Schbath J, Boissel J P, Mathy B, Ville D, Benveniste E, Sanchini B, Leizorovicz A, Belleville J, Dechavanne M, Maitre P
Thromb Haemost. 1984 Feb 28;51(1):45-9.
A prospective randomized trial of the effects of 2 antiplatelet aggregating drugs, dipyridamole (375 mg/d), a related substance RA 233 (1500 mg/d) and placebo, concomitantly with oral anticoagulants, was carried out in patients with prior valvular replacement. The study was aimed to determine effect on platelet survival time (PST) of these 2 agents. The trial sample consisted of 40 males and 15 females aged 40-70 years (average 53 years). 32 received Björk-Shiley valve in aortic position, 23 underwent mitral valve replacement: 3 with Cooley-Cutter, 11 with Lillehei-Kaster 500 and 9 with Starr-Edwards 6120 prostheses; 28 patients had aortic stenosis, 21 aortic insufficiency. All the PST measured after 3 months of treatment were within normal ranges and not different between placebo, dipyridamole or RA 233 treated subjects: averages in days were, respectively, 7.49, 7.11 and 6.88. The present study did not support the claim that modern valve prosthesis could lead to a shortened PST.
在既往接受瓣膜置换术的患者中进行了一项前瞻性随机试验,以研究两种抗血小板聚集药物双嘧达莫(375毫克/天)、相关物质RA 233(1500毫克/天)和安慰剂与口服抗凝剂同时使用的效果。该研究旨在确定这两种药物对血小板存活时间(PST)的影响。试验样本包括40名男性和15名女性,年龄在40至70岁之间(平均53岁)。32人接受了主动脉位置的 Björk-Shiley 瓣膜,23人接受了二尖瓣置换术:3人使用Cooley-Cutter瓣膜,11人使用Lillehei-Kaster 500瓣膜,9人使用Starr-Edwards 6120瓣膜;28例患者有主动脉瓣狭窄,21例有主动脉瓣关闭不全。治疗3个月后测量的所有PST均在正常范围内,安慰剂组、双嘧达莫组或RA 233组受试者之间无差异:天数平均值分别为7.49、7.11和6.88。本研究不支持现代瓣膜假体可导致PST缩短的说法。