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Updated: Nov 5, 2025

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
COVID-19 Mortality in a Pediatric Patient with Hemoglobin SC Disease and Alpha-Thalassemia Trait
Joshua E Motelow1, Stacie Kahn1, Patrick T Wilson1
1Department of Pediatrics, Division of Critical Care and Hospital Medicine, Columbia University Irving Medical Center, New York-Presbyterian Morgan Stanley Children's Hospital of New York, New York, NY, USA.
Insights
This case highlights a severe COVID-19 infection in a pediatric patient with HbSC disease and alpha-thalassemia trait. Vigilance is crucial when treating children with hemoglobinopathies during the pandemic.
Area of Science:
- Pediatric Hematology
- Infectious Diseases
- Critical Care Medicine
Background:
- The ongoing COVID-19 pandemic presents unique challenges in pediatric populations.
- Patients with hemoglobinopathies may be at increased risk for severe outcomes from SARS-CoV-2 infection.
Observation:
- A 12-year-old boy with HbSC disease and alpha-thalassemia trait presented with fever and respiratory distress.
- He rapidly progressed to respiratory failure requiring mechanical ventilation and exchange transfusion.
- Despite initial improvement, he experienced acute hypoxemia and cardiac arrest.
Findings:
- The patient tested positive for SARS-CoV-2, with chest imaging concerning for acute chest syndrome.
- Treatment included hydroxychloroquine, antibiotics, and enoxaparin for DVT prophylaxis.
- This case illustrates a severe and unusual presentation of COVID-19 in a pediatric patient with a complex hemoglobinopathy.
Implications:
- Healthcare providers must maintain high vigilance for severe COVID-19 presentations in pediatric patients with hemoglobinopathies.
- Early recognition and aggressive management are critical for improving outcomes.
- This case underscores the need for tailored treatment strategies in this vulnerable population.
Abstract:
As the pandemic continues to evolve, more cases of COVID-19 in pediatric patients are being detected. A 12-year-old boy with HbSC disease alpha-thalassemia trait presented to a pediatric emergency room with fever and weakness. His vital signs were notable for fever, tachypnea, and tachycardia. His physical exam was concerning for increased work of breathing. He tested positive for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by PCR although his hemoglobin level remained near his baseline. His chest radiograph showed a retrocardiac opacity concerning for evolving acute chest syndrome. He decompensated quickly requiring invasive mechanical ventilation and exchange transfusion. He received hydroxychloroquine, broad-spectrum antibiotics, and enoxaparin for DVT prophylaxis. Despite showing clinical signs of improvement, he became acutely hypoxemic and suffered a cardiac arrest. We believe this to be an unusual case of a pediatric patient with HbSC disease and COVID-19. We outline clearly the course of illness and treatments trialed, which can prove beneficial to providers facing similar challenges as this virus continues to strike areas around the world. Although children have significantly better outcomes than adults, providers must remain vigilant while treating any patient with a hemoglobinopathy in the setting of severe COVID-19.
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