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Hydrocortisone administration for reducing post-traumatic stress symptoms: A systematic review and meta-analysis

Authors :
Oswald D. Kothgassner
Susanne Fischer
Paul L. Plener
Joy Edobor
Marie Pellegrini
Vito Giordano
Andreas Goreis
Mercedes M. Huscsava
University of Zurich
Kothgassner, Oswald D
Source :
Psychoneuroendocrinology. 126
Publication Year :
2020

Abstract

Background Post-traumatic stress disorder (PTSD) is a debilitating disorder that is often accompanied by alterations in the hypothalamic-pituitary (HPA) axis. While there is abundant evidence for the efficacy of psychological therapies in reducing post-traumatic stress symptoms, barely anything is known about pharmacological interventions. Given the role of the HPA axis in the pathophysiology of PTSD, the aim of this study was to provide the first meta-analysis of Hydrocortisone as a potential treatment for this condition. Method A systematic review of randomized-controlled trials (RCTs) was conducted to investigate the efficacy of hydrocortisone in the prevention and curative treatment of post-traumatic stress symptoms. This study was pre-registered with the OSF (doi:10.17605/OSF.IO/GJAZF). Findings Eight studies (9 effect sizes) covering 362 participants met our inclusion criteria. We found that Hydrocortisone as compared to placebo significantly reduced PTSD symptoms (d = 0.96, 95% Cl 0.22–1.69 p = 0.011) and PTSD incidence (logRR = 0.85, 95% CI 1.12–1.59, p = 0.023). Subgroup analyses revealed a significant effect of Hydrocortisone when it was administered in a preventative context (d = 1.50; 95%CI 0.30–2.69, p = 0.014), but not when it was administered in a curative context (d = 0.28; 95%CI −0.11 to 0.66, p = 0.161). Conclusion Hydrocortisone appears to be a promising and efficient low-cost medication for the prevention of PTSD. However, the small number of included studies and their limited methodological quality emphasize the need for further rigorous studies in this field.

Details

ISSN :
18733360
Volume :
126
Database :
OpenAIRE
Journal :
Psychoneuroendocrinology
Accession number :
edsair.doi.dedup.....ac3fc1f250bba9f98a4f59cdbab8128f