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充血性心力衰竭:初始治疗应该是什么以及为什么?

Congestive heart failure: what should be the initial therapy and why?

作者信息

Chatterjee Kanu

机构信息

Chatterjee Center for Cardiac Research, Moffitt/Long Hospital, University of California, San Francisco, California 94143-0124, USA.

出版信息

Am J Cardiovasc Drugs. 2002;2(1):1-6. doi: 10.2165/00129784-200202010-00001.

Abstract

Left ventricular systolic dysfunction is associated with neurohormonal activation which contributes to progressive ventricular remodeling and worsening clinical heart failure. Renin-angiotensin-aldosterone and sympathetic nervous systems are activated, not only in patients with clinically overt heart failure, but also in patients with asymptomatic or minimally symptomatic left ventricular systolic dysfunction. Activation of the angiotensin and adrenergic systems produces deleterious effects on systemic and coronary hemodynamics, promotes myocyte hypertrophy and fibroblast growth, and myocyte necrosis and apoptosis. Thus, therapy of heart failure should consist of pharmacologic agents not only to relieve symptoms but also to prevent and attenuate ventricular remodeling and progressive heart failure, thereby improving prognosis. In patients who are symptomatic, ACE inhibitors along with digitalis and diuretics as initial therapy (triple therapy) have the greater potential to improve exercise tolerance and decrease the incidence of treatment failure compared with diuretics alone or a combination of diuretics and digitalis. Diuretics alone should not be considered for long-term therapy as plasma renin activity, angiotensin II, aldosterone, norepinephrine and vasopressin levels may increase. ACE inhibitors decrease mortality in patients with heart failure resulting from left ventricular systolic dysfunction. The results of presently available studies indicate that angiotensin II receptor blockers (ARBs) do not provide any advantage over ACE inhibitors regarding survival benefit but may be better tolerated. Long-term adrenergic inhibition with the use of ss-adrenoceptor antagonists added to ACE inhibitors is associated with attenuation of ventricular remodeling, improvement in ventricular function and clinical class and survival of patients with symptomatic systolic left ventricular failure. Thus, initial pharmacotherapy for systolic heart failure should consist of: maximal tolerated dosages of ACE inhibitors;ARBs if ACE inhibitors are not tolerated because of intractable cough or angioedema;adequate dosages of hydralazine and isosorbide dinitrate if ACE inhibitors or ARBs are not tolerated; relatively low dosages of digoxin (serum concentrations of < or = 1.0 ng/dl) if not contraindicated; and diuretics to relieve congestive symptoms. Addition of spironolactone to ACE inhibitors can result in a significant reduction in the risk of sudden death in patients with symptomatic severe heart failure. Myocardial infarction resulting from ischemic heart disease is the most common cause of systolic left ventricular failure and the therapeutic modalities with potential to reduce the risks of myocardial infraction, such as risk factor modification, adequate control of diabetes and hypertension, antiplatelet agents and lipid-lowering agents, should also be included in the initial therapy.

摘要

左心室收缩功能障碍与神经激素激活有关,这会导致进行性心室重塑和临床心力衰竭恶化。肾素 - 血管紧张素 - 醛固酮系统和交感神经系统被激活,不仅在临床上明显心力衰竭的患者中如此,在无症状或症状轻微的左心室收缩功能障碍患者中也是如此。血管紧张素和肾上腺素能系统的激活对全身和冠状动脉血流动力学产生有害影响,促进心肌细胞肥大和成纤维细胞生长,以及心肌细胞坏死和凋亡。因此,心力衰竭的治疗应包括药物治疗,不仅要缓解症状,还要预防和减轻心室重塑及进行性心力衰竭,从而改善预后。对于有症状的患者,与单独使用利尿剂或利尿剂与洋地黄联合使用相比,初始治疗采用血管紧张素转换酶抑制剂(ACE抑制剂)联合洋地黄和利尿剂(三联疗法)更有潜力提高运动耐量并降低治疗失败的发生率。单独使用利尿剂不应被视为长期治疗方法,因为血浆肾素活性、血管紧张素II、醛固酮、去甲肾上腺素和加压素水平可能会升高。ACE抑制剂可降低因左心室收缩功能障碍导致心力衰竭患者的死亡率。目前现有研究结果表明,血管紧张素II受体阻滞剂(ARB)在生存获益方面并不比ACE抑制剂有任何优势,但可能耐受性更好。在ACE抑制剂基础上使用β - 肾上腺素能受体拮抗剂进行长期肾上腺素能抑制与心室重塑的减轻、心室功能改善、临床分级改善以及有症状的收缩性左心室衰竭患者的生存率提高有关。因此,收缩性心力衰竭的初始药物治疗应包括:最大耐受剂量的ACE抑制剂;如果因顽固性咳嗽或血管性水肿而不能耐受ACE抑制剂,则使用ARB;如果不能耐受ACE抑制剂或ARB,则使用足够剂量的肼屈嗪和硝酸异山梨酯;如果无禁忌证,使用相对低剂量的地高辛(血清浓度≤1.0 ng/dl);以及使用利尿剂缓解充血症状。在ACE抑制剂基础上加用螺内酯可显著降低有症状的严重心力衰竭患者猝死的风险。缺血性心脏病导致的心肌梗死是收缩性左心室衰竭最常见的原因,初始治疗还应包括有可能降低心肌梗死风险的治疗方法,如危险因素修正、充分控制糖尿病和高血压、抗血小板药物和降脂药物。

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