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dc.contributor.authorCoyle, Caoimhe M.
dc.contributor.authorLaws, K.R.
dc.date.accessioned2015-12-20T16:00:12Z
dc.date.available2015-12-20T16:00:12Z
dc.date.issued2015-04-21
dc.identifier.citationCoyle , C M & Laws , K R 2015 , ' The use of ketamine as an antidepressant: A systematic review and meta-analysis ' , Human Psychopharmacology: Clinical and Experimental , vol. 30 , no. 3 , pp. 152-163 . https://doi.org/10.1002/hup.2475
dc.identifier.issn0885-6222
dc.identifier.otherORCID: /0000-0002-5065-0867/work/124446514
dc.identifier.urihttp://hdl.handle.net/2299/16556
dc.descriptionThis is the peer reviewed version of the following article: Caoimhe M. Coyle, and Keith R. Laws, ‘The use of ketamine as an antidepressant: a systematic review and meta-analysis’, Human Psychopharmacology, Vol. 30 (3): 152-163, May 2015, which has been published in final form at https://doi.org/10.1002/hup.2475. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.
dc.description.abstractObjective The current meta-analysis examines the effects of ketamine infusion on depressive symptoms over time in major depressive disorder (MDD) and bipolar disorder (BD). Methods Following a systematic review of the literature, data were extracted from 21 studies (n = 437 receiving ketamine) and analysed at four post-infusion time points (4 h, 24 h, 7 days and 12-14 days). The moderating effects of several factors were assessed including: repeat/single infusion, diagnosis, open-label/participant-blind infusion, pre-post/placebo-controlled design and the sex of patients. Results Effect sizes were significantly larger for repeat than single infusion at 4 h, 24 h and 7 days. For single infusion studies, effect sizes were large and significant at 4 h, 24 h and 7 days. The percentage of males was a predictor of antidepressant response at 7 days. Effect sizes for open-label and participant-blind infusions were not significantly different at any time point. Conclusions Single ketamine infusions elicit a significant antidepressant effect from 4 h to 7 days; the small number of studies at 12-14 days post infusion failed to reach significance. Results suggest a discrepancy in peak response time depending upon primary diagnosis - 24 h for MDD and 7 days for BD. The majority of published studies have used pre-post comparison; further placebo-controlled studies would help to clarify the effect of ketamine over time.en
dc.format.extent12
dc.format.extent846038
dc.language.isoeng
dc.relation.ispartofHuman Psychopharmacology: Clinical and Experimental
dc.subjectbipolar disorder
dc.subjectdepression
dc.subjectketamine
dc.subjectmajor depressive disorder
dc.subjectClinical Neurology
dc.subjectPsychiatry and Mental health
dc.subjectNeurology
dc.subjectPharmacology (medical)
dc.titleThe use of ketamine as an antidepressant: : A systematic review and meta-analysisen
dc.contributor.institutionHealth & Human Sciences Research Institute
dc.contributor.institutionSchool of Life and Medical Sciences
dc.contributor.institutionDepartment of Psychology
dc.contributor.institutionPsychology
dc.contributor.institutionCognitive Neuropsychology
dc.description.statusPeer reviewed
rioxxterms.versionofrecord10.1002/hup.2475
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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