Pediatric pulmonary hypertension: diagnosis and management

被引:4
|
作者
Dadlani, Gul H. [1 ,2 ]
Sosa, Phil [2 ]
Cobb, Harrison [2 ]
Akshatha, Akshatha [2 ]
机构
[1] Johns Hopkins All Childrens Heart Inst, St Petersburg, FL 33701 USA
[2] Univ S Florida, Dept Pediat, Morsani Coll Med, Tampa, FL 33620 USA
关键词
endothelin-receptor antagonists; pediatrics; phosphodiesterase; 5; inhibitors; prostanoids; pulmonary hypertension; ARTERIAL-HYPERTENSION; RIGHT VENTRICLE; CHILDREN; TREPROSTINIL; METABOLISM; SILDENAFIL; SURVIVAL;
D O I
10.1097/HCO.0000000000000243
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of reviewThe article is intended to provide an overview of the most current modalities for the diagnosis and management of pulmonary hypertension in the pediatric population.Recent findingsThe WHO has recently updated the classification for pulmonary hypertension to include an expanded range of pediatric disease cohorts. We continue to gain knowledge of traditional pulmonary hypertension therapies (phosphodiesterase inhibitors, endothelin-receptor antagonists, and prostanoids) and remain optimistic that new therapeutic modalities [cyclic guanosine monophosphate (cGMP) stimulators, oral prostacyclins, and gene therapy] will lead to improved outcomes in pediatric patients.SummaryPediatric pulmonary hypertension is a heterogeneous disorder that has the potential to improve in some cases as children grow throughout childhood. Utilization of dedicated multidisciplinary teams of medical providers is necessary to deliver the highest level of medical care to this complex patient population. Ongoing development of enhanced screening protocols, novel disease-specific therapeutic targets, and comprehensive registries will hopefully lead to improved morbidity and mortality in the future.
引用
收藏
页码:78 / 87
页数:10
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