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

被引:279
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
相关论文
共 50 条
  • [1] Tigecycline Population Pharmacokinetics in Patients with Community- or Hospital-Acquired Pneumonia
    Rubino, Christopher M.
    Forrest, Alan
    Bhavnani, Sujata M.
    Dukart, Gary
    Cooper, Angel
    Korth-Bradley, Joan
    Ambrose, Paul G.
    ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2010, 54 (12) : 5180 - 5186
  • [2] Randomized Phase 2 Trial To Evaluate the Clinical Efficacy of Two High-Dosage Tigecycline Regimens versus Imipenem-Cilastatin for Treatment of Hospital-Acquired Pneumonia
    Ramirez, Julio
    Dartois, Nathalie
    Gandjini, Hassan
    Yan, Jean Li
    Korth-Bradley, Joan
    McGovern, Paul C.
    ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2013, 57 (04) : 1756 - 1762
  • [3] Efficacy and Safety of Tigecycline for Patients with Hospital-Acquired Pneumonia
    Xu, Li
    Wang, Ya-Li
    Du, Shuai
    Chen, Lin
    Long, Li-Hui
    Wu, Yan
    CHEMOTHERAPY, 2015, 61 (06) : 323 - 330
  • [4] Cost-effectiveness of imipenem/cilastatin/relebactam for hospital-acquired and ventilator-associated bacterial pneumonia
    Naik, Jaesh
    Dillon, Ryan
    Massello, Matthew
    Ralph, Lewis
    Yang, Zhuo
    JOURNAL OF COMPARATIVE EFFECTIVENESS RESEARCH, 2023, 12 (03)
  • [5] Guidelines for treatment of hospital-acquired pneumonia
    Brun-Buisson, C
    SEMINARS IN RESPIRATORY AND CRITICAL CARE MEDICINE, 2002, 23 (05) : 457 - 469
  • [6] Clinical experience with tigecycline in the treatment of hospital-acquired pneumonia caused by multidrug resistant Acinetobacter baumannii
    Zhou, Yangang
    Chen, Xumin
    Xu, Ping
    Zhu, Yan
    Wang, Kuangguo
    Xiang, Daxiong
    Wang, Feng
    Hoan Linh Banh
    BMC PHARMACOLOGY & TOXICOLOGY, 2019, 20 (1)
  • [7] Current and Future Considerations for the Treatment of Hospital-Acquired Pneumonia
    Montravers, Philippe
    Harpan, Adela
    Guivarch, Elise
    ADVANCES IN THERAPY, 2016, 33 (02) : 151 - 166
  • [8] Population pharmacokinetic/pharmacodynamic assessment of imipenem/cilastatin/relebactam in patients with hospital-acquired/ventilator-associated bacterial pneumonia
    Patel, Munjal
    Bellanti, Francesco
    Daryani, Naveen M.
    Noormohamed, Nadia
    Hilbert, David W.
    Young, Katherine
    Kulkarni, Pooja
    Copalu, William
    Gheyas, Ferdous
    Rizk, Matthew L.
    CTS-CLINICAL AND TRANSLATIONAL SCIENCE, 2022, 15 (02): : 396 - 408
  • [9] Hospital-Acquired Pneumonia: Pathophysiology, Diagnosis, and Treatment
    Kieninger, Alicia N.
    Lipsett, Pamela A.
    SURGICAL CLINICS OF NORTH AMERICA, 2009, 89 (02) : 439 - +
  • [10] Cefiderocol (Fetroja) as a Treatment for Hospital-Acquired Pneumonia
    Plaisance, Connor J.
    Borne, Grant E.
    Daniel, Charles P.
    Wagner, Maxwell J.
    Shelvan, Anitha
    Mathew, Jibin
    Ahmadzadeh, Shahab
    Paladini, Antonella
    Varrassi, Giustino
    Shekoohi, Sahar
    Kaye, Alan D.
    CUREUS JOURNAL OF MEDICAL SCIENCE, 2024, 16 (01)