Psilocybin with psychological support for treatment-resistant depression: six-month follow-up. Carhart-Harris, R., L., Bolstridge, M., Day, C., M., Rucker, J., J., Watts, R., Erritzoe, D., Kaelen, M., Giribaldi, B., Bloomfield, M., Pilling, S., Rickard, J., A., Forbes, B., Feilding, A., Taylor, D., Curran, H., V., & Nutt, D., J. Psychopharmacology, 235(2):399-408, 2018.
Psilocybin with psychological support for treatment-resistant depression: six-month follow-up. [link]Website  abstract   bibtex   
RATIONALE Recent clinical trials are reporting marked improvements in mental health outcomes with psychedelic drug-assisted psychotherapy. OBJECTIVES Here, we report on safety and efficacy outcomes for up to 6 months in an open-label trial of psilocybin for treatment-resistant depression. METHODS Twenty patients (six females) with (mostly) severe, unipolar, treatment-resistant major depression received two oral doses of psilocybin (10 and 25 mg, 7 days apart) in a supportive setting. Depressive symptoms were assessed from 1 week to 6 months post-treatment, with the self-rated QIDS-SR16 as the primary outcome measure. RESULTS Treatment was generally well tolerated. Relative to baseline, marked reductions in depressive symptoms were observed for the first 5 weeks post-treatment (Cohen's d = 2.2 at week 1 and 2.3 at week 5, both p < 0.001); nine and four patients met the criteria for response and remission at week 5. Results remained positive at 3 and 6 months (Cohen's d = 1.5 and 1.4, respectively, both p < 0.001). No patients sought conventional antidepressant treatment within 5 weeks of psilocybin. Reductions in depressive symptoms at 5 weeks were predicted by the quality of the acute psychedelic experience. CONCLUSIONS Although limited conclusions can be drawn about treatment efficacy from open-label trials, tolerability was good, effect sizes large and symptom improvements appeared rapidly after just two psilocybin treatment sessions and remained significant 6 months post-treatment in a treatment-resistant cohort. Psilocybin represents a promising paradigm for unresponsive depression that warrants further research in double-blind randomised control trials.
@article{
 title = {Psilocybin with psychological support for treatment-resistant depression: six-month follow-up.},
 type = {article},
 year = {2018},
 identifiers = {[object Object]},
 keywords = {5-HT2AR,Depression,Hallucinogen,Mood,Psilocybin,Psychedelic,Psychotherapy,Serotonin,Treatment-resistant depression},
 pages = {399-408},
 volume = {235},
 websites = {https://doi.org/10.1007/s00213-017-4771-x,http://www.ncbi.nlm.nih.gov/pubmed/29119217%0Ahttp://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=PMC5813086},
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 last_modified = {2019-10-23T13:46:51.508Z},
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 abstract = {RATIONALE Recent clinical trials are reporting marked improvements in mental health outcomes with psychedelic drug-assisted psychotherapy. OBJECTIVES Here, we report on safety and efficacy outcomes for up to 6 months in an open-label trial of psilocybin for treatment-resistant depression. METHODS Twenty patients (six females) with (mostly) severe, unipolar, treatment-resistant major depression received two oral doses of psilocybin (10 and 25 mg, 7 days apart) in a supportive setting. Depressive symptoms were assessed from 1 week to 6 months post-treatment, with the self-rated QIDS-SR16 as the primary outcome measure. RESULTS Treatment was generally well tolerated. Relative to baseline, marked reductions in depressive symptoms were observed for the first 5 weeks post-treatment (Cohen's d = 2.2 at week 1 and 2.3 at week 5, both p < 0.001); nine and four patients met the criteria for response and remission at week 5. Results remained positive at 3 and 6 months (Cohen's d = 1.5 and 1.4, respectively, both p < 0.001). No patients sought conventional antidepressant treatment within 5 weeks of psilocybin. Reductions in depressive symptoms at 5 weeks were predicted by the quality of the acute psychedelic experience. CONCLUSIONS Although limited conclusions can be drawn about treatment efficacy from open-label trials, tolerability was good, effect sizes large and symptom improvements appeared rapidly after just two psilocybin treatment sessions and remained significant 6 months post-treatment in a treatment-resistant cohort. Psilocybin represents a promising paradigm for unresponsive depression that warrants further research in double-blind randomised control trials.},
 bibtype = {article},
 author = {Carhart-Harris, Robin Lester and Bolstridge, Mark and Day, Camilla M.J. and Rucker, James J.H. and Watts, Rosalind and Erritzoe, David and Kaelen, Mendel and Giribaldi, B and Bloomfield, Michael and Pilling, Steve and Rickard, James A. and Forbes, Ben and Feilding, Amanda and Taylor, David and Curran, H. Valerie and Nutt, David J.},
 journal = {Psychopharmacology},
 number = {2}
}

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