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Medical Cannabis and AASM Position Statement: The Don't Ask, Don't Tell Wishing Well

机译:医疗大麻和AASM立场声明:不要问,不要告诉心愿

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We were puzzled by the 2018 American Academy of Sleep Medicine (AASM) position statement recommending obstructive sleep apnea (OSA) be struck from the list of medical conditions for state medical cannabis programs on account of unreliable delivery methods and insufficient evidence of treatment effectiveness, tolerability and safety.1 While positive airway pressure (PAP) will likely remain the gold standard therapy for OSA in the foreseeable future, there should be room for studying and integrating pharmacologic treatment strategiesnot just endorsing expensive devicesthat can lead to improved and more personalized disease modification. The contrary AASM stance bans members from recommending potential medical alternativesspecifically admonishing cannabis-based therapiesbut also implying that failure of PAP in OSA is not an option, even though device nonadherence occurs in roughly half of the patients to whom it is initially prescribed. The AASM stance also implies that AASM affiliates had best be in lockstep with OSA-coupled diagnostic testing and device-driven management at accredited sleep centers because the alternative of ceding the management of patients with OSA who are nonadherent to PAP therapy is not allowed by the position statement authors1 (including FDA-approved medications [ie, dronabinol] studied for off-label indications).Carley et al.,2 in an elegant placebo-controlled randomized clinical trial in patients with moderate or severe OSA found opposite results debunking the criticisms of the AASM's primary assertions including: Epworth Sleepiness Scale scores were reduced in the treatment group; the incidence of adverse events was not significantly different from placebo; and there was no evidence of decreased tolerability as measured by missed doses after 6 weeks of treatment using a 10 mg dose of dronabinol delivered reliably and safely in a pill form taken orally 1 hour before bedtime. Moreover, with respect to documenting alleged harms that outweigh benefits for medical cannabis therapies (including synthetic extracts like dronabinol) to justify the position statement, the authors of the AASM position statement1 fail to cite any relevant evidence to substantiate their ethical claims despite the existing context of ample medical cannabis research reported in humans.3 This glaring failure may further erode organizational credibility and may be the driving force behind patients with OSA seeking out cannabis program affiliates to discuss alternatives therapies especially when standard treatment is challenged by non-adherence and a nondisclosure policy pertaining to medical cannabis becomes the new norm of accredited sleep centers across the United States.DISCLOSURE STATEMENTWork for this study was performed at The Heller School for Social Policy and Management, Brandeis University, Waltham, MA. All authors have viewed and approved the manuscript. The authors report no conflicts of interest.
机译:我们对2018年美国睡眠医学科学院(AASM)的立场声明感到困惑,该声明建议将阻塞性睡眠呼吸暂停(OSA)从州医疗大麻计划的医疗条件清单中剔除,原因是输送方法不可靠以及治疗效果,耐受性的证据不足1虽然在可预见的将来,气道正压(PAP)可能仍将是OSA的金标准疗法,但应该有研究和整合药物治疗策略的空间,而不仅仅是认可昂贵的设备,这些设备可以导致改善的和更个性化的疾病改变。相反,AASM的立场禁止成员推荐可能的医学替代方法,特别是建议基于大麻的疗法,但也暗示即使在最初使用处方药的患者中约有一半发生器械不依从,也不能选择在OSA中失败PAP。 AASM的立场还意味着,AASM关联公司最好与经过认可的睡眠中心进行OSA耦合的诊断测试和设备驱动的管理保持同步,因为对于不遵循PAP疗法的OSA患者,不得让其管理。立场声明的作者1(包括经FDA批准的药物[即,屈大麻酚]用于标签外适应症的研究)。Carley等[2]在一项优雅的安慰剂对照随机临床试验中,对中度或重度OSA患者进行了研究,发现相反的结果掩盖了批评AASM的主要主张包括:治疗组的Epworth嗜睡量表分数降低;不良事件的发生率与安慰剂无明显差异;并且没有证据表明耐受性降低是通过在就寝前1小时口服10毫克剂量的Dronabinol可靠,安全地以丸剂的形式治疗6周后通过错过剂量来衡量的。此外,关于记录声称的伤害超过医疗大麻疗法(包括诸如屈大麻酚的合成提取物)的收益以证明立场声明的合理性,尽管现有背景,AASM立场声明的作者1仍未引用任何相关证据来证明其道德主张在人类中进行的大量医用大麻研究报告。3这种明显的失败可能会进一步削弱组织的信誉,并且可能是OSA患者寻求大麻计划分支机构讨论替代疗法的动力,尤其是当标准治疗受到不遵守和不公开的挑战时与医疗大麻有关的政策已成为美国认可的睡眠中心的新规范。所有作者均已查看并批准了该手稿。作者说没有侵犯他的权益。

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