Finn Waagstein and the paradigm shift in the treatment of heart failure with β-adrenergic receptor antagonists ('β-blockers').

IF 3.1 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Kristina Lorenz, Ursula Ravens
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引用次数: 0

Abstract

Beta-adrenergic receptor antagonists, formerly called 'β-blockers' (which name will be used throughout this historical review), were initially used for their antihypertensive, anti-ischemic, and antiarrhythmic effects. In the early 1970s, the Swedish cardiologist Finn Waagstein opposed the paradigm that β-blockers were contraindicated in patients with decompensated heart failure. This review retraces the exciting paths of Waagstein's personal fight for recognition of his successful therapy of cardiac decompensation in patients with acute myocardial infarction and also of heart failure. In the second part, we summarise the clinical trials that led to the slow acceptance by the scientific community of the paradigm shift from contraindication to first-line treatment with β-blockers in heart failure.

Finn Waagstein和β-肾上腺素能受体拮抗剂(“β-阻滞剂”)治疗心力衰竭的范式转变。
-肾上腺素能受体拮抗剂,以前称为“β受体阻滞剂”(该名称将在整个历史回顾中使用),最初用于抗高血压,抗缺血和抗心律失常作用。在20世纪70年代早期,瑞典心脏病学家芬恩·瓦格斯坦(Finn Waagstein)反对β受体阻滞剂禁忌用于失代偿性心力衰竭患者的范式。这篇综述回顾了Waagstein为获得对急性心肌梗死和心力衰竭患者心脏失代偿的成功治疗的认可而进行的激动人心的个人斗争。在第二部分中,我们总结了导致科学界缓慢接受从禁忌症到使用β受体阻滞剂治疗心力衰竭的一线治疗的临床试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.20
自引率
5.60%
发文量
142
审稿时长
4-8 weeks
期刊介绍: Naunyn-Schmiedeberg''s Archives of Pharmacology was founded in 1873 by B. Naunyn, O. Schmiedeberg and E. Klebs as Archiv für experimentelle Pathologie und Pharmakologie, is the offical journal of the German Society of Experimental and Clinical Pharmacology and Toxicology (Deutsche Gesellschaft für experimentelle und klinische Pharmakologie und Toxikologie, DGPT) and the Sphingolipid Club. The journal publishes invited reviews, original articles, short communications and meeting reports and appears monthly. Naunyn-Schmiedeberg''s Archives of Pharmacology welcomes manuscripts for consideration of publication that report new and significant information on drug action and toxicity of chemical compounds. Thus, its scope covers all fields of experimental and clinical pharmacology as well as toxicology and includes studies in the fields of neuropharmacology and cardiovascular pharmacology as well as those describing drug actions at the cellular, biochemical and molecular levels. Moreover, submission of clinical trials with healthy volunteers or patients is encouraged. Short communications provide a means for rapid publication of significant findings of current interest that represent a conceptual advance in the field.
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