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A Lower Dose of Intravitreal Bevacizumab Effectively Treats Retinopathy of Prematurity Publisher Pubmed



Khodabande A1 ; Niyousha MR1 ; Roohipoor R1
Authors
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Authors Affiliations
  1. 1. Fabrabi Eye Research Center, Tehran University of Medical Sciences (TUMS), Tehran, Iran

Source: Journal of AAPOS Published:2016


Abstract

Purpose To determine whether a low dose (0.25 mg/0.01 mL) of intravitreal bevacizumab is effective in the treatment of type 1 retinopathy of prematurity (ROP). Methods This prospective, noncomparative, interventional case series included all consecutive infants who received 0.25 mg/0.01 mL of intravitreal bevacizumab for type 1 ROP. Infants were followed for ROP persistence/recurrence until 90 weeks’ postmenstrual age. Results A total of 49 eyes of 25 infants (24 bilateral and 1 unilateral) underwent intravitreal injection of a reduced dose (0.25 mg/0.01 mL) of intravitreal bevacizumab. ROP regressed in all eyes. Follow-up continued until 90 weeks’ postmenstrual age and showed no recurrences of plus disease or neovascularization. Conclusions All eyes treated with 0.25mg/0.01ml intravitreal bevacizumab showed complete regression, with no recurrence of plus disease or neovascularization. No safety issues were attributable to bevacizumab during the study period. © 2016 American Association for Pediatric Ophthalmology and Strabismus