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血管紧张素转换酶抑制。治疗高血压和充血性心力衰竭的独特而有效的疗法。

Angiotensin converting enzyme inhibition. Unique and effective therapy for hypertension and congestive heart failure.

作者信息

DiBianco R

出版信息

Postgrad Med. 1985 Oct;78(5):229-41, 244, 247-8. doi: 10.1080/00325481.1985.11699167.

Abstract

Major developments in the use of angiotensin converting enzyme (ACE) inhibition for the treatment of hypertension and congestive heart failure have occurred since the discovery of captopril in June 1975. Early in the past decade, this oral ACE inhibitor was restricted to refractory and severe cases of hypertension. By July 1985, the Food and Drug Administration approved its use not only for all degrees of hypertension but also for the initial treatment of hypertensive patients with uncomplicated disease. New information has confirmed the effectiveness of twice-daily administration (which favorably influences compliance) and the lack of a need to monitor blood or urine levels to assure safety. The renin-mediated and non-renin-mediated mechanisms of action of captopril-induced ACE inhibition have been fully delineated, as has its side effect profile, which does not include various CNS, sympathetic reflex, and metabolic side effects seen with other antihypertensive agents. As the first vasodilator to prove its efficacy in the acute and chronic treatment of congestive heart failure to the FDA, captopril is now widely used throughout the United States. ACE inhibition reduces symptoms, enhances exercise capacity, and favorably affects sodium, water, and potassium homeostasis in patients with heart failure. Also, recent but as yet unconfirmed evidence suggests that ACE inhibition may prolong survival in these patients. The success of captopril, the first oral agent of this class, promises to hold true for other ACE inhibitors (such as enalapril), which have similar activities but differing pharmacokinetic properties and will soon be available for clinical use. Further information on these newer agents is anxiously awaited. In the near future, the clinician will undoubtedly be able to choose from a large selection of ACE inhibitors for the treatment of hypertension and heart failure. Therefore, it is important to learn about any meaningful differences among ACE inhibitors and to contrast this class of agents with older, standard therapies. This learning process is crucial as we assess whether newer agents offer clinical advantages over the old.

摘要

自1975年6月发现卡托普利以来,血管紧张素转换酶(ACE)抑制剂在治疗高血压和充血性心力衰竭方面取得了重大进展。在过去十年的早期,这种口服ACE抑制剂仅限于难治性和重度高血压病例。到1985年7月,美国食品药品监督管理局批准其不仅可用于所有程度的高血压,还可用于无并发症高血压患者的初始治疗。新的信息证实了每日两次给药的有效性(这有利于提高依从性),并且无需监测血液或尿液水平来确保安全性。卡托普利诱导的ACE抑制的肾素介导和非肾素介导的作用机制已得到充分阐明,其副作用谱也是如此,该副作用谱不包括其他抗高血压药物所见的各种中枢神经系统、交感反射和代谢副作用。作为第一个向美国食品药品监督管理局证明其在充血性心力衰竭急性和慢性治疗中疗效的血管扩张剂,卡托普利现在在美国广泛使用。ACE抑制可减轻症状、增强运动能力,并对心力衰竭患者的钠、水和钾稳态产生有利影响。此外,最近但尚未得到证实的证据表明,ACE抑制可能会延长这些患者的生存期。这类药物中的第一个口服制剂卡托普利的成功,有望适用于其他具有相似活性但药代动力学特性不同且即将用于临床的ACE抑制剂(如依那普利)。人们急切期待有关这些新型药物的更多信息。在不久的将来,临床医生无疑将能够从众多ACE抑制剂中进行选择,用于治疗高血压和心力衰竭。因此,了解ACE抑制剂之间的任何有意义的差异,并将这类药物与旧的标准疗法进行对比非常重要。在我们评估新型药物是否比旧药物具有临床优势时,这个学习过程至关重要。

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