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Chinese Medical Injections for Acute Exacerbation of Chronic Obstructive Pulmonary Disease: A Network Meta-analysis

BACKGROUND: The World Health Organization has indicated that chronic obstructive pulmonary disease (COPD) may become the third leading cause of death by 2030. Acute exacerbation of COPD (AECOPD) is an important process in clinical treatment. Recent studies have shown that Chinese medical injections...

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Autores principales: Hu, Haiyin, Ji, Zhaochen, Qiang, Xiaoyu, Liu, Shigang, Sheng, Xiaodi, Chen, Zhe, Liu, Fanqi, Wang, Hui, Zhang, Junhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8691136/
https://www.ncbi.nlm.nih.gov/pubmed/34949918
http://dx.doi.org/10.2147/COPD.S335579
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author Hu, Haiyin
Ji, Zhaochen
Qiang, Xiaoyu
Liu, Shigang
Sheng, Xiaodi
Chen, Zhe
Liu, Fanqi
Wang, Hui
Zhang, Junhua
author_facet Hu, Haiyin
Ji, Zhaochen
Qiang, Xiaoyu
Liu, Shigang
Sheng, Xiaodi
Chen, Zhe
Liu, Fanqi
Wang, Hui
Zhang, Junhua
author_sort Hu, Haiyin
collection PubMed
description BACKGROUND: The World Health Organization has indicated that chronic obstructive pulmonary disease (COPD) may become the third leading cause of death by 2030. Acute exacerbation of COPD (AECOPD) is an important process in clinical treatment. Recent studies have shown that Chinese medical injections (CMI) are effective against AECOPD, but the effective difference among different CMIs remains unclear. The aim of this network meta-analysis (NMA) is to compare the therapeutic effect of various CMIs. METHODS: We conducted an overall, systematic literature search in the China National Knowledge Infrastructure, Wanfang, VIP, SinoMed, PubMed, Embase, Cochrane Library, and Web of Science databases to retrieve randomized controlled trials (RCTs) of CMIs for AECOPD published up to January 2021. The Cochrane risk of bias tool was used to assess the risk of bias. Stata 13.1 and WinBUGS 14.3 were used for data analyses. RESULTS: In total, 103 RCTs involving 8767 participants and 23 CMIs were included. The results indicated that among all treatments conventional Western medical therapy (WM) plus Dengzhanxixin injection (DZXX) led to the best improvement in the clinical efficacy and the ratio of forced expiratory volume in one second (FEV(1)) to forced vital capacity (FVC) (FEV(1)/FVC), with surface under the cumulative ranking curve (SUCRA)=80.47% and 98.55%, respectively. Moreover, Shenmai injection (SM) plus WM and Reduning injection (RDN) plus WM led to the best improvement in the FEV(1) (SUCRA=80.18%) and the ratio of forced expiratory volume in one second to the predicted value (FEV(1)%, SUCRA=87.28%). Shengmai injection (SGM) plus WM led to the most considerable shortening in the length of hospital stay (SUCRA=94.70%). Cluster analysis revealed that WM+DZXX had the most favorable response for clinical efficacy and FEV(1), as well as clinical efficacy and FEV(1)/FVC, WM+RDN had the most favorable response for clinical efficacy and FEV(1)%, WM+SGM had the most favorable response for clinical efficacy and length of hospital stay. CONCLUSION: WM+DZXX, WM+RDN, and WM+SGM were noted to be the optimum treatment regimens for improving in clinical efficacy, FEV(1), FEV(1)/FVC, FEV(1)% and reducing the hospital stay length of AECOPD patients. Considering the limitations this NMA may have, the current results warrant further verification via additional high-quality studies.
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spelling pubmed-86911362021-12-22 Chinese Medical Injections for Acute Exacerbation of Chronic Obstructive Pulmonary Disease: A Network Meta-analysis Hu, Haiyin Ji, Zhaochen Qiang, Xiaoyu Liu, Shigang Sheng, Xiaodi Chen, Zhe Liu, Fanqi Wang, Hui Zhang, Junhua Int J Chron Obstruct Pulmon Dis Review BACKGROUND: The World Health Organization has indicated that chronic obstructive pulmonary disease (COPD) may become the third leading cause of death by 2030. Acute exacerbation of COPD (AECOPD) is an important process in clinical treatment. Recent studies have shown that Chinese medical injections (CMI) are effective against AECOPD, but the effective difference among different CMIs remains unclear. The aim of this network meta-analysis (NMA) is to compare the therapeutic effect of various CMIs. METHODS: We conducted an overall, systematic literature search in the China National Knowledge Infrastructure, Wanfang, VIP, SinoMed, PubMed, Embase, Cochrane Library, and Web of Science databases to retrieve randomized controlled trials (RCTs) of CMIs for AECOPD published up to January 2021. The Cochrane risk of bias tool was used to assess the risk of bias. Stata 13.1 and WinBUGS 14.3 were used for data analyses. RESULTS: In total, 103 RCTs involving 8767 participants and 23 CMIs were included. The results indicated that among all treatments conventional Western medical therapy (WM) plus Dengzhanxixin injection (DZXX) led to the best improvement in the clinical efficacy and the ratio of forced expiratory volume in one second (FEV(1)) to forced vital capacity (FVC) (FEV(1)/FVC), with surface under the cumulative ranking curve (SUCRA)=80.47% and 98.55%, respectively. Moreover, Shenmai injection (SM) plus WM and Reduning injection (RDN) plus WM led to the best improvement in the FEV(1) (SUCRA=80.18%) and the ratio of forced expiratory volume in one second to the predicted value (FEV(1)%, SUCRA=87.28%). Shengmai injection (SGM) plus WM led to the most considerable shortening in the length of hospital stay (SUCRA=94.70%). Cluster analysis revealed that WM+DZXX had the most favorable response for clinical efficacy and FEV(1), as well as clinical efficacy and FEV(1)/FVC, WM+RDN had the most favorable response for clinical efficacy and FEV(1)%, WM+SGM had the most favorable response for clinical efficacy and length of hospital stay. CONCLUSION: WM+DZXX, WM+RDN, and WM+SGM were noted to be the optimum treatment regimens for improving in clinical efficacy, FEV(1), FEV(1)/FVC, FEV(1)% and reducing the hospital stay length of AECOPD patients. Considering the limitations this NMA may have, the current results warrant further verification via additional high-quality studies. Dove 2021-12-17 /pmc/articles/PMC8691136/ /pubmed/34949918 http://dx.doi.org/10.2147/COPD.S335579 Text en © 2021 Hu et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Review
Hu, Haiyin
Ji, Zhaochen
Qiang, Xiaoyu
Liu, Shigang
Sheng, Xiaodi
Chen, Zhe
Liu, Fanqi
Wang, Hui
Zhang, Junhua
Chinese Medical Injections for Acute Exacerbation of Chronic Obstructive Pulmonary Disease: A Network Meta-analysis
title Chinese Medical Injections for Acute Exacerbation of Chronic Obstructive Pulmonary Disease: A Network Meta-analysis
title_full Chinese Medical Injections for Acute Exacerbation of Chronic Obstructive Pulmonary Disease: A Network Meta-analysis
title_fullStr Chinese Medical Injections for Acute Exacerbation of Chronic Obstructive Pulmonary Disease: A Network Meta-analysis
title_full_unstemmed Chinese Medical Injections for Acute Exacerbation of Chronic Obstructive Pulmonary Disease: A Network Meta-analysis
title_short Chinese Medical Injections for Acute Exacerbation of Chronic Obstructive Pulmonary Disease: A Network Meta-analysis
title_sort chinese medical injections for acute exacerbation of chronic obstructive pulmonary disease: a network meta-analysis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8691136/
https://www.ncbi.nlm.nih.gov/pubmed/34949918
http://dx.doi.org/10.2147/COPD.S335579
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