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Acceptance of pharmaceutical cannabis substitution by cannabis using patients with schizophrenia
BACKGROUND: Cannabis-smoking patients with a psychotic disorder have poorer disease outcomes than non-cannabis-smoking patients with poorest outcomes in patients smoking high-potency cannabis (HPC) containing high Δ9-tetrahydrocannabinol (THC) and low cannabidiol (CBD). Quitting cannabis smoking or...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149068/ https://www.ncbi.nlm.nih.gov/pubmed/30236118 http://dx.doi.org/10.1186/s12954-018-0253-7 |
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author | van Amsterdam, Jan Vervloet, Jojanneke de Weert, Gerdien Buwalda, Victor J. A. Goudriaan, Anna E. van den Brink, Wim |
author_facet | van Amsterdam, Jan Vervloet, Jojanneke de Weert, Gerdien Buwalda, Victor J. A. Goudriaan, Anna E. van den Brink, Wim |
author_sort | van Amsterdam, Jan |
collection | PubMed |
description | BACKGROUND: Cannabis-smoking patients with a psychotic disorder have poorer disease outcomes than non-cannabis-smoking patients with poorest outcomes in patients smoking high-potency cannabis (HPC) containing high Δ9-tetrahydrocannabinol (THC) and low cannabidiol (CBD). Quitting cannabis smoking or substitution of HPC by cannabis variants containing less THC and/or more CBD may benefit these patients. The present study explores whether daily HPC-smoking patients with schizophrenia accept smoking such variants. METHODS: Twelve male patients were asked to smoke on six different occasions one joint: on two occasions, the cannabis they routinely smoke (HPC; not blind), and blind in random order; on two occasions, cannabis containing low THC and no CBD; and on two occasions, cannabis containing low THC and high CBD. RESULTS: Both substitute variants were appreciated, but patients preferred the HPC they usually smoked. The effect of the low THC/high CBD variant was reported by 32% to be too short and by 36% to be not strong enough, whereas this was reported by 5% and 64%, respectively, for the low THC cannabis variant. CONCLUSIONS: Based on these findings, a larger and longer study on the efficacy of cannabis substitution treatment in HPC-smoking patients with schizophrenia seems feasible and should be considered. TRIAL REGISTRATION: 2014-005540-17NL. Registered 22 October 2014, 2014-005540-17NL 20141215 CTA.xml |
format | Online Article Text |
id | pubmed-6149068 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61490682018-09-26 Acceptance of pharmaceutical cannabis substitution by cannabis using patients with schizophrenia van Amsterdam, Jan Vervloet, Jojanneke de Weert, Gerdien Buwalda, Victor J. A. Goudriaan, Anna E. van den Brink, Wim Harm Reduct J Brief Report BACKGROUND: Cannabis-smoking patients with a psychotic disorder have poorer disease outcomes than non-cannabis-smoking patients with poorest outcomes in patients smoking high-potency cannabis (HPC) containing high Δ9-tetrahydrocannabinol (THC) and low cannabidiol (CBD). Quitting cannabis smoking or substitution of HPC by cannabis variants containing less THC and/or more CBD may benefit these patients. The present study explores whether daily HPC-smoking patients with schizophrenia accept smoking such variants. METHODS: Twelve male patients were asked to smoke on six different occasions one joint: on two occasions, the cannabis they routinely smoke (HPC; not blind), and blind in random order; on two occasions, cannabis containing low THC and no CBD; and on two occasions, cannabis containing low THC and high CBD. RESULTS: Both substitute variants were appreciated, but patients preferred the HPC they usually smoked. The effect of the low THC/high CBD variant was reported by 32% to be too short and by 36% to be not strong enough, whereas this was reported by 5% and 64%, respectively, for the low THC cannabis variant. CONCLUSIONS: Based on these findings, a larger and longer study on the efficacy of cannabis substitution treatment in HPC-smoking patients with schizophrenia seems feasible and should be considered. TRIAL REGISTRATION: 2014-005540-17NL. Registered 22 October 2014, 2014-005540-17NL 20141215 CTA.xml BioMed Central 2018-09-20 /pmc/articles/PMC6149068/ /pubmed/30236118 http://dx.doi.org/10.1186/s12954-018-0253-7 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Brief Report van Amsterdam, Jan Vervloet, Jojanneke de Weert, Gerdien Buwalda, Victor J. A. Goudriaan, Anna E. van den Brink, Wim Acceptance of pharmaceutical cannabis substitution by cannabis using patients with schizophrenia |
title | Acceptance of pharmaceutical cannabis substitution by cannabis using patients with schizophrenia |
title_full | Acceptance of pharmaceutical cannabis substitution by cannabis using patients with schizophrenia |
title_fullStr | Acceptance of pharmaceutical cannabis substitution by cannabis using patients with schizophrenia |
title_full_unstemmed | Acceptance of pharmaceutical cannabis substitution by cannabis using patients with schizophrenia |
title_short | Acceptance of pharmaceutical cannabis substitution by cannabis using patients with schizophrenia |
title_sort | acceptance of pharmaceutical cannabis substitution by cannabis using patients with schizophrenia |
topic | Brief Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149068/ https://www.ncbi.nlm.nih.gov/pubmed/30236118 http://dx.doi.org/10.1186/s12954-018-0253-7 |
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