The Effect of 0.01% Atropine Eye Drops on the Ocular Surface in Children for the Control of Myopia—The Primary Results from a Six-Month Prospective Study
Received 8 June 2020
Accepted for publication 27 July 2020
Published 10 August 2020 Volume 2020:16 Pages 735—740
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Professor Deyun Wang
Jingyi Cheng,1– 3,* Yujing Yang,1– 3,* Xiehe Kong,4 Li Zeng,1– 3 Zhi Chen,1– 3 Jianjiang Xu,1– 3 Chaoran Zhang1– 3
1Department of Ophthalmology and Visual Science, Eye, Ear, Nose and Throat Hospital, Shanghai Medical College of Fudan University, Shanghai, People’s Republic of China; 2Key Laboratory of Myopia, Ministry of Health (Fudan University), Shanghai, People’s Republic of China; 3Shanghai Key Laboratory of Visual Impairment and Restoration (Fudan University), Shanghai, People’s Republic of China; 4Shanghai Research Institute of Acupuncture and Meridian, Shanghai, People’s Republic of China
*These authors contributed equally to this work
Correspondence: Chaoran Zhang
Department of Ophthalmology and Visual Science, Eye, Ear, Nose and Throat Hospital, Shanghai Medical College of Fudan University, 83 Fenyang Road, Shanghai 200031, People’s Republic of China
Tel/ Fax +86 2164377134
Email [email protected]
Purpose: To evaluate the effect of 0.01% atropine eye drops on the ocular surface in children for the control of myopia.
Methods: A total of 72 participants were recruited for this prospective study. Prior to and after 1, 3, and 6 months of 0.01% atropine administration, an ocular surface disease index (OSDI) questionnaire was obtained, Keratograph 5M was used for the measurement of the tear meniscus height (TMH), noninvasive keratographic tear film break-up time (NK-BUT, the first keratographic break-up time, [NK-BUTfirst] and the average keratographic break-up time, [NK-BUTave]), bulbar redness (BR), meiboscore (MS), and anterior segment optical coherence tomography (AS-OCT) was used to calculate the inferior tear meniscus area (TMA).
Results: After using the 0.01% atropine eye drops for 1 month, 9 subjects complained of discomfort immediately after administration, but this quickly subsided, and 1 subject was temporarily dazzled. All the ocular surface symptoms were mild and occurred rarely. After 3 months, these complaints no longer occurred. Compared with the baseline values, the OSDI scores (0.08 ± 0.28), values of TMH (0.23 ± 0.04 mm), TMA (0.0420 ± 0.0444 mm2), NK-BUTfirst (9.39 ± 5.25 s), NK-BUTave (10.49 ± 4.94 s), BR (0.63 ± 0.37), and MS (0.89 ± 0.70) did not change significantly after 6 months of 0.01% atropine eye drop administration (P > 0.05).
Conclusion: In this 6-month prospective study, no side effects were observed on the ocular surface after using 0.01% atropine in children.
Keywords: 0.01% atropine eye drops, ocular surface, children, myopia control
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