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Updated: Jul 16, 2026

Corneal Donor Tissue Preparation for Descemet's Membrane Endothelial Keratoplasty
Published on: September 17, 2014
Five-Year Endothelial Cell Density Outcomes After DMEK Using Peripherally Versus Centrally Trephinated Donor Tissue
1Cornea Department, Disha Eye Hospitals, Barrackpore, Kolkata, India.
Purpose:
To compare 5-year endothelial cell density (ECD) outcomes after Descemet membrane endothelial keratoplasty (DMEK) using peripherally trephinated donor tissue (DMEK-pD) versus centrally trephinated donor tissue (DMEK-cD) in eyes with corneal endothelial dysfunction of various etiologies.
Methods:
This retrospective comparative nonrandomized interventional cohort study included 428 eyes of 383 patients who underwent DMEK-pD (n = 205) or DMEK-cD (n = 223), with assignment based on surgeon preference, performed either alone or combined with cataract surgery using a standardized no-touch technique. All grafts were surgeon-prepared intraoperatively. ECD was measured at 6 months and annually up to 5 years. Corrected distance visual acuity, postoperative complications, and secondary graft failure (SGF) were recorded. Comparative and subgroup analyses were performed according to underlying diagnosis.
Results:
Mean ECD was significantly higher in the DMEK-pD group at all postoperative time points: 2368 ± 224 versus 2024 ± 312 cells/mm2 at 6 months, 1942 ± 284 versus 1698 ± 352 cells/mm2 at 2 years, and 1534 ± 279 versus 1280 ± 394 cells/mm2 at 5 years (all P < 0.001). Visual acuity improvement was comparable between groups (P = 0.15). Subgroup analysis demonstrated the greatest long-term ECD preservation in eyes with Fuchs endothelial corneal dystrophy undergoing DMEK-pD (P < 0.001). Postoperative complication rates were similar in both groups. SGF occurred more frequently in DMEK-cD (10.8%) than DMEK-pD (5.9%), although the difference was not statistically significant (P = 0.13).
Conclusions:
DMEK using DMEK-pD demonstrates sustained long-term ECD advantages over centrally trephinated DMEK in heterogeneous endothelial diseases, without compromising visual outcomes or safety. This suggests that a simple donor preparation modification may enhance graft longevity without altering surgical technique.

