Journal
JOURNAL OF GENERAL INTERNAL MEDICINE
Volume 33, Issue 9, Pages 1512-1519Publisher
SPRINGER
DOI: 10.1007/s11606-018-4532-5
Keywords
potentially inappropriate prescribing; overdose; opioids; mortality
Funding
- GE Foundation
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Potentially inappropriate prescribing (PIP) may contribute to opioid overdose. To examine the association between PIP and adverse events. Cohort study. Three million seventy-eight thousand thirty-four individuals age ae 18, without disseminated cancer, who received prescription opioids between 2011 and 2015. We defined PIP as (a) morphine equivalent dose ae 100 mg/day in ae 3 months; (b) overlapping opioid and benzodiazepine prescriptions in ae 3 months; (c) ae 4 opioid prescribers in any quarter; (d) ae 4 opioid-dispensing pharmacies in any quarter; (e) cash purchase of prescription opioids on ae 3 occasions; and (f) receipt of opioids in 3 consecutive months without a documented pain diagnosis. We used Cox proportional hazards models to identify PIP practices associated with non-fatal opioid overdose, fatal opioid overdose, and all-cause mortality, controlling for covariates. All six types of PIP were associated with higher adjusted hazard for all-cause mortality, four of six with non-fatal overdose, and five of six with fatal overdose. Lacking a documented pain diagnosis was associated with non-fatal overdose (adjusted hazard ratio [AHR] 2.21, 95% confidence interval [CI] 2.02-2.41), as was high-dose opioids (AHR 1.68, 95% CI 1.59-1.76). Co-prescription of benzodiazepines was associated with fatal overdose (AHR 4.23, 95% CI 3.85-4.65). High-dose opioids were associated with all-cause mortality (AHR 2.18, 95% CI 2.14-2.23), as was lacking a documented pain diagnosis (AHR 2.05, 95% CI 2.01-2.09). Compared to those who received opioids without PIP, the hazard for fatal opioid overdose with one, two, three, and ae four PIP subtypes were 4.24, 7.05, 10.28, and 12.99 (test of linear trend, p < 0.001). PIP was associated with higher hazard for all-cause mortality, fatal overdose, and non-fatal overdose. Our study implies the possibility of creating a risk score incorporating multiple PIP subtypes, which could be displayed to prescribers in real time.
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