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266. Implementation and Evaluation of a Pharmacist-Managed Pediatric Vancomycin Protocol

BACKGROUND: Pediatric studies have shown that pharmacist-guided vancomycin dosing leads to reduction in time to initial target vancomycin trough, duration of vancomycin therapy, time to clinical stability, and shorter hospital stay. At Boston Medical Center, 65% of pediatric patients receiving vanco...

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Autores principales: Vu, Christine, Brade, Karrine, Farrell, Camilla, Mancuso, Michelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255126/
http://dx.doi.org/10.1093/ofid/ofy210.277
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author Vu, Christine
Brade, Karrine
Farrell, Camilla
Mancuso, Michelle
author_facet Vu, Christine
Brade, Karrine
Farrell, Camilla
Mancuso, Michelle
author_sort Vu, Christine
collection PubMed
description BACKGROUND: Pediatric studies have shown that pharmacist-guided vancomycin dosing leads to reduction in time to initial target vancomycin trough, duration of vancomycin therapy, time to clinical stability, and shorter hospital stay. At Boston Medical Center, 65% of pediatric patients receiving vancomycin did not achieve initial therapeutic troughs between 10 and 20 μg/mL from October 1, 2016 to September 30, 2017. Through implementation of a pharmacist-managed pediatric vancomycin protocol, the project aim was to increase the percentage of patients achieving initial therapeutic troughs from 35% to 60% and percentage of patients achieving therapeutic troughs within 3 days from 67% to 90% by May 1, 2018. Secondary aims included reducing the incidence of supratherapeutic troughs from 10% to 5% and maintaining the incidence of vancomycin-associated nephrotoxicity (VAN) at 0%. METHODS: A quality improvement (QI) initiative based on the Institute for Healthcare Improvement Model was utilized, testing change through Plan-Do-Study-Act (PDSA) cycles. In PDSA cycle 1, pharmacists designed and implemented a standardized vancomycin dosing protocol for pediatric patients. In PDSA cycle 2, the addition of area under the curve (AUC)-guided dosing was implemented in select patients. Process and balancing measures included percentage of appropriately drawn vancomycin troughs, provider adherence to the new dosing protocol, and incidence of supratherapeutic troughs. RESULTS: A total of 32 pediatric patients were assessed. Compared with baseline data, percentage of patients achieving initial therapeutic troughs increased from 35% to 44% and percentage of patients achieving therapeutic troughs within 3 days increased from 67% to 92%. The incidence of supratherapeutic troughs decreased from 10% to 0% and the incidence of vancomycin-associated nephrotoxicity was maintained at 0%. CONCLUSION: Standardized initial vancomycin dosing with increased pharmacy involvement led to more patients achieving initial therapeutic troughs, shorter times to therapeutic troughs, and a reduction in supratherapeutic troughs. Next steps include hospital-wide implementation of a pediatric vancomycin per pharmacy protocol. DISCLOSURES: All authors: No reported disclosures.
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spelling pubmed-62551262018-11-28 266. Implementation and Evaluation of a Pharmacist-Managed Pediatric Vancomycin Protocol Vu, Christine Brade, Karrine Farrell, Camilla Mancuso, Michelle Open Forum Infect Dis Abstracts BACKGROUND: Pediatric studies have shown that pharmacist-guided vancomycin dosing leads to reduction in time to initial target vancomycin trough, duration of vancomycin therapy, time to clinical stability, and shorter hospital stay. At Boston Medical Center, 65% of pediatric patients receiving vancomycin did not achieve initial therapeutic troughs between 10 and 20 μg/mL from October 1, 2016 to September 30, 2017. Through implementation of a pharmacist-managed pediatric vancomycin protocol, the project aim was to increase the percentage of patients achieving initial therapeutic troughs from 35% to 60% and percentage of patients achieving therapeutic troughs within 3 days from 67% to 90% by May 1, 2018. Secondary aims included reducing the incidence of supratherapeutic troughs from 10% to 5% and maintaining the incidence of vancomycin-associated nephrotoxicity (VAN) at 0%. METHODS: A quality improvement (QI) initiative based on the Institute for Healthcare Improvement Model was utilized, testing change through Plan-Do-Study-Act (PDSA) cycles. In PDSA cycle 1, pharmacists designed and implemented a standardized vancomycin dosing protocol for pediatric patients. In PDSA cycle 2, the addition of area under the curve (AUC)-guided dosing was implemented in select patients. Process and balancing measures included percentage of appropriately drawn vancomycin troughs, provider adherence to the new dosing protocol, and incidence of supratherapeutic troughs. RESULTS: A total of 32 pediatric patients were assessed. Compared with baseline data, percentage of patients achieving initial therapeutic troughs increased from 35% to 44% and percentage of patients achieving therapeutic troughs within 3 days increased from 67% to 92%. The incidence of supratherapeutic troughs decreased from 10% to 0% and the incidence of vancomycin-associated nephrotoxicity was maintained at 0%. CONCLUSION: Standardized initial vancomycin dosing with increased pharmacy involvement led to more patients achieving initial therapeutic troughs, shorter times to therapeutic troughs, and a reduction in supratherapeutic troughs. Next steps include hospital-wide implementation of a pediatric vancomycin per pharmacy protocol. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2018-11-26 /pmc/articles/PMC6255126/ http://dx.doi.org/10.1093/ofid/ofy210.277 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
Vu, Christine
Brade, Karrine
Farrell, Camilla
Mancuso, Michelle
266. Implementation and Evaluation of a Pharmacist-Managed Pediatric Vancomycin Protocol
title 266. Implementation and Evaluation of a Pharmacist-Managed Pediatric Vancomycin Protocol
title_full 266. Implementation and Evaluation of a Pharmacist-Managed Pediatric Vancomycin Protocol
title_fullStr 266. Implementation and Evaluation of a Pharmacist-Managed Pediatric Vancomycin Protocol
title_full_unstemmed 266. Implementation and Evaluation of a Pharmacist-Managed Pediatric Vancomycin Protocol
title_short 266. Implementation and Evaluation of a Pharmacist-Managed Pediatric Vancomycin Protocol
title_sort 266. implementation and evaluation of a pharmacist-managed pediatric vancomycin protocol
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255126/
http://dx.doi.org/10.1093/ofid/ofy210.277
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