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Effects of Ketamine vs. Midazolam in Adolescent Treatment Resistant Depression.

Andrea Macejova, Veronika Kovacova, Ingrid Tonhajzerova, Zuzana Visnovcova, Nikola Ferencova, Zuzana Mlyncekova, Tomas Kukucka, Igor Ondrejka

Pharmaceuticals (Basel, Switzerland) December 4, 2024 DOI: 10.3390/ph17121627 via PubMed

Summary

AI-generated from the abstract

In a sample of 55 adolescent females with treatment-resistant depression, intravenous ketamine reduced depressive and anxiety symptoms over a short-term period, with particular efficacy in alleviating inner tension compared to midazolam. At 2 hours after the initial infusion, 33% of the ketamine group and 14% of the midazolam group responded on the Montgomery-Åsberg Depression Rating Scale; at 24 hours after treatment ended, 59% and 46% responded, respectively. Both groups showed significant reductions in symptoms from baseline at both time points. The findings suggest ketamine may offer specific advantages for symptom relief in this rarely studied population.

Study at a glance

Characteristics Randomized controlled trial Peer reviewed
Sample size 55
Population Adolescent females with treatment-resistant depression
Intervention Intravenous ketamine
Duration 2 hours after initial infusion and 24 hours after the end of treatment
Topics Depression Ketamine
Keywords Adolescent age Midazolam Novel antidepressants #mental-health mental wellness
Citations 7
Key finding Ketamine reduced depressive and anxiety symptoms over a short-term period and was particularly effective at alleviating inner tension compared to midazolam in adolescent females with treatment-resistant depression.

Abstract

Background: Adolescent treatment resistant depression (TRD) is increasing in recent years. While ketamine showed rapid antidepressant effects in adult TRD studies, research on its effectiveness in adolescents is limited. Methods: This study examines the effects of intravenous ketamine vs. midazolam on depressive and anxiety symptomatology assessed by the Montgomery-Åsberg Depression Rating Scale (MADRS), Hamilton Anxiety Rating Scale (HAM-A), and Children's Depression Inventory (CDI) at two time points-2 h after initial infusion (T0+2h) and 24 h after the end of the treatment (Te+24h) in a sample of 55 adolescent TRD females (27 receiving ketamine, 28 midazolam). Results: At T0+2h, within-group comparisons revealed a significant reduction in MADRS and HAM-A scores compared to baseline in the ketamine and midazolam groups. At Te+24h, both groups demonstrated similar significant reductions in MADRS, HAM-A, and CDI scores compared to baseline. The MADRS assessment in the ketamine group showed 33% and 59% responders, and in the midazolam group, 14% and 46% responders at T0+2h and Te+24h, respectively. HAM-A evaluation in the ketamine group revealed 33% and 56% responders, and in the midazolam group, 11% and 39% responders at T0+2h and at Te+24h, respectively. CDI rating discovered 11% and 44% responders in the ketamine group and 4% and 21% responders in the midazolam group at T0+2h and Te+24h, respectively. Moreover, inner tension significantly decreased in ketamine compared to the midazolam group at Te+24h. Conclusions: Ketamine showed a reduction in depressive and anxiety symptoms during a short-term period with particular efficacy in alleviating inner tension over midazolam, suggesting its potential advantages in specific symptom relief in rarely studied adolescent TRD.

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