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Brief Report

Evaluation of U.S. state opioid prescribing restrictions using patient opioid consumption patterns from a single, urban, academic institution

, MD MPH, , MDORCID Icon, , PhDORCID Icon, , MD, MBAORCID Icon, , MPH, , MEng, , MD & , MD MPH show all
Pages 932-936 | Published online: 11 Apr 2022
 

Abstract

Background: Since 2017, states, insurers, and pharmacies have placed blanket limits on the duration and quantity of opioid prescriptions. In many states, overlapping duration and daily dose limits yield maximum prescription limits of 150–350 morphine milligram equivalents (MMEs). There is limited knowledge of how these restrictions compare with actual patient opioid consumption; while changes in prescription patterns and opioid misuse rates have been studied, these are, at best, weak proxies for actual pain control consumption. We sought to determine how patients undergoing surgery would be affected by opioid prescribing restrictions using actual patient opioid consumption data. Methods: We constructed a prospective database of post-discharge opioid consumption: patients undergoing surgery at one institution were called after discharge to collect opioid consumption data. Patients whose opioid consumption exceeded 150 and 350 MME were identified. Results: Two thousand nine hundred and seventy-one patients undergoing 54 common surgical procedures were included in our study. Twenty-one percent of patients consumed more than the 150 MME limit. Only 7% of patients consumed above the 350 MME limit. Typical (non-outlier) opioid consumption, defined as less than the 75th percentile of consumption for any given procedure, exceeded the 150 MME and 350 MME limits for 41 and 7% of procedures, respectively. Orthopedic, spinal/neurosurgical, and complex abdominal procedures most commonly exceeded these limits. Conclusions: While most patients undergoing surgery are unaffected by recent blanket prescribing limits, those undergoing a specific subset of procedures are likely to require more opioids than the restrictions permit; providers should be aware that these patients may require a refill to adequately control post-surgical pain. Real consumption data should be used to guide these restrictions and inform future interventions so the risk of worsened pain control (and its troublesome effects on opioid misuse) is minimized. Procedure-specific prescribing limits may be one approach to prevent misuse, while also optimizing post-operative pain control.

Author contributions

KR, JM, CK, LN, and GB: study conception and design. KR, JM, CK, AF, JY, LN, and GB: data acquisition. KR, JM, CK, BB, AF, JY, and GB: analysis and data interpretation. KR, JM, CK, BB, AF, JY, and GB: drafting of the manuscript. JM, CK, BB, LN, and GB: critical revision.

Additional information

Funding

GB and KR were funded by grants from the CRICO/Risk Management Foundation of the Harvard Medical Institutions and a Blavatnik Biomedical Accelerator Pilot Grant of Harvard University. JM and BB are supported by a grant from the National Library of Medicine/National Institutes of Health (T15LM007092) and the Biomedical Informatics and Data Science Research Training (BIRT) Program of Harvard University. None of the funding organizations had any role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.

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