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Effects of Intravenous Ketamine on Posttraumatic Stress Disorder (PTSD): A Systematic Review

  • Liyang Yin
  • , Andy Lu
  • , Gia Han Le
  • , Christine E. Dri
  • , Sabrina Wong
  • , Kayla M. Teopiz
  • , Heidi Xu
  • , Roger Ho
  • , Taeho Greg Rhee
  • , Heidi Ka Ying Lo
  • , Maria Christina Sioufi
  • , Yang Jing Zheng
  • , Hezekiah C.T. Au
  • , Hernan F. Guillen-Burgos
  • , Bing Cao
  • , Roger S. McIntyre
  • Brain and Cognition Discovery Foundation
  • The University of Western Ontario
  • University of Toronto
  • University Health Network
  • National University of Singapore
  • Hong Kong University of Science and Technology
  • Yale University
  • University of Connecticut
  • The University of Hong Kong
  • Universidad Simón Bolívar
  • Center for Clinical and Translational Research
  • Southwest University

Research output: Contribution to journalReview articlepeer-review

Abstract

Introduction: Posttraumatic stress disorder (PTSD) is a mental disorder resulting from exposure to traumatic events. Evidence suggests that ketamine may be efficacious in treating PTSD, however, ketamine's mechanisms in treating PTSD remain unclear. Herein, this review aims to evaluate the clinical outcomes of ketamine treatment in persons with PTSD and investigate the possible neurobiological mechanisms underlying ketamine's therapeutic effect in PTSD. Methods: A systematic search was conducted on PubMed and OVID (MEDLINE, Embase, PsychINFO) from inception until September 2025. Randomized controlled trials reporting on the effects of intravenous ketamine to treat PTSD were included. Results: Seven studies with a total of 323 participants were included in this review. Ketamine administration meaningfully improved PTSD symptoms in two trials as evidenced by significant improvement on the Clinician-Administered PTSD Scale for DSM-5 (CAPS-5) and the Impact of Event Scale-Revised (IES-R) compared to control/placebo. Multi-infusion administration schedules achieved greater clinical outcomes when compared to single-dose administration schedules. Preliminary evidence suggests that repeated lower doses (0.2mg/kg) of ketamine were more efficacious in sustaining treatment effects than standard doses (0.5mg/kg). For persons receiving ketamine, an association was observed between top-down inhibition of the amygdala originating in the ventromedial prefrontal cortex (vmPFC) and symptom improvement. Conclusion: Our results suggest that intravenous ketamine may be efficacious in the treatment of PTSD. Subsequent studies should attempt to evaluate the additive effect of combining ketamine with psychotherapeutic interventions as well as determining mechanistic pathways mediating symptom relief in persons with PTSD.

Original languageEnglish
Pages (from-to)95-107
Number of pages13
JournalActa Psychiatrica Scandinavica
Volume153
Issue number2
DOIs
StatePublished - Feb 2026

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Ketalar
  • N-methyl-D-aspartate (NMDA) receptor
  • ketamine
  • post-traumatic stress disorder
  • posttraumatic stress symptoms
  • trauma-related stress
  • Administration, Intravenous
  • Ketamine/administration & dosage
  • Stress Disorders, Post-Traumatic/drug therapy
  • Humans
  • Randomized Controlled Trials as Topic

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