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首页> 外文期刊>Medicine. >Posterior chamber collagen copolymer phakic intraocular lens with a central hole for moderate-to-high myopia: First experience in China
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Posterior chamber collagen copolymer phakic intraocular lens with a central hole for moderate-to-high myopia: First experience in China

机译:具有中央孔的后房胶原共聚物晶状体人工晶状体,用于中度至高度近视:中国首次体验

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The purpose of this article is to evaluate the clinical outcomes of a posterior chamber phakic intraocular lens (pIOL) (Visian Implantable Collamer Lens V4c) for the correction of moderate to high myopia in Chinese eyes. The article is designed as a retrospective case series. This study included the first consecutive eyes that had implantation of a new pIOL design with a central hole, at our department by the same surgeon. The safety, efficacy, predictability, stability, and adverse events of the surgery were evaluated over 6 months. The study enrolled 63 eyes (32 patients). The mean spherical equivalent decreased from ?12.81?±?3.11 diopters (D) preoperatively to ?0.05?±?0.27?D 6 months postoperatively; 96.8% of eyes were within ±0.50?D of the target and 100% of eyes were within ±1.00?D. All eyes had a decimal uncorrected distance visual acuity of 0.5 (20/40) or better at every follow-up visit. The safety and efficacy indices were 1.42?±?0.34 and 1.11?±?0.19, respectively. Postoperatively, the intraocular pressure (IOP) remained stable over time. No significant rises in IOP (including pupillary block) and no secondary cataract were found. After 6 months, the mean vault was 505.2?±?258.9?μm (range 120–990?μm), and the mean endothelial cell loss was 2.0%. Implantation of the pIOL was safe, effective, predictable, and stable in the correction of moderate-to-high myopia in Han Chinese patients, even without peripheral iridectomy.
机译:本文的目的是评估后房型有晶状体人工晶状体(pIOL)(Visian Implantable Collamer Lens V4c)的临床效果,以矫正中国人眼的中度至高度近视。本文被设计为回顾性案例系列。这项研究包括由同一位外科医生在我们科室首次植入具有中心孔的新pIOL设计的眼睛。在6个月内评估了手术的安全性,有效性,可预测性,稳定性和不良事件。该研究招募了63只眼(32例患者)。平均球当量从术前的12.81±3.11屈光度(D)降至术后6个月的0.05±0.27±D。 96.8%的眼睛在目标的±0.50?D以内,100%的眼睛在目标的±1.00?D以内。每次随访时,所有眼睛的小数未校正远视力为0.5(20/40)或更好。安全性和有效性指数分别为1.42±0.34和1.11±0.19。术后,眼内压(IOP)随时间保持稳定。眼压(包括瞳孔阻滞)没有明显升高,也没有继发性白内障。 6个月后,平均穹ault为505.2?±?258.9?μm(范围为120-990?μm),平均内皮细胞损失为2.0%。即使没有进行周边虹膜切除术,pIOL的植入在纠正汉族中重度至高度近视方面是安全,有效,可预测和稳定的。

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