Medical Director Norway, Memira Eye Center, Oslo, Norway
Clinical Excellence and Development Manager, Memira Eye Center, Oslo, Norway.
Br J Ophthalmol. 2023 Jul;107(7):912-919. doi: 10.1136/bjophthalmol-2021-319732. Epub 2022 Feb 2.
To evaluate the safety and effectiveness of bilateral refractive lens exchange (RLE) with trifocal intraocular lens (IOL) as the surgical treatment of presbyopia.
Memira AS. Norway, Sweden and Denmark.
Multicentric retrospective interventional case series.
17 603 consecutive patients submitted to bilateral presbyopic RLE with trifocal IOLs from 2013 to 2019. The main outcomes were manifest refraction spherical equivalent (MRSE), uncorrected distance (UDVA) and near (UNVA) visual acuity, corrected distance visual acuity (CDVA), vision gain/loss, safety and efficacy indices, IOL power calculation accuracy and rate of excimer laser enhancements.
Three months postoperatively, the mean MRSE was 0.00±0.40 diopters (D), mean binocular UDVA was -0.03±0.09, with 14 470 patients (82.2%) with combined binocular UDVA and UNVA equal or better than 0.00 and Jaeger 3. Approximately 86% (n=30.124) of the eyes were within 0.50D of MRSE. Enhancement surgery was performed in 5810 eyes (16.5%). IOL power calculation refining improved accuracy and reduced enhancements rate from 20% in 2013 to 12% in 2019. Safety and efficacy indices were 0.98±0.11 and 0.85±0.18, respectively. Myopic eyes presented significant higher safety (1.00±0.19) and efficacy indices (0.87±0.19), with p<0.005. Approximately 0.38% (n=130) of the eyes lost two or more lines of CDVA, with cystoid macular oedema (n=53, 40.8%) and posterior capsular opacification (n=35, 26.9%) as the main causes. After proper care, the final incidence of two or more lines of vision loss was 0.08% (28 eyes).
Presbyopic RLE with trifocal IOL is a safe and effective modality of treatment for patients with presbyopia.
评估双眼折射性晶状体置换(RLE)联合三焦点人工晶状体(IOL)作为治疗远视的手术的安全性和有效性。
Memira AS,挪威、瑞典和丹麦。
多中心回顾性干预性病例系列。
2013 年至 2019 年,17603 例连续接受双眼远视性 RLE 联合三焦点 IOL 治疗的患者。主要结果是明显的屈光球镜等效值(MRSE)、未矫正距离(UDVA)和近(UNVA)视力、矫正距离视力(CDVA)、视力增益/损失、安全性和有效性指数、IOL 屈光力计算准确性和准分子激光增强的比率。
术后 3 个月,平均 MRSE 为 0.00±0.40 屈光度(D),平均双眼 UDVA 为-0.03±0.09,14470 例(82.2%)患者双眼 UDVA 和 UNVA 联合视力等于或优于 0.00 和 Jaeger 3。约 86%(n=30124)的眼睛在 0.50D 的 MRSE 范围内。5810 只眼(16.5%)接受了增强手术。IOL 屈光力计算细化提高了准确性,并降低了增强的比率,从 2013 年的 20%降至 2019 年的 12%。安全性和有效性指数分别为 0.98±0.11 和 0.85±0.18。近视眼的安全性(1.00±0.19)和疗效指数(0.87±0.19)显著更高,p<0.005。约 0.38%(n=130)的眼睛失去了两行或更多的 CDVA,主要原因是囊样黄斑水肿(n=53,40.8%)和后囊混浊(n=35,26.9%)。经过适当的治疗,两行或更多视力丧失的最终发生率为 0.08%(28 只眼)。
三焦点 IOL 联合双眼折射性晶状体置换术是治疗远视患者的一种安全有效的方法。