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1.
Cornea ; 32(9): 1189-92, 2013 Sep.
Article in English | MEDLINE | ID: mdl-23860430

ABSTRACT

PURPOSE: To determine the prevalence of herpes simplex virus type 1 (HSV-1) DNA in failed Descemet membrane stripping automated endothelial keratoplasty (DSAEK) grafts. METHODS: A retrospective interventional case series of patients with DSAEK graft failure treated at the New York Eye and Ear Infirmary between January 2009 and July 2012 was performed. Repeat DSAEK, penetrating keratoplasty, or keratoprosthesis procedure was subsequently performed on eyes with failed grafts. All failed grafts were examined immunohistochemically and with qualitative real-time polymerase chain reaction for HSV-1 DNA. In HSV-1-positive cases, corneoscleral donor rims from the original DSAEK procedures were also examined immunohistochemically and with polymerase chain reaction. RESULTS: Fifty-one failed DSAEK grafts from 50 eyes of 49 patients were identified. Indications for DSAEK were pseudophakic bullous keratopathy (28/51, 55%), Fuchs corneal endothelial dystrophy (12/51, 23%), failed penetrating keratoplasty (7/51, 14%), corneal decompensation from glaucoma (2/51, 4%), herpetic endotheliitis (1/51, 2%), and failed DSAEK (1/51, 2%). Forty-three grafts (83%) were primary DSAEK graft failure. HSV-1 DNA was isolated from 2 of 51 failed DSAEK grafts (4.0%). The corresponding corneoscleral donor rims did not demonstrate the presence of HSV-1. CONCLUSIONS: Based on our results, HSV-1 infection plays a minor role in DSAEK graft failure. The data suggest that recipient reactivation, rather than donor transmission, plays a role in HSV infection.


Subject(s)
Corneal Endothelial Cell Loss/virology , Descemet Stripping Endothelial Keratoplasty , Graft Rejection/virology , Herpesvirus 1, Human/isolation & purification , Keratitis, Herpetic/virology , Aged , Aged, 80 and over , Corneal Dystrophies, Hereditary/surgery , Corneal Endothelial Cell Loss/diagnosis , DNA, Viral/analysis , Descemet Membrane/virology , Endothelium, Corneal/virology , Female , Graft Rejection/diagnosis , Herpesvirus 1, Human/genetics , Humans , Keratitis, Herpetic/diagnosis , Male , Middle Aged , Real-Time Polymerase Chain Reaction , Reoperation , Retrospective Studies , Treatment Failure
2.
Br J Ophthalmol ; 94(3): 336-40, 2010 Mar.
Article in English | MEDLINE | ID: mdl-19734135

ABSTRACT

AIM: The aim of the study was to investigate the correlation between the clinical manifestation and the cytomegalovirus (CMV) viral load in the aqueous humour of patients with CMV anterior uveitis. METHODS: Seven patients with CMV-associated iridocyclitis and four patients with CMV-associated corneal endotheliitis were enrolled. Presence of CMV, but not other human herpes viruses, was confirmed by multiplex polymerase chain reaction (PCR). Viral load was measured using real-time PCR. Clinical manifestations were examined using a slit-lamp microscope and ophthalmoscope, applanation tonometer and specular microscope. RESULTS: All 11 patients had unilateral recurrent anterior uveitis with high intraocular pressure and mutton fat keratic precipitates with pigmentation. Stromal oedema of the cornea was found in CMV-associated endotheliitis, but not in CMV-associated iridocyclitis patients. A significant corneal endothelium cell loss was recorded in all 11 patients with CMV-associated endotheliitis and iridocyclitis patients. High viral loads of CMV were detected in the aqueous humour of all 11 patients. A significant association was found between the corneal endothelial cell loss intensity and CMV viral load in the aqueous humour. CONCLUSION: There is a significant correlation between the CMV viral load and corneal endothelial cell loss in both CMV-associated iridocyclitis and corneal endotheliitis.


Subject(s)
Corneal Endothelial Cell Loss/virology , Cytomegalovirus Infections/complications , Eye Infections, Viral/virology , Iridocyclitis/virology , Viral Load , Adult , Aged , Aqueous Humor/virology , Corneal Endothelial Cell Loss/pathology , Cytomegalovirus/isolation & purification , Cytomegalovirus Infections/virology , DNA, Viral/analysis , Female , Humans , Male , Middle Aged , Polymerase Chain Reaction/methods
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