Recommendations for starting a grown up congenital heart disease (GUCH) unit.

Fernando Tadeu Vasconcelos Amaral, Paulo Henrique Manso, André Schmidt, Ricardo Nilson Sgarbieri, Walter Villela de Andrade Vicente, Clovis Carbone Junior, Jane Somerville
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Abstract

During the last decades, advances in diagnosis and treatment of congenital heart disease have allowed many individuals to reach adulthood. Due mainly to the great diagnostic diversity and to the co-morbidities usually present in this age group, these patients demand assistance in a multidisciplinary facility if an adequate attention is aimed. In this paper we reviewed, based in the international literature and also on the authors' experience, the structural conditions that should be available for these patients. We highlighted aspects like the facility characteristics, the criteria usually adopted for patient transfer from the paediatric setting, the composition of the medical and para- medical staff taking into account the specific problems, and also the model of outpatient and in-hospital assistance. We also emphasized the importance of patient data storage, the fundamental necessity of institutional support and also the compromise to offer professional training. The crucial relevance of clinical research is also approached, particularly the development of multicenter studies as an appropriate methodology for this heterogeneous patient population.

关于设立长大成人先天性心脏病(GUCH)病房的建议。
在过去的几十年里,先天性心脏病诊断和治疗的进步使许多人得以长大成人。主要由于诊断的多样性和这个年龄组通常存在的并发症,这些患者需要在多学科设施中得到帮助,才能得到足够的关注。在本文中,我们根据国际文献和作者的经验,回顾了这些患者应具备的结构条件。我们着重强调了设施的特点、从儿科转院病人通常采用的标准、考虑到特殊问题的医务人员和辅助医务人员的组成,以及门诊和院内援助模式等方面。我们还强调了病人数据储存的重要性、机构支持的基本必要性以及提供专业培训的折衷方案。此外,我们还探讨了临床研究的重要意义,特别是多中心研究的发展,将其作为针对这一异质性患者群体的适当方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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