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美国国立心肺血液研究所成人先天性心脏病研究工作组报告。

Report of the National Heart, Lung, and Blood Institute Working Group on research in adult congenital heart disease.

作者信息

Williams Roberta G, Pearson Gail D, Barst Robyn J, Child John S, del Nido Pedro, Gersony Welton M, Kuehl Karen S, Landzberg Michael J, Myerson Merle, Neish Steven R, Sahn David J, Verstappen Amy, Warnes Carole A, Webb Catherine L

机构信息

Department of Pediatrics, Children's Hospital Los Angeles, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.

出版信息

J Am Coll Cardiol. 2006 Feb 21;47(4):701-7. doi: 10.1016/j.jacc.2005.08.074. Epub 2006 Jan 26.

Abstract

The Working Group on research in adult congenital heart disease (ACHD) was convened in September 2004 under the sponsorship of National Heart, Lung, and Blood Institute (NHLBI) and the Office of Rare Diseases, National Institutes of Health, Department of Health and Human Services, to make recommendations on research needs. The purpose of the Working Group was to advise the NHLBI on the current state of the science in ACHD and barriers to optimal clinical care, and to make specific recommendations for overcoming those barriers. The members of the Working Group were chosen to provide expert input on a broad range of research issues from both scientific and lay perspectives. The Working Group reviewed data on the epidemiology of ACHD, long-term outcomes of complex cardiovascular malformations, issues in assessing morphology and function with current imaging techniques, surgical and catheter-based interventions, management of related conditions including pregnancy and arrhythmias, quality of life, and informatics. After research and training barriers were discussed, the Working Group recommended outreach and educational programs for adults with congenital heart disease, a network of specialized adult congenital heart disease regional centers, technology development to support advances in imaging and modeling of abnormal structure and function, and a consensus on appropriate training for physicians to provide care for adults with congenital heart disease.

摘要

成人先天性心脏病(ACHD)研究工作组于2004年9月在美国国立卫生研究院(NIH)下属的国立心肺血液研究所(NHLBI)和罕见病办公室的赞助下召开会议,就研究需求提出建议。工作组的目的是就ACHD领域的科学现状和优化临床护理的障碍向NHLBI提供建议,并就克服这些障碍提出具体建议。工作组的成员经过挑选,以便从科学和非专业角度就广泛的研究问题提供专家意见。工作组审查了有关ACHD流行病学、复杂心血管畸形的长期预后、当前成像技术在评估形态和功能方面的问题、手术和基于导管的干预措施、包括妊娠和心律失常在内的相关病症的管理、生活质量以及信息学等方面的数据。在讨论了研究和培训障碍之后,工作组建议为先天性心脏病成人开展宣传和教育项目,建立一个成人先天性心脏病专科区域中心网络,开发支持异常结构和功能成像及建模进展的技术,并就为先天性心脏病成人提供护理的医生的适当培训达成共识。

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