Winther K, Bondesen S, Hansen S H, Hvidberg E F
Department of Oral and Maxillofacial Surgery, Royal Dental College, Copenhagen, Denmark.
Eur J Clin Pharmacol. 1987;33(4):419-22. doi: 10.1007/BF00637641.
We have studied platelet aggregation and fibrinolytic activity in six patients with chronic inflammatory bowel disease treated with 5-aminosalicylic acid (mesalazine). There were no changes in these measurements during normal treatment, i.e. 1.5 g per day with a slow-release formulation, nor after an intravenous dose of 250 mg. Also in vitro tests were negative, in contrast to the inhibition seen with aspirin (acetylsalicylic acid). We conclude that treatment with mesalazine does not constitute a hazard to these patients in regard to prolonged bleeding time caused by an influence on platelet aggregation or fibrinolytic activity.
我们研究了6例接受5-氨基水杨酸(美沙拉嗪)治疗的慢性炎症性肠病患者的血小板聚集和纤溶活性。在常规治疗期间,即每天服用1.5 g缓释制剂时,以及静脉注射250 mg后,这些测量值均无变化。体外试验结果也为阴性,这与阿司匹林(乙酰水杨酸)所见的抑制作用形成对比。我们得出结论,就美沙拉嗪对血小板聚集或纤溶活性的影响导致出血时间延长而言,该药物治疗对这些患者不构成风险。