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61. Evaluation of the Impact of a Micafungin Time-Out Protocol for Hospitalized Patients

BACKGROUND: Echinocandin overuse is associated with increased prevalence of non-albicans Candida spp, resistance, and high costs. Prospective review of micafungin prescribing by an Antimicrobial Stewardship Pharmacist (ASP) has shown reduced rates of inappropriate therapy. The aim of this study was...

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Autores principales: Williams, Kelsey N, Elshaboury, Ramy H, Letourneau, Alyssa R, Adamsick, Meagan L, Gandhi, Ronak G, Paras, Molly L, Bidell, Monique R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7777059/
http://dx.doi.org/10.1093/ofid/ofaa439.106
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author Williams, Kelsey N
Elshaboury, Ramy H
Letourneau, Alyssa R
Adamsick, Meagan L
Gandhi, Ronak G
Paras, Molly L
Bidell, Monique R
author_facet Williams, Kelsey N
Elshaboury, Ramy H
Letourneau, Alyssa R
Adamsick, Meagan L
Gandhi, Ronak G
Paras, Molly L
Bidell, Monique R
author_sort Williams, Kelsey N
collection PubMed
description BACKGROUND: Echinocandin overuse is associated with increased prevalence of non-albicans Candida spp, resistance, and high costs. Prospective review of micafungin prescribing by an Antimicrobial Stewardship Pharmacist (ASP) has shown reduced rates of inappropriate therapy. The aim of this study was to describe ASP’s interventions following introduction of a micafungin time out (MTO) protocol. METHODS: The approved MTO protocol was implemented in November 2019. Active micafungin orders for hospitalized patients were reviewed Monday through Friday at initiation and on day five. The MTO algorithm assessed micafungin use based on patient risk factors for Candida infection and de-escalation was guided by clinical status, culture data, and susceptibility testing. Micafungin use and ASP’s interventions were reviewed post-implementation between 12/01/2019 and 02/29/2020. Micafungin use was also characterized between 12/01/2018 and 02/28/2019 to serve as a control. RESULTS: A random sample of 50 patients who received micafungin for ≥ 48 hours during the pre- and post- protocol periods were included. 39 (78%) and 38 (76%) patients in the pre- and post-MTO cohort had indications for micafungin initiation according to algorithm. In the post-MTO group, 9 (75%) of the 12 micafungin initiations outside of algorithm approval were intervened on successfully by the ASP, increasing appropriate antifungal therapy to 47 (94%) patients. On day five, 18 (50%) and 25 (65.8%) (p=0.17) micafungin orders were according to algorithm in the pre- and post-MTO groups, respectively. Culture data on day five revealed 18 (50%) in the pre-MTO and 13 (34.2%) in the post-MTO group were eligible for de-escalation. An ASP-initiated MTO on day five identified 23 opportunities for antifungal therapy optimization in the post-MTO group. Interventions included de-escalation (13; 61.9%), discontinuation (6; 28.6%), and dose optimization (4; 19%). Of the 23 ASP interventions on day 5, 10 (43.4%) led to micafungin discontinuation or de-escalation, increasing the overall antifungal appropriateness to 35 (92.1%) patients. CONCLUSION: An ASP-initiated MTO can facilitate appropriate and timely optimization of antifungal therapy. The most frequent interventions were de-escalation from micafungin or therapy discontinuation. DISCLOSURES: All Authors: No reported disclosures
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spelling pubmed-77770592021-01-07 61. Evaluation of the Impact of a Micafungin Time-Out Protocol for Hospitalized Patients Williams, Kelsey N Elshaboury, Ramy H Letourneau, Alyssa R Adamsick, Meagan L Gandhi, Ronak G Paras, Molly L Bidell, Monique R Open Forum Infect Dis Poster Abstracts BACKGROUND: Echinocandin overuse is associated with increased prevalence of non-albicans Candida spp, resistance, and high costs. Prospective review of micafungin prescribing by an Antimicrobial Stewardship Pharmacist (ASP) has shown reduced rates of inappropriate therapy. The aim of this study was to describe ASP’s interventions following introduction of a micafungin time out (MTO) protocol. METHODS: The approved MTO protocol was implemented in November 2019. Active micafungin orders for hospitalized patients were reviewed Monday through Friday at initiation and on day five. The MTO algorithm assessed micafungin use based on patient risk factors for Candida infection and de-escalation was guided by clinical status, culture data, and susceptibility testing. Micafungin use and ASP’s interventions were reviewed post-implementation between 12/01/2019 and 02/29/2020. Micafungin use was also characterized between 12/01/2018 and 02/28/2019 to serve as a control. RESULTS: A random sample of 50 patients who received micafungin for ≥ 48 hours during the pre- and post- protocol periods were included. 39 (78%) and 38 (76%) patients in the pre- and post-MTO cohort had indications for micafungin initiation according to algorithm. In the post-MTO group, 9 (75%) of the 12 micafungin initiations outside of algorithm approval were intervened on successfully by the ASP, increasing appropriate antifungal therapy to 47 (94%) patients. On day five, 18 (50%) and 25 (65.8%) (p=0.17) micafungin orders were according to algorithm in the pre- and post-MTO groups, respectively. Culture data on day five revealed 18 (50%) in the pre-MTO and 13 (34.2%) in the post-MTO group were eligible for de-escalation. An ASP-initiated MTO on day five identified 23 opportunities for antifungal therapy optimization in the post-MTO group. Interventions included de-escalation (13; 61.9%), discontinuation (6; 28.6%), and dose optimization (4; 19%). Of the 23 ASP interventions on day 5, 10 (43.4%) led to micafungin discontinuation or de-escalation, increasing the overall antifungal appropriateness to 35 (92.1%) patients. CONCLUSION: An ASP-initiated MTO can facilitate appropriate and timely optimization of antifungal therapy. The most frequent interventions were de-escalation from micafungin or therapy discontinuation. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2020-12-31 /pmc/articles/PMC7777059/ http://dx.doi.org/10.1093/ofid/ofaa439.106 Text en © The Author 2020. 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 Poster Abstracts
Williams, Kelsey N
Elshaboury, Ramy H
Letourneau, Alyssa R
Adamsick, Meagan L
Gandhi, Ronak G
Paras, Molly L
Bidell, Monique R
61. Evaluation of the Impact of a Micafungin Time-Out Protocol for Hospitalized Patients
title 61. Evaluation of the Impact of a Micafungin Time-Out Protocol for Hospitalized Patients
title_full 61. Evaluation of the Impact of a Micafungin Time-Out Protocol for Hospitalized Patients
title_fullStr 61. Evaluation of the Impact of a Micafungin Time-Out Protocol for Hospitalized Patients
title_full_unstemmed 61. Evaluation of the Impact of a Micafungin Time-Out Protocol for Hospitalized Patients
title_short 61. Evaluation of the Impact of a Micafungin Time-Out Protocol for Hospitalized Patients
title_sort 61. evaluation of the impact of a micafungin time-out protocol for hospitalized patients
topic Poster Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7777059/
http://dx.doi.org/10.1093/ofid/ofaa439.106
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