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A prospective randomized trial of azithromycin versus trimethoprim/sulfamethoxazole in treatment of toxoplasmic retinochoroiditis
PURPOSE: To assess the efficacy of oral azithromycin in the treatment of toxoplasmic retinochoroiditis. METHODS: A randomized interventional comparative study was conducted on 14 patients with ocular toxoplasmosis who were treated with oral azithromycin and 13 patients who were treated with oral tri...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5463001/ https://www.ncbi.nlm.nih.gov/pubmed/28626822 http://dx.doi.org/10.1016/j.joco.2016.10.002 |
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author | Lashay, Alireza Mirshahi, Ahmad Parandin, Najaf Riazi Esfahani, Hamid Mazloumi, Mehdi Reza Lashay, Mohammad Johari, Mohammad Karim Ashrafi, Elham |
author_facet | Lashay, Alireza Mirshahi, Ahmad Parandin, Najaf Riazi Esfahani, Hamid Mazloumi, Mehdi Reza Lashay, Mohammad Johari, Mohammad Karim Ashrafi, Elham |
author_sort | Lashay, Alireza |
collection | PubMed |
description | PURPOSE: To assess the efficacy of oral azithromycin in the treatment of toxoplasmic retinochoroiditis. METHODS: A randomized interventional comparative study was conducted on 14 patients with ocular toxoplasmosis who were treated with oral azithromycin and 13 patients who were treated with oral trimethoprim/sulfamethoxazole for 6–12 weeks. The achievement of treatment criteria in the two groups and lesion size reduction were considered as primary outcome measures. RESULTS: The resolution of inflammatory activity, decrease in the size of retinochoroidal lesions, and final best corrected visual acuity (BCVA) did not differ between the two treatment groups. The lesion size declined significantly in all patients (P = 0.001). There was no significant difference in the reduction of the size of retinal lesions between the two treatment groups (P = 0.17). Within each group, there was a significant improvement in BCVA after treatment; BCVA increased by 0.24 logMAR in the azithromycin group (P = 0.001) and by 0.3 logMAR in the trimethoprim/sulfamethoxazole group (P = 0.001). CONCLUSIONS: Drug efficacy in terms of reducing the size of retinal lesions and visual improvement was similar in a regimen of trimethoprim/sulfamethoxazole or azithromycin treatment. Therefore, if confirmed with further studies, therapy with azithromycin seems to be an acceptable alternative for the treatment of ocular toxoplasmosis. |
format | Online Article Text |
id | pubmed-5463001 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-54630012017-06-16 A prospective randomized trial of azithromycin versus trimethoprim/sulfamethoxazole in treatment of toxoplasmic retinochoroiditis Lashay, Alireza Mirshahi, Ahmad Parandin, Najaf Riazi Esfahani, Hamid Mazloumi, Mehdi Reza Lashay, Mohammad Johari, Mohammad Karim Ashrafi, Elham J Curr Ophthalmol Original Research PURPOSE: To assess the efficacy of oral azithromycin in the treatment of toxoplasmic retinochoroiditis. METHODS: A randomized interventional comparative study was conducted on 14 patients with ocular toxoplasmosis who were treated with oral azithromycin and 13 patients who were treated with oral trimethoprim/sulfamethoxazole for 6–12 weeks. The achievement of treatment criteria in the two groups and lesion size reduction were considered as primary outcome measures. RESULTS: The resolution of inflammatory activity, decrease in the size of retinochoroidal lesions, and final best corrected visual acuity (BCVA) did not differ between the two treatment groups. The lesion size declined significantly in all patients (P = 0.001). There was no significant difference in the reduction of the size of retinal lesions between the two treatment groups (P = 0.17). Within each group, there was a significant improvement in BCVA after treatment; BCVA increased by 0.24 logMAR in the azithromycin group (P = 0.001) and by 0.3 logMAR in the trimethoprim/sulfamethoxazole group (P = 0.001). CONCLUSIONS: Drug efficacy in terms of reducing the size of retinal lesions and visual improvement was similar in a regimen of trimethoprim/sulfamethoxazole or azithromycin treatment. Therefore, if confirmed with further studies, therapy with azithromycin seems to be an acceptable alternative for the treatment of ocular toxoplasmosis. Elsevier 2016-12-28 /pmc/articles/PMC5463001/ /pubmed/28626822 http://dx.doi.org/10.1016/j.joco.2016.10.002 Text en Copyright © 2017, 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 | Original Research Lashay, Alireza Mirshahi, Ahmad Parandin, Najaf Riazi Esfahani, Hamid Mazloumi, Mehdi Reza Lashay, Mohammad Johari, Mohammad Karim Ashrafi, Elham A prospective randomized trial of azithromycin versus trimethoprim/sulfamethoxazole in treatment of toxoplasmic retinochoroiditis |
title | A prospective randomized trial of azithromycin versus trimethoprim/sulfamethoxazole in treatment of toxoplasmic retinochoroiditis |
title_full | A prospective randomized trial of azithromycin versus trimethoprim/sulfamethoxazole in treatment of toxoplasmic retinochoroiditis |
title_fullStr | A prospective randomized trial of azithromycin versus trimethoprim/sulfamethoxazole in treatment of toxoplasmic retinochoroiditis |
title_full_unstemmed | A prospective randomized trial of azithromycin versus trimethoprim/sulfamethoxazole in treatment of toxoplasmic retinochoroiditis |
title_short | A prospective randomized trial of azithromycin versus trimethoprim/sulfamethoxazole in treatment of toxoplasmic retinochoroiditis |
title_sort | prospective randomized trial of azithromycin versus trimethoprim/sulfamethoxazole in treatment of toxoplasmic retinochoroiditis |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5463001/ https://www.ncbi.nlm.nih.gov/pubmed/28626822 http://dx.doi.org/10.1016/j.joco.2016.10.002 |
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