Comparison of tigecycline with imipenem/cilastatin for the treatment of hospital-acquired pneumonia

被引:277
作者
Freire, Antonio T. [2 ]
Melnyk, Vasyl [3 ]
Kim, Min Ja [4 ]
Datsenko, Oleksiy [5 ]
Dzyublik, Oleksandr [6 ]
Glumcher, Felix [7 ]
Chuang, Yin-Ching [8 ]
Maroko, Robert T.
Dukart, Gary
Cooper, C. Angel
Korth-Bradley, Joan M.
Dartois, Nathalie [1 ,9 ]
Gandjini, Hassan [9 ]
机构
[1] Pfizer Inc, Clin Res, Collegeville, PA 19426 USA
[2] Santa Casa Misericordia Belo Horizonte, Belo Horizonte, MG, Brazil
[3] Kyiv City TB & Pulmonol Hosp, Kiev, Ukraine
[4] Korea Univ, Med Ctr, Anam Hosp, Seoul, South Korea
[5] City Clin Multidiscipline Hosp, Kharkiv Med Acad Postgrad Educ, Kharkov, Ukraine
[6] Cent Mil Hosp, Dept Pulmonol, Kiev, Ukraine
[7] Resuscitat & Emergency Med Care Natl Med Univ, Kyiv Municipal Clin Hosp, Kiev, Ukraine
[8] Chi Mei Med Ctr, Dept Med Res, Yung Kang, Taiwan
[9] Pfizer Inc, Paris, France
关键词
Nosocomial; Pneumonia; Glycylcycline; Ventilator/non-ventilator-associated pneumonia; Antimicrobial; VENTILATOR-ASSOCIATED PNEUMONIA; EXPOSURE-RESPONSE ANALYSES; SKIN-STRUCTURE INFECTIONS; NOSOCOMIAL PNEUMONIA; ANTIMICROBIAL ACTIVITY; COMPLICATED SKIN; CLINICAL-TRIAL; EFFICACY; MULTICENTER; IMIPENEM;
D O I
10.1016/j.diagmicrobio.2010.05.012
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
To compare efficacy and safety of a tigecycline regimen with an imipenem/cilastatin regimen in hospital-acquired pneumonia patients, a phase 3, multicenter, randomized, double-blind, study evaluated 945 patients. Coprimary end points were clinical response in clinically evaluable (CE) and clinical modified intent-to-treat (c-mITT) populations at test-of-cure. Cure rates were 67.9% for tigecycline and 78.2% for imipenem (CE patients) and 62.7% and 67.6% (c-mITT patients), respectively. A statistical interaction occurred between ventilator-associated pneumonia (VAP) and non-VAP subgroups, with significantly lower cure rates in tigecycline VAP patients compared to imipenem; in non-VAP patients, tigecycline was noninferior to imipenem. Overall mortality did not differ between the tigecycline (14.1%) and imipenem regimens (12.2%), although more deaths occurred in VAP patients treated with tigecycline than imipenem. Overall, the tigecycline regimen was noninferior to the imipenem/cilastatin regimen for the c-mITT but not the CE population; this difference appears to have been driven by results in VAP patients. (C) 2010 Published by Elsevier Inc.
引用
收藏
页码:140 / 151
页数:12
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