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Section III · Management

Chapter 31: Adrenergic Stimulators

Shields' Textbook of Glaucoma, 6th edition

Showing 1–20 of 157 articles

3.
Basic Science

A Mathematical Model of Aqueous Humor Production and Composition.

Dvoriashyna Mariia, Foss Alexander J E, Gaffney Eamonn A et al.

Invest Ophthalmol Vis SciAug 20227 citations

A mathematical model predicted aqueous humor production and composition, identifying key ion channels and transporters (e.g., K+, Cl-, Na+/H+, Na+/K+/2Cl-, carbonic anhydrase) as targets for manipulating outflow and glaucoma treatment.

12.
Review

Pediatric pseudotumor cerebri.

Rook Brita S, Phillips Paul H

Curr Opin OphthalmolSep 2016

This review highlights pediatric PTC differences from adults, noting revised diagnostic criteria (CSF >28cm H2O) and risk factors like obesity, guiding improved diagnosis and treatment strategies.

19.
Clinical Trial

Fixed-combination brinzolamide 1%/brimonidine 0.2% vs monotherapy with brinzolamide or brimonidine in patients with open-angle glaucoma or ocular hypertension: results of a pooled analysis of two phase 3 studies.

Realini T, Nguyen Q H, Katz G et al.

Eye (Lond)Jul 201320 citations

Pooled data showed fixed-combination brinzolamide/brimonidine significantly lowered intraocular pressure more than its individual components in glaucoma/ocular hypertension patients, offering superior efficacy with a consistent safety profile.

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The all-polymer microfluidic theranostic smart contact lens (AP-TSCL) demonstrated pressure-triggered delivery of timolol or brimonidine above preset thresholds in in vitro (artificial eye model), ex vivo (enucleated bovine eyes), and in vivo (rabbit ocular hypertension) studies.

TreatmentBasic SciencePreclinical studyn=Not specified (in vitro, ex vivo, in vivo models)

Brimonidine, a selective α2-adrenergic agonist, was transported by organic cation transporter 2 (OCT2) and multidrug and toxin extrusion protein 1 (MATE1) but not by OCT1, OCT3, or MATE2K in HEK293 cells.

MechanismBasic ScienceIn vitro studyn=HEK293 cells stably expressing OCT1, OCT2, OCT3, MATE1, and MATE2K

The uptake of brimonidine by OCT2 and MATE1 was time- and concentration-dependent in HEK293 cells.

MechanismBasic ScienceIn vitro studyn=HEK293 cells stably expressing OCT2 and MATE1

Organic cation transporter 2 (OCT2) and multidrug and toxin extrusion protein 1 (MATE1) may play a role in brimonidine uptake into the human eye.

MechanismBasic ScienceIn vitro and immunohistochemistry studyn=HEK293 cells and glaucomatous human eyes

Organic cation transporter 2 (OCT2) and multidrug and toxin extrusion protein 1 (MATE1) may contribute to the interindividual variability of brimonidine concentrations and effects.

MechanismBasic ScienceIn vitro and immunohistochemistry studyn=HEK293 cells and glaucomatous human eyes

Other topical agents, such as beta blocker, prostaglandin, or carbonic anhydrase inhibitors, age, sex, race, or glaucoma severity, did not show an increased or decreased hazard of high intraocular pressure (IOP) surgical failure in adult glaucoma patients (n=501 eyes) undergoing primary trabeculectomy.

PrognosisCohortRetrospective Observational Cohort Studyn=501 eyes of adult glaucoma patients

Topical carbonic anhydrase inhibitor (CAI) users had new-onset depression more frequently than controls at 3 months (1.42% vs. 0.77%), 6 months (2.46% vs. 1.41%), and 1 year (4.05% vs. 2.47%; all P < 0.001) in glaucoma patients aged ≥40 years.

PrognosisCohortRetrospective Cohort Studyn=Glaucoma patients aged ≥40 years, propensity score matched

Antidepressant prescriptions were more frequent in topical carbonic anhydrase inhibitor (CAI) users compared to controls at 3 months (3.57% vs. 1.28%), 6 months (5.0% vs. 2.49%), and 1 year (7.7% vs. 4.4%; all P < 0.001) in glaucoma patients aged ≥40 years.

PrognosisCohortRetrospective Cohort Studyn=Glaucoma patients aged ≥40 years, propensity score matched

Anxiety disorders occurred more often in topical carbonic anhydrase inhibitor (CAI) users across all time points (all P < 0.001) compared to controls in glaucoma patients aged ≥40 years.

PrognosisCohortRetrospective Cohort Studyn=Glaucoma patients aged ≥40 years, propensity score matched

Topical carbonic anhydrase inhibitor (CAI) use was associated with increased hazards of depression (aHR 1.36 at 3 months; 1.28 at 6 months; 1.27 at 1 year) in glaucoma patients aged ≥40 years.

PrognosisCohortRetrospective Cohort Studyn=Glaucoma patients aged ≥40 years, propensity score matched

Topical carbonic anhydrase inhibitor (CAI) use was associated with increased hazards of antidepressant initiation (aHR 2.45 at 3 months; 2.03 at 6 months; 1.83 at 1 year) in glaucoma patients aged ≥40 years.

PrognosisCohortRetrospective Cohort Studyn=Glaucoma patients aged ≥40 years, propensity score matched

Topical carbonic anhydrase inhibitor (CAI) use was associated with increased hazards of anxiety disorders (aHR range 1.30-1.48; all P < 0.001) in glaucoma patients aged ≥40 years.

PrognosisCohortRetrospective Cohort Studyn=Glaucoma patients aged ≥40 years, propensity score matched