Three-Month Outcomes of SMILE Pro with the VISUMAX 800 for Myopic Astigmatism in a Large Population.

Clinical ophthalmology (Auckland, N.Z.) Pub Date : 2025-02-07 eCollection Date: 2025-01-01 DOI:10.2147/OPTH.S502915
Hong Son Cung, Lan Huong Thi Tran, Thanh Ngoc Tran
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引用次数: 0

Abstract

Purpose: To report the visual and refractive outcomes of small-incision lenticule extraction (SMILE) Pro using a 2 MHz femtosecond laser for myopic astigmatism in a large population of Vietnamese patients.

Methods: This was a retrospective clinical study of subjects that underwent keratorefractive lenticule extraction (KLEx) with the VISUMAX 800 at Hong Son Eye Hospital (Ha Noi, Vietnam) between June 2023 and October 2023. Primary outcome measures of monocular uncorrected distance visual acuity (UDVA), corrected distance visual acuity (CDVA), and refraction, including vector analysis, were evaluated at 3-months postoperatively. Secondary outcome measures of intraoperative and postoperative complications were also recorded.

Results: A total of 765 eyes from 389 patients (60.66% women, mean age of 23.54±5.20 years) were analyzed 3 months after surgery. The mean preoperative spherical equivalent refraction was -5.98±2.26 D. The postoperative spherical equivalent refraction was within ±0.50 D of the intended target in 81% and within ±1.00 D in 97% of eyes. The mean spherical equivalent refraction was -0.11±0.45 D. UDVA was 20/25 or better in 92% and 20/32 or better in 97% of eyes. The mean postoperative UDVA and CDVA values were 0.05±0.09 and 0.00±0.02 logMAR, respectively. There was no change in CDVA in 99% of eyes. Efficacy index was 0.92, and safety index was 1.00. One eye (0.13%) had a suction loss, which resulted in a lenticule remnant. No other complications were reported during surgery or the postoperative follow-up period.

Conclusion: The current study, carried out on a large cohort of Asian patients, showed SMILE Pro with the VISUMAX 800 was safe and effective for treating myopic astigmatism.

SMILE Pro与VISUMAX 800在大量人群中治疗近视散光的三个月疗效
目的:报道使用2mhz飞秒激光小切口晶状体摘除(SMILE) Pro治疗越南大量近视散光患者的视力和屈光效果。方法:这是一项回顾性临床研究,研究对象是2023年6月至2023年10月在越南河内的Hong Son眼科医院使用VISUMAX 800进行角膜屈光性晶状体摘除(KLEx)的患者。术后3个月评估单眼未矫正距离视力(UDVA)、矫正距离视力(CDVA)和屈光,包括矢量分析。记录术中及术后并发症的次要结局指标。结果:术后3个月共分析389例患者765只眼,其中女性占60.66%,平均年龄23.54±5.20岁。术前平均球面等效屈光度为-5.98±2.26 D,术后球面等效屈光度在预期目标±0.50 D范围内的占81%,在±1.00 D范围内的占97%。平均球面等效屈光度为-0.11±0.45 d, UDVA值为20/25或更好的占92%,20/32或更好的占97%。术后UDVA和CDVA平均值分别为0.05±0.09和0.00±0.02 logMAR。99%的眼睛CDVA无变化。疗效指数为0.92,安全性指数为1.00。1只眼(0.13%)有吸力丧失,导致晶状体残留。手术及术后随访期间无其他并发症。结论:目前在亚洲患者中进行的一项大型队列研究表明,SMILE Pro与VISUMAX 800治疗近视散光安全有效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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