4.6 Article

Post-lumbar surgery prescription variation and opioid- related outcomes in a large US healthcare system: an observational study

Journal

SPINE JOURNAL
Volume 23, Issue 9, Pages 1345-1357

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.spinee.2023.05.006

Keywords

Benzodiazepines; Health services research; Opioids; Pain medication; Prescribing practices; Spinal surgery

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This study aimed to characterize factors associated with prescribing variation of opioids, non-opioid pain medications, and benzodiazepines in the US Military Health System. It found significant variation in factors such as procedure type, policy period, and medication receipt, highlighting the need for evidence-based interventions.
BACKGROUND CONTEXT: Spinal decompression and fusion procedures are one of the most common procedures performed in the United States (US) and remain associated with high postsurgical opioid burden. Despite guidelines emphasizing nonopioid pharmacotherapy strategies for postsurgical pain management, prescribing practices are likely variable and guideline-incongruent. PURPOSE: The purpose of this study was to characterize patient-, care-, and system-level factors associated with opioid, nonopioid pain medication, and benzodiazepine prescribing variation in the US Military Health System (MHS). STUDY DESIGN/SETTING: Retrospective study analyzing medical records from the US MHS Data Repository. PATIENT SAMPLE: Adult patients (N=6,625) undergoing lumbar decompression and spinal fusion procedures from 2016 to 2021 in the MHS enrolled in TRICARE at least a year prior to their procedure and had at least one encounter beyond the 90-day postprocedure period, without recent trauma, malignancy, cauda equina syndrome, and co-occurring procedures. OUTCOME MEASURES: Patient-, care-, and system-level factors influencing outcomes of discharge morphine equivalent dose (MED), 30-day opioid refill, and persistent opioid use (POU). POU was defined as dispensing of opioid prescriptions monthly for the first 3 months after surgery and then at least once between 90 and 180 days after surgery. METHODS: (Generalized) linear mixed models evaluated multilevel factors associated with discharge MED, opioid refill, and POU. RESULTS: The median discharge MED was 375 mg (IQR 225, 580) and days' supply was 7 days (IQR 4, 10); 36% received an opioid refill and 5%, overall, met criteria for POU. Discharge MED was associated with fusion procedures (+151-198 mg), multilevel procedures (+26 mg), policy release (-184 mg), opioid nai & BULL;vty (-31 mg), race (Black-21 mg, another race and ethnicity-47 mg), benzodiazepine receipt (+100 mg), opioid-only medications (+86 mg), gabapentinoid receipt (-20 mg), and nonopioid pain medications receipt (-60 mg). Longer symptom duration, fusion procedures, beneficiary category, mental healthcare, nicotine dependence, benzodiazepine receipt, and opioid naivety were associated with both opioid refill and POU. Multilevel procedures, elevated comorbidity score, policy period, antidepressant receipt, and gabapentinoid receipt, and presurgical physical therapy were also associated with opioid refill. POU increased with increasing discharge MED. CONCLUSIONS: Significant variation in discharge prescribing practices require systems-level, evidence-based intervention. Published by Elsevier Inc.

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