在人工小切口白内障手术中使用局部药剂和巩膜内药散瞳的比较 - 随机对照试验

Ibukunoluwa James Adeogun, B. Adekoya, Modupe Medina Balogun
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引用次数: 0

摘要

这项研究的目的是评估和比较巩膜内药雾化溶液与传统局部用药在完成黑人人工小切口白内障手术(MSICS)中的疗效。这项随机对照试验在 102 名接受腱膜下阻滞术的 MSICS 患者中进行。局部用药组患者在术前使用托吡卡胺 0.8%和苯肾上腺素 5%的局部扩张复合剂,而巩膜内用药组患者在不进行扩张的情况下开始手术,术中使用利多卡因 0.5%和肾上腺素 0.001%的巩膜内溶液实现瞳孔散大。在手术前和手术中的四个不同时间点,对瞳孔大小进行了连续测量。记录两组患者中需要补充散瞳剂的比例以及术后针孔视力(VA)。数据分析采用社会科学统计产品和服务解决方案(SPSS)25.0 版(伊利诺伊州芝加哥市,IBM)进行。在 95% 的置信区间内,统计显著性水平设定为 P < 0.05。局部用药组在散瞳和阻滞前的平均瞳孔直径为 2.5 ± 0.6 毫米,鞘内用药组为 2.5 ± 0.7 毫米(P = 0.752)。使用任何一种瞳孔散大剂后,瞳孔直径分别增至 7.7 ± 1.1 毫米和 7.4 ± 0.8 毫米(P = 0.134)。之后,两组患者的平均瞳孔直径都逐渐缩小,但巩膜内组在每个测量点的平均瞳孔直径都显著增大(P < 0.05)。术后,两组患者的视力无明显差异(P < 0.05)。使用利多卡因和肾上腺素的巩膜内混合物可在不进行术前散瞳的情况下为成功完成 MSICS 提供足够的瞳孔散大作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of pupil dilation in manual small incision cataract surgery using topical versus intracameral mydriatic agents – A randomised controlled trial
The purpose of this research is to assess and compare the efficacy of an intracameral mydriatic solution with conventional topical agents in the completion of manual small incision cataract surgery (MSICS) in a black population. This randomised controlled trial was conducted among 102 patients undergoing MSICS under sub-tenon’s block. Mydriasis in the topical group was achieved with a pre-operative topical dilating combination of tropicamide 0.8% and phenylephrine 5% while surgery was commenced in patients in the intracameral group without dilation, and mydriasis was achieved intraoperatively with an intracameral solution of lidocaine 0.5% and adrenaline 0.001%. Pupil sizes were measured serially, before, and at four different junctures during surgery. The proportion of patients needing supplementary mydriasis in either group was noted, as well as post-operative pinhole visual acuity (VA). Data analysis was carried out using the Statistical Package for the Social Sciences Statistical Product and Service Solutions(SPSS) version 25.0 (IBM, Chicago, Illinois). The level of statistical significance was set at P < 0.05 at a 95% confidence interval. Mean pupil diameter before dilating and blocking was 2.5 ± 0.6 mm in the topical group and 2.5 ± 0.7 mm in the intracameral group (P = 0.752). This increased to 7.7 ± 1.1 mm and 7.4 ± 0.8 mm, respectively (P = 0.134), after administering either mydriatic agents. After that, mean pupil diameter progressively reduced in both groups but was significantly higher in the intracameral group at each point of measurement (P < 0.05). Postoperatively, there was no significant difference in the VA between the two groups (P < 0.05). Using an intracameral mixture of lidocaine and adrenaline gives adequate mydriasis for the successful completion of MSICS without pre-operative dilation.
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