Kirsten R, Weidinger G
Klinikum der Universität Frankfurt, Abteilung Klinische Pharmakologie, Frankfurt/Main.
Arzneimittelforschung. 1994 Jan;44(1):13-6.
In a randomised, placebo-controlled design 40 patients with moderately severe essential hypertension were treated with bunazosin (CAS 52712-76-2) retard in increasing doses ranging between 6 and 18 mg/day. In intervals of 14 days titration steps were made, the minimal period of treatment was 4 weeks. In 34 patients (80.6%) a blood pressure response could be achieved with Bunazosin retard alone, the rest of the patients needed the additional administration of 25 mg hydrochlorothiazide daily. In all actively treated patients diastolic blood pressure could be normalised (DBP < or = 90 mmHg). After 4 weeks the mean blood pressure was lowered in the Bunazosin group by 16.2 mmHg (diastolic) and 25 mmHg (systolic). The mean heart rate at rest remained almost constant. Bunazosin was generally well tolerated; only very few adverse events occurred, and no patient collapsed. Compared to placebo the orthostatic tolerance was not influenced by bunazosin retard. Only when changing from resting to standing position the rise in heart rate was slightly more pronounced under bunazosin. Also the physiological blood pressure profile under bunazosin remained unchanged during the orthostatic tests.
在一项随机、安慰剂对照设计中,40例中度严重原发性高血压患者接受了缓释布那唑嗪(化学物质登记号52712 - 76 - 2)治疗,剂量从6毫克/天逐渐增加至18毫克/天。每14天进行一次滴定步骤,最短治疗期为4周。34例患者(80.6%)仅使用缓释布那唑嗪就能实现血压反应,其余患者需要每日额外服用25毫克氢氯噻嗪。在所有积极治疗的患者中,舒张压均可恢复正常(舒张压≤90毫米汞柱)。4周后,布那唑嗪组的平均血压舒张压降低了16.2毫米汞柱,收缩压降低了25毫米汞柱。静息时的平均心率几乎保持不变。布那唑嗪总体耐受性良好;仅发生了极少数不良事件,且无患者出现虚脱。与安慰剂相比,缓释布那唑嗪对直立耐受性无影响。仅在从静息状态转变为站立姿势时,服用布那唑嗪后心率的上升略微更为明显。在直立试验期间,布那唑嗪作用下的生理血压曲线也保持不变。