Department of Vitreo-Retinal Surgery, Center of Ophthalmology, University of Cologne, Kerpener Str 62, Cologne 50924, Germany.
Br J Ophthalmol. 2010 Aug;94(8):1040-4. doi: 10.1136/bjo.2009.161299. Epub 2009 Aug 18.
To evaluate the long-term outcome of autologous graft of retinal pigment epithelium (RPE) in patients with geographic atrophy.
Ten patients with progressive geographic atrophy underwent translocation of an autologous graft of RPE, Bruch membrane and choroid. The visual acuity (VA), reading performance, microperimetry, optical coherence tomography (OCT), fundus autofluorescence, fluorescein angiography and indocyanine green angiography were assessed.
No recurrence of RPE atrophy was seen. All but one transplant were revascularised. Vascularisation persisted throughout the 3 years' follow-up. Spectral-domain OCT in some cases showed intact photoreceptors or intact outer nuclear and outer plexiform layer overlying the graft. In three cases, the grafts were positioned eccentrically; these patients did not benefit from surgery. The mean VA decreased from 20/80 (range: 20/800 to 20/40) at baseline to 20/200 (range: perception of hand movements to 20/32) at last follow-up. In two patients, VA were stable from 20/50 to 20/32 and 20/40 at the last follow-up, respectively. Postoperative complications included retinal detachment due to proliferative vitreoretinopathy, macular pucker, iritis, branch retinal vein occlusion and secondary ocular hypertension.
Some patients benefit for at least 3 years from a functioning RPE-choroid graft. Functional outcome in most patients, however, was limited due to complications and unfavourable patient selection.
评估自体视网膜色素上皮(RPE)移植物治疗地图状萎缩患者的长期疗效。
10 名进行性地图状萎缩患者接受了自体 RPE、Bruch 膜和脉络膜移植物转位。评估了视力(VA)、阅读表现、微视野计、光学相干断层扫描(OCT)、眼底自发荧光、荧光素血管造影和吲哚青绿血管造影。
未发现 RPE 萎缩复发。除 1 例外,所有移植物均再血管化。血管化在 3 年的随访中持续存在。在一些病例中,光谱域 OCT 显示完整的光感受器或覆盖移植物的完整外核和外丛状层。在 3 例病例中,移植物偏心定位;这些患者未从手术中受益。平均 VA 从基线时的 20/80(范围:20/800 至 20/40)下降至最后随访时的 20/200(范围:手动感知至 20/32)。在 2 名患者中,VA 在最后随访时分别稳定在 20/50 至 20/32 和 20/40。术后并发症包括增生性玻璃体视网膜病变导致的视网膜脱离、黄斑皱缩、虹膜炎、分支视网膜静脉阻塞和继发性眼高压。
一些患者至少在 3 年内从功能正常的 RPE-脉络膜移植物中获益。然而,由于并发症和不利的患者选择,大多数患者的功能结果有限。