Cost-benefit analysis of G6PD screening in Lebanese newborn males

Issam Khneisser1, Salim M Adib, Jacques Loiselet

  • 1Newborn Screening Laboratory, Medical Genetic Unit, Faculty of Medicine, Saint Joseph University, B.P. 11-5076 Riad El Solh, Beirut, Lebanon. issam.khneisser@usj.edu.lb

Insights

Systematic newborn screening for Glucose-6-Phosphate Dehydrogenase (G6PD) deficiency in Lebanon is highly cost-effective. Early detection significantly reduces severe anemia crises and hospitalizations, lowering overall healthcare costs compared to managing the condition without screening.

Area of Science:

  • Medical Genetics
  • Public Health
  • Health Economics

Background:

  • Glucose-6-Phosphate Dehydrogenase (G6PD) deficiency is a prevalent genetic disorder in Lebanon, affecting 1% of males.
  • Established screening methods allow for early detection in newborns.

Purpose of the Study:

  • To evaluate the cost-effectiveness of universal G6PD deficiency screening for all male newborns in Lebanon.
  • To compare healthcare costs associated with screened versus unscreened G6PD-deficient individuals.

Main Methods:

  • A retrospective survey of 139 G6PD-deficient babies identified between 1999 and 2004 was conducted.
  • Data on acute anemia crises and hospitalizations were collected and compared to historical community data.

Main Results:

  • Screened G6PD-deficient infants experienced a 95% reduction in severe acute anemia crises requiring hospitalization compared to unscreened individuals.
  • The cost of screening (3 USD) is substantially lower than the estimated hospitalization cost (1450 USD).
  • Systematic screening is approximately 2.58 times more cost-effective than managing anemia-related hospitalizations in an unscreened population.

Conclusions:

  • Routine G6PD deficiency testing in newborns is an efficient strategy.
  • The findings support revising screening policies to include all male infants.
Abstract

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