High-risk prescribing and opioid overdose: prospects for prescription drug monitoring program–based proactive alerts
To develop a simple, valid model to identify patients at high risk of opioid overdose–related hospitalization and mortality, Oregon prescription drug monitoring program, Vital Records, and Hospital Discharge data were linked to estimate 2 logistic models; a first model that included a broad range of...
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Published in | Pain (Amsterdam) Vol. 159; no. 1; pp. 150 - 156 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Wolters Kluwer
01.01.2018
|
Subjects | |
Online Access | Get full text |
ISSN | 0304-3959 1872-6623 1872-6623 |
DOI | 10.1097/j.pain.0000000000001078 |
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Abstract | To develop a simple, valid model to identify patients at high risk of opioid overdose–related hospitalization and mortality, Oregon prescription drug monitoring program, Vital Records, and Hospital Discharge data were linked to estimate 2 logistic models; a first model that included a broad range of risk factors from the literature and a second simplified model. Receiver operating characteristic curves, sensitivity, and specificity of the models were analyzed. Variables retained in the final model were categories such as older than 35 years, number of prescribers, number of pharmacies, and prescriptions for long-acting opioids, benzodiazepines or sedatives, or carisoprodol. The ability of the model to discriminate between patients who did and did not overdose was reasonably good (area under the receiver operating characteristic curve = 0.82, Nagelkerke
R
2
= 0.11). The positive predictive value of the model was low. Computationally simple models can identify high-risk patients based on prescription history alone, but improvement of the predictive value of models may require information from outside the prescription drug monitoring program. Patient or prescription features that predict opioid overdose may differ from those that predict diversion. |
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AbstractList | In order to develop a simple, valid model to identify patients at high risk for opioid overdose-related hospitalization and mortality Oregon PDMP, Vital Records, and Hospital Discharge data were linked to estimate two logistic models; A first model that included a broad range of risk factors from the literature and a second simplified model. ROC curves, sensitivity and specificity of the models were analyzed. Variables retained in the final model were age categories over 35, number of prescribers, number of pharmacies, and prescriptions for long acting opioids, benzodiazepines/sedatives, or carisoprodol. The ability of the model to discriminate between patients who did and did not overdose was reasonably good (AUC = .82, Nagelkerke R2 = .11). The positive predictive value of the model was low. Computationally simple models can identify high risk patients based on prescription history alone, but improvement of the predictive value of models may require information from outside the PDMP. Patient or prescription features that predict opioid overdose may differ from those that predict diversion. To develop a simple, valid model to identify patients at high risk of opioid overdose-related hospitalization and mortality, Oregon prescription drug monitoring program, Vital Records, and Hospital Discharge data were linked to estimate 2 logistic models; a first model that included a broad range of risk factors from the literature and a second simplified model. Receiver operating characteristic curves, sensitivity, and specificity of the models were analyzed. Variables retained in the final model were categories such as older than 35 years, number of prescribers, number of pharmacies, and prescriptions for long-acting opioids, benzodiazepines or sedatives, or carisoprodol. The ability of the model to discriminate between patients who did and did not overdose was reasonably good (area under the receiver operating characteristic curve = 0.82, Nagelkerke R = 0.11). The positive predictive value of the model was low. Computationally simple models can identify high-risk patients based on prescription history alone, but improvement of the predictive value of models may require information from outside the prescription drug monitoring program. Patient or prescription features that predict opioid overdose may differ from those that predict diversion.To develop a simple, valid model to identify patients at high risk of opioid overdose-related hospitalization and mortality, Oregon prescription drug monitoring program, Vital Records, and Hospital Discharge data were linked to estimate 2 logistic models; a first model that included a broad range of risk factors from the literature and a second simplified model. Receiver operating characteristic curves, sensitivity, and specificity of the models were analyzed. Variables retained in the final model were categories such as older than 35 years, number of prescribers, number of pharmacies, and prescriptions for long-acting opioids, benzodiazepines or sedatives, or carisoprodol. The ability of the model to discriminate between patients who did and did not overdose was reasonably good (area under the receiver operating characteristic curve = 0.82, Nagelkerke R = 0.11). The positive predictive value of the model was low. Computationally simple models can identify high-risk patients based on prescription history alone, but improvement of the predictive value of models may require information from outside the prescription drug monitoring program. Patient or prescription features that predict opioid overdose may differ from those that predict diversion. To develop a simple, valid model to identify patients at high risk of opioid overdose-related hospitalization and mortality, Oregon prescription drug monitoring program, Vital Records, and Hospital Discharge data were linked to estimate 2 logistic models; a first model that included a broad range of risk factors from the literature and a second simplified model. Receiver operating characteristic curves, sensitivity, and specificity of the models were analyzed. Variables retained in the final model were categories such as older than 35 years, number of prescribers, number of pharmacies, and prescriptions for long-acting opioids, benzodiazepines or sedatives, or carisoprodol. The ability of the model to discriminate between patients who did and did not overdose was reasonably good (area under the receiver operating characteristic curve = 0.82, Nagelkerke R = 0.11). The positive predictive value of the model was low. Computationally simple models can identify high-risk patients based on prescription history alone, but improvement of the predictive value of models may require information from outside the prescription drug monitoring program. Patient or prescription features that predict opioid overdose may differ from those that predict diversion. To develop a simple, valid model to identify patients at high risk of opioid overdose–related hospitalization and mortality, Oregon prescription drug monitoring program, Vital Records, and Hospital Discharge data were linked to estimate 2 logistic models; a first model that included a broad range of risk factors from the literature and a second simplified model. Receiver operating characteristic curves, sensitivity, and specificity of the models were analyzed. Variables retained in the final model were categories such as older than 35 years, number of prescribers, number of pharmacies, and prescriptions for long-acting opioids, benzodiazepines or sedatives, or carisoprodol. The ability of the model to discriminate between patients who did and did not overdose was reasonably good (area under the receiver operating characteristic curve = 0.82, Nagelkerke R 2 = 0.11). The positive predictive value of the model was low. Computationally simple models can identify high-risk patients based on prescription history alone, but improvement of the predictive value of models may require information from outside the prescription drug monitoring program. Patient or prescription features that predict opioid overdose may differ from those that predict diversion. |
Author | Van Otterloo, Joshua Deyo, Richard A. Hallvik, Sara Wakeland, Wayne Hildebran, Christi Geissert, Peter O'Kane, Nicole Alley, Lindsey Carson, Jody Leichtling, Gillian |
AuthorAffiliation | Prescription Drug Monitoring Program, Oregon Health Authority, Portland, OR, USA Department of Family Medicine, Oregon Health & Science University, Portland, OR, USA HealthInsight Oregon, Portland, OR, USA Department of Systems Science, Portland State University, Portland, OR, USA |
AuthorAffiliation_xml | – name: Prescription Drug Monitoring Program, Oregon Health Authority, Portland, OR, USA – name: Department of Family Medicine, Oregon Health & Science University, Portland, OR, USA – name: HealthInsight Oregon, Portland, OR, USA – name: Department of Systems Science, Portland State University, Portland, OR, USA |
Author_xml | – sequence: 1 givenname: Peter surname: Geissert fullname: Geissert, Peter organization: Department of Systems Science, Portland State University, Portland, OR, USA – sequence: 2 givenname: Sara surname: Hallvik fullname: Hallvik, Sara organization: HealthInsight Oregon, Portland, OR, USA – sequence: 3 givenname: Joshua surname: Van Otterloo fullname: Van Otterloo, Joshua organization: Prescription Drug Monitoring Program, Oregon Health Authority, Portland, OR, USA – sequence: 4 givenname: Nicole surname: O'Kane fullname: O'Kane, Nicole organization: HealthInsight Oregon, Portland, OR, USA – sequence: 5 givenname: Lindsey surname: Alley fullname: Alley, Lindsey organization: HealthInsight Oregon, Portland, OR, USA – sequence: 6 givenname: Jody surname: Carson fullname: Carson, Jody organization: HealthInsight Oregon, Portland, OR, USA – sequence: 7 givenname: Gillian surname: Leichtling fullname: Leichtling, Gillian organization: HealthInsight Oregon, Portland, OR, USA – sequence: 8 givenname: Christi surname: Hildebran fullname: Hildebran, Christi organization: HealthInsight Oregon, Portland, OR, USA – sequence: 9 givenname: Wayne surname: Wakeland fullname: Wakeland, Wayne organization: Department of Systems Science, Portland State University, Portland, OR, USA – sequence: 10 givenname: Richard A. surname: Deyo fullname: Deyo, Richard A. organization: Department of Family Medicine, Oregon Health & Science University, Portland, OR, USA |
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Snippet | To develop a simple, valid model to identify patients at high risk of opioid overdose–related hospitalization and mortality, Oregon prescription drug... To develop a simple, valid model to identify patients at high risk of opioid overdose-related hospitalization and mortality, Oregon prescription drug... In order to develop a simple, valid model to identify patients at high risk for opioid overdose-related hospitalization and mortality Oregon PDMP, Vital... |
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SubjectTerms | Analgesics, Opioid - poisoning Chronic Pain - drug therapy Drug Overdose - prevention & control Drug Prescriptions Humans Models, Theoretical Prescription Drug Monitoring Programs Risk Factors |
Title | High-risk prescribing and opioid overdose: prospects for prescription drug monitoring program–based proactive alerts |
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