Wang Liang, Li Manhong, Zhu Jun, Yan Hongxiang, Wu Lei, Fan Jing, Zhou Yi, Gou Kaili, Zhang Zifeng, Wang Yusheng
Department of Ophthalmology, Eye Institute of Chinese PLA, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
State Key Laboratory of Cancer Biology, Institute of Digestive Diseases, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Front Med (Lausanne). 2021 Aug 31;8:731421. doi: 10.3389/fmed.2021.731421. eCollection 2021.
The aim of this study is to explore the clinical features of spontaneous regression of retinopathy of prematurity (ROP) in China, including fundus appearance, time course, and affecting factors. Data of pediatric patients in whom ROP spontaneously regressed without treatment were collected, including general demographics, medical history, zones and stages of ROP, and changes of fundus appearance. The fundus manifestations of spontaneous regression in ROP were systematically summarized. Meanwhile, the time course of spontaneous regression in ROP was further analyzed, including the onset time, completion time, and duration of regression, which were all compared across different ROP zones and stages. The associated factors were analyzed by survival analysis for their correlation with delayed regression for the first time. Two hundred thirty-seven eyes of 237 pediatric patients were included. The fundus manifestations of regression differed across stages. Lesions gradually subsided, and the retinal vessels gradually vascularized completely. However, despite ROP regression, some abnormalities remained. We observed avascular retina in the temporal periphery (19.0%), increased vascular branching (6.8%), retinal pigmentary changes (6.8%), and smaller angle between the upper and lower temporal retinal vessel trunks (3.0%). Acute ROP started to regress at a median 40 weeks of postmenstrual age (PMA) and completely regressed by median 49.0 weeks of PMA. The median duration for regression was 8.5 weeks. The zone II ROP and stage 3 ROP had a later time for onset and completion of regression, and longer duration. Anemia and retinal hemorrhage (RH) were identified as independent risk factors for delayed regression by survival analysis. During spontaneous regression, the fundus appearance is diverse, and the retinal vessels gradually vascularized completely. The time course of regression differs depending on the ROP zone and stage. Anemia and RH are independent risk factors for delayed regression. Further research of the natural course of the regression of ROP is needed to help design effective screening and follow-up plans.
本研究旨在探讨中国早产儿视网膜病变(ROP)自发消退的临床特征,包括眼底表现、病程及影响因素。收集未经治疗而ROP自发消退的儿科患者的数据,包括一般人口统计学资料、病史、ROP的分区及分期,以及眼底表现的变化。系统总结ROP自发消退的眼底表现。同时,进一步分析ROP自发消退的病程,包括消退的起始时间、完成时间及持续时间,并对不同ROP分区和分期进行比较。首次采用生存分析方法分析相关因素与消退延迟的相关性。纳入237例儿科患者的237只眼。不同分期的消退眼底表现各异。病变逐渐消退,视网膜血管逐渐完全血管化。然而,尽管ROP消退,但仍存在一些异常。我们观察到颞侧周边无血管视网膜(19.0%)、血管分支增加(6.8%)、视网膜色素改变(6.8%)以及颞侧视网膜上下血管主干夹角变小(3.0%)。急性ROP在月经龄(PMA)中位数40周时开始消退,在PMA中位数49.0周时完全消退。消退的中位持续时间为8.5周。II区ROP和3期ROP的消退起始和完成时间较晚,持续时间较长。生存分析确定贫血和视网膜出血(RH)是消退延迟的独立危险因素。在自发消退过程中,眼底表现多样,视网膜血管逐渐完全血管化。消退病程因ROP分区和分期而异。贫血和RH是消退延迟的独立危险因素。需要进一步研究ROP消退的自然病程,以帮助设计有效的筛查和随访计划。