Ophthalmic Features 5 Years after Cranioplasty in Children with Unilateral Coronal Craniosynostosis

IF 0.1 Q4 OPHTHALMOLOGY
Suji Yeo, Seung Ah Chung
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引用次数: 0

Abstract

Purpose: To investigate ocular asymmetry status 5 years after cranioplasty in children with unilateral coronal craniosynostosis.Methods: The medical records of 41 children who underwent cranioplasty at a mean age of 11.7 months were retrospectively reviewed. The cranial vault asymmetry index (CVAI) and the amount of head tilt were measured on images obtained before cranioplasty. Presence of anisometropia, aniso-astigmatism, amblyopia, and strabismus was evaluated at a mean age of 6.8 years. Correlations among the CVAI, direction of synostotic suture and ocular asymmetries were analyzed.Results: Before cranioplasty, the CVAI was 4.5%; 31 of 41 patients (75.6%) exhibited head tilting, which was contralateral to the synostotic suture site in 29 of these patients. At a mean of 5.6 years after cranioplasty, anisometropia of ≥ 1.00 diopters on the spherical equivalent was present in 9 patients (22.0%) and aniso-astigmatism of ≥ 1.00 diopters in 10 patients (24.4%). Amblyopia was in 15 patients (36.6%); the eye contralateral to the synostotic suture was more frequently affected, and anisometropic amblyopia was the most common subtype. Strabismus was present in 28 patients (68.3%); exodeviation and vertical deviation were the most common subtypes. The non-dominant eye was the eye ipsilateral to the synostotic suture in 12 of 13 patients (92.3%) with simulated superior oblique palsy and in 7 of 10 patients (70.0%) with dissociated vertical deviation. In children with CVAI of ≥ 5%, anisometropia was significantly more common than in other children (p = 0.04), but we found no relationship between any other type of ocular asymmetry and a high CVAI.Conclusions: Ocular asymmetries including anisometropia, aniso-astigmatism, amblyopia, and strabismus were observed even 5 years after successful cranioplasty treatment for unilateral coronal craniosynostosis, emphasizing the need for continuous ophthalmic follow-up.
单侧冠状动脉粥样硬化患儿颅骨成形术后5年的眼科特点
目的:探讨儿童单侧冠状面开颅术后5年的眼部不对称状况。方法:回顾性分析41例平均年龄11.7个月的儿童颅骨成形术的临床资料。在颅骨成形术前的图像上测量颅骨拱顶不对称指数(CVAI)和头部倾斜量。在平均6.8岁时评估是否存在屈光参差、散光、弱视和斜视。分析了CVAI、缝合方向和眼睛不对称性之间的相关性。结果:开颅术前CVAI为4.5%;41例患者中有31例(75.6%)表现出头部倾斜,其中29例患者的头部倾斜对侧滑膜缝合部位。颅骨成形术后平均5.6年,9例患者(22.0%)出现屈光度≥1.00屈光度的屈光参差,10例患者(24.4%)出现屈光度数≥1.00的散光,15例患者(36.6%)出现弱视;对侧滑膜缝合线的眼更容易受到影响,屈光参差性弱视是最常见的亚型。斜视28例(68.3%);外斜视和垂直偏斜是最常见的亚型。13例模拟上斜肌麻痹患者中有12例(92.3%)和10例游离垂直偏斜患者中有7例(70.0%)的非优势眼位于同侧缝。在CVAI≥5%的儿童中,屈光参差明显比其他儿童更常见(p=0.04),但我们没有发现任何其他类型的眼睛不对称与高CVAI之间的关系,甚至在单侧冠状骨颅缝闭合的颅骨成形术治疗成功5年后也观察到斜视,强调了持续眼科随访的必要性。
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来源期刊
CiteScore
0.20
自引率
0.00%
发文量
126
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