Secondary Glaucoma after Cataract Surgery Performed in Infancy in Congenital Rubella Syndrome

IF 2.8 Q1 OPHTHALMOLOGY Ophthalmology. Glaucoma Pub Date : 2024-11-01 DOI:10.1016/j.ogla.2024.07.001
Gayathri J. Panicker MS , Sumita Agarkar MS, DNB , Mona Khurana MS , Visakh Thomas DNB
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Abstract

Objective

To compare the incidence of secondary glaucoma after cataract surgery performed in infancy in children with congenital rubella syndrome (CRS) and children with nonrubella cataracts and to identify associated risk factors.

Design

Retrospective case control study.

Participants

Children with CRS who had undergone cataract surgery in infancy and age-matched infants who had undergone cataract surgery for infantile cataracts were included.

Main Outcome Measures

Incidence of glaucoma and probability of survival was compared among the 2 groups.

Methods

Risk factors for the development of glaucoma were assessed. The minimum follow-up was 1 year after cataract surgery.

Results

The study included 211 eyes of 115 children. The CRS group (cases) had 101 eyes (58 children) and the nonrubella cataract group (controls) included 110 eyes (57 children). There was no significant difference in the mean age at surgery among the 2 groups (P = 0.96). Cumulative incidence of secondary childhood glaucoma for the entire study period of 14 years was 32.7% in the CRS group and 24.5% in the control group (P = 0.19). Mean follow-up was 5.8 ± 3.7 years for CRS group and 6.4 ± 3.4 years for the nonrubella group. A significant difference in the cumulative probability of glaucoma free survival at 10 years after cataract surgery (cases 0.53 vs controls 0.8; log rank P = 0.034) was present. Both groups had no significant difference in the time of onset of secondary glaucoma, average number of intraocular pressure lowering medications and number of eyes with surgical intervention for glaucoma (P > 0.05). Microcornea was associated with the development of glaucoma (hazard ratio 2.83; 95% confidence interval, 1.44–5.57; P = 0.002) in CRS eyes.

Conclusion

There was no significant difference in the incidence of secondary glaucoma after cataract surgery performed in infants with CRS compared with infants who had undergone surgery for infantile cataracts. Because the 10-year probability of glaucoma free survival was significantly less in children with CRS, a closer and longer follow-up is recommended especially in eyes with at-risk features.

Financial Disclosure(s)

The author(s) have no proprietary or commercial interest in any materials discussed in this article.
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先天性风疹综合征婴儿期白内障手术后的继发性青光眼--病例对照研究。
目的比较先天性风疹综合征(CRS)患儿和非风疹性白内障患儿在婴儿期接受白内障手术后继发性青光眼的发生率,并确定相关风险因素:设计:回顾性病例对照研究:方法:青光眼的发病率和患病几率:比较两组患儿的青光眼发病率和存活概率。方法:比较两组婴儿的青光眼发病率和存活概率,并评估发生青光眼的风险因素。随访时间最短为白内障手术后 1 年:研究包括 115 名儿童的 211 只眼睛。CRS组(病例)有101只眼睛(58名儿童),非风疹型白内障组(对照组)有110只眼睛(57名儿童)。两组的平均手术年龄无明显差异(P=0.96)。在整个14年的研究期间,CRS组儿童继发性青光眼的累积发病率为32.7%,对照组为24.5%(P=0.19)。CRS组的平均随访时间为5.8±3.7年,非风疹组为6.4±3.4年。白内障手术后 10 年无青光眼生存的累积概率存在明显差异(病例为 0.53,对照组为 0.8;对数秩 p-0.034)。两组患者在继发性青光眼发病时间、平均使用降眼压药物次数和青光眼手术干预眼数方面均无明显差异(P>0.05)。在 CRS 患者中,小角膜与青光眼的发生有关(危险比 2.83,95% 置信区间 1.44-5.57;P=0.002):结论:与接受婴儿白内障手术的婴儿相比,CRS 婴儿接受白内障手术后继发性青光眼的发生率没有明显差异。由于CRS患儿的十年无青光眼生存概率明显较低,因此建议进行更密切、更长时间的随访,尤其是对具有高危特征的眼睛。
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来源期刊
Ophthalmology. Glaucoma
Ophthalmology. Glaucoma OPHTHALMOLOGY-
CiteScore
4.80
自引率
6.90%
发文量
140
审稿时长
46 days
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Reply Editorial Board Contents Posterior Capsular Pigment Deposition in a Case of Pigmentary Glaucoma Iridoschisis: The Shredded Iris
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