Pulmonary arterial hypertension related to congenital heart disease with a left-to-right shunt: phenotypic spectrum and approach to management

被引:3
|
作者
Ferrero, Paolo [1 ]
Constantine, Andrew [2 ]
Chessa, Massimo [1 ,3 ]
Dimopoulos, Konstantinos [4 ,5 ,6 ]
机构
[1] IRCCS Policlin San Donato, ACHD Unit, Milan, Italy
[2] Queen Elizabeth Hosp, Adult Congenital Heart Dis Unit, Birmingham, England
[3] Univ Vita Salute San Raffaele, Milan, Italy
[4] Royal Brompton Hosp, Adult Congenital Heart Ctr, London, England
[5] Royal Brompton Hosp, Ctr Pulm Hypertens, London, England
[6] Imperial Coll London, Natl Heart & Lung Inst, London, England
来源
关键词
pulmonary hypertension (PAH); congenital heart disease; left-right shunt; pathophysiology; management; EISENMENGER-SYNDROME; THERAPY; PERSPECTIVE; SURVIVAL; EXERCISE; ADULTS;
D O I
10.3389/fcvm.2024.1360555
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Patients with pulmonary hypertension associated with a left-right shunt include a wide spectrum of pathophysiological substrates, ranging from those characterized by pulmonary over-circulation to those with advanced pulmonary vascular disease. The former group may benefit from shunt repair in carefully selected cases but, when advanced pulmonary vascular disease has developed, defect closure should be avoided, and pulmonary vasodilators may be used to improve effort tolerance and hemodynamics. There is a paucity of evidence, however, to support decision-making in the care of these patients. We discuss the principles of management in patients with pulmonary hypertension and a predominant left-right shunt. The recommendations and statements made in this paper are based on pathophysiological considerations and expert opinion.
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页数:8
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