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Updated: Jun 22, 2026

Generation, Amplification, and Titration of Recombinant Respiratory Syncytial Viruses
Published on: April 4, 2019
[Respiratory syncytial virus prophylaxis among preterm infants--four seasons' experience]
Małgorzata Klimek1, Przemko Kwinta, Piotr Kruczek
1Klinika Chorób Dzieci Katedry Pediatrii, Uniwersytet Jagielloński Collegium Medium w Krakowie.
Insights
Respiratory syncytial virus (RSV) prophylaxis with palivizumab is most effective in preterm newborns with extremely low birth weight. This preventative treatment should be considered for these vulnerable infants, regardless of bronchopulmonary dysplasia status.
Area of Science:
- Neonatology
- Pediatric Infectious Diseases
- Immunology
Context:
- Respiratory syncytial virus (RSV) is a leading cause of hospitalization in infants.
- Preterm infants, especially those with bronchopulmonary dysplasia (BPD) or cardiac defects, face severe RSV infection risks.
- Palivizumab, a monoclonal antibody, is used for RSV prophylaxis.
Purpose:
- To evaluate the effectiveness of palivizumab for RSV prophylaxis in preterm newborns.
- To identify factors influencing the efficacy of RSV infection prevention in this high-risk population.
Summary:
- A study of 55 preterm infants (mean gestational age 27 weeks) receiving palivizumab showed 18% required hospitalization between doses or within 28 days post-prophylaxis.
- Only 3.6% of hospitalizations were due to severe RSV infection.
- Prophylaxis was most beneficial for extremely low birth weight infants and those not requiring respiratory support at discharge.
Impact:
- RSV prophylaxis is most beneficial for extremely low birth weight preterm infants.
- Consider palivizumab for extremely low birth weight infants with or without BPD.
- This research informs clinical decisions for RSV prevention in vulnerable preterm populations.
Background:
Respiratory syncitial virus (RSV) is the main reason of hospitalizations due to respiratory tract infection in children within the first year of life. The course of infection is more severe in children from a risk group, which includes children who were born preterm, these with bronchopulmonary dysplasia (BPD), children with heart defects significantly influencing their hemodynamics, and immunocompromised children. Palivizumab is a humanized monoclonal antibody class IgG-1 used to prevent RSV infection.
Aim:
To assess the results of treatment and to evaluate factors influencing the efficacy of RSV infection prophylaxis in preterm newborns.
Methods:
The study included 55 preterm newborns (mean birth weight-970g, mean gestational age-27 weeks), who were given a dose of palmivizumab of 15mg per kg body weight every four weeks in autumn and winter from season 2004/ 2005 to season 2007/2008.
Results:
Ten children (18%) required hospitalization between the doses and within 28 days after the last dose of palmivizumab. Among these, 2 children (3.6%) were hospitalized because of very severe RSV infection. Eight children (16%) were hospitalized due to respiratory tract infection within 12 months after completing the prophylaxis; none of them was infected with RSV. The episodes of respiratory tract infection between the doses and within 28 days after the last dose occurred in 19 children (31%), and in 26 patients included in the follow-up (51%) within 12 months after completing the prophylaxis. The effect of treatment was most beneficial in preterm neonates with extremely low birth weight and in children who did not require respiratory medications at the moment of discharge from the neonatal unit.
Conclusion:
RSV infection prophylaxis is of most benefit in children born with extremely low birth weight. In this group of children the prophylaxis should be considered both for children suffering from BPD and in children free of this disease.
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