Treatment of retinal pigment epithelial detachment with antiangiogenic therapy
| dc.contributor.author | Arias Barquet, Lluís | |
| dc.date.accessioned | 2021-02-04T15:56:25Z | |
| dc.date.available | 2021-02-04T15:56:25Z | |
| dc.date.issued | 2010-04-26 | |
| dc.date.updated | 2021-02-04T15:56:25Z | |
| dc.description.abstract | Purpose: 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.extent | 6 p. | |
| dc.format.mimetype | application/pdf | |
| dc.identifier.idgrec | 706664 | |
| dc.identifier.issn | 1177-5467 | |
| dc.identifier.pmid | 20463807 | |
| dc.identifier.uri | https://hdl.handle.net/2445/173679 | |
| dc.language.iso | eng | |
| dc.publisher | Dove Medical Press | |
| dc.relation.isformatof | Reproducció del document publicat a: https://doi.org/10.2147/OPTH.S9307 | |
| dc.relation.ispartof | Clinical Ophthalmology, 2010, vol. 26, num. 4, p. 369-374 | |
| dc.relation.uri | https://doi.org/10.2147/OPTH.S9307 | |
| dc.rights | cc-by-nc (c) Arias Barquet, Lluís, 2010 | |
| dc.rights.accessRights | info:eu-repo/semantics/openAccess | |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc/3.0/es | |
| dc.source | Articles publicats en revistes (Ciències Clíniques) | |
| dc.subject.classification | Malalties de la retina | |
| dc.subject.classification | Angiogènesi | |
| dc.subject.classification | Degeneració (Patologia) | |
| dc.subject.other | Retinal diseases | |
| dc.subject.other | Neovascularization | |
| dc.subject.other | Degeneration (Pathology) | |
| dc.title | Treatment of retinal pigment epithelial detachment with antiangiogenic therapy | |
| dc.type | info:eu-repo/semantics/article | |
| dc.type | info:eu-repo/semantics/publishedVersion |
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