Ketamine for bipolar depression: an updated systematic review

Background: The therapeutic potential of subanesthetic doses of ketamine appears promising in unipolar depression; however, its effectiveness in treating bipolar depression (BD) remains uncertain. Objective: This systematic review aimed to summarize findings on the use of ketamine for the treatment...

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Main Authors: Farhan Fancy, Sipan Haikazian, Danica E. Johnson, David C. J. Chen-Li, Anastasia Levinta, Muhammad I. Husain, Rodrigo B. Mansur, Joshua D. Rosenblat
Format: Article
Language:English
Published: SAGE Publishing 2023-09-01
Series:Therapeutic Advances in Psychopharmacology
Online Access:https://doi.org/10.1177/20451253231202723
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author Farhan Fancy
Sipan Haikazian
Danica E. Johnson
David C. J. Chen-Li
Anastasia Levinta
Muhammad I. Husain
Rodrigo B. Mansur
Joshua D. Rosenblat
author_facet Farhan Fancy
Sipan Haikazian
Danica E. Johnson
David C. J. Chen-Li
Anastasia Levinta
Muhammad I. Husain
Rodrigo B. Mansur
Joshua D. Rosenblat
author_sort Farhan Fancy
collection DOAJ
description Background: The therapeutic potential of subanesthetic doses of ketamine appears promising in unipolar depression; however, its effectiveness in treating bipolar depression (BD) remains uncertain. Objective: This systematic review aimed to summarize findings on the use of ketamine for the treatment of BD by assessing its efficacy, safety, and tolerability. Design: Systematic review. Methods: We conducted a systematic review of studies that investigated the use of ketamine for adults with BD. We searched PubMed and Embase for relevant randomized-controlled trials, open-label trials, and retrospective chart analyses published from inception to 13 March 2023. Results: Eight studies were identified [pooled n  = 235; mean (SD) age: 45.55 (5.54)]. All participants who received intravenous (IV) ketamine were administered a dose of 0.5–0.75 mg/kg as an adjunctive treatment to a mood-stabilizing agent, whereas participants who received esketamine were administered a dosage ranging from 28 to 84 mg. Flexible dosing was used in real-world analyses. A total of 48% of participants receiving ketamine achieved a response (defined as ⩾50% reduction in baseline depression severity), whereas only 5% achieved a response with a placebo. Real-world studies demonstrated lower rates of response (30%) compared to the average across clinical trials (63%). Reductions in suicidal ideation were noted in some studies, although not all findings were statistically significant. Ketamine and esketamine were well tolerated in most participants; however, six participants (2% of the overall sample pool, 5 receiving ketamine) developed hypomanic/manic symptoms after infusions. Significant dissociative symptoms were observed at the 40-min mark in some trials. Conclusion: Preliminary evidence suggests IV ketamine as being safe and effective for the treatment of BD. Future studies should focus on investigating the effects of repeated acute and maintenance infusions using a randomized study design.
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spelling doaj.art-44b33ffad39e4c3d948797754231f4ab2023-09-27T09:03:37ZengSAGE PublishingTherapeutic Advances in Psychopharmacology2045-12612023-09-011310.1177/20451253231202723Ketamine for bipolar depression: an updated systematic reviewFarhan FancySipan HaikazianDanica E. JohnsonDavid C. J. Chen-LiAnastasia LevintaMuhammad I. HusainRodrigo B. MansurJoshua D. RosenblatBackground: The therapeutic potential of subanesthetic doses of ketamine appears promising in unipolar depression; however, its effectiveness in treating bipolar depression (BD) remains uncertain. Objective: This systematic review aimed to summarize findings on the use of ketamine for the treatment of BD by assessing its efficacy, safety, and tolerability. Design: Systematic review. Methods: We conducted a systematic review of studies that investigated the use of ketamine for adults with BD. We searched PubMed and Embase for relevant randomized-controlled trials, open-label trials, and retrospective chart analyses published from inception to 13 March 2023. Results: Eight studies were identified [pooled n  = 235; mean (SD) age: 45.55 (5.54)]. All participants who received intravenous (IV) ketamine were administered a dose of 0.5–0.75 mg/kg as an adjunctive treatment to a mood-stabilizing agent, whereas participants who received esketamine were administered a dosage ranging from 28 to 84 mg. Flexible dosing was used in real-world analyses. A total of 48% of participants receiving ketamine achieved a response (defined as ⩾50% reduction in baseline depression severity), whereas only 5% achieved a response with a placebo. Real-world studies demonstrated lower rates of response (30%) compared to the average across clinical trials (63%). Reductions in suicidal ideation were noted in some studies, although not all findings were statistically significant. Ketamine and esketamine were well tolerated in most participants; however, six participants (2% of the overall sample pool, 5 receiving ketamine) developed hypomanic/manic symptoms after infusions. Significant dissociative symptoms were observed at the 40-min mark in some trials. Conclusion: Preliminary evidence suggests IV ketamine as being safe and effective for the treatment of BD. Future studies should focus on investigating the effects of repeated acute and maintenance infusions using a randomized study design.https://doi.org/10.1177/20451253231202723
spellingShingle Farhan Fancy
Sipan Haikazian
Danica E. Johnson
David C. J. Chen-Li
Anastasia Levinta
Muhammad I. Husain
Rodrigo B. Mansur
Joshua D. Rosenblat
Ketamine for bipolar depression: an updated systematic review
Therapeutic Advances in Psychopharmacology
title Ketamine for bipolar depression: an updated systematic review
title_full Ketamine for bipolar depression: an updated systematic review
title_fullStr Ketamine for bipolar depression: an updated systematic review
title_full_unstemmed Ketamine for bipolar depression: an updated systematic review
title_short Ketamine for bipolar depression: an updated systematic review
title_sort ketamine for bipolar depression an updated systematic review
url https://doi.org/10.1177/20451253231202723
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