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Epidemiology and management of massive, sub-massive, and non-massive pediatric pulmonary embolism: a systematic
Mohammed Alsabri1,2, Dina Essam Abo-Elnour3, Mohammed Ayyad4,5
1Emergency Department, Al-thawara Modern General Hospital, Sana'a, Yemen. Alsabri5000@gmail.com.
Insights
This systematic review highlights that pediatric pulmonary embolism (PE) diagnosis and management vary by severity. Early diagnosis and tailored treatment are crucial for improving outcomes in children and adolescents with PE.
Area of Science:
- Pediatric Medicine
- Cardiology
- Pulmonology
Background:
- Pediatric pulmonary embolism (PE) is a critical condition with diverse presentations.
- Understanding diagnosis, management, and outcomes is vital for this population.
Purpose of the Study:
- To systematically review evidence on pediatric PE diagnosis, management, and outcomes.
- To analyze presentations across massive, submassive, and non-massive severity classifications.
Main Methods:
- Systematic review adhering to PRISMA guidelines.
- Searches across major databases (PubMed, Scopus, Web of Science, Cochrane) up to February 2024.
- Included studies on patients ≤21 years with confirmed PE; risk of bias assessed using NIH tool.
Main Results:
- Six studies with 258 pediatric patients (mean age 14.1 years, predominantly female) were analyzed.
- Common risk factors: obesity, oral contraceptives, thrombophilia, autoimmune conditions.
- CTPA most common diagnostic tool; outcomes correlated with PE severity, with massive PE having higher mortality.
Conclusions:
- Pediatric PE necessitates individualized risk stratification and management.
- Diagnostic delays and severe presentations increase morbidity and mortality.
- Future research should standardize classifications, explore novel diagnostics, and compare therapeutic interventions.
Objective:
To evaluate the current evidence on the diagnosis, management, and outcomes of pediatric pulmonary embolism (PE) across varying severity classifications, including massive, submassive, and non-massive presentations.
Methods:
A systematic review was conducted following PRISMA guidelines. Searches were performed in PubMed, Scopus, Web of Science, and Cochrane databases up to February 17, 2024. Eligible studies included pediatric and adolescent patients (≤ 21 years) with confirmed PE diagnoses. Risk of bias was assessed using the NIH tool.
Results:
Six studies involving 258 pediatric patients with massive, submassive, or non-massive PE were included. Most patients were adolescents, with a mean age of 14.1 years and a predominance of females (62-66%). Risk factors included obesity, oral contraceptive use, thrombophilia, and autoimmune conditions. Computed tomography pulmonary angiography (CTPA) was the most frequently used diagnostic modality, showing varied lobar, segmental, and subsegmental involvement. Management strategies ranged from anticoagulation to catheter-directed thrombolysis and surgical thrombectomy. Outcomes varied by severity, with massive PE cases showing higher mortality and complications compared to submassive and non-massive cases.
Conclusion:
Pediatric PE requires tailored risk stratification and management strategies to optimize outcomes. Delays in diagnosis and severe disease presentations contribute to higher morbidity and mortality. Future research should focus on standardized severity classifications, novel diagnostic modalities, and comparative assessments of therapeutic interventions to enhance outcomes in this population.
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