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1.
Arq. bras. oftalmol ; 82(1): 12-17, Jan.-Feb. 2019. tab, graf
Artículo en Inglés | LILACS | ID: biblio-973876

RESUMEN

ABSTRACT Purpose: To investigate the frequency of toxic retinopathy in patients with lupus erythematosus and rheumatoid arthritis with long-term use of chloroquine diphosphate or hydroxychloroquine through spectral domain optical coherence tomography and the outcomes of ophthalmological exams (visual acuity - Snellen's table, color vision test - Ishihara's table, fundoscopy, and retinography - red-free). Methods: A cross-sectional study was carried out involving the ophthalmologic evaluation of patients using regular chloroquine diphosphate or hydroxychloroquine for a period of 1 year or longer. The patients completed a questionnaire on their opinions and treatment regularity. The same patients underwent ophthalmologic examination and spectral domain optical coherence tomography. Results: The prevalence of toxic retinopathy caused by antimalarials was 4.15% (9 of 217 patients), 7.4% (4 of 54 patients) following chloroquine diphosphate usage, and 0.82% (1 of 121 patients) following hydroxychloroquine usage. Only patients with advanced stage maculopathy presented abnormalities during the ophthalmologic exam: the color vision test was altered in 11.1%, and visual acuity and fundoscopy were altered in 33.3%. Identification of early toxic retinopathy, detected in six patients, was possible using spectral domain optical coherence tomography. The mean duration of antimalarial drug usage among patients with toxic retinopathy was 10.4 years. Only 31% of the patients reported some symptoms during treatment, and although 24% were afraid to use the medication, they did so as prescribed. Conclusion: Use of spectral domain optical coherence tomography was essential for the diagnosis of early-stage antimalarial toxic retinopathy in patients with the following characteristics: asymptomatic, antimalarial use 7 days a week for a period of more than 5 years, and normal clinical ophthalmologic examination.


RESUMO Objetivo: Investigar a frequência da retinopatia tóxica em pacientes com lúpus eritematoso e artrite reumatóide com uso crônico de difosfato de cloroquina ou hidroxicloroquina, através de tomografia de coerência óptica de domínio espectral e os resultados dos exames oftalmológicos (acuidade visual - tabela de Snellen, teste de visão de cor - tabela de Ishihara, fundoscopia e retinografia - red free). Métodos: Foi realizado um estudo transversal envolvendo a avaliação oftalmológica de pacientes em uso regular de difosfato de cloroquina ou hidroxicloroquina por um período de um ano ou mais. Os pacientes responderam a um questionário sobre a sua opinião e regularidade do tratamento. Os mesmos pacientes realizaram exame oftalmológico clínico e tomografia de coerência óptica de domínio espectral. Resultados: A prevalência de retinopatia tóxica por antimaláricos foi de 4,15% (9 dos 217 pacientes), 7,4% (4 de 54 pacientes) após uso de difosfato de cloroquina e 0,82% (1 de 121 pacientes) após uso de hidroxicloroquina. Apenas os pacientes com maculopatia em fase avançada apresentaram alterações durante os exames clínicos: teste de visão de cores alterado em 11,1%, e a acuidade visual e fundoscopia foram alteradas em 33,3%. A identificação de retinopatia tóxica precoce, detectada em seis pacientes, foi possível por meio da tomografia de coerência óptica de domínio espectral. A duração média do tempo de uso de drogas antimaláricas entre os pacientes com retinopatia tóxica foi de 10,4 anos. Apenas 31% dos pacientes relataram algum sintoma durante o tratamento e apesar de 24% terem medo de usar a medicação, eles o fizeram conforme prescrito. Conclusão: O uso da tomografia de coerência óptica de domínio espectral foi essencial para o diagnóstico de retinopatia tóxica antimalárica em estágio inicial em pacientes com as seguintes características: uso assintomático, antimalárico 7 dias por semana por um período maior que cinco anos e exame oftalmológico clínico normal.


Asunto(s)
Humanos , Femenino , Adulto , Persona de Mediana Edad , Enfermedades de la Retina/inducido químicamente , Enfermedades de la Retina/diagnóstico por imagen , Cloroquina/análogos & derivados , Tomografía de Coherencia Óptica/métodos , Hidroxicloroquina/efectos adversos , Antimaláricos/efectos adversos , Artritis Reumatoide/tratamiento farmacológico , Enfermedades de la Retina/epidemiología , Brasil/epidemiología , Agudeza Visual , Cloroquina/efectos adversos , Prevalencia , Estudios Transversales , Factores de Riesgo , Antirreumáticos/efectos adversos , Lupus Eritematoso Sistémico/tratamiento farmacológico
2.
Rev. bras. oftalmol ; 77(5): 261-263, set.-out. 2018. graf
Artículo en Inglés | LILACS | ID: biblio-977873

RESUMEN

Abstract Hydroxychloroquine is widely used by rheumatologists for the treatment of various diseases, such as systemic lupus erythematosus and rheumatoid arthritis because of its safety and low cost. However, it can cause retinal abnormalities. Until today, there is no Brazilian protocol for screening for retinal changes in these patients. We reviewed the medical records and optical coherence tomography of all patients who had attended at Hychloroquine Ambulatory of HFSE, in the period from March/ 2015 until November/2016.


Resumo A Hidroxicloroquina é amplamente utilizada por reumatologistas para o tratamento de várias condições, como os lúpus eritematoso sistêmico e artrite reumatoide, pelo seu baixo custo e relativa segurança. Porém, esta droga pode causar danos à retina. Até o presente momento, não há protocolo brasileiro para o screening de alterações retinianas devido ao uso desta medicação. Foi realizada revisão de prontuário e análise de imagens de tomografia de coerência óptica de pacientes atendidos no período de Março de 2015 a Novembro de 2016 no ambulatório de Hidroxicloroquina do Hospital Federal dos Servidores do Estado do Rio de Janeiro.


Asunto(s)
Humanos , Masculino , Femenino , Adulto , Persona de Mediana Edad , Anciano , Anciano de 80 o más Años , Enfermedades de la Retina/inducido químicamente , Enfermedades Reumáticas/tratamiento farmacológico , Antirreumáticos/efectos adversos , Hidroxicloroquina/efectos adversos , Retina/efectos de los fármacos , Enfermedades de la Retina/diagnóstico por imagen , Registros Médicos , Estudios Transversales , Tomografía de Coherencia Óptica
3.
Rev. panam. salud pública ; 36(6): 396-401, dic. 2014. tab
Artículo en Inglés | LILACS | ID: lil-742269

RESUMEN

This study describes the adverse drug reactions (ADRs) and their incidence in patients with rheumatoid arthritis who were treated in the Colombian health system. A retrospective cohort study was conducted using information from all patients who were diagnosed with rheumatoid arthritis and attended specialized health care centers in the cities of Bogotá, Cali, Manizales, Medellin, and Pereira between 1 December 2009 and 30 August 2013. The ADRs were obtained from medical records and the pharmacovigilance system registry and sorted by frequency and affected tissue according to World Health Organization Adverse Reaction Terminology (WHO-ART). A total of 949 reports of ADRs were obtained from 419 patients (32.8 ADRs per 100 patient-years); these patients were from a cohort of 1 364 patients being treated for rheumatoid arthritis and followed up for an average of 23.8 months (± 12.9). The cohort was mostly female (366, 87.4%) and had a mean age of 52.7 years (± 13.1). The highest numbers of ADRs were reported following the use of tocilizumab, rituximab, and infliximab (28.8, 23.1, and 13.3 reports per 100 patient-years respectively). The most frequently reported ADRs were elevated transaminase levels and dyspepsia. Overall, 87.7% of ADRs were classified as type A, 36.6% as mild, 40.7% as moderate, and 22.7% as severe. As a result, 73.2% of patients who experienced an ADR stopped taking their drugs. The occurrence of ADRs in patients treated for rheumatoid arthritis is common, especially in those associated with the use of biotechnologically produced anti-rheumatic drugs. This outcome should be studied in future research and monitoring is needed to reduce the risks in these patients.


Este estudio describe las reacciones adversas a medicamentos (RAM) y su incidencia en pacientes con artritis reumatoide y tratados en el sistema de salud colombiano. Se llevó a cabo un estudio retrospectivo de cohortes utilizando la información correspondiente a todos los pacientes con diagnóstico de artritis reumatoide que acudieron a centros especializados de atención de salud de las ciudades de Bogotá, Cali, Manizales, Medellín y Pereira entre el 1 de diciembre del 2009 y el 30 de agosto del 2013. Los casos de RAM se obtuvieron de las historias clínicas y del registro del sistema de farmacovigilancia, y se clasificaron por su frecuencia y el tejido afectado, según la Terminología de Reacciones Adversas de la Organización Mundial de la Salud ­ (WHO-ART). Se obtuvo un total de 949 informes de RAM en 419 pacientes (32,8 RAM por 100 pacientes-año); estos pacientes correspondían a una cohorte de 1 364 pacientes tratados por artritis reumatoide y seguidos durante un promedio de 23,8 meses (± 12,9). La cohorte estaba compuesta principalmente por mujeres (366, 87,4%) y la media de edad era de 52,7 años (± 13,1). El mayor número de casos de RAM se notificó tras el uso de tocilizumab, rituximab e infliximab (28,8, 23,1 y 13,3 notificaciones por 100 pacientes-año, respectivamente). Las RAM notificadas con mayor frecuencia fueron la elevación de los niveles de transaminasas y la dispepsia. En términos generales, 87,7% de las RAM se clasificaron como de tipo A, 36,6% como leves, 40,7% como moderadas y 22,7% como graves. Como consecuencia, 73,2% de los pacientes que presentaron una RAM dejaron de tomar sus medicamentos. La aparición de RAM en pacientes tratados por artritis reumatoide es frecuente, especialmente cuando se utilizan fármacos antirreumáticos de producción biotecnológica. Estos resultados deben ser objeto de estudio en futuras investigaciones y señalan la necesidad de actividades de vigilancia para reducir los riesgos en estos pacientes.


Asunto(s)
Humanos , Masculino , Femenino , Preescolar , Niño , Adolescente , Adulto , Persona de Mediana Edad , Anciano , Anciano de 80 o más Años , Adulto Joven , Antirreumáticos/efectos adversos , Artritis Reumatoide/tratamiento farmacológico , Antirreumáticos/uso terapéutico , Productos Biológicos/efectos adversos , Productos Biológicos/uso terapéutico , Biosimilares Farmacéuticos/efectos adversos , Biosimilares Farmacéuticos/uso terapéutico , Colombia/epidemiología , Erupciones por Medicamentos/epidemiología , Erupciones por Medicamentos/etiología , Enfermedad Hepática Inducida por Sustancias y Drogas/epidemiología , Enfermedad Hepática Inducida por Sustancias y Drogas/etiología , Estudios de Seguimiento , Enfermedades Gastrointestinales/inducido químicamente , Enfermedades Gastrointestinales/epidemiología , Enfermedades Hematológicas/inducido químicamente , Enfermedades Hematológicas/epidemiología , Farmacovigilancia , Enfermedades de la Retina/inducido químicamente , Enfermedades de la Retina/epidemiología , Estudios Retrospectivos
4.
Arq. bras. oftalmol ; 77(5): 321-323, Sep-Oct/2014. graf
Artículo en Inglés | LILACS | ID: lil-730378

RESUMEN

We present the unusual case of a 35 year-old woman with stage IV melanoma and widespread metastases, who was undergoing treatment with interferon alpha-2b and who presented with interferon-associated retinopathy. The patient, who had been taking interferon treatment for three months, complained of a sudden loss of visual acuity in the left eye. An ocular examination revealed multiple cotton wool spots along the retina and macular involvement. Interferon treatment was suspended. Although rare, retinopathy represents a potentially serious adverse effect of interferon treatment. Although normally patients are asymptomatic, complications derived of its use may arise, which can lead to significant visual impairment. We therefore suggest that before initiating treatment with this drug, patients should be informed of its potential ocular risks, and that regular eye examinations are conducted along with the treatment.


Apresentamos o caso de uma mulher de 35 anos com melanoma em estágio IV e metástases generalizadas tratados com interferon alpha-2b, que proporcionou uma retinopatia associada ao interferon. Mulher de 35 anos de idade tratados com interferon durante os últimos três meses apresentou uma perda súbita da acuidade visual no olho esquerdo. Exame ocular revelou vários pontos de algodão ao longo da retina e mácula. Tratamento com interferon foi parado. Retinopatia associada ao uso de interferon está entre os possíveis efeitos colaterais, embora rara, não deve ser subestimada. Embora geralmente assintomática, complicações decorrentes de seu uso podem levar à perda visual significativa. Consideramos, portanto, que antes de iniciar o tratamento com este medicamento, os pacientes devem ser informados sobre os riscos potenciais e os exames oftalmológicos são recomendados durante cada tratamento.


Asunto(s)
Humanos , Enfermedades de la Retina/inducido químicamente , Interferón-alfa/efectos adversos , Interferón-alfa/uso terapéutico , Melanoma/secundario
5.
Rev. bras. oftalmol ; 73(3): 135-137, May-Jun/2014. graf
Artículo en Inglés | LILACS | ID: lil-727179

RESUMEN

Purpose: Register and compare anatomical changes, structural and quantitative found in optical coherence tomography Stratus and Topcon 3D in chronic users of chloroquine. Methods: Five patients were diagnosed with toxic "bull's eye" maculopathy was submitted to macular optical coherence tomography examination (Stratus and Topcon 3D). Results: Both tools demonstrated an increase reflectivity of choriocapillaris unit just foveal retinal pigment epithelium atrophy. However, Topcon 3D provided to all patients better description of the line corresponding to the transition between inner and outer segments of photoreceptors. Using the possibility of assembling threedimensional images and subtraction selective retinal layers, we found a lesion with a target that reflects the greater thickness of retinal pigment epithelium in central and parafoveal region that is matched to preserve macular photoreceptors. Conclusion: it was observed better resolution and faster image capture by Topcon 3D than Stratus OCT, that provided more detailed analysis of the line corresponding to transition between outer and inner segment of photoreceptors in macular region. With Topcon 3D, it was possible to evaluate soundly the thickness of retinal pigment epithelium in central and parafoveal region that caused an increase reflectivity of choriocapillaris creating a image with a target unpublished before. .


Objetivo: Comparar e registrar as alterações quantitativas e qualitavivas na tomografia de coerência óptica nos pacientes com uso prolongado de cloroquina. Métodos: Avaliaram-se cinco pacientes com diagnóstico de bull’s eye no exame de tomografia de coerência óptica macular com dois modelos de aparelhos: Stratus e Topcon 3D. Resultados: Ambos aparelhos registraram aumento da refletividade coriocapilar foveal provocada pela atrofia do epitélio pigmentar da retina. Somente o Topcon 3D permitiu melhor visibilização da linha de transição entre o segmento interno e externo dos fotorreceptores. Este aparelho também permitiu a formação de imagens tridimensionais e subtração das camadas retinianas, com registro da diminuição da espessura do epitélio pigmentado da retina na região central e parafoveal macular. Conclusão: Foi possível observar a captação mais rápida e com melhor resolução das imagens geradas pelo Topcon 3D. A diminuição da espessura do epitélio pigmentado da retina, provocando o aumento da refletividade coriocapilar, com a formação de uma imagem linear circular cincundando a fóvea, foi mais detalhado pelos cortes realizados no Topcon 3D. .


Asunto(s)
Humanos , Enfermedades de la Retina/inducido químicamente , Enfermedades de la Retina/diagnóstico por imagen , Cloroquina/efectos adversos , Tomografía de Coherencia Óptica/métodos , Degeneración Macular/inducido químicamente , Degeneración Macular/diagnóstico por imagen , Retina/efectos de los fármacos , Retina/patología , Retina/diagnóstico por imagen , Cloroquina/administración & dosificación
6.
Arq. bras. oftalmol ; 77(3): 178-181, May-Jun/2014. tab, graf
Artículo en Inglés | LILACS | ID: lil-723838

RESUMEN

Purpose: To identify the effect of pegylated interferon α-2b and ribavirin treatment in the ocular fundus examination, visual acuity, and visual field. Methods: Prospective observational study was performed at the Hepatology Clinic of São José Regional Hospital and at the Vitreoretinal Department at the Sadalla Amin Ghanem Eye Hospital in patients with chronic hepatitis C before and during treatment with pegylated interferon α-2b together with ribavirin. Results: Six (37.5%) of 16 patients developed retinopathy during the treatment, two of which (12.5%) presented retinal hemorrhage, and four patients (6 eyes) presented cotton-wool spots (25%) that regressed during the treatment. One patient (6.25%) presented transient decrease in visual acuity during the treatment and recovered spontaneously without specific therapy. Conclusion: Recommended treatment methods for hepatitis C may cause transient retinopathy, commonly without any damage to visual function in most patients. Although ocular involvement is rare, follow-up with an ophthalmologist is recommended during the course of the hepatitis C medication. .


Objetivo: Identificar possíveis mudanças no exame de fundo de olho após o início do tratamento, bem como alterações na acuidade visual e campo visual. Métodos: Estudo observacional prospectivo realizado na Clínica de Hepatologia do Hospital Regional de São José e no Departamento de Vítreo e Retina do Hospital de Olhos Sadalla Amin Ghanem, em pacientes com hepatite C crônica antes e durante o tratamento com interferon peguilado α-2b associado à ribavirina. Resultados: Six (37,5%) dos 16 participantes desenvolveram retinopatia durante o tratamento, dois dos quais (12,5%) apresentaram hemorragia retiniana unilateral, e quatro pacientes com exsudatos algodonosos (25%), seis olhos, que regrediu durante o tratamento. Um participante (6,25%) apresentou diminuição transitória da acuidade visual durante o tratamento com recuperação espontaneamente sem tratamento específico. Conclusão: O tratamento recomendado para a hepatite C pode estar associado com o desenvolvimento de retinopatia transitória, geralmente sem dano à função visual na maioria dos pacientes. Embora o envolvimento ocular seja raro, o acompanhamento com o médico oftalmologista é recomendado durante todo o uso da medicação. .


Asunto(s)
Adulto , Femenino , Humanos , Masculino , Persona de Mediana Edad , Adulto Joven , Antivirales/efectos adversos , Fondo de Ojo , Hepatitis C Crónica/tratamiento farmacológico , Interferón-alfa/efectos adversos , Polietilenglicoles/efectos adversos , Enfermedades de la Retina/inducido químicamente , Ribavirina/efectos adversos , Angiografía con Fluoresceína , Estudios Prospectivos , Factores de Riesgo , Proteínas Recombinantes/efectos adversos , Factores de Tiempo , Resultado del Tratamiento , Agudeza Visual/efectos de los fármacos , Campos Visuales/efectos de los fármacos
7.
Korean Journal of Ophthalmology ; : 100-107, 2014.
Artículo en Inglés | WPRIM | ID: wpr-143093

RESUMEN

A 53-year-old Asian woman was treated with hydroxychloroquine and chloroquine for lupus erythematosus. Within a few years, she noticed circle-shaped shadows in her central vision. Upon examination, the patient's visual acuity was 20 / 25 in both eyes. Humphrey visual field (HVF) testing revealed a central visual defect, and fundoscopy showed a ring-shaped area of parafoveal retinal pigment epithelium depigmentation. Fundus autofluorescence imaging showed a hypofluorescent lesion consistent with bull's eye retinopathy. Adaptive optics scanning laser ophthalmoscope (AO-SLO) revealed patch cone mosaic lesions, in which cones were missing or lost. In addition, the remaining cones consisted of asymmetrical shapes and sizes that varied in brightness. Unlike previous studies employing deformable mirrors for wavefront aberration correction, our AO-SLO approach utilized dual liquid crystal on silicon spatial light modulators. Thus, by using AO-SLO, we were able to create a photographic montage consisting of high quality images. Disrupted cone AO-SLO images were matched with visual field test results and functional deficits were associated with a precise location on the montage, which allowed correlation of histological findings with functional changes determined by HVF. We also investigated whether adaptive optics imaging was more sensitive to anatomical changes compared with spectral-domain optical coherence tomography.


Asunto(s)
Femenino , Humanos , Persona de Mediana Edad , Cloroquina/efectos adversos , Diagnóstico Diferencial , Aumento de la Imagen/métodos , Lupus Eritematoso Sistémico/tratamiento farmacológico , Mácula Lútea/efectos de los fármacos , Oftalmoscopía/métodos , Enfermedades de la Retina/inducido químicamente
8.
Korean Journal of Ophthalmology ; : 100-107, 2014.
Artículo en Inglés | WPRIM | ID: wpr-143088

RESUMEN

A 53-year-old Asian woman was treated with hydroxychloroquine and chloroquine for lupus erythematosus. Within a few years, she noticed circle-shaped shadows in her central vision. Upon examination, the patient's visual acuity was 20 / 25 in both eyes. Humphrey visual field (HVF) testing revealed a central visual defect, and fundoscopy showed a ring-shaped area of parafoveal retinal pigment epithelium depigmentation. Fundus autofluorescence imaging showed a hypofluorescent lesion consistent with bull's eye retinopathy. Adaptive optics scanning laser ophthalmoscope (AO-SLO) revealed patch cone mosaic lesions, in which cones were missing or lost. In addition, the remaining cones consisted of asymmetrical shapes and sizes that varied in brightness. Unlike previous studies employing deformable mirrors for wavefront aberration correction, our AO-SLO approach utilized dual liquid crystal on silicon spatial light modulators. Thus, by using AO-SLO, we were able to create a photographic montage consisting of high quality images. Disrupted cone AO-SLO images were matched with visual field test results and functional deficits were associated with a precise location on the montage, which allowed correlation of histological findings with functional changes determined by HVF. We also investigated whether adaptive optics imaging was more sensitive to anatomical changes compared with spectral-domain optical coherence tomography.


Asunto(s)
Femenino , Humanos , Persona de Mediana Edad , Cloroquina/efectos adversos , Diagnóstico Diferencial , Aumento de la Imagen/métodos , Lupus Eritematoso Sistémico/tratamiento farmacológico , Mácula Lútea/efectos de los fármacos , Oftalmoscopía/métodos , Enfermedades de la Retina/inducido químicamente
9.
Rev. cuba. oftalmol ; 26(3): 536-541, sep.-dic. 2013.
Artículo en Español | LILACS | ID: lil-706682

RESUMEN

La cloroquina es un fármaco que puede producir disfunciones visuales, baja visión e incluso ceguera según la dosis. Una dosis acumulativa menor a 100 g de cloroquina, o una duración de tratamiento de menos de un año raramente se asocia con lesión retiniana. El riesgo de toxicidad aumenta cuando la dosis acumulativa excede los 300 g (250mg/día durante 3 años). Este medicamento es utilizado en el tratamiento de enfermedades autoinmunes. Se presenta una paciente de 44 años de edad, con antecedentes de artritis reumatoide hace 14 años para lo cual se indicó tratamiento con cloroquina (1 tableta 250 mg/diaria) desde el diagnóstico inicial, y presenta un diagnóstico de maculopatía por cloroquina hace 5 años, a consulta por presentar baja visión y solicitando una posibilidad de rehabilitación visual. Se realizó examen oftalmológico, estudios complementarios y se rehabilitó mediante el microperímetro MP1. Se concluye que la maculopatía por cloroquina es una de las causas de discapacidad visual y que la rehabilitación visual con microperimetría proporciona mejoría en varios parámetros visuales, mejorando la calidad visual del paciente


Chloroquine-induced toxic maculopathy and visual rehabilitation through the use of microperimeter MP1.Chrloroquine is a drug that may cause visual dysfunctions, low vision and even blindness depending on dose. An accumulative dose lower than 100 g of chloroquine or a length of treatment less than one year is rarely associated to retinal injure. The toxicity risk increases when the accumulative dose exceeds 300 g (250mg/day for 3 years). This drug is used in treating autoimmune diseases. Here is the case of a 44 years-old patient, with history of rheumatoid arthritis for 14 years. Chloroquine treatment was indicated (one 250 mg tablet daily) at the time of initial diagnosis. Five years ago, he was diagnosed with chloroquine-induced maculopathy when he went to the doctor's because of low vision and asked for possible visual rehabilitation. An ophthalmologic exam, some supplementary studies and rehabilitation through the microperimeter MP1 were all performed. It was concluded that chloroquine-maculopathy with microperimetry provides improvement of several visual parameters and better visual quality for the patient


Asunto(s)
Humanos , Adulto , Femenino , Baja Visión/rehabilitación , Cloroquina/efectos adversos , Enfermedades de la Retina/inducido químicamente
10.
MEAJO-Middle East African Journal of Ophthalmology. 2013; 20 (1): 89-91
en Inglés | IMEMR | ID: emr-146701

RESUMEN

Chloroquine retinopathy is a known complication of long-term use of chloroquine. This retinopathy can appear even after usage of chloroquine has stopped. The present case report describes the history and clinical features of chloroquine retinopathy developing a decade after discontinuing the drug


Asunto(s)
Humanos , Femenino , Electrorretinografía , Angiografía con Fluoresceína , Estudios de Seguimiento , Enfermedades de la Retina/inducido químicamente , Antirreumáticos/efectos adversos , Enfermedades de la Retina/diagnóstico , Tomografía de Coherencia Óptica
11.
Indian J Ophthalmol ; 2012 Jul-Aug; 60(4): 315-317
Artículo en Inglés | IMSEAR | ID: sea-144860

RESUMEN

A 29-year-old lady receiving repeated blood transfusions for β thalassemia since childhood, presented with rapidly deteriorating symptoms of night blindness and peripheral visual field loss. She was recently commenced on high-dose intravenous desferrioxamine for reducing the systemic iron overload. Clinical and investigative findings were consistent with desferrioxamine-related pigmentary retinopathy and optic neuropathy. Recovery was partial following cessation of desferrioxamine. This report highlights the ocular side-effects of desferrioxamine mesylate and the need to be vigilant in patients on high doses of desferrioxamine.


Asunto(s)
Adulto , Transfusión Sanguínea , Deferoxamina/toxicidad , Femenino , Humanos , Enfermedades de la Retina/inducido químicamente , Talasemia beta/terapia
12.
Korean Journal of Ophthalmology ; : 455-461, 2012.
Artículo en Inglés | WPRIM | ID: wpr-214933

RESUMEN

PURPOSE: We investigated whether oxygen-induced retinopathy (OIR) results in changes in the protein expression of neuronal and inducible nitric oxide synthases (nNOS and iNOS, respectively) in rat model of OIR. In addition, we evaluated whether treatment of rats with triamcinolone acetonide (TA) prevents this response. METHODS: To promote OIR, Sprague-Dawley rats were exposed to hyperoxia from postnatal day 2 (P2) to P14. They were then returned to normoxia after P15. TA was injected into the right vitreous of P15 rats, while saline was injected into the left vitreous. At P18 the expression of nNOS and iNOS was determined using Western blotting and immunostaining techniques in retinas obtained from control rats. RESULTS: In P18 OIR rats, the abundance of nNOS and iNOS protein was significantly increased compared with controls. These increases were not observed in the retinas of rats treated with TA. The change in expression of nNOS and iNOS were specific to parvalbumin and glial fibrillary acidic protein-positive cells. Treatment with TA prevented the increased expression of nNOS and iNOS in all samples. CONCLUSIONS: Hypoxia upregulates expression of nNOS and iNOS in OIR rat retinas, which is can be prevented by treatment with TA.


Asunto(s)
Animales , Femenino , Embarazo , Ratas , Animales Recién Nacidos , Hipoxia/metabolismo , Western Blotting , Modelos Animales de Enfermedad , Glucocorticoides/farmacología , Inmunohistoquímica , Neuronas/metabolismo , Óxido Nítrico Sintasa de Tipo II/biosíntesis , Oxígeno/toxicidad , Preñez , Ratas Sprague-Dawley , Retina/metabolismo , Enfermedades de la Retina/inducido químicamente , Triamcinolona Acetonida/farmacología
13.
Arq. bras. oftalmol ; 74(4): 306-310, jul.-ago. 2011. tab
Artículo en Inglés | LILACS | ID: lil-604185

RESUMEN

Interferons alpha and beta have been used worldwide for a few decades, altering the natural history of several severe diseases including hepatitis C, cancer and immune-mediated conditions such as multiple sclerosis. The adverse events profile of interferons is well established, but only isolated reports of ophthalmological complications of interferon therapy have been published. The objective of this study was to carry out a literature systematic review on the subject, bringing to light the need for careful ophthalmological monitoring of patients undergoing interferon treatment. Nearly 500 cases of ophthalmological complications related to interferon have been reported. The most frequent findings were soft exudates, hemorrhages and retina ischemia.


Os interferons alfa e beta têm sido usado em todo o mundo por algumas décadas, mudando a história natural de diversas doenças graves, como hepatite C, câncer e condições imunomediadas como a esclerose múltipla. O perfil de eventos adversos dos interferons está bem definido, porém apenas relatos isolados das complicações oftalmológicas do tratamento com interferon foram publicados. O objetivo do presente trabalho foi a realização de uma revisão sistemática da literatura sobre o tema, trazendo à luz a necessidade de cuidadosa monitorização oftalmológica dos pacientes em tratamento com interferon. Quase 500 casos de complicações oftalmológicas relacionadas ao uso de interferon foram relatados. Os achados mais frequentes foram exsudatos, hemorragias e isquemia de retina.


Asunto(s)
Humanos , Masculino , Femenino , Antineoplásicos/efectos adversos , Antivirales/efectos adversos , Interferón-alfa/efectos adversos , Interferón beta/efectos adversos , Enfermedades de la Retina/inducido químicamente
14.
Korean Journal of Ophthalmology ; : 42-47, 2011.
Artículo en Inglés | WPRIM | ID: wpr-121938

RESUMEN

PURPOSE: To identify altered patterns of retinal mRNA expression in a rat model of oxygen-induced retinopathy (OIR). METHODS: Sprague-Dawley rats from P2 to P14 were exposed to hyperoxia (80% oxygen) to induce OIR and then returned to normoxic conditions. Control rats were sustained in room air. Retinal gene expression between the rats of OIR and the controls was compared using cDNA microarray analysis. Reverse transcriptase polymerase chain reaction (RT-PCR) was used to verify the microarray results. RESULTS: Among a total of 12,731 cDNAs analyzed by mircroarray, 13 genes were strongly up- or down-regulated (>2-fold change over controls) in the OIR rats. We found a significant increase in expression of 10 genes (CaM-kinase II inhibitor; acidic nuclear phosphoprotein 32 family, member A; vascular endothelial growth factor; interferon alpha-inducible protein 27-like; similar to enthoprotin, epsin 4, clathrin interacting protein; nidogen [entactin]; tubulin, beta5; fibrillin-1; spectrin beta2; and stearoyl-coenzyme A desaturase 2) and a significant decrease in expression of 3 genes (myelin-associated oligodendrocytic basic protein, heat shock protein, and decorin) in OIR rats compared to controls. CONCLUSIONS: We confirmed changes in expressions of various retinal genes in a rat model of OIR by microarray and RT-PCR. This study should contribute to the understanding of genetic indicators associeated with OIR.


Asunto(s)
Animales , Ratas , Animales Recién Nacidos , Regulación hacia Abajo , Expresión Génica , Análisis por Micromatrices , Oxígeno , ARN Mensajero/metabolismo , Ratas Sprague-Dawley , Retina/metabolismo , Enfermedades de la Retina/inducido químicamente , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Regulación hacia Arriba
15.
Korean Journal of Ophthalmology ; : 69-71, 2011.
Artículo en Inglés | WPRIM | ID: wpr-121931

RESUMEN

A 63-year-old man with a history of liver transplantation presented to our clinic complaining of visual disturbance. He had been receiving tacrolimus (FK 506) for 30 months (6 mg/day for 2 years and 3 mg/day for 6 months); he reported that the visual disturbance began while taking tacrolimus. A full ophthalmologic examination and electrophysiologic and imaging studies were performed. The best corrected visual acuity was 0.1 in both eyes. There were no abnormal finding in the anterior segment, pupillary reflexes were normal and, there was no swelling in either optic disc. Although the foveal reflex was slightly decreased, fluorescein angiography revealed non-specific signs, with the exception of a window defect. A multifocal electro-retinogram revealed decreased amplitude of the central ring. A Swedish interactive threshold algorithm-standard 10-2 visual field test revealed a central scotoma. These findings suggest that tacrolimus may result in maculopathy. Therefore, careful ophthalmologic examination is necessary in the patients taking tacrolimus.


Asunto(s)
Humanos , Masculino , Persona de Mediana Edad , Electrorretinografía , Potenciales Evocados Visuales , Fondo de Ojo , Inmunosupresores/efectos adversos , Trasplante de Hígado , Mácula Lútea/efectos de los fármacos , Cuidados Posoperatorios , Tiempo de Reacción , Enfermedades de la Retina/inducido químicamente , Escotoma/inducido químicamente , Tacrolimus/efectos adversos , Tomografía de Coherencia Óptica
16.
Arq. bras. oftalmol ; 73(1): 28-32, Jan.-Feb. 2010. tab, ilus
Artículo en Portugués | LILACS | ID: lil-546044

RESUMEN

OBJETIVO: Analisar a camada de fibras nervosas nos usuários de cloroquina com a tomografia de coerência óptica (OCT). MÉTODOS: A espessura da camada de fibras nervosas foi mensurada pelo Stratus OCT® através do protocolo scan rápido da camada de fibras nervosas em 94 olhos de 48 pacientes usuários de cloroquina a pelo menos um ano e sem alteração macular aparente. A dose cumulativa e dose diária máxima (mg/kg/dia) e o tempo de uso da cloroquina foram correlacionadas com a espessura da camada de fibras nervosas. Os dados formam comparados com um grupo controle de 30 pacientes não usuários de cloroquina. Todos os pacientes foram submetidos a um exame oftalmológico completo incluindo medida da acuidade visual, refração, pressão intraocular, fundoscopia, retinografia e medida da escavação de papila. RESULTADOS: Comparação entre a média da espessura da camada de fibras nervosas entre usuários do antimalárico (107,60 ± 13,25 µm) e o grupo controle (99,05 ± 13,08 µm) teve uma associação estatisticamente significativa (p=0,0137). Também foi encontrada essa associação entre os quadrantes temporal, superior e inferior da camada de fibras nervosas peripapilar dos dois grupos. Ao analisar a camada de fibras nervosas através das 12 h do relógio detectou-se pelo menos um defeito focal em mais de 50 por cento dos usuários da medicação. Nos pacientes com o defeito focal foi observado uma relação com a dose diária máxima (p=0,0120). CONCLUSÃO: A tomografia de coerência óptica demonstrouse eficaz na detecção da diminuição da camada de fibras nervosas em usuários de cloroquina sem alterações fundoscópicas aparentes. Dessa forma, a tomografia de coerência óptica pode contribuir para o diagnóstico mais precoce da retinopatia por cloroquina.


PURPOSE: To evaluated the retinal nerve fiber layer in chloroquine patients with optical coherence tomography (OCT). METHODS: Nerve fibers layer thickness was measured by a proprietary OCT Stratus® through the fast retinal nerve fiber layer protocol in ninety-four eyes of 48 patients exposed to chloroquine for at least one year with no apparent macular disorder. Cumulative dose, maximum daily dose (mg/kg/day) and time of chloroquine use were correlated with the retinal nerve fiber layer thickness. Data were compared with a control group of 30 patients who did not use chloroquine. All patients underwent a complete ophthalmologic examination including visual acuity, refraction, intraocular pressure, fundoscopy, angiography and measurement of cup-to-disc ratio. RESULTS: The average thickness of retinal nerve fiber layer between antimalaric users (107.60 ± 13.25 µm) and the control group (99.05 ± 13.08 µm) had a statistically significant difference (p=0.0137). Furthermore, a positive association of the peripapillary thickness measurements between temporal, upper and lower quadrants of both groups was found. Twelve clock hours retinal nerve fiber layer analysis detected at least one focal defect in more than 50 percent of the medication users. Particularly, a statistical correlation with the maximum daily dose was found in patients with focal defects (p=0.0120). CONCLUSION: Optical coherence tomography is effective in detecting nerve fiber layer loss in chloroquine patients without apparent fundus changes. Thus, optical coherence tomography may contribute to the early diagnosis of chloroquine retinopathy.


Asunto(s)
Adolescente , Adulto , Anciano , Femenino , Humanos , Masculino , Persona de Mediana Edad , Adulto Joven , Antimaláricos/efectos adversos , Cloroquina/efectos adversos , Fibras Nerviosas/efectos de los fármacos , Enfermedades de la Retina/inducido químicamente , Células Ganglionares de la Retina/efectos de los fármacos , Tomografía de Coherencia Óptica , Antimaláricos/uso terapéutico , Estudios de Casos y Controles , Cloroquina/uso terapéutico , Relación Dosis-Respuesta a Droga , Malaria/tratamiento farmacológico , Fibras Nerviosas/patología , Enfermedades de la Retina/patología , Células Ganglionares de la Retina/patología , Factores de Tiempo , Adulto Joven
17.
Pakistan Journal of Pathology. 2010; 21 (4): 151-154
en Inglés | IMEMR | ID: emr-124680

RESUMEN

Interferon is an immunomodulating cytokine which is used to treat different diseases. Nowadays it is being commonly used for the treatment of chronic hepatitis C. Few patients develop ocular complications secondary to the use of Interferon. We report here a case in which a young soldier with no other risk factors developed retinopathy changes after five months of interferon alpha 2b therapy which included cotton wool spots at the posterior pole and dot-blot haemorrhages in both fundi. These changes gradually started resolving after cessation of treatment and completely disappeared after six months


Asunto(s)
Humanos , Masculino , Enfermedades de la Retina/inducido químicamente , Interferones/efectos adversos , Proteínas Recombinantes , Fondo de Ojo
18.
Arq. bras. oftalmol ; 72(5): 710-714, set.-out. 2009. ilus
Artículo en Portugués | LILACS | ID: lil-534198

RESUMEN

As drogas antimaláricas, como a cloroquina, são úteis no controle de doenças reumáticas, mas podem causar lesões oculares potencialmente graves como a retinopatia cloroquínica (RC). Neste relato, são descritos os achados à tomografia de coerência óptica convencional e na espectral de alta resolução (HD-OCT) em aparelho CirrusTM HD-OCT de duas pacientes com RC. Em um dos casos, chama a atenção à similaridade entre a imagem de atrofia do epitélio pigmentado retiniano (EPR) na angiofluoresceinografia e a obtida na HD-OCT por segmentação "en -face" (reconstruções coronais). Em outra paciente, com sinais clínicos de maculopatia, mas sem anormalidades na angiofluoresceinografia, os sinais de atrofia do EPR foram também observados nos "scans" da HD-OCT, levantando a possibilidade de que esta técnica possa permitir a detecção precoce desta doença.


Antimalarial drugs, such as chloroquine, are useful in the management of rheumatic diseases, but may cause a potentially blinding condition known as toxic maculopathy. This report describes the findings on standard and on high-resolution spectral domain ocular coherence tomography performed in a CirrusTM HD-OCTdevice in two patients with chloroquine maculopathy. In one case, a very similar aspect of retinal pigment epithelium (RPE) plaque atrophy occured in both angiographic and HD-OCT images obtained by "en-face" (coronal) segmentation. In another patient with clinical signs of maculopathy and no angiographic abnormalities, signs of RPE atrophy could also be observed in HD-OCT scans, raising the possibility that this technique may allow the early detection of the disease.


Asunto(s)
Femenino , Humanos , Persona de Mediana Edad , Antimaláricos/efectos adversos , Cloroquina/efectos adversos , Enfermedades de la Retina/inducido químicamente , Epitelio Pigmentado de la Retina/efectos de los fármacos , Epitelio Pigmentado de la Retina/patología , Tomografía de Coherencia Óptica/métodos
19.
Arq. bras. oftalmol ; 72(3): 313-320, May-June 2009. ilus, graf, tab
Artículo en Portugués | LILACS | ID: lil-521464

RESUMEN

OBJETIVOS: Avaliar diferentes métodos diagnósticos para a avaliação de pacientes portadores de lúpus eritematoso sistêmico, usuários crônicos do difosfato de cloroquina (DFC) e, portanto, com alto risco para retinopatia tóxica. MÉTODOS: Foram analisados 72 olhos de 36 pacientes consecutivos, seguidos no Serviço de Reumatologia do Hospital das Clínicas, Faculdade de Medicina da Universidade de São Paulo, de julho de 2007 a abril de 2008. Dados demográficos e clínicos foram avaliados com o intuito de estudar os fatores de alto risco e comparar os seguintes métodos oftalmológicos: acuidade visual, biomicroscopia da córnea, biomicroscopia do fundo, retinografia, angiofluoresceinografia da retina, campo visual macular com mira branca. RESULTADOS: Dos 36 pacientes, 34 (94,4 por cento) eram mulheres. A média de idade foi 39,9 ± 9,8 anos, com tempo de doença igual a 13,9 ± 6,6 anos. Além do uso crônico da cloroquina, os pacientes apresentaram altas doses diárias (>3 mg/kg) e cumulativas. Não foi observada relação entre estes fatores de alto risco e maior prevalência de retinopatia. Foi encontrada prevalência de retinopatia igual a 38,9 por cento, confirmada por alterações bilaterais, centrais ou paracentrais e reprodutíveis no exame de campo visual. Outros exames indicados para seguimento, como acuidade visual, biomicroscopia de fundo e angiofluoresceinografia não foram capazes de diagnosticar a maioria das alterações confirmadas pelo campo visual. CONCLUSÃO: Foi observada alta prevalência de retinopatia por cloroquina entre os pacientes com alto risco, usuários crônicos do DFC, segundo os achados do campo visual. A avaliação desses pacientes deve considerar a realização do exame de campo visual em intervalos menores que os propostos, mesmo quando não há suspeita clínica.


PURPOSE: To evaluate different diagnostic methods for high risk chloroquine retinopathy due to prolonged use of chloroquine (more than 5 years) by systemic lupus erythematosus patients. Methods: Seventy-two eyes of 36 consecutive patients, followed in the Division of Rheumatology, School of Medicine, University of São Paulo, were analyzed from July 2007 to April 2008. Demographic and clinical data were evaluated in order to study risk factors and to compare the following different ophthalmological methods: visual acuity, biomicroscopy, fundus examination, retinography, fluorescein angiogram, visual field test and, color vision tests. RESULTS: From 36 patients, 34 (94.4 percent) were female. The mean age was 39.9 ± 9.8 years and the disease duration was 13.9 ± 6.6 years. Besides chronic use of chloroquine, patients also showed high daily and cumulative doses. These high risk factors were not related to a higher retinopathy prevalence. Visual field showed 38.9 percent of retinopathy prevalence. Other ophthalmological methods failed in detecting most cases. CONCLUSION: High prevalence of retinopathy in high risk patients was observed by visual field test, but other ophthalmological methods failed in detecting alterations. Ophthalmological assessment of these patients should include visual field, even in the absence of clinical alterations.


Asunto(s)
Adulto , Anciano , Femenino , Humanos , Masculino , Persona de Mediana Edad , Adulto Joven , Antimaláricos/efectos adversos , Cloroquina/análogos & derivados , Técnicas de Diagnóstico Oftalmológico/normas , Lupus Eritematoso Sistémico/tratamiento farmacológico , Enfermedades de la Retina/inducido químicamente , Antimaláricos/administración & dosificación , Peso Corporal/fisiología , Distribución de Chi-Cuadrado , Cloroquina/administración & dosificación , Cloroquina/efectos adversos , Córnea/efectos de los fármacos , Córnea/patología , Técnicas de Diagnóstico Oftalmológico/clasificación , Angiografía con Fluoresceína , Prevalencia , Factores de Riesgo , Retina/efectos de los fármacos , Retina/patología , Enfermedades de la Retina/diagnóstico , Enfermedades de la Retina/epidemiología , Factores de Tiempo , Campos Visuales/efectos de los fármacos , Adulto Joven
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