Zaurova Milana, Hoffman Robert S, Vlahov David, Manini Alex F
Emergency Medicine Residency, The Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Division of Medical Toxicology, Ronald O. Perelman Department of Emergency Medicine, NYU School of Medicine, New York, NY, USA.
J Med Toxicol. 2016 Dec;12(4):335-340. doi: 10.1007/s13181-016-0558-4. Epub 2016 Jun 2.
Synthetic cannabinoid receptor agonists (SCRAs) are heterogeneous compounds originally intended as probes of the endogenous cannabinoid system or as potential therapeutic agents. We assessed the clinical toxicity associated with recent SCRA use in a large cohort of drug overdose patients.
This subgroup analysis of a large (n = 3739) drug overdose cohort study involved consecutive ED patients at two urban teaching hospitals collected between 2009 and 2013. Clinical characteristics of patients with the exposure to SCRAs (SRCA subgroup) were compared with those from patients who smoked traditional cannabinoids (marijuana subgroup). Data included demographics, exposure details, vital signs, mental status, and basic chemistries gathered as part of routine clinical care. Study outcomes included altered mental status and cardiotoxicity.
Eighty-seven patients reported exposure to any cannabinoid, of whom 17 reported SCRAs (17 cases, 70 controls, mean age 38.9 years, 77 % males, 31 % Hispanic). There were no significant differences between SRCA and marijuana with respect to demographics (age, gender, and race/ethnicity), exposure history (suicidality, misuse, and intent), vital signs, or serum chemistries. Mental status varied between SRCA and marijuana, with agitation significantly more likely in SCRA subgroup (OR = 3.8, CI = 1.2-11.9). Cardiotoxicity was more pronounced in the SCRA subgroup with dysrhythmia significantly more likely (OR = 9.2, CI = 1.0-108).
In the first clinical study comparing the adverse effects of SCRA overdose vs. marijuana controls in an ED population, we found that SCRA overdoses had significantly pronounced neurotoxicity and cardiotoxicity compared with marijuana.
合成大麻素受体激动剂(SCRAs)是一类异质性化合物,最初旨在作为内源性大麻素系统的探针或潜在治疗药物。我们评估了近期在一大群药物过量患者中使用SCRAs相关的临床毒性。
这项对一个大型(n = 3739)药物过量队列研究的亚组分析涉及2009年至2013年期间在两家城市教学医院连续收治的急诊科患者。将接触SCRAs的患者(SRCA亚组)的临床特征与吸食传统大麻素的患者(大麻亚组)的特征进行比较。数据包括人口统计学信息、接触细节、生命体征、精神状态以及作为常规临床护理一部分收集的基本化学指标。研究结局包括精神状态改变和心脏毒性。
87名患者报告接触过任何大麻素,其中17名报告接触过SCRAs(17例,70例对照,平均年龄38.9岁,77%为男性,31%为西班牙裔)。SRCA组和大麻组在人口统计学(年龄、性别和种族/民族)、接触史(自杀倾向、误用和意图)、生命体征或血清化学指标方面无显著差异。SRCA组和大麻组的精神状态有所不同,SRCA亚组中激越更为常见(比值比[OR]=3.8,可信区间[CI]=1.2 - 11.9)。心脏毒性在SRCA亚组中更为明显,心律失常的发生率显著更高(OR = 9.2,CI = 1.0 - 108)。
在第一项比较急诊科人群中SCRAs过量与大麻对照不良反应的临床研究中,我们发现与大麻相比,SCRAs过量具有明显更显著的神经毒性和心脏毒性。