Literature DB >> 28478395

Outcomes of penetrating keratoplasty in congenital hereditary endothelial dystrophy.

Hamed AlArrayedh1, Louis Collum1, Conor C Murphy1,2.   

Abstract

BACKGROUND/AIM: To report the outcome of penetrating keratoplasty (PKP) in Irish patients with congenital hereditary endothelial dystrophy (CHED).
METHODS: A retrospective case series review of patients with CHED who underwent PKP was conducted. The outcomes of PKP in 14 patients with CHED at the Royal Victoria Eye and Ear Hospital in Dublin from 1978 to 2013 were described following case note review. The main outcome measures were best-corrected visual acuity (BCVA) and graft survival.
RESULTS: Thirty-three corneal transplants were performed, which included 32 PKPs and one Descemet's stripping endothelial keratoplasty. Twenty-four eyes underwent primary corneal grafts and nine eyes had regrafts. The graft survival rates at final follow-up were 37.5% and 33% in the primary graft and regraft groups, respectively. Preoperative BCVA was 20/200 or worse in all patients. At the final postoperative visit, the BCVA was 20/80 or better in four eyes following primary PKP, 20/160 in one eye following regrafting and was 20/200 or worse in all other eyes. The mean time to graft failure was 16 months (range 0-37 months). The mean follow-up time was 101 months (range 12-252 months). Fifty per cent of the patients continue to attend for follow-up.
CONCLUSIONS: This study has demonstrated a poor outcome from PKP for CHED in this Irish cohort. This arises from a combination of dense amblyopia and a high risk of graft failure in the long term. © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted.

Entities:  

Keywords:  Cornea; Dystrophy; Treatment Surgery

Mesh:

Year:  2017        PMID: 28478395     DOI: 10.1136/bjophthalmol-2016-309565

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN: 0007-1161            Impact factor:   4.638


  4 in total

1.  Spontaneous regression of congenital corneal opacity.

Authors:  Sooyeon Choe; Chang Ho Yoon; Mee Kum Kim; Joon Young Hyon; Young Suk Yu; Joo Youn Oh
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2019-11-25       Impact factor: 3.117

2.  Harboyan syndrome: novel SLC4A11 mutation, clinical manifestations, and outcome of corneal transplantation.

Authors:  Napaporn Tananuvat; Rak Tananuvat; Wattana Chartapisak; Pongsak Mahanupab; Chananya Hokierti; Metawee Srikummool; Jatupol Kampuansai; Worrachet Intachai; Bjorn Olsen; James R Ketudat Cairns; Piranit Kantaputra
Journal:  J Hum Genet       Date:  2020-09-03       Impact factor: 3.172

3.  Identification and in silico analysis of a spectrum of SLC4A11 variations in Indian familial and sporadic cases of congenital hereditary endothelial dystrophy.

Authors:  Mohd Salman; Anshuman Verma; Sunita Chaurasia; Deeksha Prasad; Chitra Kannabiran; Vivek Singh; Muralidhar Ramappa
Journal:  Orphanet J Rare Dis       Date:  2022-09-17       Impact factor: 4.303

4.  Microscope Integrated Optical Coherence Tomography Guided Descemet Stripping Automated Endothelial Keratoplasty in Congenital Hereditary Endothelial Dystrophy.

Authors:  Mohamed Ibrahime Asif; Rahul Kumar Bafna; Namrata Sharma; Ananya Kaginalkar; Rajesh Sinha; Tushar Agarwal; Prafulla Kumar Maharana; Manpreet Kaur; Priya Taank; Jeewan S Titiyal
Journal:  Clin Ophthalmol       Date:  2021-07-27
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.