4.6 Article

Trifocal Intraocular Lens Implantation to Treat Visual Demands in Various Distances Following Lens Removal

Journal

AMERICAN JOURNAL OF OPHTHALMOLOGY
Volume 161, Issue -, Pages 71-77

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.ajo.2015.09.030

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Funding

  1. Abbott Medical Optics Inc, Santa Ana, California
  2. Alcon Pharma GmbH, Hurth, Germany
  3. Bausch & Lomb GmbH, Berlin, Germany
  4. Carl Zeiss Meditec Vertriebsgesellschaft mbH, Oberkochen, Germany
  5. Hoya Surgical Optics GmbH, Frankfurt am Main, Germany
  6. Oculus Optikgerate GmbH, Wetzlar, Germany
  7. Rayner Intraocular Lenses Ltd, Bamberg, Germany
  8. SCHWIND eye-tech-solutions, Kleinostheim, Germany
  9. Geuder AG, Heidelberg, Germany
  10. TearLab Corp, San Diego, California
  11. Thieme Compliance, Elangen, Germany
  12. Ziemer Ophthalmic Systems AG, Port, Switzerland
  13. Alcon Pharma GmbH, Birth, Germany

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PURPOSE: To evaluate visual and refractive outcomes after implantation of a trifocal intraocular lens (IOL). DESIGN: Prospective, nonrandomized noncomparative case series. METHODS: SETTING: Department of Ophthalmology, Goethe University, Frankfurt/Germany. PATIENT OR STUDY POPULATION: Twenty-seven patients (54 eyes) who had bilateral implantation of the AT LISA trifocal IOL (AT LISA tri839MP; Carl Zeiss Meditec, Jena, Germany) pre-enrollment. Exclusion criteria were previous ocular surgeries excluding cataract surgery and refractive lens exchange, irregular corneal astigmatism of >1.5 diopter, and ocular pathologies or corneal abnormalities. INTERVENTION OR OBSERVATION PROCEDURE(S): Postoperative examination at 1 and 3 months included manifest refraction; monocular and binocular uncorrected (UCVA) and distance-corrected (DCVA) visual acuity in 4 m, 80 cm, and 40 cm; slit-lamp examination; and tomography. At 3 months defocus testing, binocular contrast sensitivity (CS) under photopic and mesopic conditions and a questionnaire on subjective quality of vision, optical phenomena, and spectacle independence were performed. Main OUTCOME MEASURE(S): Three-months-postoperative monocular and binocular UCVA and DCVA in 4 m, 80 cm, and 40 cm (logMAR); defocus curve; CS; and quality-of-vision questionnaire results. RESULTS: Mean spherical equivalent was 0.05 +/- 0.32 D 3 months postoperatively. Binocular UCVA at distance, intermediate, and near was 0.1 +/- 0.1 logMAR, 0.0 +/- 0.1 logMAR, and 0.0 +/- 0.1 logMAR, respectively. Despite some optical phenomena, 92% of patients would choose the same IOL again. CONCLUSION: Evaluation of a trifocal IOL showed good VA (0.1 logMAR or better) at far, intermediate, and near distance; high patient satisfaction despite some optical phenomena; and high spectacle independence 3 months postoperatively. (C) 2016 by Elsevier Inc. All rights reserved.

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