PMID- 30543451 OWN - NLM STAT- MEDLINE DCOM- 20190513 LR - 20200225 IS - 1557-7708 (Electronic) IS - 1075-5535 (Print) IS - 1075-5535 (Linking) VI - 25 IP - 4 DP - 2019 Apr TI - Cannabidiol in the Treatment of Post-Traumatic Stress Disorder: A Case Series. PG - 392-397 LID - 10.1089/acm.2018.0437 [doi] AB - OBJECTIVES: Cannabidiol (CBD) is a non-psychotomimetic cannabinoid compound that is found in plants of the genus Cannabis. Preclinical research has suggested that CBD may have a beneficial effect in rodent models of post-traumatic stress disorder (PTSD). This effect is believed to be due to the action of CBD on the endocannabinoid system. CBD has seen a recent surge in research regarding its potential value in a number of neuro-psychiatric conditions. This is the first study to date examining the clinical benefit of CBD for patients with PTSD. METHODS: This retrospective case series examines the effect of oral CBD administration on symptoms of PTSD in a series of 11 adult patients at an outpatient psychiatry clinic. CBD was given on an open-label, flexible dosing regimen to patients diagnosed with PTSD by a mental health professional. Patients also received routine psychiatric care, including concurrent treatment with psychiatric medications and psychotherapy. The length of the study was 8 weeks. PTSD symptom severity was assessed every 4 weeks by patient-completed PTSD Checklist for the DSM-5 (PCL-5) questionnaires. RESULTS: From the total sample of 11 patients, 91% (n = 10) experienced a decrease in PTSD symptom severity, as evidenced by a lower PCL-5 score at 8 weeks than at their initial baseline. The mean total PCL-5 score decreased 28%, from a mean baseline score of 51.82 down to 37.14, after eight consecutive weeks of treatment with CBD. CBD was generally well tolerated, and no patients discontinued treatment due to side effects. CONCLUSIONS: Administration of oral CBD in addition to routine psychiatric care was associated with PTSD symptom reduction in adults with PTSD. CBD also appeared to offer relief in a subset of patients who reported frequent nightmares as a symptom of their PTSD. Additional clinical investigation, including double-blind, placebo-controlled trials, would be necessary to further substantiate the response to CBD that was observed in this study. FAU - Elms, Lucas AU - Elms L AD - 1 Rocky Vista University, Osteopathic Medical Student IV, Parker, CO. FAU - Shannon, Scott AU - Shannon S AD - 2 Department of Psychiatry, University of Colorado Denver, Denver, CO. FAU - Hughes, Shannon AU - Hughes S AD - 3 School of Social Work, Colorado State University College of Health and Human Sciences, Fort Collins, CO. FAU - Lewis, Nicole AU - Lewis N AD - 4 Department of Naturopathic Medicine, Wholeness Center, Fort Collins, CO. LA - eng PT - Journal Article DEP - 20181213 PL - United States TA - J Altern Complement Med JT - Journal of alternative and complementary medicine (New York, N.Y.) JID - 9508124 RN - 19GBJ60SN5 (Cannabidiol) SB - IM CIN - J Altern Complement Med. 2020 Apr;26(4):349-350. PMID: 31825237 CIN - J Altern Complement Med. 2020 Apr;26(4):259-260. PMID: 32109134 MH - Administration, Oral MH - Adult MH - Anxiety MH - Cannabidiol/administration & dosage/*therapeutic use MH - Dreams MH - Female MH - Humans MH - Male MH - Middle Aged MH - Retrospective Studies MH - Stress Disorders, Post-Traumatic/*drug therapy/epidemiology MH - Treatment Outcome MH - Young Adult PMC - PMC6482919 OTO - NOTNLM OT - PTSD OT - anxiety OT - cannabidiol OT - cannabis OT - nightmares OT - post-traumatic stress disorder COIS- S.S., MD has published four professional books in the area of Integrative Mental Health. Dr. S.S. is a Principal Investigator for a Phase III study of MDMA assisted psychotherapy for severe PTSD and receives compensation for his clinical work from a nonprofit corporation, the Multidisciplinary Association for Psychedelic Studies. Dr. S.H., Dr. N.L., and Mr. L.E. report no competing financial interests. EDAT- 2018/12/14 06:00 MHDA- 2019/05/14 06:00 PMCR- 2019/04/09 CRDT- 2018/12/14 06:00 PHST- 2018/12/14 06:00 [pubmed] PHST- 2019/05/14 06:00 [medline] PHST- 2018/12/14 06:00 [entrez] PHST- 2019/04/09 00:00 [pmc-release] AID - 10.1089/acm.2018.0437 [pii] AID - 10.1089/acm.2018.0437 [doi] PST - ppublish SO - J Altern Complement Med. 2019 Apr;25(4):392-397. doi: 10.1089/acm.2018.0437. Epub 2018 Dec 13.