影响小晶状体提取Pro®(VISUMAX 800)后视力结果的因素。

Muhammad Irfan Kamaruddin, Ucok Parlindungan Pasaribu, Tjahyono Darminto Gondhowiardjo
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引用次数: 0

摘要

目的:本研究旨在报告使用VISUMAX 800 (Carl Zeiss Meditec AG)治疗眼睛的早期经验中影响小切口晶状体摘除(SMILE)后视力结果的因素。方法:这是一项回顾性研究,在印度尼西亚雅加达JEC @Kedoya眼科医院使用VISUMAX 800进行SMILE Pro®手术。患者年龄在40岁及以下,矫正距离视力(CDVA)为bbb20 /25,明显屈光球等效(SE)≤10.0屈光度(D),圆柱体屈光。结果:分析132例患者共258眼。术后1个月未矫正距离视力(UDVA)达到20/20的94%。高度近视眼UDVA达到20/20的比例为81%,中度近视眼为97%,低度近视眼为99%。球等效折射(SER) (r = 0.273, p < 0.01)、视区(OZ) (r = 0.260, p < 0.01)、帽帽厚度(r = 0.209, p < 0.01)、残余间质厚度(RST) (r = 0.256, p < 0.01)与术后1个月UDVA的相关性较弱,但有统计学意义。结论:SMILE Pro®在术后早期具有良好的视觉效果。低中度近视患者的视力优于高度近视患者。小体积,薄帽厚度和低RST可能增加SMILE后不能获得最大视力结果的风险。为充分了解影响SMILE术后VA的因素,需要前瞻性设计和较长随访时间,包括综合变量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Factors Affecting Visual Outcome After Small Lenticule Extraction Pro® (VISUMAX 800).

Purpose: This study aimed to report factors affected visual outcome after small incision lenticule extraction (SMILE) in the early experience of treating eyes with VISUMAX 800 (Carl Zeiss Meditec AG).

Methods: This is a retrospective study with cross-sectional design of eyes underwent SMILE Pro® using VISUMAX 800 in JEC @Kedoya Eye Hospital Jakarta, Indonesia. Patients 40 years old or younger with the corrected distance visual acuity (CDVA) of >20/25, manifest refractive spherical equivalent (SE) ≤10.0 diopters (D), cylinder refraction <5.0 D were included. Evaluation of visual outcome was conducted at 1 day and 1 month postoperatively. All statistical analyses were performed using the SPSS v. 26.0 software (IBM Corp.) based on data normality.

Results: A total of 258 eyes from 132 patients were analyzed. 94% of eyes achieve uncorrected distance visual acuity (UDVA) 20/20 1-month post operatively. 81% of high myopic eye achieve UDVA 20/20 following by 97% and 99% in moderate and low myopic eyes, respectively. Spherical equivalent refraction (SER) (r = 0.273; p < 0.01), optic zone (OZ) (r = 0.260; p < 0.01), cap thickness (r = 0.209; p < 0.01), and residual stromal thickness (RST) (r = 0.256; p < 0.01) showed a statistically significant but weak correlation with UDVA 1 month postoperatively. There is increasing risk to get <20/20 UDVA in right eyes (OR 3.101; p<0.045), eyes with high myopia (OR 9.964; p<0.01), 100µm cap thickness (OR 4.578; p<0.01), ≤ 6mm OZ (OR 10.556; p<0.01), and <300µm RST (OR 9.100; p<0.01) 1-month post operatively.

Conclusions: SMILE Pro® give promising visual outcome in early post operative period. Low-moderate myopia give better visual outcome than high myopia patient. Small OZ, thin cap thickness, and low RST could increase risk for not getting a maximum visual outcome after SMILE. Study with prospective design and longer follow up time which included comprehensive variables were needed to fully understand factors affecting VA after SMILE.

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