Why the study?
Due to a limited number of robust pediatric clinical trials, treatment recommendations for pediatric pulmonary hypertension are often based on limited data or clinical experience.
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This review highlights practical aspects and expanding experience in the use of pharmacotherapies for pediatric pulmonary arterial hypertension, emphasizing the need for multidisciplinary care.
Pediatric pulmonary hypertension (PAH) is a rare disease that carries a poor prognosis if left untreated. Although there are published guidelines for the treatment of children with pulmonary hypertension, due to the limited number of robust pediatric clinical trials, recommendations are often based on limited data or clinical experience. Furthermore, many practical aspects of care, particularly for the pediatric patient, are learned through experience and best navigated with a multidisciplinary team. While newer PAH therapies have been approved for adults, there is still limited but expanding experience in pediatrics. This new information will help improve the targets of goal-oriented therapy. Lastly, this review highlights practical aspects in the use of the different therapies available for the treatment of pediatric pulmonary hypertension.
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Kam et al. (2020) studied this question.
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