J Pediatr Infect Dis 2024; 19(06): 327-333
DOI: 10.1055/s-0044-1789266
Original Article

Effect of Palivizumab Prophylaxis on Respiratory Syncytial Virus Hospitalizations in Preterm Infants Born to 290/7 to 316/7 Weeks of Gestational Age

Autoren

  • Elifcan Zamur

    1   Department of Pediatrics, Izmir Tepecik Training and Research Hospital, İzmir, Türkiye
  • Ozgun Uygur

    2   Division of Neonatology, Department of Pediatrics, Izmir Tepecik Training and Research Hospital, İzmir, Türkiye
  • Eda Karadag-Oncel

    3   Division of Pediatric Infectious Diseases, Department of Pediatrics, Dokuz Eylul University Faculty of Medicine, İzmir, Türkiye
  • Sezgin Gunes

    4   Division of Neonatology, Department of Pediatrics, Izmir Buca Seyfi Demirsoy Training and Research Hospital, İzmir, Türkiye
  • Suzan Sahin

    5   Division of Neonatology, Department of Pediatrics, Izmir Demokrasi University Faculty of Medicine, İzmir, Türkiye
  • Melike Kefeli Demirel

    2   Division of Neonatology, Department of Pediatrics, Izmir Tepecik Training and Research Hospital, İzmir, Türkiye
  • Defne Engur

    2   Division of Neonatology, Department of Pediatrics, Izmir Tepecik Training and Research Hospital, İzmir, Türkiye
  • Mehmet Yekta Oncel

    6   Division of Neonatology, Department of Pediatrics, Izmir Katip Çelebi University Faculty of Medicine, İzmir, Türkiye

Funding The authors declare the study received no funding.

Abstract

Objective In 2020, in-line with the recommendations of the Turkish Neonatal Society, a new palivizumab indication was added for preterm infants with 290/7 to 316/7 weeks of gestational age. This study aimed to determine the risk factors of hospitalizations due to lower respiratory tract infections (LRTIs) and respiratory syncytial virus (RSV) in preterm infants (290/7–316/7 weeks of gestational age) who were or were not within the scope of palivizumab indication during the first two RSV seasons (2018–2019 and 2019–2020) and the next two RSV seasons (2020–2021 and 2021–2022) to evaluate the validity of the new indication of palivizumab reimbursement scope.

Methods This study was a two-center retrospective and prospective cohort study and included all preterm infants (290/7–316/7 weeks) aged 90 days and younger during the RSV season (October–March). The primary outcome was to compare the hospitalization rates between patients who received palivizumab and those who did not. The secondary outcome was to identify the risk factors for patients hospitalized due to LRTIs.

Results Of the 122 preterm infants included in the study, 48.3% (n = 59) were in the prophylaxis group (Group 1) and 51.7% (n = 63) were in the non-prophylaxis group (Group 2). It was noteworthy that 53.8% (n = 14) of the 26 infants hospitalized due to LRTIs were in Group 1 and 46.2% (n = 12) were in Group 2 (p = 0.682). Of the RSV PCR-positive infants, 62.5%(n = 5) were in Group 1 and 37.5% (n = 3) were in Group 2 (p = 0.30). The median length of hospitalization was similar in the groups (p = 0.123).

Conclusion The indication for palivizumab prophylaxis can be determined more clearly for our country in light of national multicenter studies with an increased sample size.



Publikationsverlauf

Eingereicht: 31. Januar 2024

Angenommen: 05. August 2024

Artikel online veröffentlicht:
22. August 2024

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