Anisometropia and Amblyopia Outcomes in Early Versus Late Resolution of Congenital Nasolacrimal Duct Obstruction in Older Infants

Deion T. Sims, T. B. Gillette, Jocelyn G. Lam, Darren Liu, Calvin Lee, Leona Ding, Kristina Tarczy-Hornoch, M. T. Cabrera
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Abstract

Congenital nasolacrimal duct obstruction is a known risk factor for amblyopia and anisometropia. The purpose of this study was to investigate whether the rate of anisometropia and amblyopia development differed based on the age at CNLDO resolution in older infants. This retrospective chart review at a single tertiary children’s hospital from 2007 to 2017 compared early versus late spontaneous resolution (cutoff 12 months) and intervention (cutoff 15 months) groups presenting at ≥9 months of age, comparing visual outcomes, including anisometropia (≥1 D of sphere or cylinder) and amblyopia (≥2 levels difference in Teller acuity or optotype testing). Parents/guardians were contacted by phone for missing data on spontaneous resolution or intervention status. A total of 462 patients were included (152 early; 310 late group). The early group presented at a median age of 12.0 (interquartile range: 10.0, 13.0) months, while the late group presented at 21.0 (interquartile range: 15.0, 32.0) months. Unilateral disease occurred in 62% and 59%, respectively. Anisometropia was seen in (12/102) 12% of early versus (25/243) 10% of late patients (p = 0.686, 95% CI: –0.059, 0.088), and amblyopia in (4/131) 3% of early versus (14/286) 5% of late patients (p = 0.322, 95% CI: –0.061, 0.018). In patients presenting <24 months without undergoing surgery, spontaneous resolution occurred in 76% between 12 and 24 months (n = 41). Anisometropia and amblyopia rates did not significantly differ between early and delayed intervention for congenital nasolacrimal duct obstruction in this retrospective cohort presenting beyond 9 months of age to a children’s hospital. This study found frequent late spontaneous resolution.
大龄婴儿先天性鼻泪管阻塞早期与晚期解决的屈光参差和弱视结果
先天性鼻泪管阻塞是弱视和屈光参差的已知危险因素。本研究的目的是调查大婴儿的屈光参差和弱视的发展率是否根据CNLDO分辨率的年龄而不同。本回顾性图表回顾了一家三级儿童医院2007年至2017年的回顾性图表,比较了出现≥9月龄的早期自发分辨力组和晚期自发分辨力组(截止12个月)和干预组(截止15个月),比较了视力结果,包括屈光参差(球体或圆柱体≥1d)和弱视(泰勒视力或视型测试差异≥2个水平)。通过电话联系父母/监护人,以了解自发解决或干预状态的缺失数据。共纳入462例患者(早期152例;310后期组)。早期组发病中位年龄为12.0个月(四分位数范围:10.0,13.0),晚期组发病中位年龄为21.0个月(四分位数范围:15.0,32.0)。单侧病变发生率分别为62%和59%。(12/102) 12%的早期患者有屈光参差,(25/243)10%的晚期患者有屈光参差(p = 0.686, 95% CI: -0.059, 0.088);(4/131) 3%的早期患者有弱视,(14/286)5%的晚期患者有弱视(p = 0.322, 95% CI: -0.061, 0.018)。在未接受手术的<24个月的患者中,76%的患者在12至24个月内自发消退(n = 41)。在这个儿童医院的年龄超过9个月的回顾性队列中,先天性鼻泪管梗阻的早期干预和延迟干预对屈光参差和弱视的发生率没有显著差异。该研究发现频繁出现晚期自发消退。
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