Visual outcomes of an extended depth of focus intraocular lens in patients with high ocular axial length.

IF 3.3 4区 医学 Q1 OPHTHALMOLOGY
James Wiens, Brad Hall
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Abstract

Objective: To evaluate the visual outcomes and quality of vision in patients receiving a nondiffractive extended depth of focus (EDOF) intraocular lens (IOL), when implanted in eyes with high ocular axial length (≥24.5 mm).

Methods: This was a prospective, single-arm, single-surgeon study. Subjects were bilaterally implanted with the Vivity EDOF IOL (toric and nontoric). At 3 months postoperatively, assessments included binocular and monocular visual acuities at distance (6 m), intermediate (66 cm), and near (40 cm), manifest refraction, and administration of a visual disturbance questionnaire (QUVID) and a satisfaction questionnaire (IOLSAT).

Results: At 3 months postoperatively, 100% (20/20), 100% (20/20), and 65% (13/20) of subjects had binocular visual acuity 20/32 or better at distance, intermediate, and near, respectively. Similar visual acuities were obtained with distance correction. At 3 months postoperatively, 93% of eyes (37/40) had manifest refraction spherical equivalent 0.5 D or less. Patient reported spectacle independence was 95% (19/20), 90% (18/20), and 40% (8/20) at distance, intermediate, and near, respectively. Patient-reported satisfaction with their corrected vision was 95% (19/20). In addition, 70% (14/20), 65% (13/20), and 70% (14/20) of subjects reported never or rarely experiencing starburst, halo, and glare, respectively.

Conclusions: The results of this study suggest that the Vivity nontoric and toric IOLs can provide excellent distance and intermediate vision and functional near vision in eyes with high ocular axial length. Good spectacle independence can also be achieved at distance and intermediate, with high reported patient satisfaction and low reported visual disturbances.

高眼轴长患者应用深度聚焦人工晶状体的视觉效果。
目的:评价在高眼轴长(≥24.5 mm)眼内植入无衍射扩展焦深(EDOF)人工晶状体(IOL)患者的视力效果和视力质量。方法:这是一项前瞻性、单组、单一外科医生的研究。受试者双侧植入Vivity EDOF人工晶体(环形和非环形)。术后3个月,评估双眼和单眼视力,包括距离(6米),中间(66厘米)和近距离(40厘米),明显屈光,并进行视力障碍问卷(或QUVID)和满意度问卷(或IOLSAT)。结果:术后3个月,100%(20/20)、100%(20/20)、65%(13/20)的受试者双眼视力分别为20/32及以上(远、中、近)。距离校正后的视力相近。术后3个月,93%的眼睛(37/40)有明显的屈光球等效0.5 D或更小。患者报告的眼镜独立性分别为95%(19/20)、90%(18/20)和40%(8/20)。患者报告的矫正视力满意度为95%(19/20)。此外,70%(14/20)、65%(13/20)和70%(14/20)的受试者分别报告从未或很少经历星爆、光晕和眩光。结论:人工晶状体和非晶状体人工晶状体可为高眼轴长患者提供良好的中远视力和功能性近视力。良好的眼镜独立性也可以实现在距离和中间,高报告的患者满意度和低报告的视觉障碍。
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来源期刊
CiteScore
3.20
自引率
4.80%
发文量
223
审稿时长
38 days
期刊介绍: Official journal of the Canadian Ophthalmological Society. The Canadian Journal of Ophthalmology (CJO) is the official journal of the Canadian Ophthalmological Society and is committed to timely publication of original, peer-reviewed ophthalmology and vision science articles.
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