首页> 美国卫生研究院文献>The British Journal of Ophthalmology >A randomised controlled feasibility trial of vitrectomy versus laser for diabetic macular oedema
【2h】

A randomised controlled feasibility trial of vitrectomy versus laser for diabetic macular oedema

机译:玻璃体切除术与激光治疗糖尿病性黄斑水肿的随机对照可行性试验

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

>Aim: (1) To evaluate whether vitrectomy is preferable to further macular laser in improving visual acuity and resolving retinal thickening in patients with diabetic macular oedema (DMO) despite previous laser and no macular traction. (2) To determine the feasibility of further trials in this population in terms of magnitude of comparative clinical effect, rate of recruitment, and loss to follow up.>Methods: A randomised controlled feasibility study. Patients with DMO and a visual acuity of 0.3 logMAR (6/12) or worse after one or more macular laser treatments were randomised on a 1:1 basis to either pars plana vitrectomy (PPV) with internal limiting membrane (ILM) peeling or further macular laser. Patients with a posterior vitreous detachment, biomicroscopic evidence of retinal traction, or a taut thickened posterior hyaloid (TTPH) were excluded. Primary outcome measures were (1) best corrected logMAR visual acuity, (2) mean central macular thickness on optical coherence tomography, and (3) rate of recruitment and loss to follow up. Analysis was on an intention to treat basis.>Results: 19 patients were randomised to PPV and 21 to further macular laser. The mean baseline logMAR visual acuity was 0.65 (SD 0.28) for the group randomised to PPV and 0.60 (0.23) for the group randomised to laser. The mean change in best corrected visual acuity of the vitrectomy group was deterioration by 0.05 logMAR, while in the control group the mean change was an improvement of 0.03 logMAR. The median (interquartile range) baseline central macular thickness was 403 (337, 492) for the group randomised to PPV and 387 (298, 491) for the controls randomised to laser. The median change in central macular thickness from baseline to review in the vitrectomy group was a thinning by 73 μm (20%) and by 29 μm (10.7%) in the control laser group. This single centre was able to recruit 40 patients in 18 months with follow up of 82% at 1 year.>Conclusion: A randomised controlled trial was found to be potentially feasible in this population, the rate of recruitment was however slow and one in five patients were lost to follow up because of death and ill health. These data provide little evidence in terms of visual acuity and macular thickness of any benefit of vitrectomy over further macular laser in patients with an attached hyaloid, DMO despite previous laser, and no clinically evident macular traction or TTPH.
机译:>目标:(1)评价玻璃体切除术是否更适合于进一步的黄斑激光治疗,以改善糖尿病性黄斑水肿(DMO)患者的视力,并解决视网膜增厚,尽管先前使用了激光并且没有黄斑牵引。 (2)通过比较临床效果,募集率和随访失误的数量来确定在该人群中进行进一步试验的可行性。>方法:。在接受一种或多种黄斑激光治疗后DMO且视力为0.3 logMAR(6/12)或更差的患者,以1:1的基础被随机分配至具有内部限制膜(ILM)剥离或进一步剥离的平面玻璃体切除术(PPV)黄斑激光。玻璃体后脱离,视网膜牵引的生物显微学证据或绷紧的后玻璃样玻璃体(TTPH)绷紧的患者被排除在外。主要结局指标包括:(1)校正后的logMAR视敏度最佳;(2)光学相干断层扫描术中的平均黄斑中心厚度;(3)随访的征募率和流失率。分析是出于治疗目的。>结果:19例患者被随机分为PPV,21例被进一步黄斑激光治疗。 PPV随机分组的平均基线logMAR视力为0.65(SD 0.28),激光随机分组的平均基线logMAR视力为0.60(0.23)。玻璃体切除术组最佳矫正视力的平均变化为0.05 logMAR,而对照组的平均变化为0.03 logMAR。随机分配给PPV的组的中位(四分位间距)基线中心黄斑厚度为403(337、492),随机分配给激光的对照组的中位(四分位范围)为387(298、491)。玻璃体切除术组从基线到复查的中央黄斑中心厚度的中值变化是对照组激光组的73微米(20%)和29微米(10.7%)。这个单一中心能够在18个月内招募40名患者,并在1年内随访82%。>结论:发现该人群中有一项随机对照试验是可行的,招募率是但是由于死亡和身体欠佳,行动缓慢,五分之一的患者失去了随访。这些数据在视力和黄斑厚度方面尚无证据表明,尽管有先前的激光治疗,但附有透明质酸,DMO且没有临床明显的黄斑牵引或TTPH的患者,玻璃体切除术比进一步的黄斑激光有任何好处。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号