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Completed

NCT Number: NCT03697096

The INSPIRE-ASP UTI Trial

The INSPIRE-ASP UTI trial is a cluster-randomized controlled trial of HCA hospitals comparing routine empiric antibiotic stewardship practices with real-time precision medicine computerized physician order entry smart prompts providing the probability that a non-critically ill adult admitted with UTI is infected with a resistant pathogen.

Note: that enrolled "subjects" represents 59 individual HCA hospitals that have been randomized.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Riverside Community Hospital, Riverside, California, United States

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Who can participate

Healthy volunteers accepted: No

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

Facility Inclusion Criteria:

  • HCA hospitals admitting adults for UTI
  • Facility use of MEDITECH as their electronic health record system

Facility Exclusion Criteria:

-

Note: unit of randomization is the hospital, however the CPOE alert intervention will calculate risk estimates for adults age >=18 admitted to non-ICU wards and who are ordered to receive extended-spectrum antibiotics for UTI. Prisoners were excluded from prompts and analysis.

Treatment and study plan

Routine care

Other

Routine Antibiotic Stewardship Arm - Continuation of all antibiotic stewardship activities in accordance with national standards.

INSPIRE CPOE Smart Prompt

Other

Quality improvement intervention: computerized physician order entry (CPOE) decision support alert that provides physicians with patient-specific risk estimate of having a UTI due to a multidrug resistant organism (MDRO) and recommends appropriate antibiotic choice for non-ICU patients in the first 3 days of hospitalization.

Continuation of other antibiotic stewardship activities in accordance with national standards.

Primary outcomes

  1. Extended-Spectrum Days Of Antibacterial Therapy (ES-DOT) Per Empiric Day

    Time frame: First 3 days of hospitalization for each patient during 15-month intervention period

    The number of different extended-spectrum antibacterials received by the patient each empiric day-of-therapy (outcome measure unit), averaged over the empiric days (the first 3 days of hospitalization), summed across all participants. Note that Days-of-Therapy unit is a standardized national measure for antibacterial use in hospitals. For clarity the calculation is as follows: we define a DOT for a particular ES antibiotic as a day in which any number of doses of that antibiotic is given. Different ES antibiotics are summed across the empiric days for each patient admission, then divided by the empiric days for that patient-admission to determine each admission's DOT per at-risk day. If an admission is less than 3 days, only the number of days the patient is admitted will contribute to the numerator and denominator.

Secondary outcomes

  1. Vancomycin Days of Antibacterial Therapy Per Empiric Day

    Time frame: First 3 days of hospitalization for each patient during 15-month intervention period

    The number of days that Vancomycin is received by the patient averaged over the empiric days (the first 3 days of hospitalization), summed across all participants. Note that Days-of-Therapy unit is a standardized national measure for antibacterial use in hospitals. For clarity the calculation is as follows: we define a DOT for a particular ES antibiotic as a day in which any number of doses of that antibiotic is given. Different ES antibiotics are summed across the empiric days for each patient admission, then divided by the empiric days for that patient-admission to determine each admission's DOT per at-risk day. If an admission is less than 3 days, only the number of days the patient is admitted will contribute to the numerator and denominator.

  2. Antipseudomonal Antibiotic Days Of Therapy (ES-DOT) Per Empiric Day

    Time frame: First 3 days of hospitalization for each patient during 15-month intervention period

    The number of different antipseudomonals received by the patient each empiric day of therapy, averaged over the empiric days (the first 3 days of hospitalization), summed across all participants. Note that Days-of-Therapy unit is a standardized national measure for antibacterial use in hospitals. For clarity the calculation is as follows: we define a DOT for a particular ES antibiotic as a day in which any number of doses of that antibiotic is given. Different ES antibiotics are summed across the empiric days for each patient admission, then divided by the empiric days for that patient-admission to determine each admission's DOT per at-risk day. If an admission is less than 3 days, only the number of days the patient is admitted will contribute to the numerator and denominator.

Other outcomes

  1. Antibacterial Escalations [Safety Outcome 1]

    Time frame: 15 month intervention

    Days from start of standard-spectrum antibacterial until switch to extended-spectrum antibacterial during hospital stay, if that occurs. If it doesn't occur, the number of days is censored (capped) at the patient's hospital discharge or at the end of data collection. Almost all patients will be discharged before the end of trial data collection.

  2. ICU Transfers [Safety Outcome 2]

    Time frame: 15 month intervention

    Days from hospital admission until transfer to ICU, if that occurs. If it doesn't occur, the number of days is censored (capped) at the patient's hospital discharge or at the end of data collection. Almost all patients will be discharged before the end of trial data collection.

  3. Length-of-stay [Safety Outcome 3]

    Time frame: 15 month intervention

    Days from hospital admission until discharge. If the patient remains in the hospital at the end of the trial data collection, the number of days is censored (capped) at that time. Almost all patients will be discharged before the end of trial data collection.

  4. Extended-Spectrum Days of Therapy With Inpatient Extended-Spectrum (ES) Antibacterial Treatment After Empiric Period

    Time frame: 15 month intervention

    The summed number of different ES antibacterials received each day, measured repeatedly on or after 4 calendar days of admission and divided by the number of days from hospital day 4 through discharge.

    Note: this outcome is intended for a secondary manuscript.

  5. Empiric and Total Antibacterial Costs

    Time frame: 15 month intervention

    Empiric and total antibacterial costs for UTI during hospitalization. Note: this outcome is intended for a secondary manuscript.

  6. Incidence of Hospital-Onset C. Difficile

    Time frame: 15 month intervention

    Hospital-onset C. difficile positive tests (specimen obtained) after 3 calendar days of admission during hospitalization.

    Note: this outcome is intended for a secondary manuscript.

  7. Incidence of Hospital-Onset MDRO-Positive Cultures

    Time frame: 15 month intervention

    Newly-detected hospital-onset MDRO-positive cultures (on or after 3 calendar days of admission). Includes total MDRO and specific MDRO subsets.

    Note: this outcome is intended for a secondary manuscript.

  8. Fluoroquinolone (FQ) Days of Therapy Per Empiric and Total At-risk Days

    Time frame: 15 month intervention

    The summed number of different fluoroquinolone antibacterials received each day, measured repeatedly over (1) the first three days (empiric) of an admission and divided by the number of days of the admission) and (2) all days of an admission divided by the total number of admission days.

    Note: this outcome is intended for a secondary manuscript.

Sponsors and collaborators

Lead sponsor

Harvard Pilgrim Health Care

Other

Collaborators

  • Brigham and Women's Hospital
  • Centers for Disease Control and Prevention
  • Hospital Corporation of America
  • University of California, Irvine
  • University of Massachusetts, Amherst

Registry information

Official study title

INtelligent Stewardship Prompts to Improve Real-time Empiric Antibiotic Selection for Patients With Urinary Tract Infections (UTI)

Important dates

Study start
2018
Primary completion
2024
Study completion
2024
First posted
Oct 5, 2018
Registry last updated
Jan 30, 2025

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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