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Early phacoemulsification in patients with acute primary angle closure

PURPOSE: To compare long term efficacy of phacoemulsification in the early management of acute primary angle closure (APAC) after aborting an acute attack and performing laser peripheral iridotomy (LPI). METHODS: In this nonrandomized comparative prospective study, we included 35 subjects presenting...

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Autores principales: Moghimi, Sasan, Hashemian, Hesam, Chen, Rebecca, Johari, Mohammadkarim, Mohammadi, Massood, Lin, Shan C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4881187/
https://www.ncbi.nlm.nih.gov/pubmed/27239581
http://dx.doi.org/10.1016/j.joco.2015.12.001
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author Moghimi, Sasan
Hashemian, Hesam
Chen, Rebecca
Johari, Mohammadkarim
Mohammadi, Massood
Lin, Shan C.
author_facet Moghimi, Sasan
Hashemian, Hesam
Chen, Rebecca
Johari, Mohammadkarim
Mohammadi, Massood
Lin, Shan C.
author_sort Moghimi, Sasan
collection PubMed
description PURPOSE: To compare long term efficacy of phacoemulsification in the early management of acute primary angle closure (APAC) after aborting an acute attack and performing laser peripheral iridotomy (LPI). METHODS: In this nonrandomized comparative prospective study, we included 35 subjects presenting with APAC who had responded to medical treatment and LPI with intraocular pressure (IOP) less than 25 mmHg. Twenty patients with visually significant cataract with visual acuity of <20/30 were assigned to the “Phaco/LPI” group and underwent phacoemulsification within 6 weeks of the attack. Fifteen subjects with clear lens were assigned to the “LPI Only” group and were followed clinically. The primary measured outcome was the prevalence of IOP rise after 1 month (treatment failure), defined as 1) if a patient developed IOP rise resulting in IOP >21 mmHg with or without medication, or 2) if a patient required any medication to have IOP ≤21 mmHg after 1 month. Patients were followed for at least one year. RESULT: IOP, number of medications, gonioscopy grading, and amount of synechiae were not significantly different at baseline between the two groups. Acute attack did not recur in any patient. There was more significant failure in the LPI Only group compared with the Phaco/LPI group (40% vs. 5%; p = 0.02). There was a significant difference in final IOP between the two study groups (13.90 ± 2.17 vs. 17.8 ± 4.16 in the Phaco/LPI and LPI Only groups, respectively; p = 0.001). Patients in the Phaco-LPI group needed less medication than the other group at final follow-up. No serious complications have arisen from the immediate LPI or phacoemulsification. CONCLUSION: Phacoemulsification is a safe procedure for preventing IOP rise after aborting acute primary angle closure if performed within a few weeks of the attack.
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spelling pubmed-48811872016-05-27 Early phacoemulsification in patients with acute primary angle closure Moghimi, Sasan Hashemian, Hesam Chen, Rebecca Johari, Mohammadkarim Mohammadi, Massood Lin, Shan C. J Curr Ophthalmol Article PURPOSE: To compare long term efficacy of phacoemulsification in the early management of acute primary angle closure (APAC) after aborting an acute attack and performing laser peripheral iridotomy (LPI). METHODS: In this nonrandomized comparative prospective study, we included 35 subjects presenting with APAC who had responded to medical treatment and LPI with intraocular pressure (IOP) less than 25 mmHg. Twenty patients with visually significant cataract with visual acuity of <20/30 were assigned to the “Phaco/LPI” group and underwent phacoemulsification within 6 weeks of the attack. Fifteen subjects with clear lens were assigned to the “LPI Only” group and were followed clinically. The primary measured outcome was the prevalence of IOP rise after 1 month (treatment failure), defined as 1) if a patient developed IOP rise resulting in IOP >21 mmHg with or without medication, or 2) if a patient required any medication to have IOP ≤21 mmHg after 1 month. Patients were followed for at least one year. RESULT: IOP, number of medications, gonioscopy grading, and amount of synechiae were not significantly different at baseline between the two groups. Acute attack did not recur in any patient. There was more significant failure in the LPI Only group compared with the Phaco/LPI group (40% vs. 5%; p = 0.02). There was a significant difference in final IOP between the two study groups (13.90 ± 2.17 vs. 17.8 ± 4.16 in the Phaco/LPI and LPI Only groups, respectively; p = 0.001). Patients in the Phaco-LPI group needed less medication than the other group at final follow-up. No serious complications have arisen from the immediate LPI or phacoemulsification. CONCLUSION: Phacoemulsification is a safe procedure for preventing IOP rise after aborting acute primary angle closure if performed within a few weeks of the attack. Elsevier 2016-01-12 /pmc/articles/PMC4881187/ /pubmed/27239581 http://dx.doi.org/10.1016/j.joco.2015.12.001 Text en Copyright © 2015, Iranian Society of Ophthalmology. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Moghimi, Sasan
Hashemian, Hesam
Chen, Rebecca
Johari, Mohammadkarim
Mohammadi, Massood
Lin, Shan C.
Early phacoemulsification in patients with acute primary angle closure
title Early phacoemulsification in patients with acute primary angle closure
title_full Early phacoemulsification in patients with acute primary angle closure
title_fullStr Early phacoemulsification in patients with acute primary angle closure
title_full_unstemmed Early phacoemulsification in patients with acute primary angle closure
title_short Early phacoemulsification in patients with acute primary angle closure
title_sort early phacoemulsification in patients with acute primary angle closure
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4881187/
https://www.ncbi.nlm.nih.gov/pubmed/27239581
http://dx.doi.org/10.1016/j.joco.2015.12.001
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