Konidaris Vasileios, Al-Hubeshy Zahra, Tsaousis Konstantinos T, Gorgoli Konstantina, Banerjee Somnath, Empeslidis Theodoros
Leicester Royal Infirmary, University Hospitals of Leicester, Infirmary Square, Leicester, LE1 5WW, UK.
Int Ophthalmol. 2018 Feb;38(1):207-213. doi: 10.1007/s10792-017-0512-8. Epub 2017 Apr 12.
To assess the treatment outcome of switching from ranibizumab to aflibercept intravitreal injections in patients with macular oedema secondary to central retinal vein occlusion (CRVO).
A prospective interventional study was conducted in a tertiary retina service in Leicester Royal Infirmary, UK, where patients with CRVO and associated macular oedema were recruited. First-line treatment involved three monthly ranibizumab injections. Non-responders were defined as patients who despite a minimum of three consecutive injections had persistent intraretinal fluid one month after the last injection. In these cases, a treatment change to aflibercept injections on a per-needed basis was decided. Best-corrected visual acuity (BCVA) and central retinal thickness (CRT) were measured before and after switching of treatment. Follow-up period lasted for a minimum of 24 weeks after switching.
Twenty-nine eyes of 29 patients with refractory macular oedema secondary to CRVO were included. All eyes had an average of 4.5 ranibizumab intravitreal injections in a mean period of 6 months without reduction in intraretinal fluid and/or no visual acuity gain. A significant decrease in mean CRT from 633.67 ± 242.42 to 234.62 ± 78.28 μm and improvement in mean BCVA from 1.34 ± 0.66 log MAR to 0.91 ± 0.73 log MAR were noticed after switching treatment to aflibercept. The average number of aflibercept injections needed for oedema resolution was 2.19.
Aflibercept is an effective alternative treatment for macular oedema secondary to CRVO refractory to ranibizumab. Good anatomical and functional result can be achieved with few injections. The maintenance of these results after 6 months is yet to be investigated.
评估视网膜中央静脉阻塞(CRVO)继发黄斑水肿患者从雷珠单抗转换为阿柏西普玻璃体内注射的治疗效果。
在英国莱斯特皇家医院的三级视网膜服务中心进行了一项前瞻性干预研究,招募了患有CRVO及相关黄斑水肿的患者。一线治疗包括每三个月注射一次雷珠单抗。无反应者定义为尽管连续至少注射三次,但在最后一次注射后一个月仍有持续性视网膜内液的患者。在这些情况下,决定根据需要改为注射阿柏西普。在治疗转换前后测量最佳矫正视力(BCVA)和视网膜中央厚度(CRT)。转换后随访期至少持续24周。
纳入了29例CRVO继发难治性黄斑水肿患者的29只眼。所有眼睛平均在6个月内接受了4.5次雷珠单抗玻璃体内注射,视网膜内液未减少和/或视力未提高。转换为阿柏西普治疗后,平均CRT从633.67±242.42μm显著降至234.62±78.28μm,平均BCVA从1.34±0.66 log MAR提高到0.91±0.73 log MAR。水肿消退所需的阿柏西普平均注射次数为2.19次。
阿柏西普是治疗对雷珠单抗难治的CRVO继发黄斑水肿的有效替代疗法。注射次数少即可取得良好的解剖和功能效果。6个月后这些结果的维持情况尚待研究。