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睫状沟植入型人工晶状体的屈光效果改善。

Improved refractive outcome for ciliary sulcus-implanted intraocular lenses.

机构信息

The University of Sydney, Department of Ophthalmology, Sydney Eye Hospital, Save Sight Institute, 8 Macquarie Street, Sydney, NSW 2000 Australia.

出版信息

Ophthalmology. 2012 Feb;119(2):261-5. doi: 10.1016/j.ophtha.2011.07.050. Epub 2011 Dec 23.

DOI:10.1016/j.ophtha.2011.07.050
PMID:22196976
Abstract

OBJECTIVE

To investigate the ideal correction of intraocular lens (IOL) power for sulcus implantation.

DESIGN

Retrospective, comparative case series.

PARTICIPANTS

The records of 679 patients undergoing cataract surgery from June 2007 to June 2008 were reviewed.

INTERVENTION

Eyes in this series underwent phacoemulsification and IOL implantation with local anesthesia. Patients in our study population had their IOL power reduced by 0.5 or 1 diopter (D) from that calculated by the SRK-T formula for in-the-bag implantation. The IOL implanted was the foldable 3-piece acrylic Acrysof MA60AC (Alcon Laboratories Inc., Fort Worth, TX).

MAIN OUTCOME MEASURES

In each case, the difference between actual spherical equivalent (SE) refraction and that predicted by biometry using the SRK-T formula was calculated.

RESULTS

Posterior capsule tears requiring implantation of IOL in the ciliary sulcus occurred in 36 eyes. When comparing eyes in which the power was reduced by 0.5 D with those in which the reduction was 1.0 D, those with a power reduction of 1.0 D had significantly less unexpected error (0.49 vs. 1.01 D SE). After stratifying eyes by axial length (AL), we found higher unexpected refractive error in short eyes (<22 mm AL). Likewise, eyes with a predicted IOL power >25 D had a greater postoperative refractive error.

CONCLUSIONS

This is the first comparative clinical review examining adjustment of power of the sulcus-implanted IOL. We found that the IOL power should be adjusted according to the measured AL and predicted IOL power. For patients with a predicted IOL power from 18 to 25 D, power should be reduced by at least 1 D; for lenses >25 D, power should be reduced by 1.5 to 2 D.

摘要

目的

探讨囊袋内植入人工晶状体(IOL)时理想的 IOL 屈光力矫正方法。

设计

回顾性、对比病例系列研究。

参与者

回顾了 2007 年 6 月至 2008 年 6 月期间行白内障手术的 679 例患者的病历。

干预措施

本系列患者均在局麻下行白内障超声乳化吸除术和 IOL 植入术。在本研究人群中,我们将患者的 IOL 屈光力较 SRK-T 公式计算的植入囊袋内的 IOL 屈光力降低 0.5 或 1 屈光度(D)。植入的 IOL 为折叠式丙烯酸 3 件式 Acrysof MA60AC(爱尔康公司,得克萨斯州沃思堡)。

主要观察指标

在每种情况下,计算实际球镜等效(SE)屈光度与 SRK-T 公式生物测量预测值之间的差异。

结果

36 只眼发生后发性白内障,需植入睫状沟内的 IOL。与屈光力降低 0.5 D 的眼相比,降低 1.0 D 的眼的意外误差显著较小(SE 为 0.49 与 1.01 D)。对眼轴(AL)进行分层后,我们发现短眼(<22 mm AL)的术后屈光误差更高。同样,预测 IOL 屈光力>25 D 的眼术后屈光误差更大。

结论

这是首次对睫状沟内植入的 IOL 屈光力调整进行比较的临床回顾。我们发现,IOL 屈光力应根据测量的 AL 和预测的 IOL 屈光力进行调整。对于预测 IOL 屈光力为 18 至 25 D 的患者,至少应降低 1 D;对于>25 D 的镜片,应降低 1.5 至 2 D。

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