Journal List > J Korean Ophthalmol Soc > v.59(2) > 1010851

Lee, Cho, Lim, Choi, and Cho: Clinical Outcomes of Diffractive Aspheric Trifocal Intraocular Lens Implantation

Abstract

Purpose

To evaluate the clinical outcomes of patients with diffractive aspheric trifocal intraocular lens FineVision Pod F IOL (PhysIOL, Liège, Belgium) implantation.

Methods

Thirty eight eyes received phacoemulsification and implantation of FineVision Pod F IOL. Uncorrected distant visual acuity (UDVA), uncorrected intermediate visual acuity (UIVA), uncorrected near visual acuity (UNVA), refractive values, and defocus curve were evaluated at postoperative 1 month and 3 months. Optical quality was evaluated with the contrast sensitivity test, OQAS® (Optical Quality Analysis System, Visiometrics, Cerdanyola del Vallès, Spain) and questionnaire.

Results

At the 3-month postoperative follow-up, the mean spherical equivalent was 0.01 ± 0.31 D and the mean UDVA, UIVA and UNVA were 0.04 ± 0.07, 0.19 ± 0.12, and 0.04 ± 0.07, respectively. Mean contrast sensitivities at 0.75, 1.5, 3, 6, 12, and 18 cycles per degrees were 2.00 ± 1.54, 2.16 ± 1.60, 2.25 ± 1.76, 2.16 ± 1.83, 1.52 ± 1.47 and 1.03 ± 0.95 respectively and mean objective scatter index by OQAS® (Optical Quality Analysis System, Visiometrics) was 1.54 ± 0.74. In satisfaction analysis, general satisfaction with surgery was 89% and spectacle independence were 89% at far, 78% at intermediate and 83% at near distance. Postoperative dissatisfaction factors were dryness (36%), glare at night (32%), halo (18%).

Conclusions

The FineVision Pod F IOL showed excellent distant and near visual acuities with an effective intermediate visual acuity. The eyes with FineVision Pod F IOL expected to achieve the favorable visual outcome and patient satisfaction.

Figures and Tables

Figure 1

PhysIOL FineVision Pod F intraocular lens. This is a diffractive trifocal intraocular lens (the manufacturer approved the use of the photograph of their product officially).

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Figure 2

Mean monocular defocus curve at 1 and 3 months after surgery. Two peaks were observed at both far and near distances. There was no considerable decrease in the corrected visual acuity in the intermediate distance range. PL = plano.

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Figure 3

Contrast sensitivity test for patients underwent cataract surgery using FineVision trifocal intraocular lens at 4 m distance in photopic condition at 3 months after the surgery. The results of the contrast sensitivity test in the photopic condition at 3 months after the cataract surgery were measured within the normal range.

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Table 1

Patient demographics and clinical information

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Values are presented as mean ± SD (range). ‘K2–K1’ means ‘corneal cylinder’.

UCDVA = uncorrected distance visual acuity; logMAR = logarithm of the minimal angle of resolution; CDVA = corrected distance visual acuity; D = diopter; S.E = spherical equivalent; K = keratometry; IOL = intraocular lens.

Table 2

Refractive value and visual acuity (logMAR) at preoperative, postoperative 1 month, and postoperative 3 months

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Values are presented as mean ± SD (range).

logMAR = logarithm of the minimal angle of resolution; Preop = preoperation; Postop = postoperation; M = month; S.E = spherical equivalent; D = diopter; UCDVA = uncorrected distance visual acuity; CDVA = corrected distance visual acuity; UCIVA = uncorrected intermediate visual acuity at 80 cm; UCNVA = uncorrected near visual acuity at 40 cm distance.

*p-value was acquired from Wilcoxon signed rank test; p-value was acquired from paired T test.

Notes

Conflicts of Interest The authors have no conflicts to disclose.

Appendices

Appendix 1

Postoperative questionnaires on satisfaction

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Appendix 2

Survey results for postoperative satisfaction and glasses dependence

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Appendix 3

Survey results for postoperative unsatisfaction

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