Chhabra Manik, Paul Arun, Abulannaz Omaymah, Lê Mê-Linh, Mansell Holly, Finkelstein Yaron, Huntsman Richard J, Kelly Lauren E
Department of Pharmacology and Therapeutics, Max Rady College of Medicine, University of Manitoba, Winnipeg, Canada.
Department of Pharmacology, Faculty of Medicine, Jordan University of Science and Technology, Ar-Ramtha, Jordan.
Acta Paediatr. 2025 Sep;114(9):2148-2159. doi: 10.1111/apa.70140. Epub 2025 May 28.
We developed a living systematic review (LSR) that will continuously map the safety and reported benefit data related to cannabinoid use for medical purposes in children.
MEDLINE, Embase, PsycInfo, and the Cochrane Library were searched from inception to April 2023. Studies involving at least one child < 18 years who was administered plant-derived or pharmaceutical cannabinoids as an intervention or treatment for medical conditions were included.
Of 37 189 identified citations, 276 studies were included: 84 interventional, 131 observational, 54 surveys, and 7 qualitative studies. Among interventional and observational studies, common indications for cannabinoids in children were refractory epilepsy (n = 146 studies, 188 726 participants), cancer and cancer symptoms (n = 30 studies, 208 753 participants), and autism spectrum disorder (n = 18 studies, 1285 participants). Common cannabinoids identified in interventional studies were purified cannabidiol (CBD) (78.6%, n = 66 studies, 5235 participants) with dose range of 2-50 mg/kg/day, tetrahydrocannabinol (6%, n = 5 studies, 148 participants) with dose range of 2.5-10 mg/day (max dose of tetrahydrocannabinol in nabiximols 32.4 mg) and nabilone (6%, n = 5 studies, 267 participants) with dose range of 0.5-2 mg/day. In randomised controlled trials, purified cannabidiol was reported to reduce seizure frequency ranging between 30% and 50%. Common adverse events (> 20% studies) in studies enrolling children were somnolence, diarrhoea, vomiting, and decreased appetite.
These findings will continue to be updated to inform practice and reveal knowledge gaps for future research.
我们开展了一项实时系统评价(LSR),该评价将持续梳理与儿童医用大麻素使用相关的安全性及已报道的获益数据。
检索了MEDLINE、Embase、PsycInfo和Cochrane图书馆数据库,检索时间从建库至2023年4月。纳入了至少涉及一名18岁以下儿童的研究,这些儿童接受了植物源性或药用大麻素作为医疗状况的干预或治疗。
在37189条检索到的文献中,纳入了276项研究:84项干预性研究、131项观察性研究、54项调查研究和7项定性研究。在干预性和观察性研究中,儿童使用大麻素的常见适应证为难治性癫痫(n = 146项研究,188726名参与者)、癌症及癌症症状(n = 30项研究,208753名参与者)和自闭症谱系障碍(n = 18项研究,1285名参与者)。干预性研究中确定的常见大麻素为纯化大麻二酚(CBD)(78.6%,n = 66项研究,5235名参与者),剂量范围为2 - 50mg/kg/天,四氢大麻酚(6%,n = 5项研究,148名参与者),剂量范围为2.5 - 10mg/天(纳布西莫尔中四氢大麻酚的最大剂量为32.4mg),以及纳布酮(6%,n = 5项研究,267名参与者),剂量范围为0.5 - 2mg/天。在随机对照试验中,据报道纯化大麻二酚可使癫痫发作频率降低30%至50%。纳入儿童研究中常见的不良事件(>20%的研究)为嗜睡、腹泻、呕吐和食欲减退。
这些发现将持续更新,以指导实践并揭示未来研究的知识空白。