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儿童失代偿性心力衰竭综合征的药物治疗:现状与新方法

Pharmaceutical management of decompensated heart failure syndrome in children: current state of the art and a new approach.

作者信息

Gazit Avihu Z, Oren Phineas P

机构信息

Avihu Z. Gazit, MD Pediatric Critical Care, Washington University School of Medicine, St. Louis Children's Hospital, Campus Box 8116-NWT, St. Louis, MO 63110, USA.

出版信息

Curr Treat Options Cardiovasc Med. 2009 Oct;11(5):403-9. doi: 10.1007/s11936-009-0042-4.

Abstract

Prompt initiation of appropriate and intensive treatment in children with decompensated heart failure is crucial to avoid irreversible end-organ dysfunction. Initial management of these children includes transfer to the pediatric cardiac intensive care unit, basic hemodynamic monitoring, and establishment of intravenous access. Inotropic support should be instituted peripherally before obtaining central venous and arterial access. The team should be prepared for emergent intubation and initiation of mechanical circulatory support. Two experienced physicians should work together to obtain vascular access and manage sedation, airway control, and cardiovascular support. Acute heart failure syndrome in children may be related to cardiomyopathy, myocarditis, congenital heart disease, and acute rejection post heart transplantation. Each of these causes requires a different approach. Fulminant myocarditis may lead to severe morbidity and requires intensive support, although its outcome is considered to be good. Acute heart failure related to newly diagnosed dilated cardiomyopathy may represent end-stage heart failure; therefore, long-term mechanical circulatory support and heart transplantation may be considered to avoid other end-organ dysfunction. Hypertrophic cardiomyopathy may lead to acute decompensation due to 1) left ventricular outflow obstruction, 2) restrictive physiology leading to pulmonary hypertension, or 3) myocardial ischemia associated with coronary artery bridging. Decompensated heart failure associated with congenital heart disease usually represents end-stage heart failure and requires thorough evaluation for heart transplantation. Children with single-ventricle physiology who develop decompensated heart failure after a Fontan procedure are not candidates for mechanical circulatory support and therefore may not survive to heart transplantation. Acute heart failure due to posttransplantation acute rejection requires aggressive antirejection treatment, which places these patients at significant risk for overwhelming opportunistic infections. In our opinion, mechanical circulatory support should be initiated early in children who present with end-stage heart failure associated with hemodynamic instability to avoid end-organ damage.

摘要

对失代偿性心力衰竭患儿及时启动恰当且强化的治疗对于避免不可逆的终末器官功能障碍至关重要。这些患儿的初始管理包括转至儿科心脏重症监护病房、进行基本的血流动力学监测以及建立静脉通路。在获得中心静脉和动脉通路之前,应先在外周给予正性肌力支持。团队应做好紧急插管和启动机械循环支持的准备。两名经验丰富的医生应共同努力获取血管通路并管理镇静、气道控制和心血管支持。儿童急性心力衰竭综合征可能与心肌病、心肌炎、先天性心脏病以及心脏移植后的急性排斥反应有关。这些病因中的每一种都需要不同的处理方法。暴发性心肌炎可能导致严重的发病情况,需要强化支持,尽管其预后被认为良好。与新诊断的扩张型心肌病相关的急性心力衰竭可能代表终末期心力衰竭;因此,可考虑长期机械循环支持和心脏移植以避免其他终末器官功能障碍。肥厚型心肌病可能由于以下原因导致急性失代偿:1)左心室流出道梗阻;2)导致肺动脉高压的限制性生理状态;或3)与冠状动脉桥接相关的心肌缺血。与先天性心脏病相关的失代偿性心力衰竭通常代表终末期心力衰竭,需要对心脏移植进行全面评估。在Fontan手术后发生失代偿性心力衰竭的单心室生理患儿不适合机械循环支持,因此可能无法存活至心脏移植。移植后急性排斥反应导致的急性心力衰竭需要积极的抗排斥治疗,这使这些患者面临严重的机会性感染风险。我们认为,对于出现与血流动力学不稳定相关的终末期心力衰竭的儿童,应尽早启动机械循环支持以避免终末器官损伤。

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