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首页> 外文期刊>Journal of cataract and refractive surgery >Fellow-eye comparison of posterior capsule opacification between 2 aspheric microincision intraocular lenses
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Fellow-eye comparison of posterior capsule opacification between 2 aspheric microincision intraocular lenses

机译:2个非球面微切口人工晶状体后囊混浊的前瞻性比较

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摘要

Purpose: To compare posterior capsule opacification (PCO) between 2 microincision hydrophilic intraocular lenses (IOLs) and with a conventional spherical hydrophobic IOL. Setting: St. Thomas' Hospital, London, United Kingdom. Design: Prospective randomized comparative study. Methods: A microincision Acri.Smart 36A (negatively aspheric) or Akreos MI-60 (aspherically neutral) IOL was randomized to the first eye of patients with the alternative IOL implanted in the fellow eye within 3 weeks. Postoperatively, 100% and 9% logMAR corrected distance visual acuity (CDVA) were assessed. Retroillumination photographs were analyzed using the posterior capsule opacity software system. The data on PCO scores were compared with those of a conventional spherical hydrophobic IOL (Acrysof SN60AT). Results: One hundred percent CDVA was significantly better at 12 months and 9% CDVA was better at 6, 12, and 24 months (P<.05) with the negatively aspheric IOL. One eye in each group with microincision IOLs developed capsule phimosis at 1 month. Neodymium:YAG capsulotomies were required by 2 years in 2 eyes with a negatively aspheric IOL and 8 eyes with an aspherically neutral IOL. At 24 months, the mean PCO score remained less than 10% with the conventional spherical IOL, whereas it increased with time in the negatively aspheric IOL (up to 16%) and the aspherically neutral IOL (up to 23%). Conclusions: The negatively aspheric IOL had a better PCO profile than the aspherically neutral IOL. This may be attributed to the difference in the edge design between the IOLs. The microincision IOLs had more PCO than the conventional 1-piece hydrophobic IOL. Financial Disclosure: Dr. Nanavaty was supported by an unrestricted research grant from Alcon Laboratories, Inc. Drs. Spalton and Boyce were consultants to Alcon Laboratories, Inc. at the time of this study. No author has a financial or proprietary interest in any material or method mentioned.
机译:目的:比较2个微切口亲水性人工晶状体(IOL)与常规球形疏水性人工晶状体之间的后囊混浊(PCO)。地点:英国伦敦圣托马斯医院。设计:前瞻性随机比较研究。方法:将微切口Acri.Smart 36A(负非球面)或Akreos MI-60(非球面中性)IOL随机分配给患者的第一只眼,并在3周内将另一只IOL植入另一只眼。术后评估100%和9%logMAR校正的远视力(CDVA)。使用后囊不透明软件系统分析后照照。将PCO分数数据与常规球形疏水性IOL(Acrysof SN60AT)进行了比较。结果:负性非球面IOL在12个月时CDVA显着好于100%,在6、12和24个月时CDVA显着好于9%(P <.05)。每组有微切口IOL的一只眼睛在1个月时出现包囊包茎。负非球面IOL的2眼和非球面中性IOL的8眼需要2年的钕:YAG囊切术。在第24个月时,常规球形IOL的平均PCO得分仍低于10%,而在非球面IOL(高达16%)和非球面中性IOL(高达23%)中,PCO得分随时间增加。结论:负非球面IOL具有比非球面中性IOL更好的PCO轮廓。这可能归因于IOL之间边缘设计的差异。微切口IOL比传统的1件式疏水IOL具有更多的PCO。财务披露:Nanavaty博士得到了Alcon Laboratories,Inc.的无限制研究资助。在本研究进行时,Spalton和Boyce是Alcon Laboratories,Inc.的顾问。没有任何作者在提及的任何材料或方法上具有财务或所有权利益。

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