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Treatment of retinal pigment epithelial detachment with antiangiogenic therapy

dc.contributor.authorArias Barquet, Lluís
dc.date.accessioned2021-02-04T15:56:25Z
dc.date.available2021-02-04T15:56:25Z
dc.date.issued2010-04-26
dc.date.updated2021-02-04T15:56:25Z
dc.description.abstractPurpose: evaluate the efficacy of pegaptanib, a selective anti-vascular endothelial growth factor (VEGF) agent, and bevacizumab, a nonselective anti-VEGF agent, for retinal pigment epithelial detachment (PED) associated with occult choroidal neovascularization (CNV) secondary to age-related macular degeneration (AMD). Methods: prospective, comparative, nonrandomized pilot study included patients with PED comprising >50% of total lesion in subfoveal location with visual acuity (VA) 20/40-20/400 and lesions either previously untreated or treated only with photodynamic therapy/verteporfin. Seven patients received pegaptanib 0.3 mg intravitreally (IVT); eight received IVT bevacizumab 1.25 mg. Follow-up occurred every 4-6 weeks for 6 months. Reinjection of initial medication occurred if there was intra- or subretinal fluid observed by optical coherence tomography (OCT) or increased PED. Endpoints were mean changes from baseline to month 6 in VA (ETDRS) and foveal thickness. Results: at baseline, mean VA was lower, and mean foveal thickness was greater in pegaptanib versus bevacizumab-treated patients (36.1 vs 49.5 letters; 470.4 vs 321.1 mum). Mean improvements to month 6 in VA and foveal thickness were greater for pegaptanib (VA: +9.1 vs +7.2 letters; foveal thickness: -88.2 vs -52.9 mum). On average, pegaptanib-treated patients had slower but more sustained improvement in VA and foveal thickness; bevacizumab-treated patients showed rapid improvement with a slow return towards baseline. Both agents were well tolerated. Conclusion: intravitreal injections of pegaptanib or bevacizumab are both efficacious and safe treatments for PED associated with occult CNV secondary to AMD.
dc.format.extent6 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec706664
dc.identifier.issn1177-5467
dc.identifier.pmid20463807
dc.identifier.urihttps://hdl.handle.net/2445/173679
dc.language.isoeng
dc.publisherDove Medical Press
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.2147/OPTH.S9307
dc.relation.ispartofClinical Ophthalmology, 2010, vol. 26, num. 4, p. 369-374
dc.relation.urihttps://doi.org/10.2147/OPTH.S9307
dc.rightscc-by-nc (c) Arias Barquet, Lluís, 2010
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/es
dc.sourceArticles publicats en revistes (Ciències Clíniques)
dc.subject.classificationMalalties de la retina
dc.subject.classificationAngiogènesi
dc.subject.classificationDegeneració (Patologia)
dc.subject.otherRetinal diseases
dc.subject.otherNeovascularization
dc.subject.otherDegeneration (Pathology)
dc.titleTreatment of retinal pigment epithelial detachment with antiangiogenic therapy
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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