Background: Patients with sickle cell disease (SCD) have been part of the
population 'high-risk' group since the COVID‐19 pandemic. This study
focused to understand impact ofCOVID-19 on clinical outcomes in SCD.
Methods: Data were taken at the baseline and clinical course of this prospective
one-center intervention in SCD patients diagnosed with COVID-19 in isolation
centers (associated with Sevagram Hospital) dedicated for COVID-19 patients
in Wardha, Maharashtra, India. Patients were followed uppost-hospital
discharge for up to 1 month. Results: Of 120 SCD patients with COVID-19, 88
patients (73.33%) required hospitalization, and 32 died (26.67%). Vasocclusive
pain was the most common symptom. In 36.36% of hospitalised people and all
those who died, acute chest syndrome occurred. Older and recent
hypertension records, congestion and stroke, and elevated levels of creatinine
and bilirubin were common among patients who died. Conclusion: The risk for
morbidity, including ACS, seems the greatest among older patients with sickle
cell status, particularly those who have chronic end-organ diseases, including
brain, heart and lung
Keywords: COVID-19, Sickle cell disease, India, Hematology