Hutton R A, Hales M, Kernoff P B
Katharine Dormandy Haemophilia Centre, Academic Department of Haematology, Royal Free Hospital, London, England.
Thromb Haemost. 1988 Dec 22;60(3):506-7.
Nine patients with clinically moderate or severe Type I von Willebrand's disease were treated for 2 weeks with ethamsylate (2 g/day in four equal doses) and with a matched placebo in a randomised double-blind trial. Template bleeding time, von Willebrand factor activity (ristocetin co-factor) and antigen, euglobulin lysis time and type I tissue plasminogen activator inhibitor were determined before and at the end of each treatment period. None of these parameters showed any significant change attributable to ethamsylate. Thus, despite the fact that five patients thought subjectively that their bleeding symptoms improved during ethamsylate treatment compared to only one while on placebo, we obtained no evidence that the drug was of benefit to patients with von Willebrand's disease.
9名临床诊断为中度或重度I型血管性血友病的患者,在一项随机双盲试验中,接受了2周的酚磺乙胺治疗(每日2克,分4等份剂量服用),并服用匹配的安慰剂。在每个治疗期开始前及结束时,测定了模板出血时间、血管性血友病因子活性(瑞斯托霉素辅因子)和抗原、优球蛋白溶解时间以及I型组织纤溶酶原激活物抑制剂。这些参数均未显示出任何可归因于酚磺乙胺的显著变化。因此,尽管有5名患者主观认为与服用安慰剂时只有1人感觉出血症状改善相比,他们在酚磺乙胺治疗期间出血症状有所改善,但我们没有获得证据表明该药物对血管性血友病患者有益。