新型亲水人工晶状体植入术治疗白内障无晶状体的实验与临床研究

E.V. Kalinina, A. Grinev, M. B. Sviridova, A. M. Danilov, A.A. Grinev, V. Bachurikhin
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引用次数: 0

摘要

目的。目的评价新型亲水人工晶状体植入术治疗白内障术后无晶状体的实验及临床研究结果。材料和方法。实验部分采用电子扫描显微镜进行。研究了“海蓝宝石”人工晶状体光学边缘的表面和角度。临床部分分析500例海蓝宝石人工晶状体,随访1个月(第一组),其中200例随访1年(第二组)。人工晶体表面无表面缺陷。光学边缘的直角大于360°。与理想矩形形状的偏差面积在半径为40 um时为49.06-175.50 um²,在半径为60 um时为75.29-264.70 um²。海蓝宝石亲水晶状体的植入使89.6%的患者有可能获得0.5以上的高视力。结论。一项临床研究显示,海蓝宝石人工晶状体具有较高的膜层和囊层生物相容性,并且在长达1年的随访期间具有稳定的屈光数据。关键词:电子扫描显微镜;人工晶状体“海蓝宝石”;临床研究;
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Results of an experimental and clinical study of new hydrophilic intraocular lens implantation for aphakia correction in cataract surgery
Purpose. To evaluate results of an experimental and clinical study of new hydrophilic intraocular lens implantation for aphakia correction in cataract surgery. Material and methods. Experimental part was performed using electron scanning microscopy. Surface and angle of the optical edge of the IOL «Aquamarine» were studied. Clinical part included analysis of 500 implantations of Aquamarine IOL with a followup period up to 1 month (group 1), 200 of those implantations had a follow-up period up to one year (group 2). Results. Surface of the IOL had no superficial defects. Optical edge had a rectangular angle over 360°. Area of deviation from the ideal rectangular shape varied between 49.06–175.50 um²at a radius of 40 um and 75.29–264.70 um² at a radius of 60 um. Implantation of Aquamarine hydrophilic lenses made it possible to obtain a high visual acuity of 0.5 or more in 89.6% of cases. Conclusion. A clinical study revealed high uveal and capsule biocompatibility of the Aquamarine IOL, and stable refractive data in the follow up period up to 1 year. Key word:: electron scanning microscopy, IOL «Aquamarine», clinical research, cataract surgery.
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