pubmed-article:18343748 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:18343748 | lifeskim:mentions | umls-concept:C0032285 | lld:lifeskim |
pubmed-article:18343748 | lifeskim:mentions | umls-concept:C0087111 | lld:lifeskim |
pubmed-article:18343748 | lifeskim:mentions | umls-concept:C0052796 | lld:lifeskim |
pubmed-article:18343748 | lifeskim:mentions | umls-concept:C0054066 | lld:lifeskim |
pubmed-article:18343748 | lifeskim:mentions | umls-concept:C0036043 | lld:lifeskim |
pubmed-article:18343748 | lifeskim:mentions | umls-concept:C0585361 | lld:lifeskim |
pubmed-article:18343748 | lifeskim:mentions | umls-concept:C1707455 | lld:lifeskim |
pubmed-article:18343748 | lifeskim:mentions | umls-concept:C0332173 | lld:lifeskim |
pubmed-article:18343748 | lifeskim:mentions | umls-concept:C1442459 | lld:lifeskim |
pubmed-article:18343748 | lifeskim:mentions | umls-concept:C1547085 | lld:lifeskim |
pubmed-article:18343748 | pubmed:issue | 1 | lld:pubmed |
pubmed-article:18343748 | pubmed:dateCreated | 2008-3-17 | lld:pubmed |
pubmed-article:18343748 | pubmed:abstractText | This randomised, open-label, non-inferiority study was designed to demonstrate that a 3-day course of oral azithromycin 1 g once daily was at least as effective as a standard 7-day course of oral amoxicillin-clavulanate 875/125 mg twice daily in the treatment of outpatients with community-acquired pneumonia (Fine class I and II). In total, 267 patients with clinically and radiologically confirmed community-acquired pneumonia were randomly assigned to receive either the azithromycin (n=136) or the amoxicillin-clavulanate (n=131) regimen. At screening, 60/136 (58.8%) and 61/131 (62.9%) respectively had at least one pathogen identified by sputum culture, PCR, or serology. The primary endpoint was the clinical response in the intent-to-treat population at the end of therapy (day 8 to 12). Clinical success rates were 126/136 (92.6%) for azithromycin and 122/131 (93.1%) for amoxicillin-clavulanate (treatment difference: - 0.48%; 95% confidence interval: - 5.66%; 4.69%). Clinical and radiological success rates at follow-up (day 22-26) were consistent with the end of therapy results, no patient reporting clinical relapse. Bacteriological success rates at the end of therapy were 32/35 (91.4%) for azithromycin and 30/33 (90.9%) for amoxicillin-clavulanate (treatment difference: 0.52%; 95% confidence interval - 10.81%; 11.85%). Both treatment regimens were well tolerated: the overall incidence of adverse events was 34/136 (25.0%) for azithromycin and 22/132 (16.7%) for amoxicillin-clavulanate. In both treatment groups, the most commonly reported events were gastrointestinal symptoms. Azithromycin 1g once daily for 3 days is at least as effective as amoxicillin-clavulanate 875/125 mg twice daily for 7 days in the treatment of adult patients with community-acquired pneumonia. | lld:pubmed |
pubmed-article:18343748 | pubmed:language | eng | lld:pubmed |
pubmed-article:18343748 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18343748 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:18343748 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18343748 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18343748 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18343748 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:18343748 | pubmed:month | Feb | lld:pubmed |
pubmed-article:18343748 | pubmed:issn | 1973-9478 | lld:pubmed |
pubmed-article:18343748 | pubmed:author | pubmed-author:Dal NegroRR | lld:pubmed |
pubmed-article:18343748 | pubmed:author | pubmed-author:PernaGG | lld:pubmed |
pubmed-article:18343748 | pubmed:author | pubmed-author:MolWW | lld:pubmed |
pubmed-article:18343748 | pubmed:author | pubmed-author:ParisRR | lld:pubmed |
pubmed-article:18343748 | pubmed:author | pubmed-author:TodiscoTT | lld:pubmed |
pubmed-article:18343748 | pubmed:author | pubmed-author:ConfalonieriM... | lld:pubmed |
pubmed-article:18343748 | pubmed:author | pubmed-author:LigiaG PGP | lld:pubmed |
pubmed-article:18343748 | pubmed:author | pubmed-author:RastelliVV | lld:pubmed |
pubmed-article:18343748 | pubmed:author | pubmed-author:CepparuloMM | lld:pubmed |
pubmed-article:18343748 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:18343748 | pubmed:volume | 20 | lld:pubmed |
pubmed-article:18343748 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:18343748 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:18343748 | pubmed:pagination | 77-86 | lld:pubmed |
pubmed-article:18343748 | pubmed:dateRevised | 2009-8-4 | lld:pubmed |
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pubmed-article:18343748 | pubmed:year | 2008 | lld:pubmed |
pubmed-article:18343748 | pubmed:articleTitle | Efficacy and safety of azithromycin 1 g once daily for 3 days in the treatment of community-acquired pneumonia: an open-label randomised comparison with amoxicillin-clavulanate 875/125 mg twice daily for 7 days. | lld:pubmed |
pubmed-article:18343748 | pubmed:affiliation | Dept. of General Medicine, Gubbio Hospital, Italy. | lld:pubmed |
pubmed-article:18343748 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:18343748 | pubmed:publicationType | Comparative Study | lld:pubmed |
pubmed-article:18343748 | pubmed:publicationType | Randomized Controlled Trial | lld:pubmed |
pubmed-article:18343748 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |