First versus second year respiratory syncytial virus prophylaxis in chronic lung disease (2005-2015)

Daniel Y Wang1, Abby Li1, Bosco Paes2

  • 1Medical Outcomes and Research in Economics (MORE®) Research Group, Sunnybrook Health Sciences Centre, University of Toronto, 2075 Bayview Avenue, Room FG-21, Toronto, ON, M4N 3M5, Canada.

Insights

Children with chronic lung disease (CLD) receiving palivizumab in their second year of life face similar hospitalization risks for respiratory illness and respiratory syncytial virus (RSV) as those in their first year. This supports continued prophylaxis for high-risk infants based on neonatal severity.

Area of Science:

  • Pediatrics
  • Infectious Diseases
  • Respiratory Medicine

Background:

  • Infants with chronic lung disease (CLD) have a significantly higher risk of hospitalization due to respiratory syncytial virus (RSV) compared to healthy infants.
  • Palivizumab prophylaxis is a common preventative measure for RSV-related lower respiratory tract infections in high-risk children.
  • Recent guidelines recommend limiting palivizumab to specific criteria, such as gestational age or oxygen dependency in the first year of life.

Purpose of the Study:

  • To compare the risks of respiratory-related illness hospitalization (RIH) and RSV hospitalization (RSVH) in CLD children receiving palivizumab in their first year (FY) versus second year (SY) of life.
  • To evaluate the effectiveness of current selection criteria for palivizumab prophylaxis in CLD children entering their second year of life.

Main Methods:

  • Retrospective analysis of data from the Canadian Registry of Palivizumab (CARESS) from 2005 to 2015.
  • Comparison of demographic data and hospitalization events (RIH and RSVH) between FY and SY CLD children.
  • Use of Cox regression to analyze the hazards for RIH and RSVH in both groups.

Main Results:

  • SY CLD children had lower gestational age and required more neonatal respiratory support, oxygen therapy, and longer hospital stays compared to FY children.
  • RIH rates were 12.2% in FY and 18.2% in SY children.
  • RSVH rates were 2.3% in FY and 3.9% in SY children.
  • Cox regression revealed similar hazards for both RIH (HR 0.9) and RSVH (HR 1.1) between FY and SY CLD children.

Conclusions:

  • Children with CLD receiving palivizumab in their second year of life demonstrate similar risks for RIH and RSVH compared to those receiving it in their first year.
  • The findings suggest that the selection of SY children for palivizumab prophylaxis, based on neonatal illness severity, is appropriate.
  • Palivizumab prophylaxis in the second year of life appears warranted for CLD children identified as high-risk based on their neonatal course.

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