Institute of Vision Research, Department of Ophthalmology, Yonsei University College of Medicine, Seoul, South Korea.
Am J Ophthalmol. 2013 Oct;156(4):652-60. doi: 10.1016/j.ajo.2013.05.038. Epub 2013 Jul 24.
To evaluate long-term visual outcome and investigate the prognostic factors after anti-vascular endothelial growth factor (VEGF) therapy for polypoidal choroidal vasculopathy (PCV).
Retrospective study.
Analyses were done among 36 eyes (36 patients) with naïve PCV that were treated with intravitreal ranibizumab injections and completed at least 3-year follow-up. All clinical data, including baseline characteristics; imaging data from fluorescein angiography, indocyanine green angiography, and optical coherence tomography; presence of recurrence; and best-corrected visual acuity (BCVA) were investigated.
During mean follow-up of 42.58 ± 12.59 months, mean numbers of anti-VEGF injection were 11.45 ± 7.81. Twenty-four eyes (66.7%) showed at least 1 recurrence during follow-up. Mean baseline BCVA was 0.68 ± 0.43 logMAR (20/95 Snellen equivalent), and 0.78 ± 0.53 logMAR (20/120 Snellen equivalent) at 36 months (P = .307). Mean BCVA was significantly improved at 1 month (P = .018), and improvement was maintained until 12 months (P = .044), then deteriorated. Among baseline characteristics, greatest lesion diameter (B = 0.219, P = .001) and pigment epithelial detachment (B = 0.362, P = .025) were significantly correlated with long-term visual outcome. Recurrence during follow-up (B = 0.371, P = .024) was also significantly correlated with long-term visual outcome.
Significant visual improvement by anti-VEGF therapy was maintained during the first year of initial treatment; however, vision then deteriorated during long-term follow-up. Smaller lesion size, absence of pigment epithelial detachment at baseline, and no recurrence during follow-up were significantly correlated with better long-term visual outcome.
评估抗血管内皮生长因子(VEGF)治疗后息肉状脉络膜血管病变(PCV)的长期视力结果,并探讨预后因素。
回顾性研究。
对 36 只眼(36 例)接受玻璃体腔雷珠单抗注射治疗的初治 PCV 患者进行分析,这些患者完成了至少 3 年的随访。研究了所有临床数据,包括基线特征;荧光素血管造影、吲哚青绿血管造影和光学相干断层扫描的影像学数据;是否有复发;以及最佳矫正视力(BCVA)。
在平均 42.58 ± 12.59 个月的随访中,平均注射抗 VEGF 药物 11.45 ± 7.81 次。在随访过程中,24 只眼(66.7%)至少有 1 次复发。基线时的平均 BCVA 为 0.68 ± 0.43 logMAR(20/95 视力等价物),36 个月时为 0.78 ± 0.53 logMAR(20/120 视力等价物)(P =.307)。1 个月时的平均 BCVA 显著改善(P =.018),改善一直持续到 12 个月(P =.044),然后恶化。在基线特征中,最大病变直径(B = 0.219,P =.001)和色素上皮脱离(B = 0.362,P =.025)与长期视力结果显著相关。随访期间的复发(B = 0.371,P =.024)也与长期视力结果显著相关。
抗 VEGF 治疗后的视力显著改善在初始治疗的第一年得到维持;然而,在长期随访中视力随后恶化。病变较小、基线时无色素上皮脱离以及随访期间无复发与长期视力结果更好显著相关。