Stodulka Pavel, Pracharova Zuzana
Gemini Eye Clinic, U Gemini 360, Prague, Zlin 760 01, Czech Republic; 3rd Faculty of Medicine at Charles University, Prague, Czech Republic.
Gemini Eye Clinic, Vyskov, Czech Republic.
Ther Adv Ophthalmol. 2023 Oct 3;15:25158414231200108. doi: 10.1177/25158414231200108. eCollection 2023 Jan-Dec.
Extended depth-of-focus (EDOF) intraocular lenses (IOLs) provide a continuous range of uncorrected vision at different distances.
To assess visual acuity, refractive outcomes, and patient satisfaction after cataract surgery using the LuxSmart EDOF IOL (Bausch+Lomb).
A two-center, prospective observational clinical study.
This study includes patients who have undergone bilateral phacoemulsification with bilateral implantation of the LuxSmart EDOF IOL, with the aim of achieving emmetropia. Visual acuity (VA) and subjective refraction were obtained in all patients preoperatively and at 1 week, 1 month, 3 months, and 6 months postoperatively. Subjective measures were obtained using the Catquest-9SF questionnaire and the Patient-Reported Spectacle Independence Questionnaire (PRSIQ). Contrast sensitivity and a glare assessment were undertaken postoperatively. Safety outcomes were additionally assessed.
Sixty eyes from thirty patients were recruited for this study. The mean spherical equivalent was 1.04 ± 1.67 D preoperatively and -0.30 ± 0.46 D at 6 months. Monocular uncorrected distance VA was 0.57 ± 0.32 (logMAR) preoperatively and 0.09 ± 0.12 (logMAR) at 6 months. Mean 6-month monocular uncorrected VA was 0.11 ± 0.13, 0.12 ± 0.15, and 0.31 ± 0.15 (logMAR) at 80, 66, and 40 cm, respectively. More than 90% of patients were either fairly or very satisfied with their vision. There was one case of suspected vitreomacular traction postoperatively.
The LuxSmart EDOF IOL offers good refractive, VA, and safety outcomes. The single elongated focal point designed to enhance the DOF shows good results for VA and patient satisfaction.
扩展焦深(EDOF)人工晶状体(IOL)可在不同距离提供连续的未矫正视力范围。
评估使用LuxSmart EDOF人工晶状体(博士伦公司)进行白内障手术后的视力、屈光结果和患者满意度。
一项双中心前瞻性观察性临床研究。
本研究纳入接受双侧超声乳化白内障吸除术并双侧植入LuxSmart EDOF人工晶状体以实现正视化的患者。在所有患者术前以及术后1周、1个月、3个月和6个月时获取视力(VA)和主观验光结果。使用Catquest-9SF问卷和患者报告的眼镜独立问卷(PRSIQ)获取主观测量结果。术后进行对比敏感度和眩光评估。此外,评估安全性结果。
本研究招募了30例患者的60只眼。术前平均等效球镜度为1.04±1.67D,6个月时为-0.30±0.46D。术前单眼未矫正远视力为0.57±0.32(logMAR),6个月时为0.09±0.12(logMAR)。6个月时,单眼未矫正视力在80cm、66cm和40cm处的平均值分别为0.11±0.13、0.12±0.15和0.31±0.15(logMAR)。超过90%的患者对其视力相当满意或非常满意。术后有1例疑似玻璃体黄斑牵拉病例。
LuxSmart EDOF人工晶状体提供了良好的屈光、视力和安全性结果。为增强焦深而设计的单个拉长焦点在视力和患者满意度方面显示出良好的效果。