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The characteristics of premature infants with transient corneal haze

BACKGROUND: The etiology of transient corneal haze in premature infants is not known and how it relates to clinical outcomes in premature infants is not clear. OBJECTIVES: To study associated factors of transient corneal haze in premature infants. METHODS: We performed a retrospective study of 261 p...

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Autores principales: Lai, Yu-Hung, Chen, Hsiu-Lin, Yang, San-Nan, Chang, Shun-Jen, Chuang, Lea-Yea, Wu, Wen-Chuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5875869/
https://www.ncbi.nlm.nih.gov/pubmed/29596534
http://dx.doi.org/10.1371/journal.pone.0195300
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author Lai, Yu-Hung
Chen, Hsiu-Lin
Yang, San-Nan
Chang, Shun-Jen
Chuang, Lea-Yea
Wu, Wen-Chuan
author_facet Lai, Yu-Hung
Chen, Hsiu-Lin
Yang, San-Nan
Chang, Shun-Jen
Chuang, Lea-Yea
Wu, Wen-Chuan
author_sort Lai, Yu-Hung
collection PubMed
description BACKGROUND: The etiology of transient corneal haze in premature infants is not known and how it relates to clinical outcomes in premature infants is not clear. OBJECTIVES: To study associated factors of transient corneal haze in premature infants. METHODS: We performed a retrospective study of 261 premature infants from retinopathy of prematurity (ROP) screening in the neonatal intensive care unit at a tertiary referral hospital. Characteristics of premature infants with and without corneal haze were analyzed by correlation tests, Chi-square tests, and logistic regressions were used for statistical analyses. Associations between corneal haze and birth weight (BW), gestational age at birth (GA), central corneal thickness, intraocular pressure, and other systemic and ophthalmic data were evaluated. RESULTS: The incidence of corneal haze was 13.4%. Lower BW, lower GA, packed red blood cells (RBC) transfusion, more days on oxygen, older maternal age, bronchopulmonary disease, and stage 3 ROP are associated with corneal haze. The severity of corneal haze decreased with infants’ postmenstrual age. Multivariate logistic regression analyses revealed that BW and maternal age are the most important predictors of corneal haze. CONCLUSION: Low BW and older maternal age are the most important predictors of corneal haze in premature infants. Premature infants with corneal haze could carry more systemic and ocular morbidities. Hence they may require more clinical attention. Corneal haze is unlikely to hinder the treatment of ROP. However, it is possible that corneal haze could hinder the examination of ROP in some infants. If corneal haze does interfere with ROP screening, a closer, more conservative follow-up schedule with a senior ophthalmologist experienced in managing ROP is recommended.
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spelling pubmed-58758692018-04-13 The characteristics of premature infants with transient corneal haze Lai, Yu-Hung Chen, Hsiu-Lin Yang, San-Nan Chang, Shun-Jen Chuang, Lea-Yea Wu, Wen-Chuan PLoS One Research Article BACKGROUND: The etiology of transient corneal haze in premature infants is not known and how it relates to clinical outcomes in premature infants is not clear. OBJECTIVES: To study associated factors of transient corneal haze in premature infants. METHODS: We performed a retrospective study of 261 premature infants from retinopathy of prematurity (ROP) screening in the neonatal intensive care unit at a tertiary referral hospital. Characteristics of premature infants with and without corneal haze were analyzed by correlation tests, Chi-square tests, and logistic regressions were used for statistical analyses. Associations between corneal haze and birth weight (BW), gestational age at birth (GA), central corneal thickness, intraocular pressure, and other systemic and ophthalmic data were evaluated. RESULTS: The incidence of corneal haze was 13.4%. Lower BW, lower GA, packed red blood cells (RBC) transfusion, more days on oxygen, older maternal age, bronchopulmonary disease, and stage 3 ROP are associated with corneal haze. The severity of corneal haze decreased with infants’ postmenstrual age. Multivariate logistic regression analyses revealed that BW and maternal age are the most important predictors of corneal haze. CONCLUSION: Low BW and older maternal age are the most important predictors of corneal haze in premature infants. Premature infants with corneal haze could carry more systemic and ocular morbidities. Hence they may require more clinical attention. Corneal haze is unlikely to hinder the treatment of ROP. However, it is possible that corneal haze could hinder the examination of ROP in some infants. If corneal haze does interfere with ROP screening, a closer, more conservative follow-up schedule with a senior ophthalmologist experienced in managing ROP is recommended. Public Library of Science 2018-03-29 /pmc/articles/PMC5875869/ /pubmed/29596534 http://dx.doi.org/10.1371/journal.pone.0195300 Text en © 2018 Lai et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Lai, Yu-Hung
Chen, Hsiu-Lin
Yang, San-Nan
Chang, Shun-Jen
Chuang, Lea-Yea
Wu, Wen-Chuan
The characteristics of premature infants with transient corneal haze
title The characteristics of premature infants with transient corneal haze
title_full The characteristics of premature infants with transient corneal haze
title_fullStr The characteristics of premature infants with transient corneal haze
title_full_unstemmed The characteristics of premature infants with transient corneal haze
title_short The characteristics of premature infants with transient corneal haze
title_sort characteristics of premature infants with transient corneal haze
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5875869/
https://www.ncbi.nlm.nih.gov/pubmed/29596534
http://dx.doi.org/10.1371/journal.pone.0195300
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