Low dose oral ketamine treatment in chronic suicidality: An open-label pilot study
Abstract Recently, low-dose ketamine has been proposed as a rapid-acting treatment option for suicidality. The majority of studies to date have utilised intravenous (IV) ketamine, however, this route of administration has limitations. On the other hand, oral ketamine can be administered in a range o...
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2021-02-01
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Series: | Translational Psychiatry |
Online Access: | https://doi.org/10.1038/s41398-021-01230-z |
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doaj-8b6d114acb28464ba4d72ade9bca35222021-02-07T12:50:52ZengNature Publishing GroupTranslational Psychiatry2158-31882021-02-011111910.1038/s41398-021-01230-zLow dose oral ketamine treatment in chronic suicidality: An open-label pilot studyAdem T. Can0Daniel F. Hermens1Megan Dutton2Cyrana C. Gallay3Emma Jensen4Monique Jones5Jennifer Scherman6Denise A. Beaudequin7Cian Yang8Paul E. Schwenn9Jim Lagopoulos10Thompson Institute, University of the Sunshine CoastThompson Institute, University of the Sunshine CoastThompson Institute, University of the Sunshine CoastThompson Institute, University of the Sunshine CoastThompson Institute, University of the Sunshine CoastThompson Institute, University of the Sunshine CoastThompson Institute, University of the Sunshine CoastThompson Institute, University of the Sunshine CoastThompson Institute, University of the Sunshine CoastThompson Institute, University of the Sunshine CoastThompson Institute, University of the Sunshine CoastAbstract Recently, low-dose ketamine has been proposed as a rapid-acting treatment option for suicidality. The majority of studies to date have utilised intravenous (IV) ketamine, however, this route of administration has limitations. On the other hand, oral ketamine can be administered in a range of settings, which is important in treating suicidality, although studies as to safety and feasibility are lacking. n = 32 adults (aged 22–72 years; 53% female) with chronic suicidal thoughts participated in the Oral Ketamine Trial on Suicidality (OKTOS), an open-label trial of sub-anaesthetic doses of oral ketamine over 6 weeks. Participants commenced with 0.5 mg/kg of ketamine, which was titrated to a maximum 3.0 mg/kg. Follow-up assessments occurred at 4 weeks after the final dose. The primary outcome measure was the Beck Scale for Suicide Ideation (BSS) and secondary measures included scales for suicidality and depressive symptoms, and measures of functioning and well-being. Mean BSS scores significantly reduced from a high level of suicidal ideation at the pre-ketamine (week 0) timepoint to below the clinical threshold at the post-ketamine (week 6) timepoint. The proportion of participants that achieved clinical improvement within the first 6 weeks was 69%, whereas 50% achieved a significant improvement by the follow-up (week 10) timepoint. Six weeks of oral ketamine treatment in participants with chronic suicidality led to significant reduction in suicidal ideation. The response observed in this study is consistent with IV ketamine trials, suggesting that oral administration is a feasible and tolerable alternative treatment for chronic suicidality.https://doi.org/10.1038/s41398-021-01230-z |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Adem T. Can Daniel F. Hermens Megan Dutton Cyrana C. Gallay Emma Jensen Monique Jones Jennifer Scherman Denise A. Beaudequin Cian Yang Paul E. Schwenn Jim Lagopoulos |
spellingShingle |
Adem T. Can Daniel F. Hermens Megan Dutton Cyrana C. Gallay Emma Jensen Monique Jones Jennifer Scherman Denise A. Beaudequin Cian Yang Paul E. Schwenn Jim Lagopoulos Low dose oral ketamine treatment in chronic suicidality: An open-label pilot study Translational Psychiatry |
author_facet |
Adem T. Can Daniel F. Hermens Megan Dutton Cyrana C. Gallay Emma Jensen Monique Jones Jennifer Scherman Denise A. Beaudequin Cian Yang Paul E. Schwenn Jim Lagopoulos |
author_sort |
Adem T. Can |
title |
Low dose oral ketamine treatment in chronic suicidality: An open-label pilot study |
title_short |
Low dose oral ketamine treatment in chronic suicidality: An open-label pilot study |
title_full |
Low dose oral ketamine treatment in chronic suicidality: An open-label pilot study |
title_fullStr |
Low dose oral ketamine treatment in chronic suicidality: An open-label pilot study |
title_full_unstemmed |
Low dose oral ketamine treatment in chronic suicidality: An open-label pilot study |
title_sort |
low dose oral ketamine treatment in chronic suicidality: an open-label pilot study |
publisher |
Nature Publishing Group |
series |
Translational Psychiatry |
issn |
2158-3188 |
publishDate |
2021-02-01 |
description |
Abstract Recently, low-dose ketamine has been proposed as a rapid-acting treatment option for suicidality. The majority of studies to date have utilised intravenous (IV) ketamine, however, this route of administration has limitations. On the other hand, oral ketamine can be administered in a range of settings, which is important in treating suicidality, although studies as to safety and feasibility are lacking. n = 32 adults (aged 22–72 years; 53% female) with chronic suicidal thoughts participated in the Oral Ketamine Trial on Suicidality (OKTOS), an open-label trial of sub-anaesthetic doses of oral ketamine over 6 weeks. Participants commenced with 0.5 mg/kg of ketamine, which was titrated to a maximum 3.0 mg/kg. Follow-up assessments occurred at 4 weeks after the final dose. The primary outcome measure was the Beck Scale for Suicide Ideation (BSS) and secondary measures included scales for suicidality and depressive symptoms, and measures of functioning and well-being. Mean BSS scores significantly reduced from a high level of suicidal ideation at the pre-ketamine (week 0) timepoint to below the clinical threshold at the post-ketamine (week 6) timepoint. The proportion of participants that achieved clinical improvement within the first 6 weeks was 69%, whereas 50% achieved a significant improvement by the follow-up (week 10) timepoint. Six weeks of oral ketamine treatment in participants with chronic suicidality led to significant reduction in suicidal ideation. The response observed in this study is consistent with IV ketamine trials, suggesting that oral administration is a feasible and tolerable alternative treatment for chronic suicidality. |
url |
https://doi.org/10.1038/s41398-021-01230-z |
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