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Fontan 悖论的持续影响。

The Relentless Effects of the Fontan Paradox.

作者信息

Rychik Jack

机构信息

Single Ventricle Survivorship Program, The Children's Hospital of Philadelphia, Philadelphia, PA.

出版信息

Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu. 2016;19(1):37-43. doi: 10.1053/j.pcsu.2015.11.006.

Abstract

The Fontan operation is the anticipated palliative strategy for children born with single-ventricle type of congenital heart disease. As a result of important circulatory limitations, a series of end-organ complications are now increasingly recognized. Elevated central venous pressure and impaired cardiac output are the hallmarks of cavo-pulmonary flow, which result in a cascade of pathophysiological consequences. The Fontan circulation likely impacts all organ systems in an indolent and relentless manner, with progressive decline in functionality likely to occur in many. Liver fibrosis, altered bone density, decreased muscle mass, renal dysfunction, lymphatic insufficiency, and a host of other conditions are present. Standardized screening and evaluation of survivors as they grow through childhood and beyond is indicated and can be facilitated through dedicated multidisciplinary clinical programs. Invasive assessment at specific milestones can provide important actionable information to optimize individual status. More detailed characterization and understanding of these end-organ complications is necessary to contribute to the goal of achieving a normal duration and quality of life for these unique individuals.

摘要

Fontan手术是针对患有单心室型先天性心脏病儿童的预期姑息治疗策略。由于存在重要的循环限制,现在越来越多地认识到一系列终末器官并发症。中心静脉压升高和心输出量受损是腔肺分流的特征,会导致一系列病理生理后果。Fontan循环可能以隐匿且持续的方式影响所有器官系统,许多器官的功能可能会逐渐下降。存在肝纤维化、骨密度改变、肌肉量减少、肾功能不全、淋巴功能不全以及许多其他情况。建议对幸存者在童年及以后的成长过程中进行标准化筛查和评估,并且可以通过专门的多学科临床项目来促进。在特定时间节点进行侵入性评估可以提供重要的可采取行动的信息,以优化个体状况。为了实现这些特殊个体正常的寿命和生活质量这一目标,有必要对这些终末器官并发症进行更详细的特征描述和了解。

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