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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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Detalles Bibliográficos
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
Descripción
Sumario: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.