Trajectories of prescription opioid dose and risk of opioid-related adverse events among older Medicare beneficiaries in the United States: A nested case–control study

Abstract

Background Despite the rising number of older adults with medical encounters for opioid misuse, dependence, and poisoning, little is known about patterns of prescription opioid dose and their association with risk for opioid-related adverse events (ORAEs) in older patients. The study aims to compare trajectories of prescribed opioid doses in 6 months preceding an incident ORAE for cases and a matched control group of older patients with chronic noncancer pain (CNCP). Methods and findings We conducted a nested case–control study within a cohort of older (≥65 years) patients diagnosed with CNCP who were new users of prescription opioids, assembled using a 5% national random sample of Medicare beneficiaries from 2011 to 2018. From the cohort with a mean follow-up of 2.3 years, we identified 3,103 incident ORAE cases with ≥1 opioid prescription in 6 months preceding the event, and 3,103 controls matched on sex, age, and time since opioid initiation. Key exposure was trajectories of prescribed opioid morphine milligram equivalent (MME) daily dosage over 6 months before the incident ORAE or matched controls. Among the cases and controls, 2,192 (70.6%) were women, and the mean (SD) age was 77.1 (7.1) years. Four prescribed opioid trajectories before the incident ORAE diagnosis or matched date emerged: gradual dose discontinuation (from ≤3 to 0 daily MME, 1,456 [23.5%]), gradual dose increase (from 0 to >3 daily MME, 1,878 [30.3%]), consistent low dose (between 3 and 5 daily MME, 1,510 [24.3%]), and consistent moderate dose (>20 daily MME, 1,362 [22.0%]). Few older patients (Conclusions In this sample of older patients who are Medicare beneficiaries, 4 prescription opioid dose trajectories were identified, with most prescribed doses below 90 daily MME within 6 months before ORAE or matched date. An increased risk for ORAE was observed among older patients with a gradual increase in dose or among those with a consistent low-to-moderate dose of prescribed opioids when compared to patients with opioid dose discontinuation. Whether older patients are susceptible to low opioid doses warrants further investigations. Yu-Jung Jenny Wei and colleagues study patterns of prescribed opioid doses in the 6 months before an opioid-related adverse event among Medicare beneficiaries with chronic non-cancer pain in the US. Author summary Why was this study done? The number of older adults with medical encounters for opioid-related adverse events (ORAEs) has increased over the past decade. Yet, little is known about patterns of prescription opioid dose and their association with risk for ORAEs among older patients. What did the researchers do and find? We assessed trajectories of opioid morphine milligram equivalent (MME) dose prescribed during the 6 months before an incident ORAE for 3,103 cases and during the 6 months before the equivalent date for 3,103 controls who did not experience an ORAE, selected from a cohort of Medicare older patients diagnosed with chronic noncancer pain who were new users of prescription opioids. We found four prescription opioid dose trajectories, with most prescribed doses below 90 daily MME before ORAE or matched date. We also found that compared to patients with gradual dose discontinuation (from ≤3 to 0 daily MME), those with gradual dose increase (from 0 to >3 daily MME), consistent low dose (between 3 and 5 daily MME), and consistent moderate low (>20 daily MME) had a higher risk for ORAEs. What do these findings mean? An increased risk for ORAE was observed among older patients who had a gradual increase in dose or among those who had a consistent low-to-moderate dose of prescribed opioids when compared to patients with opioid dose discontinuation. Whether older patients are susceptible to low opioid doses warrants further investigations.