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A retrospective study of azithromycin and ceftizoxime for the management of children with Mycoplasma pneumoniae pneumonia
The aim of this study was to compare the clinical efficacy of azithromycin and ceftizoxime (AC) and erythromycin and amoxicillin/sulbactam (EAS) in the treatment of children with Mycoplasma pneumoniae pneumonia (MPP). In this retrospective study, a total of 92 eligible children with MPP were include...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Lippincott Williams & Wilkins
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8568348/ https://www.ncbi.nlm.nih.gov/pubmed/34871221 http://dx.doi.org/10.1097/MD.0000000000027564 |
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author | Han, Li-ping Xiao, Han-yan Fang, Li-li |
author_facet | Han, Li-ping Xiao, Han-yan Fang, Li-li |
author_sort | Han, Li-ping |
collection | PubMed |
description | The aim of this study was to compare the clinical efficacy of azithromycin and ceftizoxime (AC) and erythromycin and amoxicillin/sulbactam (EAS) in the treatment of children with Mycoplasma pneumoniae pneumonia (MPP). In this retrospective study, a total of 92 eligible children with MPP were included, and they were divided into a treatment group (n = 46) and a control group (n = 46). All patients were treated with intravenous ambroxol, and nebulized inhalation of budesonide and terbutaline. In addition, patients in the treatment group received AC. Patients in the control group underwent EAS. All patients in both groups were treated for a total of 10 days. Outcomes consist of erythrocyte sedimentation rate, C-reactive protein, serum lactate dehydrogenase, and interleukin 6, fever clearance time, time of cough disappearance, time of rale disappearance, time of signs disappeared by X-ray, and adverse events. All outcomes were measured after 10-day treatment. After treatment, patients who received AC exerted better improvements in erythrocyte sedimentation rate (P < .01), C-reactive protein (P < .01), serum lactate dehydrogenase (P < .01), interleukin 6 (P < .01), fever clearance time (P < .01), time of cough disappearance (P < .01), time of rale disappearance (P < .01), and time of signs disappeared by X-ray (P < .01), than those in patients who received EAS. In addition, there were not significant differences in adverse events between 2 groups. The results of this study showed that AC may benefit more than EAS for the children with MPP. |
format | Online Article Text |
id | pubmed-8568348 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-85683482021-11-06 A retrospective study of azithromycin and ceftizoxime for the management of children with Mycoplasma pneumoniae pneumonia Han, Li-ping Xiao, Han-yan Fang, Li-li Medicine (Baltimore) 3800 The aim of this study was to compare the clinical efficacy of azithromycin and ceftizoxime (AC) and erythromycin and amoxicillin/sulbactam (EAS) in the treatment of children with Mycoplasma pneumoniae pneumonia (MPP). In this retrospective study, a total of 92 eligible children with MPP were included, and they were divided into a treatment group (n = 46) and a control group (n = 46). All patients were treated with intravenous ambroxol, and nebulized inhalation of budesonide and terbutaline. In addition, patients in the treatment group received AC. Patients in the control group underwent EAS. All patients in both groups were treated for a total of 10 days. Outcomes consist of erythrocyte sedimentation rate, C-reactive protein, serum lactate dehydrogenase, and interleukin 6, fever clearance time, time of cough disappearance, time of rale disappearance, time of signs disappeared by X-ray, and adverse events. All outcomes were measured after 10-day treatment. After treatment, patients who received AC exerted better improvements in erythrocyte sedimentation rate (P < .01), C-reactive protein (P < .01), serum lactate dehydrogenase (P < .01), interleukin 6 (P < .01), fever clearance time (P < .01), time of cough disappearance (P < .01), time of rale disappearance (P < .01), and time of signs disappeared by X-ray (P < .01), than those in patients who received EAS. In addition, there were not significant differences in adverse events between 2 groups. The results of this study showed that AC may benefit more than EAS for the children with MPP. Lippincott Williams & Wilkins 2021-11-05 /pmc/articles/PMC8568348/ /pubmed/34871221 http://dx.doi.org/10.1097/MD.0000000000027564 Text en Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) |
spellingShingle | 3800 Han, Li-ping Xiao, Han-yan Fang, Li-li A retrospective study of azithromycin and ceftizoxime for the management of children with Mycoplasma pneumoniae pneumonia |
title | A retrospective study of azithromycin and ceftizoxime for the management of children with Mycoplasma pneumoniae pneumonia |
title_full | A retrospective study of azithromycin and ceftizoxime for the management of children with Mycoplasma pneumoniae pneumonia |
title_fullStr | A retrospective study of azithromycin and ceftizoxime for the management of children with Mycoplasma pneumoniae pneumonia |
title_full_unstemmed | A retrospective study of azithromycin and ceftizoxime for the management of children with Mycoplasma pneumoniae pneumonia |
title_short | A retrospective study of azithromycin and ceftizoxime for the management of children with Mycoplasma pneumoniae pneumonia |
title_sort | retrospective study of azithromycin and ceftizoxime for the management of children with mycoplasma pneumoniae pneumonia |
topic | 3800 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8568348/ https://www.ncbi.nlm.nih.gov/pubmed/34871221 http://dx.doi.org/10.1097/MD.0000000000027564 |
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