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Clinical Trials/NCT07748143
NCT07748143CompletedNot Applicable

The Effect of MRSA Nasal Screen Implementation on Duration of Therapy and Cost Associated With Vancomycin Use.

Methodist Health System1 site in 1 country21 target enrollmentStarted: October 1, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
21
Locations
1
Primary Endpoint
Duration of therapy

Study Overview

Brief Summary

To evaluate the impact of MRSA nasal screen implementation on duration of therapy and cost associated with vancomycin use.

Detailed Description

Routine blood and sputum cultures are often obtained inpatient for critically ill pneumonia patients. These tests, however, tend to have a high yield of false positives, leading to an increase in the use of broad spectrum antibiotics, specifically vancomycin. The Methicillin-resistant Staphylococcus aureus(MRSA) nasal screen is an antimicrobial stewardship tool that can be used to guide the treatment of community-acquired, hospital-acquired and ventilator-associated pneumonia. Due to its strong negative predictive value; a negative result can accurately indicate the absence of an MRSA infection in 96% of cases. Long-term treatment with vancomycin in patients with pneumonia is nephrotoxic and not always warranted. The implementation of an MRSA nasal screen in all patients with pneumonia treated with vancomycin has the potential to reduce vancomycin duration of therapy, decrease the risk of adverse effects and decrease the cost associated with vancomycin use.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Retrospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Age > 18 years
  • Diagnosis of pneumonia
  • Admission inpatient to Methodist Richardson Medical Center
  • Treatment with vancomycin empirically

Exclusion Criteria

  • Age ≤ 18 years
  • Patients with other confirmed gram positive infections

Arms & Interventions

The direct cost of vancomycin

The direct cost of vancomycin for each patient will then be calculated. An average duration of therapy and the average cost of therapy per patient will be calculated.

Intervention: Duration of therapy (Other)

The direct cost of vancomycin

The direct cost of vancomycin for each patient will then be calculated. An average duration of therapy and the average cost of therapy per patient will be calculated.

Intervention: Direct Cost (Other)

The direct cost of vancomycin

The direct cost of vancomycin for each patient will then be calculated. An average duration of therapy and the average cost of therapy per patient will be calculated.

Intervention: Pharmacokinectic Monitoring (Other)

The direct cost of vancomycin

The direct cost of vancomycin for each patient will then be calculated. An average duration of therapy and the average cost of therapy per patient will be calculated.

Intervention: Hospital stay (Other)

Outcomes

Primary Outcomes

Duration of therapy

Time Frame: 1 year

To analyze duration of vancomycin in days.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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