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.