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An Improved and High Throughput Respiratory Syncytial Virus (RSV) Micro-neutralization Assay
Published on: January 26, 2019
Prevention of respiratory syncytial virus infection with palivizumab
M Thomas1, A Bedford-Russell, M Sharland
1Neonatal Unit, St. George's Hospital, London, UK.
Insights
Palivizumab reduces hospitalizations for premature infants with chronic lung disease (CLD) due to respiratory syncytial virus (RSV). However, its high cost limits use to specific high-risk infants, requiring further efficacy audits.
Area of Science:
- Pediatric infectious diseases
- Respiratory medicine
- Pharmacoeconomics
Background:
- Respiratory syncytial virus (RSV) is a common childhood infection, posing significant risks to premature infants with chronic lung disease (CLD).
- Hospitalization rates for RSV in this vulnerable group have shown a declining trend over the last decade.
- Palivizumab, a monoclonal antibody, offers prophylaxis against RSV infection.
Purpose of the Study:
- To evaluate the efficacy and cost-effectiveness of palivizumab for preventing RSV-related hospitalizations in premature infants with CLD.
- To identify specific subgroups of premature infants with CLD who may benefit most from palivizumab prophylaxis.
Main Methods:
- Analysis of data from the IMpact trial, assessing the impact of palivizumab on RSV hospital admissions.
- Cost-effectiveness analyses were conducted to determine the economic viability of palivizumab use.
- Identification of specific patient criteria for palivizumab consideration.
Main Results:
- The IMpact trial showed a 39% relative risk reduction in RSV hospital admissions with palivizumab use in premature infants with CLD.
- Cost-effectiveness analyses indicate that palivizumab is not cost-effective for the majority of premature infants, including those with or without CLD.
- Palivizumab use is primarily recommended for premature infants with CLD who are receiving home oxygen therapy during their first RSV season.
Conclusions:
- Palivizumab demonstrates efficacy in reducing RSV hospitalizations for a select group of high-risk premature infants with CLD.
- The high cost of palivizumab necessitates a targeted approach, limiting its use to infants with CLD on home oxygen.
- Further post-licensing audits are crucial to validate the real-world efficacy of palivizumab in this specific high-risk population.
Abstract:
Respiratory syncytial virus (RSV) infects virtually all children by the age of 2 yrs. Premature infants with chronic lung disease (CLD) are at risk of greater morbidity due to RSV infection. However, these infants represent a small proportion of all infants admitted to hospital with RSV infection, and hospitalization rates for this group appear to have decreased over the past decade. Prophylaxis against RSV infection has recently become available in the form of palivizumab, a humanized monoclonal antibody preparation. The IMpact trial demonstrated a 39% relative risk reduction in hospital admissions for RSV in cases in which palivizumab was administered to premature infants with CLD. However, palivizumab is a very expensive drug and cost-effectiveness analyses do not support its use in the majority of premature infants with or without CLD. The only group in which palivizumab should even be considered for use is premature infants with chronic lung disease at home on oxygen during their first respiratory syncytial virus season. In this group of infants, a detailed postlicensing audit needs to be performed to determine efficacy.
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