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Evaluation and optimization of take-home naloxone in an academic medical center

With the United States in the midst of an opioid overdose epidemic, efforts to reduce overdose deaths have increased. Expanding access to the opioid antagonist naloxone can combat the epidemic. A pilot project in a psychiatric hospital resulted in the development of a screening tool in the electroni...

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Autores principales: Cooler, Jordan, Ross, Clint A, Robert, Sophie, Linder, Lauren, Ruhe, Ann Marie, Philip, Achsah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: College of Psychiatric & Neurologic Pharmacists 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6398357/
https://www.ncbi.nlm.nih.gov/pubmed/30842919
http://dx.doi.org/10.9740/mhc.2019.03.105
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author Cooler, Jordan
Ross, Clint A
Robert, Sophie
Linder, Lauren
Ruhe, Ann Marie
Philip, Achsah
author_facet Cooler, Jordan
Ross, Clint A
Robert, Sophie
Linder, Lauren
Ruhe, Ann Marie
Philip, Achsah
author_sort Cooler, Jordan
collection PubMed
description With the United States in the midst of an opioid overdose epidemic, efforts to reduce overdose deaths have increased. Expanding access to the opioid antagonist naloxone can combat the epidemic. A pilot project in a psychiatric hospital resulted in the development of a screening tool in the electronic medical record (EMR) to help pharmacists identify adult inpatients at high risk of opioid overdose. Pharmacists can facilitate these patients being discharged with take-home naloxone. The purpose of this project was to optimize the screening tool for nonpsychiatric adult inpatient areas. Prior to implementation, a team of pharmacists familiar with the screening tool and take-home naloxone met with stakeholders to assess need for modification of the tool, determine barriers to implementation, and provide insight into the new service. In addition to expanding the tool into nonpsychiatric areas, a morphine-equivalents calculator was developed to identify patients receiving at least 100 mg of morphine equivalents per day to capture an additional at-risk population. Four short educational videos were developed to provide training to pharmacists. Initial performance of the screening tool was evaluated in general medicine patients over a 5-day period. Out of 44 admissions, 8 (18.2%) screened positive. The majority of those patients (5/8, 62.5%) screened positive for morphine equivalents greater than 100 mg. Anecdotally, the educational videos have been well received by pharmacy staff. Opioid overdose risk factors can be applied to nonpsychiatric inpatients for screening purposes in the EMR. Educational videos can be used to disseminate information to pharmacists on take-home naloxone and opioid overdose.
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spelling pubmed-63983572019-03-06 Evaluation and optimization of take-home naloxone in an academic medical center Cooler, Jordan Ross, Clint A Robert, Sophie Linder, Lauren Ruhe, Ann Marie Philip, Achsah Ment Health Clin Innovative Practice With the United States in the midst of an opioid overdose epidemic, efforts to reduce overdose deaths have increased. Expanding access to the opioid antagonist naloxone can combat the epidemic. A pilot project in a psychiatric hospital resulted in the development of a screening tool in the electronic medical record (EMR) to help pharmacists identify adult inpatients at high risk of opioid overdose. Pharmacists can facilitate these patients being discharged with take-home naloxone. The purpose of this project was to optimize the screening tool for nonpsychiatric adult inpatient areas. Prior to implementation, a team of pharmacists familiar with the screening tool and take-home naloxone met with stakeholders to assess need for modification of the tool, determine barriers to implementation, and provide insight into the new service. In addition to expanding the tool into nonpsychiatric areas, a morphine-equivalents calculator was developed to identify patients receiving at least 100 mg of morphine equivalents per day to capture an additional at-risk population. Four short educational videos were developed to provide training to pharmacists. Initial performance of the screening tool was evaluated in general medicine patients over a 5-day period. Out of 44 admissions, 8 (18.2%) screened positive. The majority of those patients (5/8, 62.5%) screened positive for morphine equivalents greater than 100 mg. Anecdotally, the educational videos have been well received by pharmacy staff. Opioid overdose risk factors can be applied to nonpsychiatric inpatients for screening purposes in the EMR. Educational videos can be used to disseminate information to pharmacists on take-home naloxone and opioid overdose. College of Psychiatric & Neurologic Pharmacists 2019-03-01 /pmc/articles/PMC6398357/ /pubmed/30842919 http://dx.doi.org/10.9740/mhc.2019.03.105 Text en © 2019 CPNP. The Mental Health Clinician is a publication of the College of Psychiatric and Neurologic Pharmacists. http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License, which permits non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Innovative Practice
Cooler, Jordan
Ross, Clint A
Robert, Sophie
Linder, Lauren
Ruhe, Ann Marie
Philip, Achsah
Evaluation and optimization of take-home naloxone in an academic medical center
title Evaluation and optimization of take-home naloxone in an academic medical center
title_full Evaluation and optimization of take-home naloxone in an academic medical center
title_fullStr Evaluation and optimization of take-home naloxone in an academic medical center
title_full_unstemmed Evaluation and optimization of take-home naloxone in an academic medical center
title_short Evaluation and optimization of take-home naloxone in an academic medical center
title_sort evaluation and optimization of take-home naloxone in an academic medical center
topic Innovative Practice
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6398357/
https://www.ncbi.nlm.nih.gov/pubmed/30842919
http://dx.doi.org/10.9740/mhc.2019.03.105
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