Duration of Antibiotic Treatment for Early VAP (DATE) Trial

Sponsor
Denver Health and Hospital Authority (Other)
Overall Status
Suspended
CT.gov ID
NCT01994980
Collaborator
(none)
100
1
2
133
0.8

Study Details

Study Description

Brief Summary

Hypothesis: 4 days of antibiotic therapy, as compared to 8 days, is equally effective and results in decreased antibiotic exposure among surgical ICU patients with early VAP.

Condition or Disease Intervention/Treatment Phase
  • Drug: Default 4 days antibiotic therapy
N/A

Detailed Description

The prevalence of multi-drug resistant (MDR) pathogens in intensive care units (ICUs) worldwide has reached epidemic proportions. In some cases, the choice of potential therapy is limited or even non-existent. Antibiotic prescription, through selection pressure, represents the main mechanism by which resistance emerges. Limitations in the development of new antibiotics underscores the importance of adherence to the principles of antibiotic stewardship.

Ventilator associated pneumonia (VAP) is the most common serious infection in mechanically ventilated, critically ill patients. Approximately one half of antibiotic prescription in the ICU is related to VAP, including prophylactic, empiric, and definitive therapy. The development of evidence-based algorithms for the rational use of antibiotics in the management of patients with both suspected and confirmed VAP is pivotal to decreasing the emergence of MDR pathogens.

Shortening the duration of antimicrobial therapy for VAP represents one strategy to curtail the emergence of MDR pathogens. Although current guidelines recommend a treatment course of 8-14 days, both clinical and microbiologic resolution (MR) of infection typically occur much sooner [10, 11]. In one study of ICU patients ventilated for > 5 days who developed VAP, 8 days of antimicrobial therapy was equally as effective as 14 days, provided VAP was not caused by a non-lactose fermenting gram negative bacillus. Favorable results following shorter courses of therapy for VAP have been observed, albeit in small, uncontrolled series.

One subset of patients for whom a decreased duration of antimicrobial therapy may be particularly effective is those who develop VAP ≤ 5 days after intubation (early VAP). Early VAP comprises approximately one half of cases of pneumonia diagnosed in the ICU. Furthermore, as compared to patients who develop late VAP, patients who develop early VAP are more likely to be infected with community-acquired pathogens sensitive to narrow spectrum antibiotics. Finally, nearly all cases of early VAP caused by sensitive pathogens demonstrate MR after relatively short (3-5 days) courses of therapy.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
A Randomized Clinical Trial of 4 vs. 8 Days of Definitive Antibiotic Therapy for Early Ventilator-Associated Pneumonia in the Surgical Intensive Care Unit
Study Start Date :
Dec 1, 2013
Anticipated Primary Completion Date :
Jan 1, 2022
Anticipated Study Completion Date :
Jan 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Default 4 days antibiotic therapy

Default 4 days antibiotic therapy

Drug: Default 4 days antibiotic therapy
The intervention for this trial involves a shorter duration of antibiotic therapy. Specifically, a default of 4 vs. 8 days.
Other Names:
  • Antibiotic for 4 days
  • No Intervention: Default 8 days antibiotic therapy

    Default 8 days antibiotic therapy

    Outcome Measures

    Primary Outcome Measures

    1. Clinical Response [Daily for 28 days]

      CPIS score

    Secondary Outcome Measures

    1. Biomarker response [Daily for either 4 or 8 days, dependent upon treatment arm]

      Procalcitonin

    2. Microbiologic response [1 Day after last day of treatment]

      BAP culture <10^3 cfu/mL

    3. Infection with MDR pathogen [28 days]

      The patient has growth of a multidrug resistant pathogen on culture

    4. Recurrence [28 days]

      The patient has another occurrence of VAP after treatment

    5. Ventilator free days [28 days]

      The number of day the patient does need mechanical ventilation

    6. Mortality [28 days]

      The patient has died

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Surgical patient

    2. VAP, defined as clinical suspicion plus a bronchoalveolar lavage (BAL) culture showing ≥105 cfu/mL of at least one pathogen. The quantitative microbiology threshold will be lowered to ≥104 cfu/mL if the patient was being treated with antibiotics to which the pathogen is sensitive at the time of the BAL. Clinical suspicion of VAP is defined as at least one point for ≥ 2 variables in the Clinical Pulmonary Infection Score (CPIS, described below).

    3. Ventilated ≤ 5 days at the time that the BAL was obtained.

    4. Hospital LOS ≤ 5 days at the time that the BAL was obtained.

    Exclusion Criteria:
    1. Age < 18 years.

    2. Prior episode of VAP for the index admission (the patient may have had prior BALs sent for culture, but these cannot have met the above mentioned diagnostic criteria for VAP).

    3. VAP caused by a MDR pathogen: Early VAP is rarely caused by a MDR pathogen; in a recent analysis of our surgical ICU, 94% of cases of early VAP were caused by a highly sensitive pathogen (MSSA 39%, H flu 35%, S. pneumo 16%, E. coli 9%) (Pieracci in press). Patients with early VAP caused by the following MDR pathogens will be excluded: Methicillin-resistant Staphylococcus aureus (MRSA), Vancomycin-intermediate Staphylococcus aureus (VISA), pseudomonas aeruginosa, Vancomycin-resistant enterococcus (VRE), Acinetobacter baumannii, Stenotrophomonas maltophilia, and extended-spectrum beta lactamase producing gram negative bacilli.

    4. Antibiotic therapy for ≥ 5 of the last 10 days preceding the BAL.

    5. Septic shock, defined as evidence of tissue hypoperfusion after adequate volume expansion, due to infection, and requiring ≥ 1 vasopressor.

    6. Current or recent (within 30 days) use of immunosuppressive medications.

    7. Length of stay ≥ 48 hours in a transferring facility.

    8. Inpatient hospitalization within 30 days of admission.

    9. Pregnancy or lactation.

    10. Legal arrest or incarceration.

    11. Moribund state in which death is imminent.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Denver Health Medical Center Denver Colorado United States 80204

    Sponsors and Collaborators

    • Denver Health and Hospital Authority

    Investigators

    • Principal Investigator: Fredric Pieracci, MD MPH, Denver Health and Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Fredric Pieracci, Assistant Professor of Surgery, Denver Health and Hospital Authority
    ClinicalTrials.gov Identifier:
    NCT01994980
    Other Study ID Numbers:
    • 13-0205
    First Posted:
    Nov 26, 2013
    Last Update Posted:
    Aug 27, 2020
    Last Verified:
    Aug 1, 2020

    Study Results

    No Results Posted as of Aug 27, 2020