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Published in: Current Cardiology Reports 12/2019

01-12-2019 | Bosentan | Congenital Heart Disease (RA Krasuski, Section Editor)

Management of Pulmonary Arterial Hypertension in the Pediatric Patient

Authors: Jordan E. Ezekian, Kevin D. Hill

Published in: Current Cardiology Reports | Issue 12/2019

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Abstract

Purpose of Review

Pediatric pulmonary arterial hypertension (PAH) is associated with significant morbidity and mortality. Herein we review the diagnosis and classification for pediatric PAH and detail the current therapeutic options available for use in the pediatric PAH population.

Recent Findings

Classification and treatment of pediatric PAH is guided by adult criteria and treatment algorithms, yet the distribution of factors contributing to PAH in children differs significantly from that seen in adults. It is necessary to understand these differences in order to appropriately tailor therapy to the needs of the child or adolescent. An expanding array of targeted PAH drugs are now approved for use in adults, and many of these drugs are used “off-label” to treat children and adolescents with PAH. Use of these novel therapies has coincided with marked improvement in outcomes, suggesting significant benefit. However, because most of these drugs have not been studied in rigorous randomized, controlled trials in children, it is critical that physicians understand their mechanisms of action, potential benefits, and safety profiles.

Summary

Pediatric PAH outcomes have improved substantially in the modern era, coinciding with the “off-label” use of targeted PAH drugs in children and adolescents. Ideally, care should be provided at centers with specialized expertise in the diagnosis and treatment of pediatric PAH by providers who understand the appropriate diagnostic algorithms, classification schemes, and treatment approaches.
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Metadata
Title
Management of Pulmonary Arterial Hypertension in the Pediatric Patient
Authors
Jordan E. Ezekian
Kevin D. Hill
Publication date
01-12-2019

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