Abstract | PURPOSE: SETTING: Department of Ophthalmology, Akdeniz University, Antalya, Turkey. METHODS: RESULTS: The mean IOP changes from baseline were not statistically different between the study groups at 1, 2, and 3 hours and 7 days (P =.109, P = .764, P =.275, and P =.879, respectively). The incidence of IOP elevation of 5 mm Hg or higher was 12.2% (7 of 57 eyes) in the brinzolamide group and 10.3% (6 of 58 eyes) in the apraclonidine group (P = .743); IOP elevations of 10 mm Hg and greater occurred in 3.5% (2 of 57 eyes) and 1.7% (1 of 58 eyes) (P = .618), respectively. There were no IOP elevations greater than 20 mm Hg in either group. CONCLUSION:
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Authors | Mustafa Unal, Iclal Yücel, Yusuf Akar |
Journal | Journal of cataract and refractive surgery
(J Cataract Refract Surg)
Vol. 32
Issue 9
Pg. 1499-502
(Sep 2006)
ISSN: 0886-3350 [Print] United States |
PMID | 16931262
(Publication Type: Comparative Study, Journal Article, Randomized Controlled Trial)
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Chemical References |
- Adrenergic alpha-Agonists
- Carbonic Anhydrase Inhibitors
- Ophthalmic Solutions
- Sulfonamides
- Thiazines
- apraclonidine
- brinzolamide
- Clonidine
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Topics |
- Adrenergic alpha-Agonists
(therapeutic use)
- Adult
- Aged
- Aged, 80 and over
- Carbonic Anhydrase Inhibitors
(therapeutic use)
- Clonidine
(analogs & derivatives, therapeutic use)
- Double-Blind Method
- Female
- Humans
- Intraocular Pressure
(drug effects)
- Laser Therapy
(adverse effects)
- Lens Capsule, Crystalline
(pathology, surgery)
- Male
- Middle Aged
- Ocular Hypertension
(etiology, prevention & control)
- Ophthalmic Solutions
(therapeutic use)
- Postoperative Complications
(prevention & control)
- Premedication
- Prospective Studies
- Sulfonamides
(therapeutic use)
- Thiazines
(therapeutic use)
- Tonometry, Ocular
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