Right ventricular function mirrors clinical improvement with use of prostacyclin analogues in pediatric pulmonary

Rachel K Hopper1, Yan Wang1, Valerie DeMatteo1

  • 11 24349 Division of Cardiology, Department of Pediatrics, The Children's Hospital of Philadelphia and Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.

Pulmonary Circulation
|February 27, 2018
PubMed

Insights

Prostacyclin analogues improved right ventricular (RV) function in children with pulmonary hypertension (PH). Echocardiography showed early and sustained improvements in RV strain and function, alongside better clinical markers of PH severity.

Area of Science:

  • Pediatric Cardiology
  • Pulmonology
  • Cardiovascular Imaging

Background:

  • Pediatric pulmonary hypertension (PH) leads to significant right ventricular (RV) failure, morbidity, and mortality.
  • RV dysfunction is a key factor in the progression and outcomes of pediatric PH.

Purpose of the Study:

  • To evaluate the impact of prostacyclin analogues on RV function in pediatric PH patients.
  • To assess changes in echocardiographic parameters and clinical markers of PH severity following prostacyclin analogue treatment.

Main Methods:

  • Retrospective cohort study of 49 children with PH treated with epoprostenol or treprostinil (2001-2015).
  • Echocardiograms (including TAPSE and RV global longitudinal strain) and clinical data collected at baseline and 1-12 months post-treatment.
  • Blinded analysis of echocardiographic measurements.

Main Results:

  • Prostacyclin analogues significantly improved TAPSE (P=0.007), RV strain (P<0.001), and qualitative RV function (P=0.037).
  • Improvements were observed in BNP levels (P<0.001), functional class (P=0.047), and 6-minute walk distance (P=0.001).
  • Early improvements in TAPSE and RV strain were noted, suggesting a rapid therapeutic effect.

Conclusions:

  • Prostacyclin analogues are associated with early and sustained improvement in RV function in children with PH.
  • RV strain emerges as a sensitive echocardiographic marker for assessing RV function in pediatric PH.
  • Treatment with prostacyclin analogues positively impacts both echocardiographic and clinical indicators of PH severity in children.

Related Concept Videos

Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists01:23

Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists

Prostacyclin receptor agonists are a class of therapeutic agents integral to managing pulmonary arterial hypertension (PAH). These drugs operate by mimicking the action of prostaglandin I2, or PGI2, a naturally occurring compound in the body.
These agonists bind to the IPR receptor situated on the plasma membrane of the pulmonary artery smooth muscle cells. This binding triggers a cascade of reactions known as the GS-AC-cAMP-PKA pathway. This pathway results in the relaxation of smooth muscle...
526
Pulmonary Hypertension: Classification and Pathogenesis01:30

Pulmonary Hypertension: Classification and Pathogenesis

Pulmonary hypertension (PH) is a severe health condition in which the mean pulmonary arterial pressure increases to 25 mmHg or more, even when the body is at rest. This high pressure in the blood vessels that transport blood from the heart to the lungs can cause various symptoms, including shortness of breath, can lead to right heart failure, and significantly affect the overall quality of life.
There are various classifications for PH, each relating to different underlying causes and also...
671
Hypertension III: Clinical Manifestations and Diagnostic Studies01:30

Hypertension III: Clinical Manifestations and Diagnostic Studies

Hypertension is asymptomatic and also referred to as the "silent killer" until it progresses to a severe stage or causes target organ disease. Patients may experience symptoms stemming from the strain on blood vessels and tissues in various organs or the heart's increased workload.Physical exams might show no abnormalities other than high blood pressure. Signs of vascular damage, when present, correspond to the organs supplied by the affected vessels, leading to target organ damage. For...
613
Treatment for Pulmonary Arterial Hypertension: Phosphodiesterase Inhibitors01:28

Treatment for Pulmonary Arterial Hypertension: Phosphodiesterase Inhibitors

Phosphodiesterase 5 (PDE5) inhibitors are potent enzymes that function to hydrolyze cyclic nucleotides to their corresponding 5' monophosphates. Their unique biochemical properties have been applied in treating Pulmonary Arterial Hypertension (PAH).
Among the PDE5 inhibitors, sildenafil (Revatio) stands out as a competitive and selective inhibitor. It operates by elevating cellular levels of cGMP and augmenting signaling through the cGMP-PKG pathway, promoting vasodilation. Upon oral...
627
Pulmonary Function Tests01:25

Pulmonary Function Tests

Pulmonary Function Tests (PFTs)
Pulmonary Function Tests are crucial diagnostic tools for assessing respiratory function, particularly in patients with chronic respiratory disorders. They comprehensively evaluate lung volumes, ventilatory function, breathing mechanics, diffusion, and gas exchange. These tests help diagnose pulmonary diseases and play a significant role in monitoring disease progression, evaluating disability, and assessing response to therapy.
PFTs involve using a spirometer, a...
864
Treatment for Pulmonary Arterial Hypertension: Endothelin Receptor Antagonists01:18

Treatment for Pulmonary Arterial Hypertension: Endothelin Receptor Antagonists

Endothelins (ETs) are potent vasoactive peptides critical in the human body's various physiological and pathological processes. One of the most promising therapeutic strategies for treating pulmonary arterial hypertension (PAH) involves counteracting the effects of these endothelins using a class of drugs known as endothelin receptor antagonists.
ETs are synthesized through a complex sequence of enzymatic steps, primarily involving an enzyme referred to as endothelin-converting enzyme...
485