Screening Corneal Tomography for the Diagnosis of Keratoconus in Pediatric Patients With Trisomy 21

IF 4.2 1区 医学 Q1 OPHTHALMOLOGY
Casey G. Smith , Rebecca G. Edwards Mayhew , Jasleen K. Singh , Jennifer L. Patnaik , Brandie D. Wagner , Ronald E. Wise , Jennifer L. Jung , Michael A. Puente , Francis Hickey , Cheryl Fonteh , Emily A. McCourt
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引用次数: 0

Abstract

Purpose

The goal of this study is to describe the rates of successful corneal tomography in children with Down Syndrome (DS) and to determine whether high levels of astigmatism or myopia are reliable indicators of keratoconus in children with DS.

Design

Retrospective, cross-sectional study.

Subjects and controls

Patients aged 4 to 18 years old with and without DS who underwent corneal tomography to evaluate for keratoconus at a tertiary pediatric hospital from July 2018-January 2020.

Methods

Main observation performed was identifying keratoconus and the success of tomography in patients with down syndrome.

Main Outcome Measures

Refractive error at the time of keratoconus diagnosis.

Results

358 patients with DS were seen during the study period, and 96 patients without DS were evaluated for keratoconus. Among the patients with DS screened for keratoconus, useful images were obtained in at least 1 eye in 75.9% of patients. We compared patients with and without DS who were diagnosed with keratoconus or keratoconus suspect. At the time of keratoconus diagnosis, children with DS had less astigmatism and myopia than children without DS. Within the group of patients with DS, there was no significant difference in refractive error in the patients who were diagnosed with keratoconus versus those who were not.

Conclusions

Children with DS diagnosed with keratoconus often have lower amounts of astigmatism and less myopic spherical equivalents than children with keratoconus without DS at the time of diagnosis; therefore, relying on high astigmatism as a clinical indicator for disease in patients with DS is likely inadequate. Tomographic screening should be employed even when the patient with DS is young or has low amounts of refractive error as earlier detection and treatment is crucial to favorable outcomes in children with DS.
筛查角膜断层扫描诊断小儿21三体圆锥角膜。
目的本研究的目的是描述唐氏综合征(DS)儿童角膜断层扫描成功率,并确定高度散光或近视是否是唐氏综合征儿童圆锥角膜的可靠指标。设计:回顾性、横断面研究。研究对象和对照组:2018年7月至2020年1月在一家三级儿科医院接受角膜断层扫描以评估圆锥角膜的年龄在4至18岁,有或没有退行性椎体滑移的患者。方法主要观察唐氏综合征患者圆锥角膜的识别和断层扫描的成功率。主要观察指标圆锥角膜诊断时的屈光不正。结果研究期间共观察到358例退行性椎体滑移患者,96例非退行性椎体滑移患者被评估为圆锥角膜。在筛查圆锥角膜的DS患者中,75.9%的患者至少有一只眼获得了有用的图像。我们比较了诊断为圆锥角膜或疑似圆锥角膜的DS患者和非DS患者。在圆锥角膜诊断时,退行性椎体滑移患儿的散光和近视均少于非退行性椎体滑移患儿。在退行性椎体滑移患者组中,被诊断为圆锥角膜的患者与未被诊断为圆锥角膜的患者在屈光不正方面没有显著差异。结论诊断为圆锥角膜的退行性椎体滑移患儿在诊断时散光量和近视球当量均低于无退行性椎体滑移的圆锥角膜患儿;因此,依赖高度散光作为退行性椎体滑移患者疾病的临床指标可能是不充分的。即使是年龄较小或屈光不正程度较低的退行性椎体滑移患者也应进行断层扫描筛查,因为早期发现和治疗对于退行性椎体滑移患儿的良好预后至关重要。
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来源期刊
CiteScore
9.20
自引率
7.10%
发文量
406
审稿时长
36 days
期刊介绍: The American Journal of Ophthalmology is a peer-reviewed, scientific publication that welcomes the submission of original, previously unpublished manuscripts directed to ophthalmologists and visual science specialists describing clinical investigations, clinical observations, and clinically relevant laboratory investigations. Published monthly since 1884, the full text of the American Journal of Ophthalmology and supplementary material are also presented online at www.AJO.com and on ScienceDirect. The American Journal of Ophthalmology publishes Full-Length Articles, Perspectives, Editorials, Correspondences, Books Reports and Announcements. Brief Reports and Case Reports are no longer published. We recommend submitting Brief Reports and Case Reports to our companion publication, the American Journal of Ophthalmology Case Reports. Manuscripts are accepted with the understanding that they have not been and will not be published elsewhere substantially in any format, and that there are no ethical problems with the content or data collection. Authors may be requested to produce the data upon which the manuscript is based and to answer expeditiously any questions about the manuscript or its authors.
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