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Ketamine Treatment for Pediatric Refractory Obsessive: Five Open Label Cases.

Hannah S Ishimuro, Paula K Yanes-Lukin, Pablo H Goldberg, H Blair Simpson, Moira A Rynn

Journal of child and adolescent psychopharmacology April 1, 2025 DOI: 10.1089/cap.2024.0127 via PubMed

Summary

AI-generated from the abstract

In a small pilot trial, five adolescents with obsessive-compulsive disorder (OCD) who had not responded to first-line treatments received a single intravenous infusion of ketamine. All participants experienced mild dissociative symptoms in the 40 minutes after the infusion, but there were no abnormal vital signs, deaths, or suicidal thoughts during the two-week follow-up. Obsessive-compulsive symptom severity decreased immediately after the infusion but was not sustained over the study period. The average score on the Children's Yale-Brown Obsessive Compulsive Scale fell from 29 before treatment to 26.2 fourteen days later. The results suggest ketamine is well-tolerated in this population and warrants further testing of its efficacy.

Study at a glance

Characteristics Clinical pilot trial Open-label Pilot study Peer reviewed
Sample size 5
Population Adolescents with OCD who had failed first-line treatments
Intervention IV ketamine infusion
Dose 0.5 mg/kg
Duration Single infusion, 14-day follow-up
Topics Ketamine
Keywords Obsessive-compulsive disorder Ketamine therapy Adolescent mental health OCD Treatment Psychiatric research
Citations 6
Registration NCT02422290
Key finding Ketamine was well-tolerated in adolescents with refractory OCD, but the initial reduction in obsessive-compulsive symptom severity was not maintained over two weeks.

Abstract

Importance: Selective serotonin reuptake inhibitors (SSRIs) and cognitive behavioral therapy are the first-line treatments for pediatric obsessive-compulsive disorder (OCD) populations. Due to their limited effectiveness, additional treatment options are needed. A new potential pharmacological medication treatment avenue for OCD is intravenous (IV) ketamine. Objective: This study aimed to establish the feasibility, acceptability, and preliminary efficacy of an IV ketamine infusion for the treatment of refractory OCD in adolescents. Design: In this clinical pilot trial, every participant received IV ketamine infusion. Symptom severity and side effects were assessed daily for 2 weeks following the infusion. Setting: Study procedures were conducted at the New York State Psychiatric Institute, including a combination of in-person visits and phone calls. Participants: Five adolescents with OCD (age M, SD: 16.6 ± 1.5), who had previously failed trials of first-line treatments were enrolled. Intervention: All participants received an IV infusion of 0.5 mg/kg ketamine hydrochloride. Main Outcomes and Measures: A multimethod approach was applied, including physiological, self-report, and clinician-rated measures. To assess feasibility and acceptability, vital signs, electrocardiogram suicidality, self-reported adverse events, and dissociative symptoms were obtained. Obsessive-compulsive (OC) (Yale-Brown Obsessive Compulsive Challenge Scale, CY-BOCS) and depressive symptom severity, as well as global clinical impression, were assessed to investigate preliminary efficacy. Results: The mean (SD) pre- and 14-day posttreatment CY-BOCS were 29 (5.5) and 26.2 (5.6). There were no incidents of abnormal vital signs, mortality, or suicidal ideation in the 2 weeks following the infusion. All participants experienced mild dissociative symptoms in the 40 minutes after the IV ketamine infusion. Descriptively, OC symptom severity decreased immediately after the infusion but was not maintained over the course of the study. Conclusions and Clinical Significance: Ketamine is well-tolerated in adolescents with OCD and therefore appropriate for further efficacy testing. Trial Registration: ClinicalTrials.gov Identifier: NCT02422290.

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