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在一项系统性筛查项目中1型糖尿病患者中威胁视力的视网膜病变发病率

Incidence of sight-threatening retinopathy in Type 1 diabetes in a systematic screening programme.

作者信息

Younis N, Broadbent D M, Harding S P, Vora J P

机构信息

Department of Diabetes and Endocrinology, Royal Liverpool University Hospital, Liverpool, UK.

出版信息

Diabet Med. 2003 Sep;20(9):758-65. doi: 10.1046/j.1464-5491.2003.01035.x.

Abstract

AIM

To measure the cumulative incidence of any retinopathy, maculopathy and sight-threatening diabetic retinopathy (STDR), and calculate optimal screening intervals by retinopathy grade at baseline for patients with Type 1 diabetes attending an established systematic retinal screening programme.

METHODS

All patients with Type 1 diabetes registered with enrolled general practitioners, excluding only those attending an ophthalmologist, were studied if retinopathy data was available at baseline and at least one further screen event. Screening utilized non-stereoscopic 3-field mydriatic photography and modified Wisconsin grading. STDR was defined as moderate pre-proliferative retinopathy or greater and/or significant maculopathy in any eye.

RESULTS

Patients (n=501) underwent 2742 screen events. Cumulative incidence of STDR in patients without baseline retinopathy was 0.3% (95% CI 0.0-0.9) at 1 year, rising to 3.9% (1.4-5.4) at 5 years. Rates of progression to STDR in patients with background and mild pre-proliferative retinopathy at 1 year were 3.6% (0.5-6.6) and 13.5% (4.2-22.7), respectively. Progression to STDR was greater in patients with a higher grade of baseline retinopathy (P=0.001) or a longer disease duration (P=0.003). For a 95% likelihood of remaining free of STDR, mean screening intervals by baseline status were: no retinopathy 5.7 (95% CI 3.5-7.6) years, background 1.3 (0.4-2.0) years and mild pre-proliferative 0.4 (0-0.8) years.

CONCLUSIONS

Screening at 2-3 year intervals, rather than annually, for patients without retinopathy in Type 1 diabetes is feasible because of the low risk of progression to STDR, and may result in significant cost savings for a screening programme. Patients with higher grades of retinopathy require screening at least annually or more frequent.

摘要

目的

测量1型糖尿病患者中任何视网膜病变、黄斑病变和威胁视力的糖尿病视网膜病变(STDR)的累积发病率,并根据基线时的视网膜病变分级计算最佳筛查间隔,这些患者参加了既定的系统性视网膜筛查项目。

方法

所有在注册全科医生处登记的1型糖尿病患者,不包括仅就诊于眼科医生的患者,若基线时有视网膜病变数据且至少有一次进一步的筛查事件,则纳入研究。筛查采用非立体3视野散瞳照相和改良的威斯康星分级法。STDR定义为任何一只眼中中度增殖前期视网膜病变或更严重病变和/或显著黄斑病变。

结果

患者(n = 501)共接受了2742次筛查。无基线视网膜病变的患者中,STDR的累积发病率在1年时为0.3%(95%可信区间0.0 - 0.9),5年时升至3.9%(1.4 - 5.4)。有背景性和轻度增殖前期视网膜病变的患者在1年时进展为STDR的发生率分别为3.6%(0.5 - 6.6)和13.5%(4.2 - 22.7)。基线视网膜病变分级较高(P = 0.001)或病程较长(P = 0.003)的患者进展为STDR的情况更严重。为使无STDR的可能性达到95%,根据基线状态的平均筛查间隔为:无视网膜病变5.7年(95%可信区间3.5 - 7.6),背景性病变1.3年(0.4 - 2.0),轻度增殖前期病变0.4年(0 - 0.8)。

结论

对于1型糖尿病无视网膜病变的患者,每2 - 3年进行一次筛查而非每年一次是可行的,因为进展为STDR的风险较低,这可能会为筛查项目节省大量成本。视网膜病变分级较高的患者至少需要每年或更频繁地进行筛查。

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