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dc.contributor.authorCastberg, Ingrid Mehli
dc.contributor.authorWestin, Andreas
dc.contributor.authorSkogvoll, Eirik
dc.contributor.authorSpigset, Olav
dc.date.accessioned2018-01-18T15:11:13Z
dc.date.available2018-01-18T15:11:13Z
dc.date.created2017-10-31T15:17:31Z
dc.date.issued2017
dc.identifier.citationActa Psychiatrica Scandinavica. 2017, 136 (5), 455-464.nb_NO
dc.identifier.issn0001-690X
dc.identifier.urihttp://hdl.handle.net/11250/2478239
dc.description.abstractObjective To investigate serum concentrations of second-generation antipsychotics in relation to age and gender in a population ranging from 18 to 100 years. Method Results from a routine therapeutic drug monitoring database were retrieved, and 43 079 samples from 11 968 patients were included (17 249 samples for clozapine, 16 171 samples for olanzapine, 5343 samples for risperidone, and 4316 samples for quetiapine). The dose-adjusted concentration was used as the primary target variable. A linear mixed model was used to allow the inclusion of multiple samples from each patient. Results Age had a significant impact on the concentrations of all four drugs. At the age of 80, the dose-adjusted concentrations were up to twice those of the age of 40. At the age of 90, dose-adjusted concentrations were two- to three-fold higher. Age-related increases were largest for clozapine (+108% at 80 years; +197% at 90 years) and smallest for olanzapine (+28% at 80 years; +106% at 90 years). Females generally had dose-adjusted concentrations 20–30% higher than males. Conclusion The effect of age on the serum concentrations of the antipsychotics studied becomes pronounced with advanced age. The patient population aged above 70 should be subdivided according to exact age, and considerable dose reductions are recommended.nb_NO
dc.language.isoengnb_NO
dc.publisherWileynb_NO
dc.titleEffects of age and gender on the serum levels of clozapine, olanzapine, risperidone, and quetiapinenb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionacceptedVersionnb_NO
dc.source.pagenumber455-464nb_NO
dc.source.volume136nb_NO
dc.source.journalActa Psychiatrica Scandinavicanb_NO
dc.source.issue5nb_NO
dc.identifier.doi10.1111/acps.12794
dc.identifier.cristin1509450
dc.description.localcode© 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd. This is the peer reviewed version of the article, locked until 2 September 2018 due to copyright restrictions. It has been published in final form at http://dx.doi.org/10.1111/acps.12794. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.nb_NO
cristin.unitcode194,65,15,0
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode2


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