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Benefit of Tetrahydrocannabinol versus Cannabidiol for Common Palliative Care Symptoms
Objectives: To determine the relative contributions of tetrahydrocannabinol (THC) and cannabidiol (CBD) to patients' self-ratings of efficacy for common palliative care symptoms. Design: This is an electronic record-based retrospective cohort study. Model development used logistic regression wi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mary Ann Liebert, Inc., publishers
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776252/ https://www.ncbi.nlm.nih.gov/pubmed/31386592 http://dx.doi.org/10.1089/jpm.2018.0658 |
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author | Casarett, David J. Beliveau, Jessica N. Arbus, Michelle S. |
author_facet | Casarett, David J. Beliveau, Jessica N. Arbus, Michelle S. |
author_sort | Casarett, David J. |
collection | PubMed |
description | Objectives: To determine the relative contributions of tetrahydrocannabinol (THC) and cannabidiol (CBD) to patients' self-ratings of efficacy for common palliative care symptoms. Design: This is an electronic record-based retrospective cohort study. Model development used logistic regression with bootstrapped confidence intervals (CIs), with standard errors clustered to account for multiple observations by each patient. Setting: This is a national Canadian patient portal. Participants: A total of 2,431 patients participated. Main Outcome Measures: Self-ratings of efficacy of cannabis, defined as a three-point reduction in neuropathic pain, anorexia, anxiety symptoms, depressive symptoms, insomnia, and post-traumatic flashbacks. Results: We included 26,150 observations between October 1, 2017 and November 28, 2018. Of the six symptoms, response was associated with increased THC:CBD ratio for neuropathic pain (odds ratio [OR]: 3.58; 95% CI: 1.32–9.68; p = 0.012), insomnia (OR: 2.93; 95% CI: 1.75–4.91; p < 0.001), and depressive symptoms (OR: 1.63; 95% CI: 1.07–2.49; p = 0.022). Increased THC:CBD ratio was not associated with a greater response of post-traumatic stress disorder (PTSD)-related flashbacks (OR: 1.43; 95% CI: 0.60–3.41; p = 0.415) or anorexia (OR: 1.61; 95% CI: 0.70–3.73; p = 0.265). The response for anxiety symptoms was not significant (OR: 1.13; 95% CI: 0.77–1.64; p = 0.53), but showed an inverted U-shaped curve, with maximal benefit at a 1:1 ratio (50% THC). Conclusions: These preliminary results offer a unique view of real-world medical cannabis use and identify several areas for future research. |
format | Online Article Text |
id | pubmed-6776252 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Mary Ann Liebert, Inc., publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-67762522019-10-04 Benefit of Tetrahydrocannabinol versus Cannabidiol for Common Palliative Care Symptoms Casarett, David J. Beliveau, Jessica N. Arbus, Michelle S. J Palliat Med Special Series: Medical Cannabis in Palliative Care Objectives: To determine the relative contributions of tetrahydrocannabinol (THC) and cannabidiol (CBD) to patients' self-ratings of efficacy for common palliative care symptoms. Design: This is an electronic record-based retrospective cohort study. Model development used logistic regression with bootstrapped confidence intervals (CIs), with standard errors clustered to account for multiple observations by each patient. Setting: This is a national Canadian patient portal. Participants: A total of 2,431 patients participated. Main Outcome Measures: Self-ratings of efficacy of cannabis, defined as a three-point reduction in neuropathic pain, anorexia, anxiety symptoms, depressive symptoms, insomnia, and post-traumatic flashbacks. Results: We included 26,150 observations between October 1, 2017 and November 28, 2018. Of the six symptoms, response was associated with increased THC:CBD ratio for neuropathic pain (odds ratio [OR]: 3.58; 95% CI: 1.32–9.68; p = 0.012), insomnia (OR: 2.93; 95% CI: 1.75–4.91; p < 0.001), and depressive symptoms (OR: 1.63; 95% CI: 1.07–2.49; p = 0.022). Increased THC:CBD ratio was not associated with a greater response of post-traumatic stress disorder (PTSD)-related flashbacks (OR: 1.43; 95% CI: 0.60–3.41; p = 0.415) or anorexia (OR: 1.61; 95% CI: 0.70–3.73; p = 0.265). The response for anxiety symptoms was not significant (OR: 1.13; 95% CI: 0.77–1.64; p = 0.53), but showed an inverted U-shaped curve, with maximal benefit at a 1:1 ratio (50% THC). Conclusions: These preliminary results offer a unique view of real-world medical cannabis use and identify several areas for future research. Mary Ann Liebert, Inc., publishers 2019-10-01 2019-09-30 /pmc/articles/PMC6776252/ /pubmed/31386592 http://dx.doi.org/10.1089/jpm.2018.0658 Text en © David J. Casarett et al., 2019; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. |
spellingShingle | Special Series: Medical Cannabis in Palliative Care Casarett, David J. Beliveau, Jessica N. Arbus, Michelle S. Benefit of Tetrahydrocannabinol versus Cannabidiol for Common Palliative Care Symptoms |
title | Benefit of Tetrahydrocannabinol versus Cannabidiol for Common Palliative Care Symptoms |
title_full | Benefit of Tetrahydrocannabinol versus Cannabidiol for Common Palliative Care Symptoms |
title_fullStr | Benefit of Tetrahydrocannabinol versus Cannabidiol for Common Palliative Care Symptoms |
title_full_unstemmed | Benefit of Tetrahydrocannabinol versus Cannabidiol for Common Palliative Care Symptoms |
title_short | Benefit of Tetrahydrocannabinol versus Cannabidiol for Common Palliative Care Symptoms |
title_sort | benefit of tetrahydrocannabinol versus cannabidiol for common palliative care symptoms |
topic | Special Series: Medical Cannabis in Palliative Care |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776252/ https://www.ncbi.nlm.nih.gov/pubmed/31386592 http://dx.doi.org/10.1089/jpm.2018.0658 |
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