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ZSAL-4 角支撑型有晶状体眼人工晶状体植入 190 只近视眼的临床结果。

Clinical results of ZSAL-4 angle-supported phakic intraocular lenses in 190 myopic eyes.

作者信息

Leccisotti Antonio, Fields Stefania V

机构信息

Ophthalmic Surgery Unit, Casa di Cura Rugani, Siena, Italy.

出版信息

J Cataract Refract Surg. 2005 Feb;31(2):318-23. doi: 10.1016/j.jcrs.2004.04.051.

Abstract

PURPOSE

To evaluate the efficacy and safety of angle-supported phakic intraocular lenses (IOLs) in myopia.

SETTING

Private practice, Siena, Italy.

METHODS

This prospective noncomparative single-surgeon interventional case series comprised 190 consecutive myopic eyes of 115 patients having implantation of a ZSAL-4 IOL (Morcher GmbH) through a 5.5 mm x 3.0 mm sclerocorneal tunnel along the steepest meridian with a surgical iridectomy. Preoperatively, the mean spherical equivalent was -14.37 diopters (D) +/- 4.40 (SD) and the mean astigmatism, 1.66 +/- 1.36 D.

RESULTS

Postoperatively, the mean defocus equivalent (DEQ) was 1.55 +/- 1.06 D and the mean astigmatism, 1.41 +/- 1.11 D. The mean surgically induced astigmatism (vector analysis) was 1.03 +/- 0.77 D (95% confidence interval [CI], 0.92 to 1.15); 146 eyes (77%) were within +/-2.0 D of the DEQ, 76 eyes (40%) were within +/-1.0 D, and 36 eyes (19%) were within +/-0.5 D. The safety index was 1.25 and the efficacy index, 0.78. The improvement in best spectacle-corrected visual acuity (0.17) was statistically significant (95% CI, 0.14 to 0.2). Complications were intraocular pressure spike due to topical steroids, 18%; chronic iridocyclitis, 1%; explantation of unstable IOL, 1%; explantation of IOL for iridocyclitis, 0.5%; pupil ovalization, 11%; halos, 18%; and macular hemorrhage, 1%.

CONCLUSIONS

Angle-supported IOLs can effectively correct high myopia, although residual refractive errors may require secondary procedures. The main intraoperative and postoperative complications were halos, steroid response, and incorrect IOL sizing. The role of surgery in inducing macular hemorrhages should be assessed further.

摘要

目的

评估有晶状体眼人工晶状体(IOL)在近视治疗中的有效性和安全性。

地点

意大利锡耶纳的私人诊所。

方法

本前瞻性非对照单术者干预病例系列研究纳入了115例患者的190只连续近视眼睛,通过5.5mm×3.0mm巩膜隧道沿最陡子午线植入ZSAL-4 IOL(Morcher GmbH),并进行手术虹膜切除术。术前,平均球镜等效度为-14.37屈光度(D)±4.40(标准差),平均散光为1.66±1.36 D。

结果

术后,平均离焦等效度(DEQ)为1.55±1.06 D,平均散光为1.41±1.11 D。平均手术诱导散光(矢量分析)为1.03±0.77 D(95%置信区间[CI],0.92至1.15);146只眼(77%)的DEQ在±2.0 D范围内,76只眼(40%)在±1.0 D范围内,36只眼(19%)在±0.5 D范围内。安全指数为1.25,有效指数为0.78。最佳矫正视力的改善(0.17)具有统计学意义(95% CI,0.14至0.2)。并发症包括局部使用类固醇导致的眼压升高,18%;慢性虹膜睫状体炎,1%;不稳定IOL植入,1%;因虹膜睫状体炎取出IOL,0.5%;瞳孔椭圆化,11%;光晕,18%;黄斑出血,1%。

结论

有晶状体眼人工晶状体可有效矫正高度近视,尽管残余屈光不正可能需要二次手术。主要的术中及术后并发症为光晕、类固醇反应和IOL尺寸不合适。手术导致黄斑出血的作用应进一步评估。

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