| Literature DB >> 31787111 |
Devan Kansagara1,2, William C Becker3,4, Chelsea Ayers5, Jeanette M Tetrault3.
Abstract
Cannabis use has become increasingly common in the U.S. in recent years, with legalization for medical and recreational purposes expanding to more states. With this increase in use and access, providers should be prepared to have more conversations with patients about use. This review provides an overview of cannabis terminology, pharmacology, benefits, harms, and risk mitigation strategies to help providers engage in these discussions with their patients. Current evidence for the medical use of cannabis, cannabis-related diagnoses including cannabis use disorder (CUD) and withdrawal syndromes, and the co-use of opioids and cannabis are discussed. It is crucial that providers have the tools and information they need to deliver consistent, evidence-based assessment, treatment, prevention and harm-reduction, and we offer practical guidance in these areas.Entities:
Keywords: Cannabis; Medical marijuana; Mental health; Provider-patient relationship; Risk mitigation; Substance use
Year: 2019 PMID: 31787111 PMCID: PMC6886188 DOI: 10.1186/s13722-019-0171-3
Source DB: PubMed Journal: Addict Sci Clin Pract ISSN: 1940-0632
Cannabis formulations and routes of administration
| Form | Other terms | Development | Route of administration |
|---|---|---|---|
| Plant | Flower, bud | The highest concentration of cannabinoids are found in the flower, not the leaf, of the female plant | Smoking Vaporization Topical Rectal |
| Edibles | Brownies, cookies, candy | Typically butter or oil used to extract cannabinoids and put into a variety of edible products | Oral |
| Tincture | Golden dragon, green dragon | Alcohol or glycerin used to extract active ingredients | Oral Sublingual Oromucosal |
| Oil | Alcohol used to make highly viscous concentrated extract | Oral Topical | |
| Resin | Hash, dry sift, kief | Concentrate made by mechanically separating trichomes (hair-like protrusions on flower with high concentration of cannabinoids) from the plant | Smoking Vaporization |
| Dab | Wax, shatter | Ultraconcentrated extract made with solvents such as butane; very high levels of THC, potentially dangerous | Dabbing (concentrate placed on a very metal rod and inhaled) |
| Nabiximols | Sativex | Pharmaceutically prepared whole plant extract in spray form; 1:1 THC:CBD concentration; approved for use in the EU | Oromucosal |
| Pharmaceutical cannabinoids | Dronabinol, Nabilone, Epidiolex® | Dronabinol and nabilone are FDA-approved synthetic THC (chemotherapy induced nausea/ vomiting; AIDS related cachexia); Epidiolex® is a highly purified CBD plant extract and is FDA-approved for the treatment of two rare epilepsy syndromes | Oral |
Routes of administration: compare and contrast
| Routes | Smoking | Vaporization (“vaping”) | Oral/edibles | Topical |
|---|---|---|---|---|
| Notes | Combustion of dried cannabis flower using several methods: cigarettes (joints, spliffs), pipes, water pipes (bongs) | Vaporizer is used to heat dried flower or concentrated extract (oil, resin) and the resultant vapor is inhaled | Variety of edibles available; often dose/single serving is a fraction of the product (i.e.—one part of a cookie or brownie) | Many forms available: creams, ointments, patches, poultices, oils |
| Pharmacology | Rapid onset and peak so one can gauge effect and titrate dosing | Rapid onset and peak similar to smoking; no smoke; less toxicant exposure than smoking | No inhalation; broad range of products; slower onset action | None of the pulmonary effects associated with inhalation; probably much less intoxicating |
| Cautions | Bronchial irritation; cough; sputum; production contains carcinogens; potential for adverse effects on lung function with heavy use over many years | Substantially higher blood THC concentrations achieved at a given dose than with smoking; higher risk of adverse effects in novice users; long term lung safety is unknown; need for potentially costly equipment; risk of potentially life-threatening pulmonary illness | Onset and peak are delayed, and effects can last many hours which makes it more difficult to titrate dose; oral metabolite of THC (11-OH-THC) may have fourfold more powerful psychoactive effect risk of overdose; caution especially in novice users | Very little is known about topical preparations; unknown systemic absorption; rapidly expanding topical CBD market is completely unregulated |
Stepwise assessment of cannabis use disorder
| Step 1. Do you currently use cannabis? YES/NO | ||||
| Step 2. IF YES, cannabis use disorder-short form [ | ||||
| 1. How often during the past 6 months did you find that you were not able to stop using cannabis once you had started? | ||||
| Never | Less than monthly | Monthly | Weekly | Daily or almost daily |
| 0 | 1 | 2 | 3 | 4 |
| 2. How often in the past 6 months have you devoted a great deal of your time to getting, using, or recovering from cannabis? | ||||
| Never | Less than monthly | Monthly | Weekly | Daily or almost daily |
| 0 | 1 | 2 | 3 | 4 |
| 3. How often in the past 6 months have you had a problem with your memory or concentration after using cannabis? | ||||
| Never | Less than monthly | Monthly | Weekly | Daily or almost daily |
| 0 | 1 | 2 | 3 | 4 |
| Total score _______ | ||||
| Positive Screen = 2 or higher | ||||
| Step 3: Confirm with DSM-V Criteria for Cannabis Use Disorder [ | ||||