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原发性先天性青光眼患儿失明的危险因素——登记队列随访研究

Risk Factors for Blindness in Children With Primary Congenital Glaucoma-Follow-up of a Registry Cohort.

作者信息

Alshigari Rayan, Freidi Alia, Souru Ches, Edward Deepak P, Malik Rizwan

机构信息

Glaucoma Division, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia.

Department of Mathematics, Lebanese International University, Beirut, Lebanon.

出版信息

Am J Ophthalmol. 2021 Apr;224:238-245. doi: 10.1016/j.ajo.2020.12.014. Epub 2021 Jan 6.

Abstract

PURPOSE

To evaluate the baseline features associated with blindness in a cohort of children with primary congenital glaucoma (PCG) from a hospital registry.

DESIGN

Retrospective clinical cohort study.

METHODS

Setting: Observational cohort study. StudyPopulation: The registry included all children who presented to our tertiary care institute between 1995 and 2014 with a diagnosis of childhood glaucoma. ObservationProcedure: Baseline characteristics at initial presentation of children with PCG in the registry who were blind at the last follow-up were compared with those who were not blind, using bivariate and then multivariate regressions to account for potential confounders. MainOutcomeMeasures: Blindness was defined as a best-corrected visual acuity of 3/60 (20/400) or worse in the better eye at the final follow-up.

RESULTS

The eligible sample consisted of 196 children with a mean age of 9.54 ± 22.44 months at presentation. After a mean ± standard deviation follow-up of 8.49 ± 3.85 years, 20 (10.2%) children were blind. The baseline demographic factors, intraocular pressure, horizontal corneal diameter, spherical equivalent, axial length, and corneal thickness, were similar for the "blind" and "not blind" groups (P > .05). In the multivariate regression, only the severity of corneal opacification remained significantly (P < .001) associated with the risk of blindness (odds ratio = 4.05; 95% confidence interval: 1.89-8.85).

CONCLUSION

Corneal clouding is a predictor of future blindness in children with PCG. Children with severe corneal clouding may need more aggressive intraocular pressure control, closer follow-up, and earlier counseling.

摘要

目的

通过医院登记系统评估一组原发性先天性青光眼(PCG)患儿失明相关的基线特征。

设计

回顾性临床队列研究。

方法

设置:观察性队列研究。研究人群:该登记系统纳入了1995年至2014年间在我们三级医疗机构就诊并被诊断为儿童青光眼的所有患儿。观察程序:将登记系统中最后随访时失明的PCG患儿初次就诊时的基线特征与未失明患儿的基线特征进行比较,采用双变量然后多变量回归分析以考虑潜在混杂因素。主要观察指标:失明定义为最后随访时较好眼最佳矫正视力为3/60(20/400)或更差。

结果

符合条件的样本包括196名患儿,就诊时平均年龄为9.54±22.44个月。平均±标准差随访8.49±3.85年后,20名(10.2%)患儿失明。“失明”组和“未失明”组的基线人口统计学因素、眼压、角膜水平直径、等效球镜度、眼轴长度和角膜厚度相似(P>.05)。在多变量回归中,只有角膜混浊的严重程度与失明风险仍有显著相关性(P<.001)(比值比=4.05;95%置信区间:1.89 - 8.85)。

结论

角膜混浊是PCG患儿未来失明的一个预测指标。角膜混浊严重的患儿可能需要更积极地控制眼压、更密切的随访和更早的咨询。

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