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NCT Number: NCT00950222

Impact of Imipenem With Amikacin Pharmacokinetic and Pharmacodynamic

The study is a prospective open trial conducted in 4 centers, and designed to determine if pharmacokinetic (PK) and pharmacodynamic (PD) parameters of imipenem, associated with amikacin as empirical therapy, impact microbiological and clinical outcome of patients with Gram negative bacilli (GNB) ventilator-associated pneumonia (VAP).

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Key information

About this study

Inappropriate initial antibiotherapy increases mortality of many serious infections. This is the case for ventilator-associated pneumonia, frequently occurring during intensive care unit (ICU) hospitalization, and whose 48 first hours of treatment are decisive.

It is well established that pharmacokinetic and pharmacodynamic parameters of antibiotics are correlated with their clinical and microbiological effectiveness. However in ICU patients, pharmacokinetic parameters of antibiotics suffer great variations, and bacteria responsible for these infections are usually less sensitive to antibiotics, especially Gram negative bacilli (GNB). An important pharmacodynamic variability may occur at the initial phase of the antibiotic treatment, decisive for the infection's outcome.

We propose to evaluate the correlation between pharmacokinetic and pharmacodynamic profile of the empirical antibiotic therapy and the microbiological and clinical outcome of VAP.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 18 years
  • Mechanical ventilation for more than 48 hours
  • Clinical suspicion of VAP defined by a new persistent radiological infiltrate and one of the following signs: purulent tracheal aspirations, or temperature of 38°3 or higher, or leucocyte count > 10000/ml
  • Risk of multi resistant bacteria defined as follows: at least 6 days of mechanical ventilation or antibiotic treatment in the 15 previous days
  • Distal pulmonary secretion sample obtained beforehand for microbiological diagnosis by bronchoalveolar lavage via bronchoscopy or blinded protected telescoping catheter via bronchoscopy or blindly
  • Presence of GNB on direct examination of the distal pulmonary secretion sample
  • Realization of a preliminary medical examination. 8- Written inform consent from the patient or relatives. The consent may be obtained after the enrollment if the patient is not able to give consent and if there is no relatives

Exclusion criteria

  • Time between distal pulmonary secretion sample taking and the 1st administration of imipenem exceeding 24 hours
  • Pregnancy
  • Severely impaired renal function (creatinine clearance lower than 10 mL/mn or renal replacement therapy)
  • Allergy to imipenem or amikacin
  • Treatment in progress with imipenem or amikacin
  • Death expected within 48 hours following diagnosis of VAP
  • Myasthenia
  • Simultaneous administration of others aminoglycosides
  • Association with intravenous polymyxin or botulinum toxin

Treatment and study plan

Imipenem/Amikacin

Drug

patients will received as empirical therapy for VAP imipenem associated with amikacin.

Other names: Therapy for VAP imipenem associated with amikacin

Primary outcomes

  1. Variation of numeration (cfu per ml) of GNB, for whom culture of pulmonary samples are positive (higher than defined thresholds), between the quantitative endotracheal aspiration (QAE) obtained at H0 (initiation of treatment) and QAE obtained at H48

    Time frame: Hour 48

Secondary outcomes

  1. To describe imipenem and amikacin PK parameters as empirical therapy in ICU patients treated for VAP

    Time frame: Hour 24

  2. To describe imipenem and amikacin PD parameters as empirical therapy in ICU patients treated for VAP

    Time frame: Hour 24

  3. To determine the proportion of patients for whom the pharmacodynamic targets suggested in the literature for aminoglycosides and beta lactams are achieved

    Time frame: Hour 24

  4. To identify sources of variability of imipenem and amikacin PK/PD parameters in ICU patients with VAP

    Time frame: Hour 24

  5. To assess the impact of imipenem and amikacin PK/PD parameters on GNB eradication at day 3

    Time frame: Day 3

  6. To assess the impact of imipenem and amikacin PK/PD parameters variability on the CPIS, clinical score of VAP, measured 48 hours after initiation of the treatment

    Time frame: Hour 48

  7. To assess the impact of imipenem and amikacin PK/PD parameters on the time necessary to observe a CPIS lower or equal to 6

    Time frame: Day 8

  8. To assess the impact of imipenem and amikacin PK/PD parameters on clinical evolution of the VAP after 7 days of antibiotic treatment

    Time frame: Day 8

  9. To assess the impact of imipenem and amikacin PK/PD parameters on serum procalcitonin levels evolution between the initiation of the treatment and 48 hours after the initiation of the treatment of the VAP

    Time frame: Hour 48

  10. To assess the impact of imipenem and amikacin PK/PD parameters on mortality at day 28 (Day 28) 11- to assess the impact of imipenem and amikacin PK/PD parameters on VAP relapse

    Time frame: Day 28

  11. To study emergence of less sensitive bacteria to imipenem and/or amikacin, 48 hours after the initiation of the antibiotic treatment, among GNB isolated in endotracheal aspiration before initiation of this treatment

    Time frame: Hour 48

  12. To study emergence in the tracheal and digestive flora of micro-organisms resistant to imipenem after the first 48 hours of treatment by imipenem

    Time frame: Hour 48

Sponsors and collaborators

Lead sponsor

Assistance Publique - Hôpitaux de Paris

Other

Registry information

Acronym: IMPACT

Important dates

Study start
2009
Primary completion
2011
Study completion
2012
First posted
Jul 31, 2009
Registry last updated
Jul 26, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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