Erin S Tomiyama, Martin Rickert, Pete Kollbaum, Eric R Ritchey
{"title":"Case series: Switching myopia management therapies in a real-world academic clinic.","authors":"Erin S Tomiyama, Martin Rickert, Pete Kollbaum, Eric R Ritchey","doi":"10.1097/OPX.0000000000002245","DOIUrl":null,"url":null,"abstract":"<p><strong>Significance: </strong>Slowing myopia progression is quickly becoming the clinical standard of care, but little is known about how changing treatment alters treatment effect. This case series provides insight on how changing treatment modality may affect treatment outcomes in myopia management.</p><p><strong>Purpose: </strong>Aiming to control myopia progression in children is becoming the clinical standard of care. Little is known about the effect of changing treatment on myopic progression. We present a case series of real-world myopia management patients who underwent a change in treatment method and report the observed effect on axial length.</p><p><strong>Methods: </strong>Clinical records from the University of Houston Myopia Management Service were reviewed to identify children who underwent a change in treatment. The analyzed dataset consisted of 44 clinic assessments from seven children including two who were switched from peripheral defocus soft contact lenses to orthokeratology, two who were switched from orthokeratology to peripheral defocus soft contact lenses, and three who received combination therapy following an initial period of treatment with either orthokeratology, peripheral defocus soft contact lenses, or atropine alone. Axial length measurements were adjusted by subtracting central corneal thickness from the raw axial length value and then converted to an annualized rate (mm/y) by subtracting the previous corneal thickness-adjusted from the current corneal thickness-adjusted axial length and dividing by elapsed time between the successive clinic visits.</p><p><strong>Results: </strong>Age at initial assessment ranged from 6.6 to 12.6 years (M = 9.3 ± 2.4) with follow-up times ranging between 26 and 78 months (M = 43 ± 18.5). Each individual had a minimum of two clinical visits per treatment type. The mean (SD) for central corneal thickness-annualized adjusted axial length growth in both the eyes and chronological age at the beginning of each treatment type was calculated. Estimated progression rates are summarized separately for each individual and treatment. Data are grouped by patients who switched treatments for either lack of efficacy or other clinical issues.</p><p><strong>Conclusions: </strong>In a real-world setting, there are various reasons that necessitate a change in treatment. In this sample, change in treatment continued to show slowing of myopia progression, regardless of reason for change.</p>","PeriodicalId":19649,"journal":{"name":"Optometry and Vision Science","volume":" ","pages":""},"PeriodicalIF":1.6000,"publicationDate":"2025-03-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Optometry and Vision Science","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1097/OPX.0000000000002245","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"OPHTHALMOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Significance: Slowing myopia progression is quickly becoming the clinical standard of care, but little is known about how changing treatment alters treatment effect. This case series provides insight on how changing treatment modality may affect treatment outcomes in myopia management.
Purpose: Aiming to control myopia progression in children is becoming the clinical standard of care. Little is known about the effect of changing treatment on myopic progression. We present a case series of real-world myopia management patients who underwent a change in treatment method and report the observed effect on axial length.
Methods: Clinical records from the University of Houston Myopia Management Service were reviewed to identify children who underwent a change in treatment. The analyzed dataset consisted of 44 clinic assessments from seven children including two who were switched from peripheral defocus soft contact lenses to orthokeratology, two who were switched from orthokeratology to peripheral defocus soft contact lenses, and three who received combination therapy following an initial period of treatment with either orthokeratology, peripheral defocus soft contact lenses, or atropine alone. Axial length measurements were adjusted by subtracting central corneal thickness from the raw axial length value and then converted to an annualized rate (mm/y) by subtracting the previous corneal thickness-adjusted from the current corneal thickness-adjusted axial length and dividing by elapsed time between the successive clinic visits.
Results: Age at initial assessment ranged from 6.6 to 12.6 years (M = 9.3 ± 2.4) with follow-up times ranging between 26 and 78 months (M = 43 ± 18.5). Each individual had a minimum of two clinical visits per treatment type. The mean (SD) for central corneal thickness-annualized adjusted axial length growth in both the eyes and chronological age at the beginning of each treatment type was calculated. Estimated progression rates are summarized separately for each individual and treatment. Data are grouped by patients who switched treatments for either lack of efficacy or other clinical issues.
Conclusions: In a real-world setting, there are various reasons that necessitate a change in treatment. In this sample, change in treatment continued to show slowing of myopia progression, regardless of reason for change.
期刊介绍:
Optometry and Vision Science is the monthly peer-reviewed scientific publication of the American Academy of Optometry, publishing original research since 1924. Optometry and Vision Science is an internationally recognized source for education and information on current discoveries in optometry, physiological optics, vision science, and related fields. The journal considers original contributions that advance clinical practice, vision science, and public health. Authors should remember that the journal reaches readers worldwide and their submissions should be relevant and of interest to a broad audience. Topical priorities include, but are not limited to: clinical and laboratory research, evidence-based reviews, contact lenses, ocular growth and refractive error development, eye movements, visual function and perception, biology of the eye and ocular disease, epidemiology and public health, biomedical optics and instrumentation, novel and important clinical observations and treatments, and optometric education.