[Adenosine for pulmonary vasodilator testing in children with idiopathic pulmonary arterial hypertension]

Li-jun Fu1, Ai-qing Zhou, Ying Guo

  • 1Department of Cardiology, Shanghai Children's Medical Center, Medical College of Shanghai Jiao Tong University, Shanghai 200127, China.

Insights

Adenosine effectively assesses pulmonary vasodilator reserve in pediatric idiopathic pulmonary arterial hypertension (IPAH). This safe and rapid method helps manage children with IPAH.

Area of Science:

  • Pediatric Cardiology
  • Pulmonary Hypertension Research
  • Hemodynamic Assessment

Context:

  • Idiopathic pulmonary arterial hypertension (IPAH) requires careful management, with pulmonary vascular reactivity assessment being crucial.
  • Pediatric patients with IPAH, particularly those in WHO functional classes II to III, need specific diagnostic approaches.
  • Understanding vasodilator response is key to treatment strategies in pediatric IPAH.

Purpose:

  • To investigate the indications and methodology for pulmonary vasodilator testing in children diagnosed with IPAH.
  • To evaluate the effectiveness and safety of adenosine infusion for assessing pulmonary vascular reactivity in pediatric IPAH patients.
  • To determine the response criteria and potential adverse effects of adenosine testing in this population.

Summary:

  • A cohort of 15 pediatric patients with IPAH underwent right heart catheterization with adenosine infusion for vasodilator testing.
  • Adenosine was administered incrementally, with responders defined by a significant drop in mean pulmonary artery pressure (mPAP).
  • Three patients responded to adenosine, while twelve did not; adverse effects were transient and mild.

Impact:

  • Adenosine serves as a safe and effective agent for the rapid assessment of vasodilator reserve in pediatric IPAH.
  • The findings support the use of adenosine testing in the clinical management of children with idiopathic pulmonary arterial hypertension.
  • This study contributes to optimizing diagnostic protocols for pediatric pulmonary vascular diseases.
Abstract

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