Congenital Heart Disease and Pulmonary Hypertension

被引：13

作者：

Constantine, Andrew ^{[1
,2
,3
]}

Dimopoulos, Konstantinos ^{[1
,2
,3
]}

Opotowsky, Alexander R. ^{[4
]}

机构：

[1] Royal Brompton & Harefield NHS Fdn Trust, Royal Brompton Hosp, Adult Congenital Heart Ctr, Sydney St, London SW3 6NP, England

[2] Royal Brompton & Harefield NHS Fdn Trust, Royal Brompton Hosp, Natl Ctr Pulm Hypertens, Sydney St, London SW3 6NP, England

[3] Imperial Coll London, Natl Heart & Lung Inst, Guy Scadding Bldg,Cale St, London SW3 6LY, England

[4] Univ Cincinnati, Cincinnati Childrens Hosp, Dept Pediat, Heart Inst,Coll Med, Cincinnati, OH 45229 USA

来源：

CARDIOLOGY CLINICS | 2020年 / 38卷 / 03期

关键词：

Pulmonary hypertension; Adult congenital heart disease; Precapillary; Postcapillary; Echocardiography; Cardiac catheterization; Eisenmenger syndrome; VENTRICULAR SEPTAL-DEFECTS; ARTERIAL-HYPERTENSION; EISENMENGER-SYNDROME; EXERCISE CAPACITY; DOUBLE-BLIND; FONTAN PATIENTS; ADULTS; BOSENTAN; THERAPY; IMPACT;

D O I：

10.1016/j.ccl.2020.04.008

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Pulmonary hypertension (PH) is common in adults with congenital heart disease and carries fundamental implications for management and prognosis. A high index of suspicion, combined with knowledge of the pathogenesis and pathophysiology of PH, is required to achieve a timely, accurate diagnosis, and appropriate classification and treatment. This article provides a guide on how to approach the adult with congenital heart disease and suspected PH of different types, including current management.

引用

页码：445 / +

页数：13

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