Rostamzad Parinaz, Arslan Zehra F, Mathijssen Irene M J, Koudstaal Maarten J, Pleumeekers Mieke M, Versnel Sarah L, Loudon Sjoukje E
Department of Plastic and Reconstructive Surgery, Erasmus MC, University Medical Center, 3000 CA Rotterdam, The Netherlands.
Department of Ophthalmology, Erasmus MC, University Medical Center, 3000 CA Rotterdam, The Netherlands.
J Clin Med. 2022 Feb 18;11(4):1060. doi: 10.3390/jcm11041060.
The aim of this study was to describe the ophthalmic abnormalities and their prevalence in craniosynostosis prior to craniofacial surgery.
A systematic search was conducted on Medline OVID, Embase, Cochrane, Google Scholar, Web of Science Core Collection. Inclusion criteria were English papers, children aged <18 years with non-syndromic and syndromic craniosynostosis, case reports, case series, and case-control studies. A system of domains was established consisting of an anatomic and functional ophthalmic domain. A meta-analysis of single proportions was carried out using random effects model and pooled mean proportions with 95% confidence intervals (CI) were calculated.
Thirty-two papers analyzing 2027 patients were included. Strabismus was the most common anomaly in non-syndromic craniosynostosis: Horizontal strabismus was highest prevalent in unicoronal craniosynostosis (UCS) 19% (95% CI 9-32), followed by vertical strabismus 17% (95% CI 5-33). In syndromic craniosynostosis, horizontal strabismus was most prevalent in Crouzon syndrome 52% (95 CI 26-76), followed by Apert syndrome 50% (95% CI 42-58). Vertical strabismus was most prevalent in Saethre-Chotzen 60% followed by Muenke's syndrome 36%. Furthermore, astigmatism was the second most reported outcome in non-syndromic craniosynostosis and highest prevalent in UCS 35% (95% CI 21-51). In syndromic craniosynostosis, astigmatism was most frequently seen in Crouzon syndrome 43% (95% CI 22-65), followed by Apert syndrome 34% (95% CI 14-58). Moreover, in syndromic craniosynostosis, 5-40% had a decrease in visual acuity (VA) ≤ 0.3 LogMAR in the better eye and 11-65% had a VA ≤ 0.3 LogMAR in at least one eye.
This review demonstrates the high prevalence of ocular anomalies in non-syndromic and syndromic craniosynostosis. A multidisciplinary and systematic approach is needed for the screening and optimal treatment of these conditions in a timely manner.
本研究旨在描述颅面外科手术前颅缝早闭患者的眼科异常情况及其患病率。
对医学在线数据库(Medline OVID)、荷兰医学文摘数据库(Embase)、考克兰系统评价数据库(Cochrane)、谷歌学术、科学引文索引核心合集(Web of Science Core Collection)进行系统检索。纳入标准为英文论文、年龄小于18岁的非综合征型和综合征型颅缝早闭患儿、病例报告、病例系列研究以及病例对照研究。建立了一个由解剖学和功能性眼科领域组成的领域系统。采用随机效应模型进行单一比例的荟萃分析,并计算合并平均比例及其95%置信区间(CI)。
纳入了32篇分析2027例患者的论文。斜视是非综合征型颅缝早闭最常见的异常:水平斜视在单冠状缝颅缝早闭(UCS)中最为普遍,患病率为19%(95%CI 9 - 32),其次是垂直斜视,患病率为17%(95%CI 5 - 33)。在综合征型颅缝早闭中,水平斜视在克鲁宗综合征中最为普遍,患病率为52%(95%CI 26 - 76),其次是阿佩尔综合征,患病率为50%(95%CI 42 - 58)。垂直斜视在塞特勒-乔岑综合征中最为普遍,患病率为60%,其次是蒙克综合征,患病率为36%。此外,散光是非综合征型颅缝早闭中第二常见的结果,在UCS中最为普遍,患病率为35%(95%CI 21 - 51)。在综合征型颅缝早闭中,散光在克鲁宗综合征中最常见,患病率为43%(95%CI 22 - 65),其次是阿佩尔综合征,患病率为34%(95%CI 14 - 58)。此外,在综合征型颅缝早闭中,5% - 40%的患者较好眼的视力(VA)下降至≤0.3 LogMAR,11% - 65%的患者至少一只眼的VA≤0.3 LogMAR。
本综述表明非综合征型和综合征型颅缝早闭患者眼部异常的患病率很高。需要采取多学科和系统的方法来及时筛查和优化治疗这些疾病。