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Clinical efficacy of budesonide combined with acetylcysteine in the treatment of mycoplasma pneumonia infection
OBJECTIVE: Mycoplasma pneumoniae pneumonia (MPP) is a common respiratory tract infectious disease in children. The study aimed to elucidate the therapeutic efficacy of aerosolized budesonide and N‐acetylcysteine combination therapy for MP infection in children. METHODS: One hundred and twenty childr...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10664398/ https://www.ncbi.nlm.nih.gov/pubmed/38018572 http://dx.doi.org/10.1002/iid3.1068 |
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author | Chen, Jing Zhu, Ying Zheng, Chunfeng Zhao, Wei Liu, Qi |
author_facet | Chen, Jing Zhu, Ying Zheng, Chunfeng Zhao, Wei Liu, Qi |
author_sort | Chen, Jing |
collection | PubMed |
description | OBJECTIVE: Mycoplasma pneumoniae pneumonia (MPP) is a common respiratory tract infectious disease in children. The study aimed to elucidate the therapeutic efficacy of aerosolized budesonide and N‐acetylcysteine combination therapy for MP infection in children. METHODS: One hundred and twenty children with MP infection were included and divided into the control group (received aerosol inhalation of budesonide) and the experimental group (aerosolized budesonide and N‐acetylcysteine). After treatment, the disappearance time of clinical symptoms and efficacy were contrasted between the two groups. RESULTS: With the passage of treatment time, the children's cough score of the two groups were gradually reduced. The children in the experimental group got well from the cough faster than the control group, and the difference reached a significant level on the 5th and 7th days. The time required for fever, rale, and cough to disappear in the experimental group was shorter than those in the control group. As the treatment progressed, a gradual decrease in serum interleukin‐6, tumor necrosis factor‐α, and C‐reactive protein values was detected in both groups, and the decrease was more significant in the experimental group. The total effective rate of the experimental group was 98.33%, which surpassed the control group (93.33%). CONCLUSION: Budesonide and N‐acetylcysteine combination therapy in the treatment of MP infection in children has a significant effect, and can quickly relieve the clinical symptoms of children with good safety. It is worthy of widespread clinical use. |
format | Online Article Text |
id | pubmed-10664398 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106643982023-11-22 Clinical efficacy of budesonide combined with acetylcysteine in the treatment of mycoplasma pneumonia infection Chen, Jing Zhu, Ying Zheng, Chunfeng Zhao, Wei Liu, Qi Immun Inflamm Dis Original Articles OBJECTIVE: Mycoplasma pneumoniae pneumonia (MPP) is a common respiratory tract infectious disease in children. The study aimed to elucidate the therapeutic efficacy of aerosolized budesonide and N‐acetylcysteine combination therapy for MP infection in children. METHODS: One hundred and twenty children with MP infection were included and divided into the control group (received aerosol inhalation of budesonide) and the experimental group (aerosolized budesonide and N‐acetylcysteine). After treatment, the disappearance time of clinical symptoms and efficacy were contrasted between the two groups. RESULTS: With the passage of treatment time, the children's cough score of the two groups were gradually reduced. The children in the experimental group got well from the cough faster than the control group, and the difference reached a significant level on the 5th and 7th days. The time required for fever, rale, and cough to disappear in the experimental group was shorter than those in the control group. As the treatment progressed, a gradual decrease in serum interleukin‐6, tumor necrosis factor‐α, and C‐reactive protein values was detected in both groups, and the decrease was more significant in the experimental group. The total effective rate of the experimental group was 98.33%, which surpassed the control group (93.33%). CONCLUSION: Budesonide and N‐acetylcysteine combination therapy in the treatment of MP infection in children has a significant effect, and can quickly relieve the clinical symptoms of children with good safety. It is worthy of widespread clinical use. John Wiley and Sons Inc. 2023-11-22 /pmc/articles/PMC10664398/ /pubmed/38018572 http://dx.doi.org/10.1002/iid3.1068 Text en © 2023 The Authors. Immunity, Inflammation and Disease published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Chen, Jing Zhu, Ying Zheng, Chunfeng Zhao, Wei Liu, Qi Clinical efficacy of budesonide combined with acetylcysteine in the treatment of mycoplasma pneumonia infection |
title | Clinical efficacy of budesonide combined with acetylcysteine in the treatment of mycoplasma pneumonia infection |
title_full | Clinical efficacy of budesonide combined with acetylcysteine in the treatment of mycoplasma pneumonia infection |
title_fullStr | Clinical efficacy of budesonide combined with acetylcysteine in the treatment of mycoplasma pneumonia infection |
title_full_unstemmed | Clinical efficacy of budesonide combined with acetylcysteine in the treatment of mycoplasma pneumonia infection |
title_short | Clinical efficacy of budesonide combined with acetylcysteine in the treatment of mycoplasma pneumonia infection |
title_sort | clinical efficacy of budesonide combined with acetylcysteine in the treatment of mycoplasma pneumonia infection |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10664398/ https://www.ncbi.nlm.nih.gov/pubmed/38018572 http://dx.doi.org/10.1002/iid3.1068 |
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