Background
Glaucoma is a heterogeneous group of conditions involving progressive
damage to the optic nerve, deterioration of retinal ganglion cells and
ultimately visual field loss. It is a leading cause of blindness worldwide.
Open angle glaucoma (OAG), the commonest form of glaucoma, is a chronic
condition that may or may not present with increased intraocular pressure
(IOP). Neuroprotection for glaucoma refers to any intervention intended to
prevent optic nerve damage or cell death.
Objectives
The objective of this review was to systematically examine the
evidence regarding the effectiveness of neuroprotective agents for slowing
the progression of OAG in adults.
Search methods
We searched CENTRAL (which contains the Cochrane Eyes and Vision
Group Trials Register) (The Cochrane Library 2012, Issue
9), Ovid MEDLINE, Ovid MEDLINE In-Process and Other Non-Indexed Citations,
Ovid MEDLINE Daily, Ovid OLDMEDLINE, (January 1950 to October 2012), EMBASE
(January 1980 to October 2012), Latin American and Caribbean Literature on
Health Sciences (LILACS) (January 1982 to October 2012), the
metaRegister of Controlled Trials
(mRCT) (www.controlled-trials.com), ClinicalTrials.gov (www.clinicaltrials.gov) and the WHO International Clinical
Trials Registry Platform (ICTRP) (www.who.int/ictrp/search/en). We did not use any date or
language restrictions in the electronic searches for trials. The electronic
databases were last searched on 16 October 2012.
Selection criteria
We included randomized controlled trials (RCTs) in which topical or
oral treatments were used for neuroprotection in adults with OAG. Minimum
follow up time was four years.
Data collection and analysis
Two review authors independently reviewed titles and abstracts from
the literature searches. Full-text copies of potentially relevant studies
were obtained and re-evaluated for inclusion. Two review authors
independently extracted data related study characteristics, risk of bias,
and outcome data. One trial was identified for this review, thus we
performed no meta-analysis. Two studies comparing memantine to placebo are
currently awaiting classification until additional study details are
provided. We documented reasons for excluding studies from the review.
Main results
We included one multi-center RCT of adults with low-pressure glaucoma
(Low-pressure Glaucoma Treatment Study, LoGTS) conducted in the USA. The
primary outcome was visual field progression after four years of treatment
with either brimonidine or timolol. Of the 190 adults enrolled in the study,
12 (6.3%) were excluded after randomization and 77 (40.5%)
did not complete four years of follow up. The rate of attrition was
unbalanced between groups with more participants dropping out of the
brimonidine group (55%) than the timolol group (29%). Of
those remaining in the study at four years, participants assigned to
brimonidine showed less visual field progression than participants assigned
to timolol (5/45 participants in the brimonidine group compared with 18/56
participants in the timolol...