Clinical pharmacology of the new beta-adrenergic blocking drugs. Part 5. Pindolol (LB-46) therapy for supraventricular arrhythmia: a viable alternative to propranolol in patients with bronchospasm

IF 3.5 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS American heart journal Pub Date : 1979-09-01 DOI:10.1016/0002-8703(79)90053-X
William Frishman M.D. , Richard Davis M.D., Joel Strom M.D., Uri Elkayam M.D., Morris Stampfer M.D., Hillel Ribner M.D., Jerome Weinstein M.D., Edmund Sonnenblick M.D.
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引用次数: 49

Abstract

Pindolol (LB-46) is a new beta-adrenoceptor blocking agent with intrinsic sympathomimetic activity. In order to evaluate the efficacy of pindolol in the treatment of patients with supraventricular arrhythmias and propranolol-induced bronchospasm, 18 patients with paroxysmal supraventricular tachycardia, atrial fibrillation, atrial flutter, multifocal atrial tachycardia or junctional tachycardia, were treated with placebo followed by pindolol in intravenous and then oral form. Following a no-response placebo period (in all patients), intravenous pindolol converted six out of seven patients with paroxysmal supraventricular tachycardia to normal sinus rhythm. In six patients with atrial fibrillation, three reverted to normal sinus rhythm, and three remained in atrial fibrillation but with a slower ventricular response (less than 100 beats/minute). Of two patients with atrial flutter, one converted to normal sinus rhythm, while the other patient failed to respond. Both patients with junctional tachycardia and one with multifocal atrial tachycardia converted to normal sinus rhythm. Long-term oral pindolol therapy sustained these responses in most patients, as documented by serial Holter ECG studies. There was no deterioration in indices of airway resistance (FEV1·0VC) in patients treated with pindolol (both intravenously and orally), in contrast to a marked deterioration in FEV1·0VC in the same patients treated with propranolol. Pindolol appears to be a reasonable substitute for propranolol in patients with bronchospastic illness who require beta-blockade for control of supraventricular arrhythmias.

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新型肾上腺素能阻断药的临床药理学研究。第5部分。品多洛尔(LB-46)治疗室上性心律失常:支气管痉挛患者普萘洛尔的可行替代方案
品多洛尔(LB-46)是一种具有内在拟交感神经活性的新型β -肾上腺素受体阻滞剂。为了评价品多洛尔治疗室上性心律失常和心得安诱发的支气管痉挛的疗效,对18例阵发性室上性心动过速、心房颤动、心房扑动、多灶性房性心动过速或结性心动过速患者,先给予安慰剂,再静脉滴注品多洛尔,再口服。在安慰剂无反应期(所有患者)后,静脉注射品多洛尔将7例阵发性室上性心动过速患者中的6例转化为正常窦性心律。在6例房颤患者中,3例恢复正常窦性心律,3例房颤仍存在,但心室反应较慢(小于100次/分钟)。2例心房扑动患者中,1例转为正常窦性心律,另1例无反应。2例交界性心动过速和1例多灶性房性心动过速均转化为正常窦性心律。长期口服品多洛尔治疗在大多数患者中维持了这些反应,正如一系列动态心电图研究所证明的那样。平多洛尔组(静脉和口服)气道阻力指标(FEV1·0VC)无明显恶化,而普萘洛尔组FEV1·0VC有明显恶化。对于需要β -阻断剂来控制室上性心律失常的支气管痉挛性疾病患者,品多洛尔似乎是普萘洛尔的合理替代品。
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来源期刊
American heart journal
American heart journal 医学-心血管系统
CiteScore
8.20
自引率
2.10%
发文量
214
审稿时长
38 days
期刊介绍: The American Heart Journal will consider for publication suitable articles on topics pertaining to the broad discipline of cardiovascular disease. Our goal is to provide the reader primary investigation, scholarly review, and opinion concerning the practice of cardiovascular medicine. We especially encourage submission of 3 types of reports that are not frequently seen in cardiovascular journals: negative clinical studies, reports on study designs, and studies involving the organization of medical care. The Journal does not accept individual case reports or original articles involving bench laboratory or animal research.
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