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2.
Clin Exp Ophthalmol ; 31(5): 376-91, 2003 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-14516424

RESUMO

Age-related macular degeneration (AMD) is the leading cause of legal blindness in individuals 50 years and older in the developed world. Choroidal neovascularization (CNV) in exudative AMD is responsible for the majority of severe vision loss. Until recently, laser photocoagulation was the only well-established and widely accepted treatment for CNV. However, it is beneficial only for a small subset of patients, has a high rate of CNV persistence and recurrence and results in iatrogenic, collateral damage to the overlying retina. These issues make it difficult to recommend in the case of subfoveal lesions. Consequently, numerous experimental therapeutic interventions are under investigation with the common objective of destroying the CNV but leaving the foveal neurosensory retina intact. Treatment modalities can be grouped into five major categories: photodynamic therapy; radiotherapy; transpupillary thermotherapy; anti-angiogenic and angiostatic agents; and surgical intervention. The present review aims to explain the rationale behind these new treatments, analyse the evidence for their safety and efficacy, determine their stage of development and indicate in which patients they are potentially useful.


Assuntos
Degeneração Macular/terapia , Inibidores da Angiogênese/uso terapêutico , Neovascularização de Coroide/cirurgia , Humanos , Hipertermia Induzida , Degeneração Macular/tratamento farmacológico , Degeneração Macular/radioterapia , Degeneração Macular/cirurgia , Fotoquimioterapia , Epitélio Pigmentado Ocular/transplante , Retina/cirurgia , Hemorragia Retiniana/cirurgia , Esteroides/uso terapêutico
3.
Am J Ophthalmol ; 96(1): 33-42, 1983 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-6869478

RESUMO

Fluorouracil effectively inhibits epiretinal membrane formation and traction retinal detachment after vitrectomy surgery. When 0.5 mg of fluorouracil was administered intraocularly every 24 hours for seven days, traction retinal detachment two weeks after the intraocular injection of 200,000 cultured retinal pigment epithelial cells occurred in 12 of 12 control eyes but in only six of 14 eyes treated with fluorouracil (P less than .001). Four weeks after cell injection, eight of 12 eyes treated with fluorouracil had traction retinal detachments whereas 12 of 12 control eyes did (P less than .001). The height of the traction retinal detachment four weeks after intraocular injection of 200,000 cultured retinal pigment epithelial cells was reduced 50% in eyes treated with 0.5 mg of fluorouracil every 24 hours for seven days compared to control eyes (P less than .001). When the number of injected retinal pigment epithelial cells was increased to 400,000 cells and 1.25 mg of fluorouracil was administered intraocularly every 24 hours for seven days, traction retinal detachment two weeks after injection occurred in 15 of 15 eyes in the control group but in none of ten eyes in the treated group. Four weeks after cell injection, eight of eight eyes in the control group and five of five eyes in the fluorouracil-treated group had detachments and the mean height of the detachments in the two groups was equal. Autoradiography of the epiretinal membranes in eyes injected with 200,000 cultured retinal pigment epithelial cells and labeled for two hours with tritiated thymidine showed that 0.8% of the epiretinal cell nuclei were labeled two weeks after cell injection but that no labeled cells were present in the fluorouracil-treated eyes. Tritiated thymidine labeling of epiretinal cells in the fluorouracil-treated eyes was first noted three weeks after the cell injection. The presence of tritiated thymidine labeling in the fluorouracil-treated eyes correlated with an increase in the number of epiretinal cells and an increase in the incidence of traction retinal detachment.


Assuntos
Fluoruracila/administração & dosagem , Cuidados Pós-Operatórios/métodos , Doenças Retinianas/terapia , Corpo Vítreo/cirurgia , Animais , Autorradiografia , Células Cultivadas , Modelos Animais de Doenças , Avaliação Pré-Clínica de Medicamentos , Oftalmopatias/patologia , Oftalmopatias/terapia , Microscopia Eletrônica , Epitélio Pigmentado Ocular/transplante , Epitélio Pigmentado Ocular/ultraestrutura , Coelhos , Descolamento Retiniano/prevenção & controle , Doenças Retinianas/patologia , Fatores de Tempo
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