Wang Jiangya, Ma Qingmin, Du Fangfang
Department of Pediatrics, Hebei General Hospital, Shijiazhuang, 050000, People's Republic of China.
Department of Ophthalmology, Hebei General Hospital, Shijiazhuang, 050000, People's Republic of China.
J Multidiscip Healthc. 2025 Aug 30;18:5381-5391. doi: 10.2147/JMDH.S528155. eCollection 2025.
Retinopathy of prematurity (ROP) is rising in China alongside improved neonatal intensive care. Current screening, reliant on gestational age (GA) and birth weight (BW), faces challenges of resource constraints and infant burden. Postnatal weight gain rate (WGR) is a potential predictive marker, but robust data on its value, particularly for severe ROP, and validated thresholds within the Chinese population are lacking. The study aimed to examine the risk factors linked with the incidence of retinopathy of ROP.
A retrospective cohort analysis was conducted on 230 preterm infants (GA ≤32 weeks, BW ≤2000g) admitted to a neonatal intensive care unit (2016-2020). Infants were categorized into non-ROP (n=189) and ROP (n=41) groups; the ROP group was further stratified into mild (n=32) and severe (n=9) subgroups. Clinical data, including GA, BW, comorbidities and WGR, were analyzed. Univariate analysis, multivariate logistic regression, and receiver operating characteristic (ROC) curve analysis were employed.
In the univariate analysis, the non-ROP group manifested superior values in GA, BW, and rates of weight gain in comparison to the ROP group (all P < 0.05). Multivariate analysis identified lower GA (OR=0.91, 95% CI=0.83-0.99, P=0.03), lower BW (OR=0.99, 95% CI=0.99-1.00, P=0.04), and lower WGR (OR=0.73, 95% CI=0.63-0.83, P<0.01) as independent risk factors for ROP. GA, BW, and WGR were significantly higher in the mild vs severe ROP group (all P<0.05). ROC analysis demonstrated that WGR <24.5 g/day predicted any ROP (AUC=0.939, 95% CI=0.905-0.973, sensitivity 90.2%, specificity 86.8%, P<0.05). Crucially, WGR <18 g/day predicted severe ROP (AUC=0.865, 95% CI=0.70-1.00, sensitivity 100%, specificity 66,7%, P<0.05).
Diminished GA, reduced BW, and sluggish weight gain rates have been correlated with an elevated susceptibility to ROP. Notably, a diminished rate of weight gain can serve as an anticipatory marker for severe ROP, given its heightened propensity to precipitate the onset of severe ROP.
Full name of the registry: Chinese Clinical Trial Registry, http://www.chictr.org.cn. Trial registration number: chiCTR2400087938. Date of registration: 2024-08-07.
随着新生儿重症监护水平的提高,中国早产儿视网膜病变(ROP)的发病率呈上升趋势。目前的筛查依赖于胎龄(GA)和出生体重(BW),面临资源限制和婴儿负担等挑战。出生后体重增加率(WGR)是一个潜在的预测指标,但关于其价值,尤其是对于严重ROP的价值,以及中国人群中经过验证的阈值的数据尚缺乏。本研究旨在探讨与ROP发病率相关的危险因素。
对入住新生儿重症监护病房(2016 - 2020年)的230例早产儿(GA≤32周,BW≤2000g)进行回顾性队列分析。将婴儿分为非ROP组(n = 189)和ROP组(n = 41);ROP组进一步分为轻度(n = 32)和重度(n = 9)亚组。分析临床数据,包括GA、BW、合并症和WGR。采用单因素分析、多因素逻辑回归和受试者工作特征(ROC)曲线分析。
在单因素分析中,非ROP组在GA、BW和体重增加率方面表现优于ROP组(所有P < 0.05)。多因素分析确定确定,较低的GA(OR = 0.91,95%CI = 0.83 - 0.99,P = 0.03)、较低的BW(OR = 0.99,95%CI = 0.99 - 1.00,P = 0.04)和较低的WGR(OR = 0.73,95%CI = 0.63 - 0.83,P < 0.01)是ROP的独立危险因素。轻度ROP组与重度ROP组相比,GA、BW和WGR显著更高(所有P < 0.05)。ROC分析表明,WGR < 24.5 g/天可预测任何ROP(AUC = 0.939,95%CI = 0.905 - 0.973,敏感性90.2%,特异性86.8%,P < 0.05)。至关重要的是,WGR < 18 g/天可预测严重ROP(AUC = 0.865,95%CI = 0.70 - 1.00,敏感性100%,特异性66.7%,P < 0.05)。
GA降低、BW减少和体重增加缓慢与ROP易感性增加相关。值得注意的是,体重增加率降低可作为严重ROP的预测指标,因为其更易引发严重ROP的发生。
注册机构全称:中国临床试验注册中心,http://www.chictr.org.cn。试验注册号:chiCTR2400087938。注册日期:2024 - 08 - 07。