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Updated: Nov 12, 2025

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
Impact of COVID-19 on vasooclusive crisis in patients with sickle cell anaemia
S Alkindi1, R A Elsadek2, A Al-Madhani3
1Department of Haematology, Sultan Qaboos University Hospital, Oman; College of Medicine and Health Sciences, Muscat, Oman.
Insights
COVID-19 may trigger vasooclusive crisis (VOC) in sickle cell anaemia (SCA) patients, but did not significantly increase VOC-related morbidity or mortality in this cohort.
Area of Science:
- Hematology
- Infectious Diseases
- Public Health
Background:
- Sickle cell anaemia (SCA) is a genetic blood disorder characterized by abnormal haemoglobin, leading to vasooclusive crises (VOCs).
- The impact of COVID-19 on SCA patients, particularly concerning VOCs, requires thorough investigation due to potential synergistic effects on morbidity and mortality.
Purpose of the Study:
- To evaluate the effect of COVID-19 infection on the frequency and severity of vasooclusive crises (VOCs) in patients with sickle cell anaemia (SCA).
- To assess the influence of COVID-19 on the morbidity and mortality associated with VOCs in SCA patients.
Main Methods:
- A prospective cohort study involving 100 SCA patients, divided into two groups: 50 with confirmed COVID-19 (COVID group) and 50 without (non-COVID group).
- Data collection included VOC episodes, hospitalizations, specific clinical manifestations, laboratory markers (hemoglobin, white blood cell count, platelets, lactate dehydrogenase, ferritin), and mortality rates.
Main Results:
- The COVID group experienced a higher median number of VOC episodes annually (3 vs 2, P < 0.05) and presented with more specific complications like osteonecrosis, splenic sequestration, splenomegaly, and hepatic crisis.
- While both groups showed reduced mean hemoglobin and lymphocyte subsets, the COVID group exhibited a subdued rise in white blood cell count, reticulocyte percentage, platelets, and ferritin.
- Hospitalization rates were similar between groups, and there was no statistically significant difference in mortality (2 deaths in the COVID group vs 3 in the non-COVID group).
Conclusions:
- COVID-19 infection may act as a trigger for vasooclusive crises (VOCs) in individuals with sickle cell anaemia (SCA).
- Despite increased VOC episodes and certain complications, COVID-19 did not significantly elevate overall VOC-related morbidity or mortality within this SCA cohort.
Objectives:
The study aimed to assess COVID-19 impact on the morbidity and mortality of vasooclusive crisis (VOC) in sickle cell anaemia (SCA) patients.
Methods:
A prospective cohort study of 100 SCA patients; 50 with COVID-19 (COVID group) and 50 without (non-COVID group). All patients signed written informed consent.
Results:
The COVID group had a significantly higher VOC episode median per year; 3 (IQR,1-6) vs 2 (IQR,2-12) (P < 0.05). The need for hospitalisation was similar in both groups. The non-COVID group had more history of culture-proven infection (P = 0.05). The COVID-group had more osteonecrosis (P < 0.05), splenic sequestration, splenomegaly and hepatic crisis (P = 0.05, 0.006, 0.02; respectively) and significantly higher (P < 0.05) symptoms of fever, cough, fatigue, abdominal pain and anosmia. Mean haemoglobin, lymphocyte subset, platelets, and reticulocytes were reduced in both groups, while lactate dehydrogenase and ferritin levels were significantly elevated. In the COVID group, the rise in white blood cell count, reticulocyte percentage, platelets and ferritin was subdued (P < 0.05). Two patients in the COVID group and 3 in the non-COVID group died; there was no statistically significant difference in mortality.
Conclusions:
Although COVID-19 may have triggered the onset of VOC, it did not significantly influence VOC-related morbidity or mortality in this SCA cohort.
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