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Updated: Jun 9, 2025

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
Newborn Screening for Sickle Cell Disease in Catalonia between 2015 and 2022-Epidemiology and Impact on Clinical
José Manuel González de Aledo-Castillo1, Ana Argudo-Ramírez1, David Beneitez-Pastor2
1Section of Inborn Errors of Metabolism, Department of Biochemistry and Molecular Genetics, Hospital Clínic de Barcelona, 08028 Barcelona, Spain.
Insights
Catalonia's newborn screening for sickle cell disease (SCD) led to earlier diagnosis and treatment. Screened children experienced significantly fewer clinical events, emergency visits, and hospitalizations, improving their quality of life.
Area of Science:
- Pediatrics
- Hematology
- Public Health
Background:
- Catalonia implemented newborn screening (NBS) for sickle cell disease (SCD) in 2015.
- Standard care includes penicillin, hydroxyurea, and vaccinations.
- Limited data exists on the clinical impact of SCD NBS programs.
Purpose of the Study:
- To analyze the incidence of SCD and related hemoglobinopathies in Catalonia.
- To assess the clinical impact of SCD NBS on patient outcomes.
- To evaluate changes in clinical events after NBS introduction.
Main Methods:
- Retrospective multicenter study analyzing 506,996 newborns screened from 2015-2022.
- Included 100 screened (SG) and 95 unscreened (UG) SCD patients.
- Compared SCD-related clinical events in the first six years of life.
Main Results:
- Identified 160 SCD cases, with an incidence of 1 in 3169 newborns.
- SG showed significantly earlier diagnosis (0.1 vs. 1.68 years) and treatment initiation.
- SG experienced fewer clinical events (0.19 vs. 0.77/year), ED visits (0.37 vs. 0.76/year), and hospitalizations (0.33 vs. 0.72/year).
Conclusions:
- Newborn screening for SCD in Catalonia significantly reduces morbidity.
- Early diagnosis and treatment initiation improve the quality of life for affected children.
- NBS programs are effective in managing sickle cell disease.
Abstract:
In 2015, Catalonia introduced sickle cell disease (SCD) screening in its newborn screening (NBS) program along with standard-of-care treatments like penicillin, hydroxyurea, and anti-pneumococcal vaccination. Few studies have assessed the clinical impact of introducing NBS programs on SCD patients. We analyzed the incidence of SCD and related hemoglobinopathies in Catalonia and the change in clinical events occurring after introducing NBS. Screening 506,996 newborns from 2015 to 2022, we conducted a retrospective multicenter study including 100 screened (SG) and 95 unscreened (UG) SCD patients and analyzed SCD-related clinical events over the first six years of life. We diagnosed 160 cases of SCD, with an incidence of 1 in 3169 newborns. The SG had a significantly lower median age at diagnosis (0.1 y vs. 1.68 y, p < 0.0001), and initiated penicillin prophylaxis (0.12 y vs. 1.86 y, p < 0.0001) and hydroxyurea treatment earlier (1.42 y vs. 4.5 y, p < 0.0001). The SG experienced fewer median SCD-related clinical events (vaso-occlusive crisis, acute chest syndrome, infections of probable bacterial origin, acute anemia requiring transfusion, acute splenic sequestration, and pathological transcranial Doppler echography) per year of follow-up (0.19 vs. 0.77, p < 0.0001), a reduced number of annual emergency department visits (0.37 vs. 0.76, p < 0.0001), and fewer hospitalizations (0.33 vs. 0.72, p < 0.0001). SCD screening in Catalonia's NBS program has effectively reduced morbidity and improved affected children's quality of life.
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