Neonatal screening in Hong Kong and Macau

S T S Lam1, M L Cheng

  • 1Clinical Genetic Service, Department of Health, Hong Kong.

Insights

Hong Kong

Area of Science:

  • Public Health
  • Neonatal Screening
  • Genetics

Background:

  • Neonatal screening programs require careful consideration of public health impact, system feasibility, and social factors.
  • Glucose-6-Phosphate Dehydrogenase (G6PD) deficiency and Congenital Hypothyroidism (CHT) were identified for screening in Hong Kong in the early 1980s.

Purpose of the Study:

  • To detail the implementation and evaluate the outcomes of Hong Kong's territory-wide neonatal screening program for G6PD deficiency and CHT.
  • To present the methodology and results of G6PD deficiency screening in Macau.

Main Methods:

  • A territory-wide screening program for G6PD deficiency and CHT was implemented in Hong Kong in 1984, achieving over 99% newborn coverage.
  • Pre-screening education was provided to 95% of pregnant women through Department of Health centers.
  • G6PD deficiency screening began in Macau in 1977 in one major hospital.

Main Results:

  • In Hong Kong, the incidence of CHT was 1 in 2404, and G6PD deficiency affected 4.5% of males and 0.3% of females.
  • Over 99% of Hong Kong newborns have been screened since the program's inception.
  • Macau has initiated G6PD deficiency screening but not CHT screening.

Conclusions:

  • Hong Kong's comprehensive neonatal screening program for G6PD deficiency and CHT has achieved high coverage and provided valuable incidence data.
  • The study highlights the importance of public health impact, system feasibility, and social considerations in establishing effective neonatal screening programs.
  • Comparative data on screening programs in Hong Kong and Macau are presented.

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