygous patients with VWD Vicenza (VWD-VI) carrying R1205H VWF mutation and 23 with C1130F mutation, both characterised by markedly increased VWF clearance. During 71 months of follow-up, 65% of patients with VWD-VI and 61% with C1130F required treatment. The rate of spontaneous bleeding requiring consultation/treatment was 7.5/100 patients-year in patients with C1130F mutation vs. 1.9/100 patients-year in those with R1205H (p=0.004). This difference persisted also by multivariate analysis adjusted for sex, age and blood group (hazard ratio [HR]=3.3 for C1130F, 95% confidence interval [CI] 1.16-9.27) and females were at greater risk of bleeding (HR=3, 95%CI 1.01-9.93) because of menorrhagia. Only 3/15 (20 %) women in fertile age with VWD-VI compared to 8/9 (89 %) with C1130F mutation required consultation/treatment for menorrhagia (iron supplementation, combined oral contraceptives, tranexamic acid). Almost all dental extractions, minor surgeries and deliveries occurring during follow-up were successfully managed with desmopressin. Major surgery required factor VIII/VWF concentrates, but a few cases benefited from desmopressin. In conclusion, similar to patients with type 1 VWD, also in patients with increased VWF clearance desmopressin maintains a major therapeutic role.

摘要

von Willebrand 因子(VWF)的清除加速最近被确定为导致一些血管性血友病(VWD)患者 VWF 水平降低的主要病理生理机制。这些患者的出血频率和最佳治疗方法从未在大型患者系列中进行前瞻性评估。本研究旨在前瞻性评估 60 名携带 R1205H VWF 突变的 VWD Vicenza(VWD-VI)杂合子患者和 23 名携带 C1130F 突变的患者的临床事件,这两种突变均表现出明显增加的 VWF 清除率。在 71 个月的随访期间,65%的 VWD-VI 患者和 61%的 C1130F 患者需要治疗。C1130F 突变患者自发性出血需要咨询/治疗的发生率为 7.5/100 患者年,而 R1205H 突变患者为 1.9/100 患者年(p=0.004)。通过多变量分析,在校正性别、年龄和血型后,这种差异仍然存在(C1130F 的危险比 [HR]=3.3,95%置信区间 [CI] 1.16-9.27),女性出血风险更高(HR=3,95%CI 1.01-9.93),因为月经过多。与 C1130F 突变相比,只有 15 名生育期 VWD-VI 女性中有 3 名(20%)需要咨询/治疗月经过多(补铁、联合口服避孕药、氨甲环酸)。随访期间发生的几乎所有拔牙、小手术和分娩都成功地用去氨加压素治疗。大手术需要因子 VIII/VWF 浓缩物,但少数病例受益于去氨加压素。总之,与 1 型 VWD 患者一样,在清除 VWF 增加的患者中,去氨加压素仍然具有主要的治疗作用。

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