VISION DEFECTS IN PATIENTS WITH PERI-CHIASMAL LESIONS

Citation
Tl. Blamires et Bc. Reeves, VISION DEFECTS IN PATIENTS WITH PERI-CHIASMAL LESIONS, Optometry and vision science, 73(9), 1996, pp. 572-578
Citations number
33
Categorie Soggetti
Ophthalmology
ISSN journal
10405488
Volume
73
Issue
9
Year of publication
1996
Pages
572 - 578
Database
ISI
SICI code
1040-5488(1996)73:9<572:VDIPWP>2.0.ZU;2-U
Abstract
Background. Patients with chiasmal lesions frequently suffer loss of v ision, but some may be visually asymptomatic and have little, if any, visual field loss. This study addressed two questions about the nature of such loss: (1) which tests are best able to detect visual loss and (2) what is the relation between the size of a lesion and the degree and type of visual loss. Methods. Visual acuity (VA), Goldmann perimet ry, pattern evoked potentials, contrast sensitivity (CS), and color vi sion (CV) were assessed, in addition to a full ophthalmologic examinat ion. Thirty-five patients were recruited from neurology, endocrinology , and ophthalmology departments; 31 had pituitary tumors and 4 had tum ors of other origin (1 secondary) close to the chiasm. For analysis, p atients were classified (1) according to whether they had visual sympt oms on presentation and (2) according to lesion size. Results, Sevente en patients had visual symptoms; all had visual field defects and all but one had two or more additional abnormal test results. Of the 18 vi sually asymptomatic patients, 12 had visual field defects and 14 had a t least 2 abnormal test results; 7 had tumors with less than 5 mm of s uprasellar extension, of whom 5 had field loss or at least 2 abnormal test results. CS was abnormal most often (85% of patients), followed b y Goldmann perimetry (80%), visual evoked potentials (VEPs) (57%), CV (49%), and VA (26%). Conclusion Our results support previous reports t hat asymptomatic patients and those with intrasellar tumors or only sm all amounts of suprasellar extension may have demonstrable visual dysf unction. Perimetry did not appear to be significantly worse than other more recently developed tests, which have often been regarded as bein g more sensitive, for detecting vision loss. However, VA and clinical observation of pupil reactions had poor sensitivity.