Hovanesian John A, Jones Michael, Allen Quentin
Harvard Eye Associates, Laguna Hills, CA, USA.
Quantum Vision Centers, Swansea, IL, USA.
Clin Ophthalmol. 2024 Oct 18;18:2977-2984. doi: 10.2147/OPTH.S476666. eCollection 2024.
To evaluate patient-reported outcomes of cataract surgery using the Clareon Panoptix and Panoptix Toric trifocal lenses and to compare these to the data collected previously for the AcrySof Panoptix and Panoptix Toric.
Prospective, open-label, multicenter analysis of satisfaction, spectacle independence, presence of unwanted side effects, and best-corrected visual acuity among patients undergoing cataract surgery who had been implanted at least 1 month previously with the Clareon PanOptix or PanOptix Toric trifocal IOL bilaterally. Results were compared to outcomes measured two years ago from a similar study with the AcrySof version of the same lens.
No significant differences in patient satisfaction rates were reported between the two cohorts. Spectacle independence was similar with 88% of Clareon Panoptix and 83% of AcrySof Panoptix patients having no need for any corrective lenses. Quality of vision was not statistically different with 7% of Clareon vs 15% of AcrySof patients reporting "very much" or more of glare/halo severity. Significantly more AcrySof (66%) than Clareon (42%) patients achieved a spherical equivalent outcome within 0.25 D of target. Best corrected distance visual acuity differences were not statistically significant, and no safety concerns were reported.
The Clareon PanOptix trifocal lens provides similar satisfaction and spectacle independence and has a similar side effect profile and BCVA outcome to the identical lens made of the predecessor AcrySof lens.
评估使用Clareon Panoptix和Panoptix Toric三焦点人工晶状体进行白内障手术的患者报告结局,并将这些结果与之前收集的关于AcrySof Panoptix和Panoptix Toric的数据进行比较。
对至少在1个月前双侧植入Clareon PanOptix或PanOptix Toric三焦点人工晶状体的白内障手术患者进行前瞻性、开放标签、多中心分析,评估其满意度、无需眼镜情况、不良副作用的存在情况以及最佳矫正视力。将结果与两年前对相同晶状体的AcrySof版本进行的类似研究中测量的结果进行比较。
两个队列报告的患者满意度率无显著差异。无需眼镜的情况相似,88%的Clareon PanOptix患者和83%的AcrySof PanOptix患者无需任何矫正眼镜。视力质量无统计学差异,7%的Clareon患者与15%的AcrySof患者报告眩光/光晕严重程度为“非常严重”或更严重。达到目标等效球镜度在0.25 D以内的AcrySof患者(66%)显著多于Clareon患者(42%)。最佳矫正远距离视力差异无统计学意义,且未报告安全问题。
Clareon PanOptix三焦点人工晶状体提供了相似的满意度和无需眼镜情况,并且与由前代AcrySof晶状体制成的相同晶状体具有相似的副作用特征和最佳矫正视力结果。