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

机译:建议开始长大的先天性心脏病(GUCH)单元

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摘要

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.
机译:在过去的几十年中,先天性心脏病的诊断和治疗的进步使许多人成年。由于主要的诊断多样性和该年龄段患者通常存在的合并症,因此如果要引起足够的重视,这些患者需要在多学科机构中提供帮助。在本文中,我们根据国际文献以及作者的经验,对这些患者应具备的结构条件进行了回顾。我们着重强调了以下方面:设施特征,通常从儿科环境转移患者的标准,考虑到具体问题的医务人员和准医务人员的组成以及门诊和住院协助的模式。我们还强调了患者数据存储的重要性,机构支持的基本必要性以及提供专业培训的妥协性。还探讨了临床研究的关键意义,特别是将多中心研究发展为这种异类患者群体的适当方法。

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