Medizinische Universität Graz - Research portal

Logo MUG Resarch Portal

Selected Publication:

SHR Neuro Cancer Cardio Lipid Metab Microb

Richter-Mueksch, S; Kiss, CG; Radner, W; Binder, S; Velikay-Parel, M.
Proliferative vitreoretinopathy--at what risk is the fellow eye?
Wien Klin Wochenschr. 2004; 116(1-2):32-36 Doi: 10.1007/BF03040421
Web of Science PubMed FullText FullText_MUG

 

Leading authors Med Uni Graz
Velikay-Parel Michaela
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
PURPOSE: To find out if patients with proliferative vitreoretinopathy (PVR) due to complicated retinal detachment are at risk to acquire the same disease or other vision-threatening retinal abnormalities in the fellow eye. To furthermore assess in what time-period they appear and if subgroups of patients have special risks. METHODS: 100 consecutive PVR-patients were studied retrospectively. 21 patients with PVR graded lower than C3, traumatic PVR, diabetic retinopathy or congenital vitreoretinal diseases were excluded. Age, gender, best-corrected visual acuity at the first and last visit, refraction, ocular disease in both eyes and observation-time were recorded. RESULTS: After a mean follow-up of 8.5 years, 42 of 79 patients (53.4%) showed vision-threatening abnormalities in their fellow eyes: among them, 9 patients (11.4%) had PVR, 13 (16%) simple retinal detachments and 14 (17.3%) retinal breaks. Abnormalities in the fellow eye did not develop after a certain time following surgery of the primary eye; 71.4% appeared within 5 years. Aphakic and pseudophakic patients had retinal breaks significantly more often (p = 0.011) than phakic patients. Myopia did not increase the risk for any abnormality. Men developed retinal detachment (p = 0.037) and PVR (p = 0.025) significantly more often than women. CONCLUSION: Patients with PVR have a greater than 50% risk of developing vision-threatening retinal abnormalities in their fellow eye. Because of this increased risk, these patients need regularly-scheduled long-term follow-up. SUMMARY STATEMENT: Patients with PVR have a greater than 50% risk of developing vision-threatening retinal abnormalities in their fellow eye and a 37% risk to develop PVR from rhegmatogenous retinal detachment. More than two thirds of abnormalities in the fellow eye developed within five years of surgery of the primary eye.
Find related publications in this database (using NLM MeSH Indexing)
Adult -
Aged -
Aged, 80 and over -
Comorbidity -
Female -
Follow-Up Studies -
Humans -
Male -
Mathematical Computing -
Middle Aged -
Postoperative Complications - diagnosis
Recurrence - diagnosis
Reoperation - statistics and numerical data
Retinal Detachment - complications
Retinal Perforations - complications
Retrospective Studies - complications
Risk - complications
Vitreoretinopathy, Proliferative - diagnosis

Find related publications in this database (Keywords)
proliferative vitreoretinopathy
risk factors
retinal detachment
fellow eye
visual acuity
© Med Uni GrazImprint