Clinical Study

Outcomes and Prognostic Factors of Intravitreal Bevacizumab Monotherapy in Zone I Stage 3+ and Aggressive Posterior Retinopathy of Prematurity

Figure 2

(a) Zone I disease prior to the bevacizumab injection: female infant, BW 2050 g, GA 28 w, treated with intravitreal bevacizumab at PMA of 34 weeks and PNA of 6 weeks. (b) The same case as in (a), 8 weeks after the intravitreal injection of bevacizumab showing ROP regression.
(a)
(b)