大麻和大麻素药物治疗慢性口面部疼痛:范围审查

Jory Longworth , Michael Szafron , Amanda Gruza , Keith Da Silva
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引用次数: 2

摘要

目的整理和总结口腔颌面外科医生(OMFS)、口腔医学专家(OMS)和口腔颌面疼痛专家(OPS)使用大麻和大麻素治疗慢性口腔颌面疼痛(COP)的现有证据。数据我们系统地筛选了来源,包括大麻素化合物对COP患者疼痛的影响,这些患者可能由我们的目标专家进行治疗。资料来源由两位作者独立选择。来源按国家、发表日期、目的、研究的COP条件、研究的大麻素、方法、结果、局限性和结论进行了总结。进行了主题分析和单词云,以阐明已确定来源之间的共性、重点和差距。来源检索自MEDLINE、EMBASE、Web of Science Core Collections、牙科和口腔科学、DARE、CCRCT和美国国家健康与对照试验研究所注册处。研究选择在705个检索到的标题中,有8个符合纳入/排除标准并纳入审查。纳入的资料涉及COP,归因于:头颈部癌症(3)、多发性硬化相关三叉神经痛样症状(2)、疱疹后神经痛(1)、颞下颌关节功能障碍(1)和原发性烫口综合征(1)。所研究的大麻类药物包括:自填大麻(3)、局部N-棕榈酰-乙醇胺(1)、局部大麻提取物(1),大麻籽油(1)和萘啶肟口腔粘膜喷雾剂(1)以及萘啶酮(1)。结论大多数来源得出结论,他们各自的大麻素治疗为COP提供了一些治疗益处(6/8),并且所有来源得出结论认为他们的治疗是安全的。目前的研究是全面的,记录了疼痛、焦虑、抑郁、生活质量和功能性残疾的结果。大麻类药物通常被研究为辅助和姑息治疗。临床意义大麻类药物越来越容易获得,可能使许多COP患者受益。患者和临床医生需要更多、更高质量的证据,才能就大麻或大麻素治疗COP做出自信和知情的决定。这篇综述为患者、临床医生和未来的研究人员总结了当前的证据。
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Cannabis and cannabinoid medications for the treatment of chronic orofacial pain: A scoping review

Objectives

To collate and summarize existing evidence for the use of cannabis and cannabinoids to treat chronic orofacial pain (COP) by oral and maxillofacial surgeons (OMFS), oral medicine specialists (OMS), and orofacial pain specialists (OPS).

Data

We systematically screened for sources including a measure of effect of a cannabinoid compound on pain in COP patients that might be treated by our target specialists. Sources were selected by two authors independently. Sources were summarized by country, publication date, objective(s), COP condition(s) studied, cannabinoid(s) studied, methods, results, limitations, and conclusions. A thematic analysis and word cloud were conducted to elucidate commonalities, emphases, and gaps amongst identified sources.

Sources

Retrieved from MEDLINE, EMBASE, Web of Science Core Collections, Dentistry and Oral Sciences, DARE, CCRCT, and US National Institute of Health and Controlled Trials Register.

Study Selection

Of 705 retrieved titles, 8 met inclusion/exclusion criteria and were included for review. Included sources dealt with COP attributed to: head and neck cancer (3), multiple sclerosis-related trigeminal neuralgia-like symptoms (2), post-herpetic neuralgia (1), temporomandibular dysfunction (1), and primary burning mouth syndrome (1). Cannabinoids studied included: self-administered cannabis (3), topical N-palmitoyle-thanolamine (1), topical cannabis extract (1), cannabis sativa oil (1), nabiximols oromucosal spray (1), and nabilone (1).

Conclusions

Most sources concluded their respective cannabinoid treatments to provide some therapeutic benefit for COP (6 of 8) and all concluded their treatments to be safe. Current research is wholistically focused, recording outcome measures for pain, anxiety, depression, quality of life, functional disability. Cannabinoids are most often studied as adjunctive and palliative treatments.

Clinical significance

Cannabinoids are becoming increasingly accessible and might benefit many COP patients. Patients and clinicians require more and higher quality evidence to make confident and informed decisions regarding treatment of COP with cannabis or cannabinoids. This review summarizes current evidence for patients, clinicians, and future researchers.

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