儿童青光眼的进展:8年随访的经验教训

Q2 Medicine
Farideh Sharifipour, Elahe Arasteh, Maryam Hajizadeh, Atefe Mahdian-Rad, Mohammad Sadegh Mirdehghan
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引用次数: 0

摘要

背景:外科手术是儿童青光眼的主要治疗方式之一,即使可能发生进展。在这项研究中,我们旨在探讨影响儿童青光眼进展的危险因素。方法:在这项回顾性队列研究中,我们回顾了2009年4月至2017年3月诊断为儿童青光眼的患者的医疗记录。儿童青光眼患者接受了至少1年的定期随访。记录患者的人口统计学、眼压(IOP)、角膜中央厚度(CCT)、角膜轴长(AL)、杯盘比(C/D)、角膜直径、青光眼类型、诊断时年龄、手术时年龄。进展被定义为在1年随访期间AL增加> 2mm, C/D比值> 0.2,或角膜直径> 1mm。结果:纳入46例患者83只眼:原发性先天性青光眼37只(45%),继发性青光眼46只(55%),83只眼中27只(32.5%)出现进展。PCG和继发性青光眼的进展相当(PCG, 22%;继发性青光眼,41%;P = 0.152)。随着病情进展,诊断时的年龄和首次手术时的年龄明显降低(P = 0.046和0.012)。进展眼和非进展眼的手术平均(标准差)分别为1.88(1.1)和1 (0.8)(P = 0.015)。青光眼进展患者并发全身性疾病的频率显著高于青光眼进展患者(P = 0.043)。进展眼和未进展眼在其他人口统计学特征和眼部参数方面具有可比性(P > 0.05)。结论:诊断和首次青光眼手术时年龄较小的儿童青光眼患者以及合并全身性疾病的患者青光眼进展的风险较高。这些发现对临床医生在咨询儿童青光眼患儿的父母有关疾病结果时是有用的。然而,未来需要更大样本量和更长的随访期的前瞻性研究来证实我们的发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Progression in pediatric glaucoma: lessons learnt from 8 years' follow-up.

Progression in pediatric glaucoma: lessons learnt from 8 years' follow-up.

Background: Surgical procedures are used as 1 of the main treatment modalities for pediatric glaucoma, even though progression may occur. In this study, we aimed to investigate the risk factors affecting the progression of pediatric glaucoma.

Methods: In this retrospective cohort study, we reviewed the medical records of patients diagnosed with pediatric glaucoma between April 2009 and March 2017. Pediatric glaucoma patients who underwent regular follow-up for at least 1 year were included. Demographics, intraocular pressure (IOP), central corneal thickness (CCT), axial length (AL), cup-to-disc ratio (C/D ratio), corneal diameter, type of glaucoma, age at time of diagnosis, and age at surgery were recorded. Progression was defined as an increase in AL > 2 mm, C/D ratio > 0.2, or corneal diameter > 1 mm during 1 year of follow-up.

Results: Eighty-three eyes from 46 patients were included: 37 eyes (45%) with primary congenital glaucoma (PCG), 46 eyes (55%) with secondary glaucoma, and 27 of these 83 eyes (32.5%) showed progression. Progression was comparable between eyes with PCG and secondary glaucoma (PCG, 22%; secondary glaucoma, 41%; P = 0.152). Age at the time of diagnosis and age at the time of the first surgery were significantly lower in the eyes with progression (P = 0.046 and 0.012, respectively). The mean (standard deviation) of surgeries in progressed versus non-progressed eyes was 1.88 (1.1) versus 1 (0.8) (P = 0.015). The frequency of comorbid systemic disease was significantly higher in patients with glaucoma progression (P = 0.043). The progressed and non-progressed eyes were comparable in terms of other demographic characteristics and ocular parameters (all P > 0.05).

Conclusions: Pediatric glaucoma patients who were younger at the time of diagnosis and the first glaucoma surgery and those with comorbid systemic disease are at higher risk of glaucoma progression. These findings are useful for clinicians when counseling parents of children with pediatric glaucoma about disease outcomes. However, future prospective studies with larger sample sizes and longer follow-up periods are needed to confirm our findings.

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