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A Porcine Model of Acute Autologous Pulmonary Embolism
Published on: September 6, 2024
Clinical features and outcome of pulmonary embolism in children
Tina T Biss1, Leonardo R Brandão, Walter H Kahr
1Department of Hematology/Oncology, The Hospital for Sick Children, Toronto, ON, Canada.
Insights
Childhood pulmonary embolism (PE) is under-recognized, with immobility and central lines as common risk factors. Despite treatment, significant morbidity and mortality persist, highlighting the need for further research.
Area of Science:
- Pediatric Medicine
- Cardiology
- Hematology
Background:
- Pulmonary embolism (PE) is uncommon in children but frequently underdiagnosed.
- Understanding childhood PE requires examining its unique risk factors and outcomes.
Purpose of the Study:
- To retrospectively review cases of pediatric pulmonary embolism (PE) at a tertiary center.
- To identify risk factors, diagnostic findings, treatment complications, and outcomes in children with PE.
Main Methods:
- Retrospective review of 56 children diagnosed with radiologically proven PE over 8 years.
- Analysis of patient demographics, symptoms, risk factors, thrombophilia, concurrent deep vein thrombosis (DVT), and treatment modalities.
- Evaluation of therapeutic complications, recurrence rates, and mortality.
Main Results:
- Most pediatric PE patients (84%) presented with symptoms; 96.4% had risk factors like immobility and central venous lines.
- Deep vein thrombosis (DVT) was present in 55.4% of cases. Elevated D-dimer was observed in 86.7%.
- Treatment complications included major hemorrhage (21.4%). Mortality was 21.4%, with 8.9% due to PE and 5.9% due to hemorrhage.
Conclusions:
- Childhood PE has distinct risk factors compared to adults, and carries significant morbidity and mortality.
- Current treatment strategies result in complications and persistent mortality.
- Multicenter prospective studies are essential to establish optimal treatment protocols and long-term outcomes for pediatric PE.
Abstract:
Pulmonary embolism (PE) is rare in childhood but evidence suggests it is under-recognised. Children diagnosed with PE at a large tertiary centre over an 8-year period were retrospectively reviewed. Fifty-six children with radiologically proven PE were identified, 31 males and 25 females, median age 12 years. Eighty-four per cent had symptoms of PE. Risk factors for thromboembolism were present in 54 patients (96.4%); most commonly immobility (58.9%), central venous line (35.7%) and recent surgery (28.6%). Investigation revealed a thrombophilic abnormality in 14/40 patients (35%). Concurrent deep vein thrombosis was confirmed in 31 patients (55.4%), predominantly lower limb. D dimer was elevated at presentation in 26/30 patients (86.7%). Eight patients underwent systemic thrombolysis. An inferior vena cava filter was placed in five patients. Therapy was complicated by major haemorrhage in 12 patients (21.4%). The majority (82.1%) had complete or partial resolution of PE following a median of 3 months anticoagulation. Seven patients had a recurrent thromboembolic event and 12 patients died (mortality 21.4%); five due to thromboembolism (8.9%) and two due to haemorrhage. Risk factors for PE in children are distinct from adults and morbidity and mortality is significant. Multicentre prospective studies are required to determine optimal treatment and long-term outcome of childhood PE.
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