“…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).…”