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j.pupt.2010.05.007.pdf834.01 kBAdobe PDF見る/開く
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dc.contributor.authorIto, Isaoen
dc.contributor.authorKadowaki, Seizoen
dc.contributor.authorTanabe, Naoyaen
dc.contributor.authorHaruna, Akaneen
dc.contributor.authorKase, Masahitoen
dc.contributor.authorYasutomo, Yoshiroen
dc.contributor.authorTsukino, Mitsuhiroen
dc.contributor.authorNakai, Asakoen
dc.contributor.authorMatsumoto, Hisakoen
dc.contributor.authorNiimi, Akioen
dc.contributor.authorChin, Kazuoen
dc.contributor.authorIchiyama, Satoshien
dc.contributor.authorMishima, Michiakien
dc.contributor.alternative伊藤, 功朗ja
dc.date.accessioned2010-10-12T00:56:20Z-
dc.date.available2010-10-12T00:56:20Z-
dc.date.issued2010-10-
dc.identifier.issn1094-5539-
dc.identifier.urihttp://hdl.handle.net/2433/126728-
dc.description.abstractBACKGROUND: Treatment of aspiration pneumonia is becoming an important issue due to aging of populations worldwide. Effectiveness of tazobactam/piperacillin (TAZ/PIPC) in aspiration pneumonia is not clear. PURPOSE: To compare clinical efficacy between TAZ/PIPC (1:4 compound) and imipenem/cilastatin (IPM/CS) in patients with moderate-to-severe aspiration pneumonia. PATIENTS AND METHODS: In this open-label, randomized study either TAZ/PIPC 5 g or IPM/CS 1 g was intravenously administered every 12 h to patients with moderate-to-severe community-acquired aspiration pneumonia or nursing home-acquired pneumonia with risk for aspiration pneumonia for average 11 days. The primary outcome was clinical response rate at the end of treatment (EOT) in validated per-protocol (VPP) population. Secondary outcomes were clinical response during treatment (days 4 and 7) and at the end of study (EOS) in VPP population, and survival at day 30 in modified intention-to-treat (MITT) population. RESULTS: There was no difference between the groups in primary or secondary outcome. However, significantly faster improvement as measured by axillary temperature (p < 0.05) and WBC count (p = 0.01) was observed under TAZ/PIPC treatment. In patients with gram-positive bacterial infection, TAZ/PIPC was more effective at EOT in VPP population (p = 0.03). CONCLUSION: TAZ/PIPC is as effective and safe as IPM/CS in the treatment of moderate- to-severe aspiration pneumonia.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherElsevieren
dc.rights© 2010 Elsevier Ltden
dc.rightsThis is not the published version. Please cite only the published version.en
dc.rightsこの論文は出版社版でありません。引用の際には出版社版をご確認ご利用ください。ja
dc.subjectCommunity-acquired pneumonia (CAP)en
dc.subjectNursing home-acquired pneumonia (NHAP)en
dc.subjectAspirationen
dc.subjectTazobactam/piperacillin (TAZ/PIPC)en
dc.subjectImipenem/cilastain (IPM/CS)en
dc.subjectOpen-label randomized studyen
dc.titleTazobactam/piperacillin for moderate-to-severe pneumonia in patients with risk for aspiration: comparison with imipenem/cilastatin.en
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.ncidAA1115999X-
dc.identifier.jtitlePulmonary pharmacology & therapeuticsen
dc.identifier.volume23-
dc.identifier.issue5-
dc.identifier.spage403-
dc.identifier.epage410-
dc.relation.doi10.1016/j.pupt.2010.05.007-
dc.textversionauthor-
dc.identifier.pmid20561917-
dcterms.accessRightsopen access-
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