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Intranasal Oxytocin to Prevent Posttraumatic Stress Disorder Symptoms: A Randomized Controlled Trial in Emergency Department Patients

Authors :
Jan S. K. Luitse
Saskia B. J. Koch
Dick J. Veltman
Miranda Olff
Adriaan Honig
Tessa H. Biesheuvel
J. Carel Goslings
Jessie L. Frijling
Mirjam van Zuiden
Laura Nawijn
APH - Global Health
ANS - Mood, Anxiety, Psychosis, Stress & Sleep
APH - Mental Health
Adult Psychiatry
Other departments
Surgery
AMS - Ageing & Morbidty
Other Research
Psychiatry
Amsterdam Neuroscience - Mood, Anxiety, Psychosis, Stress & Sleep
Anatomy and neurosciences
APH - Personalized Medicine
Source :
Biological psychiatry, 81(12), 1030-1040. Elsevier USA, Biological Psychiatry, 81(12), 1030-1040. Elsevier USA, van Zuiden, M, Frijling, J L, Nawijn, L, Koch, S B J, Goslings, J C, Luitse, J S, Biesheuvel, T H, Honig, A, Veltman, D J & Olff, M 2017, ' Intranasal Oxytocin to Prevent Posttraumatic Stress Disorder Symptoms : A Randomized Controlled Trial in Emergency Department Patients ', Biological Psychiatry, vol. 81, no. 12, pp. 1030-1040 . https://doi.org/10.1016/j.biopsych.2016.11.012
Publication Year :
2017

Abstract

Background There are currently few preventive interventions available for posttraumatic stress disorder (PTSD). Intranasal oxytocin administration early after trauma may prevent PTSD, because oxytocin administration was previously found to beneficially impact PTSD vulnerability factors, including neural fear responsiveness, peripheral stress reactivity, and socioemotional functioning. Therefore, we investigated the effects of intranasal oxytocin administration early after trauma on subsequent clinician-rated PTSD symptoms. We then assessed whether baseline characteristics moderated the intervention's effects. Methods We performed a multicenter, randomized, double-blind, placebo-controlled clinical trial. Adult emergency department patients with moderate to severe acute distress ( n = 120; 85% accident victims) were randomized to intranasal oxytocin (8 days/40 IU twice daily) or placebo (8 days/10 puffs twice daily), initiated within 12 days posttrauma. The Clinician-Administered PTSD Scale (CAPS) was administered at baseline (within 10 days posttrauma) and at 1.5, 3, and 6 months posttrauma. The intention-to-treat sample included 107 participants (oxytocin: n = 53; placebo: n = 54). Results We did not observe a significant group difference in CAPS total score at 1.5 months posttrauma (primary outcome) or across follow-up (secondary outcome). Secondary analyses showed that participants with high baseline CAPS scores receiving oxytocin had significantly lower CAPS scores across follow-up than participants with high baseline CAPS scores receiving placebo. Conclusions Oxytocin administration early after trauma did not attenuate clinician-rated PTSD symptoms in all trauma-exposed participants with acute distress. However, participants with high acute clinician-rated PTSD symptom severity did show beneficial effects of oxytocin. Although replication is warranted, these findings suggest that oxytocin administration is a promising preventive intervention for PTSD for individuals with high acute PTSD symptoms.

Details

Language :
English
ISSN :
00063223
Database :
OpenAIRE
Journal :
Biological psychiatry, 81(12), 1030-1040. Elsevier USA, Biological Psychiatry, 81(12), 1030-1040. Elsevier USA, van Zuiden, M, Frijling, J L, Nawijn, L, Koch, S B J, Goslings, J C, Luitse, J S, Biesheuvel, T H, Honig, A, Veltman, D J & Olff, M 2017, ' Intranasal Oxytocin to Prevent Posttraumatic Stress Disorder Symptoms : A Randomized Controlled Trial in Emergency Department Patients ', Biological Psychiatry, vol. 81, no. 12, pp. 1030-1040 . https://doi.org/10.1016/j.biopsych.2016.11.012
Accession number :
edsair.doi.dedup.....75bf1b6d5c47ba943942ebe8b5b6a64b