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Association Between Atopic Keratoconjunctivitis and the Risk of Recurrent Corneal Erosion

Purpose: To investigate the risk of recurrent corneal erosion (RCE) in patients with atopic keratoconjunctivitis (AKC). Methods: This national, retrospective, matched cohort study enrolled 184,166 newly-diagnosed AKC patients, selected from the Taiwan National Health Insurance Research Database and...

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Autores principales: Jan, Ren-Long, Weng, Shih-Feng, Wang, Jhi-Joung, Tseng, Sung-Huei, Chang, Yuh-Shin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8210667/
https://www.ncbi.nlm.nih.gov/pubmed/34150819
http://dx.doi.org/10.3389/fmed.2021.688355
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author Jan, Ren-Long
Weng, Shih-Feng
Wang, Jhi-Joung
Tseng, Sung-Huei
Chang, Yuh-Shin
author_facet Jan, Ren-Long
Weng, Shih-Feng
Wang, Jhi-Joung
Tseng, Sung-Huei
Chang, Yuh-Shin
author_sort Jan, Ren-Long
collection PubMed
description Purpose: To investigate the risk of recurrent corneal erosion (RCE) in patients with atopic keratoconjunctivitis (AKC). Methods: This national, retrospective, matched cohort study enrolled 184,166 newly-diagnosed AKC patients, selected from the Taiwan National Health Insurance Research Database and identified by the International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM) code 372.05. The control group comprised 184,166 non-AKC patients matched by age, sex, and potential comorbidities and they were selected from the Taiwan Longitudinal Health Insurance Database, 2000. Information from patients was gathered from 1 January 2004 to 31 December 2011, and both groups were traced from the index date until December 2013. The incidence and risk of RCE (ICD-9-CM code 361.42) was compared between the groups. The adjusted hazard ratio (HR) for RCE was obtained by a Cox proportional hazard regression analysis. The Kaplan–Meier analysis was performed to calculate the cumulative incidence of RCE. Results: In total, 564 AKC patients and 406 non-AKC controls developed RCE during the follow-up span. The incidence of RCE was 1.45 times higher in AKC patients than in controls (95% confidence interval [CI] = 1.27–1.64; P < 0.0001). After adjusting for potential confounders, including diabetes mellitus, keratoconjunctivitis sicca, corneal transplantation, ocular blunt trauma, corneal dystrophy, and band keratopathy, AKC patients were 1.36 times more likely to develop RCE than controls (adjusted HR, 1.36; 95% CI = 1.19–1.54; p < 0.05). Conclusions: AKC Patients had an increased risk of developing RCE and should be informed of this risk.
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spelling pubmed-82106672021-06-18 Association Between Atopic Keratoconjunctivitis and the Risk of Recurrent Corneal Erosion Jan, Ren-Long Weng, Shih-Feng Wang, Jhi-Joung Tseng, Sung-Huei Chang, Yuh-Shin Front Med (Lausanne) Medicine Purpose: To investigate the risk of recurrent corneal erosion (RCE) in patients with atopic keratoconjunctivitis (AKC). Methods: This national, retrospective, matched cohort study enrolled 184,166 newly-diagnosed AKC patients, selected from the Taiwan National Health Insurance Research Database and identified by the International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM) code 372.05. The control group comprised 184,166 non-AKC patients matched by age, sex, and potential comorbidities and they were selected from the Taiwan Longitudinal Health Insurance Database, 2000. Information from patients was gathered from 1 January 2004 to 31 December 2011, and both groups were traced from the index date until December 2013. The incidence and risk of RCE (ICD-9-CM code 361.42) was compared between the groups. The adjusted hazard ratio (HR) for RCE was obtained by a Cox proportional hazard regression analysis. The Kaplan–Meier analysis was performed to calculate the cumulative incidence of RCE. Results: In total, 564 AKC patients and 406 non-AKC controls developed RCE during the follow-up span. The incidence of RCE was 1.45 times higher in AKC patients than in controls (95% confidence interval [CI] = 1.27–1.64; P < 0.0001). After adjusting for potential confounders, including diabetes mellitus, keratoconjunctivitis sicca, corneal transplantation, ocular blunt trauma, corneal dystrophy, and band keratopathy, AKC patients were 1.36 times more likely to develop RCE than controls (adjusted HR, 1.36; 95% CI = 1.19–1.54; p < 0.05). Conclusions: AKC Patients had an increased risk of developing RCE and should be informed of this risk. Frontiers Media S.A. 2021-06-02 /pmc/articles/PMC8210667/ /pubmed/34150819 http://dx.doi.org/10.3389/fmed.2021.688355 Text en Copyright © 2021 Jan, Weng, Wang, Tseng and Chang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Jan, Ren-Long
Weng, Shih-Feng
Wang, Jhi-Joung
Tseng, Sung-Huei
Chang, Yuh-Shin
Association Between Atopic Keratoconjunctivitis and the Risk of Recurrent Corneal Erosion
title Association Between Atopic Keratoconjunctivitis and the Risk of Recurrent Corneal Erosion
title_full Association Between Atopic Keratoconjunctivitis and the Risk of Recurrent Corneal Erosion
title_fullStr Association Between Atopic Keratoconjunctivitis and the Risk of Recurrent Corneal Erosion
title_full_unstemmed Association Between Atopic Keratoconjunctivitis and the Risk of Recurrent Corneal Erosion
title_short Association Between Atopic Keratoconjunctivitis and the Risk of Recurrent Corneal Erosion
title_sort association between atopic keratoconjunctivitis and the risk of recurrent corneal erosion
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8210667/
https://www.ncbi.nlm.nih.gov/pubmed/34150819
http://dx.doi.org/10.3389/fmed.2021.688355
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