Anesthetic drugs & techniques

Opioid use in treated and untreated obstructive sleep apnoea: remifentanil pharmacokinetics and pharmacodynamics in adult volunteers

Br J AnaesthPublished Preplanned analysis of a prospective cohort study

Authors' conclusion

OSA (untreated or treated) did not influence remifentanil pharmacokinetics or pharmacodynamics (miosis, analgesia, respiratory depression).

Study context

Population
Awake adult volunteers (median age 52 yr, range 23–70) with or without obstructive sleep apnoea (OSA)
Participants
20 / 33 / 21
Exposure
Untreated OSA vs treated OSA vs no OSA
  • No OSAn = 20reference
  • Untreated OSAn = 33
  • Treated OSAn = 21
Outcome
Remifentanil PK (clearance, volume of distribution) and PD (miosis, thermal heat tolerance, end-expired CO2)
Methodological detailspharmacokinetic/pharmacodynamic, single-centre, open-label, stepped-dose TCI remifentanil infusion, population PK/PD modelling
  • Pharmacokinetic/pharmacodynamic
  • Single-centre
  • Open-label
  • Stepped-dose TCI remifentanil infusion
  • Population PK/PD modelling

Main finding

As reported in the abstract

Remifentanil PK
GroupValueVolume of distribution
No OSAmedian 147 L h-119.6 L
Untreated OSAmedian 143 L h-115.5 L
Treated OSAmedian 155 L h-117.7 L

Value

No OSAmedian 147 L h-1
Untreated OSAmedian 143 L h-1
Treated OSAmedian 155 L h-1

Volume of distribution

No OSA19.6 L
Untreated OSA15.5 L
Treated OSA17.7 L
  • No OSA: P = 0.472
  • No OSA: P = 0.473

Observational data: associations, not effects.

Further findings

Model-estimated pupil area (% of baseline) at plasma remifentanil 4 ng ml-1 · across 3 groups

P = 0.086

Model-estimated thermal heat tolerance at plasma remifentanil 4 ng ml-1 · across 3 groups

P = 0.218

Model-estimated end-expired CO2 at plasma remifentanil 4 ng ml-1 · across 3 groups

P = 0.257

Original publication

Opioid use in treated and untreated obstructive sleep apnoea: remifentanil pharmacokinetics and pharmacodynamics in adult volunteers. Br J Anaesth. Published 20 January 2025. doi:10.1016/j.bja.2024.10.042

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