患者报告了在术后高度近视的情况下实施聚焦深度增强型人工晶状体后的结果。

Maciej Gawęcki , Natalia Prądzyńska , Krzysztof Kiciński , Agnieszka Ratajczak , Izabella Karska-Basta , Andrzej Grzybowski
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引用次数: 1

摘要

背景:增强型聚焦深度人工晶状体(EDOF IOL)填补了单焦点和多焦点人工植入物之间的空白,具有单焦点晶状体的光学特性,通常是多焦点晶状体典型的轻微的耳咽炎。本研究的目的是评估需要完全近视和中等视力的患者双侧植入新型EDOF IOL后的视觉效果。方法:本研究包括15名患者(29眼为弱视),双侧植入LUXSMART EDOF IOL(Bausch&Lomb),双眼有针对性近视(-0.25至-0.50D)。在手术后1、3、6和12个月评估远、中、近和屈光结果的单核矫正和未矫正视力。此外,在最后一次随访时测量双眼视力、对比敏感度和散焦曲线。在12个月的随访中,患者完成了一份问卷调查,评估患者满意度、眼镜独立性和是否存在吞咽困难。结果:12个月随访时,双眼裸眼视力为0.13​±​0.160.06​±​0.080.07​±​0.09和0.15​±​0.09 logMAR(远距离),80​厘米,66​厘米和40​cm。12个月时矫正的双眼视觉敏锐度为0.00​±​0.00、0.05​±​0.07,0.05​±​0.060.13​±​距离分别为0.16,80​厘米,66​厘米和40​12个月随访时的自动折射球面当量为-0.70​±​0.48D,比计算的生物特征目标低0.46D,但12个月时主观折射的球面等效值等于-0.49​±​0.46D,更接近术前生物特征指标。散焦曲线具有平缓的形状,没有单焦点IOL典型的峰值。双眼对比敏感度结果优于该年龄组的平均结果,相当于1.78​±​0.16 logMAR(无校正)和1.81​±​0.13 logMAR(带校正)。近距离和中距离的眼镜独立性在所有患者中实现,远距离的眼镜独立度在73.3%的患者中实现。在任何情况下均未报告有负担性吞咽困难。结论:在大多数情况下,针对低近视的双侧EDOF IOL可以提供优异的近中视力和独立于任何光学矫正的能力。这种方法可以用于选定的专注于静止活动的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Patient reported outcomes after implementation of an enhanced depth of focus intraocular lens with low postoperative myopia

Background

Enhanced depth-of- focus intraocular lenses (EDOF IOL) have filled the gap between monofocal and multifocal intraocular implants with optical qualities of monofocal lenses and usually minor dysphotopsias typical for multifocal lenses. The purpose of this study was to evaluate visual outcomes after bilateral implantation of a new EDOF IOL in patients with requirements for perfect near and intermediate vision.

Methods

The study included 15 patients (29 eyes as one was amblyopic) with bilateral implantation of LUXSMART EDOF IOL (Bausch & Lomb) with a targeted myopia (between –0.25 and –0.50D) in both eyes. Monocular corrected and uncorrected visual acuity for far, intermediate and near as well as refractive outcomes were evaluated at 1, 3, 6 and 12 months after the surgery. Additionally, binocular visual acuity, contrast sensitivity and defocus curve were measured at the final follow-up visit. At 12 months’ visit patients completed a questionnaire evaluating patient satisfaction, spectacle independence and presence of dysphotopsias.

Results

Binocular uncorrected visual acuities at 12 month’s visit were 0.13 ​± ​0.16, 0.06 ​± ​0.08, 0.07 ​± ​0.09 and 0.15 ​± ​0.09 logMAR for far distance, 80 ​cm, 66 ​cm and 40 ​cm respectively. Corrected binocular visual acuities at 12 months were 0.00 ​± ​0.00, 0.05 ​± ​0.07, 0.05 ​± ​0.06, 0.13 ​± ​0.16 respectively for distance, 80 ​cm, 66 ​cm and 40 ​cm. Automated refraction spherical equivalent at 12 months’ visit stood at –0.70 ​± ​0.48D, which was 0.46D less than calculated biometric target, however spherical equivalent of subjective refraction at 12 months equaled –0.49 ​± ​0.46D, which was closer to preoperative biometric target. Defocus curve had gentle shape without peaks typical for monofocal IOLs. Binocular contrast sensitivity results were superior to average results for that age group and equaled 1.78 ​± ​0.16 logMAR without correction and 1.81 ​± ​0.13 logMAR with correction. Spectacle independence for near and intermediate distances was achieved in all patients and for far distance in 73.3% of patients. Burdensome dysphotopsias were not reported in any case.

Conclusions

EDOF IOLs targeted bilaterally at low myopia can provide excellent near and intermediate visual acuity and independence of any optical correction in majority of cases. This approach can be used in selected patients who are focused on stationary activities.

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