Severe pulmonary hypertension with therapeutic L-lysine ibuprofen in 2 preterm neonates

Barbara Amendolia1, Madeline Lynn, Vishwanath Bhat

  • 1Department of Pediatrics, Cooper University Hospital, Camden, New Jersey 08103, USA. amendolia-barbara@cooperhealth.edu

Pediatrics
|April 12, 2012
PubMed

Insights

Ibuprofen, used to treat patent ductus arteriosus (PDA) in premature infants, can rarely cause severe pulmonary hypertension. This serious complication occurred in two infants, highlighting the need for careful monitoring during PDA treatment.

Area of Science:

  • Neonatology
  • Pediatric Cardiology
  • Pharmacology

Background:

  • Patent ductus arteriosus (PDA) is common in very low birth weight infants, leading to significant morbidity.
  • Ibuprofen is increasingly preferred over indomethacin for PDA closure due to lower risk of necrotizing enterocolitis.
  • Pulmonary hypertension is a rare but severe complication associated with ibuprofen therapy.

Observation:

  • Two preterm infants developed severe pulmonary hypertension after receiving L-lysine ibuprofen for PDA closure.
  • Both infants presented with echocardiographic evidence of increased pulmonary vascular resistance and left-to-right shunting.
  • Clinical deterioration, including refractory hypotension and hypoxemia, occurred within 48-72 hours.

Findings:

  • The infants' conditions rapidly worsened, with repeat echocardiograms confirming severe pulmonary hypertension.
  • Despite therapeutic interventions, both infants ultimately died from complications related to pulmonary hypertension.
  • This suggests a potential causal link between L-lysine ibuprofen and the development of pulmonary hypertension in susceptible preterm infants.

Implications:

  • Clinicians must be aware of the potential for severe pulmonary hypertension as a complication of ibuprofen therapy for PDA.
  • Careful echocardiographic monitoring for pulmonary hypertension is crucial in preterm infants receiving ibuprofen.
  • Further research is needed to understand the mechanism and identify risk factors for ibuprofen-induced pulmonary hypertension.

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...
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...
Pulmonary Embolism II: Diagnostic Studies and Interprofessional Care01:29

Pulmonary Embolism II: Diagnostic Studies and Interprofessional Care

Diagnosing Pulmonary EmbolismDiagnosing pulmonary embolism (PE) involves clinical assessment and advanced imaging tests. The preferred diagnostic tool is the spiral (helical) CT scan or CT angiography (CTA), which uses intravenous contrast media to visualize the pulmonary vasculature and identify emboli.A ventilation-perfusion (V/Q) scan is an alternative for patients unable to receive contrast media. This scan includes both perfusion and ventilation scanning. Perfusion scanning involves...
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...