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

This Meeting has been awarded 27 CME credits

 

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Clinical outcomes of central circular Descemetorhexis without endothelial transplantation in patients with Fuch's corneal dystrophy

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Session Details

Session Title: Cornea Surgical II

Session Date/Time: Tuesday 13/09/2016 | 08:00-10:30

Paper Time: 09:44

Venue: Hall C2

First Author: : E.Malyutina RUSSIA

Co Author(s): :    B. Malyugin   O. Antonova                 

Abstract Details

Purpose:

To assess the results of central descemetorhexis (CDR) in patients with Fuch’s corneal endothelial dystrophy

Setting:

S. Fyodorov Eye Microsurgery Federal Institution, Moscow, Russia

Methods:

8 eyes of 8 patients (2 men and 6 women) with the mean age of 65,7±11,3 years (range 51-84) having Fuch’s corneal dystrophy and cataract underwent US phacoemulsification, in-the-bag hydrophobic acrylic IOL implantation followed by CDR (3.5-4.5 mm in diameter) without endothelial transplantation. Best-corrected visual acuity (BCVA), corneal pachymetry, endothelial cell density (ECD), and confocal microscopy were evaluated preoperatively and 1 day, 1 and 3 months postoperatively

Results:

On the 1st day postop significant stromal edema corresponding to the area of removed Descemet’s membrane was observed leading to low VA. Mean preoperative BCVA was 0,34±0,19. Following the surgery BCVA was 0,07±0,06; 0,29±0,25 and 0,36±0,18 1st day, 1 and 3 months postop. Central corneal pachymety values were 596,5±53,8μm; 865,4±43,9μm; 709,6±106,2μm; and 605,0±48,3μm in the above mentioned time intervals. Complete resolution of corneal edema was achieved in 6 out of 8 cases in 3-month period. Their BCVA at the last visit was 0,47±0,22 with central corneal pachymetry 34,2±108,6μm.After 3 months ECD were counted in 2 out of 6 eyes

Conclusions:

Central descemetorhexis is a viable option for visual rehabilitation in some patients with Fuch’s corneal endothelial dystrophy and cataract eliminating the need for endothelial grafting. Further research is necessary to find out which category of patients will benefit best from that technology

Financial Disclosure:

NONE

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