Tazobactam/piperacillin for moderate-to-severe pneumonia in patients with risk for aspiration: Comparison with imipenem/cilastatin

被引:27
|
作者
Ito, Isao [1 ,2 ]
Kadowaki, Seizo [2 ]
Tanabe, Naoya [1 ]
Haruna, Akane [1 ]
Kase, Masahito [2 ]
Yasutomo, Yoshiro [2 ]
Tsukino, Mitsuhiro [3 ]
Nakai, Asako [4 ]
Matsumoto, Hisako [1 ]
Niimi, Akio [1 ]
Chin, Kazuo [5 ]
Ichiyama, Satoshi [6 ]
Mishima, Michiaki [1 ]
机构
[1] Kyoto Univ Hosp, Dept Resp Med, Sakyo Ku, Kyoto 6068507, Japan
[2] Ono Municipal Hosp, Dept Med, Ono, Hyogo 6751332, Japan
[3] Hikone Municipal Hosp, Dept Resp Med, Shiga 5228507, Japan
[4] Kyoto Univ Hosp, Dept Diagnost Imaging & Nucl Med, Sakyo Ku, Kyoto 6068507, Japan
[5] Kyoto Univ Hosp, Dept Resp Care & Sleep Med, Sakyo Ku, Kyoto 6068507, Japan
[6] Kyoto Univ Hosp, Dept Infecton Control & Prevent, Sakyo Ku, Kyoto 6068507, Japan
关键词
Community-acquired pneumonia (CAP); Nursing home-acquired pneumonia (NHAP); Aspiration; Tazobactam/piperacillin (TAZ/PIPC); Imipenem/cilastain (IPM/CS); Open-label randomized study; COMMUNITY-ACQUIRED PNEUMONIA; CARE-ASSOCIATED PNEUMONIA; PIPERACILLIN-TAZOBACTAM; NOSOCOMIAL PNEUMONIA; ELDERLY-PATIENTS; BACTERIOLOGY; CLINDAMYCIN; MONOTHERAPY; TOBRAMYCIN; RESISTANCE;
D O I
10.1016/j.pupt.2010.05.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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 perprotocol (VPP) population. Secondary outcomes were clinical response during treatment (days 4 and 7) and at the end of study (EDS) in VPP population, and survival at day 30 in modified intention-to-treat (MITI) 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. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:403 / 410
页数:8
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