J Cataract Refract Surg. 2016 Sep;42(9):1268-1275. doi: 10.1016/j.jcrs.2016.06.033.
To analyze the clinical outcomes after implantation of an extended range of vision intraocular lens (IOL), the Tecnis Symfony, in a routine clinical setting.
Forty clinical sites in Finland, France, Germany, Norway, Spain, Sweden, and the United Kingdom.
Prospective case series.
The study comprised 411 patients who had bilateral implantation of the extended range of vision IOL, with intended micro-monovision in 1 group (monovision group) and intended emmetropia in the other group (non-monovision group). Visual acuity, spectacle independence, patient and surgeon satisfaction, and photic phenomena were analyzed during the 4- to 6-month follow-up.
The monovision group comprised 112 patients and the non-monovision group, 299 patients. The mean decimal uncorrected distance (UDVA), intermediate (UIVA), and near (UNVA) visual acuities were 0.95, 0.81, and 0.69, respectively, 4 to 6 months postoperatively. Significantly better UIVA (P = .003) and UNVA (P = .011) were found in the monovision group than in the non-monovision group. Spectacle independence was high, with 14.4% of eyes requiring reading spectacles frequently. More than 90% of patients reported no or mild halos, glare, starbursts, or other photic phenomena. Patient satisfaction scores (median) for distance, intermediate, and near vision were 9.0, 10.0, and 8.0, respectively. The satisfaction score for near vision increased to 9.0 in the monovision group. More than 91% of patients said they would recommend the same procedure to their friends and family.
The extended range of vision IOL provided successful visual restoration across all distances after cataract surgery, with a minimal level of disturbing photic phenomena and high levels of patient satisfaction.
Dr. Cochener is a clinical investigator for Revision Optics, Inc., Horus Vision LLC, Alcon Laboratories, Inc., Abbott Medical Optics, Inc., Théa Pharma GmbH, and Santen, Inc.; she is also a consultant to Alcon Laboratories, Inc., Abbott Medical Optics, Inc., Théa Pharma GmbH, and Santen, Inc.
分析在常规临床环境下植入扩展视程人工晶状体(IOL) Tecnis Symfony 的临床效果。
芬兰、法国、德国、挪威、西班牙、瑞典和英国的 40 个临床地点。
前瞻性病例系列。
该研究纳入了 411 例双侧植入扩展视程 IOL 的患者,其中一组(单视组)计划进行微单眼视力,另一组(非单视组)计划实现正视。在 4 至 6 个月的随访期间,分析了视力、眼镜依赖度、患者和医生满意度以及视觉现象。
单视组包括 112 例患者,非单视组包括 299 例患者。术后 4 至 6 个月,平均未矫正远视力(UDVA)、中距离视力(UIVA)和近视力(UNVA)分别为 0.95、0.81 和 0.69。单视组的 UIVA(P=0.003)和 UNVA(P=0.011)明显优于非单视组。眼镜依赖度高,14.4%的患者经常需要阅读眼镜。超过 90%的患者报告无或轻度光晕、眩光、星爆或其他视觉现象。患者对远、中、近视力的满意度评分(中位数)分别为 9.0、10.0 和 8.0,单视组的近视力满意度评分增加到 9.0。超过 91%的患者表示愿意向朋友和家人推荐相同的手术。
扩展视程 IOL 可为白内障手术后的所有距离提供成功的视觉恢复,视觉现象干扰极小,患者满意度高。
Cochener 博士是 Revision Optics,Inc.、Horus Vision LLC、Alcon Laboratories,Inc.、Abbott Medical Optics,Inc.、Théa Pharma GmbH 和 Santen,Inc.的临床研究员;她还是 Alcon Laboratories,Inc.、Abbott Medical Optics,Inc.、Théa Pharma GmbH 和 Santen,Inc.的顾问。