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To Evaluate the Impact of MRSA Nasal Screen Implementation.

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07748143
Enrollment
21
Registered
2026-08-05
Start date
2019-10-01
Completion date
2026-06-10
Last updated
2026-08-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

MRSA

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.

Interventions

The final data will then be compared to determine if the duration of therapy and cost after implementation of the MRSA nasal screen if significantly different from before the implementation of the MRSA nasal screen.

Direct costs of vancomycin for each treatment arm (in US dollars).

OTHERPharmacokinectic Monitoring

Number of vancomycin levels drawn for pharmacokinetic monitoring.

Length of hospital stay in days

Sponsors

Methodist Health System
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Age \> 18 years 2. Diagnosis of pneumonia 3. Admission inpatient to Methodist Richardson Medical Center 4. Treatment with vancomycin empirically

Exclusion criteria

1. Age ≤ 18 years 2. Patients with other confirmed gram positive infections

Design outcomes

Primary

MeasureTime frameDescription
Duration of therapy1 yearTo analyze duration of vancomycin in days.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORDaniel Betina

Methodist Health System

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 6, 2026