Isaac M, Tehrani N, Mireskandari K
Department of Ophthalmology and Vision Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada.
Department of Ophthalmology and Vision Sciences, University of Toronto, Toronto, Ontario, Canada.
Eye (Lond). 2016 Mar;30(3):333-41. doi: 10.1038/eye.2015.289. Epub 2016 Feb 12.
To describe involution patterns following monotherapy with intravitreal bevacizumab injection (IVB) for type 1 retinopathy of prematurity (ROP) in zone I or zone II posterior.
A retrospective chart review of infants treated with IVB from January 2010-April 2014. Infants with minimum of 82 weeks postmenstrual age at last follow-up were included. Primary outcome was timing of involution of type 1 ROP for the first 12 weeks post treatment. Secondary outcomes were development of any recurrence and structural outcome at last follow-up. Retinal examination records, fundus, and flourescein angiography images were reviewed.
Twenty-eight eyes were included. Average follow-up post treatment was 33.9±9.7 months (range 21.4-61.9). Cumulative frequency of regression of plus disease was seen in 73.3, 86.7, and 100% of eyes by days 3, 5, and 8, respectively. Regression of both stage 3 and plus disease was observed in 29, 82, 88, and 100% by weeks 1, 2, 3, and 4, respectively. Within the first 3 months, 17/28 eyes developed recurrence to stage 1 or 2 after regression. None developed recurrence of plus disease. By the end of 3 months 18% of eyes vascularized into zone III. At a mean of 24±17.3 months, 39% of eyes were not vascularized into zone III as seen on flourescein angiography with scleral indentation.
Our experience suggests regression of plus disease and stage 3 are expected within the first 4 weeks after bevacizumab treatment. Recurrence may occur despite initial regression and requires careful follow-up.
描述玻璃体内注射贝伐单抗(IVB)单药治疗I区或II区后部1型早产儿视网膜病变(ROP)后的 involution 模式。
对2010年1月至2014年4月接受IVB治疗的婴儿进行回顾性病历审查。纳入末次随访时月经后年龄至少82周的婴儿。主要结局是治疗后前12周1型ROP的 involution 时间。次要结局是末次随访时任何复发的发生情况和结构结局。回顾视网膜检查记录、眼底和荧光素血管造影图像。
纳入28只眼。治疗后平均随访33.9±9.7个月(范围21.4 - 61.9个月)。分别在第3天、第5天和第8天,73.3%、86.7%和100%的眼出现附加病变消退的累积频率。分别在第1周、第2周、第3周和第4周,29%、82%、88%和100%的眼观察到3期病变和附加病变均消退。在最初3个月内,17/28只眼在消退后复发至1期或2期。无附加病变复发。到3个月末,18%的眼血管化至III区。平均24±17.3个月时,荧光素血管造影联合巩膜压陷显示39%的眼未血管化至III区。
我们的经验表明,贝伐单抗治疗后前4周内附加病变和3期病变有望消退。尽管最初消退仍可能发生复发,需要仔细随访。