Maier M, Feucht N, Huebner M, Lohmann C
Augenklinik, Klinikum rechts der Isar der TU München.
Klin Monbl Augenheilkd. 2008 Jun;225(6):582-7. doi: 10.1055/s-2008-1027474.
Intravitreal anti-VEGF therapy with Pegaptanib was effective in neovascular AMD in the VISION study. We report our experience with Macugen for the treatment of occult or minimally classic choroidal neovascularisation (CNV) due to age-related macular degeneration (AMD).
35 eyes of 35 patients with occult CNV or minimally classic CNV due to neovascular AMD not eligible for PDT were treated with intravitreal injection of 0.3 mg Pegaptanib. An average of 2.74 injections per patient was administered. Before, and every 3 months after treatment, visual acuity, intraocular pressure measurement, angiography and OCT examinations were performed. One month after treatment only visual acuity, intraocular pressure measurement, and OCT examinations were performed. Visual acuity measurements and an eye examination were done on the first and second day after injection, after 4-6 weeks and at months 3 and 6.
Intravitreal Pegaptanib was well tolerated and we had no complications. Mean visual acuity was 0.38 +/- 0.23 at baseline, after one month 0.38 +/- 0.26, at 3 months it was 0.39 +/- 0.22 and at 6 months 0.41 +/- 0.26. OCT examinations showed a decrease in central retinal thickness from 277 microm to 254 microm. In 91.4 % of the eyes the visual acuity was stabilised or improved. No patient had an elevated intraocular pressure after 6 months.
Intravitreal therapy with Pegaptanib was safe and effective. The majority of patients showed a stabilisation in all the assessed parameters. In clinical practice unselective VEGF inhibition should be considered carefully for patients with high cardiovascular risk profile or thromboembolic events in the history.
在VISION研究中,玻璃体内注射培加替尼进行抗VEGF治疗对新生血管性年龄相关性黄斑变性(AMD)有效。我们报告了使用Macugen治疗年龄相关性黄斑变性(AMD)所致隐匿性或轻微典型性脉络膜新生血管(CNV)的经验。
35例因新生血管性AMD导致隐匿性CNV或轻微典型性CNV且不符合光动力疗法(PDT)条件的患者的35只眼,接受了玻璃体内注射0.3mg培加替尼治疗。每位患者平均注射2.74次。治疗前及治疗后每3个月进行视力、眼压测量、血管造影和光学相干断层扫描(OCT)检查。治疗后1个月仅进行视力、眼压测量和OCT检查。在注射后的第1天和第2天、4 - 6周以及第3个月和第6个月进行视力测量和眼部检查。
玻璃体内注射培加替尼耐受性良好,未出现并发症。基线时平均视力为0.38±0.23,1个月后为0.38±0.26,3个月时为0.39±0.22,6个月时为0.41±0.26。OCT检查显示中心视网膜厚度从277微米降至254微米。91.4%的患眼视力稳定或提高。6个月后无患者眼压升高。
玻璃体内注射培加替尼治疗安全有效。大多数患者在所有评估参数方面均表现稳定。在临床实践中,对于有高心血管风险或有血栓栓塞事件病史的患者,应谨慎考虑非选择性VEGF抑制治疗。