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老花眼患者白内障摘除术后三焦点人工晶状体与双焦点人工晶状体的比较

Trifocal intraocular lenses versus bifocal intraocular lenses after cataract extraction among participants with presbyopia.

作者信息

Zamora-de La Cruz Diego, Zúñiga-Posselt Karla, Bartlett John, Gutierrez Mario, Abariga Samuel A

机构信息

Anterior Segment Department, Instituto de Oftalmología Fundación Conde de Valenciana, Mexico City, Mexico.

Anterior Segment Department, Hospital Mexiquense de Salud Visual, ISEM, Naucalpan de Juárez, Mexico.

出版信息

Cochrane Database Syst Rev. 2020 Jun 18;6(6):CD012648. doi: 10.1002/14651858.CD012648.pub2.

Abstract

BACKGROUND

Presbyopia occurs when the lens of the eyes loses its elasticity leading to loss of accommodation. The lens may also progress to develop cataract, affecting visual acuity and contrast sensitivity. One option of care for individuals with presbyopia and cataract is the use of multifocal or extended depth of focus intraocular lens (IOL) after cataract surgery. Although trifocal and bifocal IOLs are designed to restore three and two focal points respectively, trifocal lens may be preferable because it restores near, intermediate, and far vision, and may also provide a greater range of useful vision and allow for greater spectacle independence in individuals with presbyopia.

OBJECTIVES

To assess the effectiveness and safety of implantation with trifocal versus bifocal IOLs during cataract surgery among participants with presbyopia.

SEARCH METHODS

We searched the Cochrane Central Register of Controlled Trials (CENTRAL) (which contains the Cochrane Eyes and Vision Trials Register) (2019, Issue 9); Ovid MEDLINE; Embase.com; PubMed; ClinicalTrials.gov; and the World Health Organization (WHO) International Clinical Trials Registry Platform (ICTRP). We did not use any date or language restrictions in the electronic search for trials. We last searched the electronic databases on 26 September 2019. We searched the reference lists of the retrieved articles and the abstracts from the Annual Meeting of the Association for Research in Vision and Ophthalmology (ARVO) for the years 2005 to 2015.

SELECTION CRITERIA

We included randomized controlled trials that compared trifocal and bifocal IOLs among participants 30 years or older with presbyopia undergoing cataract surgery.

DATA COLLECTION AND ANALYSIS

We used standard Cochrane methodology.

MAIN RESULTS

We identified five studies conducted in Europe with a total of 175 participants. All five studies assessed uncorrected distance visual acuity (primary outcome of the review), while some also examined our secondary outcomes including uncorrected near, intermediate, and best-corrected distance visual acuity, as well as contrast sensitivity. Study characteristics All participants had bilateral cataracts with no pre-existing ocular pathologies or ocular surgery. Participants' mean age ranged from 58 to 64 years. Only one study reported on gender of participants, and they were mostly women. We assessed all the included studies as being at unclear risk of bias for most domains. Two studies received financial support from manufacturers of lenses evaluated in this review, and at least one author of another study reported receiving payments for delivering lectures with lens manufacturers. Findings All studies compared trifocal versus bifocal IOL implantation on visual acuity outcomes measured on a LogMAR scale. At one year, trifocal IOL showed no evidence of effect on uncorrected distance visual acuity (mean difference (MD) 0.00, 95% confidence interval (CI) -0.04 to 0.04; I = 0%; 2 studies, 107 participants; low-certainty evidence) and uncorrected near visual acuity (MD 0.01, 95% CI -0.04 to 0.06; I = 0%; 2 studies, 107 participants; low-certainty evidence). Trifocal IOL implantation may improve uncorrected intermediate visual acuity at one year (MD -0.16, 95% CI -0.22 to -0.10; I= 0%; 2 studies, 107 participants; low-certainty evidence), but showed no evidence of effect on best-corrected distance visual acuity at one year (MD 0.00, 95% CI -0.03 to 0.04; I= 0%; 2 studies, 107 participants; low-certainty evidence). No study reported on contrast sensitivity or quality of life at one-year follow-up. Data from one study at three months suggest that contrast sensitivity did not differ between groups under photopic conditions, but may be worse in the trifocal group in one of the four frequencies under mesopic conditions (MD -0.19, 95% CI -0.33 to -0.05; 1 study; I = 0%, 25 participants; low-certainty evidence). In two studies, the investigators observed that participants' satisfaction or spectacle independence may be higher in the trifocal group at six months, although another study found no evidence of a difference in participant satisfaction or spectacle independence between groups. Adverse events Adverse events reporting varied among studies. Two studies reported information on adverse events at one year. One study reported that participants showed no intraoperative or postoperative complications, while the other study reported that four eyes (11.4%) in the bifocal and three eyes (7.5%) in the trifocal group developed significant posterior capsular opacification requiring YAG capsulotomy. The certainty of the evidence was low.

AUTHORS' CONCLUSIONS: There is low-certainty of evidence that compared to bifocal IOL, implantation of trifocal IOL may improve uncorrected intermediate visual acuity at one year. However, there is no evidence of a difference between trifocal and bifocal IOL for uncorrected distance visual acuity, uncorrected near visual acuity, and best-corrected visual acuity at one year. Future research should include the comparison of both trifocal IOL and specific bifocal IOLs that correct intermediate visual acuity to evaluate important outcomes such as contrast sensitivity and quality of life.

摘要

背景

当眼睛的晶状体失去弹性导致调节功能丧失时,就会出现老花眼。晶状体也可能会进一步发展形成白内障,影响视力和对比敏感度。对于患有老花眼和白内障的个体,一种治疗选择是在白内障手术后使用多焦点或扩展焦深人工晶状体(IOL)。尽管三焦点和双焦点IOL分别设计用于恢复三个和两个焦点,但三焦点晶状体可能更可取,因为它能恢复近、中、远视力,还可能提供更大范围的有用视力,并使老花眼患者减少对眼镜的依赖。

目的

评估在患有老花眼的参与者中,白内障手术时植入三焦点与双焦点IOL的有效性和安全性。

检索方法

我们检索了Cochrane对照试验中心注册库(CENTRAL)(其中包含Cochrane眼科和视力试验注册库)(2019年第9期);Ovid MEDLINE;Embase.com;PubMed;ClinicalTrials.gov;以及世界卫生组织(WHO)国际临床试验注册平台(ICTRP)。在电子检索试验时,我们没有使用任何日期或语言限制。我们最近一次检索电子数据库是在2019年9月26日。我们检索了检索到的文章的参考文献列表以及2005年至2015年视觉与眼科研究协会(ARVO)年会的摘要。

选择标准

我们纳入了比较三焦点和双焦点IOL在30岁及以上患有老花眼且接受白内障手术的参与者中的随机对照试验。

数据收集与分析

我们采用标准的Cochrane方法。

主要结果

我们确定了在欧洲进行的5项研究,共有175名参与者。所有5项研究均评估了未矫正的远视力(本综述的主要结局),而一些研究还检查了我们的次要结局,包括未矫正的近视力、中视力以及最佳矫正远视力,以及对比敏感度。研究特征所有参与者均患有双侧白内障,且无既往眼部疾病或眼部手术史。参与者的平均年龄在58至64岁之间。只有一项研究报告了参与者的性别,且大多数为女性。我们评估所有纳入研究在大多数领域的偏倚风险均不明确。两项研究获得了本综述中评估的晶状体制造商的资金支持,另一项研究的至少一位作者报告因向晶状体制造商授课而获得报酬。结果所有研究均比较了三焦点与双焦点IOL植入对以LogMAR量表测量的视力结局的影响。在1年时,三焦点IOL对未矫正远视力无显著影响(平均差(MD)0.00,95%置信区间(CI)-0.04至0.04;I² = 0%;2项研究,107名参与者;低质量证据),对未矫正近视力也无显著影响(MD 0.01,95% CI -0.04至0.06;I² = 0%;2项研究,107名参与者;低质量证据)。三焦点IOL植入可能在1年时改善未矫正的中视力(MD -0.16,95% CI -0.22至-0.10;I² = 0%;2项研究,107名参与者;低质量证据),但在1年时对最佳矫正远视力无显著影响(MD 0.00,95% CI -0.03至0.04;I² = 0%;2项研究,107名参与者;低质量证据)。没有研究报告1年随访时的对比敏感度或生活质量。一项研究在3个月时的数据表明,在明视条件下两组之间的对比敏感度无差异,但在中视条件下四个频率中的一个频率上,三焦点组的对比敏感度可能更差(MD -0.19,95% CI -0.33至-0.05;1项研究;I² = 0%,25名参与者;低质量证据)。在两项研究中,研究者观察到三焦点组在6个月时参与者的满意度或减少对眼镜的依赖程度可能更高,尽管另一项研究未发现两组之间参与者满意度或减少对眼镜依赖程度存在差异的证据。不良事件不同研究报告的不良事件各不相同。两项研究报告了1年时的不良事件信息。一项研究报告参与者未出现术中或术后并发症,而另一项研究报告双焦点组有4只眼(11.4%)、三焦点组有3只眼(7.5%)发生了需要YAG囊切开术的显著后囊膜混浊。证据的确定性较低。

作者结论

证据质量低,表明与双焦点IOL相比,三焦点IOL植入可能在1年时改善未矫正的中视力。然而,在1年时,三焦点和双焦点IOL在未矫正远视力、未矫正近视力和最佳矫正视力方面没有差异的证据。未来的研究应包括比较三焦点IOL和能矫正中视力的特定双焦点IOL,以评估对比敏感度和生活质量等重要结局。

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