Early Pulmonary Hypertension in Preterm Infants

Srinivasan Mani1, Hussnain Mirza2, James Ziegler3

  • 1Section of Neonatology, Department of Pediatrics, The University of Toledo/ ProMedica Russell J. Ebeid Children's Hospital, Toledo, OH 43606, USA.

Clinics in Perinatology
|February 7, 2024
PubMed

Insights

Pulmonary hypertension (PH) in preterm neonates stems from lung injury and abnormal vascular development. Management strategies and the use of pulmonary vasodilators remain debated topics in neonatal care.

Area of Science:

  • Neonatology
  • Pediatric Cardiology
  • Respiratory Medicine

Background:

  • Pulmonary hypertension (PH) in preterm neonates presents unique multifactorial pathogenesis.
  • Premature lungs are susceptible to injury from ventilation and oxygen, leading to diverse PH phenotypes.
  • Early PH prevalence varies significantly, affecting 8-55% of extremely preterm infants.

Purpose of the Study:

  • To review the characteristics and pathogenesis of PH in preterm neonates.
  • To discuss the variable prevalence and contributing factors of early PH.
  • To highlight the controversies surrounding the management of PH and vasodilator use in this population.

Main Methods:

  • Literature review of studies on neonatal pulmonary hypertension.
  • Analysis of factors contributing to lung injury and vascular dysfunction in preterm infants.
  • Synthesis of current evidence on PH management strategies.

Main Results:

  • Preterm infants experience lung injury from positive pressure ventilation and high oxygen concentrations.
  • Disrupted lung development and vascular signaling pathways contribute to abnormal pulmonary vascular transition.
  • The prevalence of PH in extremely preterm infants is highly variable.

Conclusions:

  • PH in preterm neonates is characterized by multifactorial causes and unique presentations.
  • Abnormal pulmonary vascular transition is linked to disrupted lung development and signaling.
  • Current management approaches for early PH, including off-label vasodilator use, require further investigation and consensus.

Related Concept Videos

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...
180
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...
165
Treatment for Pulmonary Arterial Hypertension: Oxygen Therapy for Respiratory Failure01:16

Treatment for Pulmonary Arterial Hypertension: Oxygen Therapy for Respiratory Failure

Oxygen therapy has emerged as a significant tool in enhancing the quality of life for patients suffering from pulmonary arterial hypertension (PAH). While this therapy has principally been studied on patients with significant hypoxemia, this therapeutic approach helps prevent potential organ damage and can be administered in the comfort of one's home.
Oxygen therapy is vital in increasing and maintaining blood oxygen levels in PAH patients. As a result, it aids in reducing fatigue,...
216
Pulmonary Cycle: Exhalation01:17

Pulmonary Cycle: Exhalation

In terms of human respiration, the act of expelling air, known as exhalation (or expiration), operates on the principle of pressure gradients. During expiration, the pressure within the lungs exceeds that of the surrounding atmosphere. Under normal conditions, quiet breathing involves passive exhalation and is free of muscular contractions. This is because the exhalation process is driven by the natural elastic recoil of the lungs and chest wall, both of which have an inherent tendency to...
1.6K
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...
182