Congenital heart disease: types, pathophysiology, diagnosis, and treatment options

IF 10.7 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
MedComm Pub Date : 2024-07-05 DOI:10.1002/mco2.631
Xiao Meng, Ming Song, Kai Zhang, Weida Lu, Yunyi Li, Cheng Zhang, Yun Zhang
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引用次数: 0

Abstract

Congenital heart disease (CHD) is a structural abnormality of the heart and/or great vessels and patients with CHD are at an increased risks of various morbidities throughout their lives and reduced long-term survival. Eventually, CHD may result in various complications including heart failure, arrhythmias, stroke, pneumonia, and sudden death. Unfortunately, the exact etiology and pathophysiology of some CHD remain unclear. Although the quality of life and prognosis of patients with CHD have significantly improved following technological advancement, the influence of CHD is lifelong, especially in patients with complicated CHD. Thus, the management of CHD remains a challenge due to its high prevalence. Finally, there are some disagreements on CHD among international guidelines. In this review, we provide an update of the pathophysiology, diagnosis, and treatment in most common type of CHD, including patent foramen ovale, atrial septal defect, ventricular septal defect, atrioventricular septal defect, patent ductus arteriosus, coarctation of the aorta, transposition of the great arteries, congenitally corrected transposition of the great arteries, coronary anomalies, left and right ventricular outflow tract obstruction, tetralogy of Fallot and Ebstein anomaly. In particular, we focus on what is known and what is unknown in these areas, aiming to improve the current understanding of various types of CHD.

Abstract Image

先天性心脏病:类型、病理生理学、诊断和治疗方案
先天性心脏病(CHD)是指心脏和/或大血管的结构异常,患有先天性心脏病的患者一生中患各种疾病的风险会增加,长期存活率也会降低。最终,心脏病可能导致各种并发症,包括心力衰竭、心律失常、中风、肺炎和猝死。遗憾的是,某些心脏病的确切病因和病理生理学仍不清楚。虽然随着技术的进步,心脏瓣膜病患者的生活质量和预后得到了显著改善,但心脏瓣膜病的影响是终生的,尤其是对于复杂的心脏瓣膜病患者。因此,由于冠心病的高发病率,冠心病的治疗仍然是一项挑战。最后,国际指南对冠心病的认识也存在一些分歧。在这篇综述中,我们介绍了最常见类型的先天性心脏病的病理生理学、诊断和治疗的最新进展,包括卵圆孔未闭、房间隔缺损、室间隔缺损、房室间隔缺损、动脉导管未闭、主动脉瓣狭窄、动脉导管未闭、动脉导管未闭、动脉导管未闭、动脉导管未闭、动脉导管未闭、动脉导管未闭、动脉导管未闭、动脉导管未闭、动脉导管未闭、动脉导管未闭、大动脉转位、先天性矫正的大动脉转位、冠状动脉异常、左右心室流出道阻塞、法洛氏四联症和 Ebstein 异常。我们特别关注这些领域的已知和未知情况,旨在提高目前对各类先天性心脏病的认识。
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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来源期刊
CiteScore
6.70
自引率
0.00%
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0
审稿时长
10 weeks
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