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Surgical management of subfoveal choroidal neovascular membranes in age-related macular degeneration by macular relocation: Experiences of an early-stopped randomised clinical trial (MARAN Study)

机译:黄斑移位治疗年龄相关性黄斑变性中心凹下脉络膜新生血管膜的手术治疗:早期随机临床试验的经验(maRaN研究)

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摘要

Rationale The MARAN (Macular Relocation in Age-related Neovascular disease) trial was planned to assess the effectiveness of full macular relocation (MR) in patients with neovascular age-related macular degeneration (AMD). Design Randomised, prospective, controlled clinical trial. Methods Patients suffering from visual loss because of AMD were randomised to either surgery or a control group receiving standard treatment (observation or photodynamic therapy (PDT)). The primary end point was the change of visual acuity (VA) (ETDRS) 52 weeks after randomisation compared with initial VA, and secondary end points included reading performance, contrast sensitivity, stability of fixation, eye-specific quality of life, and the absolute number of letters read correctly at 52 weeks compared with initial examination. Results Owing to early determination, only 28 patients were included in the study. The study did not show a difference between the two groups with respect to the final visual result or any of the secondary outcomes measured. The study was limited by the low recruitment that was, at least in part, attributed to the inherent risks for those patients randomised to the surgical arm of the study as well as to the emerging new treatments for AMD. Conclusion The results of the MARAN trial failed to recruit a sufficient number of patients and a superiority of surgery over observation or PDT in patients with exudative AMD was not shown. There was a trend that the reading function was superior after surgery. In the light of the new pharmacological treatments, surgical options such as MR will be an option for only selected cases. © 2010 Macmillan Publishers Limited All rights reserved.
机译:基本原理计划进行MARAN(与年龄有关的新血管疾病的黄斑区重定位)试验,以评估在患有新血管的与年龄相关的黄斑变性(AMD)患者中进行全黄斑定位(MR)的有效性。设计随机,前瞻性,对照临床试验。方法将因AMD导致视力丧失的患者随机分为接受标准治疗(观察或光动力疗法(PDT))的手术组或对照组。主要终点是随机分配后52周的视觉敏锐度(VA)(ETDRS)与初始VA相比的变化,次要终点包括阅读性能,对比敏感度,注视稳定性,特定于眼睛的生活质量和绝对与初次检查相比,在52周时正确阅读的字母数量。结果由于及早确定,该研究仅包括28例患者。该研究没有显示出两组在最终视觉结果或所测得的任何次要结果方面的差异。这项研究受到招募人数少的限制,这至少部分归因于那些随机分配到研究手术臂的患者的固有风险以及新兴的AMD治疗。结论MARAN试验的结果未能招募足够多的患者,并且未显示渗出性AMD患者的手术优于观察或PDT的优势。术后有阅读功能优越的趋势。根据新的药理学治疗方法,仅针对特定病例,将选择MR等外科手术。 ©2010 Macmillan Publishers Limited版权所有。

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