Characteristics and outcomes of preterm infants with early pulmonary hypertension

Rachel Mullaly1,2, Aisling Smith3, Claire Murphy3

  • 1Department of Neonatology, The Rotunda Hospital, Dublin, Ireland. rachelmullaly21@rcsi.ie.

Insights

Preterm infants with early pulmonary hypertension (PH) face significantly higher mortality rates and distinct echocardiographic findings. Early detection and management of PH in premature infants are crucial for improving survival and long-term outcomes.

Area of Science:

  • Neonatal Medicine
  • Pediatric Cardiology
  • Perinatology

Background:

  • Pulmonary hypertension (PH) is a serious complication in preterm infants.
  • Understanding the incidence, outcomes, and echocardiographic features of early PH is critical for clinical management.

Purpose of the Study:

  • To investigate the incidence, outcomes, and echocardiographic characteristics of preterm infants with early pulmonary hypertension (PH).
  • To compare these features between infants with and without early PH.

Main Methods:

  • A prospective observational study included infants born before 29 weeks gestation.
  • Echocardiograms were performed at 24-48 hours and 36 weeks postmenstrual age (PMA).
  • Early PH was defined by ductal shunting (bidirectional or right-to-left).

Main Results:

  • Early PH was identified in 12% (20/166) of infants.
  • Infants with early PH exhibited significantly higher mortality (55% vs 11%).
  • Distinct echocardiographic differences in cardiac function (twist, torsion, systolic time, isovolumic relaxation time) were observed, persisting in survivors at 36 weeks PMA.

Conclusions:

  • Early PH in preterm infants is associated with increased mortality and unique echocardiographic profiles.
  • Functional cardiac alterations in survivors persist until 36 weeks PMA.
  • Timely identification and targeted interventions for early PH may enhance outcomes in preterm neonates.
Abstract

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...
115
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...
96
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,...
122
Pneumonia III: Complications and Assessment01:30

Pneumonia III: Complications and Assessment

Pneumonia poses the potential for numerous complications that warrant consideration. These complications include the following:
126
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...
114
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...
1.3K