TY - JOUR
T1 - Dorzolamide hydrochloride and visual function in normal eyes
AU - Sponsel, W. E.
AU - Harrison, J.
AU - Elliott, W. R.
AU - Trigo, Y.
AU - Kavanagh, J.
AU - Harris, A.
N1 - Funding Information:
Accepted for publication Jan 16, 1997- From the Department of Ophthalmology, University of Texas Health Science Center, San Antonio, Texas (Drs Sponsel, Harrison, and Kavanagh, Mr Elliott and Ms Trigo); and Department of Ophthalmology, Indiana University, Indianapolis, Indiana (Dr Harris). Supported by an unrestricted grant from Research to Prevent Blindness, Inc, New York, New York; a research grant from Merck Research Laboratories, Blue Bell, Pennsylvania; and contract F41624-93-905 (USAF Armstrong Laboratory, San Antonio, Texas) through Conceptual Mindworks, Inc, San Antonio, Texas, with equipment support from Humphrey-Zeiss, San Leandro, California. Presented in part at the Annual Meeting of the Association for Research in Vision and Ophthalmology, Fort Lauderdale, Florida, April 23, 1996.
PY - 1997
Y1 - 1997
N2 - PURPOSE: To determine by a pilot study whether standard treatment with the topical carbonic anhydrase inhibitor dorzolamide hydrochloride influences visual function under normal breathing conditions, during carbon dioxide inhalation, or during hyperventilation, and to establish criteria for future larger-scale studies. METHODS: We enrolled 12 normal subjects into this randomized double-masked placebo-controlled crossover study. Each subject was treated with either dorzolamide 2% or placebo, three times daily, for 4 days. After a 2-week washout period, the alternative topical agent was used under identical testing conditions. On day 2 of each treatment phase, contrast sensitivities to sinusoidal gratings of 1 and 4 cycles per degree (cpd) were assessed. On day 4, mean deviation values from full-threshold 10-2 visual fields were obtained. Three sets of each visual function test were obtained before each treatment phase, and in sequence on each testing day, during normal breathing (baseline), inhalation of carbon dioxide-enriched air, and hyperventilation while intraocular pressure was monitored. RESULTS: Contrast sensitivity at 4 cpd decreased significantly (P < .01) during carbon dioxide supplementation with placebo but showed no significant change with dorzolamide. The decrease in contrast sensitivity accompanying hyperventilation was attenuated (by nearly 50% at 1 cpd) during dorzolamide treatment. Dorzolamide treatment was associated with higher perimetry mean deviation values under each treatment condition and was statistically significant (P < .05) at baseline. CONCLUSIONS: Dorzolamide appears to enhance contrast sensitivity in normal subjects during physiologic hypercapnia and hypocapnia at 4 and 1 cpd, respectively. Also, under normal breathing conditions, dorzolamide therapy increases perimetric light sensitivity.
AB - PURPOSE: To determine by a pilot study whether standard treatment with the topical carbonic anhydrase inhibitor dorzolamide hydrochloride influences visual function under normal breathing conditions, during carbon dioxide inhalation, or during hyperventilation, and to establish criteria for future larger-scale studies. METHODS: We enrolled 12 normal subjects into this randomized double-masked placebo-controlled crossover study. Each subject was treated with either dorzolamide 2% or placebo, three times daily, for 4 days. After a 2-week washout period, the alternative topical agent was used under identical testing conditions. On day 2 of each treatment phase, contrast sensitivities to sinusoidal gratings of 1 and 4 cycles per degree (cpd) were assessed. On day 4, mean deviation values from full-threshold 10-2 visual fields were obtained. Three sets of each visual function test were obtained before each treatment phase, and in sequence on each testing day, during normal breathing (baseline), inhalation of carbon dioxide-enriched air, and hyperventilation while intraocular pressure was monitored. RESULTS: Contrast sensitivity at 4 cpd decreased significantly (P < .01) during carbon dioxide supplementation with placebo but showed no significant change with dorzolamide. The decrease in contrast sensitivity accompanying hyperventilation was attenuated (by nearly 50% at 1 cpd) during dorzolamide treatment. Dorzolamide treatment was associated with higher perimetry mean deviation values under each treatment condition and was statistically significant (P < .05) at baseline. CONCLUSIONS: Dorzolamide appears to enhance contrast sensitivity in normal subjects during physiologic hypercapnia and hypocapnia at 4 and 1 cpd, respectively. Also, under normal breathing conditions, dorzolamide therapy increases perimetric light sensitivity.
UR - https://www.scopus.com/pages/publications/0031005744
U2 - 10.1016/S0002-9394(14)71124-9
DO - 10.1016/S0002-9394(14)71124-9
M3 - Article
C2 - 9535619
AN - SCOPUS:0031005744
SN - 0002-9394
VL - 123
SP - 759
EP - 766
JO - American Journal of Ophthalmology
JF - American Journal of Ophthalmology
IS - 6
ER -