Olmos L C, Sayed M S, Moraczewski A L, Gedde S J, Rosenfeld P J, Shi W, Feuer W J, Lee R K
Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, FL, USA.
Eye (Lond). 2016 Mar;30(3):463-72. doi: 10.1038/eye.2015.259. Epub 2015 Dec 18.
To compare the outcomes of neovascular glaucoma (NVG) treated with and without intravitreal bevacizumab in a large case comparison study.
The study is a retrospective, comparative, case series of 163 eyes of 151 patients with NVG, including 99 treated without and 64 treated with intravitreal bevacizumab. Medical and surgical treatments for NVG were assessed. The main outcome measures were visual acuity (VA) and intraocular pressure (IOP).
At the time of NVG diagnosis, the median VA was count fingers (CF) in the non-bevacizumab group and 2/300 in the bevacizumab group. IOP (mean±SD) was 43.1±13.0 mm Hg in the non-bevacizumab group and 40.8±11.5 mm Hg in the bevacizumab group. IOP (mean±SD) decreased to 18.3±13.8 mm Hg in the non-bevacizumab group and 15.3±8.0 mm Hg in the bevacizumab group, and the median VA was CF in both treatment groups at a mean follow-up of 12 months. Panretinal photocoagulation (PRP) substantially reduced the need for glaucoma surgery (P<0.001) in bevacizumab treated NVG eyes.
Although bevacizumab delayed the need for glaucoma surgery, PRP was the most important factor that reduced the need for surgery. Vision and IOP in eyes with NVG treated with bevacizumab showed no long-term differences when compared with eyes that were not treated with bevacizumab. Thus, intravitreal bevacizumab serves as an effective temporizing treatment, but is not a replacement for close monitoring and definitive treatment of NVG. PRP remains the treatment modality that affects the course of NVG in terms of decreasing the need for surgery to control IOP.
在一项大型病例对照研究中比较接受和未接受玻璃体内注射贝伐单抗治疗的新生血管性青光眼(NVG)的治疗效果。
本研究为回顾性、对比性病例系列研究,纳入151例NVG患者的163只眼,其中99只眼未接受玻璃体内注射贝伐单抗治疗,64只眼接受了该治疗。对NVG的药物和手术治疗进行了评估。主要观察指标为视力(VA)和眼压(IOP)。
在NVG诊断时,非贝伐单抗治疗组的中位视力为指数(CF),贝伐单抗治疗组为2/300。非贝伐单抗治疗组的眼压(均值±标准差)为43.1±13.0 mmHg,贝伐单抗治疗组为40.8±11.5 mmHg。非贝伐单抗治疗组的眼压(均值±标准差)降至18.3±13.8 mmHg,贝伐单抗治疗组降至15.3±8.0 mmHg,在平均随访12个月时,两个治疗组的中位视力均为CF。在接受贝伐单抗治疗的NVG眼中,全视网膜光凝(PRP)显著减少了青光眼手术的需求(P<0.001)。
尽管贝伐单抗延迟了青光眼手术的需求,但PRP是减少手术需求的最重要因素。与未接受贝伐单抗治疗的眼睛相比,接受贝伐单抗治疗的NVG眼睛的视力和眼压在长期内没有差异。因此,玻璃体内注射贝伐单抗是一种有效的临时治疗方法,但不能替代对NVG的密切监测和确定性治疗。就减少控制眼压所需手术的需求而言,PRP仍然是影响NVG病程的治疗方式。