首页> 外文期刊>Journal of cataract and refractive surgery >Efficacy of topical plus intracameral anesthesia for cataract surgery in high myopia: randomized controlled trial.
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Efficacy of topical plus intracameral anesthesia for cataract surgery in high myopia: randomized controlled trial.

机译:局部加前庭麻醉在高度近视白内障手术中的功效:随机对照试验。

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PURPOSE: To assess the efficacy of intracameral lidocaine supplementation of topical anesthesia during cataract surgery in eyes with high myopia. SETTING: Department of Ophthalmology, Ospedale San Pietro-Fatebenefratelli, Rome, Italy. METHODS: This prospective double-blind study comprised 120 highly myopic eyes with an axial length (AL) greater than 26.0 mm scheduled for routine cataract surgery. Cases were divided into 2 groups of 60 eyes each. One group received a placebo of balanced salt solution (BSS) (control group) and the other group, a supplement of 0.1 mL preservative-free lidocaine hydrochloride 1% injected in the capsular bag during hydrodissection (lidocaine group). Intraoperative pain was assessed by recording spontaneous patient reports of sensation of pain or ocular discomfort during 3 surgical stages: phaco tip insertion, irrigation/aspiration (I/A) system insertion for cortical aspiration, I/A system insertion for ophthalmic viscosurgical device removal after intraocular lens implantation. Postoperative pain was assessed on a visual analog scale (range 0 to 10). Data were compared by chi-square and Mann-Whitney U tests. RESULTS: The overall mean AL was 28.58 mm (28.57 mm control group; 28.50 mm lidocaine group). Fewer patients in the lidocaine group reported intraoperative pain, ocular discomfort, or tissue manipulation (odds ratio=0.36; 95% confidence interval, 0.16-0.80; P= .019). The mean postoperative pain score was 1.88+/-2.17 (SD) in the control group and 1.36+/-2.02 in the lidocaine group; the difference was not statistically significant (P= .21). CONCLUSION: Intracameral lidocaine supplementation for cataract surgery may improve intraoperative comfort under topical anesthesia in highly myopic eyes.
机译:目的:评估在高度近视眼白内障手术期间局部麻醉中使用前房内利多卡因补充局部麻醉的疗效。地点:意大利罗马的圣彼得罗·费特内菲拉泰利医院眼科。方法:这项前瞻性双盲研究包括120例高度近视眼,其轴向长度(AL)大于26.0 mm,计划用于常规白内障手术。将病例分为两组,每组60只眼。一组接受安慰剂平衡盐溶液(BSS)(对照组),另一组接受在水解剖过程中向囊袋中注入0.1 mL不含防腐剂的盐酸利多卡因1%的补充剂(利多卡因组)。通过记录三个手术阶段中自发的疼痛或眼部不适感的患者报告来评估术中疼痛:超声乳化吸除术,用于皮层抽吸的冲洗/抽吸(I / A)系统插入,用于在手术后移除眼科内窥镜手术器械的I / A系统插入人工晶状体植入。以视觉模拟量表(0到10)评估术后疼痛。通过卡方检验和Mann-Whitney U检验比较数据。结果:总平均AL为28.58 mm(对照组为28.57 mm;利多卡因组为28.50 mm)。利多卡因组中较少的患者报告术中出现疼痛,眼部不适或组织操作(赔率= 0.36; 95%置信区间为0.16-0.80; P = 0.019)。对照组的平均术后疼痛评分为1.88 +/- 2.17(SD),利多卡因组的平均术后疼痛评分为1.36 +/- 2.02;差异无统计学意义(P = 0.21)。结论:对于高度近视眼,在白内障手术中补充前房内利多卡因可改善局部麻醉下的术中舒适度。

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