Vickery Alistair W, Finch Phillip M
Emerald Clinics, Perth, Western Australia, Australia.
School of Medicine, Notre Dame University, Notre Dame, Fremantle, Western Australia, Australia.
Intern Med J. 2020 Nov;50(11):1326-1332. doi: 10.1111/imj.15052.
Cannabis has been used as a medicine for millennia. Prohibition in the mid-20th century precluded early scientific investigation. 'Cannabis' describes three separate forms - herbal cannabis, 'hemp' products, pharmaceutical-grade regulated cannabinoid-based medical products (CBMP). In Australia, CBMP became available for prescription in November 2016. Herbal cannabis with Δ9-tetrahydrocannabinol (THC), which is illegal, and cannabidiol (CBD) in herbal extracts, are both unregulated and unreliable sources of cannabinoids. The endocannabinoid system (ECS), delineated in the late 1990s, has increased the understanding and interest in research for appropriate clinical indications. The ubiquitous ECS has homeostatic and anti-inflammatory effects and comprises cannabinoid receptors, endocannabinoids and degrading enzymes. Phytocannabinoids are partial agonists of the ECS. In pre-clinical studies, THC and CBD produce beneficial effects in chronic pain, anxiety, sleep and inflammation. Systematic reviews often conflate herbal cannabis and CBMP, confusing the evidence. Currently large randomised controlled trials are unlikely to be achieved. Other methodologies with quality end-points are required. Rich, valuable high-quality real-world evidence for the safe and effective use of CBMP provides an opportunity to examine benefits and potential harms. Evidence demonstrates benefit of CBMP in multiple sclerosis, chronic neuropathic pain, chemotherapy induced nausea and vomiting, resistant paediatric epilepsy, anxiety and insomnia. CBMP are well tolerated with few serious adverse events. Additional clinical benefits are promising in many other resistant chronic conditions. Pharmaceutical grade prescribed CBMP has proven clinical benefits and provides another clinical option in the physician's pharmacopeia.
数千年来,大麻一直被用作药物。20世纪中叶的禁令阻碍了早期的科学研究。“大麻”描述了三种不同的形式——草药大麻、“大麻”产品、医药级受监管的基于大麻素的医疗产品(CBMP)。在澳大利亚,CBMP于2016年11月开始可供处方使用。含有非法的Δ9-四氢大麻酚(THC)的草药大麻以及草药提取物中的大麻二酚(CBD),都是不受监管且不可靠的大麻素来源。20世纪90年代末划定的内源性大麻素系统(ECS),增加了人们对适用于适当临床适应症研究的理解和兴趣。无处不在的ECS具有稳态和抗炎作用,由大麻素受体、内源性大麻素和降解酶组成。植物大麻素是ECS的部分激动剂。在临床前研究中,THC和CBD在慢性疼痛、焦虑、睡眠和炎症方面产生有益效果。系统评价常常将草药大麻和CBMP混为一谈,混淆了证据。目前不太可能进行大型随机对照试验。需要其他具有高质量终点的方法。关于安全有效使用CBMP的丰富、有价值的高质量真实世界证据,为研究其益处和潜在危害提供了机会。证据表明CBMP在多发性硬化症、慢性神经性疼痛、化疗引起的恶心和呕吐、难治性小儿癫痫、焦虑和失眠方面有益处。CBMP耐受性良好,严重不良事件很少。在许多其他难治性慢性病中,额外的临床益处很有前景。医药级处方CBMP已证明具有临床益处,并在医生的药典中提供了另一种临床选择。