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用于近视散光的有晶状体眼后房型可植入式胶原晶状体和有晶状体眼虹膜固定型折叠式人工晶状体植入后的疗效和安全性。

Efficacy and Safety After Toric Posterior Chamber Implantable Collamer Lens and Toric Iris-Fixated Foldable Phakic Intraocular Lens for Myopic Astigmatism.

作者信息

Monteiro Tiago, Pinto Christophe, Franqueira Nuno, Faria-Correia Fernando, Mendes José, Alfonso Sánchez José, Vaz Fernando

出版信息

J Refract Surg. 2022 Jun;38(6):339-347. doi: 10.3928/1081597X-20220406-01. Epub 2022 Jun 1.

Abstract

PURPOSE

To compare visual, refractive, and safety outcomes of toric posterior chamber Implantable Collamer Lens (T-ICL) (STAAR Surgical) and toric iris-fixated foldable phakic intraocular lens (IOL) (T-Artiflex; Ophtec BV) implantation for the correction of myopic astigmatism.

METHODS

This retrospective cohort study included 312 eyes of 312 patients who had phakic IOL implantation for myopic astigmatism. Two groups were defined: 205 eyes that underwent T-ICL implantation and 107 eyes that underwent T-Artiflex implantation. Safety, efficacy, and predictability outcomes were evaluated preoperatively and at 12 months postoperatively. Refractive and corneal astigmatic vector analysis were performed using the Alpins method.

RESULTS

One year postoperatively, uncorrected distance visual acuity was 0.05 ± 0.18 (T-ICL) and 0.10 ± 0.16 (T-Artiflex) logMAR, with efficacy indexes of 1.16 ± 0.27 and 1.05 ± 0.31, respectively ( < .001). Safety indexes were 1.28 ± 0.30 and 1.21 ± 0.31, respectively ( = .04). Spherical equivalent was within ±0.50 diopters (D) of emmetropia in 165 (80.5%) and 88 (82.2%) eyes, respectively. Refractive astigmatic analysis showed an index of success of 0.28 ± 0.33 (T-ICL) and 0.31 ± 0.26 (T-Artiflex) ( = .07). Surgically induced corneal astigmatism was 0.48 ± 0.74 and 0.81 ± 0.61 D, respectively ( < .001). Mean endothelial loss was 1.11% and 2.05%, respectively ( = .42). Six (2.9%) eyes in the T-ICL group and 1 (0.9%) eye in the T-Artiflex group had phakic IOL repositioning due to significant misalignment. No vision-threatening complications occurred.

CONCLUSIONS

Both the T-ICL and T-Artiflex groups showed high visual and refractive efficacy with a good safety profile for the correction of myopic astigmatism. T-ICL implantation demonstrated significantly better efficacy and safety indexes after 12 months. Vector analysis showed similar refractive astigmatic correction in both groups, but T-Artiflex implantation revealed higher surgically induced corneal astigmatism. .

摘要

目的

比较用于矫正近视散光的环曲面后房型可植入式角膜接触镜(T-ICL,STAAR Surgical公司)和环曲面虹膜固定折叠型有晶状体眼人工晶状体(T-Artiflex;Ophtec BV公司)植入术后的视力、屈光及安全性结果。

方法

这项回顾性队列研究纳入了312例接受有晶状体眼人工晶状体植入术矫正近视散光的患者的312只眼。分为两组:205只眼接受T-ICL植入,107只眼接受T-Artiflex植入。术前及术后12个月评估安全性、有效性和可预测性结果。使用Alpins方法进行屈光和角膜散光矢量分析。

结果

术后1年,未矫正远视力的对数最小分辨角(logMAR)在T-ICL组为0.05±0.18,在T-Artiflex组为0.10±0.16,有效性指数分别为1.16±0.27和1.05±0.31(P<0.001)。安全性指数分别为1.28±0.30和1.21±0.31(P = 0.04)。等效球镜度在±0.50屈光度(D)范围内达到正视化的眼数在T-ICL组为165只(80.5%),在T-Artiflex组为88只(82.2%)。屈光性散光分析显示成功指数在T-ICL组为0.28±0.33,在T-Artiflex组为0.31±0.26(P = 0.07)。手术诱导的角膜散光分别为0.48±0.74 D和0.81±0.61 D(P<0.001)。平均内皮细胞损失率分别为1.11%和2.05%(P = 0.42)。T-ICL组有6只眼(2.9%)因明显移位而进行了有晶状体眼人工晶状体重新定位,T-Artiflex组有1只眼(0.9%)。未发生威胁视力的并发症。

结论

T-ICL组和T-Artiflex组在矫正近视散光方面均显示出较高的视力和屈光有效性以及良好的安全性。T-ICL植入术后12个月显示出明显更好的有效性和安全性指数。矢量分析显示两组在屈光性散光矫正方面相似,但T-Artiflex植入术后显示出更高的手术诱导角膜散光。

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