A comparison of tangent screen, Goldmann, and Humphrey perimetry in the detection and localization of occipital lesions

To compare manual kinetic perimetry with tangent screen and Goldmann techniques and automated static perimetry with the Humphrey Field Analyzer in the detection and localization of occipital lobe lesions. Prospective consecutive comparative case series. Twelve patients with well-defined occipital lo...

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Published inOphthalmology (Rochester, Minn.) Vol. 107; no. 3; pp. 527 - 544
Main Authors Wong, Agnes M.F, Sharpe, James A
Format Journal Article
LanguageEnglish
Published New York, NY Elsevier Inc 01.03.2000
Elsevier
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Summary:To compare manual kinetic perimetry with tangent screen and Goldmann techniques and automated static perimetry with the Humphrey Field Analyzer in the detection and localization of occipital lobe lesions. Prospective consecutive comparative case series. Twelve patients with well-defined occipital lobe infarcts on magnetic resonance (MR) imaging were studied. The patients were tested by tangent screen, Goldmann, and Humphrey perimetry (central 30-2 threshold program). The three visual fields were compared and correlated with MR images. All three perimetric techniques detected the presence of postchiasmal lesions. However, localization of lesions differed with perimetric technique. Visual fields obtained from tangent screen and Goldmann perimetry were similar and corresponded well with the location of lesions on MR images in all 12 patients. Humphrey perimetry inaccurately localized the lesion to the proximal part of the postchiasmal pathway by revealing incongruous fields in two patients, failed to detect sparing of the posterior occipital cortex or occipital pole in four patients, and estimated a larger extent of damage in one patient when compared with MR images and manual perimetry. All three perimetric techniques are satisfactory screening tests to detect occipital lesions. However, tangent screen and Goldmann perimetry provide information about the location and extent of lesions that is more consistent with prevailing knowledge of the effects of the lesion in the postgeniculate visual pathway.
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ISSN:0161-6420
1549-4713
DOI:10.1016/S0161-6420(99)00092-5