Mash Deborah C
Department of Neurology and Molecular and Cellular Pharmacology, University of Miami Miller School of Medicine Miami, FL, USA.
Front Physiol. 2016 Oct 13;7:435. doi: 10.3389/fphys.2016.00435. eCollection 2016.
Over the past decade, the excited delirium syndrome (ExDS) has raised continued controversy regarding the cause and manner of death of some highly agitated persons held in police custody, restrained or incapacitated by electrical devices. At autopsy, medical examiners have difficulty in identifying an anatomic cause of death, but frequently cite psychostimulant intoxication as a contributing factor. The characteristic symptoms of ExDS include bizarre and aggressive behavior, shouting, paranoia, panic, violence toward others, unexpected physical strength, and hyperthermia. Throughout the United States and Canada, these cases are most frequently associated with cocaine, methamphetamine, and designer cathinone abuse. Acute exhaustive mania and sudden death presents with behavioral symptoms that are identical to what is described for ExDS in psychostimulant abusers. Bell's mania or acute exhaustive mania was first described in the 1850's by American psychiatrist Luther Bell in institutionalized psychiatric patients. This rare disorder of violent mania, elevated body temperature and autonomic collapse continued to be described by others in the psychiatric literature, but with different names until the first cases of ExDS were seen at the beginning of the cocaine epidemic by medical examiners. The neurochemical pathology examination of brain tissues after death revealed a loss of dopamine transporter regulation together with increases in heat shock protein 70 (hsp70) expression as a biomarker of hyperthermia. The similarity in the behavioral symptoms between extremely agitated psychostimulant abusers and unmedicated psychiatric patients suggests that a genetic disorder that leads to dysregulated central dopamine transporter function could be a precipitating cause of the acute delirium and sudden death. While the precise cause and mechanism of lethality remains controversial, the likely whys and wherefores of sudden death of ExDS victims are seen to be "biological," since excessive dopamine in the brain triggers the manic excitement and delirium, which unabated, culminates in a loss of autonomic function that progresses to cardiorespiratory collapse.
在过去十年中,激越性谵妄综合征(ExDS)一直引发着持续的争议,争议焦点在于一些被警方拘留、被电子设备约束或失去行动能力的高度激动者的死因及死亡方式。尸检时,法医难以确定解剖学上的死因,但经常将精神兴奋剂中毒列为一个促成因素。ExDS的特征性症状包括怪异且具有攻击性的行为、呼喊、偏执、恐慌、对他人的暴力行为、意想不到的体力以及体温过高。在美国和加拿大各地,这些病例最常与可卡因、甲基苯丙胺和合成卡西酮滥用有关。急性耗竭性躁狂和猝死所呈现的行为症状与精神兴奋剂滥用者中ExDS的描述相同。贝尔氏躁狂或急性耗竭性躁狂最早于19世纪50年代由美国精神病学家路德·贝尔在住院精神病患者中描述。这种罕见的暴力躁狂、体温升高和自主神经衰竭的病症在精神病学文献中不断被其他人描述,但名称各异,直到法医在可卡因流行初期首次见到ExDS病例。死后对脑组织进行的神经化学病理学检查显示多巴胺转运体调节功能丧失,同时热休克蛋白70(hsp70)表达增加,作为体温过高的生物标志物。极度激动的精神兴奋剂滥用者与未接受药物治疗的精神病患者在行为症状上的相似性表明,导致中枢多巴胺转运体功能失调的遗传疾病可能是急性谵妄和猝死的诱发原因。虽然致死的确切原因和机制仍存在争议,但ExDS受害者猝死的可能原因被认为是“生物学”的,因为大脑中过多的多巴胺引发躁狂兴奋和谵妄,若不缓解,最终会导致自主神经功能丧失,进而发展为心肺功能衰竭。