Department of Ophthalmology, University of Ulsan, College of Medicine, Asan Medical Center, Seoul, South Korea.
Am J Ophthalmol. 2013 Dec;156(6):1201-1210.e2. doi: 10.1016/j.ajo.2013.08.002. Epub 2013 Sep 25.
To determine the efficacy of 1 intravitreal bevacizumab injection followed by pro re nata (1 + PRN) injection in cases of subfoveal myopic choroidal neovascularization (CNV) and to identify CNV-recurrence-related prognostic factors.
Retrospective observational case series.
In total, 103 eyes of 89 consecutive naive patients who had subfoveal myopic CNV and had been followed-up for at least 2 years were included. Of those eyes, 24 had recurrences. The remaining eyes were stable after the initial treatment.
The average patient age was 51.1 ± 15.2 years. The average follow-up duration was 44.1 ± 12.7 months. At baseline and at the 1-year, 2-year, and final visits, the average best corrected visual acuities (BCVAs) were 0.57 ± 0.45, 0.38 ± 0.51, 0.40 ± 0.52, and 0.41 ± 0.41 logMAR, respectively. The recurrence rate during follow-up was 23.3%. The BCVA improved by 0.2 logMAR after 2.7 injections in the eyes without recurrence but by only 0.08 logMAR after 6.9 injections in the eyes with recurrence. In univariate analysis, recurrence was associated with older age, more myopic refraction, thinner choroid, larger CNV lesions, and subfoveal hemorrhage at baseline. In multivariate analysis, only baseline CNV lesion size associated significantly with CNV recurrence (P = 0.002). Recurrence, baseline BCVA, choroidal thickness, and CNV size associated significantly with final BCVA (P = 0.026, <0.0001, 0.007, and 0.002, respectively). Baseline choroidal thickness, CNV size, age, and presence of lacquer cracks associated significantly with injection number (P < 0.0001, <0.0001, 0.026, and 0.035, respectively).
1 + PRN intravitreal bevacizumab monotherapy effectively stabilized subfoveal myopic CNV. The CNV size, the baseline BCVA, and the choroidal thickness were the main prognostic factors of subfoveal myopic CNV after 1 + PRN injection of bevacizumab.
确定玻璃体内单次注射贝伐单抗联合后续按需(1+PRN)注射治疗中心性浆液性脉络膜视网膜病变的疗效,并确定与脉络膜新生血管(CNV)复发相关的预测因素。
回顾性观察性病例系列。
共纳入 89 例初次接受治疗的中心性浆液性脉络膜视网膜病变且至少随访 2 年的 103 只眼。其中 24 只眼复发,其余眼在初次治疗后稳定。
患者平均年龄为 51.1±15.2 岁。平均随访时间为 44.1±12.7 个月。在基线和 1 年、2 年和最终随访时,平均最佳矫正视力(BCVA)分别为 0.57±0.45、0.38±0.51、0.40±0.52 和 0.41±0.41 logMAR。随访期间的复发率为 23.3%。无复发眼在 2.7 次注射后 BCVA 提高 0.2 logMAR,而复发眼在 6.9 次注射后仅提高 0.08 logMAR。单因素分析显示,年龄较大、近视程度较高、脉络膜较薄、CNV 病变较大、基线时存在黄斑下出血与复发相关。多因素分析显示,仅基线 CNV 病变大小与 CNV 复发显著相关(P=0.002)。复发、基线 BCVA、脉络膜厚度和 CNV 大小与最终 BCVA 显著相关(P=0.026、<0.0001、0.007 和 0.002)。基线脉络膜厚度、CNV 大小、年龄和漆裂纹的存在与注射次数显著相关(P<0.0001、<0.0001、0.026 和 0.035)。
玻璃体内单次注射贝伐单抗联合后续按需治疗可有效稳定中心性浆液性脉络膜视网膜病变下的脉络膜新生血管。在贝伐单抗 1+PRN 注射后,CNV 大小、基线 BCVA 和脉络膜厚度是中心性浆液性脉络膜视网膜病变的主要预后因素。