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首页> 外文期刊>Journal of refractive surgery >Visian toric implantable collamer lens for correction of compound myopic astigmatism.
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Visian toric implantable collamer lens for correction of compound myopic astigmatism.

机译:用于矫正复合近视散光的Visian复曲面植入式矫正镜。

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摘要

PURPOSE: To assess the safety, efficacy, predictability, and stability of a toric posterior chamber phakic intraocular lens for the correction of myopia with astigmatism. METHODS: A non-randomized, retrospective analysis of 63 eyes of 36 patients with a minimum follow-up of 6 months was performed. The STAAR Toric Implantable Collamer Lens (TICL) was implanted under topical anesthesia through a 3-mm temporal clear corneal incision. Mean preoperative spherical equivalent refraction was -10.71+/-3.55 diopters (D). Median preoperative best spectacle-corrected visual acuity (BSCVA) was 20/25, with a mean sphere of -8.78 D (range: -2.50 to -16.50 D) and mean cylinder of 3.60 D (range: 1.25 to 7.00 D). Postoperative parameters were analyzed at different time points, and vector analysis was performed to calculate surgically induced astigmatism. RESULTS: Fifty-nine (93.6%) eyes had a spherical equivalent refraction within +/-1.00 D and 52 (82.5%) eyes were within +/-0.50 D of emmetropia. Median postoperative uncorrected visual acuity was 20/25 and BSCVA was 20/20. Preoperative keratometric astigmatism was 1.99@178.2 vs 1.82@178.6 postoperative keratometric astigmatism, most likely due to the surgical incision. Preoperative refractive astigmatism was 2.17@93 whereas postoperatively it reduced to 0.38@99.6. No eye lost 2 or more lines of Snellen BSCVA. Twenty-two (34.9%) eyes gained 2 or more Snellen lines of vision. Preoperatively, 45 (71.4%) eyes had a BSCVA of 20/30 or better, whereas 60 (95.2%) eyes were within this range of BSCVA after surgery. The TICL demonstrated good rotational stability in this study. CONCLUSIONS: Implantation of the STAAR TICL was an effective, predictable, and safe method for correction of high myopia and myopic astigmatism as shown in this retrospective observational series.
机译:目的:评估复曲面后房型有晶状体人工晶状体矫正近视的安全性,有效性,可预测性和稳定性。方法:对36例患者的63只眼进行了非随机回顾性分析,至少随访了6个月。将STAAR复曲面植入式矫正镜(TICL)通过3毫米的颞透明角膜切口在局部麻醉下植入。术前平均等效球镜屈光度为-10.71 +/- 3.55屈光度(D)。术前最佳眼镜矫正视力(BSCVA)的中位数为20/25,平均球面值为-8.78 D(范围:-2.50至-16.50 D),平均圆柱度为3.60 D(范围:1.25至7.00 D)。在不同时间点分析术后参数,并进行矢量分析以计算手术引起的散光。结果:五十九(93.6%)眼球镜等效屈光度在+/- 1.00 D以内,52眼(82.5%)眼球屈光度在+/- 0.5 D以内。术后中位未矫正视力中位数为20/25,BSCVA为20/20。术前角膜散光为1.99@178.2,而术后角膜散光为1.82@178.6,最可能是由于手术切口引起的。术前屈光散光为2.17@93,而术后屈光散光降至0.38@99.6。视力不受影响的Snellen BSCVA为2行或更多行。 22眼(34.9%)的眼睛获得了2或更多的Snellen视线。术前,有45(71.4%)眼的BSCVA为20/30或更高,而术后有60(95.2%)眼在BSCVA的范围内。 TICL在这项研究中显示出良好的旋转稳定性。结论:STAAR TICL的植入是矫正高度近视和近视散光的有效,可预测和安全的方法,如该回顾性观察系列所示。

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