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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.
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.
Purpose:
This study aims to evaluate the frequency of hemorrhagic complications and identify potential risk factors in premature infants treated with intravitreal bevacizumab for retinopathy of prematurity (ROP).
Methods:
This retrospective study analyzed data from 132 premature infants treated with intravitreal bevacizumab for ROP. Hemorrhagic complications were categorized as preretinal or intravitreal based on clinical examination findings: preretinal hemorrhages were defined as bleeding confined to the ROP ridge and not exceeding two optic disc diameters, while intravitreal hemorrhages were defined as bleeding extending beyond two optic disc diameters into the vitreous cavity. Demographic and clinical variables, including gestational age, birth weight, maternal age, NICU length of stay, and the timing of anti-VEGF administration, were collected. Patients with pre-existing hemorrhages prior to treatment were excluded. Statistical analyses included descriptive methods, univariate comparisons, and binary logistic regression to identify independent risk factors for hemorrhagic complications.
Results:
Hemorrhagic complications were observed in 23 (17.4%) of the patients, with 91.3% being preretinal hemorrhages and 8.7% intravitreal hemorrhages. NICU length of stay was significantly longer in patients with bleeding (62.23 ± 12.87 days) compared to those without bleeding (45.78 ± 16.74 days, p < 0.0001). Logistic regression identified prolonged NICU stay as an independent risk factor for hemorrhagic complications, with each additional day increasing the risk by 5.1% (p = 0.008, OR = 1.051, 95% CI 1.013-1.091). Gestational age, birth weight, maternal age, and timing of anti-VEGF administration were not significantly associated with bleeding risk.
Conclusions:
This study highlights the significant role of NICU length of stay in increasing the risk of hemorrhagic complications in premature infants treated with intravitreal bevacizumab. In retinopathy. of prematurity treated with bevacizumab, preretinal and vitreous hemorrhages are common. Each additional day of NICU stay increases the risk of hemorrhagic complications.
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