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Atropine 0.01% eye drops slow myopia progression: a systematic review and Meta-analysis 被引量:10
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作者 Ying Zhao Kai Feng +4 位作者 Rui-Bao Liu Jin-Hua Pan Lai-Lin Zhang Zhu-Ping Xu Xue-Jing Lu 《International Journal of Ophthalmology(English edition)》 SCIE CAS 2019年第8期1337-1343,共7页
AIM: To evaluate the effects of atropine 0.01% on slowing myopia progression. METHODS: We searched for relevant studies in the Cochrane Library, PubMed, Embase, Ovid, CBM, CNKI, VIP and Wan Fang Data in Chinese. A sup... AIM: To evaluate the effects of atropine 0.01% on slowing myopia progression. METHODS: We searched for relevant studies in the Cochrane Library, PubMed, Embase, Ovid, CBM, CNKI, VIP and Wan Fang Data in Chinese. A supplementary search was conducted in OpenGrey(System for Information on Grey Literature in Europe), the ISRCTN registry, Clinical Trials.gov, and the WHO International Clinical Trials Registry Platform(ICTRP) from the dates of inception to June 30, 2018. RESULTS: Seven randomized controlled trials(RCTs) with a total of 1079 subjects were included(505 in the atropine 0.01% group and 574 in the control group). The results showed that the atropine 0.01% group exhibited significantly greater control of axial growth than the control group (MD=-0.12, 95%CI(-0.19,-0.06))There was also a statistically significant difference between the atropine 0.01% and control groups in the changes in axial length [MD=-0.14, 95%CI(-0.25,-0.03)], but the quality of evidence was low. There were no significant differences between the atropine 0.01% and control groups in the overall effect with respect to diopter value, change in diopter, distance vision and intraocular pressure (MD=0.08, 95%CI(-0.27, 0.42);MD=0.09, 95%CI(-0.17, 0.36);MD=-0.01, 95%CI(-0.02, 0.00);MD=0.08, 95%CI(-0.56,0.40))The sensitivity analysis showed that the conclusion of the Meta-analysis is relatively stable. With respect to adverse events, there were significant differences between the atropine 0.01% and control groups (OR=0.26, 95%CI(0.11, 0.61))CONCLUSION: Based on the available evidence, atropine 0.01% eye drops offer benefits in controlling axial growth and safety without causing significant differences in diopter values, distance vision and intraocular pressure. 展开更多
关键词 atropine 0.01% eye drops MYOPIA systematic REVIEW META-ANALYSIS
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不同浓度阿托品制剂治疗屈光不正患者的疗效及安全性 被引量:24
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作者 张晓瑾 周磊 《中国生化药物杂志》 CAS 2016年第11期106-108,111,共4页
目的探讨不同浓度阿托品制剂治疗屈光不正患者的疗效及安全性。方法选取2014年4月-2015年8月宁波市眼科医院收治的近视性屈光不正患者123例,按随机数字表法分为3组,每组各41例,高浓度组予以0.1%硫酸阿托品滴眼液治疗,低浓度组予以0.01%... 目的探讨不同浓度阿托品制剂治疗屈光不正患者的疗效及安全性。方法选取2014年4月-2015年8月宁波市眼科医院收治的近视性屈光不正患者123例,按随机数字表法分为3组,每组各41例,高浓度组予以0.1%硫酸阿托品滴眼液治疗,低浓度组予以0.01%硫酸阿托品滴眼液治疗,对照组给予人工泪液滴眼,观察1年后3组远视力、屈光度、眼压及眼轴长度变化状况。结果治疗后,3组远视力差值比较,高浓度组〉低浓度组〉对照组(P〈0.05);3组治疗前后屈光度、眼压、眼轴长度差值比较,对照组〉低浓度组〉高浓度组(P〈0.05);低浓度组总有效率85.37%与高浓度组90.24%比较差异无统计学意义;高浓度组不良反应发生率21.95%与低浓度组4.88%比较,差异具有统计学意义(P〈0.05)。结论 0.1%与0.01%浓度阿托品均有效控制近视性屈光不正屈光度、眼轴长度进展,进而提高远视力,前者效果更佳,后者安全性较高。 展开更多
关键词 0.1%浓度阿托品制剂 0.01%浓度阿托品制剂 近视性屈光不正 安全性
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