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高血压患者的吲哚洛尔与收缩期时间间期

Pindolol and systolic time intervals in patients with hypertension.

作者信息

Hammond J J, Kirkendall W M, Jacks-Nagle V L, Plotnick G D, Fisher M L, Hamilton J H, Robinson M, Carliner N H, Janoski A H, Hamilton B P

出版信息

Am Heart J. 1982 Aug;104(2 Pt 2):456-64. doi: 10.1016/0002-8703(82)90140-5.

Abstract

Two studies of systolic time intervals (STIs) in patients with mild to moderate hypertension (HBP) revealed that no mean change in systolic intervals occurred with pindolol therapy, although some patients had significant alterations in their STIs. Pindolol responders with normal pretreatment preejection period to left ventricular ejection time (PEP/LVET) ratios had a significant increase in this ratio following pindolol therapy, whereas those with abnormal pretreatment PEP/LVET ratios had improvement in this ratio on administration of the drug. Patients on propranolol showed no change in PEP/LVET ratio. Propranolol administration slowed heart rate and lengthened Q-S2, S1-S2, and LVET, however, without altering the Q-S2 and LVET index, indicating that the changes were caused by the effect of propranolol on the heart rate alone. Chlorthalidone in high doses significantly reduced the Q-S2 index and the S1-S2 index, indicating that these changes were not caused by alteration of the heart rate. The second study suggests that STIs may provide a predictive clue for clinical response to pindolol. Patients with normal cardiac function (group I) are more likely to respond to pindolol than are those with abnormal cardiac function (group II). Directionally opposite changes in STIs in the two subgroups suggest different mechanisms for changing cardiac function. Pindolol's dual role as a beta-blocking agent with intrinsic sympathomimetic activity is proposed as a possible explanation, beta-blocking effects predominating in group I and sympathomimetic activity balancing the beta effect in group II.

摘要

两项针对轻至中度高血压患者收缩期时间间期(STIs)的研究表明,使用吲哚洛尔治疗时,收缩期间期的平均变化未出现,但部分患者的STIs有显著改变。治疗前射血前期与左心室射血时间(PEP/LVET)比值正常的吲哚洛尔反应者,在接受吲哚洛尔治疗后该比值显著升高,而治疗前PEP/LVET比值异常者在用药后该比值有所改善。服用普萘洛尔的患者PEP/LVET比值无变化。然而,普萘洛尔使心率减慢,Q - S2、S1 - S2和LVET延长,但未改变Q - S2和LVET指数,这表明这些变化仅是由普萘洛尔对心率的影响所致。高剂量氯噻酮显著降低了Q - S2指数和S1 - S2指数,这表明这些变化并非由心率改变引起。第二项研究表明,STIs可能为临床对吲哚洛尔的反应提供预测线索。心功能正常的患者(I组)比心功能异常的患者(II组)更可能对吲哚洛尔有反应。两个亚组中STIs的方向相反变化提示心脏功能改变的机制不同。吲哚洛尔作为具有内在拟交感活性的β受体阻滞剂的双重作用被认为是一种可能的解释,在I组中β受体阻滞作用占主导,而在II组中拟交感活性平衡了β受体效应。

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