Efficacy and safety of intravenous infusion of doripenem versus imipenem in ventilator-associated pneumonia: A multicenter, randomized study
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Chastre, Jean
[1
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Wunderink, Richard
[2
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Prokocimer, Philippe
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Johnson & Johnson Pharmaceut Res & Dev, LLC, Mountain View, CA USAUniv Paris 06, Assistance Publ Hop Paris, Reanimat Med Grp Hosp Pieie Salpetriere, Paris, France
Prokocimer, Philippe
[3
]
Lee, Michael
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Johnson & Johnson Pharmaceut Res & Dev, LLC, Mountain View, CA USAUniv Paris 06, Assistance Publ Hop Paris, Reanimat Med Grp Hosp Pieie Salpetriere, Paris, France
Lee, Michael
[3
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Kaniga, Kone
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Johnson & Johnson Pharmaceut Res & Dev, LLC, Mountain View, CA USAUniv Paris 06, Assistance Publ Hop Paris, Reanimat Med Grp Hosp Pieie Salpetriere, Paris, France
Kaniga, Kone
[3
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Friedland, Ian
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Johnson & Johnson Pharmaceut Res & Dev, LLC, Mountain View, CA USAUniv Paris 06, Assistance Publ Hop Paris, Reanimat Med Grp Hosp Pieie Salpetriere, Paris, France
Friedland, Ian
[3
]
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[1] Univ Paris 06, Assistance Publ Hop Paris, Reanimat Med Grp Hosp Pieie Salpetriere, Paris, France
[2] Northwestern Univ, Feinberg Sch Med, Dept Med, Div Pulm & Crit Care, Chicago, IL 60611 USA
[3] Johnson & Johnson Pharmaceut Res & Dev, LLC, Mountain View, CA USA
Objective: Doripenem is an investigational carbapenem with broad-spectrum activity against Gram-negative and Gram-positive pathogens, including multidrug-resistant strains, commonly responsible for ventilator-associated pneumonia (VAP). This large, phase III study compared doripenem with imipenem for the treatment of ventilator-associated pneumonia. Design: Prospective, multicenter, parallel randomized, active-controlled, open-label study. Setting, Intensive care units. Patients. Adults (N = 531) who met clinical and radiologic criteria for ventilator-associated pneumonia. Interventions: Patients were stratified by duration of mechanical ventilation (<5 vs. >= 5 days), severity of illness (Acute Physiology and Chronic Health Evaluation II score <= 15 vs. >15), and geographic region and then randomly assigned to doripenem 500 mg every 8 hrs via a 4-hr intravenous infusion or imipenem 500 mg every 6 hrs or 1000 mg every 8 hrs via 30- or 60-min intravenous infusions, respectively, for 7-14 days. Measurements and Main Results. The primary efficacy end points were the clinical cure rates in the clinical modified intent-to-treat (cMITT) and clinically evaluable populations. Doripenem was noninferior to imipenem (lower boundary of 95% confidence interval around the difference between treatments >=-20%). Clinical cure rates were 68.3% (doripenem) and 64.2% (imipenem) in the clinically evaluable and 59.0% (doripenem) and 57.8% (imipenem) in the cMITT populations. In patients with Pseudomonas aeruginosa, clinical cure was 80.0% (doripenem) and 42.9% (imipenem) (p not significant); microbiological cure was 65.0% (doripenem) and 37.5% (imipenem). Only 18% (5 of 28) of P. aeruginosa isolates had minimum inhibitory concentration >= 8 mu g/mL at baseline or following therapy in the doripenem arm compared with 64% (16 of 25) in the imipenem treatment group (p = .001). Clinical cure rate was higher with doripenem than imipenem at higher Acute Physiology and Chronic Health Evaluation II scores and older ages. Doripenem was generally well tolerated. Conclusions: In this large, phase III study of patients with ventilator-associated pneumonia, a 4-hr intravenous infusion of doripenem was clinically efficacious and therapeutically noninferior to imipenem.