<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ragnhildstveit A</submitter><funding>US Department of Veterans Affairs, Clinical Sciences R&amp;amp;D</funding><funding>NCATS NIH HHS</funding><funding>American Foundation for Suicide Prevention</funding><funding>Beth K and Stuart Yudofsky Chair in the Neuropsychiatry of Military Post Traumatic Stress Syndrome</funding><pagination>20451253231154125</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9989422</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13</volume><pubmed_abstract>Posttraumatic stress disorder (PTSD) is a devastating condition, for which there are few pharmacological agents, often with a delayed onset of action and poor efficacy. Trauma-focused psychotherapies are further limited by few trained providers and low patient engagement. This frequently results in disease chronicity as well as psychiatric and medical comorbidity, with considerable negative impact on quality of life. As such, off-label interventions are commonly used for PTSD, particularly in chronic refractory cases. Ketamine, an &lt;i>N&lt;/i>-methyl-D-aspartate (NDMA) receptor antagonist, has recently been indicated for major depression, exhibiting rapid and robust antidepressant effects. It also shows transdiagnostic potential for an array of psychiatric disorders. Here, we synthesize clinic</pubmed_abstract><journal>Therapeutic advances in psychopharmacology</journal><pubmed_title>The potential of ketamine for posttraumatic stress disorder: a review of clinical evidence.</pubmed_title><pmcid>PMC9989422</pmcid><funding_grant_id>YIG-0-004-16</funding_grant_id><funding_grant_id>IK2CX001873</funding_grant_id><funding_grant_id>R01 DA030386</funding_grant_id><funding_grant_id>UL1 TR001863</funding_grant_id><pubmed_authors>Ragnhildstveit A</pubmed_authors><pubmed_authors>Abdallah CG</pubmed_authors><pubmed_authors>Averill LA</pubmed_authors><pubmed_authors>Bass LC</pubmed_authors><pubmed_authors>Roscoe J</pubmed_authors><pubmed_authors>Averill CL</pubmed_authors></additional><is_claimable>false</is_claimable><name>The potential of ketamine for posttraumatic stress disorder: a review of clinical evidence.</name><description>Posttraumatic stress disorder (PTSD) is a devastating condition, for which there are few pharmacological agents, often with a delayed onset of action and poor efficacy. Trauma-focused psychotherapies are further limited by few trained providers and low patient engagement. This frequently results in disease chronicity as well as psychiatric and medical comorbidity, with considerable negative impact on quality of life. As such, off-label interventions are commonly used for PTSD, particularly in chronic refractory cases. Ketamine, an &lt;i>N&lt;/i>-methyl-D-aspartate (NDMA) receptor antagonist, has recently been indicated for major depression, exhibiting rapid and robust antidepressant effects. It also shows transdiagnostic potential for an array of psychiatric disorders. Here, we synthesize clinic</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2025-04-19T02:38:45.172Z</modification><creation>2025-02-19T04:43:51.915Z</creation></dates><accession>S-EPMC9989422</accession><cross_references><pubmed>36895431</pubmed><doi>10.1177/20451253231154125</doi></cross_references></HashMap>