Abstract
The effects of cycloplegia on ocular biological parameters in children have been extensively studied, but few studies have compared these parameters between different refractive states, ages, and sexes. Therefore, the purpose of this study was to investigate the changes in ocular biometry before and after cycloplegia in different groups based on dioptre, age and sex. We examined a total of 2049 participants in this cross-sectional study. A comprehensive eye examination was conducted before cycloplegia. Cycloplegia was implemented with the application of atropine or tropicamide. Ocular biological parameters were evaluated after cycloplegia, including axial length (AL), mean keratometry (K), flat keratometry (K1), steep keratometry (K2), central corneal thickness (CCT), anterior chamber depth (ACD) and white-to-white (WTW) distance. All the participants were categorized based on dioptre, age and sex. Statistical analysis was performed with paired t tests and Wilcoxon signed-rank tests. Regarding dioptre, AL was found to be increased significantly in the Fs, Ast and FA (p < 0.05) postcycloplegia groups. We observed significant increases in K, K1, K2 and ACD in the Fs group (p < 0.05) after cycloplegia. Regarding age, we found significant increases in AL, CCT and ACD in group 1 (p < 0.05), but AL decreased significantly in groups 2 and 3 (p < 0.05) postcycloplegia. There were no significant changes found in K, K1 and K2 in the three groups after cycloplegia (p > 0.05). Regarding sex, AL and WTW were found to decrease significantly among males and increase significantly among females (p < 0.05) postcycloplegia, while K, K1 and K2 showed the opposite trends. This study showed that there were differences in some ocular biological parameters after cycloplegia across different groups; in particular, there were significant differences in AL, CCT and ACD. Attention should be devoted to the influence of cycloplegia in clinical work.
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Introduction
Short-sightedness is caused by a slight elongation of the eyeball, which means that light is focused only in front of the retina rather than on the retina. In the past 50 years, the rate of myopia in East Asian countries has increased sharply1. Myopia, especially high myopia, seriously threatens people's physical and mental health and can even lead to blindness. Approximately 2 billion people have myopia, accounting for approximately 28.3% of the global population2. Additionally, approximately 277 million people have high myopia, accounting for approximately 4.0% of the worldwide population2. It is estimated that by 2050, the number of individuals with myopia will increase to 4.76 billion, accounting for approximately 49.8% of the global population, and nearly 1 billion individuals will have high myopia2,3. Ocular disorders among children and adolescents have become a serious social problem in China, and refraction is the primary cause of vision loss in these age groups4,5,6. Therefore, the accurate diagnosis and appropriate treatment of myopia are increasingly important.
With the increasing number of myopic patients, an increasing number of children require orthokeratology, which highlights the great importance of the accuracy of preoperative optometry7,8,9. In addition, due to the increasing number of patients undergoing corneal refractive surgery, such as transepithelial photorefractive keratectomy (T-PRK), laser in situ keratomileusis (LASIK) and laser subepithelial keratomileusis (LASEK), as well as people's stringent requirements for visual quality after the surgery, it is important to accurately evaluate patients' refractive parameters before the operation10,11,12. Cycloplegia optometry is the internationally recognized and the most important method for the diagnosis of ametropia in children and adolescents13,14,15. However, the parameters of the anterior segment can be altered after the application of cycloplegia, including refractive state16,17,18,19, axial length (AL)17,19,20,21,22, corneal curvature23,24,25, central corneal thickness (CCT)16,21,22,26,27,28, anterior chamber depth (ACD)17,19,21,22,23,24,25,26,29,30,31, anterior chamber volume (ACV)26,30, and white-to-white (WTW) distance22,31. Some researchers have found that significant changes occur in higher-order aberrations (HOAs)18, subfoveal choroidal thickness (ChT)13,20 and lens thickness21,30 among children or adults after the drop in cycloplegia in the eye. Bagheri A and some other researchers found that cycloplegia causes a hyperopic shift16,17,18,19. Numerous studies have shown that ACD increases after cycloplegia21,22,30. All the parameters from the abovementioned studies showed huge differences except ACD, ACV, hyperopic shift, ChT, HOAs and lens thickness. The change in refractive state and anterior segment parameters caused by ciliary paralysis directly affects the diagnosis and treatment of ametropia. Corneal curvature, CCT and ACD are also important indices for the preoperative evaluation of many kinds of ophthalmic surgery, including corneal refractive surgery and cataract surgery. There were considerable differences in the results of previous studies on the biological parameters of the important anterior segment, such as AL, corneal curvature and CCT, even though the opposite results were obtained17,19,21,22.
At present, there is a lack of large sample studies on the effects of cycloplegia on refractive state, AL, ACD, corneal curvature and CCT in children and adolescents. The effects of mydriasis optometry after cycloplegia on corneal curvature and CCT have yet to be fully elucidated, and it is unclear whether different cycloplegic drugs have different effects on ocular biological parameters. This cross-sectional study compared changes in corneal curvature, CCT, ACD and AL in children and adolescents before and after cycloplegia based on dioptre age, and sex.
Methods
Study participants
In this cross-sectional study, we examined the right eyes of 2049 patients with ametropia. This study was conducted in accordance with the Declaration of Helsinki. This study was also approved by the ethics committee of the First People's Hospital of Jiujiang City in China. Furthermore, written informed consent was obtained from each participant of the study at the time of study enrolment. All patients were divided into groups based on dioptre, age, and sex, and we compared the changes in the ophthalmic biological measurement parameters before and after cycloplegia. We examined children aged between 1 and 21 years old (mean age was 8.99 ± 3.233 years) with ametropia in the outpatient clinic, including 1102 males and 947 females. All patients underwent systematic ophthalmological examination, including the eyelid, conjunctiva, cornea, refraction, vision, best-corrected visual acuity (BCVA), functional slit lamp biomicroscopy (FSLB), intraocular pressure (IOP) and fundus examination. The examinations were performed by an ophthalmologist to rule out organic ophthalmopathy. The inclusion criteria were as follows: (1) children and adolescents aged 1 to 21 years old in the ophthalmology clinic and (2) no eye diseases found after systematic eye examination (vision, FSLB, fundus examination, etc.). The exclusion criteria were as follows: (1) suffering from eye diseases; (2) having a history of eye diseases; (3) suffering from chronic diseases such as asthma and heart disease; and (4) wearing corneal contact lenses in the past 1 month.
Ocular examinations
Ocular examinations were performed in the hospital after patients were screened for abnormal vision when they were at school. Ocular biological characteristics of the subjects were measured before and after pupil dilation with a noncontact apparatus (AL-Scan, NIDEK CO., LTD., Aichi Prefecture, Japan). A single operating ophthalmologist performed the procedure. All patients were instructed to stare at the detected beam during the measurement. The right eye was measured first, and then the left eye was measured. The following parameters were examined only once: mean keratometry (K), flat keratometry (K1), steep keratometry (K2), CCT, ACD and WTW. AL was generated automatically 5 times, and the results were averaged. Software was used to automatically calculate the values of CCT and ACD through image analysis. ACD was measured as the distance from the anterior corneal pole to the anterior lens surface. Computer-based optometry was performed on the subjects before and after cycloplegia using a desktop autorefractor (RM8900; Topcon Corp., Tokyo, Japan), first in the right eye and then the left eye. Measurements were repeated 3 times in each eye, and then the average value was recorded. All the data were artificially extracted from the device and entered into a spreadsheet, and each patient was assigned a unique identification number.
For children with ametropia who were under 7 years of age, preliminarily diagnosed with hyperopia and merged with strabismus or amblyopia, cycloplegia was induced by 1% atropine sulfate eye gel, dropping eyes 3 times a day for 3 days, and taking the medicine again on the morning of optometry. Cycloplegia was considered complete when the pupil was dilated to at least 6 mm and a pupillary light reflex was absent. Tropicamide phenylephrine eye drops (Mydrin-P) were used for the children aged 7–12 years old, adolescents aged over 12 years old who were preliminary diagnosed with hyperopia, and children or adolescents under 16 years old who had a change of dioptre upon revisit. The dropping was administered 4 times continuously for one day and 5 min apart. We evaluated cycloplegia and pupil dilation of the patients after an additional 30 min. When the pupil was dilated to at least 6 mm and a pupillary light reflex was absent, cycloplegia was considered complete. Patients without complete cycloplegia were not included in the subsequent biometric analysis. Eventually, the following indices were evaluated: AL, K, K1, K2, CCT, ACD and WTW.
Statistical analysis
All descriptive statistics are expressed as the mean ± standard deviation (‾x ± s). The Kolmogorov‒Smirnov test was performed to detect the normality of the data. A paired-samples t test was used for statistical analysis before and after cycloplegia when the continuous data were normally distributed; otherwise, the Wilcoxon signed-rank test was used. Two-tailed p values were used in all analyses. The 95% confidence intervals (CIs) were calculated for pairwise comparisons of different paired samples. A p value of < 0.05 was considered statistically significant. All statistical analyses were performed in SPSS 22.0 software (IBM Corp., Armonk, New York, USA).
Ethical approval and consent to participate
The implementation of this study followed the Declaration of Helsinki. This study was also supported by the ethics committee of Jiujiang No 1 Peoples Hospital (Affiliated Jiujiang Hospital of Nanchang University) in China. Permit Number: JJSDYRMYY-YXLL-2022–243.
Consent to participate
Written informed consent for study participation was obtained from the parents or legal guardians of the participants in this study at the time of study enrolment.
Results
This study contained a larger sample size than previous studies. A total of 2049 individuals participated in the study, including 1102 males (53.8%) and 947 females (46.2%). One of the patients was excluded due to the incomplete collection of parameters in the eye. Only data from the right eyes of the patients were analysed. The average age of the 2048 included patients was 8.99 ± 3.234 years (range from 1 to 21 years) (Supplementary Table 1). In this study, the biometric parameters of the eyes of patients were as follows: AL, K, K1, K2, CCT, ACD and WTW. Patients were divided into groups based on differences in dioptre, age and sex. The groups had different numbers of patients because there was some missing information due to different levels of cooperation among the patients. The general data of patients in each group, such as the number of patients, sex distribution, and age, is shown in Supplementary Table 1.
Overall situation
After studying the changes in biometric parameters among the 2048 subjects before and after cycloplegia, we found that there was a significant increase in CCT and ACD after cycloplegia (p < 0.05, 95% CI − 11.787 to − 7.728, − 0.094 to − 0.047, respectively) (Table 1). However, AL, K, K1, K2 and WTW did not change significantly in this overall population (p > 0.05) (Table 1), which is different from previous studies.
Delaminated by dioptre
In this study, we divided the patients into six groups according to their dioptre, as follows: Fs (farsightedness, 122 patients), Ss (shortsightedness, 360 patients), Ast (astigmatism, 171 patients), EmP (emmetropia, 12 patients), FA (farsightedness combined with astigmatism, 661 patients), and SA (shortsightedness combined with astigmatism, 671 patients).
We observed different results across the refractive conditions. AL changed significantly in all groups (p < 0.05) except the EmP group (p > 0.05): it increased in the Fs, Ast, and FA groups and decreased in the Ss and SA groups (Tables 2, 3). No significant difference was found in any of the parameters in the EmP group, which may be due to the inclusion of an extremely small number of patients (Table 3). In the remaining five groups, we found significant increases in K, K1, K2 and ACD after cycloplegia (p < 0.05), whereas CCT and WTW were not changed significantly in the Fs group (p > 0.05) (Table 2). In the Ss group, K1 and ACD significantly decreased and K2 and CCT significantly increased postcycloplegia (p < 0.05), but K and WTW did not change significantly (p > 0.05) (Table 2). In the Ast group, significant increases in CCT and ACD and significant decreases in K and K2 were observed postcycloplegia (p < 0.05), while the changes in K1 and WTW were not significant (p > 0.05) (Table 2). In the FA group, there was a significant increase in K1, CCT and ACD after cycloplegia (p < 0.05), whereas K, K2 and WTW did not change significantly (p > 0.05) (Table 3). In the SA group, K and K1 significantly decreased and CCT significantly increased postcycloplegia (p < 0.05), but K2, ACD and WTW did not change significantly (p > 0.05) (Table 3).
Delaminated by age
We divided the individuals into three age groups: 1 to 7 years old (group 1, 703 patients), 8 to 14 years old (group 2, 1252 patients), and 15 to 21 years old (group 3, 94 patients). AL increased significantly in group 1 and decreased in groups 2 and 3 (p < 0.05) (Table 4). No other parameters were found to be significantly changed in group 3 (p > 0.05) (Table 4) except AL. Additionally, K, K1, K2 and WTW were not found to be significantly changed in any of the three groups (Table 4). Significant increases in CCT and ACD were observed in group 1 postcycloplegia (p < 0.05). However, in group 2, only CCT increased significantly (p < 0.05); the change in ACD was not significant (p > 0.05) (Table 4).
Delaminated by sex
We divided the participants into two groups according to their sex: male (group A, 1102 patients) and female (group B, 947 patients). There was a significant decrease in AL in group A and an increase in group B after cycloplegia (p < 0.05). K, K1 and K2 increased significantly in group A and decreased in group B postcycloplegia (p < 0.05). CCT increased significantly in both groups after cycloplegia (p < 0.05). ACD was not changed significantly in group A (p > 0.05) but increased significantly in group B after cycloplegia (p < 0.05). WTW decreased significantly in group A but increased in group B postcycloplegia (p < 0.05) (Table 5).
Discussion
Among the 2048 patients included in this study, we found that there were no significant changes in AL, K, K1, K2 and WTW after cycloplegia, but CCT and ACD increased significantly. After grouping patients based on their dioptre, age and sex, we found that only CCT and ACD increased significantly. Regarding dioptre, a significant increase in AL was observed in the Fs and Ast groups, while significant decreases were observed in the Ss and SA groups. There were significant increases in K in the Fs group, significant increases in K1 in the Fs and FA groups, and significant increases in K2 in the Fs and Ss groups. There were significant decreases in K in the Ast and SA groups, significant decreases in K1 in the Ss and SA groups, and significant decreases in K2 in the Ast group. There were no significant changes in K in the Ss and FA groups, K1 in the Ast group, or K2 in the FA and SA groups. Regarding age, we found that AL increased prominently after cycloplegia among younger patients. No differences were observed in K, K1 and K2 based on age. Regarding sex, AL decreased among males and increased among females postcycloplegia. The same trend was observed for K, K1 and K2 among males and females. CCT and ACD both increased significantly among males and females, bin the two groups, but the change in ACD among males was an exception. Interestingly, WTW began to show a significant trend of change in the two groups (decreased in the male group and increased in the female group).
A series of correct management strategies for myopia and control strategies can counteract its high prevalence and damage. Early diagnosis and prevention associated with effective therapeutic measures are needed to improve public eye health2. In regard to the early diagnosis of myopia, postcycloplegia optometry is an important process that has been recognized by scholars all over the world4,5,14,32. Cycloplegia has a certain effect on the biometric parameters of the eye that will further affect the accuracy of optometry and refractive surgery, for example, the calculation of the degree of intraocular lens22.
In previous studies, some scholars confirmed that cycloplegia in children could lead to changes in AL, K, CCT and ACD; in fact, many studies have reported increases in ACD13,17,19,20,21,22,23,24,25,27,28,29,30,31,33. Similar conclusions were obtained in our study, but the results varied based on the groups. Because of the large sample size, only CCT and ACD increased significantly after cycloplegia in all individuals. In general, an increase in CCT will lead to the prolongation of AL, which is contrary to our study. When accommodation of the eye is eliminated by cycloplegia, the crystalline lens becomes thinner and moves posteriorly in myopia compared to emmetropia and hyperopia after cycloplegia34. Therefore, AL does not transform with changes in CCT and ACD. Nevertheless, Cheng HC17, Bahar A20 and Tuncer I22 still detected a positive shift, and Ho MC19 and Raina UK21 detected a negative shift after cycloplegia. Ho MC19 pointed out in his research that the mean AL was reduced by 0.023 mm in those with an emmetropic or hyperopic shift, whereas it was elevated by 0.026 mm in those with a myopic shift of the eye (p = 0.003). This type of phenomenon of AL in the study of Ho MC19 was different from the observation in our study, in which the mean AL increased by 1.359 mm in the Fs group and decreased by 1.009 mm in the Ss group (p < 0.001). Although many studies showed no effect of cycloplegia on AL measurement, most have been done on adult eyes. We believe that children with stronger accommodative ability may be more vulnerable to cycloplegia, resulting in a greater change in the average refractive index and a significant impact on the calculation of AL. Many studies have shown that K decreases after cycloplegia17,23,24,25. Similar to previous studies, we found that K, K1 and K2 increased significantly after cycloplegia in the Fs group, and the greatest increase was found in K2. Some of the above studies were conducted in children and on myopic eyes; therefore, we believe that the low ocular tissue rigidity in the groups of patients in these studies is the cause of the results. The weak corneal biomechanics in children suggests that it may be affected by the contraction of the adjacent ciliary muscles. We are confident that the change in corneal curvature is a mechanical response to the relaxation of the ciliary muscle, but this effect was not significant in our study. Unlike ACD, which was increased in almost all previous studies, changes in CCT were different. Bagheri A16, Zeng Y28 and Tuncer I22 found that CCT increased markedly after cycloplegia; in contrast, Palamar M26 and Raina UK21 found that CCT decreased significantly postcycloplegia. Three hypotheses have been proposed for the increase in CCT after cycloplegia. The first is that eye drops containing benzalkonium chloride as a preservative may damage corneal epithelial and endothelial cells and cause corneal stroma oedema35. The second hypothesis is that reflex tearing after eye drops may lead to an overestimation of corneal thickness. In addition, the antimuscarinic effect of cycloplegic agents may inhibit or reduce the secretion of reflex tears, which probably decreases tear film thickness and reduces central corneal thickness measurements23. The third hypothesis is related to the possible effects of contraction or relaxation of ciliary muscles on the cornea, which can also lead to changes in corneal curvature. Cycloplegic agents may increase or decrease corneal thickness but mainly increased in our study. As an exception, ACD was slightly reduced in the Ss group. We speculate that this may be related to the decrease in AL in this group. We did not find significant changes in AL, K, K1, K2 and WTW as a whole, which may be due to the increase in sample size and the inclusion of all kinds of refractive error.
Currently, cataract surgery has gradually become a refractive surgery along with the application of high-quality lenses. There are many reasons for the prediction error for refractive state after cataract surgery, such as the selection of the intraocular lens (IOL) power formula and the accuracy of the various devices used to measure the eye (intraoperative aberrometry [IA] included)36. In the calculation of intraocular lenses in cataract surgery, both the Hill-radial basis function (RBF) formula and the Kane formula use the AL, K, ACD, CCT, and even biological sex to make their predictions36. As mentioned in the formula and IOL studies, ACD is measured from the corneal epithelium to the lens. Surprisingly, AL, CCT and ACD increased markedly in almost all groups, which will obviously have an adverse effect on the calculation of the intraocular lens.
The effects of cycloplegia on biometric parameters also varied across different age groups. Tuncer I22 divided patients into three age groups (50–60 years, 30–40 years and 10–20 years). He found that ACD was signally increased postcycloplegia in all groups, and the greatest increase was in the 10- to 20-year-old age group22. This is consistent with our findings that ACD was significantly increased after cycloplegia in the 1- to 7-year-old age group, whereas almost no change was observed in the 8- to 14-year-old and 15- to 21-year-old age groups. Özyol P37 pointed out that with increasing age, lens sclerosis reduces the elasticity of the lens capsule, increases the size and weight of the lens, and reduces the reaction of the lens to cycloplegic agents. Our results support the hypothesis mentioned above. We also found that AL and CCT increased more with age, which has not been found in previous studies. Huang J31 and Tuncer I22 reported a significant increase in WTW postcycloplegia, although these changes appeared to be unverifiable33,37. Similar to their results, we found that WTW increased significantly among females and decreased among males. Many biometric devices locate the limbus on the basis of the change in the contrast from paler sclera to darker cornea. However, the borderline between them is not very distinct; furthermore, the contrast difference can be influenced by the illumination and quality of the image. Under the circumstances described above, WTW measurements after cycloplegia could be larger than those obtained previously37.
Because of the larger sample size of our study, the results of this study are more reliable. Additionally, we grouped patients according to the type of refraction, age and sex for the first time. The results obtained herein were inconsistent with previous findings. The conclusions we obtained have certain reference value. The limitations of our study were that the age group was too young, and this topic remains to be further explored. It was difficult to dilate pupils in emmetropic children due to the worries of parents; consequently, this group did not include more patients for the trial. We applied different cycloplegic drugs in different age stages; the differences between these drugs need to be examined in future studies. This study demonstrated that many biological parameters of the eye changed after cycloplegia, even when grouped by refractive error, age and sex. CCT and ACD revealed significant increases in almost all classified groups. In view of the significance of this study, we hope to include more patients of other ages in future studies.
Data availability
All data generated or analysed during this study are included in this published article. All data are available upon request. Requests for the data should be directed to Yulin Tao.
References
Dolgin, E. The myopia boom. Nature 519, 276–278. https://doi.org/10.1038/519276a (2015).
Baird, P. N. et al. Myopia. Nat. Rev. Dis. Primers 6, 99. https://doi.org/10.1038/s41572-020-00231-4 (2020).
Holden, B. A. et al. Global prevalence of myopia and high myopia and temporal trends from 2000 through 2050. Ophthalmology 123, 1036–1042. https://doi.org/10.1016/j.ophtha.2016.01.006 (2016).
Guo, X. et al. Significant axial elongation with minimal change in refraction in 3- to 6-Year-Old Chinese Preschoolers: The Shenzhen kindergarten eye study. Ophthalmology 124, 1826–1838. https://doi.org/10.1016/j.ophtha.2017.05.030 (2017).
Li, T., Jiang, B. & Zhou, X. Axial length elongation in primary school-age children: A 3-year cohort study in Shanghai. BMJ Open 9, e029896. https://doi.org/10.1136/bmjopen-2019-029896 (2019).
Wang, S. K. et al. Incidence of and factors associated with Myopia and high Myopia in Chinese children, based on refraction without cycloplegia. JAMA Ophthalmol. 136, 1017–1024. https://doi.org/10.1001/jamaophthalmol.2018.2658 (2018).
Cho, P. & Tan, Q. Myopia and orthokeratology for myopia control. Clin. Exp. Optom. 102, 364–377. https://doi.org/10.1111/cxo.12839 (2019).
Bullimore, M. A. & Johnson, L. A. Overnight orthokeratology. Cont. Lens Anterior Eye 43, 322–332. https://doi.org/10.1016/j.clae.2020.03.018 (2020).
Vincent, S. J. et al. CLEAR—Orthokeratology. Cont. Lens Anterior Eye 44, 240–269. https://doi.org/10.1016/j.clae.2021.02.003 (2021).
Toda, I. Dry eye after LASIK. Invest. Ophthalmol. Vis. Sci. 59, 109–115. https://doi.org/10.1167/iovs.17-23538 (2018).
Ambrosio, R. Jr. & Wilson, S. LASIK vs LASEK vs PRK: Advantages and indications. Semin. Ophthalmol. 18, 2–10. https://doi.org/10.1076/soph.18.1.2.14074 (2003).
Mimouni, M., Pokroy, R., Rabina, G. & Kaiserman, I. LASIK versus PRK for high astigmatism. Int. Ophthalmol. 41, 2091–2098. https://doi.org/10.1007/s10792-021-01766-5 (2021).
Ye, L. et al. Comparisons of atropine versus cyclopentolate cycloplegia in myopic children. Clin. Exp. Optom. 104, 143–150. https://doi.org/10.1111/cxo.13128 (2021).
Major, E., Dutson, T. & Moshirfar, M. Cycloplegia in Children: An optometrist’s perspective. Clin Optom 12, 129–133. https://doi.org/10.2147/OPTO.S217645 (2020).
Li, T., Zhou, X., Zhu, J., Tang, X. & Gu, X. Effect of cycloplegia on the measurement of refractive error in Chinese children. Clin. Exp. Optom. 102, 160–165. https://doi.org/10.1111/cxo.12829 (2019).
Bagheri, A. et al. Effect of cycloplegia on corneal biometrics and refractive state. J. Ophthalmic. Vis. Res. 13, 101–109. https://doi.org/10.4103/jovr.jovr_196_17 (2018).
Cheng, H. C. & Hsieh, Y. T. Short-term refractive change and ocular parameter changes after cycloplegia. Optom. Vis. Sci. 91, 1113–1117. https://doi.org/10.1097/OPX.0000000000000339 (2014).
Hiraoka, T. et al. Influences of cycloplegia with topical atropine on ocular higher-order aberrations. Ophthalmology 120, 8–13. https://doi.org/10.1016/j.ophtha.2012.07.057 (2013).
Ho, M. C., Hsieh, Y. T., Shen, E. P., Hsu, W. C. & Cheng, H. C. Short-term refractive and ocular parameter changes after topical atropine. Taiwan J. Ophthalmol. 10, 111–115. https://doi.org/10.4103/tjo.tjo_110_18 (2020).
Bahar, A. & Pekel, G. The effects of pharmacological accommodation and cycloplegia on axial length and choroidal thickness. Arq. Bras. Oftalmol. 84, 107–112. https://doi.org/10.5935/0004-2749.20210015 (2021).
Raina, U. K., Gupta, S. K., Gupta, A., Goray, A. & Saini, V. Effect of cycloplegia on optical biometry in pediatric eyes. J. Pediatr. Ophthalmol. Strabismus 55, 260–265. https://doi.org/10.3928/01913913-20180327-05 (2018).
Tuncer, I., Zengin, M. O. & Yildiz, S. The effect of cycloplegia on the ocular biometry and intraocular lens power based on age. Eye 35, 676–681. https://doi.org/10.1038/s41433-020-01131-3 (2021).
Chang, S. W., Lo, A. Y. & Su, P. F. Anterior segment biometry changes with cycloplegia in myopic adults. Optom. Vis. Sci. 93, 12–18. https://doi.org/10.1097/OPX.0000000000000748 (2016).
Polat, N. & Gunduz, A. Effect of cycloplegia on keratometric and biometric parameters in keratoconus. J. Ophthalmol. 2016, 3437125. https://doi.org/10.1155/2016/3437125 (2016).
Saitoh, K., Yoshida, K., Hamatsu, Y. & Tazawa, Y. Changes in the shape of the anterior and posterior corneal surfaces caused by mydriasis and miosis: Detailed analysis. J. Cataract Refract. Surg. 30, 1024–1030. https://doi.org/10.1016/j.jcrs.2003.10.040 (2004).
Palamar, M., Egrilmez, S., Uretmen, O., Yagci, A. & Kose, S. Influences of cyclopentolate hydrochloride on anterior segment parameters with Pentacam in children. Acta Ophthalmol. 89, e461-465. https://doi.org/10.1111/j.1755-3768.2011.02122.x (2011).
Gao, L., Fan, H., Cheng, A. C., Wang, Z. & Lam, D. S. The effects of eye drops on corneal thickness in adult myopia. Cornea 25, 404–407. https://doi.org/10.1097/01.ico.0000214205.29823.f6 (2006).
Zeng, Y. & Gao, J. H. Effects of Mydrin eye-drops on central corneal thickness values in adult patients with myopia. Clin. Exp. Optom. 100, 151–154. https://doi.org/10.1111/cxo.12465 (2017).
Rodriguez-Raton, A., Jimenez-Alvarez, M., Arteche-Limousin, L., Mediavilla-Pena, E. & Larrucea-Martinez, I. Effect of pupil dilation on biometry measurements with partial coherence interferometry and its effect on IOL power formula calculation. Eur. J. Ophthalmol. 25, 309–314. https://doi.org/10.5301/ejo.5000568 (2015).
Momeni-Moghaddam, H. et al. The effect of cycloplegia on the ocular biometric and anterior segment parameters: A cross-sectional study. Ophthalmol. Ther. 8, 387–395. https://doi.org/10.1007/s40123-019-0187-5 (2019).
Huang, J. et al. The effect of cycloplegia on the lenstar and the IOL master biometry. Optom. Vis. Sci. 89, 1691–1696. https://doi.org/10.1097/OPX.0b013e3182772f4f (2012).
Doyle, L. A., McCullough, S. J. & Saunders, K. J. Cycloplegia and spectacle prescribing in children: Attitudes of UK optometrists. Ophthalmic Physiol. Opt. 39, 148–161. https://doi.org/10.1111/opo.12612 (2019).
Ozcaliskan, S. & Yenerel, N. M. The effect of cycloplegia on biometric measurements using swept-source optical coherence tomography-based biometry. Clin. Exp. Optom. 102, 501–505. https://doi.org/10.1111/cxo.12888 (2019).
Yuan, Y. et al. Responses of the ocular anterior segment and refraction to 0.5% tropicamide in Chinese school-aged Children of Myopia, emmetropia, and hyperopia. J. Ophthalmol. 2015, 612728. https://doi.org/10.1155/2015/612728 (2015).
Chen, W. et al. Corneal alternations induced by topical application of benzalkonium chloride in rabbit. PLoS One 6, e26103. https://doi.org/10.1371/journal.pone.0026103 (2011).
Kane, J. X. & Chang, D. F. Intraocular lens power formulas, biometry, and intraoperative aberrometry: A review. Ophthalmology 128, e94–e114. https://doi.org/10.1016/j.ophtha.2020.08.010 (2021).
Özyol, P., Özyol, E. & Baldemir, E. Changes in ocular parameters and intraocular lens powers in aging cycloplegic eyes. Am. J. Ophthalmol. 173, 76–83. https://doi.org/10.1016/j.ajo.2016.09.032 (2017).
Acknowledgements
The authors would like to thank all the donors enrolled in the present study.
Funding
This work was supported by the General Project of the Key R & D Program of the Department of Science and Technology of Jiangxi Province (No. 005062833097), the Science and Technology Plan Project of the Health Commission of Jiangxi Province (No. 202140286), and the Science and Technology Program of Administration of Traditional Chinese Medicine of Jiangxi Province (No. 2021A151).
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J. OY. conceived of this study and obtained financial support. J. OY., Q. Z., YL. T. and XK. C. contributed to the study design. XK. C., C. OY., XY. Q. and WJ. L. conducted material preparation, sample selection and data analysis. The first draft of the manuscript was written by YL. T., and all authors gave input for revising the manuscript. All authors read and approved the final manuscript. The parents or legal guardians of the participants in this study consented to the submission of the case report to the journal.
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Tao, Y., Cheng, X., Ouyang, C. et al. Changes in ocular biological parameters after cycloplegia based on dioptre, age and sex. Sci Rep 12, 22470 (2022). https://doi.org/10.1038/s41598-022-25462-1
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DOI: https://doi.org/10.1038/s41598-022-25462-1
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