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首页> 外文期刊>Clinical and experimental ophthalmology >Spherical implantable collamer lenses for myopia and hyperopia: 126 eyes with 1-year follow up.
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Spherical implantable collamer lenses for myopia and hyperopia: 126 eyes with 1-year follow up.

机译:用于近视和远视的球形植入式矫正眼镜:126眼,随访一年。

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摘要

BACKGROUND: To report on 1-year follow up of a series of 126 eyes implanted with a spherical implantable collamer lens (ICL). METHODS: Retrospective case note review of 126 eyes (68 patients) undergoing ICL placement by a single surgeon (TG) to correct preoperative mean spherical equivalents between +8.88 and -20.50 D. Main outcome measures included uncorrected visual acuity (UCVA), refraction, best spectacle-corrected VA, unaided binocular vision, adverse events, operative/postoperative complications and patient symptoms. RESULTS: Complete data were available at 1 year on 121 of the 126 eyes (65 out of 68 patients). At 12 months 86% (104/121) had postoperative UCVA better than or equal to preoperative best spectacle-corrected VA, and 98% (118/121) had UCVA within one line of preoperative best spectacle-corrected VA. Ninety-six per cent (116/121) had postoperative UCVA of 6/9 or better, and 100% had postoperative best-corrected visual acuity of 6/12 or better. Ninety-eight per cent (64/65) patients had unaided binocular vision at 1 year of 6/7.5 or better. Average myopia treated was -8.83 D (116 patients), and average hyperopia +7.14 D (10 patients). Two ICLs were replaced because of high vaulting; one eye had increased intraocular pressure that resolved with smaller ICL placement. Four patients had visually insignificant pigment deposits on the ICL at 3/12, but no pigmentary glaucoma. Five patients noticed haloes around lights at night, none preventing driving. CONCLUSIONS: One-year results from this study, the largest reported clinical investigation of the use of ICLs in New Zealand, support the safety, efficacy and predictability of ICL to treat both hyperopic and myopic spherical refractive errors.
机译:背景:要对1年来植入一系列球状可植入矫正晶状体(ICL)的126眼进行随访。方法:回顾性病例记录回顾了由单名外科医生(TG)进行ICL植入以校正术前平均球镜当量+8.88至-20.50 D的126眼(68例)。主要结局指标包括未矫正视力(UCVA),屈光,最佳的眼镜矫正视力,无双眼视力,不良事件,手术/术后并发症和患者症状。结果:126眼中的121眼在1年时可获得完整数据(68例患者中的65例)。在12个月时,有86%(104/121)的UCVA优于或等于术前最佳眼镜矫正的VA,而98%(118/121)的UCVA在术前最佳眼镜矫正的一线之内。 96%(116/121)的术后UCVA为6/9或更高,而100%的术后最佳矫正视力为6/12或更高。百分之九十八(64/65)的患者在1年内没有双眼视力达到6 / 7.5或更好。治疗的平均近视为-8.83 D(116例),平均远视+7.14 D(10例)。由于跳高,更换了两个ICL;一只眼睛的眼内压升高,可通过较小的ICL放置来解决。 4名患者在3/12时ICL上的色素沉着微不足道,但无色素性青光眼。五名患者在夜间发现灯光周围的光环,无一妨碍驾驶。结论:这项研究的一年结果是新西兰使用ICL的最大的临床研究报告,支持ICL治疗远视和近视球面屈光不正的安全性,有效性和可预测性。

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