Evaluation of a pharmacy-driven methicillin-resistant Staphylococcus aureus surveillance protocol in pneumonia
Autor: | Kara W. Orwig, Sarah Dunaway, Zachary L Myers, Stephanie E. Giancola, James A. Sizemore, Zachary Q Arbogast |
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Rok vydání: | 2018 |
Předmět: |
Adult
Male Methicillin-Resistant Staphylococcus aureus 0301 basic medicine medicine.medical_specialty Time Factors Adolescent 030106 microbiology Pharmaceutical Science Pharmacy Toxicology medicine.disease_cause Patient Readmission Young Adult 03 medical and health sciences 0302 clinical medicine Vancomycin Internal medicine Humans Medicine Pharmacology (medical) Hospital Mortality 030212 general & internal medicine Aged Retrospective Studies Aged 80 and over Pharmacology business.industry Retrospective cohort study Pneumonia Length of Stay Middle Aged Antimicrobial medicine.disease Methicillin-resistant Staphylococcus aureus Anti-Bacterial Agents Community-Acquired Infections Withholding Treatment Staphylococcus aureus Nasal Swab Pharmaceutical Services Female business medicine.drug |
Zdroj: | International Journal of Clinical Pharmacy. 40:526-532 |
ISSN: | 2210-7711 2210-7703 |
DOI: | 10.1007/s11096-018-0647-3 |
Popis: | Background Methicillin-resistant Staphylococcus aureus (MRSA) is an important cause of pneumonia and clinicians must determine when empiric antimicrobial therapy directed toward MRSA is needed. Objective To evaluate the effect of a pharmacy-driven protocol utilizing the nasal swab MRSA polymerase chain reaction (PCR) test to discontinue vancomycin on duration of vancomycin therapy and clinical outcomes in patients with suspected community-acquired pneumonia (CAP) or healthcare-associated pneumonia (HCAP). Setting A teaching hospital in Huntington, WV, USA. Methods This retrospective study included adult patients who received at least one dose of vancomycin for suspected CAP or HCAP. The pre-intervention group consisted of patients prior to the addition of the nasal swab MRSA PCR test to the CAP/HCAP order set. The post-intervention group consisted of patients after the addition of the nasal swab MRSA PCR test to the CAP/HCAP order set. Main outcome measure The primary outcome was vancomycin hours of therapy. Results Of the 196 patients included in the study, 121 patients were in the pre-intervention group and 75 patients were in the post-intervention group. The median duration of vancomycin therapy was significantly shorter in the post-intervention group than the pre-intervention group (49 vs. 18 h, p |
Databáze: | OpenAIRE |
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