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Cost effectiveness of establishing a neonatal screening programme for phenylketonuria in Libya
Erikas Sladkevicius1, Rodney J Pollitt, Ali Mgadmi
1CATALYST Health Economics Consultants Ltd, Northwood, Middlesex, UK.
Insights
Introducing neonatal screening for phenylketonuria (PKU) in Libya is a cost-effective strategy. This initiative is projected to save millions and significantly improve public health outcomes by detecting PKU early.
Area of Science:
- Public Health
- Metabolic Disorders
- Health Economics
Background:
- Inborn errors of metabolism (IEM) contribute significantly to morbidity and mortality in North Africa and the Middle East.
- Libya is considering implementing neonatal screening for phenylketonuria (PKU), with future plans to expand to other IEMs.
Purpose of the Study:
- To evaluate the cost-effectiveness of neonatal screening for PKU in Libya compared to no screening.
- To provide economic data to support the potential implementation of a national PKU screening program.
Main Methods:
- A decision model was developed to analyze the cost-effectiveness from a societal perspective.
- Expert opinion was utilized to determine healthcare resource use and other input parameters for the model.
Main Results:
- Neonatal screening for PKU is estimated to save Libyan society approximately $US107.6 million over the lifetime of patients.
- The screening program is projected to gain 6947 life-years, with a negative cost per life-year gained (-$US15,500).
- The program demonstrates a 90% return on investment and has a high probability (0.95) of being cost-effective.
Conclusions:
- Neonatal screening for PKU presents a cost-effective strategy for Libyan society.
- The findings support the implementation of a national PKU screening program in Libya.
Background:
Inborn errors of metabolism (IEM) are a significant cause of morbidity and mortality in North Africa and the Middle East. With the evident success of neighbouring countries in initiating neonatal screening for IEM, the Libyan Authorities are now considering introducing neonatal screening for phenylketonuria (PKU) in Libya in the first instance, with the prospect of expanding the programme to cover other IEM in the future.
Objective:
To estimate the cost effectiveness of neonatal screening for PKU compared with no neonatal screening in Libya.
Methods:
A decision model was constructed to estimate the cost effectiveness of neonatal screening for PKU, from the perspective of Libyan society. Healthcare resource use and other input parameters were based on expert opinion.
Results:
The expected discounted cost to Libyan society of screening over 15 years and managing ∼374 patients with detected PKU over their lifetime was estimated to be $US213.6 (95% CI 211.9, 214.3) million (year 2007-8 values). The current expected discounted cost of managing these same PKU patients over their lifetime as a result of not screening was estimated to be $US321.2 (95% CI 318.0, 322.7) million. Hence, screening would save Libyan society $US107.6 (95% CI 105.5, 109.1) million over the lifetime of PKU patients and lead to an additional 6947 life-years (95% CI 6837, 7056). The expected cost per undiscounted life-year gained was estimated to be -$US15,500 (95% CI -16,600, 1100). There would be a 90% return on investment in the screening programme since society would gain $US1.9 for every $US1 invested. Probabilistic sensitivity analysis demonstrated that the screening programme has a 0.95 probability of being cost effective even at a willingness-to-pay threshold of $US4000 per life-year gained.
Conclusions:
Within the model's limitations, neonatal screening for PKU appears to offer Libyan society a strategy that is cost effective compared with no neonatal screening.
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