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首页> 外文期刊>Journal of cataract and refractive surgery >Rate of posterior capsule opacification in eyes with the Akreos intraocular lens.
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Rate of posterior capsule opacification in eyes with the Akreos intraocular lens.

机译:Akreos人工晶状体在眼后囊混浊的发生率。

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PURPOSE: To determine the rate of posterior capsule opacification (PCO) in eyes with an Akreos Adapt or Akreos Fit intraocular lens (IOL) (Bausch & Lomb) over a minimum follow-up of 18 months. SETTING: Department of Ophthalmology, Worthing and Southlands Hospital NHS Trust, Worthing, United Kingdom. METHOD: This was a retrospective analysis of 102 patients who had uneventful phacoemulsification with implantation of an Akreos Adapt IOL or Akreos Fit IOL from September 2001 to May 2004. Patients from a single surgeon's operating list were recruited into the study. Exclusion criteria included posterior subcapsular cataract, history of uveitis, diabetic retinopathy, glaucoma, and age-related macular degeneration. The protocol included the determination of logMAR best corrected visual acuity (BCVA) and PCO scoring using the Evaluation of Posterior Capsular Opacification System (EPCO 2000) by digital photography of the posterior capsule. The number of patients having a neodymium:YAG (Nd:YAG) capsulotomy was also recorded. RESULTS: The mean follow-up was 30 months +/- 10.3 (SD). The mean BCVA was 20/32 (0.2 logMAR). The mean EPCO score at the central 6.0 mm of the posterior capsule was 0.39 +/- 0.53 and at the central 3.0 mm, 0.18 +/- 0.40. The Nd:YAG capsulotomy rate was 8.8%. CONCLUSIONS: All patients had stable visual acuity with low rates of PCO 2.5 years after surgery. The PCO rate with the Akreos IOL was similar to that with other acrylic IOLs reported in the literature.
机译:目的:在至少18个月的随访中,使用Akreos Adapt或Akreos Fit人工晶状体(IOL)(Bausch&Lomb)确定眼睛后囊混浊(PCO)的比率。地点:英国沃辛,沃辛和南国医院NHS Trust眼科。方法:这是一项回顾性分析,分析了2001年9月至2004年5月间使用Akreos Adapt人工晶状体或Akreos Fit人工晶状体植入的超声乳化正常的102例患者。该患者来自单个手术医生的手术清单。排除标准包括后囊性白内障,葡萄膜炎病史,糖尿病性视网膜病,青光眼和年龄相关性黄斑变性。该方案包括使用后囊数字化摄影技术对后囊不透明化系统进行评估(EPCO 2000),确定logMAR最佳矫正视力(BCVA)和PCO评分。还记录了进行钕:YAG(Nd:YAG)囊切开术的患者人数。结果:平均随访时间为30个月+/- 10.3(SD)。平均BCVA为20/32(0.2 logMAR)。在后囊中央6.0 mm处的平均EPCO得分为0.39 +/- 0.53,在中央3.0 mm处为0.18 +/- 0.40。 Nd:YAG囊切开术率为8.8%。结论:所有患者术后2。5年的视力稳定,PCO率低。 Akreos IOL的PCO率与文献中报道的其他丙烯酸IOL的PCO率相似。

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