2015, Volume 8, Issue 1, pp 90 – 93

Hydroxyapatite ocular implant and non-integrated implants in eviscerated patients

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Authors and Affiliations

Correspondence to:Ciuluvica R, MD Anatomy Department “Carol Davila” University of Medicine and Pharmacy, 8 Eroilor Sanitari Blvd, Bucharest, Romania, Mobile phone: +40 744 618 555, E-mail: raduciuluvica@yahoo.com

Abstract

Introduction: This study compares the outcomes and complications of hydroxyapatite ocular implant and non-integrated ocular implants following evisceration.

Materials and Methods: This is a retrospective study of 90 patients who underwent evisceration for different ocular affections, in the Ophthalmology Department of the University Emergency Hospital Bucharest, between January 2009 and December 2013. The outcomes measured were conjunctival dehiscence, socket infection, implant exposure and extrusion rate.

Results: Forty-three patients had the hydroxyapatite implant (coralline–Integrated Ocular Implants, USA or synthetic–FCI, France) and forty-seven received non-integrated ocular implants (24 acrylic and 23 silicone). Five cases of socket infection, thirteen cases of extrusion and two cases of conjunctival dehiscence were encountered.

Conclusions: There was a higher rate of conjunctival dehiscence with hydroxyapatite ocular implant, but implant extrusion and socket infection were found in non-integrated ocular implants.

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About this article

PMC ID: 4397530
PubMed ID: 25914747
DOI: 

Article Publishing Date (print): Jan-Mar 2015
Available Online: 

Journal information

ISSN Printing: 1844-122X
ISSN Online: 1844-3117
Journal Title: Journal of Medicine and Life

Copyright License: Open Access

This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use and redistribution provided that the original author and source are credited.


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