Absorption pharmacokinetics and feasibility of intranasal dexmedetomidine in patients under general anaesthesia

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dc.contributor.author Tiainen, Suvi-Maria
dc.contributor.author Anderson, Brian J
dc.contributor.author Rinne, Ella
dc.contributor.author Tornio, Aleksi
dc.contributor.author Engström, Marica T
dc.contributor.author Saari, Teijo I
dc.contributor.author Uusalo, Panu
dc.coverage.spatial England
dc.date.accessioned 2024-07-12T02:50:23Z
dc.date.available 2024-07-12T02:50:23Z
dc.date.issued 2024-06-19
dc.identifier.citation (2024). Acta Anaesthesiologica Scandinavica (Early view).
dc.identifier.issn 0001-5172
dc.identifier.uri https://hdl.handle.net/2292/69218
dc.description.abstract BACKGROUND: The use of intranasal dexmedetomidine is hampered by a limited understanding of its absorption pharmacokinetics. METHODS: We examined the pharmacokinetics and feasibility of intranasal dexmedetomidine administered in the supine position to adult patients undergoing general anaesthesia. Twenty-eight patients between 35 and 80 years of age, ASA 1-3 and weight between 50 and 100 kg, who underwent elective unilateral total hip or knee arthroplasty under general anaesthesia were recruited. All patients received 100 μg of intranasal dexmedetomidine after anaesthesia induction. Six venous blood samples (at 0, 5, 15, 45, 60, 240 min timepoints from dexmedetomidine administration) were collected from each patient and dexmedetomidine plasma concentrations were measured. Concentration-time profiles after nasal administration were pooled with earlier data from a population analysis of intravenous dexmedetomidine (n = 202) in order to estimate absorption parameters using nonlinear mixed effects. Peak concentration (CMAX) and time (TMAX) were estimated using simulation (n = 1000) with parameter estimates and their associated variability. RESULTS: There were 28 adult patients with a mean (SD) age of 66 (8) years and weight of 83 (10) kg. The mean weight-adjusted dose of dexmedetomidine was 1.22 (0.15) μg kg-1. CMAX 0.273 μg L-1 was achieved at 98 min after intranasal administration (TMAX). The relative bioavailability of dexmedetomidine was 80% (95% CI 75-91%). The absorption half-time (TABS = 120 min; 95% CI 90-147 min) was slower than that in previous pharmacokinetic studies on adult patients. Perioperative haemodynamics of all patients remained stable. CONCLUSIONS: Administration of intranasal dexmedetomidine in the supine position during general anaesthesia is feasible with good bioavailability. This administration method has slower absorption when compared to awake patients in upright position, with consequent concentrations attained after TMAX for several hours.
dc.language eng
dc.publisher Wiley
dc.relation.ispartofseries Acta Anaesthesiol Scand
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher.
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm
dc.rights.uri https://creativecommons.org/licenses/by/4.0/
dc.subject alpha2‐agonists
dc.subject extravascular administration
dc.subject intranasal administration
dc.subject pharmacokinetics
dc.subject 1103 Clinical Sciences
dc.subject 1109 Neurosciences
dc.subject 1116 Medical Physiology
dc.subject 3202 Clinical sciences
dc.subject 3209 Neurosciences
dc.title Absorption pharmacokinetics and feasibility of intranasal dexmedetomidine in patients under general anaesthesia
dc.type Journal Article
dc.identifier.doi 10.1111/aas.14473
dc.date.updated 2024-06-22T03:30:00Z
dc.rights.holder Copyright: The authors en
pubs.author-url https://onlinelibrary.wiley.com/doi/10.1111/aas.14473
pubs.publication-status Published online
dc.rights.accessrights http://purl.org/eprint/accessRights/OpenAccess en
pubs.subtype Journal Article
pubs.elements-id 1033981
pubs.org-id Medical and Health Sciences
pubs.org-id School of Medicine
pubs.org-id Anaesthesiology
dc.identifier.eissn 1399-6576
pubs.record-created-at-source-date 2024-06-22
pubs.online-publication-date 2024-06-19


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