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Modeling buprenorphine reduction of fentanyl-induced respiratory depression
Erik Olofsen, … , Albert Dahan, Celine M. Laffont
Erik Olofsen, … , Albert Dahan, Celine M. Laffont
Published March 22, 2022
Citation Information: JCI Insight. 2022;7(9):e156973. https://doi.org/10.1172/jci.insight.156973.
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Clinical Research and Public Health Clinical trials Neuroscience

Modeling buprenorphine reduction of fentanyl-induced respiratory depression

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Abstract

BACKGROUND Potent synthetic opioids, such as fentanyl, are increasingly abused, resulting in unprecedented numbers of fatalities from respiratory depression. Treatment with the high-affinity mu-opioid receptor partial agonist buprenorphine may prevent fatalities by reducing binding of potent opioids to the opioid receptor, limiting respiratory depression.METHODS To characterize buprenorphine-fentanyl interaction at the level of the mu-opioid receptor in 2 populations (opioid-naive individuals and individuals who chronically use high-dose opioids), the effects of escalating i.v. fentanyl doses with range 0.075–0.35 mg/70 kg (opioid naive) and 0.25–0.70 mg/70 kg (chronic opioid use) on iso-hypercapnic ventilation at 2–3 background doses of buprenorphine (target plasma concentrations range: 0.2–5 ng/mL) were quantified using receptor association/dissociation models combined with biophase distribution models.RESULTS Buprenorphine produced mild respiratory depression, while high doses of fentanyl caused pronounced respiratory depression and apnea in both populations. When combined with fentanyl, buprenorphine produced a receptor binding–dependent reduction of fentanyl-induced respiratory depression in both populations. In individuals with chronic opioid use, at buprenorphine plasma concentrations of 2 ng/mL or higher, a protective effect against high-dose fentanyl was observed.CONCLUSION Overall, the results indicate that when buprenorphine mu-opioid receptor occupancy is sufficiently high, fentanyl is unable to activate the mu-opioid receptor and consequently will not cause further respiratory depression in addition to the mild respiratory effects of buprenorphine.TRIAL REGISTRATION Trialregister.nl, no. NL7028 (https://www.trialregister.nl/trial/7028)FUNDING Indivior Inc., North Chesterfield, Virginia, USA.

Authors

Erik Olofsen, Marijke Hyke Algera, Laurence Moss, Robert L. Dobbins, Geert J. Groeneveld, Monique van Velzen, Marieke Niesters, Albert Dahan, Celine M. Laffont

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Figure 7

Prediction- and variability-corrected visual predictive checks of the pharmacodynamic model with a Kalman filter in individuals with chronic opioid use for the various drug administrations and probabilities of apnea for the same conditions.

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Prediction- and variability-corrected visual predictive checks of the ph...
(A and B) Fentanyl given at the background of placebo infusion. (C and D) Fentanyl given at the background of buprenorphine infusion. The dots in A and C are the 1-minute ventilation averages; the broken lines are the observed percentiles (dark orange: median, dark blue: 2.5th and 97.5th percentiles); the bins are the 95% confidence intervals of simulated percentiles (orange bins: median, blue bins: 2.5th and 97.5th percentiles). The right panels (B and D) give the probability of apnea. The red symbols are the probabilities of the observed apneic episodes; the orange bins are the simulated 95% confidence intervals of the probability of apnea.

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