Department of Ophthalmology, Xinhua Hospital Affiliated to Shanghai JiaoTong University School of Medicine, Shanghai, China.
Acta Ophthalmol. 2013 Jun;91(4):e304-10. doi: 10.1111/aos.12055. Epub 2013 May 7.
To evaluate the effect of early vitreoretinal surgery on vascularly active stage 4 ROP through the preoperative use of intravitreal bevacizumab.
This was a retrospective study. Eighteen patients with vascularly active stage 4 ROP who underwent primary vitrectomy from April 2007 to March 2010 were enrolled. Twelve eyes from eight patients received one-time intravitreal injection of 0.625 mg bevacizumab 7 days prior to vitrectomy (bevacizumab group), and 11 eyes from 10 patients underwent the surgical procedure without bevacizumab (control group). Demographical information of all patients was recorded. The patients were followed up for 12-36 months after the surgery. The postmenstrual age at vitrectomy, surgical procedure, anatomical and visual outcome, adverse effects and surgical complications were compared.
There was no statistically significant difference between the two groups in gender, birthweight and gestational age. The bevacizumab group showed remarkable regression of vascular activity after the injection. The mean postmenstrual age at the time of vitrectomy was significantly earlier in the bevacizumab group (40 versus 47 weeks, p = 0.002) compared with the controls. The mean surgery time was shorter in the bevacizumab group (74.81 versus 101.70 min, bevacizumab group versus control, p = 0.002). At the final follow-up, all patients in the bevacizumab group achieved anatomical retinal attachment, compared with 70% in the control group. Eighty-eight per cent patients in the bevacizumab group obtained pattern vision, while it was 30% in the control group (p = 0.015).
Intravitreal bevacizumab administrated prior to vitrectomy effectively reduced active neovascularization in vascularly active stage 4 ROP patients, thus advancing the timing of vitrectomy and facilitating pars plicata vitrectomy (PPV).
通过术前玻璃体腔内注射bevacizumab,评估早期玻璃体视网膜手术对活跃期 4 期 ROP 的疗效。
这是一项回顾性研究。2007 年 4 月至 2010 年 3 月,我们收治了 18 例接受初次玻璃体切除术的活跃期 4 期 ROP 患者。其中 8 例患者的 12 只眼在玻璃体切除术前 7 天单次玻璃体腔内注射 0.625mg bevacizumab(bevacizumab 组),10 例患者的 11 只眼未行 bevacizumab 治疗(对照组)。记录所有患者的人口统计学信息。术后随访 12-36 个月。比较两组患者的手术时胎龄、手术过程、解剖和视力结果、不良反应和手术并发症。
两组患者在性别、出生体重和胎龄方面无统计学差异。bevacizumab 组注射后血管活性显著消退。bevacizumab 组玻璃体切除时的平均胎龄明显早于对照组(40 周与 47 周,p = 0.002)。bevacizumab 组的平均手术时间较短(74.81 分钟与 101.70 分钟,bevacizumab 组与对照组,p = 0.002)。最终随访时,bevacizumab 组所有患者均实现解剖视网膜附着,而对照组为 70%。bevacizumab 组 88%的患者获得了图案视力,而对照组为 30%(p = 0.015)。
玻璃体腔内注射 bevacizumab 可有效减少活跃期 4 期 ROP 患者的新生血管活性,从而提前玻璃体切除术的时机,并促进扁平部玻璃体切除术(PPV)。