A Comparative Study on Efficacy of Intraocular Pressure Lowering of Two Fixed-Dose Antiglaucoma Drug Combination Brinzolamide-Brimonidine Versus Latanoprost-Timolol in Primary Open-Angle Glaucoma and Ocular Hypertension
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作者:
Mishra, Avinash
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机构:
Mil Hosp, Dept Ophthalmol, Jalandhar 144001, Punjab, IndiaMil Hosp, Dept Ophthalmol, Jalandhar 144001, Punjab, India
Mishra, Avinash
[1
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Agrawal, Mohini
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Mil Hosp, Dept Ophthalmol, Jalandhar 144001, Punjab, IndiaMil Hosp, Dept Ophthalmol, Jalandhar 144001, Punjab, India
Agrawal, Mohini
[1
]
Tripathi, Anchal
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Mil Hosp, Dept Ophthalmol, Jammu, IndiaMil Hosp, Dept Ophthalmol, Jalandhar 144001, Punjab, India
Tripathi, Anchal
[2
]
Bhirud, Atul
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Mil Hosp, Dept Ophthalmol, Jalandhar 144001, Punjab, IndiaMil Hosp, Dept Ophthalmol, Jalandhar 144001, Punjab, India
Bhirud, Atul
[1
]
Kumar, Lt Col Rajnish
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Mil Hosp, Dept Ophthalmol, Danapur, IndiaMil Hosp, Dept Ophthalmol, Jalandhar 144001, Punjab, India
glaucoma;
ocular hypertension;
open angle;
fixed-drug combination;
Brinzolamide-Brimonidine;
Latanoprost-Timolol;
RESIDENT COMPLIANCE;
AMERICAN ACADEMY;
PERSISTENCE;
SAFETY;
0.2-PERCENT;
PATTERNS;
THERAPY;
TRIAL;
D O I:
10.1089/jop.2023.0186
中图分类号:
R77 [眼科学];
学科分类号:
100212 ;
摘要:
Purpose: To compare the efficacy of Brinzolamide-Brimonidine (BB) (1%+0.2%) with the gold standard Latanoprost-Timolol (LT) (0.005%+0.5%) in treating primary open-angle glaucoma (POAG) and ocular hypertension (OHT). Methods: A 1-year prospective study, spanning from May 2022 to May 2023, conducted at a tertiary eye-care hospital. Participants, aged 40-60, with a baseline intraocular pressure (IOP) >21 mm Hg, requiring a >30% reduction, were enrolled. Group A (n = 100) received BB, and Group B (n = 100) received LT. Outcomes were assessed at 1 month (IOP difference from baseline), 3 and 6 months (mean diurnal variations). Results: The mean age at presentation was 55.5 +/- 4.5 years in Group A and 54.7 +/- 4.2 years in Group B. At 1 month, Group A exhibited a mean IOP of 18.7 mm Hg, while Group B had 17.6 mm Hg, with no statistically significant difference (P = 0.53). No significant diurnal variation was observed in either group (P = 0.07). Target pressure was achieved in 88% of patients in Group A and slightly higher at 92% in Group B. Moreover, no serious side effects were reported, and compliance was higher in Group B (98%) compared to Group A (96%). Conclusion: Although LT showed slightly better and sustained IOP reduction, the difference was not statistically significant. Both BB and LT demonstrated comparable outcomes for managing POAG and OHT.
机构:
Univ Clin Ctr Kosovo, Pristina, KosovoUniv Pristina Hasan Prishtina, Fac Med, Prishtina, Kosovo
Hoxha, Gentian
Hoxha, Fellanza Ismajli
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Univ Clin Ctr Kosovo, Pristina, KosovoUniv Pristina Hasan Prishtina, Fac Med, Prishtina, Kosovo
Hoxha, Fellanza Ismajli
Shoshi, Flaka
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机构:
Univ Pristina Hasan Prishtina, Fac Med, Prishtina, Kosovo
Univ Clin Ctr Kosovo, Pristina, KosovoUniv Pristina Hasan Prishtina, Fac Med, Prishtina, Kosovo