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波吲洛尔,一种新型长效β肾上腺素能受体拮抗剂——与普萘洛尔治疗高血压患者的随机对照研究

Bopindolol, a new long-acting beta-adrenoceptor antagonist--a randomized comparison against propranolol in hypertensive patients.

作者信息

Kirch W, Axthelm T

出版信息

Int J Clin Pharmacol Res. 1983;3(2):89-93.

PMID:6148312
Abstract

In a randomized parallel-group trial the blood-pressure lowering effect of a new beta-adrenoceptor blocker bopindolol (LT 31-200) in a dose of 1-4 mg once daily (eight patients) was compared with that of propranolol in a dose of 40-120 mg t.i.d. (nine patients). The average blood pressure fell in the bopindolol group from 185/113 mmHg to 135/90 mmHg and in the propranolol group from 183/120 mmHg to 147/102 mmHg. Both changes were statistically significant. This was achieved during a nine week treatment period at the end of which the average dose of bopindolol was 3 mg per day and of propranolol 330 mg per day. One patient receiving bopindolol interrupted the trial because of restlessness and insomnia, and one receiving propranolol because of bronchospasm. Side-effects were, otherwise, mild in both groups. During a one-year treatment period following the comparative trial, the seven patients who had received bopindolol showed no evidence of tachyphylaxia, the blood-pressure remaining well controlled while the dosage was slightly reduced. No new side-effects were reported and the ANA and AMA tests remained negative in all patients.

摘要

在一项随机平行组试验中,将每日一次服用剂量为1 - 4毫克的新型β - 肾上腺素能受体阻滞剂波吲洛尔(LT 31 - 200)(8例患者)的降压效果与每日三次服用剂量为40 - 120毫克的普萘洛尔(9例患者)的降压效果进行了比较。波吲洛尔组的平均血压从185/113毫米汞柱降至135/90毫米汞柱,普萘洛尔组从183/120毫米汞柱降至147/102毫米汞柱。两种变化均具有统计学意义。这是在为期9周的治疗期内实现的,在此治疗期结束时,波吲洛尔的平均剂量为每日3毫克,普萘洛尔为每日330毫克。一名接受波吲洛尔治疗的患者因烦躁不安和失眠中断了试验,一名接受普萘洛尔治疗的患者因支气管痉挛中断了试验。除此之外,两组的副作用均较轻。在对比试验后的一年治疗期内,接受波吲洛尔治疗的7例患者未出现快速耐受性迹象,血压在剂量略有减少的情况下仍得到良好控制。未报告新的副作用,所有患者的抗核抗体(ANA)和抗线粒体抗体(AMA)检测仍为阴性。

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