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Updated: Dec 15, 2025

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
Coronavirus Disease among Persons with Sickle Cell Disease, United States, March 20-May 21, 2020
Insights
Sickle cell disease (SCD) impacts Black or African American individuals, causing organ damage and shorter lives. A US registry found 69% of SCD patients were hospitalized and 7% died from COVID-19.
Area of Science:
- Hematology
- Infectious Diseases
- Public Health
Background:
- Sickle cell disease (SCD) disproportionately affects Black or African American populations in the US.
- SCD can lead to severe multisystem organ damage and a reduced lifespan.
- Understanding COVID-19 outcomes in SCD patients is critical due to potential disease severity.
Purpose of the Study:
- To analyze the impact of COVID-19 on individuals with sickle cell disease in the United States.
- To determine hospitalization and mortality rates for SCD patients with COVID-19.
Main Methods:
- Data collected from an SCD-coronavirus disease case registry in the US.
- Analysis of reported cases including hospitalization and death outcomes.
- Descriptive statistics to summarize patient data.
Main Results:
- 178 individuals with SCD and COVID-19 were reported to the registry.
- 69% (122) of these patients were hospitalized.
- 7% (13) of these patients died.
Conclusions:
- COVID-19 poses a significant risk to individuals with sickle cell disease.
- High rates of hospitalization and mortality underscore the vulnerability of the SCD population to COVID-19.
- Further research and public health interventions are needed to protect this population.
Abstract:
Sickle cell disease (SCD) disproportionately affects Black or African American persons in the United States and can cause multisystem organ damage and reduced lifespan. Among 178 persons with SCD in the United States who were reported to an SCD-coronavirus disease case registry, 122 (69%) were hospitalized and 13 (7%) died.
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