Clinical data registry comparing outcomes of two light adjustable lenses

比较两种光可调镜片疗效的临床数据注册研究

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Abstract

PURPOSE: To compare the clinical performance of the light adjustable lenses (LALs) with the LAL+ with an increased central power to have broader depth of focus (DoF). SETTING: Private practice clinics. DESIGN: Prospective, nonrandomized, nonmask, multicenter. METHODS: Clinical data collection registry of patients bilaterally implanted with the LAL or LAL+. Outcome measures included subjective manifest refraction; monocular corrected distance, intermediate and near visual acuity; binocular uncorrected distance, intermediate, and near visual acuity; and binocular uncorrected best focus visual acuity at differing contrast levels. RESULTS: 91.1% and 93.5% of LAL and LAL+ eyes had a manifest refraction spherical equivalent within 0.50 diopter of target, respectively. 92.0% and 89.0% of LAL and LAL+ patients had a binocular uncorrected distance visual acuity of 20/20 or better after adjustment, respectively. 86.0% and 93.0% of LAL and LAL+ patients had binocular uncorrected best focus visual acuity of J1 or better at 100% contrast, respectively. Distance corrected intermediate and near visual acuity was better with the LAL+ compared with the LAL, consistent with its further broadened DoF. Best corrected distance vision was only slightly reduced for LAL+ (1 letter), with both lenses achieving high levels. CONCLUSIONS: Both LAL and LAL+ achieved excellent refractive and binocular visual outcomes at distance, intermediate, and near. The broadened DoF of the LAL+ was clinically evident and led to less anisometropia. The ability of patients to binocularly select and adjust their refraction according to their visual goal is a unique therapeutic approach to cataract refractive patients.

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