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Oral versus intravenous clarithromycin in moderate to severe community-acquired pneumonia: an observational study

OBJECTIVES: British Thoracic Society guidelines recommend clarithromycin in addition to beta-lactam antibiotics for patients with community-acquired pneumonia and CURB-65 score 2–5. Intravenous therapy is commonly used but there are few data on whether oral therapy is equally effective. METHODS: Thi...

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Autores principales: Rae, Nikolas, Singanayagam, Aran, Schembri, Stuart, Chalmers, James D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5471852/
https://www.ncbi.nlm.nih.gov/pubmed/28702304
http://dx.doi.org/10.1186/s41479-017-0025-2
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author Rae, Nikolas
Singanayagam, Aran
Schembri, Stuart
Chalmers, James D.
author_facet Rae, Nikolas
Singanayagam, Aran
Schembri, Stuart
Chalmers, James D.
author_sort Rae, Nikolas
collection PubMed
description OBJECTIVES: British Thoracic Society guidelines recommend clarithromycin in addition to beta-lactam antibiotics for patients with community-acquired pneumonia and CURB-65 score 2–5. Intravenous therapy is commonly used but there are few data on whether oral therapy is equally effective. METHODS: This observational study used propensity matching to compare two groups of patients with moderate to severe community-acquired pneumonia (CURB-65 score 2–5) treated with oral (n = 226) or intravenous (n = 226) clarithromycin on admission. Outcomes were 30-day mortality, intensive care unit admission, time to clinical stability, and length of hospital stay. RESULTS: There was no significant difference in 30-day mortality (16.8% for intravenous [IV] group vs. 14.6% for oral group, hazard ratio for IV group 1.11 95% CI 0.70–1.78), ICU admission (10.6% in both groups) or complications (10.6% for IV group and 9.3% for oral group) between the groups. The time to clinical stability in both cohorts was a median of 5 days (interquartile range 3–7 days, p = 0.3). The median length of hospital stay was 8 days in the IV group (interquartile range 4–14 days) and 7 days in the oral group (interquartile range 4–13 days), p = 0.5. No other differences were observed between oral and IV groups. CONCLUSION: Where the oral route is not compromised, oral macrolides appear to be equivalent to IV in treating moderate to severe CAP.
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spelling pubmed-54718522017-07-12 Oral versus intravenous clarithromycin in moderate to severe community-acquired pneumonia: an observational study Rae, Nikolas Singanayagam, Aran Schembri, Stuart Chalmers, James D. Pneumonia (Nathan) Brief Report OBJECTIVES: British Thoracic Society guidelines recommend clarithromycin in addition to beta-lactam antibiotics for patients with community-acquired pneumonia and CURB-65 score 2–5. Intravenous therapy is commonly used but there are few data on whether oral therapy is equally effective. METHODS: This observational study used propensity matching to compare two groups of patients with moderate to severe community-acquired pneumonia (CURB-65 score 2–5) treated with oral (n = 226) or intravenous (n = 226) clarithromycin on admission. Outcomes were 30-day mortality, intensive care unit admission, time to clinical stability, and length of hospital stay. RESULTS: There was no significant difference in 30-day mortality (16.8% for intravenous [IV] group vs. 14.6% for oral group, hazard ratio for IV group 1.11 95% CI 0.70–1.78), ICU admission (10.6% in both groups) or complications (10.6% for IV group and 9.3% for oral group) between the groups. The time to clinical stability in both cohorts was a median of 5 days (interquartile range 3–7 days, p = 0.3). The median length of hospital stay was 8 days in the IV group (interquartile range 4–14 days) and 7 days in the oral group (interquartile range 4–13 days), p = 0.5. No other differences were observed between oral and IV groups. CONCLUSION: Where the oral route is not compromised, oral macrolides appear to be equivalent to IV in treating moderate to severe CAP. BioMed Central 2017-02-05 /pmc/articles/PMC5471852/ /pubmed/28702304 http://dx.doi.org/10.1186/s41479-017-0025-2 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Brief Report
Rae, Nikolas
Singanayagam, Aran
Schembri, Stuart
Chalmers, James D.
Oral versus intravenous clarithromycin in moderate to severe community-acquired pneumonia: an observational study
title Oral versus intravenous clarithromycin in moderate to severe community-acquired pneumonia: an observational study
title_full Oral versus intravenous clarithromycin in moderate to severe community-acquired pneumonia: an observational study
title_fullStr Oral versus intravenous clarithromycin in moderate to severe community-acquired pneumonia: an observational study
title_full_unstemmed Oral versus intravenous clarithromycin in moderate to severe community-acquired pneumonia: an observational study
title_short Oral versus intravenous clarithromycin in moderate to severe community-acquired pneumonia: an observational study
title_sort oral versus intravenous clarithromycin in moderate to severe community-acquired pneumonia: an observational study
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5471852/
https://www.ncbi.nlm.nih.gov/pubmed/28702304
http://dx.doi.org/10.1186/s41479-017-0025-2
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