<abstract xmlns="http://www.w3.org/1999/xhtml">

<p>More than half of patients with opioid use disorder for chronic non-cancer pain (CNCP) reduced their dose through a progressive opioid withdrawal supported by a rotation to buprenorphine and/or tramadol. The aim of this research is to analyse the long-term effectiveness of opioid deprescription taking into account the impact of sex and pharmacogenetics on the inter-individual variability. A cross-sectional study was carried out from October 2019 to June 2020 on CNCP patients who had previously undergone an opioid deprescription (<italic>n</italic> = 119 patients). Demographic, clinical (pain, relief and adverse events) and therapeutic (analgesic use) outcomes were collected. Effectiveness (&lt; 50 mg per day of morphine equivalent daily dose without any aberrant opioid use behaviour) and safety (number of side-effects) were analysed in relation to sex differences and pharmacogenetic markers impact [<italic>OPRM1</italic> genotype (rs1799971) and CYP2D6 phenotypes]. Long-term opioid deprescription was achieved in 49 % of the patients with an increase in pain relief and a reduction of adverse events. CYP2D6 poor metabolizers showed the lowest long-term opioid doses. Here, women showed a higher degree of opioid deprescription, but increased use of tramadol and neuromodulators, as well as an increased number of adverse events. Long-term deprescription was successful in half of the cases. Understanding sex and gender interaction plus a genetic impact could help to design more individualized strategies for opioid deprescription.</p>
</abstract>

More than half of patients with opioid use disorder for chronic non-cancer pain (CNCP) reduced their dose through a progressive opioid withdrawal supported by a rotation to buprenorphine and/or tramadol. The aim of this research is to analyse the long-term effectiveness of opioid deprescription taking into account the impact of sex and pharmacogenetics on the inter-individual variability. A cross-sectional study was carried out from October 2019 to June 2020 on CNCP patients who had previously undergone an opioid deprescription (n = 119 patients). Demographic, clinical (pain, relief and adverse events) and therapeutic (analgesic use) outcomes were collected. Effectiveness (< 50 mg per day of morphine equivalent daily dose without any aberrant opioid use behaviour) and safety (number of side-effects) were analysed in relation to sex differences and pharmacogenetic markers impact [OPRM1 genotype (rs1799971) and CYP2D6 phenotypes]. Long-term opioid deprescription was achieved in 49 % of the patients with an increase in pain relief and a reduction of adverse events. CYP2D6 poor metabolizers showed the lowest long-term opioid doses. Here, women showed a higher degree of opioid deprescription, but increased use of tramadol and neuromodulators, as well as an increased number of adverse events. Long-term deprescription was successful in half of the cases. Understanding sex and gender interaction plus a genetic impact could help to design more individualized strategies for opioid deprescription.

Long-term deprescription in chronic pain and opioid use disorder patients: Pharmacogenetic and sex differences

Pain Unit, Dr. Balmis General University Hospital

Dr. Balmis General University Hospital ISABIAL

Acta Pharmaceutica

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

More than half of patients with opioid use disorder for chronic non-cancer pain (CNCP) reduced their dose through a progressive opioid withdrawal supported by...

Long-term deprescription in chronic pain and opioid use disorder patients: Pharmacogenetic and sex differences

Online veröffentlicht: 12. Juni 2023

Seitenbereich: 227 - 241

Akzeptiert: 17. Nov. 2022

DOI: https://doi.org/10.2478/acph-2023-0018

Schlüsselwörter
chronic pain, drug deprescription, opioid use disorder, long-term monitoring, pharmacogenetics, sex differences

© 2023 Javier Muriel et al., published by Sciendo

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

Long-term deprescription in chronic pain and opioid use disorder patients: Pharmacogenetic and sex differences

Online veröffentlicht: 12. Juni 2023

Seitenbereich: 227 - 241

Akzeptiert: 17. Nov. 2022

DOI: https://doi.org/10.2478/acph-2023-0018

Schlüsselwörterchronic pain, drug deprescription, opioid use disorder, long-term monitoring, pharmacogenetics, sex differences

© 2023 Javier Muriel et al., published by Sciendo

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

Schlüsselwörter
chronic pain, drug deprescription, opioid use disorder, long-term monitoring, pharmacogenetics, sex differences