2014
DOI: 10.1167/iovs.14-14309
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Surface Metrology and 3-Dimensional Confocal Profiling of Femtosecond Laser and Mechanically Dissected Ultrathin Endothelial Lamellae

Abstract: Confocal microscopy allows quantitative surface roughness analysis and 3-dimensional reconstruction of human corneal lamellae. Femtosecond-laser photodisruption at 60 kHz results in rougher surfaces compared with mechanical dissection. The motor-driven linear microkeratome allows single-pass dissection of ultrathin endothelial lamellae with a standard deviation ≤20 μm.

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Cited by 7 publications
(7 citation statements)
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“…The DSAEK donor tissue was then dissected using a Gebauer SLc microkeratome (Gebauer Medizintechniek GmbH, Neuhausen, Germany) using the single‐pass technique, with the goal of achieving a central residual stromal bed thickness of 100 ± 40 μ m for ultrathin DSAEK (Dickman et al. , ). The donor (pre‐dissection) and lamellar (post‐dissection) central corneal thickness values were measured using a Casia SS‐1000 anterior segment OCT (Tomey, Nagoya, Japan).…”
Section: Methodsmentioning
confidence: 99%
“…The DSAEK donor tissue was then dissected using a Gebauer SLc microkeratome (Gebauer Medizintechniek GmbH, Neuhausen, Germany) using the single‐pass technique, with the goal of achieving a central residual stromal bed thickness of 100 ± 40 μ m for ultrathin DSAEK (Dickman et al. , ). The donor (pre‐dissection) and lamellar (post‐dissection) central corneal thickness values were measured using a Casia SS‐1000 anterior segment OCT (Tomey, Nagoya, Japan).…”
Section: Methodsmentioning
confidence: 99%
“…After a short hypothermic storage between recovery and arrival at the bank, corneoscleral buttons were dissected and stored in organ culture comprising minimum essential medium (Biowest, Nuaillé, France) supplemented with 25 mmol/l 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid, 26 mmol/l sodium bicarbonate, 5.5 mmol/l glucose, 2 mmol/l L-glutamine, 1 mmol/l pyruvate, 2% (vol/vol) newborn calf serum, 10 IU/ml penicillin, 0.1 mg/ml streptomycin, and 0.25 mg/ml amphotericin at 31 C. To allow deturgescence, corneoscleral buttons were transferred to a transport medium supplemented with 6% dextran (Sigma Aldrich, St. Louis, MO) before and immediately after dissection. Graft dissection was performed with the Gebauer SLc microkeratome system (Gebauer Medizintechniek GmbH, Neuhausen, Germany) using a single-pass technique, 12,13 aiming at a central residual stromal bed thickness of 200AE20 mm for DSAEK and 100AE20 mm for UT-DSAEK. Donor and lamellar central corneal thickness were measured at the cornea bank using anterior-segment optical coherence tomography (AS-OCT; Cassia SS-1000; Tomey, Nagoya, Japan).…”
Section: Donor Preparationmentioning
confidence: 99%
“…To date there have been a number of articles investigating this. [6][7][8][9][10][11][12][13][14][15] Several authors have developed subjective (observer based grading) and objective (e.g. texture analysis) scores to quantify the smoothness of stromal beds using primarily scanning electron microscopy (SEM) images for comparison.…”
Section: Scanning Electronic Microscopy Evaluation Of the Roughness Omentioning
confidence: 99%