[1]王博,吴京,马明,等. 玻璃体内注射雷珠单抗与曲安奈德治疗糖尿病黄斑水肿的疗效对比分析[J].眼科新进展,2015,35(3):246-249.[doi:10.13389/j.cnki.rao.2015.0066]
 WANG Bo,WU Jing,MA Ming,et al. Clinictid effect comparison of intravitreal lucentis and triamcinolone acetonide for diabetic macular edema[J].Recent Advances in Ophthalmology,2015,35(3):246-249.[doi:10.13389/j.cnki.rao.2015.0066]
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 玻璃体内注射雷珠单抗与曲安奈德治疗糖尿病黄斑水肿的疗效对比分析
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《眼科新进展》[ISSN:1003-5141/CN:41-1105/R]

卷:
35卷
期数:
2015年3期
页码:
246-249
栏目:
应用研究
出版日期:
2015-03-05

文章信息/Info

Title:
 Clinictid effect comparison of intravitreal lucentis and triamcinolone acetonide for diabetic macular edema
作者:
 王博吴京马明李萍萍于健
 510515 广东省广州市,南方医科大学南方医院眼科
Author(s):
 WANG Bo WU Jing MA Ming LI Ping-Ping YU Jian
 Department of Ophthalmology , Nanfang Hospital of Southem Medical University, Guangzhou 5 105 15 , Guangdong Province , China
关键词:
 糖尿病黄斑水肿雷珠单抗曲安奈德玻璃体内注射
Keywords:
 diabetic macular edema lucentis triamcinolone acetonide intravitreal injection
DOI:
10.13389/j.cnki.rao.2015.0066
文献标志码:
A
摘要:
 目的 对比分析玻璃体内注射雷珠单抗与曲安奈德治疗糖尿病黄斑水肿的临床疗效。方法 选取就诊于我院眼科的糖尿病黄斑水肿患者47例(48眼),病程6~14个月;分为雷珠单抗组24例24眼,曲安奈德组23例24眼;分别给予玻璃体内注射雷珠单抗0.05mL与曲安奈德0.05mg,比较两组治疗1周、1个月、3个月、6个月患眼的最佳矫正视力、黄斑中心凹视网膜厚度、眼压及眼底黄斑区荧光素渗漏情况,观察治疗后的效果。结果 雷珠单抗组与曲安奈德组治疗后1周、1个月、3个月患眼的最佳矫正视力均得到提高,分别为0.08±0.02与0.06±0.03、0.21±0.03与0.17±0.05、0.29±0.07与0.27±0.04,治疗后短期内两组间差异无统计学意义(P值分别为0.082、0.092、0.320);治疗6个月后,曲安奈德组患眼的最佳矫正视力(0.18±0.03)有5例出现回降现象;而雷珠单抗组患眼的最佳矫正视力(0.28±0.09)变化趋于稳定,两组间的差异有统计学意义(P=0.003)。治疗后1周、1个月、3个月、6个月雷珠单抗组与曲安奈德组患眼的黄斑中心凹视网膜厚度分别为(336.00±94.71)μm与(378.00±89.74)μm、(251.00±63.55)μm与(273.00±81.29)μm、(263.00±59.42)μm与(267.00±49.32)μm、(238.00±42.61)μm与(298.00±33.27)μm,治疗后各时间点两组间的差异均无统计学意义(P=0.127、0.071、0.053、0.058)。另外,治疗后各时间点两组的眼压均在正常范围内,并且黄斑区荧光渗漏均无明显增强现象。结论 玻璃体内注射雷珠单抗和曲安奈德治疗糖尿病黄斑水肿,均能有效控制糖尿病视网膜病变患者病情发展并能改善视力。两种疗法的疗效在短期内差异无统计学意义,治疗6个月后,雷珠单抗疗效的稳定性优于曲安奈德。
Abstract:
 Objective To compare clinical effects of intravitreal lucentis ( LU ) and triamcinolone acetonide ( TA) for diabetic macular edema ( DME ). Methods Randomized controlled clinical retrospective study. Forty-seven patients ( 48 eyes) with DME in our hospital were chosen and divided into two groups , which were respectively intravitreal injected TA ( 0. 05 mg) and lucentis ( 0. 05 mL) . The duration was from 6 months t0 14 months. the changes of best corrected visual acuity ( BCVA) , central macular thickness ( CMT) .intraocular pressure and fundus fluorescein angiography ( FFA) in two groups at I week,l month,3 months and 6 months after treatment were compared between two groups, and clinical effects were observed. Results BCVA was improved in two groups at I week. I month ,3 months after treatment of lucentis and TA groups ,which were 0. 08 + 0. 02 and 0. 06 + 0. 03 .0. 21 + 0. 03 and 0. 17 + 0. 05 , 0. 29 + 0. 07 and 0. 27 + 0. 04 , respectively , there was no sigruficant difference ( P = 0. 082 ,0. 092 . 0. 320) . BCVA in TA group at 6 months after treatment was 0. 18 + 0. 03 .5 cases were decreased . while lucentis group kept stable vision acuity ( 0. 28 + 0. 09 ) , there was sigruficant difference(P = 0. 003) . CMT of lucentis group and TA group at I week.l month.3 months and 6 months after treatment were ( 336. 00 + 94. 71 ) ym and ( 378. 00 + 89. 74 ) ym , ( 251. 00 +63. 55 ) ym and ( 273. 00 +81. 29) ym , ( 263. 00 +59. 42) ym and ( 267. 00 + 49. 32 ) ym , ( 238. 00 + 42. 61 ) Vm and ( 298. 00 + 33. 27 ) Vm , respectively , there was no significant difference ( P = 0. 127 .0. 071 . 0. 053 , 0. 058 ) . A1l intraocular pressures were in the normal range and macular areas had no enhancing fluorescence leakage phenomenon after treatment in two groups. Conclusion Both intravitreal injection of lucentis and TA for DME can effectively control disease progression and improve visual acuity. Therapeutic effect is not significant between two methods in the short term . but after 6 months of treatment , the stability of lucentis is much better than that of TA.

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备注/Memo

备注/Memo:
 广东省自然科学基金(编号:S2012010008946、S201301001664)
更新日期/Last Update: 2015-03-04