Department of Ophthalmology, Medical University of Vienna, Vienna, Austria.
Department of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.
PLoS One. 2022 Jul 12;17(7):e0271166. doi: 10.1371/journal.pone.0271166. eCollection 2022.
To evaluate the effect of intravitreal aflibercept monotherapy on arterial and venous oxygen saturation, retinal vessel diameter and flicker response in patients with newly diagnosed specific subtypes of exudative maculopathy.
This prospective study included forty-four eyes of 44 patients with treatment-naïve polypoidal choroidal vasculopathy (PCV, n = 12), hemorrhagic choroidal neovascularization (hCNV, n = 12), pigment epithelium detachment (PED, n = 9) and type 3 MNV (RAP, n = 11). All patients received three initial aflibercept 2mg/0.05ml injections (Eylea®) in monthly intervals (loading phase) and were subsequently treated until month 12. Measurements of arterial and venous oxygen saturation, vessel diameters and flicker response were performed using the Dynamic Vessel Analyzer (DVA; IMEDOS, Jena, Germany). Statistical analysis was performed on the total population at baseline, after loading dose and at the last follow-up visit.
The arterial oxygen saturation was 94.01±2.14% and showed no change after loading dose (93.94±2.88%, p = 0.4; estimated difference [confidence interval] -0.38 [-1.24; 0.48]) and at the last visit (95.48±1.90%; p = 0.1; -1.29 [-0.34; 2.91]). The venous oxygenation during treatment was 78.49±6.93% at baseline, 80.94±7.71% after 3-monthly injections (p = 0.7; -0.43 [-2.72; 1.86]) and 80.56±7.33% at month 12 (p = 0.5; 1.07 [-2.10; 4.24). The arterial and venous vessel diameters were 94±22μm and 131±19μm at baseline, and remained unchanged following aflibercept loading dose and at the last follow-up visit (p-value: p = 0.5; 2.30 [-5.00; 9.59] p = 0.8; 0.59 [-3.17; 4.34]). During stimulation with flicker light, arterial diameter changed by +1.24±4.93% at baseline and remained stable at month 3 (+2.70±5.95%; p = 0.5; 1.43 [-2.54; 5.41]) while the change in venous diameter during flicker stimulation was +4.52±4.45% at baseline and +4.13±3.65% after loading dose (p = 0.4, 5.18 [1.73; 8.63]).
During intravitreal aflibercept treatment oxygen saturation, vessel diameter and flicker response did not change in the total population of patients with specific subtypes of exudative maculopathy.
评估玻璃体内注射阿柏西普单药治疗对新诊断的特定渗出性黄斑病变亚型患者的动脉和静脉血氧饱和度、视网膜血管直径和闪烁反应的影响。
本前瞻性研究纳入了 44 例(44 只眼)未经治疗的息肉样脉络膜血管病变(PCV,n = 12)、出血性脉络膜新生血管(hCNV,n = 12)、色素上皮脱离(PED,n = 9)和 3 型脉络膜新生血管(RAP,n = 11)患者的 44 只眼。所有患者均接受了三次初始阿柏西普 2mg/0.05ml 注射(艾力雅®),每月一次(加载阶段),随后治疗至第 12 个月。使用动态血管分析仪(DVA;IMEDOS,耶拿,德国)测量动脉和静脉血氧饱和度、血管直径和闪烁反应。在基线、加载剂量后和最后一次随访时对总人群进行了统计学分析。
动脉血氧饱和度为 94.01±2.14%,加载剂量后无变化(93.94±2.88%,p = 0.4;估计差值[置信区间]-0.38[-1.24;0.48])和最后一次随访时(95.48±1.90%;p = 0.1;-1.29[-0.34;2.91])。治疗期间静脉氧合为 94.49±6.93%在基线时,3 个月后注射时为 80.94±7.71%(p = 0.7;-0.43[-2.72;1.86]),在第 12 个月时为 80.56±7.33%(p = 0.5;1.07[-2.10;4.24])。动脉和静脉血管直径在基线时分别为 94±22μm 和 131±19μm,在阿柏西普加载剂量后和最后一次随访时均无变化(p 值:p = 0.5;2.30[-5.00;9.59] p = 0.8;0.59[-3.17;4.34])。在闪烁光刺激下,动脉直径在基线时变化+1.24±4.93%,在第 3 个月时保持稳定(+2.70±5.95%;p = 0.5;1.43[-2.54;5.41]),而静脉直径在闪烁刺激期间的变化在基线时为+4.52±4.45%,在加载剂量后为+4.13±3.65%(p = 0.4,5.18[1.73;8.63])。
在玻璃体内注射阿柏西普治疗期间,特定渗出性黄斑病变亚型患者的总人群的血氧饱和度、血管直径和闪烁反应均未发生变化。