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Azithromycin combination therapy for community-acquired pneumonia: propensity score analysis

Whether macrolide combination therapy reduces the mortality of patients with severe community-acquired pneumonia (CAP) hospitalized in the non-intensive care unit (ICU) remains unclear. Therefore, we investigated the efficacy of adding azithromycin to β-lactam antibiotics for such patients. This pro...

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Autores principales: Ito, Akihiro, Ishida, Tadashi, Tachibana, Hiromasa, Tokumasu, Hironobu, Yamazaki, Akio, Washio, Yasuyoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895050/
https://www.ncbi.nlm.nih.gov/pubmed/31804572
http://dx.doi.org/10.1038/s41598-019-54922-4
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author Ito, Akihiro
Ishida, Tadashi
Tachibana, Hiromasa
Tokumasu, Hironobu
Yamazaki, Akio
Washio, Yasuyoshi
author_facet Ito, Akihiro
Ishida, Tadashi
Tachibana, Hiromasa
Tokumasu, Hironobu
Yamazaki, Akio
Washio, Yasuyoshi
author_sort Ito, Akihiro
collection PubMed
description Whether macrolide combination therapy reduces the mortality of patients with severe community-acquired pneumonia (CAP) hospitalized in the non-intensive care unit (ICU) remains unclear. Therefore, we investigated the efficacy of adding azithromycin to β-lactam antibiotics for such patients. This prospective cohort study enrolled consecutive patients with CAP hospitalized in the non-ICU between October 2010 and November 2016. The 30-day mortality between β-lactam and azithromycin combination therapy and β-lactam monotherapy was compared in patients classified as mild to moderate and severe according to the CURB-65, Pneumonia Severity Index (PSI), and Infectious Diseases Society of America (IDSA)/American Thoracic Society (ATS) criteria. Inverse probability of treatment weighting (IPTW) analysis was used to reduce biases. Based on the CURB-65 and PSI, combination therapy did not significantly reduce the 30-day mortality in either group (179 patients in the combination group, 952 in the monotherapy group). However, based on the IDSA/ATS criteria, combination therapy significantly reduced the 30-day mortality in patients with severe (odds ratio [OR] 0.12, 95% confidence interval [CI] 0.007–0.57), but not non-severe pneumonia (OR 1.85, 95% CI 0.51–5.40); these results were similar after IPTW analysis. Azithromycin combination therapy significantly reduced the mortality of patients with severe CAP who met the IDSA/ATS criteria.
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spelling pubmed-68950502019-12-11 Azithromycin combination therapy for community-acquired pneumonia: propensity score analysis Ito, Akihiro Ishida, Tadashi Tachibana, Hiromasa Tokumasu, Hironobu Yamazaki, Akio Washio, Yasuyoshi Sci Rep Article Whether macrolide combination therapy reduces the mortality of patients with severe community-acquired pneumonia (CAP) hospitalized in the non-intensive care unit (ICU) remains unclear. Therefore, we investigated the efficacy of adding azithromycin to β-lactam antibiotics for such patients. This prospective cohort study enrolled consecutive patients with CAP hospitalized in the non-ICU between October 2010 and November 2016. The 30-day mortality between β-lactam and azithromycin combination therapy and β-lactam monotherapy was compared in patients classified as mild to moderate and severe according to the CURB-65, Pneumonia Severity Index (PSI), and Infectious Diseases Society of America (IDSA)/American Thoracic Society (ATS) criteria. Inverse probability of treatment weighting (IPTW) analysis was used to reduce biases. Based on the CURB-65 and PSI, combination therapy did not significantly reduce the 30-day mortality in either group (179 patients in the combination group, 952 in the monotherapy group). However, based on the IDSA/ATS criteria, combination therapy significantly reduced the 30-day mortality in patients with severe (odds ratio [OR] 0.12, 95% confidence interval [CI] 0.007–0.57), but not non-severe pneumonia (OR 1.85, 95% CI 0.51–5.40); these results were similar after IPTW analysis. Azithromycin combination therapy significantly reduced the mortality of patients with severe CAP who met the IDSA/ATS criteria. Nature Publishing Group UK 2019-12-05 /pmc/articles/PMC6895050/ /pubmed/31804572 http://dx.doi.org/10.1038/s41598-019-54922-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ito, Akihiro
Ishida, Tadashi
Tachibana, Hiromasa
Tokumasu, Hironobu
Yamazaki, Akio
Washio, Yasuyoshi
Azithromycin combination therapy for community-acquired pneumonia: propensity score analysis
title Azithromycin combination therapy for community-acquired pneumonia: propensity score analysis
title_full Azithromycin combination therapy for community-acquired pneumonia: propensity score analysis
title_fullStr Azithromycin combination therapy for community-acquired pneumonia: propensity score analysis
title_full_unstemmed Azithromycin combination therapy for community-acquired pneumonia: propensity score analysis
title_short Azithromycin combination therapy for community-acquired pneumonia: propensity score analysis
title_sort azithromycin combination therapy for community-acquired pneumonia: propensity score analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895050/
https://www.ncbi.nlm.nih.gov/pubmed/31804572
http://dx.doi.org/10.1038/s41598-019-54922-4
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