Hypertension in neonates treated with intravitreal bevacizumab for retinopathy of prematurity

J Perinatol. 2021 Jun;41(6):1426-1431. doi: 10.1038/s41372-021-01021-w. Epub 2021 Mar 8.

Abstract

Objective: To investigate if preterm neonates developed systemic hypertension after intravitreal bevacizumab for retinopathy of prematurity.

Methods: Patients who received treatment between January 1, 2011 and January 31, 2019 were eligible for inclusion. Patients with pre-existing hypertension, congenital eye disease, or who were discharged within 72 h of treatment were excluded. Charts were reviewed for baseline data, co-morbidities, and the development of systemic hypertension within 4 weeks post treatment.

Results: After exclusions, 64 patients were analyzed. New-onset systemic hypertension was identified in 44 (69%) infants. There were no statistical differences in the demographic characteristics or presence of co-morbidities between the hypertensive and non-hypertensive groups. Of those who developed hypertension, the majority presented within the first week post treatment (55%).

Conclusions: The majority of infants who received intravitreal bevacizumab developed new-onset systemic hypertension after treatment. Further studies may explore hypertension as a potential side effect of bevacizumab in the neonatal population.

MeSH terms

  • Bevacizumab / adverse effects
  • Humans
  • Hypertension* / chemically induced
  • Hypertension* / drug therapy
  • Hypertension* / epidemiology
  • Infant, Newborn
  • Retinopathy of Prematurity* / drug therapy

Substances

  • Bevacizumab