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Incomplete Vitreomacular Traction Release Using Intravitreal Ocriplasmin

PURPOSE: To report the clinical course of our first 7 consecutive patients treated with intravitreal ocriplasmin (Jetrea(®)). METHODS: Retrospective case series of the first 7 patients treated with ocriplasmin between January and December 2013 at an academic tertiary care center. RESULTS: The averag...

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Autores principales: Chin, Eric K., Almeida, David R.P., Sohn, Elliott H., Boldt, H. Culver, Mahajan, Vinit B., Gehrs, Karen M., Russell, Stephen R., Folk, James C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4296250/
https://www.ncbi.nlm.nih.gov/pubmed/25606039
http://dx.doi.org/10.1159/000370024
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author Chin, Eric K.
Almeida, David R.P.
Sohn, Elliott H.
Boldt, H. Culver
Mahajan, Vinit B.
Gehrs, Karen M.
Russell, Stephen R.
Folk, James C.
author_facet Chin, Eric K.
Almeida, David R.P.
Sohn, Elliott H.
Boldt, H. Culver
Mahajan, Vinit B.
Gehrs, Karen M.
Russell, Stephen R.
Folk, James C.
author_sort Chin, Eric K.
collection PubMed
description PURPOSE: To report the clinical course of our first 7 consecutive patients treated with intravitreal ocriplasmin (Jetrea(®)). METHODS: Retrospective case series of the first 7 patients treated with ocriplasmin between January and December 2013 at an academic tertiary care center. RESULTS: The average age was 78.4 years (range: 63–92). Five patients were pseudophakic and 2 patients were phakic in the injected eye. The median baseline visual acuity (VA) was 20/60 (range: 20/25 to 20/200). The median 1-month postinjection VA was 20/70, with a mean loss of 2 lines of VA among all patients. None of the patients had complete resolution of their vitreomacular traction or macular hole at 1 month of follow-up. Three patients had subsequent pars plana vitrectomy and membrane peeling surgery. The mean follow-up period for those who did not undergo vitrectomy was 9 months (range: 1–13). One patient with known ocular hypertension had an increase in intraocular pressure requiring topical pressure-lowering eyedrops. There were no cases of postinjection uveitis, endophthalmitis, retinal tears, or retinal detachment. CONCLUSIONS: While ocriplasmin may be a viable pharmacological agent for vitreolysis, we present a series of patients that all had incomplete resolution of vitreomacular traction with and without full-thickness macular hole. There was an associated reduction in VA after ocriplasmin treatment at 1 month of follow-up. Careful analysis of the vitreoretinal interface and comorbid eye conditions is required to optimize outcome success with ocriplasmin.
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spelling pubmed-42962502015-01-20 Incomplete Vitreomacular Traction Release Using Intravitreal Ocriplasmin Chin, Eric K. Almeida, David R.P. Sohn, Elliott H. Boldt, H. Culver Mahajan, Vinit B. Gehrs, Karen M. Russell, Stephen R. Folk, James C. Case Rep Ophthalmol Published online: December, 2014 PURPOSE: To report the clinical course of our first 7 consecutive patients treated with intravitreal ocriplasmin (Jetrea(®)). METHODS: Retrospective case series of the first 7 patients treated with ocriplasmin between January and December 2013 at an academic tertiary care center. RESULTS: The average age was 78.4 years (range: 63–92). Five patients were pseudophakic and 2 patients were phakic in the injected eye. The median baseline visual acuity (VA) was 20/60 (range: 20/25 to 20/200). The median 1-month postinjection VA was 20/70, with a mean loss of 2 lines of VA among all patients. None of the patients had complete resolution of their vitreomacular traction or macular hole at 1 month of follow-up. Three patients had subsequent pars plana vitrectomy and membrane peeling surgery. The mean follow-up period for those who did not undergo vitrectomy was 9 months (range: 1–13). One patient with known ocular hypertension had an increase in intraocular pressure requiring topical pressure-lowering eyedrops. There were no cases of postinjection uveitis, endophthalmitis, retinal tears, or retinal detachment. CONCLUSIONS: While ocriplasmin may be a viable pharmacological agent for vitreolysis, we present a series of patients that all had incomplete resolution of vitreomacular traction with and without full-thickness macular hole. There was an associated reduction in VA after ocriplasmin treatment at 1 month of follow-up. Careful analysis of the vitreoretinal interface and comorbid eye conditions is required to optimize outcome success with ocriplasmin. S. Karger AG 2014-12-12 /pmc/articles/PMC4296250/ /pubmed/25606039 http://dx.doi.org/10.1159/000370024 Text en Copyright © 2014 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article licensed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported license (CC BY-NC) (www.karger.com/OA-license), applicable to the online version of the article only. Users may download, print and share this work on the Internet for noncommercial purposes only, provided the original work is properly cited, and a link to the original work on http://www.karger.com and the terms of this license are included in any shared versions.
spellingShingle Published online: December, 2014
Chin, Eric K.
Almeida, David R.P.
Sohn, Elliott H.
Boldt, H. Culver
Mahajan, Vinit B.
Gehrs, Karen M.
Russell, Stephen R.
Folk, James C.
Incomplete Vitreomacular Traction Release Using Intravitreal Ocriplasmin
title Incomplete Vitreomacular Traction Release Using Intravitreal Ocriplasmin
title_full Incomplete Vitreomacular Traction Release Using Intravitreal Ocriplasmin
title_fullStr Incomplete Vitreomacular Traction Release Using Intravitreal Ocriplasmin
title_full_unstemmed Incomplete Vitreomacular Traction Release Using Intravitreal Ocriplasmin
title_short Incomplete Vitreomacular Traction Release Using Intravitreal Ocriplasmin
title_sort incomplete vitreomacular traction release using intravitreal ocriplasmin
topic Published online: December, 2014
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4296250/
https://www.ncbi.nlm.nih.gov/pubmed/25606039
http://dx.doi.org/10.1159/000370024
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