Characteristics of pulmonary hypertension in preterm neonates

V H Kumar1, A A Hutchison, S Lakshminrusimha

  • 1Department of Pediatrics (Neonatology), State University of New York (SUNY) at Buffalo, Women and Children's Hospital of Buffalo, Buffalo, New York 14222, USA. vkumar@upa.chob.edu

Insights

Pulmonary hypertension (PHT) in preterm infants is linked to low Apgar scores and certain prenatal conditions. Response to inhaled nitric oxide (iNO) therapy improves with increasing gestational age (GA) in these vulnerable infants.

Area of Science:

  • Neonatal Medicine
  • Pediatric Cardiology
  • Respiratory Medicine

Background:

  • Pulmonary hypertension (PHT) in preterm infants is a significant concern with limited data on risk factors and treatment response.
  • Understanding PHT development and inhaled nitric oxide (iNO) efficacy is crucial for improving outcomes in premature neonates.

Purpose of the Study:

  • To identify risk factors for PHT in infants born before 37 weeks gestational age (GA).
  • To evaluate the response to inhaled nitric oxide (iNO) therapy in preterm infants diagnosed with PHT.

Main Methods:

  • Retrospective chart review of infants (<37 weeks GA) with echocardiographic diagnosis of PHT within the first 4 weeks of life.
  • Matched control group (no PHT) for comparison, analyzing prenatal/postnatal characteristics, iNO response, and mortality.
  • Statistical analysis to determine independent predictors of PHT and factors associated with mortality.

Main Results:

  • Low Apgar scores, preterm premature rupture of membranes, oligohydramnios, pulmonary hypoplasia, and sepsis were independent predictors of PHT.
  • Mortality was significantly higher in the PHT group (26.2%) compared to controls (4.1%).
  • Response to iNO therapy increased with gestational age (GA), with infants <29 weeks GA showing poor response.

Conclusions:

  • Low Apgar scores, oligohydramnios, and pulmonary hypoplasia are associated with PHT development in preterm infants.
  • The efficacy of inhaled nitric oxide (iNO) for PHT in preterm infants is dependent on gestational age, improving with increased GA.
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...
Pulmonary Embolism I: Introduction01:29

Pulmonary Embolism I: Introduction

Pulmonary embolism (PE) occurs when a thrombus, fat or air embolus, amniotic fluid, or tumor tissue blocks one or more pulmonary arteries. These blockages originate in the venous system or the right side of the heart.EtiologyPE primarily arises from deep vein thrombosis (DVT) and other hypercoagulable states, such as inherited thrombophilias. Additional etiological factors include venous stasis, commonly seen in obesity, and endothelial injury from surgery and trauma. Less common causes include...
Pulmonary Embolism I: Introduction01:19

Pulmonary Embolism I: Introduction

A blood clot, or thrombus, is a semi-solid mass composed of fibrin, platelets, and red blood cells. When it forms within a vessel, it can obstruct blood flow, known as thrombosis. If part of the clot detaches, it becomes an embolus that can travel and block distant vessels. When this occurs in the pulmonary arteries, it causes a condition known as pulmonary embolism (PE).Origin and ImpactMost often, the embolus originates from a thrombus in the deep veins of the lower limbs, a condition called...
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...
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 (ECE). Of...
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, improving...