Li Li, Gao Yanlin, Lu Yuhan, Chen Wei, Han Mei
Tianjin Eye Hospital, Tianjin Key Laboratory of Ophthalmology and Visual Science, Tianjin, China.
School of Medicine, Nankai University, Tianjin, China.
Front Pediatr. 2025 Jun 4;13:1509106. doi: 10.3389/fped.2025.1509106. eCollection 2025.
To evaluate the effectiveness and applicability of the postnatal growth and retinopathy of prematurity (G-ROP) screening criteria in a Chinese neonatal cohort.
Data pertaining to the retinal screening of premature infants admitted to the neonatal intensive care unit from January 2021 through December 2021 were retrospectively analyzed. The severity of ROP was graded on the basis of the International Classification of Retinopathy of Prematurity criteria established in 2005. Treatment decisions for ROP were guided by the recommendations of the Early Treatment for Retinopathy of Prematurity Cooperative Group. The presence of six key variables that comprise the G-ROP screening criteria were carefully documented. The sensitivity and specificity of the G-ROP predictive algorithm in identifying infants with ROP requiring treatment were calculated.
A total of 352 infants with complete records were included in this study, among whom 120 infants (34.1%) were diagnosed with ROP. Of those, 21 infants (6.0%) received treatment. By applying the 6 criteria of the G-ROP model, all infants with severe ROP were successfully identified. The sensitivity of the G-ROP model in predicting treatment-requiring ROP was 100% (CI, 0.808-1.00), and the specificity was 47.8% (CI, 0.413-0.545). By applying the G-ROP criteria, the number of infants who required ROP screening would have been reduced by 122 (34.7%), while the number of screenings (1967) would have been reduced by 537 (27.3%).
The prevalence of ROP (34.1%) and treatment-requiring ROP (6.0%) were relatively high in our cohort. Application of the G-ROP prediction model can improve the sensitivity and specificity of ROP screening. All infants with treatment-requiring ROP were correctly identified. The G-ROP screening criteria seemed to be effective and appropriate for predicting ROP in infants living in Tianjin, China.
评估早产新生儿生长发育及早产儿视网膜病变(G-ROP)筛查标准在中国新生儿队列中的有效性和适用性。
对2021年1月至2021年12月入住新生儿重症监护病房的早产儿视网膜筛查数据进行回顾性分析。ROP严重程度根据2005年制定的国际早产儿视网膜病变分类标准进行分级。ROP的治疗决策遵循早产儿视网膜病变早期治疗协作组的建议。仔细记录构成G-ROP筛查标准的六个关键变量的存在情况。计算G-ROP预测算法在识别需要治疗的ROP婴儿中的敏感性和特异性。
本研究共纳入352例记录完整的婴儿,其中120例(34.1%)被诊断为ROP。其中,21例(6.0%)接受了治疗。通过应用G-ROP模型的6项标准,所有重度ROP婴儿均被成功识别。G-ROP模型预测需要治疗的ROP的敏感性为100%(CI,0.808-1.00),特异性为47.8%(CI,0.413-0.545)。应用G-ROP标准,需要进行ROP筛查的婴儿数量将减少122例(34.7%),而筛查次数(1967次)将减少537次(27.3%)。
在我们的队列中,ROP患病率(34.1%)和需要治疗的ROP患病率(6.0%)相对较高。应用G-ROP预测模型可提高ROP筛查的敏感性和特异性。所有需要治疗的ROP婴儿均被正确识别。G-ROP筛查标准似乎对预测中国天津地区婴儿的ROP有效且适用。