Publication:
The role of negative methicillin-resistant staphylococcus aureus nasal surveillance swabs in predicting the need for empiric vancomycin therapy in intensive care unit patients

dc.contributor.authorDarunee Chotiprasitsakulen_US
dc.contributor.authorPranita D. Tammaen_US
dc.contributor.authorAvinash Gadalaen_US
dc.contributor.authorSara E. Cosgroveen_US
dc.contributor.otherFaculty of Medicine, Ramathibodi Hospital, Mahidol Universityen_US
dc.contributor.otherJohns Hopkins Hospitalen_US
dc.contributor.otherThe Johns Hopkins School of Medicineen_US
dc.date.accessioned2019-08-28T06:21:49Z
dc.date.available2019-08-28T06:21:49Z
dc.date.issued2018-03-01en_US
dc.description.abstract© 2018 by The Society for Healthcare Epidemiology of America. All rights reserved. OBJECTIVES The role of methicillin-resistant Staphylococcus aureus (MRSA) nasal surveillance swabs (nasal swabs) in guiding decisions about prescribing vancomycin is unclear. We aimed to determine the likelihood that patients with negative MRSA nasal swabs develop subsequent MRSA infections; to assess avoidable vancomycin days for patients with negative nasal swabs; and to identify risk factors for having a negative nasal swab and developing a MRSA infection during the intensive care unit (ICU) stay. METHODS This retrospective cohort study was conducted in 6 ICUs at a tertiary-care hospital from December 2013 through June 2015. The negative predictive value (NPV), defined as the ability of a negative nasal swab to predict no subsequent MRSA infection, was calculated. Days of vancomycin continued or restarted after 3 days from the collection time of the first negative nasal swab were determined. A matched case-control study identified risk factors for having a negative nasal swab and developing MRSA infection. RESULTS Of 11,441 patients with MRSA-negative nasal swabs, the rate of subsequent MRSA infection was 0.22%. A negative nasal swab had a NPV of 99.4% (95% confidence interval [CI], 99.1%-99.6%). Vancomycin was continued or started after nasal swab results were available in 1,431 patients, translating to 7,364 vancomycin days. No risk factors associated with MRSA infection were identified. CONCLUSIONS In our hospital with a low prevalence of MRSA transmission, a negative MRSA nasal swab was helpful in identifying patients with low risk of MRSA infection in whom empiric vancomycin therapy could be stopped and in whom the subsequent initiation of vancomycin therapy during an ICU admission could be avoided.en_US
dc.identifier.citationInfection Control and Hospital Epidemiology. Vol.39, No.3 (2018), 290-296en_US
dc.identifier.doi10.1017/ice.2017.308en_US
dc.identifier.issn15596834en_US
dc.identifier.issn0899823Xen_US
dc.identifier.other2-s2.0-85051358740en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/46904
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85051358740&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleThe role of negative methicillin-resistant staphylococcus aureus nasal surveillance swabs in predicting the need for empiric vancomycin therapy in intensive care unit patientsen_US
dc.typeConference Paperen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85051358740&origin=inwarden_US

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