The Cannabis and Health Research Initiative will help integrate medicinal cannabis in healthcare

Johannes Thrul, Ryan Vandrey
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Abstract

In the USA, there are more than 5.5 million registered patients in state-regulated medicinal cannabis programs and many people use hemp products (sourced from cannabis containing <0.3% delta-9-tetrahydrocannabinol (THC) by dry weight) for therapeutic purposes. However, clinical research on non-pharmaceutical cannabis products remains limited1, healthcare providers feel inadequately trained on integrating medicinal cannabis into their practice2, and medicinal cannabis use is poorly documented in electronic medical records (EMRs)3. These issues highlight the need for patient-level data on the impacts of medicinal cannabis use4.

With legalization of retail cannabis sales in some US states, the diversity of cannabis products available to consumers has substantially increased5. Products vary in chemical composition6, dose and intended route of administration, all of which can affect clinical effect, safety and abuse liability, and should be considered in clinical decision making. The diversity in cannabis products and the use of poorly defined nomenclature contributes to difficulty in assessing the health effects of medicinal cannabis.

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大麻与健康研究计划将帮助把药用大麻纳入医疗保健中
在美国,有超过 550 万名注册患者参加了州政府监管的药用大麻计划,许多人将大麻产品(源自干重含 0.3% δ-9-四氢大麻酚(THC)的大麻)用于治疗目的。然而,对非药用大麻产品的临床研究仍然有限1 ,医疗服务提供者在将药用大麻纳入其实践方面感到培训不足2 ,电子病历(EMR)中对药用大麻的使用记录很少3。 这些问题凸显了对有关药用大麻使用影响的患者层面数据的需求4。随着美国一些州的大麻零售合法化,消费者可获得的大麻产品种类大幅增加5。产品的化学成分6 、剂量和预期给药途径各不相同,所有这些都会影响临床效果、安全性和滥用责任,在临床决策中应加以考虑。大麻产品种类繁多,使用的术语定义不清,给评估药用大麻对健康的影响造成了困难。
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