Abstract 99. Jahrestagung der DOG, 29. 9. - 2. 10. 01 im ICC, Berlin

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Laser epithelial keratomileusis (LASEK): histological investigations for the vitality of corneal epithelial cells after alcohol exposure.

1,2Dreiss A. K., 3Winkler von Mohrenfels C. W., 3Gabler B., 2Kohnen T., 1Marshall J., 1,3Lohmann C. P.

1Dept of Ophthalmology, The Rayne Institute, ST Thomas' Hospital London; 2Zentrum für Augenheilkunde, Universität Frankfurt/Main; 3Universitäts-Augenklinik Regensburg

Background: Laser epithelial keratomileusis (LASEK) is a new surgical procedure to treat myopia. An epithelial flap is created after the exposure to 20% alcohol and following the laser ablation the epithelium is repositioned to its original location. The advantage of LASEK is that the ablated corneal surface is covered by a full thickness epithelium immediately after surgery. It is hypothesised that this epithelial coverage inhibits the wound healing response of the cornea. However, this concept will only work if the epithelial cells are still vital after the exposure to alcohol.
Material and Methods: The vitality of the corneal epithelial cells was investigated in 3 human cadaver eyes after the exposure to 20% alcohol over 30 to 120 sec. The vitality of the corneal epithelial cells was assessed by soaking the specimen in a 0.1% trypan blue solution and incubated at 37oC for 2 min. At this stage the all cells would have taken up trypan blue and would appear blue. After a wash with BSS the specimen were reincubated at 37oC for 30 min in culture medium. After one more wash with BSS the cells were observed with a standard light microscope. Cells, which retained the blue colour would be dead and vital cells would appear clear again because of the ability to pump out the trypan blue.
Results: Vital corneal epithelial cells were seen up to an alcohol exposure time of 45 sec. In particular the basal epithelial cells appeared alive. Longer exposition times showed, that most cells were dead.
Conclusion: In LASEK the exposure time of 20% alcohol is between 20 and 30 sec. Based on our results we can conclude that after such exposure time most cells are alive, which is the basis for inhibiting the postoperative wound healing response.




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