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Updated: Jun 28, 2025

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
Case Report: Obstetric and COVID-19-Related Morbidity and Mortality in Three Patients with Sickle Hemoglobinopathy
Shanea Gibson1, Tiffany Hunter1,2, Nadine Johnson1,2
1Department of Obstetrics and Gynaecology, University Hospital of the West Indies, Kingston, Jamaica.
Pregnant women with sickle cell disease (SCD) face severe risks from COVID-19. This study highlights adverse maternal and neonatal outcomes, including deaths, in Jamaican patients with SCD and SARS-CoV-2 infection.
Area of Science:
- Obstetrics and Gynecology
- Hematology
- Infectious Diseases
Background:
- Sickle cell disease (SCD) affects approximately 3% of pregnant women globally.
- The COVID-19 pandemic (caused by SARS-CoV-2) poses significant risks, particularly for immunocompromised individuals.
- Limited research exists on the impact of COVID-19 on pregnant women of Afro-Caribbean descent with SCD.
Observation:
- A retrospective case series analyzed three pregnant patients with SCD who contracted COVID-19 at the University Hospital of the West Indies between 2020 and 2022.
- Complications included vaso-occlusive crisis, need for ventilatory support, and severe adverse outcomes.
- Two patients had hemoglobin SC disease, and one had hemoglobin SS disease.
Findings:
- The study documented severe maternal and neonatal complications, including the demise of both a mother and her newborn.
- Vaso-occlusive crisis was a frequent presentation among these patients.
- Two out of three patients required mechanical ventilation due to respiratory compromise.
Implications:
- Pregnant women with SCD are at high risk for adverse outcomes when infected with SARS-CoV-2.
- Maternal and neonatal mortality are possible sequelae, even with supportive care.
- Further research is crucial to understand and mitigate these risks in vulnerable populations.
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05:23Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
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