Neonatal/newborn haemoglobinopathy screening in Europe and Africa

B J Bain1

  • 1Department of Haematology, St Mary's Hospital, London, UK. b.bain@ic.ac.uk

Insights

Neonatal screening for haemoglobinopathy, including sickle cell disease, is expanding globally. Early detection improves infant care through education and infection prevention strategies.

Area of Science:

  • Medical Science
  • Public Health
  • Genetics

Background:

  • Changing immigration patterns increase the number of neonates at risk for sickle cell disease in Europe.
  • Haemoglobinopathy screening programs vary, with some standalone and others integrated into metabolic disorder screening.

Purpose of the Study:

  • To outline the growing implementation of neonatal haemoglobinopathy screening.
  • To highlight the benefits of early detection for managing sickle cell disease.

Main Methods:

  • Review of current neonatal screening practices for haemoglobinopathies.
  • Analysis of program integration and standalone approaches.

Main Results:

  • Increasing adoption of neonatal haemoglobinopathy screening in European countries.
  • Gradual introduction of screening programs in African nations despite challenges.

Conclusions:

  • Neonatal haemoglobinopathy screening is crucial for early intervention in sickle cell disease.
  • Screening programs are expanding despite logistic and economic constraints.