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2073. Positive Clinical Impact of MALDI-TOF for the Management of Inpatient Pneumonia Without Additional Antimicrobial Stewardship (AS) Support
BACKGROUND: Matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF) mass spectrometry decreases time to identification (ID) and has been shown to improve antibiotic utilization when combined with real-time AS intervention. We assessed the impact of MALDI-TOF without additional AS supp...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253337/ http://dx.doi.org/10.1093/ofid/ofy210.1729 |
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author | Porreca, Ann Marie Gallagher, Jason Sullivan, Kaede Ota |
author_facet | Porreca, Ann Marie Gallagher, Jason Sullivan, Kaede Ota |
author_sort | Porreca, Ann Marie |
collection | PubMed |
description | BACKGROUND: Matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF) mass spectrometry decreases time to identification (ID) and has been shown to improve antibiotic utilization when combined with real-time AS intervention. We assessed the impact of MALDI-TOF without additional AS support in patients with inpatient pneumonia. METHODS: This was a single-center quasi-experimental study of adult patients with a pneumonia who had a positive respiratory culture with bacteria that were identified by MALDI-TOF from August 2016–February 2017 (Pre-MALDI-TOF) and August–February 2018 (Post-MALDI-TOF). The primary endpoint was the time to initiation of optimal therapy before and after MALDI-TOF. The secondary endpoints included: clinical cure at 7 days; inpatient antibiotic duration; infection-related length of stay (LOS); overall LOS; excess antibiotic days; and costs. T-tests, Mann–Whitney U, and chi-squared tests were used for comparisons where appropriate. RESULTS: CONCLUSION: The implementation of MALDI-TOF without AS support for pneumonia patients reduced the time to ID and optimal therapy but there were no significant differences in clinical outcomes. It did not positively impact excess antibiotic doses or costs. DISCLOSURES: J. Gallagher, Achaogen: Consultant, Consulting fee; Merck: Consultant, Grant Investigator and Speaker’s Bureau, Consulting fee and Research grant; Allergan: Consultant and Speaker’s Bureau, Consulting fee; Astellas: Consultant and Speaker’s Bureau, Consulting fee; Cempra: Consultant, Consulting fee; Cidara: Consultant, Consulting fee; CutisPharma: Consultant, Consulting fee; Paratek: Consultant, Consulting fee; Shionogi: Consultant, Consulting fee; Tetraphase: Consultant, Consulting fee; Theravance: Consultant, Consulting fee; The Medicines Company: Consultant, Consulting fee; Melinta: Speaker’s Bureau, Consulting fee. |
format | Online Article Text |
id | pubmed-6253337 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62533372018-11-28 2073. Positive Clinical Impact of MALDI-TOF for the Management of Inpatient Pneumonia Without Additional Antimicrobial Stewardship (AS) Support Porreca, Ann Marie Gallagher, Jason Sullivan, Kaede Ota Open Forum Infect Dis Abstracts BACKGROUND: Matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF) mass spectrometry decreases time to identification (ID) and has been shown to improve antibiotic utilization when combined with real-time AS intervention. We assessed the impact of MALDI-TOF without additional AS support in patients with inpatient pneumonia. METHODS: This was a single-center quasi-experimental study of adult patients with a pneumonia who had a positive respiratory culture with bacteria that were identified by MALDI-TOF from August 2016–February 2017 (Pre-MALDI-TOF) and August–February 2018 (Post-MALDI-TOF). The primary endpoint was the time to initiation of optimal therapy before and after MALDI-TOF. The secondary endpoints included: clinical cure at 7 days; inpatient antibiotic duration; infection-related length of stay (LOS); overall LOS; excess antibiotic days; and costs. T-tests, Mann–Whitney U, and chi-squared tests were used for comparisons where appropriate. RESULTS: CONCLUSION: The implementation of MALDI-TOF without AS support for pneumonia patients reduced the time to ID and optimal therapy but there were no significant differences in clinical outcomes. It did not positively impact excess antibiotic doses or costs. DISCLOSURES: J. Gallagher, Achaogen: Consultant, Consulting fee; Merck: Consultant, Grant Investigator and Speaker’s Bureau, Consulting fee and Research grant; Allergan: Consultant and Speaker’s Bureau, Consulting fee; Astellas: Consultant and Speaker’s Bureau, Consulting fee; Cempra: Consultant, Consulting fee; Cidara: Consultant, Consulting fee; CutisPharma: Consultant, Consulting fee; Paratek: Consultant, Consulting fee; Shionogi: Consultant, Consulting fee; Tetraphase: Consultant, Consulting fee; Theravance: Consultant, Consulting fee; The Medicines Company: Consultant, Consulting fee; Melinta: Speaker’s Bureau, Consulting fee. Oxford University Press 2018-11-26 /pmc/articles/PMC6253337/ http://dx.doi.org/10.1093/ofid/ofy210.1729 Text en © The Author(s) 2018. 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 Porreca, Ann Marie Gallagher, Jason Sullivan, Kaede Ota 2073. Positive Clinical Impact of MALDI-TOF for the Management of Inpatient Pneumonia Without Additional Antimicrobial Stewardship (AS) Support |
title | 2073. Positive Clinical Impact of MALDI-TOF for the Management of Inpatient Pneumonia Without Additional Antimicrobial Stewardship (AS) Support |
title_full | 2073. Positive Clinical Impact of MALDI-TOF for the Management of Inpatient Pneumonia Without Additional Antimicrobial Stewardship (AS) Support |
title_fullStr | 2073. Positive Clinical Impact of MALDI-TOF for the Management of Inpatient Pneumonia Without Additional Antimicrobial Stewardship (AS) Support |
title_full_unstemmed | 2073. Positive Clinical Impact of MALDI-TOF for the Management of Inpatient Pneumonia Without Additional Antimicrobial Stewardship (AS) Support |
title_short | 2073. Positive Clinical Impact of MALDI-TOF for the Management of Inpatient Pneumonia Without Additional Antimicrobial Stewardship (AS) Support |
title_sort | 2073. positive clinical impact of maldi-tof for the management of inpatient pneumonia without additional antimicrobial stewardship (as) support |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253337/ http://dx.doi.org/10.1093/ofid/ofy210.1729 |
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