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j.pupt.2010.05.007.pdf834.01 kBAdobe PDF見る/開く
タイトル: Tazobactam/piperacillin for moderate-to-severe pneumonia in patients with risk for aspiration: comparison with imipenem/cilastatin.
著者: Ito, Isao  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0003-3109-898X (unconfirmed)
Kadowaki, Seizo
Tanabe, Naoya  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0002-7481-0212 (unconfirmed)
Haruna, Akane
Kase, Masahito
Yasutomo, Yoshiro
Tsukino, Mitsuhiro
Nakai, Asako
Matsumoto, Hisako  KAKEN_id
Niimi, Akio
Chin, Kazuo  KAKEN_id
Ichiyama, Satoshi  KAKEN_id
Mishima, Michiaki
著者名の別形: 伊藤, 功朗
キーワード: Community-acquired pneumonia (CAP)
Nursing home-acquired pneumonia (NHAP)
Aspiration
Tazobactam/piperacillin (TAZ/PIPC)
Imipenem/cilastain (IPM/CS)
Open-label randomized study
発行日: Oct-2010
出版者: Elsevier
誌名: Pulmonary pharmacology & therapeutics
巻: 23
号: 5
開始ページ: 403
終了ページ: 410
抄録: BACKGROUND: 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.
著作権等: © 2010 Elsevier Ltd
This is not the published version. Please cite only the published version.
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。
URI: http://hdl.handle.net/2433/126728
DOI(出版社版): 10.1016/j.pupt.2010.05.007
PubMed ID: 20561917
出現コレクション:学術雑誌掲載論文等

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