Taneri Suphi, Feit Rachel, Azar Dimitri T
Department of Ophthalmology, Massachusetts Eye and Ear Infirmary and the Schepens Eye Research Institute, Harvard Medical School, Boston, MA 02114, USA.
J Cataract Refract Surg. 2004 Oct;30(10):2130-7. doi: 10.1016/j.jcrs.2004.02.070.
To evaluate the visual outcomes and complications in low to moderate levels of myopia and astigmatism treated with laser-assisted subepithelial keratectomy (LASEK) with a focus on postoperative recovery.
Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, Massachusetts, USA.
A retrospective analysis of a case series of eyes treated with LASEK from 1996 to July 2002 with a follow-up of 2 years was performed. The LASEK technique involved creating an epithelial flap with 25 to 45 seconds of exposure to 20% alcohol, ablating the corneal surface using 3 different excimer lasers and nomogram adjustment, and repositioning the flap and applying a bandage contact lens. The main outcome measures were uncorrected visual acuity (UCVA), efficacy index, manifest refraction, best spectacle-corrected visual acuity (BSCVA), safety index, retreatment rate, and complications.
One hundred seventy-one eyes (85 right eyes and 86 left eyes) of 105 patients were studied. Preoperatively, the mean spherical equivalent was -2.99 diopters (D) +/- 1.43 (SD) (range -0.38 to -7.75 D) and the mean cylinder, -0.78 +/- 0.73 D. The UCVA ranged from 20/800 to 20/32, and the BSCVA ranged from 20/63 to 20/16; the median was 20/20. One week postoperatively, 96% of eyes had a UCVA of 20/40 or better but definitive visual recovery took more than 4 weeks in some eyes. Approximately 95% of eyes were within +/-1.0 D of emmetropia after 4 to 52 weeks; the remaining 5% did not show major deviations. At 4 to 52 weeks, only 1 eye was overcorrected by more than 1.0 D of manifest refraction. The safety index remained close to 1.0 for the follow-up after 4 weeks. The efficacy index displayed a plateau at 0.9 from 1 month to 1 year. No serious complication (including recurrent erosion syndrome) was encountered. The mean follow-up was 31 weeks, and the retreatment rate was 2.9% up to 2 years of follow-up.
The long-term safety and effectiveness of LASEK for the correction of low to moderate myopia and astigmatism were demonstrated. The treatment effect stabilized after 4 weeks.
评估激光辅助上皮下角膜磨镶术(LASEK)治疗低度至中度近视和散光的视觉效果及并发症,重点关注术后恢复情况。
美国马萨诸塞州波士顿哈佛医学院麻省眼耳医院。
对1996年至2002年7月接受LASEK治疗且随访2年的一系列病例进行回顾性分析。LASEK技术包括用20%酒精暴露25至45秒制作上皮瓣,使用3种不同的准分子激光和调整列线图消融角膜表面,重新定位瓣并佩戴绷带接触镜。主要观察指标为裸眼视力(UCVA)、疗效指数、显验光、最佳矫正视力(BSCVA)、安全指数、再次治疗率和并发症。
研究了105例患者的171只眼(85只右眼和86只左眼)。术前,平均等效球镜度为-2.99屈光度(D)±1.43(标准差)(范围-0.38至-7.75 D),平均柱镜度为-0.78±0.73 D。UCVA范围为20/800至20/32,BSCVA范围为20/63至20/16;中位数为20/20。术后1周,96% 的眼睛UCVA达到20/40或更好,但部分眼睛明确的视力恢复超过4周。4至52周后,约95% 的眼睛等效球镜度在正视眼±1.0 D范围内;其余5% 无明显偏差。4至52周时,仅1只眼显验光过矫超过1.0 D。4周后的随访中,安全指数接近1.0。1个月至1年,疗效指数稳定在0.9。未出现严重并发症(包括复发性糜烂综合征)。平均随访31周,随访2年的再次治疗率为2.9%。
证明了LASEK矫正低度至中度近视和散光的长期安全性和有效性。4周后治疗效果稳定。