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Implantable Collamer Lens Versus Iris-Fixed Phakic Intraocular Lens Implantation to Correct Myopia: A Meta-Analysis

机译:植入式护目镜与虹膜固定的带眼眼内晶状体植入以矫正近视:一项荟萃分析

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摘要

This study is a meta-analysis comparing the efficacy, predictability, and safety of correcting myopia via implantation of two types of phakic intraocular lens (PIOLs): the implantable collamer lens (ICL) and iris-fixed PIOL. The Cochrane library, Pubmed, and EMBASE were searched. Study selection, data exclusion, and quality assessment were performed by two independent observers. The pooled relative risk (RR), pooled standardized mean difference (SMD), and their 95% confidence intervals (CIs) were used to compare lenses. Seven studies, involving 511 eyes, were included. The pooled SMD in postoperative uncorrected distance visual acuity (UDVA) comparing ICLs to iris-fixed PIOLs was −0.22 (95% CI, −0.58 to 0.13; P = .22). The pooled RR values of UDVA of 20/20 or better and of 20/40 or better comparing ICLs to iris-fixed PIOLs were 1.15 (95% CI, 0.89 to 1.47; P = .29) and 1.01 (95% CI, 0.95 to 1.08; P = .75), respectively. The pooled RR of loss of best spectacle-corrected visual acuity (BSCVA) and gain in BSCVA comparing ICLs to iris-fixed PIOLs were 1.20 (95% CI, 0.24 to 6.00; P = .82) and 1.14 (95% CI, 0.89 to 1.48; P = .31), respectively. The pooled RR comparing ICLs to iris-fixed PIOLs was 0.78 (95% CI, 0.29 to 2.12; P = .63) for all reported complications and 2.80 (95% CI, 1.04 to 7.52; P = .04) for severe complications. The pooled RR of achieving a result within ±0.5 D (diopter) of the intended target comparing ICLs to iris-fixed PIOLs was 1.35 (95% CI, 1.04 to 1.77; P = .03). Overall, there is no significant difference in efficacy between the two types of PIOLs or in safety, except that the ICL is associated with a greater incidence of severe complications, especially anterior subcapsular cataract, primarily in the Version 2 and Version 3 groups. However, ICL has better predictability.
机译:这项研究是一项荟萃分析,比较了通过植入两种类型的有晶状体人工晶状体(PIOL):近视眼固定透镜和虹膜固定PIOL来矫正近视的功效,可预测性和安全性。搜索Cochrane库,Pubmed和EMBASE。研究选择,数据排除和质量评估由两名独立的观察员进行。合并的相对风险(RR),合并的标准平均差(SMD)及其95%置信区间(CIs)用于比较镜片。包括511眼的七项研究被纳入。比较ICL和虹膜固定PIOL的术后未矫正远视力(UDVA)中的SMD汇总为-0.22(95%CI,-0.58至0.13; P; = .22)。比较ICL与虹膜固定PIOL的UDVA汇总RR值为20/20或更高,以及20/40或更高,分别为1.15(95%CI,0.89至1.47; P = .29)和1.01(95%CI,0.95)至1.08; P = .75)。与ICL和虹膜固定PIOL相比,最佳眼镜矫正视力丧失(BSCVA)和BSCVA增益的合并RR为1.20(95%CI,0.24至6.00; P = .82)和1.14(95%CI,0.89)至1.48; P; = .31)。对于所有报告的并发症,合并的ICL与虹膜固定PIOL的RR比较为0.78(95%CI,0.29至2.12; P = .63),对于严重并发症,其为2.80(95%CI,1.04至7.52; P = .04)。与ICL和虹膜固定PIOL相比,在预期目标的±0.5 D(屈光度)范围内达到结果的合并RR为1.35(95%CI,1.04至1.77; P = .03)。总体而言,两种类型的PIOL的疗效或安全性无显着差异,只是ICL与严重并发症(尤其是前囊膜白内障)的发生率较高相关,主要在第2版和第3版组中。但是,ICL具有更好的可预测性。

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