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Fall 2011
Newsletter

MICHAEL V. DRAKE, M.D.

Professor of Ophthalmology
Vice President for Health Affairs
University of California, Office of the Presi
dent
 


Research Summary

Glaucoma Screening

Glaucoma is among the leading causes of blindness in the U.S., and it is the leading cause of blindness among African Americans. There are presently no consistent guidelines in the U.S. or internationally for treating patients with "ocular hypertension" - those who have pressures between 24 and 32 mm Hg, when the ophthalmic examination is normal in other aspects. In Great Britain, surgery is advocated at the first evidence of glaucoma. Previous studies are inconsistent: they are often flawed methodologically, the definition of glaucoma differs from one study to another, sample size is often small, and follow-up
periods are variable. As a result, great confusion exists in the ophthalmic community regarding the need to treat patients with elevated intraocular pressure but otherwise normal ocular examinations.

Evaluating Glaucoma Risk.
If we can define precisely which patients are at greatest risk of developing glaucoma, we will be able to initiate reasonable treatment for the greatest number of patients. I am principal investigator for a randomized prospective
multicenter trial that we have designed to evaluate the relative risk of developing glaucomatous visual field loss for patients who have pressures between 24 and 32 mm Hg, and who do not presently have glaucoma. This study will be important in determining whether we should expose these patients to a lifetime of expensive medications or surgery, or if they are better off if we follow them until glaucomatous visual loss appears.

This study will closely follow selected patients with ocular hypertension, between 40 and 80 years of age, in order to determine whether treatment will change the rates at which these patients develop glaucoma. Patients are randomly assigned to a treatment group or to a nontreatment group; patients in both treatment and nontreatment groups will be followed every six months, but patients in the treatment group will have intraocular pressure lowered 20% or more, using topical antiglaucoma drops. Because of the increased evidence of glaucoma among African-Americans, 30% of patients will be African-American. If any patient
progresses to glaucamatous loss, they will be treated fully for glaucoma in a standard fashion.

This study is designed in a way that it should be successful in determining in a scientific fashion the relative risk of developing glaucomatous visual field loss for patients with pressures between 24 and 32 mm Hg. This new data will help in directing practice patterns.

The Glaucoma Service at UCSF boasts an international reputation for excellence in glaucoma research, diagnosis and care. In the last decade, I have participated in numerous multi-center collaborative trials at UCSF that have focused on glaucoma. I have also served on the NIH/NEI Panel that reviews multi-center collaborative glaucoma studies.

 

 

©2011 University of California, San Francisco, Department of Ophthalmology
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