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治疗左心发育不全综合征的资源与成本考量

Resource and cost considerations in treating hypoplastic left heart syndrome.

作者信息

Urencio Miguel, Greenleaf Chris, Salazar Jorge D, Dodge-Khatami Ali

机构信息

Division of Cardiothoracic Surgery.

Children's Heart Center, University of Mississippi Medical Center, Jackson, MS, USA.

出版信息

Pediatric Health Med Ther. 2016 Nov 16;7:149-153. doi: 10.2147/PHMT.S98327. eCollection 2016.

Abstract

Hypoplastic left heart syndrome (HLHS) was a uniformly fatal diagnosis before 1983, when surgical treatment was first undertaken with the Norwood I operation as the first of 3-staged operations. Since then, operative survival rate of stage I has risen from 53% to over 90% in the current era, not only thanks to technical advances in surgery but also through prenatal diagnosis and imaging, enhanced cardiopulmonary bypass technology, better perioperative intensive care, and closer interstage monitoring. The improvements in patient outcomes achieved through rigorous multidisciplinary teamwork have come at a tremendous cost in manpower and resources, making HLHS still a challenge to all congenital heart programs, established or emerging. We review the various surgical steps to treat HLHS and their current expected outcomes, and put into perspective cost considerations compared to other more "simple" congenital heart defects.

摘要

左心发育不全综合征(HLHS)在1983年以前一直是一种必死无疑的诊断,当时首次采用诺伍德I型手术作为三期手术中的第一步进行外科治疗。从那时起,I期手术的生存率在当前时代已从53%提高到90%以上,这不仅得益于外科技术的进步,还得益于产前诊断和成像、改进的体外循环技术、更好的围手术期重症监护以及更密切的阶段间监测。通过严格的多学科团队合作实现的患者预后改善付出了巨大的人力和资源成本,这使得HLHS对所有先天性心脏病项目(无论是已成熟的还是新兴的)来说仍然是一个挑战。我们回顾了治疗HLHS的各种手术步骤及其当前预期结果,并与其他更“简单”的先天性心脏病缺陷相比,对成本考量进行了分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cf4/5683290/d23b92cc1503/phmt-7-149Fig1.jpg

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