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dc.contributor.authorWestin, Andreas
dc.contributor.authorBrekke, Malin
dc.contributor.authorMolden, Espen
dc.contributor.authorSkogvoll, Eirik
dc.contributor.authorCastberg, Ingrid Mehli
dc.contributor.authorSpigset, Olav
dc.date.accessioned2019-01-30T14:25:27Z
dc.date.available2019-01-30T14:25:27Z
dc.date.created2018-01-03T11:31:39Z
dc.date.issued2017
dc.identifier.citationClinical Pharmacology and Therapeutics. 2017, 103 (3), 477-484.nb_NO
dc.identifier.issn0009-9236
dc.identifier.urihttp://hdl.handle.net/11250/2583180
dc.description.abstractAlthough pregnancy is known to cause changes in drug pharmacokinetics, little is known about its impact on serum levels of antipsychotics. In this study we retrospectively assessed 201 routine serum antipsychotic therapeutic drug monitoring concentration measurements obtained from a total of 110 pregnancies in 103 women, and 512 measurements from the same women before and after pregnancy. Serum concentrations in the third trimester were significantly lower than baseline for quetiapine (−76%; confidence interval (CI), −83%, −66%; P < 0.001) and aripiprazole (−52%; CI, −62%, −39%; P < 0.001), but not for olanzapine (−9%; CI, −28%, +14%; P = 0.40). For the remaining antipsychotics (perphenazine, haloperidol, ziprasidone, risperidone, and clozapine), our dataset was limited, but it indicates that concentrations may decline at least for perphenazine and possibly also for haloperidol. Even though the clinical consequence of the serum concentrations decline remains to be elucidated, our results warrant close clinical monitoring throughout pregnancy, preferentially supported by therapeutic drug monitoring.nb_NO
dc.language.isoengnb_NO
dc.publisherAmerican Society for Clinical Pharmacology and Therapeuticsnb_NO
dc.rightsNavngivelse-Ikkekommersiell 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/deed.no*
dc.titleTreatment with antipsychotics in pregnancy: changes in drug dispositionnb_NO
dc.title.alternativeTreatment with antipsychotics in pregnancy: changes in drug dispositionnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.pagenumber477-484nb_NO
dc.source.volume103nb_NO
dc.source.journalClinical Pharmacology and Therapeuticsnb_NO
dc.source.issue3nb_NO
dc.identifier.doi10.1002/cpt.770
dc.identifier.cristin1534600
dc.description.localcode© 2017 The Authors. Clinical Pharmacology & Therapeutics published by Wiley Periodicals, Inc. on behalf of American Society for Clinical Pharmacology and Therapeutics This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial License.nb_NO
cristin.unitcode194,65,25,0
cristin.unitcode194,65,15,0
cristin.unitnameInstitutt for sirkulasjon og bildediagnostikk
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2


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Navngivelse-Ikkekommersiell 4.0 Internasjonal
Except where otherwise noted, this item's license is described as Navngivelse-Ikkekommersiell 4.0 Internasjonal