Chatziralli Irini, Theodossiadis George, Kabanarou Stamatina A, Parikakis Efstratios, Xirou Tina, Mitropoulos Panagiotis, Theodossiadis Panagiotis
2nd Department of Ophthalmology, "Attikon" Hospital, National and Kapodistrian University of Athens, Athens, Greece.
, 1 Rimini Street, Haidari, 12462, Athens, Greece.
Graefes Arch Clin Exp Ophthalmol. 2017 Oct;255(10):1899-1905. doi: 10.1007/s00417-017-3719-5. Epub 2017 Jun 15.
To compare intravitreal ranibizumab and dexamethasone implant in patients with macular edema (ME) secondary to central retinal vein occlusion (CRVO).
Participants were 42 treatment naive patients with ME due to CRVO, who received either intravitreal 0.5 mg ranibizumab (n = 25) or intravitreal 0.7 mg dexamethasone implant (n = 17). The main outcomes included the mean change in best corrected visual acuity (BCVA) and central subfield thickness (CST) at month 12 compared to baseline in the two groups.
At month 12, there was no statistically significant difference in BCVA and CST change between the two groups. However, there was recurrence in ME at month 5 in the dexamethasone group.
Both ranibizumab and dexamethasone implant were found to be safe and effective at the 12-month follow-up in patients with ME secondary to CRVO. Since there was a recurrence in ME at month 5 in the dexamethasone group, we suggested that intravitreal injection of dexamethasone implant should be potentially administered sooner than 6 months.
比较玻璃体内注射雷珠单抗和地塞米松植入物治疗视网膜中央静脉阻塞(CRVO)继发黄斑水肿(ME)的效果。
42例因CRVO继发ME且未接受过治疗的患者,分别接受玻璃体内注射0.5mg雷珠单抗(n = 25)或玻璃体内植入0.7mg地塞米松(n = 17)。主要观察指标包括两组患者12个月时与基线相比最佳矫正视力(BCVA)和中心子野厚度(CST)的平均变化。
12个月时,两组患者的BCVA和CST变化无统计学差异。然而,地塞米松组在第5个月时出现ME复发。
在CRVO继发ME患者的12个月随访中,雷珠单抗和地塞米松植入物均安全有效。由于地塞米松组在第5个月时出现ME复发,我们建议玻璃体内注射地塞米松植入物的时间可能应早于6个月。