Cargando…

1191. The Implementation of Nasal MRSA PCR for Pneumonia and Association with Antibiotic Use and Clinical Outcomes

BACKGROUND: Nasal MRSA PCR testing has been successfully implemented at many centers and limits vancomycin exposure among hospitalized patients with pneumonia. There are few studies of a Best Practice Alert (BPA) to direct nasal MRSA PCR use and vancomycin de-escalation in the absence of other stewa...

Descripción completa

Detalles Bibliográficos
Autores principales: Fenlon, Luke A, Fong, Karen, Spivak, Emily S, Imlay, Hannah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10678713/
http://dx.doi.org/10.1093/ofid/ofad500.1031
Descripción
Sumario:BACKGROUND: Nasal MRSA PCR testing has been successfully implemented at many centers and limits vancomycin exposure among hospitalized patients with pneumonia. There are few studies of a Best Practice Alert (BPA) to direct nasal MRSA PCR use and vancomycin de-escalation in the absence of other stewardship oversight. On 1/2/2020, nasal MRSA PCR and a BPA were implemented at our institution. Providers ordering vancomycin for patients with an indication of pneumonia or undifferentiated sepsis were directed to order a nasal MRSA PCR and recommended to stop vancomycin if negative (Figure 1). Our aim was to examine the impact of BPAs implementation on vancomycin duration among patients with suspected pneumonia. [Figure: see text] METHODS: A retrospective chart review was conducted among hospitalized patients without prior MRSA PCR performed during their admission who had a listed indication of pneumonia or sepsis at the time of vancomycin order. Patients were categorized into “pre” (9/17/2018 – 1/1/2020) and “post” (1/2/2020 – 3/20/2021) cohorts based on date of vancomycin order. Demographics, comorbidities, and antibiotic duration were electronically extracted. Uni- and multivariable logistic models were used to examine the proportion of patients in the pre and post cohorts whose vancomycin was stopped within 24 hours of initial order. RESULTS: A total of 2,195 patients were included, 1210 in the pre-intervention and 985 in the post-intervention cohort. After BPA implementation, 771/985 (78%) patients received a nasal MRSA PCR. Vancomycin was discontinued within 24 hours after initiation in 384/1210 (32%) patients pre-intervention and 559/985 (57%) patients post-intervention (adjusted OR 2.92 [95% CI 2.44 – 3.49], p < 0.001) (Table 1). Although “high risk” patient factors (e.g. need for mechanical ventilation) were associated with longer durations, vancomycin duration was significantly shorter in the post-implementation cohort for all “high risk” sub-groups (Figure 2). [Figure: see text] [Figure: see text] CONCLUSION: BPA directed nasal MRSA PCR testing and vancomycin de-escalation effectively shortened duration of therapy among patients with suspected pneumonia. Utilizing a BPA directed approach can improve decision efficiency and allow valuable stewardship team resources to be allocated elsewhere. DISCLOSURES: All Authors: No reported disclosures