EPV580 - Clinical Outcomes of Ketamine Therapy for Depression, Anxiety, and PTSD in Post-TBI Patients
EPV580
Clinical Outcomes of Ketamine Therapy for Depression, Anxiety, and PTSD in Post-TBI Patients
W. Aldulaimy 1, A. Shah 2,*
1Psychiatry, 2Texas Institute for Graduate Medical Education and Research , San Antonio, United States
Introduction: TBI patients often suffer from severe, treatment-resistant depression and PTSD. Ketamine shows promise in non-TBI populations, but its efficacy in TBI patients needs exploration for efficacy and tolerability.
Objectives: Evaluate ketamine's clinical effectiveness and safety (PHQ-9, GAD-7, PCL-5 scores) in post-TBI patients, comparing IM, intranasal, and oral routes.
Methods: Design: Retrospective chart review of 35 adult TBI patients (mean age 38.4; TBI 3.5 years prior).
Formulations: IM (0.5-0.75 mg/kg), Intranasal (84 mg esketamine), and Oral Dissolving Tablets (100-300 mg).
Measures: PHQ-9, GAD-7, and PCL-5 scores.
Analysis: Efficacy by % reduction, response (≥50% reduction), and remission (PHQ-9 < 5, PCL-5 < 20).
Results: Magnitude: Large effect sizes
observed (32.7% GAD-7/ODT to 65.6%
PCL-5/Nasal).
Clinical: 72% response, 45% remission
rates.
Route-Dependent: Parenteral
(IM/Nasal) outperformed ODT due to better bioavailability.
Rapid Onset: Initial improvement within 5-10 days.
Safety: Favorable profile with mild, transient adverse events.
Conclusions: Magnitude: Large effect sizes
observed (32.7% GAD-7/ODT to 65.6%
PCL-5/Nasal).
Clinical: 72% response, 45% remission
rates.
Route-Dependent: Parenteral
(IM/Nasal) outperformed ODT due to better bioavailability.
Rapid Onset: Initial improvement within 5-10 days.
Safety: Favorable profile with mild, transient adverse events.
1. Directions
Disclosure of Interest: None Declared
