Initial outcomes following intravitreal ocriplasmin for treatment of symptomatic vitreomacular adhesion

Copyright 2013, SLACK Incorporated.

Détails bibliographiques
Publié dans:Ophthalmic surgery, lasers & imaging retina. - 2013. - 44(2013), 4 vom: 12. Juli, Seite 334-43
Auteur principal: Kim, Brian T (Auteur)
Autres auteurs: Schwartz, Stephen G, Smiddy, William E, Doshi, Rishi R, Kovach, Jaclyn L, Berrocal, Audina M, Moshfeghi, Andrew A, Fortun, Jorge A
Format: Article en ligne
Langue:English
Publié: 2013
Accès à la collection:Ophthalmic surgery, lasers & imaging retina
Sujets:Journal Article Fibrinolytic Agents Peptide Fragments microplasmin 7V6HE3DM5A Fibrinolysin EC 3.4.21.7
Description
Résumé:Copyright 2013, SLACK Incorporated.
BACKGROUND AND OBJECTIVE: When delivered via a single intravitreal injection, ocriplasmin can effect proteolytic resolution of symptomatic vitreomacular adhesion (VMA). The authors describe their initial clinical experience with ocriplasmin at a large academic center
PATIENTS AND METHODS: Retrospective review of all patients with symptomatic VMA treated with ocriplasmin from January 2013 through May 2013 at a single center
RESULTS: Nineteen patients with symptomatic VMA received intravitreal ocriplasmin. Eight patients (42%) exhibited resolution of VMA. Macular holes in three of six patients (50%) closed after injection. A higher proportion of VMA resolution was observed in patients with the following baseline characteristics: age less than 65 years, focal adhesions less than or equal to 1,500 μm, presence of macular hole, phakic status, and absence of epiretinal membrane
CONCLUSION: Initial clinical outcomes using ocriplasmin in this study are consistent with those reported in the phase 3 clinical trials. Improved clinical results can be achieved with careful case selection based on specific baseline characteristics
Description:Date Completed 06.02.2014
Date Revised 25.11.2016
published: Print
CommentIn: Ophthalmic Surg Lasers Imaging Retina. 2013 Jul-Aug;44(4):319. doi: 10.3928/23258160-20130715-01. - PMID 23883265
Citation Status MEDLINE
ISSN:2325-8179
DOI:10.3928/23258160-20130715-05