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1.
Neurology ; 74(15): 1184-90, 2010 Apr 13.
Article in English | MEDLINE | ID: mdl-20385890

ABSTRACT

OBJECTIVE: To determine the diagnostic accuracy of confrontation visual field testing and to compare the accuracy of confrontation tests both individually and in combination. METHODS: Patients were prospectively recruited from ophthalmology clinics over a 6-month period. All patients underwent SITA-standard 24-2 Humphrey visual field analysis. Two examiners, masked to the automated perimetry results and the results of the other examiner, assessed patients using 7 common confrontation visual field tests. The order of testing was randomized to reduce any learning effect. For each individual test and combination of tests, the sensitivity, specificity, positive predictive value, and negative predictive value were calculated. RESULTS: A total of 301 eyes from 163 patients were included in the study. The average mean deviation was -5.91 +/- 7.72 (SD) dB. Most confrontation tests were insensitive to the identification of field loss. The sensitivity and specificity varied depending on the type, density, and cause of the visual field defect. Kinetic testing with a red target provided the highest sensitivity (74.4%) and specificity (93.0%) of any individual test and when combined with static finger wiggle testing achieved a sensitivity of 78.3% while retaining a specificity of 90.1%. CONCLUSIONS: Confrontation visual field tests are insensitive at detecting visual field loss when performed individually and are therefore a poor screening test. Combining confrontation tests is a simple and practical method of improving the sensitivity of confrontation testing.


Subject(s)
Eye Diseases/diagnosis , Visual Field Tests/methods , Visual Fields/physiology , Adult , Aged , Diagnosis, Differential , Female , Humans , Male , Middle Aged , Neurologic Examination/methods , Patient Selection , Prospective Studies , Sensitivity and Specificity , Sensory Thresholds/physiology
2.
J Clin Neurosci ; 16(10): 1263-8, 2009 Oct.
Article in English | MEDLINE | ID: mdl-19586772

ABSTRACT

Giant cell arteritis (GCA) is an immune-mediated vasculitis affecting individuals over 50 years of age. It is characterised by granulomatous inflammation that affects medium-sized and large arteries. The wide spectrum of clinical manifestations can be divided into those related to tissue ischemia from vascular lesions and those related to a systemic inflammatory response. The pathogenesis of these groups also appears distinct, with vascular lesion formation thought to be an adaptive immune response, and the systemic inflammatory reaction an innate immune response. Clinical suspicion of GCA must remain especially high in those with neurological or visual symptoms and if warranted, prompt treatment with high-dose corticosteroids is invaluable in halting disease progression.


Subject(s)
Giant Cell Arteritis/physiopathology , Giant Cell Arteritis/therapy , Giant Cell Arteritis/diagnosis , Giant Cell Arteritis/epidemiology , Humans
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