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1.
Br J Ophthalmol ; 88(11): 1380-6, 2004 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-15489477

RESUMO

AIM: To evaluate the efficacy of periocular triamcinolone acetonide for the treatment of thyroid associated ophthalmopathy (TAO), and the presence of ocular or systemic adverse effects. METHODS: A multicentre prospective pilot study was performed on patients diagnosed with Graves' ophthalmopathy less than 6 months before entry to the study. Patients were admitted to the study and were randomised into two groups: treatment and control. The treatment group received four doses of 20 mg of triamcinolone acetate 40 mg/ml in a peribulbar injection to the inferolateral orbital quadrant. Both groups were evaluated by measuring the area of binocular vision without diplopia on a Goldmann perimeter and the size of the extraocular muscles on computed tomography (CT) scans. Ophthalmological and systemic examinations were done to rule out ocular and systemic adverse effects. Follow up was 6 months for both groups. RESULTS: 50 patients were eligible for the study. 41 patients completed the study. There was an increase in the area of binocular vision without diplopia in the treatment group (Sigma initial: mean 231.1 (SD 99.9) and final absolute change, mean 107.1 (SD 129.0)) compared to the control group (Sigma initial: mean 350.7 (SD 86.5) and final absolute change, mean -4.5 (SD 67.6)). The sizes of the extraocular muscles were reduced in the treatment group (mean (inferior rectus initial values): 1.3 (0.7), final percentage change: -13.2 (25.7), medial rectus initial values: 1.2 (0.6), final percentage change: -8.2 (20.7), superior rectus-levator palpebrae initial values: 1.2 (0.6), final percentage change: -9.5 (29.1), lateral rectus initial values: 1.0 (0.4), final percentage change: -11.5 (20.6)) compared to the control group (inferior rectus initial values: 0.9 (0.3), final percentage change: -4.0 (21.5), medial rectus initial values: 0.9 (0.3), final percentage change: 0.6 (22.4), superior rectus-levator palpebrae initial values: 0.9 (0.3), final percentage change: 12.5 (37.5), lateral rectus initial values: 0.9 (0.4), final percentage change: -0.5 (31.6)). Both measurements (degree of diplopia and muscle thickness) were statistically significant between groups (initial - final). No systemic or ocular adverse effects were found. CONCLUSIONS: Triamcinolone administered as a periocular injection is effective in reducing diplopia and the sizes of extraocular muscles in TAO ophthalmopathy of recent onset. This form of treatment is not associated with systemic or ocular side effects.


Assuntos
Anti-Inflamatórios/administração & dosagem , Glucocorticoides/administração & dosagem , Doença de Graves/tratamento farmacológico , Triancinolona Acetonida/administração & dosagem , Adulto , Idoso , Anti-Inflamatórios/efeitos adversos , Diplopia/prevenção & controle , Movimentos Oculares , Feminino , Glucocorticoides/efeitos adversos , Doença de Graves/patologia , Doença de Graves/fisiopatologia , Humanos , Injeções/métodos , Masculino , Pessoa de Meia-Idade , Projetos Piloto , Estudos Prospectivos , Tomografia Computadorizada por Raios X , Resultado do Tratamento , Triancinolona Acetonida/efeitos adversos , Visão Binocular/fisiologia
2.
J Pediatr (Rio J) ; 77(4): 327-30, 2001.
Artigo em Português | MEDLINE | ID: mdl-14647866

RESUMO

OBJECTIVE: To compare standard color vision test results (Ishihara test) with a new test developed by the authors ("crayon" test) for the detection of congenital dyschromatopsia. METHODS: Cross-sectional study of 712 children from three public schools and one private school in the city of Porto Alegre, state of Rio Grande do Sul. Children with learning disabilities, or systemic and ocular diseases were excluded from this random sample. Two color vision tests, Ishihara test (short version with 14 plates) and crayon test (developed by the authors) were sequentially applied. Each test was applied by different evaluators and analyzed by a third evaluator. RESULTS: The crayon test showed a specificity of 100% (99.3-100%) and sensitivity of 38.5% (15.1-67.7%) when compared to Ishihara test. The prevalence of congenital dyschromatopsia in this population sample was 2.6% for male children, and 0.9% for female children. CONCLUSIONS: The crayon test results showed greater specificity than Ishihara test in the studied group; however, sensitivity was not adequate for a screening test. It is necessary to improve the sensitivity so that congenital dyschromatopsia can be detected by the crayon test.

3.
Surv Ophthalmol ; 42(6): 571-6, 1998.
Artigo em Inglês | MEDLINE | ID: mdl-9635905

RESUMO

Divergence paralysis is a rare clinical entity that causes a comitant esotropia at distance. While this is usually benign and self-limited, there are reports of divergence paralysis associated with brain tumors, central nervous system syphilis, trauma, and multiple sclerosis. We studied a 14-year-old girl who presented with diplopia and was found to have divergence paralysis. Magnetic resonance imaging disclosed a large pontomedullary glioma.


Assuntos
Neoplasias Encefálicas/complicações , Esotropia/etiologia , Glioma/complicações , Doenças do Nervo Oculomotor/etiologia , Doença Aguda , Adolescente , Biópsia , Neoplasias Encefálicas/diagnóstico , Neoplasias Encefálicas/terapia , Terapia Combinada , Diplopia/diagnóstico , Diplopia/etiologia , Diplopia/terapia , Esotropia/diagnóstico , Esotropia/terapia , Feminino , Seguimentos , Glioma/diagnóstico , Glioma/terapia , Humanos , Imageamento por Ressonância Magnética , Bulbo/patologia , Doenças do Nervo Oculomotor/diagnóstico , Doenças do Nervo Oculomotor/terapia , Ponte/patologia
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