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Evaluation of drug-drug interactions in hospitalized patients on medications for OUD

INTRODUCTION: Medications used to treat OUD have common metabolic pathways and pharmacodynamic properties that can lead to drug-drug interactions (DDIs) that may go unnoticed in the inpatient setting. The purpose of this study was to identify the frequency of DDIs between medications prescribed for...

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Autores principales: Berger, Olivia, Rector, Katherine, Meredith, Jacqueline, Sebaaly, Jamielynn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: College of Psychiatric & Neurologic Pharmacists 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8287868/
https://www.ncbi.nlm.nih.gov/pubmed/34316418
http://dx.doi.org/10.9740/mhc.2021.07.231
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author Berger, Olivia
Rector, Katherine
Meredith, Jacqueline
Sebaaly, Jamielynn
author_facet Berger, Olivia
Rector, Katherine
Meredith, Jacqueline
Sebaaly, Jamielynn
author_sort Berger, Olivia
collection PubMed
description INTRODUCTION: Medications used to treat OUD have common metabolic pathways and pharmacodynamic properties that can lead to drug-drug interactions (DDIs) that may go unnoticed in the inpatient setting. The purpose of this study was to identify the frequency of DDIs between medications prescribed for OUD and commonly used inpatient medications. METHODS: This was a retrospective review of orders for buprenorphine, buprenorphine-naloxone, and methadone to identify potential DDIs. Adult inpatients with an order for one of these medications for OUD were included. Medication regimens were evaluated throughout the inpatient stay and on day of discharge for DDIs. DDIs were classified by severity and type of interaction (increased risk of QT prolongation, additive CNS effects/respiratory depression, and opioid withdrawal). The primary endpoint was the number of potential DDIs. Other endpoints included number of each classification/severity of DDI, duration of therapy of interacting medications, and modifications made to OUD medications because of DDIs. RESULTS: A total of 102 patients were included, with 215 inpatient interactions and 83 interactions at discharge identified. While inpatient, 85% of patients were on an interacting medication, and 46% of patients were on an interacting medication at discharge. The most common classification of DDI was additive CNS effects/respiratory depression (68.8% inpatient, 50.6% discharge), followed by QT prolongation (24.2% inpatient, 45.8% discharge). The majority of DDIs were classified as requiring close monitoring rather than contraindicated. DISCUSSION: There are opportunities to optimize the prescribing practices surrounding OUD medications in both the inpatient setting and at discharge to ensure patient safety.
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spelling pubmed-82878682021-07-26 Evaluation of drug-drug interactions in hospitalized patients on medications for OUD Berger, Olivia Rector, Katherine Meredith, Jacqueline Sebaaly, Jamielynn Ment Health Clin Original Research INTRODUCTION: Medications used to treat OUD have common metabolic pathways and pharmacodynamic properties that can lead to drug-drug interactions (DDIs) that may go unnoticed in the inpatient setting. The purpose of this study was to identify the frequency of DDIs between medications prescribed for OUD and commonly used inpatient medications. METHODS: This was a retrospective review of orders for buprenorphine, buprenorphine-naloxone, and methadone to identify potential DDIs. Adult inpatients with an order for one of these medications for OUD were included. Medication regimens were evaluated throughout the inpatient stay and on day of discharge for DDIs. DDIs were classified by severity and type of interaction (increased risk of QT prolongation, additive CNS effects/respiratory depression, and opioid withdrawal). The primary endpoint was the number of potential DDIs. Other endpoints included number of each classification/severity of DDI, duration of therapy of interacting medications, and modifications made to OUD medications because of DDIs. RESULTS: A total of 102 patients were included, with 215 inpatient interactions and 83 interactions at discharge identified. While inpatient, 85% of patients were on an interacting medication, and 46% of patients were on an interacting medication at discharge. The most common classification of DDI was additive CNS effects/respiratory depression (68.8% inpatient, 50.6% discharge), followed by QT prolongation (24.2% inpatient, 45.8% discharge). The majority of DDIs were classified as requiring close monitoring rather than contraindicated. DISCUSSION: There are opportunities to optimize the prescribing practices surrounding OUD medications in both the inpatient setting and at discharge to ensure patient safety. College of Psychiatric & Neurologic Pharmacists 2021-07-16 /pmc/articles/PMC8287868/ /pubmed/34316418 http://dx.doi.org/10.9740/mhc.2021.07.231 Text en © 2021 CPNP. The Mental Health Clinician is a publication of the College of Psychiatric and Neurologic Pharmacists. https://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 Original Research
Berger, Olivia
Rector, Katherine
Meredith, Jacqueline
Sebaaly, Jamielynn
Evaluation of drug-drug interactions in hospitalized patients on medications for OUD
title Evaluation of drug-drug interactions in hospitalized patients on medications for OUD
title_full Evaluation of drug-drug interactions in hospitalized patients on medications for OUD
title_fullStr Evaluation of drug-drug interactions in hospitalized patients on medications for OUD
title_full_unstemmed Evaluation of drug-drug interactions in hospitalized patients on medications for OUD
title_short Evaluation of drug-drug interactions in hospitalized patients on medications for OUD
title_sort evaluation of drug-drug interactions in hospitalized patients on medications for oud
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8287868/
https://www.ncbi.nlm.nih.gov/pubmed/34316418
http://dx.doi.org/10.9740/mhc.2021.07.231
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