PMID- 31293419 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20200930 IS - 1663-9812 (Print) IS - 1663-9812 (Electronic) IS - 1663-9812 (Linking) VI - 10 DP - 2019 TI - Efficacy and Safety of Brinzolamide as Add-On to Prostaglandin Analogues or beta-Blocker for Glaucoma and Ocular Hypertension: A Systematic Review and Meta-Analysis. PG - 679 LID - 10.3389/fphar.2019.00679 [doi] LID - 679 AB - Background: Brinzolamide as a carbonic anhydrase inhibitor could be combined with other intraocular pressure (IOP) lowering drugs for glaucoma and ocular hypertension (OHT), but the efficacy was controversial. So, this study was used to assess the efficacy and safety of brinzolamide as add-on to prostaglandin analogues (PGAs) or beta-blocker in treating patients with glaucoma or OHT who fail to adequately control IOP. Methods: We searched PubMed, Embase, MEDLINE, Cochrane Library, and clinicaltrials.gov from inception to October 4, 2018. Randomized controlled trials of brinzolamide as add-on to PGAs or beta-blocker for glaucoma and OHT were included. Meta-analysis was conducted by RevMan 5.3 software. Results: A total of 26 trials including 5,583 patients were analyzed. Brinzolamide produced absolute reductions of IOP as an adjunctive therapy for patients with glaucoma or OHT. Brinzolamide and timolol were not significantly different in lowering IOP as add-on to PGAs (9 am: P = 0.07; 12 am: P = 0.66; 4 pm: P = 0.66). Likewise, brinzolamide was as effective as dorzolamide in depressing IOP (9 am: P = 0.59; 12 am: P = 0.94; 4 pm: P = 0.95). For the mean diurnal IOP at the end of treatment duration, there were no statistical differences in above comparisons (P > 0.05). Compared with brimonidine (b.i.d.), there was a significant reduction of IOP in brinzolamide (b.i.d.) at 9 am (P < 0.0001); however, the difference was cloudy in thrice daily subgroup (P = 0.44); at 12 am, brinzolamide (b.i.d.) was similar to brimonidine (b.i.d.) in IOP-lowering effect (P = 0.23), whereas brimonidine (t.i.d.) led to a greater effect than brinzolamide (t.i.d.) (P = 0.02). At 4 pm, brinzolamide (b.i.d.) was superior IOP-lowering effect compared with brimonidine (b.i.d.) (P = 0.0003); conversely, the effect in brinzolamide (t.i.d.) was lower than brimonidine (t.i.d.) (P < 0.0001). For the mean diurnal IOP, brinzolamide was lower in twice daily subgroup (P < 0.00001); brimonidine was lower in thrice daily subgroup (P < 0.00001). With regard to the safety, brinzolamide and dorzolamide had a higher incidence of taste abnormality; moreover, brinzolamide resulted in more frequent blurred vision; dorzolamide resulted in more frequent ocular discomfort and eye pain. Timolol resulted in more frequent blurred vision and less conjunctival hyperemia. Brimonidine resulted in more frequent ocular hyperemia. As to other adverse events (AEs) (conjunctivitis, eye pruritus, foreign body sensation in eyes, and treatment-related AEs), brinzolamide was similar to other three active comparators. Conclusions: Brinzolamide, as add-on to PGAs or beta-blocker, significantly decreased IOP of patients with refractory glaucoma or OHT and the AEs were tolerable. FAU - Liu, Yuanzhi AU - Liu Y AD - Department of Pharmacy, The Affiliated Hospital of Southwest Medical University, Luzhou, China. FAU - Zhao, Junyi AU - Zhao J AD - Department of Pharmacy, The Affiliated Hospital of Southwest Medical University, Luzhou, China. AD - College of Pharmacy, Southwest Medical University, Luzhou, China. FAU - Zhong, Xiaoyan AU - Zhong X AD - Department of Pharmacy, The Affiliated Hospital of Southwest Medical University, Luzhou, China. FAU - Wei, Qiming AU - Wei Q AD - Department of Pharmacy, The Affiliated Hospital of Southwest Medical University, Luzhou, China. FAU - Huang, Yilan AU - Huang Y AD - Department of Pharmacy, The Affiliated Hospital of Southwest Medical University, Luzhou, China. LA - eng PT - Systematic Review DEP - 20190625 PL - Switzerland TA - Front Pharmacol JT - Frontiers in pharmacology JID - 101548923 PMC - PMC6603202 OTO - NOTNLM OT - brinzolamide OT - glaucoma OT - ocular hypertension OT - prostaglandin analogues OT - systematic review OT - beta-blocker EDAT- 2019/07/12 06:00 MHDA- 2019/07/12 06:01 PMCR- 2019/06/25 CRDT- 2019/07/12 06:00 PHST- 2019/02/11 00:00 [received] PHST- 2019/05/24 00:00 [accepted] PHST- 2019/07/12 06:00 [entrez] PHST- 2019/07/12 06:00 [pubmed] PHST- 2019/07/12 06:01 [medline] PHST- 2019/06/25 00:00 [pmc-release] AID - 10.3389/fphar.2019.00679 [doi] PST - epublish SO - Front Pharmacol. 2019 Jun 25;10:679. doi: 10.3389/fphar.2019.00679. eCollection 2019.