Original article
A Randomized Trial of Brimonidine Versus Timolol in Preserving Visual Function: Results From the Low-pressure Glaucoma Treatment Study

https://doi.org/10.1016/j.ajo.2010.09.026Get rights and content

Purpose

To compare the alpha2-adrenergic agonist brimonidine tartrate 0.2% to the beta-adrenergic antagonist timolol maleate 0.5% in preserving visual function in low-pressure glaucoma.

Design

Randomized, double-masked, multicenter clinical trial.

Methods

Exclusion criteria included untreated intraocular pressure (IOP) >21 mm Hg, visual field mean deviation worse than −16 decibels, or contraindications to study medications. Both eyes received twice-daily monotherapy randomized in blocks of 7 (4 brimonidine to 3 timolol). Standard automated perimetry and tonometry were performed at 4-month intervals. Main outcome measure was field progression in either eye, defined as the same 3 or more points with a negative slope ≥−1 dB/year at P < 5%, on 3 consecutive tests, assessed by pointwise linear regression. Secondary outcome measures were progression based on glaucoma change probability maps (GCPM) of pattern deviation and the 3-omitting method for pointwise linear regression.

Results

Ninety-nine patients were randomized to brimonidine and 79 to timolol. Mean (± SE) months of follow-up for all patients was 30.0 ± 2. Statistically fewer brimonidine-treated patients (9, 9.1%) had visual field progression by pointwise linear regression than timolol-treated patients (31, 39.2%, log-rank 12.4, P = .001). Mean treated IOP was similar for brimonidine- and timolol-treated patients at all time points. More brimonidine-treated (28, 28.3%) than timolol-treated (9, 11.4%) patients discontinued study participation because of drug-related adverse events (P = .008). Similar differences in progression were observed when analyzed by GCPM and the 3-omitting method.

Conclusion

Low-pressure glaucoma patients treated with brimonidine 0.2% who do not develop ocular allergy are less likely to have field progression than patients treated with timolol 0.5%.

Section snippets

Methods

Methods are fully described elsewhere.15

Results

Recruitment15 was between April 28, 1998 and June 19, 2000, with 193 individuals assessed for enrollment (Figure 1). A total of 178 randomized participants were followed: 99 (55.6%) were allocated to brimonidine and 79 (44.4%) to timolol. There were no significant differences at baseline in demographics, ocular parameters, or systemic factors between the 2 treatment groups (Table 1).

Statistically more subjects assigned to brimonidine (36/99, 36.4%) dropped out prior to the year-1 examination

Discussion

Low-pressure glaucoma patients randomized to monotherapy with brimonidine were statistically less likely to have progressive visual field loss than those patients randomized to monotherapy with timolol, despite known similar IOP lowering.13, 14, 16, 24 Determination of field progression by pointwise linear regression required the same 3 or more individual test locations to be progressing on 3 consecutive examinations over an 8-month interval.25 Therefore, the first detection of field

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