Related Experiment Video
Updated: Nov 29, 2025

Hemodynamic Characterization of Rodent Models of Pulmonary Arterial Hypertension
Published on: April 11, 2016
Mineralocorticoid receptor blockade improves pulmonary hypertension and right ventricular function in
Roberto Giagnorio1, Georg Hansmann1
1Department of Pediatric Cardiology and Critical Care, Hannover Medical School, Hannover, Germany.
Insights
This study shows that adding spironolactone and hydrochlorothiazide improved a premature infant's chronic lung disease and pulmonary hypertension. Biomarkers and echocardiography confirmed rapid recovery of heart function.
Area of Science:
- Pediatric Pulmonology
- Neonatology
- Cardiology
Background:
- Bronchopulmonary dysplasia (BPD) is a leading cause of chronic lung disease in infants.
- Persistent pulmonary hypertension (PH) in BPD significantly elevates mortality risk.
- Right heart failure is a severe complication associated with BPD and PH.
Observation:
- A 4-month-old infant, previously preterm, presented with BPD, severe PH, and right heart failure.
- The infant's clinical status and right ventricular (RV) function were monitored.
- Blood biomarkers (NT-pro-BNP, troponin T) and echocardiography were utilized for assessment.
Findings:
- Addition of spironolactone and hydrochlorothiazide to the infant's regimen led to rapid clinical improvement.
- Significant enhancement in right ventricular function was observed post-treatment.
- Biomarker levels and echocardiographic data corroborated the positive therapeutic response.
Implications:
- Spironolactone and hydrochlorothiazide may offer a novel therapeutic approach for infants with BPD and PH.
- This treatment strategy shows potential for improving outcomes in severe BPD cases.
- Further research is warranted to explore the efficacy and safety of these diuretics in BPD-PH management.
Abstract:
Bronchopulmonary dysplasia (BPD) is a combined pulmonary vascular and parenchymal disease, representing the most common cause of chronic lung disease (CLD) in infancy. Pulmonary hypertension (PH) is frequently associated with BPD and-if persistent-substantially increases mortality. We report on a 4-month-old, former preterm infant with BPD, severe PH and right heart failure who greatly and rapidly improved clinical status and right ventricular (RV) function by means of blood biomarkers [N-terminal prohormone of brain natriuretic peptide (NT-pro-BNP), cardiac troponin T] and transthoracic echocardiography, following the addition of spironolactone and hydrochlorothiazide to the treatment regimen.
More Related Videos
07:41A Model of Reverse Vascular Remodeling in Pulmonary Hypertension Due to Left Heart Disease by Aortic Debanding in Rats
Published on: March 1, 2022
09:23Shunt Surgery, Right Heart Catheterization, and Vascular Morphometry in a Rat Model for Flow-induced Pulmonary Arterial Hypertension
Published on: February 11, 2017
Related Concept Videos
Treatment for Pulmonary Arterial Hypertension: Receptor Tyrosine Kinase Inhibitors and Calcium Channel Blockers
TKIs, such as imatinib (Gleevec), are particularly effective in tackling the growth and mitogenic factors that become upregulated in PAH patients. These factors contribute to the...
COPD: Management Using Bronchodilators and Corticosteroids
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System
Pulmonary Hypertension: Classification and Pathogenesis
There are various classifications for PH, each relating to different underlying causes and also...
Treatment for Pulmonary Arterial Hypertension: Endothelin Receptor Antagonists
ETs are synthesized through a complex sequence of enzymatic steps, primarily involving an enzyme referred to as endothelin-converting enzyme...
Heart Failure Drugs: β-Blockers