Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 5 de 5
Filtrar
Mais filtros











Base de dados
Intervalo de ano de publicação
2.
Br J Ophthalmol ; 86(10): 1109-13, 2002 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-12234888

RESUMO

AIM: To evaluate the utility of measuring the optic nerve sheath diameter in children with shunted hydrocephalus, suspected of having raised intracranial pressure. METHODS: 23 children with shunted hydrocephalus were examined, six had well controlled ICP, 17 however manifested symptoms suggestive of intracranial hypertension. A clinical history was taken from all patients and their parents or carers. The shunt valve was examined clinically, and signs of raised intracranial pressure were sought. Ultrasound examination was performed in both eyes to measure the optic nerve sheath diameters 3 mm behind the globe. These measurements were compared with control data obtained from 102 children who attended the radiology department for unrelated renal ultrasound examination. RESULTS: Control data suggested that the upper limit of normal for optic nerve sheath diameter is 4.5 mm (measured 3 mm behind the globe) in patients over 1 year of age, and 4.0 mm in children less than 1 year of age. Those patients with functioning ventriculoperitoneal shunts had a mean optic nerve sheath diameter of 2.9 (SD 0.5) mm; those with raised intracranial pressure had a mean optic nerve sheath diameter of 5.6 (0.6) mm (p<0.0001). These results confirm that optic nerve sheath diameters in excess of the control data are strongly suggestive of raised intracranial pressure. CONCLUSION: The evaluation of the optic nerve sheath diameter is a simple non-invasive procedure, which is a potentially useful tool in the assessment and monitoring of children with hydrocephalus suspected of having raised intracranial pressure.


Assuntos
Hidrocefalia/diagnóstico por imagem , Pressão Intracraniana , Nervo Óptico/diagnóstico por imagem , Adolescente , Fatores Etários , Criança , Pré-Escolar , Humanos , Hidrocefalia/patologia , Hidrocefalia/fisiopatologia , Lactente , Recém-Nascido , Doenças do Recém-Nascido/diagnóstico por imagem , Doenças do Recém-Nascido/patologia , Doenças do Recém-Nascido/fisiopatologia , Nervo Óptico/patologia , Ultrassonografia
3.
Eye (Lond) ; 16(5): 567-71, 2002 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-12194070

RESUMO

PURPOSE: To survey clinical visual function including quantitative manual perimetry results in a group of patients taking vigabatrin; to assess the severity of any field defects; to tabulate cumulative and daily doses of medication and to assess possible changes in visual function over time. METHOD: A prevalence study of 100 out of 183 patients currently attending a tertiary referral epilepsy centre who were taking or had recently discontinued vigabatrin (duration 83-3570 days; mean 1885 days) as part of combination anticonvulsant therapy. Complete neuro-ophthalmic examination including Goldmann kinetic perimetry was performed and monocular mean radial degrees (MRD) to the I/4e isopter calculated. Patients were followed up at 6-monthly intervals for not less than 18 months. RESULTS: Acuity and colour vision remained stable in all patients regardless of changes in visual fields. Twenty per cent of patients had significant constriction of their visual field defined as a monocular MRD of 30 degrees or less. Males were significantly more likely to be severely affected than females (P < 0.01). Twenty one patients were followed after discontinuing vigabatrin treatment. Only three of these showed a change in MRD of 10 degrees or more with two deteriorating and one improving. No correlation between treatment duration or cumulative dosage/kg and the severity of defects could be demonstrated. CONCLUSIONS: Earlier reports of a high prevalence of both moderate and more serious field defects were confirmed in patients taking vigabatrin but not in epileptic patients taking other anti-convulsants. We found no evidence of progression or resolution of visual field defects on discontinuing the drug, and no relationship between dose history and visual deficit field loss. An idiosyncratic drug reaction within the neurosensory retina may underlie the pathogenesis of the visual field loss in some patients.


Assuntos
Anticonvulsivantes/efeitos adversos , Vigabatrina/efeitos adversos , Transtornos da Visão/induzido quimicamente , Campos Visuais/efeitos dos fármacos , Adulto , Idoso , Inglaterra/epidemiologia , Feminino , Seguimentos , Humanos , Masculino , Auditoria Médica , Pessoa de Meia-Idade , Razão de Chances , Fatores Sexuais , Transtornos da Visão/epidemiologia , Transtornos da Visão/fisiopatologia , Testes de Campo Visual
4.
J Neuroophthalmol ; 16(1): 7-8, 1996 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-8963424

RESUMO

Anterior ischemic optic neuropathy (AION) is a condition more commonly found in later life. We present a case of unilateral AION in a 13-year-old boy with small discs and ipsilateral optic nerve head drusen.


Assuntos
Oftalmopatias/diagnóstico por imagem , Drusas do Disco Óptico/diagnóstico por imagem , Adolescente , Humanos , Masculino , Tomografia Computadorizada por Raios X
5.
Eye (Lond) ; 7 ( Pt 1): 89-94, 1993.
Artigo em Inglês | MEDLINE | ID: mdl-8325431

RESUMO

Pyoderma gangrenosum is an uncommon chronic ulcerative condition, the aetiology of which is poorly understood. Ophthalmic involvement is rare. The case presented in this paper involves destruction of the orbital contents with subsequent perforation of the eye despite conventional therapy. Evisceration was performed with the patient being subjected to hyperbaric oxygen therapy pre- and post-operatively, with resultant cessation of the disease process.


Assuntos
Doenças Orbitárias/diagnóstico , Pioderma Gangrenoso/diagnóstico , Idoso , Oftalmopatias/etiologia , Evisceração do Olho , Feminino , Humanos , Oxigenoterapia Hiperbárica , Doenças Orbitárias/complicações , Doenças Orbitárias/diagnóstico por imagem , Doenças Orbitárias/patologia , Pioderma Gangrenoso/diagnóstico por imagem , Pioderma Gangrenoso/patologia , Tomografia Computadorizada por Raios X
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA