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An Improved and High Throughput Respiratory Syncytial Virus (RSV) Micro-neutralization Assay
Published on: January 26, 2019
Respiratory syncytial virus immunoprophylaxis in high-risk infants with heart disease
Peta M A Alexander1, Lucas Eastaugh, Jenny Royle
1Department of Cardiology, The Royal Children's Hospital, Melbourne, Victoria, Australia. peta.alexander@rch.org.au
Insights
Palivizumab significantly reduced hospitalizations for respiratory syncytial virus (RSV) in infants with heart disease. This passive immunisation strategy offers a cost-effective approach to managing RSV in this vulnerable population.
Area of Science:
- Pediatric Cardiology
- Infectious Diseases
- Neonatal Care
Background:
- Infants with hemodynamically significant cardiac disease face severe respiratory syncytial virus (RSV) bronchiolitis.
- Passive immunisation with palivizumab is a recommended intervention for these high-risk infants.
Purpose of the Study:
- To evaluate the effectiveness of palivizumab in reducing RSV hospital admissions in infants with cardiac disease.
- To assess the impact of palivizumab on the course and cost of RSV bronchiolitis in this population.
Main Methods:
- Retrospective analysis of RSV admissions from 2005-2009.
- Examination of infants with cardiac disease who received palivizumab during 2008-2009.
Main Results:
- Infants with cardiac disease experienced more severe RSV bronchiolitis, including longer hospital stays and increased intensive care needs.
- Palivizumab use was associated with a reduction in RSV hospital admissions (2% per year) compared to pre-intervention rates (5-9% per year).
- Intensive care admissions for RSV bronchiolitis remained unchanged, potentially due to late diagnosis or presentation from other centers.
Conclusions:
- Palivizumab effectively reduced RSV hospitalizations in infants with hemodynamically significant cardiac disease.
- Targeted palivizumab use demonstrated cost-effectiveness.
- Regional consideration of immunoprophylaxis is recommended to impact intensive care admissions.
Aim:
Passive immunisation with palivizumab is recommended in many countries for children with haemodynamically significant cardiac disease. We trialled respiratory syncytial virus (RSV) immunoprophylaxis in such infants during 2008–2009.
Methods:
We identified all RSV admissions between 2005–2009 and examined all patients with significant cardiac disease who received palivizumab in 2008–2009.
Results:
Infants with symptomatic cardiac disease had a more complicated course of RSV bronchiolitis with longer hospital stay, more frequent intensive care admission, longer intensive care stay and were more likely to receive respiratory support (all P < 0.05). One hundred seventeen infants with symptomatic cardiac disease received palivizumab. Of these, two (1.7%) required admission for RSV bronchiolitis. Overall, there was a reduction in admission of infants with symptomatic cardiac disease with RSV bronchiolitis in 2008–2009 (2% per year) compared with 2005–2007 (5–9% per year; P < 0.03). The number of patients with symptomatic cardiac disease who required intensive care for RSV bronchiolitis in the same period was unchanged, as a number presented to our service with RSV infection prior to commencing immunoprophylaxis or having had their cardiac diagnosis made in other centres.
Conclusions:
Compared with other infants, those with haemodynamically significant cardiac disease have a more complicated course of illness with RSV bronchiolitis. In these infants, palivizumab reduced the number of hospitalisations because of RSV. Cohorting patients for maximal palivizumab use reduced overall cost. To significantly impact on intensive care admissions overall, immunoprophylaxis should be considered at a regional level.
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