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卡托普利在低肾素性充血性心力衰竭中的疗效:持续性反应性高肾素血症在区分反应者与无反应者中的重要性。

Efficacy of captopril in low-renin congestive heart failure: importance of sustained reactive hyperreninemia in distinguishing responders from nonresponders.

作者信息

Packer M, Medina N, Yushak M

出版信息

Am J Cardiol. 1984 Oct 1;54(7):771-7. doi: 10.1016/s0002-9149(84)80206-4.

DOI:10.1016/s0002-9149(84)80206-4
PMID:6091434
Abstract

To determine the efficacy of converting-enzyme inhibition in patients with low-renin congestive heart failure (CHF), the long-term hemodynamic and clinical responses to captopril were evaluated in 26 consecutive patients with severe, chronic CHF whose pretreatment plasma renin activity (PRA) was less than 2 ng/ml/hour. After 2 to 8 weeks of continuous treatment with captopril, 14 patients (54%) showed long-term hemodynamic benefits, of whom 13 (50%) improved clinically by at least 1 New York Heart Association functional class. To distinguish responders from nonresponders, patients were grouped based on the presence or absence of sustained reactive hyperreninemia (PRA during chronic therapy greater than 4 ng/ml/hour). After 2 to 8 weeks of therapy with captopril, 14 patients had sustained reactive hyperreninemia. Their cardiac index increased by 0.33 liters/min/m2 (p less than 0.01), left ventricular filling pressure decreased by 12.6 mm Hg (p less than 0.001), mean right atrial pressure decreased by 4.9 mm Hg (p less than 0.001) and systemic vascular resistance decreased by 529 dyne s cm-5 (p less than 0.001). Twelve of these 14 patients improved clinically. Twelve other patients had no reactive increase in PRA, and these patients showed no significant improvement in any hemodynamic variable after 2 to 8 weeks of treatment with captopril; only 1 of the 12 patients improved clinically (p less than 0.001 between groups). The 2 groups were otherwise similar with regard to pretreatment demographic, hemodynamic and hormonal variables.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

为了确定转换酶抑制对低肾素性充血性心力衰竭(CHF)患者的疗效,我们对26例严重慢性CHF患者进行了研究,这些患者治疗前血浆肾素活性(PRA)低于2 ng/ml/小时,评估了他们对卡托普利的长期血流动力学和临床反应。在接受卡托普利持续治疗2至8周后,14例患者(54%)显示出长期血流动力学益处,其中13例(50%)临床改善至少达1个纽约心脏协会功能分级。为了区分反应者和无反应者,根据慢性治疗期间是否存在持续性反应性高肾素血症(PRA大于4 ng/ml/小时)对患者进行分组。在接受卡托普利治疗2至8周后,14例患者出现持续性反应性高肾素血症。他们的心脏指数增加了0.33升/分钟/平方米(p<0.01),左心室充盈压降低了12.6毫米汞柱(p<0.001),平均右心房压降低了4.9毫米汞柱(p<0.001),全身血管阻力降低了529达因·秒/厘米⁻⁵(p<0.001)。这14例患者中有12例临床改善。另外12例患者PRA无反应性升高,在接受卡托普利治疗2至8周后,这些患者的任何血流动力学变量均无显著改善;12例患者中只有1例临床改善(两组间p<0.001)。两组在治疗前的人口统计学、血流动力学和激素变量方面其他方面相似。(摘要截断于250字)

相似文献

1
Efficacy of captopril in low-renin congestive heart failure: importance of sustained reactive hyperreninemia in distinguishing responders from nonresponders.卡托普利在低肾素性充血性心力衰竭中的疗效:持续性反应性高肾素血症在区分反应者与无反应者中的重要性。
Am J Cardiol. 1984 Oct 1;54(7):771-7. doi: 10.1016/s0002-9149(84)80206-4.
2
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Quantitative differences in the hemodynamic effects of captopril and nitroprusside in severe chronic heart failure.卡托普利和硝普钠对重度慢性心力衰竭血流动力学影响的定量差异。
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Coronary hemodynamic effects of angiotensin inhibition by captopril and teprotide in patients with congestive heart failure.卡托普利和替普罗肽对充血性心力衰竭患者血管紧张素抑制的冠状动脉血流动力学效应。
Am J Cardiol. 1982 Nov;50(5):967-72. doi: 10.1016/0002-9149(82)90403-9.

引用本文的文献

1
Effect of captopril on renin and blood pressure in cirrhosis.卡托普利对肝硬化患者肾素及血压的影响。
Eur J Clin Pharmacol. 1987;33(3):249-54. doi: 10.1007/BF00637557.
2
Captopril. An update of its pharmacodynamic and pharmacokinetic properties, and therapeutic use in hypertension and congestive heart failure.卡托普利。其药效学和药代动力学特性的最新进展,以及在高血压和充血性心力衰竭中的治疗应用。
Drugs. 1988 Nov;36(5):540-600. doi: 10.2165/00003495-198836050-00003.
3
Enalapril: a review of human pharmacology.依那普利:人体药理学综述。
Drugs. 1985;30 Suppl 1:13-24. doi: 10.2165/00003495-198500301-00004.
4
Vasodilator therapy without converting-enzyme inhibition in congestive heart failure--usefulness and limitations.充血性心力衰竭中不使用血管紧张素转换酶抑制剂的血管扩张剂治疗——效用与局限性
Cardiovasc Drugs Ther. 1989 Jun;3(3):375-96. doi: 10.1007/BF01858109.
5
Acute hemodynamic effects of converting enzyme inhibition in children with intracardiac shunts.
Pediatr Cardiol. 1992 Jul;13(3):129-35. doi: 10.1007/BF00793943.