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心力衰竭的管理与新疗法的范围:xamoterol 起什么作用?

The management of heart failure and the scope for new therapies: what role for xamoterol?

作者信息

Campbell R W

机构信息

Department of Cardiology, Freeman Hospital, Newcastle upon Tyne.

出版信息

Br J Clin Pharmacol. 1989;28 Suppl 1(Suppl 1):59S-64S. doi: 10.1111/j.1365-2125.1989.tb03574.x.

DOI:10.1111/j.1365-2125.1989.tb03574.x
PMID:2572256
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1379877/
Abstract
  1. Current therapy of heart failure leaves much to be desired. Not all patients respond, and many agents lose their effects with time. 2. Newer agents may be effective but toxic, and some which have a beneficial action when given intravenously have proved disappointing when used orally. 3. The value of digoxin in patients in sinus rhythm is open to debate, and diuretics, although useful acutely in reducing fluid overload, do not appear to improve prognosis. 4. Vasodilators increase effort capacity and reduce symptoms, possibly conferring some long-term benefit, and angiotensin converting enzyme (ACE) inhibitors improve symptoms and decrease mortality in a wide range of patients. 5. Positive inotropes may be effective in the short term, but they increase myocardial oxygen demand and show tachyphylaxis with no prognostic benefit. 6. Xamoterol (Corwin, Carwin, Corwil, Xamtol, ICI 118,587) is a partial sympathetic agonist with approximately 50% of the activity of a pure agonist, which provides inotropic support at rest, and protection against excess sympathetic activity on exercise. 7. It is compatible with other therapies and has shown no serious toxicity. 8. It should be considered at present as an adjunct to diuretic and/or ACE inhibitor therapy, although it may be useful alone; its role will become clearer as its effects on mortality are established.
摘要
  1. 目前心力衰竭的治疗仍有许多不尽人意之处。并非所有患者都有反应,而且许多药物会随着时间推移失去疗效。2. 新型药物可能有效但有毒性,一些静脉给药时有有益作用的药物经口服使用后却令人失望。3. 地高辛对窦性心律患者的价值存在争议,利尿剂虽然在急性情况下有助于减轻液体负荷过重,但似乎并不能改善预后。4. 血管扩张剂可增加运动耐力并减轻症状,可能带来一些长期益处,而血管紧张素转换酶(ACE)抑制剂可改善症状并降低各类患者的死亡率。5. 正性肌力药短期内可能有效,但会增加心肌氧需求并出现快速耐受性,且对预后无益处。6. 扎莫特罗(科温、卡温、科尔威尔、扎姆托尔、ICI 118,587)是一种部分交感神经激动剂,其活性约为纯激动剂的50%,可在静息时提供正性肌力支持,并防止运动时交感神经活动过度。7. 它可与其他疗法联合使用,且未显示出严重毒性。8. 目前应将其视为利尿剂和/或ACE抑制剂治疗的辅助药物,尽管它单独使用可能也有用;随着其对死亡率影响的确立,其作用将更加明确。

相似文献

1
The management of heart failure and the scope for new therapies: what role for xamoterol?心力衰竭的管理与新疗法的范围:xamoterol 起什么作用?
Br J Clin Pharmacol. 1989;28 Suppl 1(Suppl 1):59S-64S. doi: 10.1111/j.1365-2125.1989.tb03574.x.
2
Long-term studies with xamoterol in heart failure.关于xamoterol治疗心力衰竭的长期研究。
Br J Clin Pharmacol. 1989;28 Suppl 1(Suppl 1):53S-58S. doi: 10.1111/j.1365-2125.1989.tb03573.x.
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Xamoterol, a beta 1-adrenoceptor partial agonist: review of the clinical efficacy in heart failure.扎莫特罗,一种β1肾上腺素能受体部分激动剂:心力衰竭临床疗效综述
Br J Clin Pharmacol. 1989;28 Suppl 1(Suppl 1):23S-30S. doi: 10.1111/j.1365-2125.1989.tb03570.x.
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Focus on diastolic dysfunction: a new approach to heart failure therapy.关注舒张功能障碍:心力衰竭治疗的新方法。
Br J Clin Pharmacol. 1989;28 Suppl 1(Suppl 1):41S-52S. doi: 10.1111/j.1365-2125.1989.tb03572.x.
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Clinical experience of therapy with xamoterol in patients with severe systolic and diastolic dysfunction.沙美特罗治疗严重收缩和舒张功能障碍患者的临床经验。
Eur Heart J. 1990 Apr;11 Suppl A:33-8. doi: 10.1093/eurheartj/11.suppl_a.33.
6
Effects of xamoterol on resting and exercise haemodynamics in patients with chronic heart failure.羟甲异丁肾上腺素对慢性心力衰竭患者静息和运动血流动力学的影响。
Br J Clin Pharmacol. 1989;28 Suppl 1(Suppl 1):15S-22S.
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The pharmacology of xamoterol: a basis for modulation of the autonomic control of the heart.昔莫特罗的药理学:心脏自主控制调节的基础。
Br J Clin Pharmacol. 1989;28 Suppl 1(Suppl 1):3S-13S. doi: 10.1111/j.1365-2125.1989.tb03569.x.
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[Role of adrenergic beta receptor partial agonists in left ventricular failure of ischemic origin. Value of xamoterol (ICI 118,587, Corwin)].肾上腺素能β受体部分激动剂在缺血性左心室衰竭中的作用。扎莫特罗(ICI 118,587,科温)的价值
Ann Med Interne (Paris). 1985;136(3):247-50.
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Beta, partial agonists to treat heart failure: effects of xamoterol upon cardiac function and clinical status.β受体部分激动剂治疗心力衰竭:扎莫特罗对心功能和临床状况的影响。
Clin Cardiol. 1990 Mar;13(3):171-6. doi: 10.1002/clc.4960130305.
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Treatment of congestive heart failure--state of the art and future trends.充血性心力衰竭的治疗——现状与未来趋势。
Br J Clin Pharmacol. 1989;28 Suppl 1(Suppl 1):31S-39S. doi: 10.1111/j.1365-2125.1989.tb03571.x.

本文引用的文献

1
Vasodilator drug therapy in congestive heart failure.充血性心力衰竭的血管扩张剂药物治疗
Curr Probl Cardiol. 1982 Nov;7(8):1-42. doi: 10.1016/0146-2806(82)90017-2.
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Activity of the sympathetic nervous system and renin-angiotensin system assessed by plasma hormone levels and their relation to hemodynamic abnormalities in congestive heart failure.通过血浆激素水平评估交感神经系统和肾素-血管紧张素系统的活性及其与充血性心力衰竭血流动力学异常的关系。
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Heart failure in outpatients: a randomized trial of digoxin versus placebo.门诊患者的心力衰竭:地高辛与安慰剂的随机试验。
N Engl J Med. 1982 Mar 25;306(12):699-705. doi: 10.1056/NEJM198203253061202.
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Mechanisms governing the postural response and baroreceptor abnormalities in chronic congestive heart failure: effects of acute and long-term converting-enzyme inhibition.慢性充血性心力衰竭中姿势反应和压力感受器异常的调控机制:急性和长期血管紧张素转换酶抑制的作用
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Effects of intravenous nitroglycerin on ventricular ectopic beats in acute myocardial infarction.
Am Heart J. 1984 May;107(5 Pt 1):940-4. doi: 10.1016/0002-8703(84)90832-9.
6
Captopril in heart failure. A double blind controlled trial.卡托普利治疗心力衰竭。一项双盲对照试验。
Br Heart J. 1984 Nov;52(5):530-5. doi: 10.1136/hrt.52.5.530.
7
Plasma norepinephrine as a guide to prognosis in patients with chronic congestive heart failure.血浆去甲肾上腺素作为慢性充血性心力衰竭患者预后的一项指标。
N Engl J Med. 1984 Sep 27;311(13):819-23. doi: 10.1056/NEJM198409273111303.
8
Increased plasma arginine vasopressin levels in patients with congestive heart failure.充血性心力衰竭患者血浆精氨酸加压素水平升高。
J Am Coll Cardiol. 1983 Jun;1(6):1385-90. doi: 10.1016/s0735-1097(83)80040-0.
9
Decreased catecholamine sensitivity and beta-adrenergic-receptor density in failing human hearts.衰竭的人类心脏中儿茶酚胺敏感性和β-肾上腺素能受体密度降低。
N Engl J Med. 1982 Jul 22;307(4):205-11. doi: 10.1056/NEJM198207223070401.
10
Beneficial effects of long-term beta-blockade in congestive cardiomyopathy.长期使用β受体阻滞剂对充血性心肌病的有益作用。
Br Heart J. 1980 Aug;44(2):117-33. doi: 10.1136/hrt.44.2.117.