COVID- 19 in patients affected by red blood cell disorders, results from the European registry ERN-EuroBloodNet
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Pablo Velasco Puyo1, Soteroula Christou2, Saveria Campisi3
1Pediatric Oncology and Hematology, Vall d'Hebron Barcelona Hospital, Passeig Vall Hebron 129, 08035, Barcelona, Spain. Pablo.velascopuyo@vallhebron.cat.
Insights
COVID-19 infections in sickle cell disease (SCD) and red blood cell disease (RBCD) patients are generally mild with low mortality. International registries like ERN-EuroBloodNet are crucial for rare disease research during health crises.
Area of Science:
- Hematology
- Infectious Diseases
- Epidemiology
Background:
- No international registry existed for COVID-19 in red blood cell diseases (RBCD).
- ERN-EuroBloodNet established a registry for real-time SARS-CoV-2 patient data during the pandemic.
- This facilitated timely, disease-specific knowledge sharing for rare blood disorders.
Purpose of the Study:
- To analyze patient distribution and COVID-19 infection across different RBCDs.
- To identify risk factors for COVID-19 severity in RBCD patients.
- To evaluate the impact of vaccination and comorbidities on COVID-19 outcomes.
Main Methods:
- Data collected via ERN-EuroBloodNet's REDCap platform from April 2020 to April 2023.
- Analysis of patient demographics, infection incidence, and severity factors.
- Comparison of COVID-19 outcomes between sickle cell disease (SCD) and thalassemia (TDT/NTDT) patients.
Main Results:
- 681 infections recorded in 663 RBCD patients (373 TDT/NTDT, 269 SCD).
- SCD patients had higher COVID-19 incidence than TDT/NTDT (10.5 vs. 4.8 per 100 patients).
- 92% of cases were mild; comorbidities (obesity, hypertension) and specific complications (ACS, kidney failure) increased severity. Vaccination showed a protective effect. Mortality (0.7%) was similar to the general population.
Conclusions:
- SARS-CoV-2 infection in SCD and TDT/NTDT patients is generally mild with no increased mortality compared to the general population.
- International registries are vital for rare disease management during health emergencies.
- Collaborative efforts like ERN-EuroBloodNet are essential for rare disease research and patient care.
Background:
Despite several publications covering patients from multiple centers, no international registry covered all patients with red blood cell diseases (RBCD) affected by COVID- 19. The ERN-EuroBloodNet's registry provided real-time registration of SARS-CoV- 2 patients with RBCD, promoting timely disease-specific knowledge sharing during the pandemic's early stages.
Procedures:
The study evaluated patient distribution, the infection across different RBCDs, and severity risk factors across similar healthcare systems, using data collected from the ERN-EuroBloodNet's REDCap platform.
Results:
From April 2020 to April 2023, 681 infections were recorded among 663 patients, of which 373 had transfusion-dependent thalassemia or non-transfusion-dependent thalassemia (TDT/NTDT), and 269 had sickle cell disease (SCD). SCD patients had a higher incidence of COVID- 19 than those with TDT/NTDT (10.5 vs. 4.8 COVID/100 patients). Notably, 92% of the cases were mild, with neither age nor the specific RBCD affecting severity. The number of comorbidities, notably obesity and hypertension, that patients had prior to infection was associated with more severe COVID- 19. During the infection, the presence of vaso-occlusive crises, acute chest syndrome, kidney failure, and ground-glass opacities on chest tomography scans were associated with a more severe clinical picture. The vaccination rate (32%) mirrored that of the general population and showed a protective effect against severe COVID- 19. The observed mortality rate was 0.7%, aligning with Europe's general population.
Conclusion:
SARS-CoV- 2 infection in SCD and TDT/NTDT patients is mild and without higher mortality than the general population. The ERN-Eurobloodnet's registry collaborative structure exemplifies the power of international cooperation in tackling rare diseases, especially during health emergencies.
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