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Time of maximum cycloplegia after instillation of cyclopentolate 1% in children with brown irises

PURPOSE: We aimed to 1) determine the time of maximum cycloplegia after instillation of cyclopentolate 1% in children with brown irises, 2) evaluate the correlation between the pupillary reaction and time of maximum cycloplegia, and 3) identify any side effects of the medication. PATIENTS AND METHOD...

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Autores principales: Laojaroenwanit, Sittikorn, Layanun, Vimontip, Praneeprachachon, Pokpong, Pukrushpan, Parnchat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4876091/
https://www.ncbi.nlm.nih.gov/pubmed/27274191
http://dx.doi.org/10.2147/OPTH.S102611
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author Laojaroenwanit, Sittikorn
Layanun, Vimontip
Praneeprachachon, Pokpong
Pukrushpan, Parnchat
author_facet Laojaroenwanit, Sittikorn
Layanun, Vimontip
Praneeprachachon, Pokpong
Pukrushpan, Parnchat
author_sort Laojaroenwanit, Sittikorn
collection PubMed
description PURPOSE: We aimed to 1) determine the time of maximum cycloplegia after instillation of cyclopentolate 1% in children with brown irises, 2) evaluate the correlation between the pupillary reaction and time of maximum cycloplegia, and 3) identify any side effects of the medication. PATIENTS AND METHODS: This was a prospective analytical study involving children aged 5 to 14 years who were attending refraction clinic. Cyclopentolate 1% was instilled three times at 10-minute intervals. The spherical equivalent, pupillary reaction, and pupillary diameter were recorded before the first drop and nine times after the last drop at 10-minute intervals. Side effects were assessed. Time of maximum cycloplegia was determined from the time point at which the 95% confidence interval of the differences between the mean spherical equivalent at each point and its final value at 110 minutes was reached and remained within the equivalence limit (±0.25 D). RESULTS: Sixty children were enrolled in this study. Their mean age was 9.8 years (range: 5–4 years). Time of maximum cycloplegia was reached at 30 minutes after the first instillation of cyclopentolate. A poor correlation was observed between the pupillary reaction and the time of maximum cycloplegia (r=−0.07). The mean pupillary diameter at 30 minutes was 3.7±1.3 mm, and further dilation occurred thereafter. No side effects were observed. CONCLUSION: In most children, maximum cycloplegia was reached 30 minutes after the first instillation of cyclopentolate. The absence of a pupillary reaction should not be used as an indicator of maximum cycloplegia.
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spelling pubmed-48760912016-06-07 Time of maximum cycloplegia after instillation of cyclopentolate 1% in children with brown irises Laojaroenwanit, Sittikorn Layanun, Vimontip Praneeprachachon, Pokpong Pukrushpan, Parnchat Clin Ophthalmol Original Research PURPOSE: We aimed to 1) determine the time of maximum cycloplegia after instillation of cyclopentolate 1% in children with brown irises, 2) evaluate the correlation between the pupillary reaction and time of maximum cycloplegia, and 3) identify any side effects of the medication. PATIENTS AND METHODS: This was a prospective analytical study involving children aged 5 to 14 years who were attending refraction clinic. Cyclopentolate 1% was instilled three times at 10-minute intervals. The spherical equivalent, pupillary reaction, and pupillary diameter were recorded before the first drop and nine times after the last drop at 10-minute intervals. Side effects were assessed. Time of maximum cycloplegia was determined from the time point at which the 95% confidence interval of the differences between the mean spherical equivalent at each point and its final value at 110 minutes was reached and remained within the equivalence limit (±0.25 D). RESULTS: Sixty children were enrolled in this study. Their mean age was 9.8 years (range: 5–4 years). Time of maximum cycloplegia was reached at 30 minutes after the first instillation of cyclopentolate. A poor correlation was observed between the pupillary reaction and the time of maximum cycloplegia (r=−0.07). The mean pupillary diameter at 30 minutes was 3.7±1.3 mm, and further dilation occurred thereafter. No side effects were observed. CONCLUSION: In most children, maximum cycloplegia was reached 30 minutes after the first instillation of cyclopentolate. The absence of a pupillary reaction should not be used as an indicator of maximum cycloplegia. Dove Medical Press 2016-05-18 /pmc/articles/PMC4876091/ /pubmed/27274191 http://dx.doi.org/10.2147/OPTH.S102611 Text en © 2016 Laojaroenwanit et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Laojaroenwanit, Sittikorn
Layanun, Vimontip
Praneeprachachon, Pokpong
Pukrushpan, Parnchat
Time of maximum cycloplegia after instillation of cyclopentolate 1% in children with brown irises
title Time of maximum cycloplegia after instillation of cyclopentolate 1% in children with brown irises
title_full Time of maximum cycloplegia after instillation of cyclopentolate 1% in children with brown irises
title_fullStr Time of maximum cycloplegia after instillation of cyclopentolate 1% in children with brown irises
title_full_unstemmed Time of maximum cycloplegia after instillation of cyclopentolate 1% in children with brown irises
title_short Time of maximum cycloplegia after instillation of cyclopentolate 1% in children with brown irises
title_sort time of maximum cycloplegia after instillation of cyclopentolate 1% in children with brown irises
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4876091/
https://www.ncbi.nlm.nih.gov/pubmed/27274191
http://dx.doi.org/10.2147/OPTH.S102611
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