Cost-benefit analysis of newborn screening for galactosemia in the Philippines

Carmencita D Padilla1, Leonila F Dans, Sylvia C Estrada

  • 1Department of Pediatrics, Philippine General Hospital, University of the Philippines, Manila, Philippines.

Insights

Newborn screening for galactosemia (GAL) in the Philippines found an incidence of 1 in 106,006. The current screening program

Area of Science:

  • Medical Genetics
  • Public Health
  • Health Economics

Background:

  • Galactosemia (GAL) is a rare genetic disorder.
  • Early detection and treatment are crucial to prevent severe health complications.
  • Newborn screening programs aim to identify infants with GAL shortly after birth.

Purpose of the Study:

  • To determine the incidence of galactosemia in the Philippines.
  • To evaluate the cost-benefit of newborn screening for GAL from a societal perspective.

Main Methods:

  • Cost-benefit analysis was performed.
  • Newborn screening utilized the Beutler test after 24 hours of life.
  • Incidence rates from the Philippine Newborn Screening Program (PNSP) were used to compare costs and benefits.

Main Results:

  • Screening of 157,186 newborns identified 2 cases of galactosemia, yielding an incidence of 1 in 106,006.
  • Projected costs for the screening program were $1.1M, with benefits of $0.2M, resulting in a net cost of $0.9M.
  • The cost-benefit analysis indicated that program costs outweigh the benefits at the observed incidence rate.

Conclusions:

  • The current newborn screening for galactosemia in the Philippines is not cost-beneficial based on the determined incidence.
  • Further research into the true incidence of GAL in the Philippine population is needed.
  • Adjusting screening strategies or considering a higher incidence rate may improve the program's net benefits.