Suppr超能文献

布林佐胺/噻吗洛尔固定复方制剂用于曾使用溴莫尼定/噻吗洛尔固定复方制剂的拉丁美洲开角型青光眼或高眼压症患者的疗效和耐受性

Efficacy and tolerability of fixed-combination brinzolamide/timolol in Latin American patients with open-angle glaucoma or ocular hypertension previously on brimonidine/timolol fixed combination.

作者信息

Alezzandrini Arturo, Hubatsch Douglas, Alfaro Rene

机构信息

University of Buenos Aires, Buenos Aires, Argentina,

出版信息

Adv Ther. 2014 Sep;31(9):975-85. doi: 10.1007/s12325-014-0145-5. Epub 2014 Aug 20.

Abstract

INTRODUCTION

Fixed-combination glaucoma medications are commonly used to achieve target intraocular pressure (IOP) reduction in patients uncontrolled with monotherapy; however, ocular discomfort associated with eye drops can decrease adherence. This study assessed the efficacy and tolerability of twice-daily fixed-combination brinzolamide 1%/timolol 0.5% (BRINZ/TIM-FC) in Latin American patients transitioned from fixed-combination brimonidine 0.2%/timolol 0.5% (BRIM/TIM-FC) because of insufficient IOP control or treatment intolerance.

METHODS

This 8-week, open-label, prospective study was conducted at six sites in Argentina, Chile, and Mexico. Enrolled patients were aged ≥18 years with open-angle glaucoma (including primary, exfoliative, or pigment-dispersion glaucoma) or ocular hypertension with IOP of 19-35 mmHg in ≥1 eye at baseline (on BRIM/TIM-FC). Patients self-administered BRINZ/TIM-FC to both eyes at 8 a.m. and 8 p.m. daily for 8 weeks. The primary and secondary efficacy endpoints were mean IOP change from baseline at week 8 and percentage of patients achieving target IOP (≤18 mmHg) at week 8, respectively. Exploratory endpoints included patient and investigator preference for treatment at week 8. Adverse events (AEs) were assessed as the safety endpoint.

RESULTS

Fifty patients (mean ± SD age, 66.7 ± 11.5 years) received BRINZ/TIM-FC, and 49 were included in the intent-to-treat population. Mean ± SD IOP was significantly reduced from baseline after 8 weeks of treatment with BRINZ/TIM-FC (-3.6 ± 3.0 mmHg; P < 0.0001, Wilcoxon signed-rank test; 17.1% reduction). Overall, 55.3% of patients achieved IOP ≤18 mmHg at week 8. Significantly more patients (89.4%) and investigators (95.7%) preferred BRINZ/TIM-FC to BRIM/TIM-FC (both P < 0.0001, exact binomial test). Of the 13 AEs observed, 8 were related to BRINZ/TIM-FC; the most common treatment-related AEs were eye irritation (n = 4) and abnormal sensation in the eye (n = 2).

CONCLUSION

BRINZ/TIM-FC provides an effective and well-tolerated treatment option for patients transitioned from BRIM/TIM-FC.

摘要

引言

固定复方青光眼药物常用于降低单药治疗无法控制眼压(IOP)的患者的目标眼压;然而,滴眼液引起的眼部不适会降低依从性。本研究评估了每日两次的固定复方布林佐胺1%/噻吗洛尔0.5%(BRINZ/TIM-FC)对因眼压控制不佳或治疗不耐受而从固定复方溴莫尼定0.2%/噻吗洛尔0.5%(BRIM/TIM-FC)转换过来的拉丁美洲患者的疗效和耐受性。

方法

这项为期8周的开放标签前瞻性研究在阿根廷、智利和墨西哥的六个地点进行。入选患者年龄≥18岁,患有开角型青光眼(包括原发性、剥脱性或色素性青光眼)或眼压升高,基线时(使用BRIM/TIM-FC)至少一只眼睛的眼压为19-35 mmHg。患者每天上午8点和晚上8点自行将BRINZ/TIM-FC滴入双眼,持续8周。主要和次要疗效终点分别是第8周时眼压相对于基线的平均变化以及第8周时达到目标眼压(≤18 mmHg)的患者百分比。探索性终点包括第8周时患者和研究者对治疗的偏好。不良事件(AE)被评估为安全性终点。

结果

50名患者(平均±标准差年龄,66.7±11.5岁)接受了BRINZ/TIM-FC治疗,49名患者被纳入意向性分析人群。使用BRINZ/TIM-FC治疗8周后,眼压平均±标准差较基线显著降低(-3.6±3.0 mmHg;P<0.0001,Wilcoxon符号秩检验;降低17.1%)。总体而言,55.3%的患者在第8周时眼压≤18 mmHg。明显更多的患者(89.4%)和研究者(95.7%)更喜欢BRINZ/TIM-FC而非BRIM/TIM-FC(两者P<0.0001,精确二项式检验)。在观察到的13例不良事件中,8例与BRINZ/TIM-FC相关;最常见的与治疗相关的不良事件是眼部刺激(n = 4)和眼部异常感觉(n = 2)。

结论

对于从BRIM/TIM-FC转换过来的患者,BRINZ/TIM-FC提供了一种有效且耐受性良好的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a993/4177101/bbec37545ad3/12325_2014_145_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验