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缓释美托洛尔对冠心病室性心律失常患者的剂量依赖性抗心律失常作用

[Dose-dependent anti-arrhythmia effect of retard metoprolol in coronary disease patients with ventricular arrhythmia].

作者信息

Hartwig C A, Bethge K P, Wenzlaff P, Lichtlen P R

机构信息

Abt. für Kardiologie, Medizinische Hochschule Hannover.

出版信息

Z Kardiol. 1988 Nov;77(11):704-12.

PMID:2463717
Abstract

The antiarrhythmic efficacy of a slow-release form of metoprolol was studied in 13 male coronary patients, mean age 47 years (39-59 years) with frequent and complex ventricular arrhythmias (couplets, salvos). The prospective, single-blind trial was based on 24 h Holter monitoring. In each case, the extent of coronary heart disease and the presence of old myocardial infarction was documented by coronary angiography. Initial treatment with placebo was followed by active treatment with 200 and 400 mg metoprolol per day, respectively, and placebo again during one week each. Thereafter, 200 mg metoprolol/24 h were administered over a period of one month. At the end of each treatment period, metoprolol plasma levels were determined simultaneously with the assessment of cardiac arrhythmias by Holter monitoring. Under a daily dose of 400 mg metoprolol, plasma levels increased from 235 +/- 326 (under 200 mg) to 841 +/- 613 mumol/l (p less than 0.001), and mean heart rate decreased from 75 to 63 bpm (p less than 0.001), the average number of ventricular extrasystoles decreased from 1,722 to 480/24 h (p less than 0.05) and the number of couplets from 38 to 7/24 h (p less than 0.05) when compared to the placebo period. After one month's treatment with 200 mg metoprolol per day, a significant reduction in heart rate from 75 to 67 bpm was observed (p less than 0.05); however, antiarrhythmic efficacy with regard to the number of premature ventricular contractions and couplets was insignificant.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对13名男性冠心病患者(平均年龄47岁,范围39 - 59岁)进行了缓释美托洛尔抗心律失常疗效的研究,这些患者有频发且复杂的室性心律失常(成对室早、短阵室速)。该前瞻性单盲试验基于24小时动态心电图监测。在每种情况下,通过冠状动脉造影记录冠心病的程度和陈旧性心肌梗死的情况。最初给予安慰剂治疗,随后分别给予每天200毫克和400毫克美托洛尔进行积极治疗,每种治疗后再给予一周安慰剂治疗。此后,每天200毫克美托洛尔持续给药一个月。在每个治疗期结束时,通过动态心电图监测评估心律失常的同时测定美托洛尔血浆水平。在每天400毫克美托洛尔剂量下,血浆水平从200毫克时的235±326微摩尔/升升至841±613微摩尔/升(p<0.001),平均心率从75次/分钟降至63次/分钟(p<0.001),与安慰剂期相比,室性早搏平均数量从每24小时1722次降至480次(p<0.05),成对室早数量从每24小时38次降至7次(p<0.05)。每天200毫克美托洛尔治疗一个月后,心率从75次/分钟显著降至67次/分钟(p<0.05);然而,关于室性早搏和成对室早数量的抗心律失常疗效不显著。(摘要截短于250字)

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