Selected results of a post-registration observational study on the clinical efficacy and tolerability of Bimicombi Antiglau ECO and Brim Antiglau ECO in different stages of primary open-angle glaucoma in real-world clinical practice (Brim Bimicombi Antiglau Real World Ophthalmology, BRAWO)

Q4 Medicine
A. Kuroyedov, M. V. Kosakovskaya, O. V. Gapon’ko, V. Gorodnichiy, D. Lovpache, I. A. Bulakh
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引用次数: 0

Abstract

Aim: to assess the clinical efficacy and tolerability of bimatoprost/timolol (Bimicombi Antiglau ECO) and brimonidine (Brim Antiglau ECO) in different stages of primary open-angle glaucoma (POAG) compared with prior therapy. Patients and Methods: data from 1036 patients were included in the final protocol of the multicenter combined scientific and clinical study. All patients were diagnosed with POAG or were glaucoma suspects (GS) with ocular hypertension (OHT). All patients underwent a complex eye examination. Treatment with the drugs studied should have lasted 2 to 4 months. Treatment choice resulted from the lack of efficacy, ineffectiveness, or intolerance of prior therapies. The control study was conducted once not less than a month after inclusion in the study. Results: POAG (any stage) was diagnosed in 982 patients (94.8%), and GS with OHT were 54 patients (5.2%). Changing treatment regimen (in a planned manner) prevented tachyphylaxis and tolerance to previously prescribed drugs, which was established by IOP measurements (a 20% reduction in IOP compared with prior data). If the regimen was changed for any reason (overall, 6 reasons were analyzed), three most common reasons were poor clinical efficacy (36.6%), discomfort (26.6%), and poor tolerability (23.9%). Prescription of preservative-free IOP-lowering medications (eye drops studied) for 1 month after the washout period significantly (by 19 times) reduced the number of these complaints. Preservative-free medications significantly increase the maximum satisfaction with prescribed treatment regimens (Likert score 4.61 of 5) and largely meet the expectations of doctors in terms of drug efficacy and tolerability (Likert score 4.67 of 5). Conclusion: preservative-free IOP-lowering medications (eye drops studied) are effective and well tolerated. KEYWORDS: glaucoma therapy, efficacy, tolerability, bimatoprost/timolol, brimonidine, primary open-angle glaucoma, real-world clinical practice, BRAWO. FOR CITATION: Kuroyedov A.V., Kosakovskaya M.V., Gapon'ko O.V., Gorodnichiy V.V., Lovpache D.N., Bulakh I.A. Selected results of a post- registration observational study on the clinical efficacy and tolerability of Bimicombi Antiglau ECO and Brim Antiglau ECO in different stages of primary open-angle glaucoma in real-world clinical practice (Brim Bimicombi Antiglau Real World Ophthalmology, BRAWO). Russian Journal of Clinical Ophthalmology. 2023;23(3):129–135 (in Russ.). DOI: 10.32364/2311-7729-2023-23-3-4.
Bimicombi Antiglau ECO和Brim Antiglau ECO在不同阶段原发性开角型青光眼临床实践中的临床疗效和耐受性的注册后观察研究(Brim Bimicombi Antiglau Real World Ophthalmology, BRAWO)
目的:比较比马前列素/替莫洛尔(Bimicombi Antiglau ECO)和溴莫尼定(Brim Antiglau ECO)治疗不同阶段原发性开角型青光眼(POAG)的临床疗效和耐受性。患者和方法:1036例患者的数据被纳入多中心科学与临床联合研究的最终方案。所有患者均被诊断为POAG或疑似青光眼(GS)伴高眼压(OHT)。所有患者都接受了复杂的眼部检查。所研究的药物治疗应持续2至4个月。治疗选择是由于缺乏疗效、无效或先前治疗的不耐受。对照研究在纳入研究后不少于一个月进行一次。结果:POAG(任何分期)982例(94.8%),GS合并OHT 54例(5.2%)。改变治疗方案(以计划的方式)可以防止快速反应和对先前处方药物的耐受性,这是通过IOP测量(与先前的数据相比,IOP降低了20%)确定的。如果因任何原因改变方案(总共分析了6个原因),最常见的三个原因是临床疗效差(36.6%)、不适(26.6%)和耐受性差(23.9%)。洗脱期后1个月服用不含防腐剂的降低眼压药物(研究了眼药水),显著(减少了19倍)减少了这些投诉的数量。无防腐剂药物显著提高了患者对处方治疗方案的最大满意度(Likert评分为4.61(5分)),在药物疗效和耐受性方面基本符合医生的预期(Likert评分为4.67(5分))。结论:无防腐剂降眼压药物(研究滴眼液)有效且耐受性良好。关键词:青光眼治疗,疗效,耐受性,比马前列素/替莫洛尔,溴莫尼定,原发性开角型青光眼,现实世界的临床实践,BRAWO。引文:Kuroyedov a.v., Kosakovskaya m.v., Gapon'ko o.v., Gorodnichiy v.v., Lovpache D.N, Bulakh I.A.注册后观察性研究的结果,研究了Bimicombi Antiglau ECO和Brim Antiglau ECO在现实世界临床实践中不同阶段原发性开角型青光眼的临床疗效和耐受性(Brim Bimicombi Antiglau Real World Ophthalmology, BRAWO)。俄罗斯临床眼科学杂志。2023;23(3):129-135。DOI: 10.32364 / 2311-7729-2023-23-3-4。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.60
自引率
0.00%
发文量
21
审稿时长
20 weeks
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