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dc.contributor.advisorKennedy, Amy
dc.contributor.advisorEdwards, Christopher
dc.contributor.authorEllis, Danielle
dc.contributor.authorFleury, Molly
dc.contributor.authorMcDermott, Logan
dc.contributor.authorWelch, Haley
dc.date.accessioned2025-09-26T19:53:39Z
dc.date.available2025-09-26T19:53:39Z
dc.date.issued2024
dc.identifier.urihttp://hdl.handle.net/10150/678607
dc.descriptionClass of 2024 Abstract and Posteren_US
dc.description.abstractSpecific Aims: Describe the population at high risk for opioid overdose that are receiving naloxone orders with concurrent prescriptions with a morphine milliequivalent (MME) ≥ 50, concurrent prescriptions for benzodiazepines or opioid use disorder, and/or a history of opioid overdose. Methods: This is a descriptive, observational, retrospective, cross-sectional study from October 2022 using data extracted from El Rio charts. To be eligible for this study, patients must have been treated at El Rio Clinic during October 2022, and meet certain Centers for Disease Control and Prevention (CDC) criteria for being at high risk for opioid overdose. A sample size of 773 was provided for data analysis. A total of 77 patients were excluded due to a lack of combined MME available, leaving a total of 696 patients analyzed. Results: Of the sample size analyzed (n=696), there were 367 naloxone orders prescribed. For MME >50, 238 patients were analyzed and 159 were prescribed concurrent naloxone (66.8%). For patients with medications used for opioid use disorder (OUD) and/or substance use disorder (SUD), 186 patients were analyzed and 130 were prescribed concurrent naloxone (69.9%). For patients with an OUD/SUD diagnosis, 239 patients were analyzed and 148 had concurrent naloxone (61.9%). For patients with concurrent benzodiazepines and opioids, 143 patients were analyzed and 65 had concurrent naloxone (45.4%). For patients with orders for benzodiazepines, muscle relaxants, and opioids, 75 patients were analyzed and 38 had concurrent naloxone (50.6%). Conclusions: There were 881 total opportunities to provide naloxone that met CDC recommendations. On average, 2 out of every 5 patients could have received naloxone that did not. Patients with OUD/SUD history or relevant medications were most commonly co-prescribed naloxone. The most overlooked group were those on opioids and benzodiazepines concurrently.en_US
dc.language.isoen_USen_US
dc.publisherThe University of Arizona.en_US
dc.rightsCopyright © is held by the author.en_US
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/
dc.subjectNaloxoneen_US
dc.subjectOpioid Overdoseen_US
dc.subjectMedication managementen_US
dc.subjectOpioid use disorderen_US
dc.subjectSubstance use disorderen_US
dc.subject.meshNaloxoneen_US
dc.subject.meshRisk Assessmenten_US
dc.subject.meshMedication Therapy Managementen_US
dc.subject.meshOpioid-Related Disordersen_US
dc.subject.meshDrug Therapy, Combinationen_US
dc.titleNaloxone: A Pain to Co-Prescribe? Evaluating naloxone co-prescribing practices for patients at an increased risk of opioid overdose at a federally qualified health centeren_US
dc.typePosteren_US
dc.typetexten_US
dc.contributor.departmentCollege of Pharmacy, The University of Arizonaen_US
dc.description.collectioninformationThis item is part of the Pharmacy Student Research Projects collection, made available by the College of Pharmacy and the University Libraries at the University of Arizona. For more information about items in this collection, please contact Jennifer Martin, Librarian and Clinical Instructor, Pharmacy Practice and Science, jenmartin@arizona.edu.en_US
refterms.dateFOA2025-09-26T19:53:42Z


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