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Cost-effectiveness analysis of palivizumab in premature infants without chronic lung disease
Nahed O Elhassan1, Melony E S Sorbero, Caroline B Hall
1Division of Neonatology, Department of Pediatrics, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, USA.
Insights
Palivizumab prophylaxis for premature infants is generally not cost-effective for preventing respiratory syncytial virus. However, it may be cost-effective for some infants if severe asthma risk is considered.
Area of Science:
- Pediatric infectious diseases
- Health economics
- Respiratory medicine
Background:
- Respiratory syncytial virus (RSV) is a common cause of lower respiratory tract infections in infants.
- Palivizumab is an antibody used for RSV prophylaxis in high-risk infants.
- The cost-effectiveness of palivizumab in premature infants without chronic lung disease requires evaluation.
Purpose of the Study:
- To assess the cost-effectiveness of palivizumab for RSV prophylaxis in premature infants.
- To determine the impact of reduced asthma risk on palivizumab's cost-effectiveness.
Main Methods:
- Two decision analytic models were used: one including and one excluding the risk of asthma post-RSV infection.
- Hypothetical cohorts of premature infants (26-32 weeks gestation) without chronic lung disease were analyzed.
- Cost-effectiveness was measured by the incremental cost-effectiveness ratio (ICER) per quality-adjusted life-year (QALY).
Main Results:
- Palivizumab prophylaxis incurred higher costs than no prophylaxis.
- ICERs were generally high, exceeding the $200,000/QALY threshold, indicating limited cost-effectiveness.
- Models were sensitive to palivizumab cost and the quality of life impact of childhood asthma.
Conclusions:
- The study suggests more restrictive guidelines for palivizumab prophylaxis.
- Palivizumab demonstrated cost-effectiveness for certain infants when severe asthma risk following RSV infection was factored into the analysis.
Objectives:
To evaluate the cost-effectiveness of palivizumab as respiratory syncytial virus prophylaxis in premature infants without chronic lung disease and to evaluate the impact on cost-effectiveness of a potential reduction in risk of asthma following respiratory syncytial virus infection among infants receiving palivizumab.
Design:
Two decision analytic models were designed, one with and the other without accounting for increased risk of asthma following respiratory syncytial virus infection.
Setting:
A hypothetical community or university hospital.
Participants:
Hypothetical cohorts of infants without chronic lung disease born at 26 to 32 weeks' gestation.
Interventions:
Palivizumab prophylaxis vs no prophylaxis.
Main Outcome Measures:
Expected costs and incremental cost-effectiveness ratio expressed as cost per quality-adjusted life-year.
Results:
The expected costs were higher for palivizumab prophylaxis as compared with no prophylaxis. The incremental cost-effectiveness ratios were high for all gestations and are not considered cost-effective by today's standards (<$200 000 per quality-adjusted life-year). Both models were sensitive to variation in the cost of palivizumab. The model that included asthma was sensitive to variation in quality of life for children with asthma. In instances where asthma was considered severe with profound worsening in quality of life compared with life without asthma, some infants had an incremental cost per quality-adjusted life-year that was less than $200 000.
Conclusions:
Our model supports implementing more restrictive guidelines for palivizumab prophylaxis. Palivizumab was cost-effective for some infants in an analysis that accounted for increased risk of severe asthma following respiratory syncytial virus infection.
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