有早产儿视网膜病变史的儿童中央窝发育不全的评价。

IF 2.3 2区 医学 Q2 OPHTHALMOLOGY Retina-The Journal of Retinal and Vitreous Diseases Pub Date : 2024-12-02 DOI:10.1097/IAE.0000000000004362
Gökhan Çelik, Bilge Batu Oto, Osman Kızılay, Murat Gunay
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引用次数: 0

摘要

目的:评价早产儿视网膜病变(ROP)患者的视网膜中央凹发育情况,探讨治疗是否会影响早产儿视网膜病变患者的视网膜中央凹发育。方法:本横断面研究纳入有ROP病史的患者。比较自发性退行眼和治疗眼的中央凹发育情况。此外,还评估了治疗时的胎龄、出生体重、ROP区和分期以及经后胎龄。根据中央凹发育不全(FH)严重程度分析最终视力。结果:本研究纳入83例患者166只眼。治疗组与自发性消退组中央凹发育差异有统计学意义,且治疗组FH更为严重。自发性消退组的中央凹发育正常率高于治疗组。这表明ROP治疗可能在中央凹发育过程中引起形态学改变。胎龄、治疗时经后年龄、ROP分期、ROP区与FH严重程度相关。轻度FH不影响视力,88.5%的患者视力为logmar0。结论:ROP患者早期中央凹发育无明显中断,ROP患者无明显与FH相关的视觉障碍。然而,用激光光凝或玻璃体内抗血管内皮生长因子治疗ROP的眼睛比自发消退的眼睛表现出更严重的发育不全。
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Evaluation of Foveal Hypoplasia in Children with a History of Retinopathy of Prematurity.

Purpose: To evaluate the foveal development in patients diagnosed with retinopathy of prematurity (ROP) and to evaluate whether foveal development was affected by treatment in ROP patients.

Methods: This cross-sectional study included patients with a history of ROP. Foveal development was compared between eyes with spontaneous regression and treated eyes. Additionally, gestational age, birth weight, ROP zone and stage, and postmenstrual gestational age at the time of treatment, were evaluated. The final visual acuity was analyzed according to the foveal hypoplasia (FH) severity.

Results: This study included 166 eyes from 83 patients. Foveal development was significantly different among the treatment and spontaneous regression groups, and FH was more severe in the treatment group. The prevalence of normal foveal development was higher in the spontaneous regression group than in the treatment groups. This suggests that ROP treatment may induce morphological alterations during foveal development. Gestational age, postmenstrual age at the time of treatment, ROP stage, and ROP zone were correlated with FH severity. Visual acuity was not affected by mild FH, and 88.5% of the patients had a visual acuity of LogMAR 0.

Conclusion: Early stage foveal development is not significantly disrupted in patients with ROP, and patients with ROP show no significant visual disturbance associated with FH. However,eyes treated for ROP either with laser photocoagulation or intravitreal anti-vascular endothelial growth factor demonstrated more severe hypoplasia compared to that with spontaneous regression.

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来源期刊
CiteScore
5.70
自引率
9.10%
发文量
554
审稿时长
3-6 weeks
期刊介绍: ​RETINA® focuses exclusively on the growing specialty of vitreoretinal disorders. The Journal provides current information on diagnostic and therapeutic techniques. Its highly specialized and informative, peer-reviewed articles are easily applicable to clinical practice. In addition to regular reports from clinical and basic science investigators, RETINA® publishes special features including periodic review articles on pertinent topics, special articles dealing with surgical and other therapeutic techniques, and abstract cards. Issues are abundantly illustrated in vivid full color. Published 12 times per year, RETINA® is truly a “must have” publication for anyone connected to this field.
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