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Endothelial cell loss rate after penetrating keratoplasty: optical versus therapeutic grafts

BACKGROUND: This study aimed to compare the rate of endothelial cell loss (ECL) after penetrating keratoplasty (PKP) for optical versus therapeutic grafts at 3-, 6-, and 12-month postoperatively. Furthermore, the study aimed to investigate postoperative graft viability and the rate of graft rejectio...

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Autores principales: Shams, Abdelrhman, Abdelmoneim Gaafar, Ayman, Elkitkat, Rania Serag, Omar Yousif, Mohamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Virtual Ophthalmic Research Center 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10460226/
https://www.ncbi.nlm.nih.gov/pubmed/37641612
http://dx.doi.org/10.51329/mehdiophthal1424
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author Shams, Abdelrhman
Abdelmoneim Gaafar, Ayman
Elkitkat, Rania Serag
Omar Yousif, Mohamed
author_facet Shams, Abdelrhman
Abdelmoneim Gaafar, Ayman
Elkitkat, Rania Serag
Omar Yousif, Mohamed
author_sort Shams, Abdelrhman
collection PubMed
description BACKGROUND: This study aimed to compare the rate of endothelial cell loss (ECL) after penetrating keratoplasty (PKP) for optical versus therapeutic grafts at 3-, 6-, and 12-month postoperatively. Furthermore, the study aimed to investigate postoperative graft viability and the rate of graft rejection during the first year of follow-up for both indications. METHODS: This was a prospective, observational, comparative study that included patients who sought medical advice at the cornea outpatient clinic of Ain Shams University Hospitals, Cairo, Egypt. The study recruited 60 patients: group 1 included 30 transplanted corneas of 30 patients who underwent optical PKP for various indications, while group 2 included 30 transplanted corneas of 30 patients who underwent therapeutic PKP for unhealed, resistant infectious keratitis. Specular microscopy was performed for all patients at the 3-, 6-, and 12-month follow-up visits using Nidek CEM-530 specular microscopy. Postoperative clinical examinations were performed at the same follow-up visits to detect graft rejection. RESULTS: There were no statistically significant differences between the groups concerning the postoperative timing of graft clarity or the rate of ECL at 3- and 6-months postoperatively; however, the rate of ECL was significantly greater in group 2 than in group 1 at 12-months postoperatively (P = 0.03), although the difference was small from a clinical point of view. Moreover, there was no statistically significant difference between the groups in terms of the graft rejection rate. CONCLUSIONS: Therapeutic PKP results were comparable to optical PKP with respect to graft viability, the rate of ECL, and the rate of graft rejection 1 year after grafting.
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spelling pubmed-104602262023-08-28 Endothelial cell loss rate after penetrating keratoplasty: optical versus therapeutic grafts Shams, Abdelrhman Abdelmoneim Gaafar, Ayman Elkitkat, Rania Serag Omar Yousif, Mohamed Med Hypothesis Discov Innov Ophthalmol Original Article BACKGROUND: This study aimed to compare the rate of endothelial cell loss (ECL) after penetrating keratoplasty (PKP) for optical versus therapeutic grafts at 3-, 6-, and 12-month postoperatively. Furthermore, the study aimed to investigate postoperative graft viability and the rate of graft rejection during the first year of follow-up for both indications. METHODS: This was a prospective, observational, comparative study that included patients who sought medical advice at the cornea outpatient clinic of Ain Shams University Hospitals, Cairo, Egypt. The study recruited 60 patients: group 1 included 30 transplanted corneas of 30 patients who underwent optical PKP for various indications, while group 2 included 30 transplanted corneas of 30 patients who underwent therapeutic PKP for unhealed, resistant infectious keratitis. Specular microscopy was performed for all patients at the 3-, 6-, and 12-month follow-up visits using Nidek CEM-530 specular microscopy. Postoperative clinical examinations were performed at the same follow-up visits to detect graft rejection. RESULTS: There were no statistically significant differences between the groups concerning the postoperative timing of graft clarity or the rate of ECL at 3- and 6-months postoperatively; however, the rate of ECL was significantly greater in group 2 than in group 1 at 12-months postoperatively (P = 0.03), although the difference was small from a clinical point of view. Moreover, there was no statistically significant difference between the groups in terms of the graft rejection rate. CONCLUSIONS: Therapeutic PKP results were comparable to optical PKP with respect to graft viability, the rate of ECL, and the rate of graft rejection 1 year after grafting. International Virtual Ophthalmic Research Center 2021-08-05 /pmc/articles/PMC10460226/ /pubmed/37641612 http://dx.doi.org/10.51329/mehdiophthal1424 Text en © Author(s). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.
spellingShingle Original Article
Shams, Abdelrhman
Abdelmoneim Gaafar, Ayman
Elkitkat, Rania Serag
Omar Yousif, Mohamed
Endothelial cell loss rate after penetrating keratoplasty: optical versus therapeutic grafts
title Endothelial cell loss rate after penetrating keratoplasty: optical versus therapeutic grafts
title_full Endothelial cell loss rate after penetrating keratoplasty: optical versus therapeutic grafts
title_fullStr Endothelial cell loss rate after penetrating keratoplasty: optical versus therapeutic grafts
title_full_unstemmed Endothelial cell loss rate after penetrating keratoplasty: optical versus therapeutic grafts
title_short Endothelial cell loss rate after penetrating keratoplasty: optical versus therapeutic grafts
title_sort endothelial cell loss rate after penetrating keratoplasty: optical versus therapeutic grafts
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10460226/
https://www.ncbi.nlm.nih.gov/pubmed/37641612
http://dx.doi.org/10.51329/mehdiophthal1424
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