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10 - 14 Sept. 2016, Bella Center, Copenhagen, Denmark

This Meeting has been awarded 27 CME credits

 

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Preliminary results of posterior capsule opacification following cataract surgery with implantation of the MICS-IOL L313

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Session Details

Session Title: Posterior Capsule Opacification

Session Date/Time: Sunday 11/09/2016 | 08:30-10:00

Paper Time: 09:30

Venue: Hall C2

First Author: : H.Höh GERMANY

Co Author(s): :    U. Holland   C. Stylianides                 

Abstract Details

Purpose:

To collect intra- and postoperative data and evaluate the rate of posterior capsule opacification (PCO) following implantation of the MICS-IOL L313.

Setting:

Monocenter retrospective study at the Department of Ophthalmology of Dietrich-Bonhoeffer Klinikum in Neubrandenburg, Teaching Hospital of Ernst-Moritz-Arndt University Greifswald, Germany

Methods:

The data of 5.564 eyes, who had cataract surgery in our Hospital Outpatient Center between Sept. 2009 and Dec. 2013 with implantation of the MICS IOL L313 (Oculentis GmbH, Berlin, Germany) were collected between May 2013 and March 2016. Only the data of patients with their written informed consent were included. It was approved by the Ethics Committee of the University of Greifswald, Germany. Evaluation was performed using Kaplan-Meier-Statistics with STATISTICA (StatSoft, Hamburg, Germany). We could use the data sets of 2.171 eyes for an interim evaluation. Patients with posterior capsule tear were excluded.

Results:

Mean age of all patients at the time of surgery was 73,76 ± 9,06 (range 5 to 101, n=5.564). 59,16 % of the patients are female. The proportion of return of patients surveys until now is 36,7 %. Based on 2.171 data sets the rate of PCO was 4,5 % after 365 days, 7,3 % after 730 days, 13,3 % after 1460 days and 13,8% after 2190 days.

Conclusions:

After 850 days the 9,9% PCO rate of the L313 IOL is lower than the PCO rate of ThinLens (33,33%), of CareFlex (32,56%), of AcriSmart (20,0%) and of AcriFlex (11,36%).

Financial Disclosure:

... research is funded, fully or partially, by a company producing, developing or supplying the product or procedure presented

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