Furino Claudio, Boscia Francesco, Recchimurzo Nicola, Besozzi Gianluca, Cardascia Nicola, Sborgia Luigi, Niro Alfredo, Sborgia Carlo
Department of Ophthalmology and Otorhinolaryngology, University of Bari, Piazza Giulio Cesare 11, Bari, Italy.
Acta Ophthalmol. 2009 Jun;87(4):404-7. doi: 10.1111/j.1755-3768.2008.01262.x. Epub 2008 Sep 8.
This study aimed to evaluate the efficacy of multiple injections of intravitreal bevacizumab for treatment-naïve subfoveal occult choroidal neovascularization (CNV) in age-related macular degeneration (AMD).
Twelve eyes of 12 patients (mean age 76 +/- 6 years) with mean best corrected visual acuity (BCVA) of 20/100 and occult subfoveal CNV at fluorescein angiography (FA), indocyanine-green (ICG) angiography and optical coherence tomography (OCT), showing intra- or subretinal fluid with or without retinal pigment epithelial detachment (PED), underwent multiple intravitreal injections (mean 2.4 +/- 0.7) of 1.25 mg (0.05 ml) bevacizumab. Visual acuity and OCT findings were assessed at the end of follow-up.
After a mean follow-up of 5.7 +/- 2 months, BCVA improved from 20/100 (range 20/50-20/303) to 20/60 (range 20/28-20/200) (p = 0.038). Five eyes (42%) increased BCVA by > or = 3 lines, six eyes (50%) increased BCVA by < 3 lines and one eye (8%) remained stable. Macular thickness decreased from 298 +/- 71 microm to 223 +/- 72 microm (p = 0.017). No ocular or systemic side-effects were observed.
Short-term results suggest that multiple intravitreal injections of 1.25 mg bevacizumab are well tolerated and associated with significant improvements in BCVA and decreased retinal thickness by OCT in most patients with treatment-naïve occult CNV. Further evaluation of intravitreal bevacizumab for the treatment of occult CNV is warranted.
本研究旨在评估多次玻璃体内注射贝伐单抗治疗初治的年龄相关性黄斑变性(AMD)所致的中心凹下隐匿性脉络膜新生血管(CNV)的疗效。
12例患者(平均年龄76±6岁)的12只眼,平均最佳矫正视力(BCVA)为20/100,荧光素血管造影(FA)、吲哚菁绿(ICG)血管造影及光学相干断层扫描(OCT)显示中心凹下隐匿性CNV,伴有或不伴有视网膜色素上皮脱离(PED)的视网膜内或视网膜下液,接受了1.25mg(0.05ml)贝伐单抗的多次玻璃体内注射(平均2.4±0.7次)。在随访结束时评估视力和OCT检查结果。
平均随访5.7±2个月后,BCVA从20/100(范围20/50 - 20/303)提高到20/60(范围20/28 - 20/200)(p = 0.038)。5只眼(42%)BCVA提高≥3行,6只眼(50%)BCVA提高<3行,1只眼(8%)保持稳定。黄斑厚度从298±71μm降至223±72μm(p = 0.017)。未观察到眼部或全身副作用。
短期结果表明,多次玻璃体内注射1.25mg贝伐单抗耐受性良好,大多数初治隐匿性CNV患者的BCVA有显著改善,且OCT显示视网膜厚度降低。有必要对玻璃体内注射贝伐单抗治疗隐匿性CNV进行进一步评估。