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Three-quarter DMEK in eyes with glaucoma draining devices to avoid secondary graft failure
O. Oganesyan, P. Makarov, A. Grdikanyan, C. Oganesyan, V. Getadaryan, GRJ. Melles
Language English Country Great Britain
Document type Case Reports, Journal Article
NLK
Free Medical Journals
from 2008 to 1 year ago
Medline Complete (EBSCOhost)
from 2008-02-01 to 1 year ago
Wiley Free Content
from 2008 to 1 year ago
PubMed
33124201
DOI
10.1111/aos.14645
Knihovny.cz E-resources
- MeSH
- Time Factors MeSH
- Glaucoma Drainage Implants * MeSH
- Glaucoma etiology physiopathology surgery MeSH
- Humans MeSH
- Follow-Up Studies MeSH
- Graft Survival MeSH
- Prospective Studies MeSH
- Prosthesis Design MeSH
- Pseudophakia complications MeSH
- Refraction, Ocular MeSH
- Graft Rejection prevention & control MeSH
- Endothelium, Corneal transplantation MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Descemet Stripping Endothelial Keratoplasty methods MeSH
- Visual Acuity * MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Case Reports MeSH
PURPOSE: To present a case series of a modified three-quarter Descemet's membrane endothelial keratoplasty (3/4-DMEK) technique to treat pseudophakic bullous keratopathy in the presence of a glaucoma drainage device (GDD) tube in the anterior chamber by reducing the risk of donor endothelial damage due to absence of donor endothelial cells overlying the GGD tube area. METHODS: In this prospective case series, four eyes of three patients with stable glaucoma underwent 3/4-DMEK surgery for pseudophakic bullous keratopathy after GDD insertion. The patients were followed up to 24 ± 2.5 months postoperatively. RESULTS: No intraoperative or postoperative complications were noted. The average central endothelial cell density (ECD) was 1093 ± 74 cells/mm2 at 12 months postoperatively, corresponding to an ECD decrease of 58 (±6)% as compared to preoperative values. Average best-corrected visual acuity increased from finger counting before surgery to 20/60 (logMar 0.5) at 12 months after 3/4-DMEK and remained stable up to 24 months postoperatively. All corneas remained clear at the last available follow-up. CONCLUSION: This case series demonstrates the technical feasibility of 3/4-DMEK in eyes with pseudophakic bullous keratopathy in the presence of a GDD tube. The absence of a donor DM and donor cells above the silicone tube excludes direct tube contact with the graft. Longer term studies are needed to show the effect of this modified graft pattern and dimensions on transplant survival.
Netherlands Institute for Innovative Ocular Surgery Rotterdam The Netherlands
The Charles University Prague Czech Republic
The Helmholtz Moscow Institute of Eye Diseases Moscow Russia
References provided by Crossref.org
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