Department of Ophthalmology, Sungkyunkwan University School of Medicine, Samsung Medical Center, Seoul, Republic of Korea.
Department of Medicine, The Graduate School, Sungkyunkwan University, Seoul, Republic of Korea.
Sci Rep. 2020 Sep 9;10(1):14832. doi: 10.1038/s41598-020-69318-y.
This study compared the visual outcome, visual quality, and satisfaction following implantation of the Mix-and-Match bifocal IOLs (+ 2.75 D and + 3.25 D add power Tecnis Multifocal Model), EDOF IOL (Tecnis Symfony IOL), and Trifocal IOL (FineVision PodFT, PhysIOL). All outcomes were compared among the three groups. The manifest refraction indicated that the EDOF group had significantly higher myopic spherical equivalent values than did the others. In the terms of visual acuity, there were no significant differences in far or intermediate visual acuity among the three groups. Only in near (33 cm), the EDOF group had significantly worse binocular visual acuity than did the Trifocal group (p = 0.002). Regarding to defocus curve, the Trifocal group had better defocus curves at near distances (- 2.0 to - 3.5 D; p = 0.001 vs. EDOF) than did the other two groups. In contrast sensitivity test, the EDOF group had relatively lower value than did the other two groups. In reading speed, only at 0.3 logMAR (6.5-point font), Mix-and-Match group had a significantly higher reading speed than did the other two groups (p = < 0.001 vs. EDOF, p = 0.007 vs. Trifocal). also Mix-and-Match group showed significantly fewer visual artifacts. There were no differences between the three groups in terms of patient satisfaction.ClinicalTrials.gov number: NCT04019691.
本研究比较了植入混合匹配双焦点人工晶状体(+2.75D 和+3.25D 附加光焦度 Tecnis 多焦点型号)、扩展景深人工晶状体(Tecnis Symfony 人工晶状体)和三焦点人工晶状体(FineVision PodFT,PhysIOL)后的视觉结果、视觉质量和满意度。所有结果在三组之间进行比较。 显性折射表明,EDOF 组的近视等效球镜值明显高于其他两组。 在远视力和中间视力方面,三组之间没有显著差异。 只有在近视力(33cm)时,EDOF 组的双眼视力明显低于三焦点组(p=0.002)。 在离焦曲线方面,三焦点组在近距(-2.0 至-3.5D;p=0.001 与 EDOF 相比)具有更好的离焦曲线。 在对比敏感度测试中,EDOF 组的相对值低于其他两组。 在阅读速度方面,只有在 0.3logMAR(6.5 点字体)时,混合匹配组的阅读速度明显高于其他两组(p<0.001 与 EDOF 相比,p=0.007 与三焦点相比)。 混合匹配组还显示出明显较少的视觉伪影。 在患者满意度方面,三组之间没有差异。临床试验注册号:NCT04019691。