Hemorrhagic complications in premature infants treated with intravitreal bevacizumab

Esra Kızıldağ Özbay1, Şenol Sabancı2, Mehmet Fatih Küçük2

  • 1Antalya Training and Research Hospital, Varlık, Kazım Karabekir Cd., Muratpaşa, Antalya, 07100, Turkey. esrakizildag.md@gmail.com.

PubMed

Insights

Prolonged NICU stays increase hemorrhagic complications in premature infants receiving intravitreal bevacizumab for retinopathy of prematurity. Each extra day in the NICU elevates the risk of bleeding events.

Area of Science:

  • Ophthalmology
  • Neonatology
  • Pharmacology

Background:

  • Retinopathy of prematurity (ROP) is a leading cause of visual impairment in premature infants.
  • Intravitreal bevacizumab is an off-label treatment for severe ROP, but carries potential risks.

Purpose of the Study:

  • To determine the incidence of hemorrhagic complications following intravitreal bevacizumab treatment for ROP.
  • To identify risk factors associated with these hemorrhagic complications in premature infants.

Main Methods:

  • Retrospective analysis of 132 premature infants treated with intravitreal bevacizumab for ROP.
  • Hemorrhagic complications were classified as preretinal or intravitreal.
  • Logistic regression analysis was used to identify independent risk factors.

Main Results:

  • Hemorrhagic complications occurred in 17.4% of infants.
  • Prolonged NICU length of stay was a significant independent risk factor for bleeding (p=0.008).
  • Each additional day in NICU increased bleeding risk by 5.1% (OR=1.051).

Conclusions:

  • NICU length of stay is a critical factor influencing hemorrhagic complications after intravitreal bevacizumab for ROP.
  • Preretinal and vitreous hemorrhages are common sequelae.
  • Minimizing NICU stay may reduce bleeding risk in these vulnerable infants.
Abstract