You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


ABOUT ARCHIVES
Advanced Search

Welcome   | My Account | E-mail Alerts | Access Rights | Sign In


  Vol. 125 No. 3, March 2007 TABLE OF CONTENTS
  Archives
  •  Online Features
  Clinical Trial
 This Article
 •Full text
 •PDF
 • Reply to article
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Citing articles on HighWire
 •Citing articles on ISI (13)
 •Contact me when this article is cited
 Related Content
 •Similar articles in this journal
 Topic Collections
 •Drug Therapy, Other
 •Randomized Controlled Trial
 •Articles for Residents
 •Macular Disorders
 •Drug Therapy
 •Alert me on articles by topic

Randomized Controlled Study of an Intravitreous Dexamethasone Drug Delivery System in Patients With Persistent Macular Edema

Baruch D. Kuppermann, MD, PhD; Mark S. Blumenkranz, MD; Julia A. Haller, MD; George A. Williams, MD; David V. Weinberg, MD; Connie Chou, PhD; Scott M. Whitcup, MD; for the Dexamethasone DDS Phase II Study Group

Arch Ophthalmol. 2007;125(3):309-317.

Objective  To evaluate a dexamethasone intravitreous drug delivery system (DDS) in patients with persistent (≥90 days despite treatment) macular edema.

Methods  This 6-month study randomized 315 patients with persistent macular edema with best-corrected visual acuity (BCVA) of 20/40 to 20/200 in the study eye to observation or a single treatment with dexamethasone DDS, 350 or 700 µg.

Main Outcome Measures  Proportion of patients achieving a BCVA improvement of 10 or more letters or 15 or more letters, safety measures, change in fluorescein angiographic leakage, and central retinal thickness.

Results  At day 90 (primary end point), an improvement in BCVA of 10 letters or more was achieved by a greater proportion of patients treated with dexamethasone DDS, 700 µg (35%) or 350 µg (24%), than observed patients (13%; P<.001 vs 700-µg group; P = .04 vs 350-µg group); an improvement in BCVA of 15 letters or more was achieved in 18% of patients treated with dexamethasone DDS, 700 µg, vs 6% of observed patients (P = .006). Results were similar in patients with diabetic retinopathy, vein occlusion, or uveitis or Irvine-Gass syndrome. During 3 months of observation, 11% of treated patients and 2% of observed patients had intraocular pressure increases of 10 mm Hg or higher.

Conclusion  In persistent macular edema, a single dexamethasone DDS treatment produced statistically significant BCVA improvements 90 days after treatment and was well tolerated for 180 days.

Application to Clinical Practice  Dexamethasone DDS, 700 µg, may have potential as a treatment for persistent macular edema.

Trial Registration  clinicaltrials.gov Identifier: NCT00035906


Author Affiliations: Departments of Ophthalmology, University of California, Irvine (Dr Kuppermann), Stanford University, Stanford, Calif (Dr Blumenkranz), and Wilmer Eye Institute, Johns Hopkins University, Baltimore, Md (Dr Haller); Associated Retinal Consultants, Beaumont Eye Institute, Royal Oak, Mich (Dr Williams); The Eye Institute, Medical College of Wisconsin, Milwaukee (Dr Weinberg); and Allergan Inc, Irvine (Drs Chou and Whitcup).



THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Dexamethasone Inhibits High Glucose-, TNF-{alpha}-, and IL-1{beta}-Induced Secretion of Inflammatory and Angiogenic Mediators from Retinal Microvascular Pericytes
Nehme and Edelman
IOVS 2008;49:2030-2038.
ABSTRACT | FULL TEXT  

Safety Evaluation of Ocular Drug Delivery Formulations: Techniques and Practical Considerations
Short
Toxicol Pathol 2008;36:49-62.
ABSTRACT | FULL TEXT  

From the Library
Br. J. Ophthalmol. 2007;91:846-846.
FULL TEXT  





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 2007 American Medical Association. All Rights Reserved.