Long-Term Peripheral Vitreoretinal Interface Abnormalities of Retinopathy of Prematurity: Ultra-Wide Field Optical Coherence Tomography Findings.

IF 5.6 2区 医学 Q1 OPHTHALMOLOGY
Gökhan Çelik, Bilge Batu Oto, Osman Kızılay, Murat Gunay, Aslan Aykut
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引用次数: 0

Abstract

Background: Evaluation of long-term changes in the vitreoretinal interface in patients with retinopathy of prematurity (ROP) using ultrawide-field optical coherence tomography (OCT). This cross-sectional single-centre study included children with a history of ROP treated with either a single dose of intravitreal bevacizumab (IVB), laser photocoagulation (LPC), or those with spontaneous regression (SR).

Methods: Ultrawide-field OCT imaging was performed using an Optos Silverstone Swept Source-OCT device. Vitreoretinal abnormalities, including those in the former ridge area, vitreous veils, tractions, and adhesions, were grouped as 'vitreoretinal interface abnormalities'. The images were evaluated for these abnormalities.

Results: This study enrolled 188 eyes of 94 patients (76 eyes of 38 children, IVB group; 40 eyes of 28 children, LPC group; 72 eyes of 44 children, SR group). The prevalence of vitreoretinal interface abnormalities was 73.2% and 44.4% in the IVB and SR groups, respectively. All the patients in the LPC group showed abnormalities in laser and non-laser retinal areas.

Conclusion: Ultrawide-field OCT revealed various vitreoretinal interface abnormalities in patients with a history of ROP. Long-term follow-up and OCT evaluation of the peripheral retina, even without structural abnormalities on following examinations, may help prevent outcomes such as retinal detachment. Treatment of detected lesions remains uncertain.

早产儿视网膜病变的长期外周玻璃体视网膜界面异常:超宽视场光学相干断层扫描结果。
背景:应用超宽视场光学相干断层扫描(OCT)评价早产儿视网膜病变(ROP)患者玻璃体视网膜界面的长期变化。这项横断面单中心研究纳入了接受单剂量玻璃体内贝伐单抗(IVB)、激光光凝(LPC)或自发性消退(SR)治疗的有ROP病史的儿童。方法:采用Optos Silverstone扫描源OCT设备进行超宽视场OCT成像。玻璃体视网膜异常,包括前脊区、玻璃体膜、牵拉和粘连,被归类为“玻璃体视网膜界面异常”。对这些异常图像进行评估。结果:本研究共纳入94例患者188眼(IVB组38例76眼;LPC组28例40眼;SR组44例72眼)。IVB组和SR组玻璃体视网膜界面异常发生率分别为73.2%和44.4%。LPC组患者均出现激光及非激光视网膜病变。结论:超宽视场OCT显示有ROP病史的患者有多种玻璃体视网膜界面异常。对周围视网膜的长期随访和OCT评估,即使在后续检查中没有结构异常,也可能有助于预防视网膜脱离等结果。检测到的病变的治疗仍不确定。
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来源期刊
CiteScore
7.60
自引率
12.50%
发文量
150
审稿时长
4-8 weeks
期刊介绍: Clinical & Experimental Ophthalmology is the official journal of The Royal Australian and New Zealand College of Ophthalmologists. The journal publishes peer-reviewed original research and reviews dealing with all aspects of clinical practice and research which are international in scope and application. CEO recognises the importance of collaborative research and welcomes papers that have a direct influence on ophthalmic practice but are not unique to ophthalmology.
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