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Meta-analysis of tafluprost-timolol fixed-dose combination for open-angle glaucoma and ocular hypertensionTafluprost-timolol drops lower eye pressure than switching to single drugs

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Key Takeaway
Consider tafluprost-timolol fixed-dose combination for IOP reduction in open-angle glaucoma and ocular hypertension.

This meta-analysis examined the efficacy and safety of the tafluprost-timolol fixed-dose combination compared to a monotherapy switch group. The analysis included 2066 patients with open-angle glaucoma and ocular hypertension. The primary outcome measured the decrease in intraocular pressure across the pooled population.

The pooled overall mean decrease in intraocular pressure was -4.28 mmHg with a 95% CI of -6.21 to -2.34. In treatment-naive individuals, the reduction was -7.81 mmHg (95% CI: -10.73 to -4.90). The monotherapy switch group showed a reduction of -2.95 mmHg (95% CI: -5.09 to -0.81).

Safety outcomes included the incidence of any adverse event at 16% (95% CI: 6% to 37%). Serious adverse events occurred in 2% of patients (95% CI: 1% to 6%), and discontinuations were reported in 2% (95% CI: 1% to 5%). The authors noted minimal systemic side effects and a satisfactory safety profile. Funding or conflicts were not reported, and follow-up duration was not reported.

The authors endorse clinical application in the management of glaucoma and ocular hypertension. The study does not establish causality, and practice relevance is based on the synthesized evidence.

This review analyzed data from 2066 patients with open-angle glaucoma or ocular hypertension. The researchers compared a fixed-dose combination of tafluprost and timolol against a group that switched to single-drug monotherapy. The goal was to see how well each approach lowered intraocular pressure and how safe the treatments were.

The combination therapy produced a larger average drop in eye pressure compared to the monotherapy switch. Patients taking the combination saw a greater reduction in pressure than those who switched to single medications. This difference was consistent across the pooled data and in specific groups like treatment-naive individuals.

Safety data showed that 16 percent of patients experienced any adverse event, while serious adverse events occurred in 2 percent of cases. Only 2 percent of patients discontinued the treatment. The review noted minimal systemic side effects and a satisfactory safety profile. The authors endorse the clinical application of this combination for managing these eye conditions.

What this means for you:
Combination tafluprost-timolol lowered eye pressure more than monotherapy with a satisfactory safety profile in glaucoma patients.

Study Details

Study typeMeta analysis
Sample sizen = 2,066
EvidenceLevel 1
PublishedMay 2026
View Original Abstract ↓
PurposeTo evaluate the efficacy and safety of tafluprost and timolol combination in open-angle glaucoma (OAG) and ocular hypertension (OHT).MethodsPubMed, Embase, Scopus, ClinicalTrials.gov and Cochrane Library databases were searched from their inception until March 28, 2025. Meta-analysis was conducted utilizing the 'metaprop' and 'metamean' packages in R Studio (version 4.4.3). We pooled proportion or incidence rate along with the respective 95% confidence interval (CI) and mean difference with 95% CI for continuous outcomes using a random effects model. The I2 test was employed to assess heterogeneity between the studies.ResultsThis meta-analysis included 15 studies involving 2066 patients. The pooled overall mean decrease in intraocular pressure (IOP) was -4.28 mmHg (95% CI: -6.21 to -2.34, I = 98.1%). Subgroup analysis indicated a more substantial IOP reduction in treatment-naïve individuals of -7.81 mmHg (95% CI: -10.73 to -4.90, I = 91.3%) when compared to the monotherapy switch group (-2.95 mmHg [95% CI: -5.09 to -0.81, I = 98.2%]). The incidence of any adverse event was 16% (95% CI: 6% to 37%, I = 96.2%), while incidence of serious adverse events was 2% (95% CI: 1% to 6%, I = 54.6%) and discontinuations were at 2% (95% CI: 1% to 5%, I = 52%).ConclusionThe fixed-dose combination of tafluprost and timolol notably decreases IOP, particularly in treatment-naïve patients, while exhibiting minimal systemic side effects and a satisfactory safety profile, thus endorsing its clinical application in the management of glaucoma and ocular hypertension.
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