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Latanoprost, a Prostaglandin Analog, for Glaucoma Therapy

Authors :
C.J. Pollack-Rundle
Ronald M. Caronia
H. Aasved
Mark B. Sherwood
M. Sloper
Robert D. Fechtner
Frank D. Green
M. Potts
R. Halseide
Martin B. Wax
R. Fenton
V. Gates
M. Bailey
B. Kaplan
Jacob T. Wilensky
A. Vegge
P. Watson
Paul L. Kaufman
C. Davey
Robert Ritch
D. Neeley
M. Juzych
S.E. Nilsson
J. Airaksinen
B. Ehinger
I. Spencer
B. Lindblom
A. Ringvold
A. Chatterjee
B. Mills
M.A. Vanderhof-Young
D. Steinberger
C.B. Camras
P. Jangard
A. Heijl
J. Fenton
Alan L. Robin
Michael E. Yablonski
F. Valenzuela
Peter G. Watson
R. Coakes
M. Austin
B. Friström
S.M. Podos
M. Arroyo
R.A. Schumer
Jeanette A. Stewart
Christina Lindén
A.T. Johnson
A. Jones
Gregg A Heatley
K.G. Gundersen
J. M. Liebmann
S. Murray
Paul P. Lee
S. Roxburgh
S. Nagasubramanian
Zanna I. Currie
Lisa F. Rosenberg
Dale K. Heuer
D. Hillman
J.M. Rudermann
J. Hickman-Casey
E. Bengtsson-Stigmar
Peter K. Wishart
Albert Alm
Johan Stjernschantz
E.M. Van Buskirk
D.W. Stokes
I. Widengard
S. Nitzberg
M.H. Tannenbaum
E. Weiss
R. Sanders
Eve J. Higginbotham
William C. Stewart
C. Nail
Carl B. Camras
A. Luff
H. Lund-Andersen
M. Blackmore
A. Elkington
K. Clarkson
J. Lustgarten
C. Holmin
Anja Tuulonen
I.F. Whyte
E. Ohia
Stephen A Vernon
Marlene R. Moster
P. Reynolds
M. F. Smith
Z.S. Zam
M. Brummett
P. Flesner
M. Söderström
R. Ochabsi
G.A. Cioffi
G. Abundo
L. Beck
M. Padea
L. J. Katz
Donald S. Minckler
S. Longstaff
B. Parker
T. J. Zimmerman
Robert N. Weinreb
A. Alm
F. Ibrahim
J. Fraser
M K Birch
J. Thygesen
Theodore Krupin
Source :
Ophthalmology. 103:1916-1924
Publication Year :
1996
Publisher :
Elsevier BV, 1996.

Abstract

Purpose: To determine efficacy and safety of latanoprost, a prostaglandin analog for glaucoma, during 1 year of treatment. Methods: After baseline measurements, 0.005% latanoprost was topically applied once daily for 12 months in patients from Scandinavia, the United Kingdom, and the United States who had elevated intraocular pressure (IOP). Diagnoses included ocular hypertension, chronic open-angle glaucoma, exfoliation syndrome, and pigment dispersion syndrome. Treatment was masked for the first 6 months and open-label during the second 6 months. Results: Of the 272 patients initially enrolled, withdrawals were due to inadequate IOP control (1 %), increased iris pigmentation (5%), other ocular problems (3%), systemic medical problems (3%), and nonmedical reasons (14%). Latanoprost significantly ( P Conclusion: Latanoprost safely and effectively reduces IOP for 1 year in patients of diverse nationalities, providing further evidence for its usefulness in chronic glaucoma therapy.

Details

ISSN :
01616420
Volume :
103
Database :
OpenAIRE
Journal :
Ophthalmology
Accession number :
edsair.doi...........fe3ecd679e2bbedf2bc138eadd88b60b
Full Text :
https://doi.org/10.1016/s0161-6420(96)30407-7