Cluster Randomized Trial of Hospitals to Assess Impact of Targeted Versus Universal Strategies to Reduce Methicillin-resistant Staphylococcus Aureus (MRSA) in Intensive Care Units (ICUs)

Overview

The Randomized Evaluation of Decolonization versus Universal Clearance to Eliminate MRSA (REDUCE MRSA) Trial is a cluster randomized trial of the comparative effectiveness of three strategies to prevent methicillin-resistant Staphylococcus aureus (MRSA) in intensive care units. The three strategies to be evaluated are: – screening on admission followed by isolation of MRSA+ patients – screening on admission followed by isolation and decolonization of MRSA+ patients – universal decolonization on admission with no screening. The decolonization regimen involves bathing with chlorhexidine plus intra-nasal application of mupirocin. The main outcome will be MRSA+ clinical cultures. The study is a partnership between the CDC, the CDC Prevention Epicenters, and the Hospital Corporation of America.

Full Title of Study: “Cluster Randomized Trial of Hospitals to Assess Impact of Targeted Versus Universal”

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Randomized
    • Primary Purpose: Prevention
  • Study Primary Completion Date: September 2011

Detailed Description

Baseline data involving 12 months of data for participating hospitals (July 2008 – June 2009) was collected prior to randomization to account for size and ICU baseline prevalence of MRSA in randomization scheme. Randomization occurred at the hospital level. Eligibility survey was conducted to determine exclusion criteria. As of May 2010, enrollment has been closed. 45 hospitals were randomized, but two were found to meet exclusion criteria and were excluded. As-randomized (or as-assigned) analysis included 43 hospitals, representing 74 ICUs. Individual (patient-level) subject enrollment during intervention is 74,256.

Interventions

  • Drug: Chlorhexidine bath and nasal mupirocin
    • The intervention / decolonization regimen will consist of the most commonly used topical regimen in the US – a combination of daily baths with 2% chlorhexidine cloths , plus 5 days of topical intranasal mupirocin ointment (bilateral nares, twice daily)

Arms, Groups and Cohorts

  • No Intervention: Arm 1: Usual Care-Active Surveillance
    • Active Surveillance in All Adult ICUs, Contact Precautions for MRSA+
  • Active Comparator: Arm 2: Targeted Decolonization
    • Continue Active Surveillance (AS), MRSA decolonization based on AS, Continue Contact Precautions for MRSA+
  • Active Comparator: Arm 3: Universal Decolonization
    • Chlorhexidine bath and nasal mupirocin for all, Discontinuation of Active Surveillance, Continuation of Contact Precautions for MRSA+

Clinical Trial Outcome Measures

Primary Measures

  • Main Outcome: Patients With Nosocomial MRSA Clinical Cultures
    • Time Frame: The 30-month time frame represents 12-month baseline and 18-month intervention periods. During these time periods, outcomes are defined as events occurring during attributed ICU time: from day 3 of the ICU stay until 2 days after ICU discharge.
    • Hazard ratio for ICU-attributable MRSA+ clinical cultures comparing Baseline to Intervention period, by Arm, accounting for clustering by hospital.

Secondary Measures

  • MRSA Bloodstream Infection
    • Time Frame: The 30-month time frame represents 12-month baseline and 18-month intervention periods. During these time periods, outcomes are defined as events occurring during attributed ICU time: from day 3 of the ICU stay until 2 days after ICU discharge.
    • Hazard ratio for ICU-attributable MRSA+ blood cultures comparing Baseline to Intervention period, by Arm, accounting for clustering by hospital.
  • ICU-attributable All-pathogen Bloodstream Infection
    • Time Frame: The 30-month time frame represents 12-month baseline and 18-month intervention periods. During these time periods, outcomes are defined as events occurring during attributed ICU time: from day 3 of the ICU stay until 2 days after ICU discharge.
    • Hazard ratio for ICU-attributable positive blood culture from any pathogen, comparing Baseline to Intervention period, by Arm, accounting for clustering by hospital.
  • Intervention Impact on Healthcare Costs
    • Time Frame: 12-month period
    • Costs (in dollars) per 1000 ICU-admissions associated with 3 ICU strategies to reduce ICU Bloodstream infection (BSI), (Arms 1-3).
  • Blood Culture Contamination Rates
    • Time Frame: 24-month time frame for this analysis represents a 6-month baseline and 18-month intervention period.
    • Odds ratio for ICU-attributable blood culture contamination rates, comparing Baseline to Intervention period across Arms, accounting for clustering by hospital.
  • Intervention Impact on Bacteriuria and Candiduria
    • Time Frame: 30-month time frame represents 12-month baseline and 18-month intervention periods.
    • Proportional hazard ratio for as-randomized, unadjusted, ICU-attributable bacteriuria, comparing Baseline to Intervention period across Arms, accounting for clustering by hospital. High-level bacteriuria is defined as ≥50,000 CFU/mL, high-level candiduria is defined as ≥50,000 CFU/mL.
  • Intervention Impact on Mupirocin Susceptibility of MRSA Isolates
    • Time Frame: 25-month time frame represents 7-month baseline and 18-month intervention periods
    • Odds ratio for MRSA+ isolates from ICU patients expressing low-level mupirocin resistance (LLMR) and high-level mupirocin resistance (HLMR), comparing baseline to intervention period across arms, accounting for clustering by hospital.
  • Intervention Impact on Chlorhexidine Susceptibility of MRSA Isolates
    • Time Frame: 25-month time frame represents 7-month baseline and 18-month intervention periods
    • Frequency of MRSA+ isolates from ICU patients with reduced susceptibility to chlorhexidine (CHG) (MIC >4 μg/ml), comparing baseline to intervention period across arms, accounting for clustering by hospital.

Participating in This Clinical Trial

Inclusion Criteria

Inclusion criteria will include all HCA hospitals that reside in US states where physicians do NOT routinely prescribe decolonization for MRSA + ICU patients. Exclusion Criteria:

Exclusion criteria will include hospitals where ICU physicians often prescribe decolonization for MRSA+ ICU patients.

  • Dedicated burn ICUs will also be excluded due to the inability to perform routine bathing. – Finally, since the intent is to assess the intervention in adult ICUs, pediatric hospitals will be excluded although patients <13 years old that are admitted to participating adult ICUs will be included in the unit-based intervention.

Gender Eligibility: All

Minimum Age: 13 Years

Maximum Age: N/A

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • Harvard Pilgrim Health Care
  • Collaborator
    • Agency for Healthcare Research and Quality (AHRQ)
  • Provider of Information About this Clinical Study
    • Principal Investigator: Richard Platt, Professor and Department Chair – Harvard Pilgrim Health Care
  • Overall Official(s)
    • Richard Platt, MD, MS, Principal Investigator, Department of Population Medicine, Harvard Medical School / Harvard Pilgrim Healthcare Institute
    • Edward Septimus, MD, Principal Investigator, Hospital Corporation of America (HCA)
    • Susan Huang, MD MPH, Principal Investigator, University of California, Irvine

References

Platt R, Takvorian SU, Septimus E, Hickok J, Moody J, Perlin J, Jernigan JA, Kleinman K, Huang SS. Cluster randomized trials in comparative effectiveness research: randomizing hospitals to test methods for prevention of healthcare-associated infections. Med Care. 2010 Jun;48(6 Suppl):S52-7. doi: 10.1097/MLR.0b013e3181dbebcf.

Huang SS, Septimus E, Platt R. Targeted decolonization to prevent ICU infections. N Engl J Med. 2013 Oct 10;369(15):1470-1. doi: 10.1056/NEJMc1309704. No abstract available.

Citations Reporting on Results

Huang SS, Septimus E, Kleinman K, Moody J, Hickok J, Avery TR, Lankiewicz J, Gombosev A, Terpstra L, Hartford F, Hayden MK, Jernigan JA, Weinstein RA, Fraser VJ, Haffenreffer K, Cui E, Kaganov RE, Lolans K, Perlin JB, Platt R; CDC Prevention Epicenters Program; AHRQ DECIDE Network and Healthcare-Associated Infections Program. Targeted versus universal decolonization to prevent ICU infection. N Engl J Med. 2013 Jun 13;368(24):2255-65. doi: 10.1056/NEJMoa1207290. Epub 2013 May 29. Erratum In: N Engl J Med. 2013 Aug 8;369(6):587. N Engl J Med. 2014 Feb 27;370(9):886.

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