Caimi G, Francavilla G, Romano A, Catania A, Santonocito G, Sarno A
Br J Clin Pract. 1988 Nov;42(11):456-8.
To evaluate the effect of bezafibrate on the haemorheological pattern, 30 atherosclerotic non-diabetic patients were enlisted in a double-blind, comparative, parallel group trial with bezafibrate (600 mg daily) or placebo being randomly assigned. The 45-day treatment period was preceded by a three week pharmacological wash-out. Haemorheological parameters such as whole-blood, plasma and serum viscosity, haematocrit, fibrinogen, fibrinogen/albumin ratio and erythrocyte filterability were evaluated before and at the end of treatment. The results showed no change in haemorheological determinants in the placebo-treated group but a significant reduction in whole-blood viscosity, in haematocrit, in fibrinogen and fibrinogen/albumin ratio was observed in the bezafibrate treated patients. No variation was present in the plasma and serum viscosity and in the erythrocyte filterability.
为评估苯扎贝特对血液流变学模式的影响,30例非糖尿病动脉粥样硬化患者被纳入一项双盲、对照、平行组试验,随机分配接受苯扎贝特(每日600毫克)或安慰剂治疗。在为期45天的治疗期之前,有为期三周的药物洗脱期。在治疗前和治疗结束时评估血液流变学参数,如全血、血浆和血清粘度、血细胞比容、纤维蛋白原、纤维蛋白原/白蛋白比值和红细胞滤过率。结果显示,安慰剂治疗组的血液流变学指标无变化,但苯扎贝特治疗的患者全血粘度、血细胞比容、纤维蛋白原和纤维蛋白原/白蛋白比值显著降低。血浆和血清粘度以及红细胞滤过率无变化。