Working… Menu
Trial record 32 of 752 for:    Anti-Infective Agents AND Antibiotics, Antitubercular AND culture

Pilot Study of the Utility of Empiric Antibiotic Therapy for Suspected ICU-Acquired Infection

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00438269
Recruitment Status : Completed
First Posted : February 22, 2007
Last Update Posted : February 22, 2007
The Physicians' Services Incorporated Foundation
Information provided by:
Canadian Critical Care Trials Group

Brief Summary:

Infection developing in the intensive care unit is a common complication of critical illness, but notoriously difficult to diagnose. A definite diagnosis based on the most reliable tests usually is not possible for at least two days. It is unclear what the optimal management approach should be while awaiting the results of diagnostic tests. In some circumstances, broad spectrum antibiotics are started with a plan to adjust them once the results of cultures are available. Observational studies show that this results in greater antibiotic use, and the risk of superinfection and resistance. In other circumstances, antibiotics may be withheld pending the results of cultures, a strategy that leads to a delay in therapy when cultures are positive, and that may be associated with a worse clinical outcome.

We undertook a randomized pilot study to address the question: "In a critically ill patient for whom clinicians are uncertain whether infection may be present, and in whom potential sites of infection have been managed by removing or changing invasive devices, can a policy of delaying antibiotic treatment until cultures are available reduce the risks of excessive antibiotic use, without increasing the risks associated with delayed therapy?"

Recognizing that the question has not been formally addressed before, and that approaches to clinical management are both widely divergent and passionately held, our pilot study tested the feasibility and acceptability of undertaking a larger trial with sufficient power to determine equivalence.

Condition or disease Intervention/treatment Phase
Nosocomial Infection Pneumonia Systemic Inflammatory Response Syndrome Critical Illness Pyrexia Drug: Site-specific empiric regimens included: Meropenem Drug: Piperacillin/tazobactam Drug: Ciprofloxacin and cefazolin +/- metronidazole Phase 2

Detailed Description:

We randomized critically ill patients who had been in hospital for at least 72 hours, and in the ICU for at least 24 hours, and who manifested either a temperature >38.5 degrees, or a temperature>38.0 degrees and a white cell count >12,000, and in whom clinicians entertained the possibility of infection as a diagnosis, to either site-specific broad spectrum empiric antibiotics or the corresponding placebo. All patients underwent a comprehensive series of investigations to identify an infectious focus, and all patients had full source control, including changes of central lines and urinary catheters, and change of nasogastric to orogastric tubes.

Patients were maintained in assigned study arm for seven days, or until culture data were available, at which time they were switched to culture-guided narrow spectrum therapy

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Enrollment : 80 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double
Primary Purpose: Treatment
Official Title: Appropriate Antimicrobial Therapy in Critical Care: A Pilot Randomized Controlled Trial
Study Start Date : February 2003
Study Completion Date : March 2005

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Antibiotics

Primary Outcome Measures :
  1. Feasibility: = % of eligible patients who were consented and randomized
  2. Acceptability: = % of patients in each study arm who were switched to open label therapy prior to culture results

Secondary Outcome Measures :
  1. Mortality (14, 30, 90 day)
  2. Microbial resistance patterns
  3. ICU-free days
  4. Antibiotic-free days
  5. Change in organ dysfunction (MOD scores)

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

Layout table for eligibility information
Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • In hospital > 72 hrs and in ICU > 24hrs, and
  • Core temperature ≥38.5°C, or temperature ≥ 38.0°C with a WBC>12,000/mm3, or temperature ≤ 36.0°C with a WBC > 12,000/mm3
  • Suspicion of infection

Exclusion Criteria:

  • Age < 18 years
  • Imminent death (within 24 hrs) or withdrawal of aggressive therapy
  • Prosthetic heart valve or vascular graft
  • Neutropenia (Absolute neutrophil count < 1000/mm3)
  • Received > 16 hours of a broad spectrum antibiotic in the last 24 hours (3rd gen cephalosporin, fluoroquinolone, carbapenem, anti-pseudomonal penicillin) or any combination therapy
  • History of allergic reaction to both study medications
  • New physical findings consistent with infection:

    • Meningeal signs
    • Peritonitis + free air on Abdo x-ray
    • Soft tissue infection / cellulitis
    • Murmur & suspicion of endocarditis
  • Newly available (within past 24 hours) culture results consistent with infection

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00438269

Layout table for location information
Canada, Ontario
University Health Network
Toronto, Ontario, Canada, M5G 2C4
Sponsors and Collaborators
Canadian Critical Care Trials Group
The Physicians' Services Incorporated Foundation
Layout table for investigator information
Principal Investigator: Mary-Anne W Aarts, MD MSc University of Toronto
Principal Investigator: John C Marshall, MD University of Toronto

Layout table for additonal information Identifier: NCT00438269     History of Changes
Other Study ID Numbers: AATICC Pilot Study
First Posted: February 22, 2007    Key Record Dates
Last Update Posted: February 22, 2007
Last Verified: February 2007
Keywords provided by Canadian Critical Care Trials Group:
Additional relevant MeSH terms:
Layout table for MeSH terms
Piperacillin, Tazobactam Drug Combination
Anti-Bacterial Agents
Anti-Infective Agents
Antiprotozoal Agents
Antiparasitic Agents
Antineoplastic Agents
Communicable Diseases
Cross Infection
Critical Illness
Systemic Inflammatory Response Syndrome
Lung Diseases
Respiratory Tract Diseases
Respiratory Tract Infections
Disease Attributes
Pathologic Processes
Iatrogenic Disease
Body Temperature Changes
Signs and Symptoms
Topoisomerase II Inhibitors