Annals of Thoracic Medicine (Jan 2014)

Saudi Guidelines on the Diagnosis and Treatment of Pulmonary Hypertension: Pulmonary hypertension in children

  • Maha Al Dabbagh,
  • Hanna Banjar,
  • Nasser Galal,
  • Amjad Kouatli,
  • Hammam Kandil,
  • May Chehab

DOI
https://doi.org/10.4103/1817-1737.134053
Journal volume & issue
Vol. 9, no. 5
pp. 113 – 120

Abstract

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Pulmonary hypertension (PH) is relatively uncommon in children. Pulmonary arterial hypertension (PAH) in pediatric comprises a wide spectrum of diseases, from a transient neonatal condition to a progressive disease associated with morbidity and mortality. Most common PAH in pediatric are idiopathic (IPAH) or PAH associated with congenital heart disease (PAH-CHD), while other associated conditions, such as connective tissue disease (CTD), are less common in pediatrics. Despite better understanding of PH and the availability of new medications during recent decades; the diagnosis, investigation and choice of therapy remain a challenge in children, as evidence-based recommendations depend mainly on adult studies. In this review, we provide a detailed discussion about the distinctive features of PAH in pediatric, mainly emphacysing on classification and diagnostic algorithm.

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