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首页> 外文期刊>Journal of cataract and refractive surgery >Visual outcome and complications after posterior iris-claw aphakic intraocular lens implantation
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Visual outcome and complications after posterior iris-claw aphakic intraocular lens implantation

机译:后虹膜爪无晶状体人工晶状体植入术后的视觉结果和并发症

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摘要

Purpose: To evaluate the indications, visual outcomes, and complication rate after implantation of a posterior chamber iris-claw aphakic intraocular lens (IOL). Setting: Department of Ophthalmology, University Medicine Charité Berlin, Berlin, Germany. Design: Retrospective case series. Methods: Eyes without adequate capsule support had posterior chamber iris-claw aphakic IOL implantation (Verisyse/Artisan) between 2005 and 2010. Results: The study comprised 137 eyes (126 patients). The mean follow-up was 5 months (range 1 to 48 months). The IOLs were inserted during primary lens surgery in 10 eyes (7.3%), during an IOL exchange procedure for dislocated posterior chamber IOLs in 95 eyes (69.4%), and as a secondary procedure in 32 aphakic eyes (23.3%). The final mean corrected distance visual acuity (CDVA) (0.38 ± 0.31 [SD] logMAR) was significantly better than preoperatively (0.65 ± 0.58 logMAR) (P <.05). In 128 eyes (93.4%), postoperative refractive errors were within ±2.00 diopters (D) of emmetropia. Complications included slight temporary pupil ovalization in 34 eyes (24.8%), cystoid macular edema in 12 eyes (8.7%), hyphema in 3 eyes (2.1%), early postoperative hypotony in 7 eyes (5.1%) and elevated intraocular pressure in 6 eyes (4.3%), chronic uveitis in 1 eye (0.7%), toxic anterior segment syndrome in 1 eye (0.7%), and endophthalmitis in 1 eye (0.7%). Iris-claw IOL disenclavation occurred in 12 eyes (8.7%); all IOLs could be easily repositioned. Conclusion: The retropupillary iris-claw IOL provided good visual outcomes with a favorable complication rate and can be used for a wide range of indications in eyes without adequate capsule support. Financial Disclosure: No author has a financial or proprietary interest in any material or method mentioned.
机译:目的:评估后房虹膜-爪无晶状体人工晶状体(IOL)植入后的适应症,视觉效果和并发症发生率。地点:德国柏林大学医学夏尔特医学院眼科。设计:回顾案系列。方法:2005年至2010年之间,没有足够胶囊支持的眼睛进行了后房虹膜爪无晶状体人工晶状体植入(Verisyse / Artisan)。结果:该研究包括137眼(126例患者)。平均随访时间为5个月(1到48个月)。在初次晶状体手术中,将IOL插入10眼(7.3%),在进行IOL置换手术后,将后房IOL插入95眼(69.4%),并将其作为继发性手术在32例无晶状体眼中插入(23.3%)。最终平均矫正距离视力(CDVA)(0.38±0.31 [SD] logMAR)明显优于术前(0.65±0.58 logMAR)(P <.05)。在128只眼(93.4%)中,术后屈光不正在正视眼的±2.00屈光度(D)以内。并发症包括轻微的暂时性瞳孔卵圆形化34眼(24.8%),囊状黄斑水肿12眼(8.7%),前房积血3眼(2.1%),术后早期低眼压7眼(5.1%)和眼压升高6眼(4.3%),慢性葡萄膜炎1眼(0.7%),中毒性眼前节综合征1眼(0.7%)和眼内炎1眼(0.7%)。虹膜爪人工晶体剥夺发生在12只眼中(8.7%);所有IOL都可以轻松地重新定位。结论:瞳孔后虹膜爪人工晶状体可提供良好的视觉效果,并具有良好的并发症发生率,并且在没有足够胶囊支持的情况下可用于多种眼部适应症。财务披露:没有任何作者对所提及的任何材料或方法有财务或专有利益。

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