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N/A N=43 Randomized Prevention

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)

Methicillin-resistant Staphylococcus Aureus

Enrolled (actual)
43
Serious AEs
0.0%
Results posted
Jul 2014
Primary outcome: Primary: Main Outcome: Patients With Nosocomial MRSA Clinical Cultures — 0.92; 0.75; 0.63 hazard ratio — p=0.01

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Chlorhexidine bath and nasal mupirocin (Drug)
Age
Pediatric, Adult, Older Adult · 13+ yrs
Sex
All
Sponsor
Harvard Pilgrim Health Care
Primary completion
Sep 2011

Outcome Measures

OutcomeResultp-value
PRIMARY
Main Outcome: Patients With Nosocomial MRSA Clinical Cultures
0.92; 0.75; 0.63 0.01 sig
SECONDARY
MRSA Bloodstream Infection
1.23; 1.23; 0.72
SECONDARY
ICU-attributable All-pathogen Bloodstream Infection
0.99; 0.78; 0.56
SECONDARY
Intervention Impact on Healthcare Costs
9,120; 9,120; 0; 69,010; 68,830; 24,890
SECONDARY
Blood Culture Contamination Rates
0.74; 0.94; 0.56; 0.73; 0.93; 0.55
SECONDARY
Intervention Impact on Bacteriuria and Candiduria
1.02; 0.88; 0.87; 0.97; 0.83; 0.93
SECONDARY
Intervention Impact on Mupirocin Susceptibility of MRSA Isolates
1.0; 1.4; 0.5; 0.8; 0.9; 0.7
SECONDARY
Intervention Impact on Chlorhexidine Susceptibility of MRSA Isolates
2; 0; 0

Summary

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.

Eligibility Criteria

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.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00980980). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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