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The hypothetical impact of Accelerate Pheno™ system on time to effective therapy and time to definitive therapy in an institution with an established antimicrobial stewardship programme currently utilizing rapid genotypic organism/resistance marker identification

BACKGROUND: Rapid organism identification and antimicrobial susceptibility testing (AST) can optimize antimicrobial therapy in patients with bacteraemia. The Accelerate Pheno™ system (ACC) can provide identification and AST results within 7 h of a positive culture. OBJECTIVES: To assess the hypothet...

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Autores principales: Henig, Oryan, Cooper, Christopher C, Kaye, Keith S, Lephart, Paul, Salimnia, Hossein, Taylor, Maureen, Hussain, Noman, Hussain, Zara, Deeds, Kathryn, Hayat, Umar, Patel, Jinit, Pogue, Jason M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6382028/
https://www.ncbi.nlm.nih.gov/pubmed/30690538
http://dx.doi.org/10.1093/jac/dky533
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author Henig, Oryan
Cooper, Christopher C
Kaye, Keith S
Lephart, Paul
Salimnia, Hossein
Taylor, Maureen
Hussain, Noman
Hussain, Zara
Deeds, Kathryn
Hayat, Umar
Patel, Jinit
Pogue, Jason M
author_facet Henig, Oryan
Cooper, Christopher C
Kaye, Keith S
Lephart, Paul
Salimnia, Hossein
Taylor, Maureen
Hussain, Noman
Hussain, Zara
Deeds, Kathryn
Hayat, Umar
Patel, Jinit
Pogue, Jason M
author_sort Henig, Oryan
collection PubMed
description BACKGROUND: Rapid organism identification and antimicrobial susceptibility testing (AST) can optimize antimicrobial therapy in patients with bacteraemia. The Accelerate Pheno™ system (ACC) can provide identification and AST results within 7 h of a positive culture. OBJECTIVES: To assess the hypothetical impact of ACC on time to effective therapy (TTET), time to definitive therapy (TTDT) and antimicrobial usage at the Detroit Medical Center (DMC). METHODS: Patients with positive blood cultures from 29 March to 24 June 2016 were included. ACC was performed in parallel with normal laboratory procedures, but results were not made available to the clinicians. The potential benefit of having ACC results was determined if clinicians modified therapy based on actual AST results. Potential changes in TTET, TTDT and antibiotic usage were calculated. RESULTS: One hundred and sixty-seven patients were included. The median TTET was 2.4 h (IQR 0.5, 15.1). Had ACC results been available, TTET could have been improved in four patients (2.4%), by a median decrease of 18.9 h (IQR 11.3, 20.4). The median TTDT was 41.4 h (IQR 21.7, 73.3) and ACC results could have improved TTDT among 51 patients (30.5%), by a median decrease of 25.4 h (IQR 18.7, 37.5). ACC implementation could have led to decreases in usage of cefepime (16% reduction), aminoglycosides (23%), piperacillin/tazobactam (8%) and vancomycin (4%). CONCLUSIONS: ACC results could potentially improve time to de-escalation and reduce use of antimicrobials. The impact of ACC on TTET was small, likely related to the availability of other rapid diagnostic tests at DMC.
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spelling pubmed-63820282019-02-25 The hypothetical impact of Accelerate Pheno™ system on time to effective therapy and time to definitive therapy in an institution with an established antimicrobial stewardship programme currently utilizing rapid genotypic organism/resistance marker identification Henig, Oryan Cooper, Christopher C Kaye, Keith S Lephart, Paul Salimnia, Hossein Taylor, Maureen Hussain, Noman Hussain, Zara Deeds, Kathryn Hayat, Umar Patel, Jinit Pogue, Jason M J Antimicrob Chemother Supplement Papers BACKGROUND: Rapid organism identification and antimicrobial susceptibility testing (AST) can optimize antimicrobial therapy in patients with bacteraemia. The Accelerate Pheno™ system (ACC) can provide identification and AST results within 7 h of a positive culture. OBJECTIVES: To assess the hypothetical impact of ACC on time to effective therapy (TTET), time to definitive therapy (TTDT) and antimicrobial usage at the Detroit Medical Center (DMC). METHODS: Patients with positive blood cultures from 29 March to 24 June 2016 were included. ACC was performed in parallel with normal laboratory procedures, but results were not made available to the clinicians. The potential benefit of having ACC results was determined if clinicians modified therapy based on actual AST results. Potential changes in TTET, TTDT and antibiotic usage were calculated. RESULTS: One hundred and sixty-seven patients were included. The median TTET was 2.4 h (IQR 0.5, 15.1). Had ACC results been available, TTET could have been improved in four patients (2.4%), by a median decrease of 18.9 h (IQR 11.3, 20.4). The median TTDT was 41.4 h (IQR 21.7, 73.3) and ACC results could have improved TTDT among 51 patients (30.5%), by a median decrease of 25.4 h (IQR 18.7, 37.5). ACC implementation could have led to decreases in usage of cefepime (16% reduction), aminoglycosides (23%), piperacillin/tazobactam (8%) and vancomycin (4%). CONCLUSIONS: ACC results could potentially improve time to de-escalation and reduce use of antimicrobials. The impact of ACC on TTET was small, likely related to the availability of other rapid diagnostic tests at DMC. Oxford University Press 2019-01 2019-01-25 /pmc/articles/PMC6382028/ /pubmed/30690538 http://dx.doi.org/10.1093/jac/dky533 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Supplement Papers
Henig, Oryan
Cooper, Christopher C
Kaye, Keith S
Lephart, Paul
Salimnia, Hossein
Taylor, Maureen
Hussain, Noman
Hussain, Zara
Deeds, Kathryn
Hayat, Umar
Patel, Jinit
Pogue, Jason M
The hypothetical impact of Accelerate Pheno™ system on time to effective therapy and time to definitive therapy in an institution with an established antimicrobial stewardship programme currently utilizing rapid genotypic organism/resistance marker identification
title The hypothetical impact of Accelerate Pheno™ system on time to effective therapy and time to definitive therapy in an institution with an established antimicrobial stewardship programme currently utilizing rapid genotypic organism/resistance marker identification
title_full The hypothetical impact of Accelerate Pheno™ system on time to effective therapy and time to definitive therapy in an institution with an established antimicrobial stewardship programme currently utilizing rapid genotypic organism/resistance marker identification
title_fullStr The hypothetical impact of Accelerate Pheno™ system on time to effective therapy and time to definitive therapy in an institution with an established antimicrobial stewardship programme currently utilizing rapid genotypic organism/resistance marker identification
title_full_unstemmed The hypothetical impact of Accelerate Pheno™ system on time to effective therapy and time to definitive therapy in an institution with an established antimicrobial stewardship programme currently utilizing rapid genotypic organism/resistance marker identification
title_short The hypothetical impact of Accelerate Pheno™ system on time to effective therapy and time to definitive therapy in an institution with an established antimicrobial stewardship programme currently utilizing rapid genotypic organism/resistance marker identification
title_sort hypothetical impact of accelerate pheno™ system on time to effective therapy and time to definitive therapy in an institution with an established antimicrobial stewardship programme currently utilizing rapid genotypic organism/resistance marker identification
topic Supplement Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6382028/
https://www.ncbi.nlm.nih.gov/pubmed/30690538
http://dx.doi.org/10.1093/jac/dky533
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