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普齐地洛(SK&F 92657),一种具有β受体阻滞特性的新型血管扩张剂,用于治疗原发性高血压。

Prizidilol (SK & F 92657), a new vasodilator with beta-blocking properties in the treatment of essential hypertension.

作者信息

Lüscher T, Havelka J, Greminger P, Tuma J, Täuber M, Siegenthaler W, Vetter W

出版信息

Eur J Clin Pharmacol. 1982;23(5):411-5. doi: 10.1007/BF00605990.

Abstract

The antihypertensive effect of a new vasodilator with betablocking properties (SK & F 92657) was investigated in 10 patients with mild to moderate essential hypertension. After a mean treatment period of 26,5 weeks (6,5-49 weeks) blood pressure was significantly reduced, from 168 +/- 22/106 +/- 6 mmHg to 144 +/- 19/94 +/- 12 mmHg (p less than 0.05 and 0.025). The mean dose was 410 mg (100-700 mg). Heart rate decreased slightly from 77 +/- 12 to 70 +/- 8 beats/min. Plasma renin activity and plasma aldosterone showed only minor changes. Nausea, heavy dreams, facial and hand flushing and mild depression were reported as side effects. In most patients the symptoms disappeared without reduction in the dose. In one patient anaemia developed after 7 weeks and treatment with prizidilol was stopped. A slight but statistically significant decrease in haemoglobin concentration of 1.1 +/- 0.6 g/dl was observed in 5 of the 10 patients (p less than 0.02). Thus, a mean dose of prizidilol of 410 +/- 242 mg/day had a mean blood pressure lowering effect of 24/12 mmHg. In 7 of the 10 patients (70%) diastolic blood pressure could be reduced to 95 mmHg or less. However, the observed haematological side-effects should be carefully monitored in further studies and may limit the clinical use of prizidilol.

摘要

对10例轻度至中度原发性高血压患者研究了一种具有β受体阻滞特性的新型血管扩张剂(SK&F 92657)的降压效果。平均治疗期26.5周(6.5 - 49周)后,血压显著降低,从168±22/106±6 mmHg降至144±19/94±12 mmHg(p<0.05和0.025)。平均剂量为410 mg(100 - 700 mg)。心率从77±12次/分钟略有下降至70±8次/分钟。血浆肾素活性和血浆醛固酮仅显示轻微变化。报告的副作用有恶心、多梦、面部和手部潮红以及轻度抑郁。大多数患者症状未减少剂量就消失了。1例患者在7周后出现贫血,停用了普齐地洛治疗。在这10例患者中有5例观察到血红蛋白浓度轻微但有统计学意义的下降,下降了1.1±0.6 g/dl(p<0.02)。因此,普齐地洛平均剂量410±242 mg/天平均降压效果为24/12 mmHg。10例患者中有7例(70%)舒张压可降至95 mmHg或更低。然而,在进一步研究中应仔细监测观察到的血液学副作用,其可能会限制普齐地洛的临床应用。

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