Shah Alpesh R, Diwan Rasesh P, Vasavada Abhay R, Keng Manzoor Qadir
Iladevi Cataract & IOL Research Centre, Ahmedabad, India.
Indian J Ophthalmol. 2004 Jun;52(2):133-8.
To evaluate the effect of intracameral preservative-free 1% xylocaine on the corneal endothelium as an adjuvant to topical anaesthesia during phacoemulsification and Acrysof foldable IOL implantation.
MATERIAL & METHODS: This is a prospective, controlled, randomised, double-masked study. 106 patients with soft to moderately dense (Grade 1-3) senile cataract and corneal endothelial cell density of >1500/mm2 were randomised to the xylocaine group (n=53) and control group(n=53). Central endothelial specular microscopy and ultrasound corneal pachymetry were performed preoperatively. On the first postoperative day the eyes were evaluated for corneal oedema and Descemet's folds. Ultrasound corneal pachymetry was performed at 1, 3 and 12 months. Specular microscopy was performed at 3 and 12 months. Cell loss was expressed as a percentage of preoperative cell density. Six patients could not complete one year follow-up. Chi-square and paired t test (2 tail) statistical tests were applied for analysis.
Four (7.54%) patients in the xylocaine group and 5 (9.43%) in the control group had a few Descemet's folds associated with mild central stromal oedema. Corneal thickness increased from 549.3micro +/- 37.2micro to 555.5micro +/- 36.5micro in the xylocaine group and from 553.1micro +/- 36.2micro to 559.3micro +/- 40.5micro in the control group at the one-month postoperative visit. Thickness returned to the preoperative level in xylocaine group 549.6micro +/- 34.5micro and control group 554.7micro +/- 41.1micro at three months. (P=0.484) The percentage of cell loss was 4.47 +/- 2.53% in the xylocaine group and 4.49 +/- 3.09% in the control group at one year. (P=0.97)
Intracameral preservative-free 1% xylocaine does not appear to affect corneal endothelium adversely during phacoemulsification.
评估前房内注射不含防腐剂的1%利多卡因作为超声乳化白内障吸除术及Acrysof可折叠人工晶状体植入术中表面麻醉辅助用药时对角膜内皮的影响。
这是一项前瞻性、对照、随机、双盲研究。106例患有软性至中度致密(1-3级)老年性白内障且角膜内皮细胞密度>1500/mm²的患者被随机分为利多卡因组(n=53)和对照组(n=53)。术前进行中央内皮细胞镜检查和超声角膜测厚。术后第一天评估眼睛的角膜水肿和后弹力层皱襞情况。在术后1个月、3个月和12个月时进行超声角膜测厚。在术后3个月和12个月时进行内皮细胞镜检查。细胞丢失以术前细胞密度的百分比表示。6例患者未能完成一年的随访。采用卡方检验和配对t检验(双侧)进行统计分析。
利多卡因组有4例(7.54%)患者和对照组有5例(9.43%)患者出现一些与轻度中央基质水肿相关的后弹力层皱襞。术后1个月时,利多卡因组角膜厚度从549.3μm±37.2μm增加至555.5μm±36.5μm,对照组从553.1μm±36.2μm增加至559.3μm±40.5μm。术后3个月时,利多卡因组角膜厚度恢复至术前水平549.6μm±34.5μm,对照组为554.7μm±41.1μm。(P=0.484)一年时,利多卡因组细胞丢失百分比为4.47±2.53%,对照组为4.49±3.09%。(P=0.97)
前房内注射不含防腐剂的1%利多卡因在超声乳化白内障吸除术中似乎不会对角膜内皮产生不良影响。