Pulmonary endarterectomy in a 12-year-old boy with multiple comorbidities

Tom Verbelen1, Bjorn Cools2, Zina Fejzic3

  • 1Department of Cardiac Surgery, University Hospitals Leuven, Leuven, Belgium.

Pulmonary Circulation
|April 15, 2020
PubMed

Insights

Pulmonary endarterectomy is a feasible and well-tolerated treatment for pediatric chronic thromboembolic pulmonary hypertension (CTEPH), even with comorbidities. Early surgical consideration improves outcomes for children with CTEPH.

Area of Science:

  • Cardiology
  • Pediatric Surgery
  • Pulmonary Medicine

Background:

  • Chronic thromboembolic pulmonary hypertension (CTEPH) is a rare but serious condition in children.
  • Early diagnosis and intervention are crucial for improving patient prognosis.

Observation:

  • A 10-year-old boy with multiple comorbidities presented with symptoms of severe pulmonary hypertension.
  • Initial medical management with anticoagulation, antibiotics, and oxygen provided temporary relief.
  • Despite progressive symptoms and severe right ventricular dysfunction, the patient was deemed inoperable in his country of residence.

Findings:

  • Pulmonary endarterectomy was successfully performed in a 12-year-old boy with severe CTEPH and comorbidities.
  • Post-surgery, significant improvements were observed in mean pulmonary artery pressure (mPAP) and cardiac output.
  • The patient experienced a remarkable recovery, returning to normal activities without supplemental oxygen within months.

Implications:

  • This case demonstrates the feasibility and efficacy of pulmonary endarterectomy in young pediatric patients with CTEPH.
  • CTEPH should be strongly considered in children with risk factors such as hypercoagulable states or a history of thromboembolism.
  • Timely surgical referral is essential, as it represents the only potentially curative treatment and delays may worsen prognosis.