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Opioid Drug-Drug-Drug Interactions and Unintentional Traumatic Injury: Screening to Detect Three-Way Drug Interaction Signals

Growing evidence suggests that drug interactions may be responsible for much of the known association between opioid use and unintentional traumatic injury. While prior research has focused on pairwise drug interactions, the role of higher-order (i.e., drug-drug-drug) interactions (3DIs) has not bee...

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Autores principales: Acton, Emily K., Hennessy, Sean, Brensinger, Colleen M., Bilker, Warren B., Miano, Todd A., Dublin, Sascha, Horn, John R., Chung, Sophie, Wiebe, Douglas J., Willis, Allison W., Leonard, Charles E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9127150/
https://www.ncbi.nlm.nih.gov/pubmed/35620282
http://dx.doi.org/10.3389/fphar.2022.845485
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author Acton, Emily K.
Hennessy, Sean
Brensinger, Colleen M.
Bilker, Warren B.
Miano, Todd A.
Dublin, Sascha
Horn, John R.
Chung, Sophie
Wiebe, Douglas J.
Willis, Allison W.
Leonard, Charles E.
author_facet Acton, Emily K.
Hennessy, Sean
Brensinger, Colleen M.
Bilker, Warren B.
Miano, Todd A.
Dublin, Sascha
Horn, John R.
Chung, Sophie
Wiebe, Douglas J.
Willis, Allison W.
Leonard, Charles E.
author_sort Acton, Emily K.
collection PubMed
description Growing evidence suggests that drug interactions may be responsible for much of the known association between opioid use and unintentional traumatic injury. While prior research has focused on pairwise drug interactions, the role of higher-order (i.e., drug-drug-drug) interactions (3DIs) has not been examined. We aimed to identify signals of opioid 3DIs with commonly co-dispensed medications leading to unintentional traumatic injury, using semi-automated high-throughput screening of US commercial health insurance data. We conducted bi-directional, self-controlled case series studies using 2000–2015 Optum Data Mart database. Rates of unintentional traumatic injury were examined in individuals dispensed opioid-precipitant base pairs during time exposed vs unexposed to a candidate interacting precipitant. Underlying cohorts consisted of 16–90-year-olds with new use of opioid-precipitant base pairs and ≥1 injury during observation periods. We used conditional Poisson regression to estimate rate ratios adjusted for time-varying confounders, and semi-Bayes shrinkage to address multiple estimation. For hydrocodone, tramadol, and oxycodone (the most commonly used opioids), we examined 16,024, 8185, and 9330 drug triplets, respectively. Among these, 75 (0.5%; hydrocodone), 57 (0.7%; tramadol), and 42 (0.5%; oxycodone) were significantly positively associated with unintentional traumatic injury (50 unique base precipitants, 34 unique candidate precipitants) and therefore deemed potential 3DI signals. The signals found in this study provide valuable foundations for future research into opioid 3DIs, generating hypotheses to motivate crucially needed etiologic investigations. Further, this study applies a novel approach for 3DI signal detection using pharmacoepidemiologic screening of health insurance data, which could have broad applicability across drug classes and databases.
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spelling pubmed-91271502022-05-25 Opioid Drug-Drug-Drug Interactions and Unintentional Traumatic Injury: Screening to Detect Three-Way Drug Interaction Signals Acton, Emily K. Hennessy, Sean Brensinger, Colleen M. Bilker, Warren B. Miano, Todd A. Dublin, Sascha Horn, John R. Chung, Sophie Wiebe, Douglas J. Willis, Allison W. Leonard, Charles E. Front Pharmacol Pharmacology Growing evidence suggests that drug interactions may be responsible for much of the known association between opioid use and unintentional traumatic injury. While prior research has focused on pairwise drug interactions, the role of higher-order (i.e., drug-drug-drug) interactions (3DIs) has not been examined. We aimed to identify signals of opioid 3DIs with commonly co-dispensed medications leading to unintentional traumatic injury, using semi-automated high-throughput screening of US commercial health insurance data. We conducted bi-directional, self-controlled case series studies using 2000–2015 Optum Data Mart database. Rates of unintentional traumatic injury were examined in individuals dispensed opioid-precipitant base pairs during time exposed vs unexposed to a candidate interacting precipitant. Underlying cohorts consisted of 16–90-year-olds with new use of opioid-precipitant base pairs and ≥1 injury during observation periods. We used conditional Poisson regression to estimate rate ratios adjusted for time-varying confounders, and semi-Bayes shrinkage to address multiple estimation. For hydrocodone, tramadol, and oxycodone (the most commonly used opioids), we examined 16,024, 8185, and 9330 drug triplets, respectively. Among these, 75 (0.5%; hydrocodone), 57 (0.7%; tramadol), and 42 (0.5%; oxycodone) were significantly positively associated with unintentional traumatic injury (50 unique base precipitants, 34 unique candidate precipitants) and therefore deemed potential 3DI signals. The signals found in this study provide valuable foundations for future research into opioid 3DIs, generating hypotheses to motivate crucially needed etiologic investigations. Further, this study applies a novel approach for 3DI signal detection using pharmacoepidemiologic screening of health insurance data, which could have broad applicability across drug classes and databases. Frontiers Media S.A. 2022-05-10 /pmc/articles/PMC9127150/ /pubmed/35620282 http://dx.doi.org/10.3389/fphar.2022.845485 Text en Copyright © 2022 Acton, Hennessy, Brensinger, Bilker, Miano, Dublin, Horn, Chung, Wiebe, Willis and Leonard. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Acton, Emily K.
Hennessy, Sean
Brensinger, Colleen M.
Bilker, Warren B.
Miano, Todd A.
Dublin, Sascha
Horn, John R.
Chung, Sophie
Wiebe, Douglas J.
Willis, Allison W.
Leonard, Charles E.
Opioid Drug-Drug-Drug Interactions and Unintentional Traumatic Injury: Screening to Detect Three-Way Drug Interaction Signals
title Opioid Drug-Drug-Drug Interactions and Unintentional Traumatic Injury: Screening to Detect Three-Way Drug Interaction Signals
title_full Opioid Drug-Drug-Drug Interactions and Unintentional Traumatic Injury: Screening to Detect Three-Way Drug Interaction Signals
title_fullStr Opioid Drug-Drug-Drug Interactions and Unintentional Traumatic Injury: Screening to Detect Three-Way Drug Interaction Signals
title_full_unstemmed Opioid Drug-Drug-Drug Interactions and Unintentional Traumatic Injury: Screening to Detect Three-Way Drug Interaction Signals
title_short Opioid Drug-Drug-Drug Interactions and Unintentional Traumatic Injury: Screening to Detect Three-Way Drug Interaction Signals
title_sort opioid drug-drug-drug interactions and unintentional traumatic injury: screening to detect three-way drug interaction signals
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9127150/
https://www.ncbi.nlm.nih.gov/pubmed/35620282
http://dx.doi.org/10.3389/fphar.2022.845485
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