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Communicating Microbiology Results. It’s Not Just What You Say, But How You Say It

BACKGROUND: Gaps in microbiology communication can lead to suboptimal antibiotic prescribing. In May 2016, our laboratory modified reporting of respiratory cultures growing commensal flora only to specify “no methicillin-resistant Staphylococcus aureus/MRSA or Pseudomonas aeruginosa” (PA). The purpo...

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Autores principales: Musgrove, Mary, Kenney, Rachel M, Kendall, Ronald, Tibbetts, Robert, Samuel, Linoj, Peters, Mike, Davis, Susan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5632025/
http://dx.doi.org/10.1093/ofid/ofx162.069
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author Musgrove, Mary
Kenney, Rachel M
Kendall, Ronald
Tibbetts, Robert
Samuel, Linoj
Peters, Mike
Davis, Susan
author_facet Musgrove, Mary
Kenney, Rachel M
Kendall, Ronald
Tibbetts, Robert
Samuel, Linoj
Peters, Mike
Davis, Susan
author_sort Musgrove, Mary
collection PubMed
description BACKGROUND: Gaps in microbiology communication can lead to suboptimal antibiotic prescribing. In May 2016, our laboratory modified reporting of respiratory cultures growing commensal flora only to specify “no methicillin-resistant Staphylococcus aureus/MRSA or Pseudomonas aeruginosa” (PA). The purpose of this study was to compare MRSA and PA antibiotic therapy utilization before and after the change. METHODS: IRB approved, quasi-experiment at four hospitals with an antimicrobial stewardship program. Dates: August 1, 2015–January 31, 2016 and August 1, 2016–January 31, 2017. Included: ≥18 years, commensal flora only respiratory culture, empiric MRSA and PA antibiotic for treatment of lower respiratory infection. Excluded: non-respiratory infection. Primary outcome: MRSA or PA therapy de-escalated. Secondary outcomes: time to culture result, MRSA and PA antibiotic days of therapy, length of stay. Safety outcomes: acute kidney injury (AKI), C. difficile (CDI), subsequent multi-drug-resistant organism (MDRO), in-hospital all-cause mortality. RESULTS: Two hundred and ten patients included, 105 per group. Median age 64 and 61 years, male sex 52% and 56% in pre- and post-group, respectively. Empiric antibiotics, pre vs. post: vancomycin 94% vs. 95%; cefepime 66% vs. 36%; piperacillin–tazobactam 10% vs. 46%. MRSA or PA antibiotics de-escalated: 39% pre and 73% post (P < 0.001). See Table 1 for variables associated with antibiotic de-escalation. Days of therapy: 7 vs. 5 days (P < 0.001). AKI 31% vs. 14% (P = 0.003). Eight subsequent MDRO in pre and one in post (P = 0.035). No differences: time to culture result, length of stay, mortality, CDI. CONCLUSION: Improved microbiology communication to assist prescriber interpretation of commensal respiratory flora was associated with a reduction in the proportion of patients that received antibiotics targeting MRSA and PA. DISCLOSURES: S. Davis, Merck: Received grant through college that I’m faculty for, Grant recipient; Allergan: Speaker’s Bureau, Consulting fee; Allergan: Consultant and Scientific Advisor, Consulting fee; Medicines Company: Consultant and Scientific Advisor, Consulting fee; Zavante: Consultant and Scientific Advisor, Consulting fee.
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spelling pubmed-56320252017-11-07 Communicating Microbiology Results. It’s Not Just What You Say, But How You Say It Musgrove, Mary Kenney, Rachel M Kendall, Ronald Tibbetts, Robert Samuel, Linoj Peters, Mike Davis, Susan Open Forum Infect Dis Abstracts BACKGROUND: Gaps in microbiology communication can lead to suboptimal antibiotic prescribing. In May 2016, our laboratory modified reporting of respiratory cultures growing commensal flora only to specify “no methicillin-resistant Staphylococcus aureus/MRSA or Pseudomonas aeruginosa” (PA). The purpose of this study was to compare MRSA and PA antibiotic therapy utilization before and after the change. METHODS: IRB approved, quasi-experiment at four hospitals with an antimicrobial stewardship program. Dates: August 1, 2015–January 31, 2016 and August 1, 2016–January 31, 2017. Included: ≥18 years, commensal flora only respiratory culture, empiric MRSA and PA antibiotic for treatment of lower respiratory infection. Excluded: non-respiratory infection. Primary outcome: MRSA or PA therapy de-escalated. Secondary outcomes: time to culture result, MRSA and PA antibiotic days of therapy, length of stay. Safety outcomes: acute kidney injury (AKI), C. difficile (CDI), subsequent multi-drug-resistant organism (MDRO), in-hospital all-cause mortality. RESULTS: Two hundred and ten patients included, 105 per group. Median age 64 and 61 years, male sex 52% and 56% in pre- and post-group, respectively. Empiric antibiotics, pre vs. post: vancomycin 94% vs. 95%; cefepime 66% vs. 36%; piperacillin–tazobactam 10% vs. 46%. MRSA or PA antibiotics de-escalated: 39% pre and 73% post (P < 0.001). See Table 1 for variables associated with antibiotic de-escalation. Days of therapy: 7 vs. 5 days (P < 0.001). AKI 31% vs. 14% (P = 0.003). Eight subsequent MDRO in pre and one in post (P = 0.035). No differences: time to culture result, length of stay, mortality, CDI. CONCLUSION: Improved microbiology communication to assist prescriber interpretation of commensal respiratory flora was associated with a reduction in the proportion of patients that received antibiotics targeting MRSA and PA. DISCLOSURES: S. Davis, Merck: Received grant through college that I’m faculty for, Grant recipient; Allergan: Speaker’s Bureau, Consulting fee; Allergan: Consultant and Scientific Advisor, Consulting fee; Medicines Company: Consultant and Scientific Advisor, Consulting fee; Zavante: Consultant and Scientific Advisor, Consulting fee. Oxford University Press 2017-10-04 /pmc/articles/PMC5632025/ http://dx.doi.org/10.1093/ofid/ofx162.069 Text en © The Author 2017. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Musgrove, Mary
Kenney, Rachel M
Kendall, Ronald
Tibbetts, Robert
Samuel, Linoj
Peters, Mike
Davis, Susan
Communicating Microbiology Results. It’s Not Just What You Say, But How You Say It
title Communicating Microbiology Results. It’s Not Just What You Say, But How You Say It
title_full Communicating Microbiology Results. It’s Not Just What You Say, But How You Say It
title_fullStr Communicating Microbiology Results. It’s Not Just What You Say, But How You Say It
title_full_unstemmed Communicating Microbiology Results. It’s Not Just What You Say, But How You Say It
title_short Communicating Microbiology Results. It’s Not Just What You Say, But How You Say It
title_sort communicating microbiology results. it’s not just what you say, but how you say it
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5632025/
http://dx.doi.org/10.1093/ofid/ofx162.069
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