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集合不足的非手术干预措施。

Non-surgical interventions for convergence insufficiency.

作者信息

Scheiman Mitchell, Gwiazda Jane, Li Tianjing

机构信息

Pennsylvania College of Optometry, 1200 West Godfrey Avenue, Philadelphia, Pennsylvania, USA, 19141.

出版信息

Cochrane Database Syst Rev. 2011 Mar 16(3):CD006768. doi: 10.1002/14651858.CD006768.pub2.

Abstract

BACKGROUND

Convergence insufficiency is a common eye muscle co-ordination problem in which the eyes have a strong tendency to drift outward (exophoria) when reading or doing close work. Symptoms may include eye strain, headaches, double vision, print moving on the page, frequent loss of place when reading, inability to concentrate, and short attention span.

OBJECTIVES

To systematically assess and synthesize evidence from randomized controlled trials (RCTs) on the effectiveness of non-surgical interventions for convergence insufficiency.

SEARCH STRATEGY

We searched The Cochrane Library, MEDLINE, EMBASE, Science Citation Index, the metaRegister of Controlled Trials (mRCT) (www.controlled-trials.com) and ClinicalTrials.gov (www.clinicaltrials.gov ) on 7 October 2010. We manually searched reference lists and optometric journals.

SELECTION CRITERIA

We included RCTs examining any form of non-surgical intervention against placebo, no treatment, sham treatment, or each other.

DATA COLLECTION AND ANALYSIS

Two authors independently assessed eligibility, risk of bias, and extracted data. We performed meta-analyses when appropriate.

MAIN RESULTS

We included six trials (three in children, three in adults) with a total of 475 participants. We graded four trials at low risk of bias.Evidence from one trial (graded at low risk of bias) suggests that base-in prism reading glasses was no more effective than placebo reading glasses in improving clinical signs or symptoms in children.Evidence from one trial (graded at high risk of bias) suggests that base-in prism glasses using a progressive addition lens design was more effective than progressive addition lens alone in decreasing symptoms in adults. At three weeks of therapy, the mean difference in Convergence Insufficiency Symptoms Survey (CISS) score was -10.24 points (95% confidence interval (CI) -15.45 to -5.03).Evidence from two trials (graded at low risk of bias) suggests that outpatient (or office-based as used in the US) vision therapy/orthoptics was more effective than home-based convergence exercises (or pencil push-ups as used in the US) in children. At 12 weeks of therapy, the mean difference in change in near point of convergence, positive fusional vergence, and CISS score from baseline was 3.99 cm (95% CI 2.11 to 5.86), 13.13 diopters (95% CI 9.91 to 16.35), and 9.86 points (95% CI 6.70 to 13.02), respectively.In a young adult population, evidence from one trial (graded at low risk of bias) suggests outpatient vision therapy/orthoptics was more effective than home-based convergence exercises in improving positive fusional vergence at near (7.7 diopters, 95% CI 0.82 to 14.58), but not the other outcomes.Evidence from one trial (graded at low risk of bias) comparing four interventions, also suggests that outpatient vision therapy/orthoptics was more effective than home-based computer vision therapy/orthoptics in children. At 12 weeks, the mean difference in change in near point of convergence, positive fusional vergence, and CISS score from baseline was 2.90 cm (95% CI 0.96 to 4.84), 7.70 diopters (95% CI 3.94 to 11.46), and 8.80 points (95% CI 5.26 to 12.34), respectively. Evidence was less consistent for other pair-wise comparisons.

AUTHORS' CONCLUSIONS: Current research suggests that outpatient vision therapy/orthoptics is more effective than home-based convergence exercises or home-based computer vision therapy/orthoptics for children. In adult population, evidence of the effectiveness of various non-surgical interventions is less consistent.

摘要

背景

集合不足是一种常见的眼肌协调问题,即眼睛在阅读或进行近距离工作时极易向外偏斜(外隐斜)。症状可能包括眼睛疲劳、头痛、复视、页面上的文字移动、阅读时频繁跳读、注意力不集中以及注意力持续时间短。

目的

系统评价和综合随机对照试验(RCT)中关于非手术干预集合不足有效性的证据。

检索策略

2010年10月7日,我们检索了考克兰图书馆、MEDLINE、EMBASE、科学引文索引、对照试验元注册库(mRCT)(www.controlled-trials.com)和临床试验.gov(www.clinicaltrials.gov)。我们还手动检索了参考文献列表和验光期刊。

入选标准

我们纳入了比较任何形式的非手术干预与安慰剂、无治疗、假治疗或相互比较的RCT。

数据收集与分析

两位作者独立评估纳入标准、偏倚风险并提取数据。我们在适当的时候进行荟萃分析。

主要结果

我们纳入了6项试验(3项针对儿童,3项针对成人),共475名参与者。我们将4项试验评定为低偏倚风险。一项试验(评定为低偏倚风险)的证据表明,在改善儿童临床体征或症状方面,底向内棱镜阅读眼镜并不比安慰剂阅读眼镜更有效。一项试验(评定为高偏倚风险)的证据表明,采用渐进多焦点镜片设计的底向内棱镜眼镜在减轻成人症状方面比单独使用渐进多焦点镜片更有效。在治疗3周时,集合不足症状调查(CISS)评分的平均差异为-10.24分(95%置信区间(CI)-15.45至-5.03)。两项试验(评定为低偏倚风险)的证据表明,在儿童中,门诊(或美国使用的基于办公室的)视觉治疗/视光学比家庭式集合训练(或美国使用的铅笔推近法)更有效。在治疗12周时,与基线相比,集合近点、正融合性聚散度和CISS评分变化的平均差异分别为3.99厘米(95%CI 2.11至5.86)、13.13棱镜度(95%CI 9.91至16.35)和9.86分(95%CI 6.70至13.02)。在年轻成人中,一项试验(评定为低偏倚风险)的证据表明,门诊视觉治疗/视光学在改善近距离正融合性聚散度方面(7.7棱镜度,95%CI 0.82至14.58)比家庭式集合训练更有效,但在其他结果方面并非如此。一项试验(评定为低偏倚风险)比较了四种干预措施,其证据还表明,在儿童中,门诊视觉治疗/视光学比家庭式计算机视觉治疗/视光学更有效。在12周时,与基线相比,集合近点、正融合性聚散度和CISS评分变化的平均差异分别为2.90厘米(95%CI 0.96至4.84)、7.70棱镜度(95%CI 3.94至11.46)和8.80分(95%CI 5.26至12.34)。其他两两比较的证据不太一致。

作者结论

目前的研究表明,对于儿童,门诊视觉治疗/视光学比家庭式集合训练或家庭式计算机视觉治疗/视光学更有效。在成人中,各种非手术干预有效性的证据不太一致。

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