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A Porcine Model of Acute Autologous Pulmonary Embolism
Published on: September 6, 2024
Idiopathic acute massive pulmonary embolism in childhood
H M Caliskan1, S C Ozbek2, B Celik1
1Department of Emergency Medicine, Medical Faculty, Ahi Evran University, Kirsehir, Turkey.
Insights
Acute massive pulmonary embolism (PE) in a child is rare but critical. This case highlights the importance of considering PE in pediatric emergencies presenting with respiratory distress, even without prior medical history.
Area of Science:
- Pediatric Emergency Medicine
- Cardiology
- Radiology
Background:
- Acute pulmonary embolism (PE) is infrequently diagnosed in pediatric populations.
- Early recognition and management are crucial for favorable outcomes.
Observation:
- A 10-year-old child presented with acute massive PE, characterized by dyspnea and perioral cyanosis.
- Diagnostic workup included arterial blood gas analysis, electrocardiography, and contrast-enhanced pulmonary computed tomography.
- CT scan confirmed a large thrombus in the right pulmonary artery, obstructing blood flow to lobar arteries.
Findings:
- The patient received initial treatment with intravenous fluids, oxygen therapy, and subcutaneous enoxaparin.
- Due to the severity and need for advanced care, the patient was transferred to a tertiary care center for potential pharmacological thrombolysis.
Implications:
- This case underscores the necessity of including PE in the differential diagnosis for pediatric patients presenting with acute respiratory symptoms in emergency departments.
- Prompt diagnostic imaging and timely transfer to specialized centers are vital for managing pediatric PE.
Abstract:
Acute pulmonary embolism (PE) is an uncommon clinical condition in childhood. We hereby present a case report of a 10-year-old child who presented to the emergency department with an acute massive PE. He was transferred by ambulance to our emergency department for dyspnea and perioral cyanosis. His parents denied any previous history of illness or familial disease. Arterial blood gas analysis, electrocardiography, and clinical symptoms and signs collectively raised a suspicion of a probable PE. A contrast-enhanced pulmonary computed tomography scan revealed a massive thrombus in the distal part of the right pulmonary artery with no contrast passage into upper, middle, and lower lobar arteries. Upon ascertaining, the diagnosis of PE, intravenous saline infusion, 3 L/min oxygen through nasal route, and subcutaneous enoxaparin 0.4 cc was administered promptly. As our hospital lacked a pediatric intensive care unit and a further need for administration of pharmacological thrombolysis was anticipated, we transferred the patient to a tertiary care center. PE should always be kept in mind as a differential diagnosis in emergency departments even in pediatric patients.
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