延焦深度眼内透镜对青光眼患者的临床疗效。

IF 1.4 4区 医学 Q3 OPHTHALMOLOGY International Ophthalmology Pub Date : 2024-11-27 DOI:10.1007/s10792-024-03361-w
Reem Amir Kamal Dessouky, Amr Aref, André Mermoud
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引用次数: 0

摘要

目的:评估混合型屈光/延伸焦距眼内透镜(Lucidis;Swiss Advanced Vision,SAV-IOL SA,瑞士纳沙泰尔)在青光眼患者中的临床效果,并比较对比敏感度结果与青光眼控制方法的关系:这项回顾性多中心研究纳入了 28 名视力受损白内障患者,他们都是在 2021 年 6 月至 2023 年 7 月期间接受过超声乳化术和 Lucidis 眼内晶体植入术的早期至中度原发性开角型青光眼患者。对医疗记录进行审查,以了解基线特征、青光眼的严重程度、控制的充分性和方法、白内障手术的详细情况以及术后结果。对术后 3 个月的临床结果进行了分析,包括未矫正和最佳矫正的近、中、远视力、屈光表现、对比敏感度和患者满意度(改编自 Catquest-9SF 问卷):共纳入 28 名患者的 42 只眼睛,男女比例为 1:1.8。术后未矫正视力和最佳矫正近、中、远视力均有非常明显的改善(p 结论:Lucidis IOL 是一种有效的人工晶体:Lucidis IOL 对白内障和要求独立配戴眼镜的早期至中度 POAG 患者有效且安全。无论采用哪种控制方法,充分的青光眼控制和较好的术前平均偏差都能确保良好的临床效果:ZU-IRB#11,295-28-11-2023,2023 年 11 月 28 日 "回顾性注册"。
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Clinical outcomes of an extended depth-of-focus intraocular lens in patients with glaucoma.

Purpose: to evaluate the clinical outcomes of a hybrid refractive/extended depth-of-focus intraocular lens (Lucidis; Swiss Advanced Vision, SAV-IOL SA, Neuchâtel, Switzerland) in glaucoma patients and to compare the contrast sensitivity results as regards to method of glaucoma control.

Methods: This retrospective multicenter study included 28 patients with visually impairing cataract and controlled early to moderate primary open angle glaucoma who underwent phacoemulsification and Lucidis intraocular lens implantation during the period from June 2021 to July 2023. Medical records were reviewed for baseline characteristics, severity, adequacy and method of control of glaucoma, details of cataract surgery and postoperative findings. Clinical outcomes were analysed at 3 months postoperatively and included uncorrected and best corrected near, intermediate and distance visual acuities, manifest refraction, contrast sensitivity, and patient satisfaction (adapted from the Catquest-9SF questionnaire).

Results: 42 eyes of 28 patients were included, with a male to female ratio of 1:1.8. There was a highly significant improvement in postoperative uncorrected and best corrected near, intermediate, and distance visual acuities (p < 0.001). Mean postoperative contrast sensitivity was 1.56 ± 0.11 log and there was no significant difference between medically and surgically controlled glaucoma (P = 0.08). There was a highly significant correlation between preoperative mean deviation and postoperative contrast sensitivity (p < 0.001). 26 (92.9%) patients were very satisfied. One (2.4%) eye developed dysphotopsia and no serious complications occurred throughout the study.

Conclusions: Lucidis IOL is effective and safe in patients with cataract and early to moderate POAG requesting spectacle independence. Adequate glaucoma control, regardless the method of control, and better preoperative mean deviation ensure good clinical outcomes.

Trial registration: ZU-IRB#11,295-28-11-2023, 28/11/2023 'retrospectively registered'.

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来源期刊
CiteScore
3.20
自引率
0.00%
发文量
451
期刊介绍: International Ophthalmology provides the clinician with articles on all the relevant subspecialties of ophthalmology, with a broad international scope. The emphasis is on presentation of the latest clinical research in the field. In addition, the journal includes regular sections devoted to new developments in technologies, products, and techniques.
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