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Evaluation effects of nebulized gentamicin in exacerbation of chronic obstructive lung disease
BACKGROUND: Chronic obstructive pulmonary disease (COPD) is a major cause of chronic morbidity and mortality throughout the world. Exacerbation of COPD has negative effect on quality of life. Therapeutic effect of nebulized antibiotics in pulmonary infections has been reported previously. Hence, we...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5122183/ https://www.ncbi.nlm.nih.gov/pubmed/27904601 http://dx.doi.org/10.4103/1735-1995.187278 |
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author | Soltaninejad, Forogh Kheiri, Soleiman Habibian, Roya Amra, Arshia Asgari-Savadjani, Shahin |
author_facet | Soltaninejad, Forogh Kheiri, Soleiman Habibian, Roya Amra, Arshia Asgari-Savadjani, Shahin |
author_sort | Soltaninejad, Forogh |
collection | PubMed |
description | BACKGROUND: Chronic obstructive pulmonary disease (COPD) is a major cause of chronic morbidity and mortality throughout the world. Exacerbation of COPD has negative effect on quality of life. Therapeutic effect of nebulized antibiotics in pulmonary infections has been reported previously. Hence, we evaluated the effect of nebulized gentamicin in acute exacerbation of COPD (AECOPD). MATERIALS AND METHODS: In this clinical trial study, 86 hospitalized patients with AECOPD were divided into two groups for using nebulized gentamicin twice daily (case group) and placebo (control group) for 5 days in addition to standard treatment. On admission and on the 6(th) day, respiratory rate (RR), white blood cell (WBC), spirometry, and SPO(2) (arterial O(2) saturation by pulse oxymetry) were measured in groups. The severity of dyspnea was evaluated by the Medical Research Council scale. RESULTS: In both groups, changes of SpO(2), RR, forced an expiratory volume of first second (FEV1), and forced vital capacity (FVC) were significant during the times of intervention (P < 0.05). However, changes of FEV1 and FVC were significantly different between two groups (P < 0.05). So that increments of FEV1 and FVC were higher in the case group than control group. WBC decreased significantly in the case group (P < 0.05) compared to control group. There was no significant difference between groups in severity of dyspnea after intervention (P > 0.05). CONCLUSION: Treatment with Nebulized Gentamicin in AECOPD exacerbation resulted in further improvement of FVC and FEV1 on the 6(th) day. |
format | Online Article Text |
id | pubmed-5122183 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-51221832016-11-30 Evaluation effects of nebulized gentamicin in exacerbation of chronic obstructive lung disease Soltaninejad, Forogh Kheiri, Soleiman Habibian, Roya Amra, Arshia Asgari-Savadjani, Shahin J Res Med Sci Original Article BACKGROUND: Chronic obstructive pulmonary disease (COPD) is a major cause of chronic morbidity and mortality throughout the world. Exacerbation of COPD has negative effect on quality of life. Therapeutic effect of nebulized antibiotics in pulmonary infections has been reported previously. Hence, we evaluated the effect of nebulized gentamicin in acute exacerbation of COPD (AECOPD). MATERIALS AND METHODS: In this clinical trial study, 86 hospitalized patients with AECOPD were divided into two groups for using nebulized gentamicin twice daily (case group) and placebo (control group) for 5 days in addition to standard treatment. On admission and on the 6(th) day, respiratory rate (RR), white blood cell (WBC), spirometry, and SPO(2) (arterial O(2) saturation by pulse oxymetry) were measured in groups. The severity of dyspnea was evaluated by the Medical Research Council scale. RESULTS: In both groups, changes of SpO(2), RR, forced an expiratory volume of first second (FEV1), and forced vital capacity (FVC) were significant during the times of intervention (P < 0.05). However, changes of FEV1 and FVC were significantly different between two groups (P < 0.05). So that increments of FEV1 and FVC were higher in the case group than control group. WBC decreased significantly in the case group (P < 0.05) compared to control group. There was no significant difference between groups in severity of dyspnea after intervention (P > 0.05). CONCLUSION: Treatment with Nebulized Gentamicin in AECOPD exacerbation resulted in further improvement of FVC and FEV1 on the 6(th) day. Medknow Publications & Media Pvt Ltd 2016-07-29 /pmc/articles/PMC5122183/ /pubmed/27904601 http://dx.doi.org/10.4103/1735-1995.187278 Text en Copyright: © 2016 Journal of Research in Medical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Soltaninejad, Forogh Kheiri, Soleiman Habibian, Roya Amra, Arshia Asgari-Savadjani, Shahin Evaluation effects of nebulized gentamicin in exacerbation of chronic obstructive lung disease |
title | Evaluation effects of nebulized gentamicin in exacerbation of chronic obstructive lung disease |
title_full | Evaluation effects of nebulized gentamicin in exacerbation of chronic obstructive lung disease |
title_fullStr | Evaluation effects of nebulized gentamicin in exacerbation of chronic obstructive lung disease |
title_full_unstemmed | Evaluation effects of nebulized gentamicin in exacerbation of chronic obstructive lung disease |
title_short | Evaluation effects of nebulized gentamicin in exacerbation of chronic obstructive lung disease |
title_sort | evaluation effects of nebulized gentamicin in exacerbation of chronic obstructive lung disease |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5122183/ https://www.ncbi.nlm.nih.gov/pubmed/27904601 http://dx.doi.org/10.4103/1735-1995.187278 |
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