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Comparative effects of dexmedetomidine, propofol, sevoflurane, and S-ketamine on regional cerebral glucose metabolism in humans: a positron emission tomography study
University of Turku, Turku, Finland / Turku University Hospital, Turku, Finland.
Turku University Hospital, Turku, Finland.
Tampere University Hospital, Tampere, Finland.
Turku University Hospital, Turku, Finland.
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2018 (Engelska)Ingår i: British Journal of Anaesthesia, ISSN 0007-0912, E-ISSN 1471-6771, Vol. 121, nr 1, s. 281-290Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

IntroductionThe highly selective α2-agonist dexmedetomidine has become a popular sedative for neurointensive care patients. However, earlier studies have raised concern that dexmedetomidine might reduce cerebral blood flow without a concomitant decrease in metabolism. Here, we compared the effects of dexmedetomidine on the regional cerebral metabolic rate of glucose (CMRglu) with three commonly used anaesthetic drugs at equi-sedative doses.

MethodsOne hundred and sixty healthy male subjects were randomised to EC50 for verbal command of dexmedetomidine (1.5 ng ml−1n=40), propofol (1.7 μg ml−1n=40), sevoflurane (0.9% end-tidal; n=40) or S-ketamine (0.75 μg ml−1n=20) or placebo (n=20). Anaesthetics were administered using target-controlled infusion or vapouriser with end-tidal monitoring. 18F-labelled fluorodeoxyglucose was administered 20 min after commencement of anaesthetic administration, and high-resolution positron emission tomography with arterial blood activity samples was used to quantify absolute CMRglu for whole brain and 15 brain regions.

ResultsAt the time of [F18]fluorodeoxyglucose injection, 55% of dexmedetomidine, 45% of propofol, 85% of sevoflurane, 45% of S-ketamine, and 0% of placebo subjects were unresponsive. Whole brain CMRglu was 63%, 71%, 71%, and 96% of placebo in the dexmedetomidine, propofol, sevoflurane, and S-ketamine groups, respectively (P<0.001 between the groups). The lowest CMRglu was observed in nearly all brain regions with dexmedetomidine (P<0.05 compared with all other groups). With S-ketamine, CMRgludid not differ from placebo.

ConclusionsAt equi-sedative doses in humans, potency in reducing CMRglu was dexmedetomidine>propofol>ketamine=placebo. These findings alleviate concerns for dexmedetomidine-induced vasoconstriction and cerebral ischaemia.

Ort, förlag, år, upplaga, sidor
Elsevier, 2018. Vol. 121, nr 1, s. 281-290
Nationell ämneskategori
Övrig annan medicin och hälsovetenskap
Forskningsämne
Kognitiv neurovetenskap och filosofi
Identifikatorer
URN: urn:nbn:se:his:diva-15615DOI: 10.1016/j.bja.2018.04.008ISI: 000439025500072PubMedID: 29935583Scopus ID: 2-s2.0-85046622088OAI: oai:DiVA.org:his-15615DiVA, id: diva2:1219082
Konferens
10th International Symposium on Memory and Awareness in Anesthesia (MAA), Helsinki, Finland, June 19-21, 2017
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CC BY-NC-ND 4.0

Tillgänglig från: 2018-06-15 Skapad: 2018-06-15 Senast uppdaterad: 2020-11-02Bibliografiskt granskad

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Valli, KatjaRevonsuo, Antti

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