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首页> 外文期刊>Journal of cataract and refractive surgery >New supplementary intraocular lens for refractive enhancement in pseudophakic patients.
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New supplementary intraocular lens for refractive enhancement in pseudophakic patients.

机译:用于假晶状体患者屈光增强的新型辅助眼内镜。

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摘要

PURPOSE: To assess the efficacy and safety of implanting a secondary intraocular lens (IOL) in the ciliary sulcus to correct pseudophakic ametropia. SETTING: Department of Ophthalmology, Medical University of Vienna, Vienna, Austria. METHODS: This prospective nonrandomized study included patients who had implantation of a secondary IOL (Sulcoflex 653L) to correct residual refractive error after phacoemulsification with IOL implantation in the capsular bag. After implantation of the secondary IOL in the ciliary sulcus, visual and refractive outcomes were evaluated. Inflammation was measured with a laser flare-cell meter. The position and rotation of the IOLs were documented at all control visits, and Scheimpflug images were taken. Postoperative follow-up was at 1 week and 1, 6, 12, and 17 months. RESULTS: Twelve eyes of 10 patients were evaluated. The mean spherical equivalent decreased from -1.25 diopters (D) +/- 0.25 (SD) (range -2.00 to +4.00 D) preoperatively to -0.25 +/- 0.40 D (range -0.50 to +0.25 D) postoperatively. Uncorrected distance visual acuity improved in all cases. There were no significant intraoperative or postoperative complications. CONCLUSIONS: Sulcus implantation of the secondary IOL to correct pseudophakic refractive error was safe and predictable. The IOL was well tolerated in all eyes. FINANCIAL DISCLOSURE: Neither author has a financial or proprietary interest in any material or method mentioned. Additional disclosures are found in the footnotes.
机译:目的:评估在睫状沟内植入二级人工晶状体(IOL)以纠正假晶状体屈光不正的疗效和安全性。地点:奥地利维也纳医科大学眼科。方法:这项前瞻性非随机研究包括接受二次IOL(Sulcoflex 653L)植入以矫正超声乳化并在囊袋中植入IOL的残余屈光不正的患者。在睫状沟中植入继发IOL后,评估视觉和屈光结局。用激光耀斑细胞仪测量炎症。在所有对照访视中记录IOL的位置和旋转,并拍摄Scheimpflug图像。术后随访时间为1周,1、6、12和17个月。结果:对10名患者的十二只眼进行了评估。平均球当量从术前的-1.25屈光度(D)+/- 0.25(SD)(范围-2.00至+4.00 D)降至术后的-0.25 +/- 0.40 D(范围-0.50至+0.25 D)。在所有情况下,未矫正的远距离视力均得到改善。没有明显的术中或术后并发症。结论:为了矫正假晶状体屈光不正,二次人工晶状体的沟内植入术是安全且可预测的。所有人均对IOL耐受良好。财务披露:两位作者都没有提及任何材料或方法的财务利益或专有利益。在脚注中可以找到其他披露内容。

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