Evaluation and comparison of the safety profile of topical anti-glaucoma drugs in patients of primary open angle glaucoma or ocular hypertension or normal tension glaucoma

P. Bhagat, Kinjal Y Trivedi
{"title":"Evaluation and comparison of the safety profile of topical anti-glaucoma drugs in patients of primary open angle glaucoma or ocular hypertension or normal tension glaucoma","authors":"P. Bhagat, Kinjal Y Trivedi","doi":"10.15713/INS.CLEVER.51","DOIUrl":null,"url":null,"abstract":"Aim: The aim of the the study was to evaluate and to compare the side effects of topical anti-glaucoma drugs in patients of POAG, OHT, ad NTG. Introduction: Topical drugs are the mainstay of glaucoma management but are associated with various adverse effects which can influence compliance and quality of life of the patient. Materials and Methods: We studied 308 eyes of 154 patients above 15 years, having POAG, OHT, or NTG and using at least one anti-glaucoma medication. A structured validated questionnaire was used followed by ocular examination to collect data which were analyzed statistically. Results: Out of 308 eyes of 154 patients, 80.51% patients experienced at least one side effect, more in females. The incidence increased to 72.52%, 92.10%, 91.66%, and 100% among 50–59, 60–69, 70–79, and 80–89 age groups, respectively. TBUT was normal in 62.79% eyes when duration of therapy was ≤ 5 years but not when beyond 11 years and normal only in 34% eyes exposed to benzalkonium chloride. Only 8.45% patients experienced systemic side effects but none required emergency care. Change of therapy due to side effects occurred in 8.11% patients. Conclusion: Topical anti-glaucoma drugs are quite safe but incidence of side effects increases with age, duration of therapy, and number of medications. Although few, they affect the quality of life and compliance potentially limiting success of the treatment. Clinical Significance: Knowledge of side effects helps us in tailoring, monitoring, and revising treatment as necessary, to minimize side effects and maximize outcomes.","PeriodicalId":130091,"journal":{"name":"Clinical and Experimental Vision and Eye Research","volume":"34 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical and Experimental Vision and Eye Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15713/INS.CLEVER.51","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2

Abstract

Aim: The aim of the the study was to evaluate and to compare the side effects of topical anti-glaucoma drugs in patients of POAG, OHT, ad NTG. Introduction: Topical drugs are the mainstay of glaucoma management but are associated with various adverse effects which can influence compliance and quality of life of the patient. Materials and Methods: We studied 308 eyes of 154 patients above 15 years, having POAG, OHT, or NTG and using at least one anti-glaucoma medication. A structured validated questionnaire was used followed by ocular examination to collect data which were analyzed statistically. Results: Out of 308 eyes of 154 patients, 80.51% patients experienced at least one side effect, more in females. The incidence increased to 72.52%, 92.10%, 91.66%, and 100% among 50–59, 60–69, 70–79, and 80–89 age groups, respectively. TBUT was normal in 62.79% eyes when duration of therapy was ≤ 5 years but not when beyond 11 years and normal only in 34% eyes exposed to benzalkonium chloride. Only 8.45% patients experienced systemic side effects but none required emergency care. Change of therapy due to side effects occurred in 8.11% patients. Conclusion: Topical anti-glaucoma drugs are quite safe but incidence of side effects increases with age, duration of therapy, and number of medications. Although few, they affect the quality of life and compliance potentially limiting success of the treatment. Clinical Significance: Knowledge of side effects helps us in tailoring, monitoring, and revising treatment as necessary, to minimize side effects and maximize outcomes.
外用抗青光眼药物治疗原发性开角型青光眼、高眼压型青光眼和正常眼压型青光眼的安全性评价与比较
目的:本研究的目的是评价和比较局部抗青光眼药物对POAG、OHT和NTG患者的副作用。外用药物是青光眼治疗的主要手段,但其副作用会影响患者的依从性和生活质量。材料和方法:我们研究了154例15岁以上患者的308只眼睛,这些患者患有POAG、OHT或NTG,并至少使用一种抗青光眼药物。采用结构化的有效问卷,然后进行眼部检查,收集数据并进行统计分析。结果:在154例患者308只眼中,80.51%的患者出现了至少一种副作用,女性患者较多。50 ~ 59岁、60 ~ 69岁、70 ~ 79岁和80 ~ 89岁年龄组的发病率分别为72.52%、92.10%、91.66%和100%。治疗时间≤5年的眼TBUT正常的有62.79%,超过11年的眼TBUT不正常,暴露于苯扎氯铵的眼TBUT正常的只有34%。只有8.45%的患者出现全身副作用,但没有人需要紧急护理。8.11%的患者因不良反应而改变治疗方案。结论:局部抗青光眼药物是相当安全的,但副作用的发生率随年龄、治疗时间和用药次数的增加而增加。虽然很少,但它们会影响生活质量和依从性,可能会限制治疗的成功。临床意义:对副作用的了解有助于我们在必要时调整、监测和修改治疗方案,以最大限度地减少副作用和提高疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信