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Published on: September 6, 2024
Pulmonary embolism in pediatric age: A retrospective study from a tertiary center
Raquel Lopes de Bragança1,2, Vanessa Gorito1,2,3, Diana Gonçalves Cibele4
1Department of Pediatrics, Centro Hospitalar Universitário de São João, Porto, Portugal.
Insights
Pediatric pulmonary embolism (PE) is rare but often missed. Adult diagnostic scores show higher sensitivity than pediatric ones, suggesting a need for improved pediatric PE diagnostic tools and consideration of family history.
Area of Science:
- Medical research
- Pediatric medicine
- Cardiology
Background:
- Pediatric pulmonary embolism (PE) is an uncommon but serious condition.
- Accurate and timely diagnosis of PE in children is challenging.
Purpose of the Study:
- To characterize pediatric pulmonary embolism cases in a tertiary hospital.
- To evaluate the sensitivity of various diagnostic prediction tools for pediatric PE.
Main Methods:
- Retrospective descriptive study of 29 PE cases (2008-2020).
- Analysis of patient demographics, risk factors, clinical presentation, management, and outcomes.
- Application and comparison of adult and pediatric PE diagnostic prediction tools.
Main Results:
- Most pediatric PE cases were central, massive, or submassive.
- Outpatient risk factors included contraceptives and thrombophilia; inpatient factors included immobilization and chronic diseases.
- Adult diagnostic scores demonstrated higher sensitivity (92.9%-96%) compared to pediatric scores (85.7%-92.9%).
Conclusions:
- Pediatric PE diagnosis is frequently delayed or missed.
- Development of pediatric-specific diagnostic tools, potentially adapted from adult scores, is warranted.
- Clinical presentation and risk factors differ between pediatric outpatients and inpatients; family history should be more broadly considered.
Introduction:
Pediatric pulmonary embolism (PE) is rare but associated with adverse outcomes. We aimed to characterize PE cases admitted in a tertiary hospital and to evaluate sensitivity of selected PE diagnostic prediction tools.
Methods:
Retrospective, descriptive study of PE cases admitted from 2008 to 2020 using data collected from hospital records. Patients were grouped according to PE severity and setting (outpatients vs. inpatients). Links and correlation with demographic characteristics, risk factors, clinical presentation, management, and outcomes were analyzed. PE diagnostic prediction tools were applied.
Results:
Twenty-nine PE episodes occurred in 27 patients, 62.9% female, mean age 14.1 years. Most PE were central and split between massive or submassive. One was diagnosed in autopsy. Twenty outpatients, all adolescents, were admitted for classic PE symptoms; in half of them the diagnosis had been previously missed. Risk factors included contraceptives (65%), thrombophilia (35%), obesity (20%) and auto-immunity (20%). Eight inpatients, diagnosed during cardiorespiratory deterioration (n = 5), or through incidental radiological findings (n = 3), were younger and had immobilization (87.5%), complex chronic diseases (75%), infections (75%) and central venous catheter (62.5%) as risk factors. Retrospectively, d -dimer testing and adult scores performed better than pediatric scores (sensitivity 92.9%-96% vs. 85.7%-92.9%). Both pediatric scores missed a case with a positive family history.
Discussion:
Pediatric PE diagnosis is often delayed or missed. Development of pediatric prediction tools from validated adult scores merits being explored. We argue clinical presentation and risk factors may be different in inpatients and outpatients and propose broader reliance on family history.
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