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Long-term outcomes after acute primary angle closure in a White Caucasian population

INTRODUCTION: Very limited data is available on the morbidity and progression to primary angle closure glaucoma (PACG) in White Caucasian individuals following acute primary angle closure (APAC). Our aim is to identify the number of eyes who developed PACG following an APAC attack and to determine t...

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Autores principales: Andreatta, Walter, Elaroud, Ibrahim, Nightingale, Peter, Nessim, Maged
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4541724/
https://www.ncbi.nlm.nih.gov/pubmed/26286533
http://dx.doi.org/10.1186/s12886-015-0100-5
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author Andreatta, Walter
Elaroud, Ibrahim
Nightingale, Peter
Nessim, Maged
author_facet Andreatta, Walter
Elaroud, Ibrahim
Nightingale, Peter
Nessim, Maged
author_sort Andreatta, Walter
collection PubMed
description INTRODUCTION: Very limited data is available on the morbidity and progression to primary angle closure glaucoma (PACG) in White Caucasian individuals following acute primary angle closure (APAC). Our aim is to identify the number of eyes who developed PACG following an APAC attack and to determine the risk factors for PACG development in a White Caucasian population in the United Kingdom (UK). We assessed the rate of blindness and visual impairment in the affected eye as defined by the World Health Organisation. METHODS: Retrospective observational study including 48 consecutive eyes of 46 White Caucasian subjects who presented with APAC to a tertiary referral unit in the United Kingdom. Eyes affected by glaucomatous optic neuropathy at presentation were excluded. We included in our analysis socio-demographic variables, ophthalmic findings, investigations and treatment. RESULTS: The mean final follow up period was 27 months ± 14 standard deviation (SD). Seven (15 %) eyes developed PACG. Statistical analysis showed that the following factors were linked to a higher risk of progression: length of symptoms before presentation and time taken to break the attack. The intraocular pressure (IOP) was significantly higher in the group who developed PACG at the one- and six-month visit compared to the group which did not develop the disease. At the final visit 3 (6 %) eyes were blind while 5 (10 %) were visually impaired. PACG was responsible for visual impairment in 2 (4 %) eyes but not for any case of blindness. CONCLUSIONS: Delayed presentation, length of time taken to break the attack and poor IOP control can result in PACG development and visual impairment. APAC causes a low long-term visual morbidity in White Caucasians.
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spelling pubmed-45417242015-08-21 Long-term outcomes after acute primary angle closure in a White Caucasian population Andreatta, Walter Elaroud, Ibrahim Nightingale, Peter Nessim, Maged BMC Ophthalmol Research Article INTRODUCTION: Very limited data is available on the morbidity and progression to primary angle closure glaucoma (PACG) in White Caucasian individuals following acute primary angle closure (APAC). Our aim is to identify the number of eyes who developed PACG following an APAC attack and to determine the risk factors for PACG development in a White Caucasian population in the United Kingdom (UK). We assessed the rate of blindness and visual impairment in the affected eye as defined by the World Health Organisation. METHODS: Retrospective observational study including 48 consecutive eyes of 46 White Caucasian subjects who presented with APAC to a tertiary referral unit in the United Kingdom. Eyes affected by glaucomatous optic neuropathy at presentation were excluded. We included in our analysis socio-demographic variables, ophthalmic findings, investigations and treatment. RESULTS: The mean final follow up period was 27 months ± 14 standard deviation (SD). Seven (15 %) eyes developed PACG. Statistical analysis showed that the following factors were linked to a higher risk of progression: length of symptoms before presentation and time taken to break the attack. The intraocular pressure (IOP) was significantly higher in the group who developed PACG at the one- and six-month visit compared to the group which did not develop the disease. At the final visit 3 (6 %) eyes were blind while 5 (10 %) were visually impaired. PACG was responsible for visual impairment in 2 (4 %) eyes but not for any case of blindness. CONCLUSIONS: Delayed presentation, length of time taken to break the attack and poor IOP control can result in PACG development and visual impairment. APAC causes a low long-term visual morbidity in White Caucasians. BioMed Central 2015-08-19 /pmc/articles/PMC4541724/ /pubmed/26286533 http://dx.doi.org/10.1186/s12886-015-0100-5 Text en © Andreatta et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Andreatta, Walter
Elaroud, Ibrahim
Nightingale, Peter
Nessim, Maged
Long-term outcomes after acute primary angle closure in a White Caucasian population
title Long-term outcomes after acute primary angle closure in a White Caucasian population
title_full Long-term outcomes after acute primary angle closure in a White Caucasian population
title_fullStr Long-term outcomes after acute primary angle closure in a White Caucasian population
title_full_unstemmed Long-term outcomes after acute primary angle closure in a White Caucasian population
title_short Long-term outcomes after acute primary angle closure in a White Caucasian population
title_sort long-term outcomes after acute primary angle closure in a white caucasian population
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4541724/
https://www.ncbi.nlm.nih.gov/pubmed/26286533
http://dx.doi.org/10.1186/s12886-015-0100-5
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