The Efficacy, Safety and Satisfaction Associated with Switching from Brinzolamide 1% and Brimonidine 0.1% to a Fixed Combination of Brinzolamide 1% and Brimonidine 0.1% in Glaucoma Patients

We evaluated glaucoma patients for the efficacy, safety and satisfaction associated with switching from brinzolamide 1% and brimonidine 0.1% to a fixed combination of brinzolamide 1% and brimonidine 0.1%. A total of 22 glaucoma patients were enrolled and completed this prospective, nonrandomized stu...

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Autores principales: Hiromitsu Onoe, Kazuyuki Hirooka, Mikio Nagayama, Atsushi Hirota, Hideki Mochizuki, Takeshi Sagara, Katsuyoshi Suzuki, Hideaki Okumichi, Yoshiaki Kiuchi
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Lenguaje:EN
Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/6fa3f659028946dfb297d7ceddd3d563
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spelling oai:doaj.org-article:6fa3f659028946dfb297d7ceddd3d5632021-11-25T18:00:40ZThe Efficacy, Safety and Satisfaction Associated with Switching from Brinzolamide 1% and Brimonidine 0.1% to a Fixed Combination of Brinzolamide 1% and Brimonidine 0.1% in Glaucoma Patients10.3390/jcm102252282077-0383https://doaj.org/article/6fa3f659028946dfb297d7ceddd3d5632021-11-01T00:00:00Zhttps://www.mdpi.com/2077-0383/10/22/5228https://doaj.org/toc/2077-0383We evaluated glaucoma patients for the efficacy, safety and satisfaction associated with switching from brinzolamide 1% and brimonidine 0.1% to a fixed combination of brinzolamide 1% and brimonidine 0.1%. A total of 22 glaucoma patients were enrolled and completed this prospective, nonrandomized study that evaluated patients who underwent treatment with at least brinzolamide 1% and brimonidine 0.1%. Patients on brinzolamide 1% and brimonidine 0.1% were switched to a brinzolamide/brimonidine fixed-combination ophthalmic suspension (BBFC). Evaluations of intraocular pressure (IOP), superficial punctate keratopathy (SPK) and conjunctival hyperemia were conducted at baseline and at 4 and 12 weeks. The Treatment Satisfaction Questionnaire for Medication-9 (TSQM-9) was utilized to assess the change in treatment satisfaction. At baseline and at 4 and 12 weeks, the IOP was 15.0 ± 4.1, 14.8 ± 4.1 and 14.8 ± 4.1 mmHg, respectively. There were no significant differences observed at any of the time points. However, the SPK score significantly decreased at 12 weeks, even though no significant differences were observed for the conjunctival hyperemia incidence at any of the time points. After switching from brinzolamide 1% and brimonidine 0.1% to BBFC, there was a significant increase in the TSQM-9 score for convenience and global satisfaction. Both an improvement in the degree of SPK and an increase in treatment satisfaction occurred after switching from brinzolamide 1% and brimonidine 0.1% to BBFC, even though there were sustained IOP values throughout the 12-week evaluation period.Hiromitsu OnoeKazuyuki HirookaMikio NagayamaAtsushi HirotaHideki MochizukiTakeshi SagaraKatsuyoshi SuzukiHideaki OkumichiYoshiaki KiuchiMDPI AGarticleglaucomabrinzolamidebrimonidinesatisfactionMedicineRENJournal of Clinical Medicine, Vol 10, Iss 5228, p 5228 (2021)
institution DOAJ
collection DOAJ
language EN
topic glaucoma
brinzolamide
brimonidine
satisfaction
Medicine
R
spellingShingle glaucoma
brinzolamide
brimonidine
satisfaction
Medicine
R
Hiromitsu Onoe
Kazuyuki Hirooka
Mikio Nagayama
Atsushi Hirota
Hideki Mochizuki
Takeshi Sagara
Katsuyoshi Suzuki
Hideaki Okumichi
Yoshiaki Kiuchi
The Efficacy, Safety and Satisfaction Associated with Switching from Brinzolamide 1% and Brimonidine 0.1% to a Fixed Combination of Brinzolamide 1% and Brimonidine 0.1% in Glaucoma Patients
description We evaluated glaucoma patients for the efficacy, safety and satisfaction associated with switching from brinzolamide 1% and brimonidine 0.1% to a fixed combination of brinzolamide 1% and brimonidine 0.1%. A total of 22 glaucoma patients were enrolled and completed this prospective, nonrandomized study that evaluated patients who underwent treatment with at least brinzolamide 1% and brimonidine 0.1%. Patients on brinzolamide 1% and brimonidine 0.1% were switched to a brinzolamide/brimonidine fixed-combination ophthalmic suspension (BBFC). Evaluations of intraocular pressure (IOP), superficial punctate keratopathy (SPK) and conjunctival hyperemia were conducted at baseline and at 4 and 12 weeks. The Treatment Satisfaction Questionnaire for Medication-9 (TSQM-9) was utilized to assess the change in treatment satisfaction. At baseline and at 4 and 12 weeks, the IOP was 15.0 ± 4.1, 14.8 ± 4.1 and 14.8 ± 4.1 mmHg, respectively. There were no significant differences observed at any of the time points. However, the SPK score significantly decreased at 12 weeks, even though no significant differences were observed for the conjunctival hyperemia incidence at any of the time points. After switching from brinzolamide 1% and brimonidine 0.1% to BBFC, there was a significant increase in the TSQM-9 score for convenience and global satisfaction. Both an improvement in the degree of SPK and an increase in treatment satisfaction occurred after switching from brinzolamide 1% and brimonidine 0.1% to BBFC, even though there were sustained IOP values throughout the 12-week evaluation period.
format article
author Hiromitsu Onoe
Kazuyuki Hirooka
Mikio Nagayama
Atsushi Hirota
Hideki Mochizuki
Takeshi Sagara
Katsuyoshi Suzuki
Hideaki Okumichi
Yoshiaki Kiuchi
author_facet Hiromitsu Onoe
Kazuyuki Hirooka
Mikio Nagayama
Atsushi Hirota
Hideki Mochizuki
Takeshi Sagara
Katsuyoshi Suzuki
Hideaki Okumichi
Yoshiaki Kiuchi
author_sort Hiromitsu Onoe
title The Efficacy, Safety and Satisfaction Associated with Switching from Brinzolamide 1% and Brimonidine 0.1% to a Fixed Combination of Brinzolamide 1% and Brimonidine 0.1% in Glaucoma Patients
title_short The Efficacy, Safety and Satisfaction Associated with Switching from Brinzolamide 1% and Brimonidine 0.1% to a Fixed Combination of Brinzolamide 1% and Brimonidine 0.1% in Glaucoma Patients
title_full The Efficacy, Safety and Satisfaction Associated with Switching from Brinzolamide 1% and Brimonidine 0.1% to a Fixed Combination of Brinzolamide 1% and Brimonidine 0.1% in Glaucoma Patients
title_fullStr The Efficacy, Safety and Satisfaction Associated with Switching from Brinzolamide 1% and Brimonidine 0.1% to a Fixed Combination of Brinzolamide 1% and Brimonidine 0.1% in Glaucoma Patients
title_full_unstemmed The Efficacy, Safety and Satisfaction Associated with Switching from Brinzolamide 1% and Brimonidine 0.1% to a Fixed Combination of Brinzolamide 1% and Brimonidine 0.1% in Glaucoma Patients
title_sort efficacy, safety and satisfaction associated with switching from brinzolamide 1% and brimonidine 0.1% to a fixed combination of brinzolamide 1% and brimonidine 0.1% in glaucoma patients
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/6fa3f659028946dfb297d7ceddd3d563
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