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Pulmonary Endarterectomy in Pediatric Patients: Institutional Experience
Çağatay Çetinkaya1, Nezih Onur Ermerak2, Ela Erdem3
1Üsküdar University School of Medicine, Department of Thoracic Surgery, Turkey, Istanbul.
The Thoracic and Cardiovascular Surgeon
|June 17, 2026
Summary
Pulmonary endarterectomy (PEA) is a viable treatment for pediatric chronic thromboembolic pulmonary hypertension (CTEPH), even with complex conditions. This surgery significantly improves patient hemodynamics and function.
Area of Science:
- Pediatric Cardiology
- Cardiovascular Surgery
- Pulmonary Hypertension Research
Background:
- Chronic thromboembolic pulmonary hypertension (CTEPH) is uncommon in children, with limited data on surgical interventions.
- Pulmonary endarterectomy (PEA) experience in pediatric patients is scarce.
Purpose of the Study:
- To evaluate the feasibility and outcomes of PEA in pediatric patients with CTEPH.
- To assess the safety and efficacy of PEA in children, including those with comorbidities.
Main Methods:
- Retrospective review of seven PEA procedures in six pediatric patients (<18 years).
- Analysis of clinical characteristics, perioperative findings, hemodynamic data, and follow-up.
- Inclusion of patients with diverse risk factors and comorbidities.
Main Results:
- Median age was 13 years; most patients presented with severe pulmonary hypertension (WHO functional class III/IV).
- Post-PEA, mean pulmonary artery pressure decreased from 39 ± 15 mmHg to 21 ± 4 mmHg, and PVRi from 7.51 ± 4.56 to 2.36 ± 1.36 U·m².
- One in-hospital mortality; other patients showed significant recovery with short ICU and hospital stays.
Conclusions:
- PEA is a safe and effective treatment for carefully selected pediatric CTEPH patients.
- The procedure leads to substantial hemodynamic and functional improvements.
- PEA offers a potentially curative option for this rare pediatric condition.

