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早产儿视网膜病变消退后的脉络膜厚度。

Choroidal thickness in regressed retinopathy of prematurity.

作者信息

Anderson M F, Ramasamy B, Lythgoe D T, Clark D

机构信息

Department of Ophthalmology, University Hospital Aintree, Liverpool, UK.

出版信息

Eye (Lond). 2014 Dec;28(12):1461-8. doi: 10.1038/eye.2014.207. Epub 2014 Oct 3.

Abstract

PURPOSE

To compare choroidal thickness in patients with regressed retinopathy of prematurity (ROP) with healthy controls using enhanced depth imaging optical coherence tomography (EDI OCT) METHODS: Twenty-four children and young adults (41 eyes) with regressed ROP≥stage 3 had undergone EDI OCT with Spectralis FD-OCT as part of their clinical record. Their refraction, best-corrected visual acuity, and ophthalmoscopic findings were recorded. Corresponding data was collected prospectively from 33 healthy controls (58 eyes) who had been born at term. Choroidal thickness was measured independently by two observers subfoveally and at 1500 μm nasal and temporal to the fovea using EDI OCT.

RESULTS

Mean subfoveal choroidal thickness, adjusted for refraction, was 271.1 μm (95% CI, 247.8-294.5) in the ex-ROP group, which was significantly thinner than 327.4 μm (95% CI, 293.8-360.9) in controls (P=0.008). Similarly, mean adjusted temporal choroidal thickness was 257.2 μm (95% CI, 240.2-274.2) in ex-ROP's vs 320.5 μm (95% CI, 288.6-352.3) in controls (P=0.001). There was no statistically significant difference in the nasal measurement. In the ex-ROP group, there was no significant correlation between subfoveal choroidal thickness and gestational age (r(s)=0.16, P=0.46) or birthweight (r(s)=0.03, P=0.90). In eyes without copathology in addition to regressed ROP (29 eyes, 19 patients), there was no significant correlation between subfoveal choroidal thickness and visual acuity.

CONCLUSIONS

Our findings of thinner subfoveal and temporal macular choroidal thickness in regressed ROP support the case for choroidal involvement in the pathogenesis of this condition.

摘要

目的

使用增强深度成像光学相干断层扫描(EDI OCT)比较早产儿视网膜病变(ROP)消退期患者与健康对照者的脉络膜厚度。方法:24例患有ROP≥3期且病变已消退的儿童和青年(41只眼)接受了Spectralis FD-OCT的EDI OCT检查,作为其临床记录的一部分。记录他们的屈光状态、最佳矫正视力和检眼镜检查结果。前瞻性收集了33例足月出生的健康对照者(58只眼)的相应数据。使用EDI OCT由两名观察者独立测量黄斑中心凹下以及中心凹鼻侧和颞侧1500μm处的脉络膜厚度。结果:经屈光矫正后,ROP消退组黄斑中心凹下脉络膜平均厚度为271.1μm(95%可信区间,247.8 - 294.5),显著薄于对照组的327.4μm(95%可信区间,293.8 - 360.9)(P = 0.008)。同样,ROP消退组经矫正后的颞侧脉络膜平均厚度为257.2μm(95%可信区间,240.2 - 274.2),对照组为320.5μm(95%可信区间,288.6 - 352.3)(P = 0.001)。鼻侧测量结果无统计学显著差异。在ROP消退组中,黄斑中心凹下脉络膜厚度与胎龄(r(s)=0.16,P = 0.46)或出生体重(r(s)=0.03,P = 0.90)之间无显著相关性。在除ROP消退外无合并病变的眼中(29只眼,19例患者),黄斑中心凹下脉络膜厚度与视力之间无显著相关性。结论:我们关于ROP消退期黄斑中心凹下和颞侧脉络膜厚度变薄的研究结果支持脉络膜参与该疾病发病机制的观点。

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