Three Patient-Reported Outcomes Questionnaires in Japanese Patients Undergoing Cataract Surgery with Trifocal IOL Implantation.

Clinical ophthalmology (Auckland, N.Z.) Pub Date : 2024-09-04 eCollection Date: 2024-01-01 DOI:10.2147/OPTH.S478292
Takayuki Akahoshi
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Abstract

Purpose: To analyze the patient-reported-outcomes obtained after trifocal intraocular lens (IOL) bilateral implantation in Japanese patients using three different validated questionnaires.

Methods: Fifty-three patients implanted with the FineVision HP IOLs (Beaver-Visitec International, Inc. USA) were enrolled in this prospective-study. At 3-months, refraction (spherical equivalent [SE] and cylinder), logMAR uncorrected distance visual acuity (UDVA), and corrected distance visual acuity (CDVA) were obtained. Specifically, patient-reported-outcomes were evaluated using the NEI VFQ-25, the Catquest-9SF, and the PRSIQ questionnaires.

Results: The mean SE and refractive cylinder were 0.00±0.22D and -0.07±0.23D, respectively. A 98.11% of eyes were within ±0.50D and 100% were within ±1.00D of the SE. A 93.40% of the eyes showed equal or less than 0.50D of astigmatism and 100% of eyes equal or less than 1.00D. The mean value for monocular UDVA was -0.05±0.07 logMAR and the mean value for monocular CDVA was -0.07±0.06 logMAR. 87.74% and 92.45% of the eyes showed 20/20 or better monocular UDVA and CDVA, respectively, with 97.17% and 98.11% showing 20/25 or better for UDVA and CDVA, respectively. The NEI VFQ-25 outcomes showed very high scores across all categories, with mean general vision, distance and near activities values of 86.70±6.35, 96.23±7.72 and 92.14±10.74, respectively. The outcomes for the Catquest-9SF questionnaire showed that 90.57% of patients did not report difficulty in their everyday-life with their sight, and 100% of them were "very or quite satisfied" with their sight at present. The PRSIQ outcomes revealed that 100%, 98.11% and 98.11% of patients did not need glasses or contacts for far, intermediate and near vision, respectively.

Conclusion: The results of the patient-reported-outcomes questionnaires indicated that patients implanted bilaterally with the FineVision HP IOL have high vision and health related quality-of-life scores, with a high spectacle independence rate and high patient satisfaction.

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三焦点人工晶体植入白内障手术日本患者的三份患者报告结果问卷。
目的:使用三种不同的有效问卷,分析日本患者双侧植入三焦点眼内人工晶体(IOL)后的患者报告结果:53名植入FineVision HP人工晶体(美国Beaver-Visitec International公司)的患者参加了这项前瞻性研究。3个月后,获得屈光度(球面等效[SE]和圆柱度)、logMAR未矫正距离视力(UDVA)和矫正距离视力(CDVA)。具体而言,使用 NEI VFQ-25、Catquest-9SF 和 PRSIQ 问卷对患者报告的结果进行了评估:结果:SE 和屈光圆柱的平均值分别为 0.00±0.22D 和 -0.07±0.23D。98.11%的眼睛视力在±0.50D以内,100%的眼睛视力在±1.00D以内。93.40%的眼睛散光等于或小于 0.50D,100%的眼睛散光等于或小于 1.00D。单眼 UDVA 平均值为-0.05±0.07 logMAR,单眼 CDVA 平均值为-0.07±0.06 logMAR。单眼 UDVA 和 CDVA 分别有 87.74% 和 92.45% 显示为 20/20 或更好,UDVA 和 CDVA 分别有 97.17% 和 98.11% 显示为 20/25 或更好。NEI VFQ-25 结果显示,所有类别的得分都很高,一般视力、远视力和近视力的平均值分别为 86.70±6.35、96.23±7.72 和 92.14±10.74。Catquest-9SF 问卷的结果显示,90.57% 的患者没有表示在日常生活中遇到视力困难,100% 的患者对目前的视力表示 "非常满意或比较满意"。PRSIQ结果显示,分别有100%、98.11%和98.11%的患者不需要佩戴远、中和近视眼镜或隐形眼镜:患者报告结果问卷调查结果表明,双侧植入 FineVision HP 人工晶体的患者视力和健康相关生活质量得分较高,眼镜独立率较高,患者满意度较高。
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