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失代偿性心力衰竭患者的药物治疗。

Drug treatment of patients with decompensated heart failure.

作者信息

Mills R M, Hobbs R E

机构信息

The Section of Clinical Cardiology and the Kaufman Center for Heart Failure, Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA.

出版信息

Am J Cardiovasc Drugs. 2001;1(2):119-25. doi: 10.2165/00129784-200101020-00005.

Abstract

Decompensated heart failure (HF) may be defined as sustained deterioration of at least one New York Heart Association functional class, usually with evidence of sodium retention. Episodes of decompensation are most commonly precipitated by sodium retention, often associated with medication noncompliance. Our therapeutic approach to hospitalized patients is based on the documented hemodynamic responses to vasodilator therapy, with redistribution of mitral regurgitant flow to forward cardiac output and decompression of the left atrium. Invasive hemodynamic monitoring is seldom required for the effective management of patients with HF and there are risks associated with pulmonary artery catheterization. The currently available parenteral vasoactive drugs for decompensated heart failure include: (i) vasodilators such as nesiritide, nitroprusside and nitroglycerin (glyceryl trinitrate); (ii) catecholamine inotropes, primarily dobutamine; and (iii) inodilators such as milrinone, a phosphodiesterase inhibitor. Vasodilators are most appropriate for those patients who are primarily volume-overloaded, but with adequate peripheral perfusion. In this class of agents, nesiritide (recombinant human B-type natriuretic peptide) offers advantages over currently available drugs. Nesiritide produces rapid and sustained decreases in right atrial and pulmonary capillary wedge pressures, with reduction in pulmonary and systemic vascular resistance and increases in cardiac index. The hemodynamic effects of nesiritide infusion were sustained over a duration of 1 week and the drug may be used without intensive monitoring in patients with decompensated HF. Treatment with dobutamine is indicated in patients in whom low cardiac output rather than elevated pulmonary pressure is the primary hemodynamic aberration. However, milrinone reduces left atrial congestion more effectively than dobutamine, and is well tolerated and effective when used in patients receiving beta-blockers. In-patient therapy for decompensated HF is a short term exercise for symptom relief and provides an opportunity to re-assess management in the continuum of care.

摘要

失代偿性心力衰竭(HF)可定义为纽约心脏协会功能分级中至少一项持续恶化,通常伴有钠潴留证据。失代偿发作最常见的诱因是钠潴留,常与药物治疗依从性差有关。我们对住院患者的治疗方法基于已记录的血管扩张剂治疗的血流动力学反应,使二尖瓣反流血流重新分布至心输出量增加,并使左心房减压。对于HF患者的有效管理,很少需要有创血流动力学监测,而且肺动脉导管插入术存在风险。目前可用于失代偿性心力衰竭的肠外血管活性药物包括:(i)血管扩张剂,如奈西立肽、硝普钠和硝酸甘油(三硝酸甘油酯);(ii)儿茶酚胺类正性肌力药,主要是多巴酚丁胺;(iii)血管扩张性正性肌力药,如米力农,一种磷酸二酯酶抑制剂。血管扩张剂最适合那些主要存在容量超负荷但外周灌注充足的患者。在这类药物中,奈西立肽(重组人B型利钠肽)比现有药物具有优势。奈西立肽可使右心房和肺毛细血管楔压迅速且持续降低,同时降低肺血管和体循环血管阻力,并增加心脏指数。奈西立肽输注的血流动力学效应可持续1周,对于失代偿性HF患者,使用该药物时无需进行强化监测。多巴酚丁胺适用于以低心输出量而非肺动脉压升高为主要血流动力学异常的患者。然而,米力农比多巴酚丁胺更有效地减轻左心房淤血,并且在用于接受β受体阻滞剂治疗的患者时耐受性良好且效果显著。失代偿性HF的住院治疗是缓解症状的短期措施,并且为在连续护理过程中重新评估管理提供了机会。

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