Observations on the Pharmacokinetics and Pharmacodynamics of Dexmedetomidine. Clinical Studies on Healthy Volunteers and Intensive Care Patients

dc.contributorInstitute of Clinical Medicine; Department of Anaesthesiology, Intensive Care, Emergency Care and Pain Medicine-
dc.contributor.authorIirola, Timo
dc.contributor.departmentfi=Kliininen laitos|en=Institute of Clinical Medicine|
dc.contributor.facultyfi=Lääketieteellinen tiedekunta|en=Faculty of Medicine|
dc.date.accessioned2012-02-27T05:11:59Z
dc.date.available2012-02-27T05:11:59Z
dc.date.issued2012-03-16
dc.description.abstractPatients treated in intensive care units require sedation and analgesia. However, sedative drugs also have potential adverse effects, and there is no single ideal sedativeanalgesic drug for these patients. Dexmedetomidine is an apha2-adrenoceptor agonist licenced for sedation of intensive care patients and patients undergoing surgery and other invasive procedures. Several routes of parenteral administration (intravenous, intramuscular, subcutaneous and intranasal) have been utilized. In the present series of studies, the pharmacokinetics and pharmacodynamics of intranasally administered dexmedetomidine as well as the gastrointestinal effects of intravenous dexmedetomidine were determined in healthy volunteers. Pharmacokinetics of dexmedetomidine during long lasting, high-dose infusions were characterized in intensive care patients. The bioavailability of intranasal dexmedetomidine was relatively good (65%), but interindividual variation was large. Dexmedetomidine significantly inhibited gastric emptying and gastrointestinal transit. In intensive care patients, the elimination half-life of dexmedetomidine was somewhat longer than reported for infusions of shorter duration and in less ill patients or healthy volunteers. Dexmedetomidine appeared to have linear pharmacokinetics up to the studied dose rate of 2.5 μg/kg/h. Dexmedetomidine clearance was decreasing with age and its volume of distribution was increased in hypoalbuminaemic patients, resulting in a longer elimination half-life and context-sensitive half-time. Intranasally administered dexmedetomidine was efficacious and well tolerated, making it appropriate for clinical situations requiring light sedation. The clinical significance of the gastrointestinal inhibitory effects of dexmedetomidine should be further evaluated in intensive care patients. The possibility of potentially altered potency and effect duration should be taken into account when administering dexmedetomidine to elderly or hypoalbuminaemic patients.-
dc.description.accessibilityfeatureei tietoa saavutettavuudesta
dc.description.notificationSiirretty Doriasta
dc.format.contentfulltext
dc.identifierISBN 978-951-29-4907-6-
dc.identifier.olddbid78954
dc.identifier.oldhandle10024/74514
dc.identifier.urihttps://www.utupub.fi/handle/11111/27310
dc.identifier.urnURN:ISBN:978-951-29-4907-6
dc.language.isoeng-
dc.publisherAnnales Universitatis Turkuensis D 1004-
dc.publisherfi=Turun yliopisto|en=University of Turku|en
dc.relation.ispartofseriesTurun yliopiston julkaisuja. Sarja D, Medica – Odontologica
dc.relation.issn2343-3213
dc.relation.numberinseries1004-
dc.source.identifierhttps://www.utupub.fi/handle/10024/74514
dc.titleObservations on the Pharmacokinetics and Pharmacodynamics of Dexmedetomidine. Clinical Studies on Healthy Volunteers and Intensive Care Patients-
dc.type.ontasotfi=Artikkeliväitöskirja|en=Doctoral dissertation (article-based)|

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