2002
DOI: 10.1016/s0149-2918(02)80034-0
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A multicenter, open-label, randomized comparison of levofloxacin and azithromycin plus ceftriaxone in hospitalized adults with moderate to severe community-acquired pneumonia

Abstract: In this study in hospitalized patients with moderate to severe CAP, levofloxacin monotherapy was at least as effective as a combination regimen of azithromycin and ceftriaxone in providing coverage against the current causative pathogens in CAP. In addition, levofloxacin was as well tolerated as the combination of azithromycin and ceftriaxone.

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Cited by 85 publications
(76 citation statements)
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“…Of the included trials, 8 trials included only patients with severe or moderate-to-severe pneumonia. 16,18,19,21,22,28,30,36 Six additional trials enrolled patients with severe pneumonia; 17,26,27,29,33,34 however, the majority of enrolled patients had mild to moderate pneumonia. The guidelines of the American Thoracic Society 37 and Pneumonia Severity Index score class IV and V 38 were mainly used for assessment of severe pneumonia.…”
Section: Included Trialsmentioning
confidence: 99%
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“…Of the included trials, 8 trials included only patients with severe or moderate-to-severe pneumonia. 16,18,19,21,22,28,30,36 Six additional trials enrolled patients with severe pneumonia; 17,26,27,29,33,34 however, the majority of enrolled patients had mild to moderate pneumonia. The guidelines of the American Thoracic Society 37 and Pneumonia Severity Index score class IV and V 38 were mainly used for assessment of severe pneumonia.…”
Section: Included Trialsmentioning
confidence: 99%
“…[14][15][16][17][18]20,21,26,27,[29][30][31][32] Isolates recovered from all patients enrolled in the studies were tested for resistance against the study antibiotics and for penicillin resistance. Only one S. aureus isolate resistant to levofloxacin was found in these 13 studies.…”
Section: Included Trialsmentioning
confidence: 99%
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“…Literatürde F ile AS ± M kullanımının karşılaştırıldığı çalışmalarda gruplar arasında farklı sonuçlar mevcuttur (10-13). F ile AS ± M alan hastaların karşılaştırıldığı birçok çalışmada mikrobiyolojik eradikasyon, semptom kontrolü ve klinik başarı tedavi grupları arasında benzer etkinlikte saptanmıştır (14)(15)(16)(17)(18)(19)(20)(21). Klinik başarı kombinasyon grubunda %79 ile %92, solunum florokinolonları grubunda %79 ile %89 arasında değiştiği görülmüştür.…”
Section: Discussionunclassified