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Septic Pulmonary Embolism in Pediatric Population: A Case Series With Literature Review
Issa Hanna1, Vincent B Gonzalez2, Pulin B Koul3
1From the Pediatric Emergency Medicine.
Insights
Septic pulmonary embolism (SPE) in children is rare, often presenting with respiratory symptoms and fever. This study identifies cavernous sinus thrombosis as a novel associated condition, stressing prompt antibiotic treatment for better outcomes.
Area of Science:
- Pediatric Infectious Diseases
- Pulmonary Medicine
- Radiology
Background:
- Septic pulmonary embolism (SPE) is a rare condition often stemming from osteomyelitis or endocarditis.
- Specific diagnostic guidelines for pediatric SPE are lacking.
- This review examines clinical, radiographic, and therapeutic aspects of SPE in children.
Purpose of the Study:
- To review clinical manifestations, radiographic findings, and antibiotic treatments in pediatric patients diagnosed with SPE.
- To identify potential new clinical associations with pediatric SPE.
Main Methods:
- A retrospective review of patients aged 1-18 years with confirmed SPE between 2000 and 2020.
- Exclusion of patients with neoplastic disease and duplicate records.
- Analysis of clinical data, imaging (chest CT), and microbiological findings.
Main Results:
- Common symptoms included shortness of breath, fever, and chest pain. Half of patients had identifiable extrapulmonary infection sources.
- Methicillin-resistant Staphylococcus aureus (MRSA) was the most common pathogen (62.5%).
- Cavernous sinus thrombosis was identified as a new associated clinical entity in this pediatric SPE series.
Conclusions:
- Cavernous sinus thrombosis is a newly recognized clinical entity associated with pediatric SPE.
- Prompt and targeted antibiotic therapy is crucial for improving outcomes in children with SPE.
Background:
Septic pulmonary embolism (SPE), resulting from infections such as osteomyelitis and endocarditis, is rare and lacks specific diagnostic guidelines. This report reviews the clinical manifestations, radiographic abnormalities and antibiotic therapy in children with SPE.
Methods:
Patients 1 to 18 years of age with confirmed SPE were identified from a database using the International Classification of Diseases-9/10 codes from 2000 to 2020. After excluding duplicates and those with neoplastic disease, 8 patients were included of 16 encounters.
Results:
Patients predominantly presented with shortness of breath, fever and chest pain. Half had identifiable extrapulmonary infection sources. Leukocytosis was present in 50% and leukopenia in 12.5%. Anemia was noted in 87.5% of patients, possibly linked to patients' acute illness. Contrasted chest computed tomography showed bilateral emboli in most patients. Echocardiograms were normal. Methicillin-resistant Staphylococcus aureus was identified in 62.5% of cases and oxacillin-sensitive staphylococcus aureus in 37.5%. While osteomyelitis was the most common infection source, our series uniquely included cavernous sinus thrombosis in children and reported for the first time. Most patients were empirically treated with vancomycin.
Conclusion:
This case series highlights cavernous sinus thrombosis as a new clinical entity associated with pediatric SPE. It emphasizes the significance of prompt, targeted antibiotic therapy for improved outcomes in children with SPE.
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