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成人青光眼筛查:美国预防服务工作组的更新证据报告和系统评价。

Screening for Glaucoma in Adults: Updated Evidence Report and Systematic Review for the US Preventive Services Task Force.

机构信息

Pacific Northwest Evidence-based Practice Center, Department of Medical Informatics and Clinical Epidemiology, Oregon Health & Science University, Portland.

Department of Family Medicine, Oregon Health & Science University, Portland.

出版信息

JAMA. 2022 May 24;327(20):1998-2012. doi: 10.1001/jama.2022.6290.

Abstract

IMPORTANCE

Two 2013 systematic reviews to inform the US Preventive Services Task Force (USPSTF) found insufficient evidence to assess benefits and harms of screening for primary open-angle glaucoma (OAG) in adults.

OBJECTIVE

To update the 2013 reviews on screening for glaucoma, to inform the USPSTF.

DATA SOURCES

Ovid MEDLINE, the Cochrane Central Register of Controlled Trials, and the Cochrane Database of Systematic Reviews (to February 2021); surveillance through January 21, 2022.

STUDY SELECTION

Randomized clinical trials (RCTs) of screening, referral, and treatment; and studies of screening test diagnostic accuracy.

DATA EXTRACTION AND SYNTHESIS

One investigator abstracted data and a second checked accuracy. Two investigators independently assessed study quality.

RESULTS

Eighty-three studies (N = 75 887) were included (30 trials and 53 diagnostic accuracy studies). One RCT (n = 616) found screening of frail elderly persons associated with no difference in vision outcomes vs no screening but with significantly greater falls risk (relative risk [RR], 1.31 [95% CI, 1.13-1.50]). No study evaluated referral to an eye health professional. For glaucoma diagnosis, spectral domain optical coherence tomography (providing high-resolution cross-sectional imaging; 15 studies, n = 4242) was associated with sensitivity of 0.79 (95% CI, 0.75-0.83) and specificity of 0.92 (95% CI, 0.87-0.96) and the Humphrey Visual Field Analyzer (for perimetry, or measurement of visual fields; 6 studies, n = 11 244) with sensitivity of 0.87 (95% CI, 0.69-0.95) and specificity 0.82 (95% CI, 0.66-0.92); tonometry (for measurement of intraocular pressure; 13 studies, n = 32 892) had low sensitivity (0.48 [95% CI, 0.31-0.66]). Medical therapy for ocular hypertension and untreated glaucoma was significantly associated with decreased intraocular pressure and decreased likelihood of glaucoma progression (7 trials, n = 3771; RR, 0.68 [95% CI, 0.49-0.96]; absolute risk difference -4.2%) vs placebo, but 1 trial (n = 461) found no differences in visual acuity, quality of life, or function. Selective laser trabeculoplasty and medical therapy had similar outcomes (4 trials, n = 957).

CONCLUSIONS AND RELEVANCE

This review found limited direct evidence on glaucoma screening, showing no association with benefits. Screening tests can identify persons with glaucoma and treatment was associated with a lower risk of glaucoma progression, but evidence of improvement in visual outcomes, quality of life, and function remains lacking.

摘要

重要性

为了向美国预防服务工作组(USPSTF)提供信息,2013 年有两项系统评价发现,原发性开角型青光眼(OAG)成人筛查的益处和危害证据不足。

目的

更新 2013 年关于青光眼筛查的综述,为 USPSTF 提供信息。

数据来源

Ovid MEDLINE、Cochrane 对照试验中心注册库和 Cochrane 系统评价数据库(截至 2021 年 2 月);2022 年 1 月 21 日进行监测。

研究选择

筛查、转诊和治疗的随机临床试验(RCT);以及筛查试验诊断准确性的研究。

数据提取和综合

一名调查员提取数据,第二名调查员核对准确性。两名调查员独立评估研究质量。

结果

共纳入 83 项研究(N=75887)(30 项 RCT 和 53 项诊断准确性研究)。一项 RCT(n=616)发现,对体弱老年人进行筛查与不筛查相比,视力结局无差异,但跌倒风险显著增加(相对风险[RR],1.31[95%CI,1.13-1.50])。没有研究评估转诊给眼科保健专业人员。对于青光眼诊断,光谱域光学相干断层扫描(提供高分辨率的横截面成像;15 项研究,n=4242)的敏感性为 0.79(95%CI,0.75-0.83),特异性为 0.92(95%CI,0.87-0.96),Humphrey 视野分析仪(用于视野检查或测量视野;6 项研究,n=11244)的敏感性为 0.87(95%CI,0.69-0.95),特异性为 0.82(95%CI,0.66-0.92);眼压测量的眼压计(tonometry;13 项研究,n=32892)的敏感性较低(0.48[95%CI,0.31-0.66])。眼部高血压和未经治疗的青光眼的药物治疗与眼压降低和青光眼进展的可能性降低显著相关(7 项 RCT,n=3771;RR,0.68[95%CI,0.49-0.96];绝对风险差异-4.2%)与安慰剂相比,但 1 项研究(n=461)发现视力、生活质量或功能没有差异。选择性激光小梁成形术和药物治疗的结果相似(4 项 RCT,n=957)。

结论和相关性

本综述发现关于青光眼筛查的直接证据有限,没有发现与益处相关的证据。筛查试验可以识别出青光眼患者,治疗与较低的青光眼进展风险相关,但改善视力结果、生活质量和功能的证据仍然缺乏。

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