Ghaffari-Rafi Arash, Eum Ki Suk, Villanueva Jesus, Jahanmir Jay
University of Hawai'i at Mānoa, John A. Burns School of Medicine, Honolulu, HI.
University College London, Queen Square Institute of Neurology, London, UK.
Medicine (Baltimore). 2020 Oct 9;99(41):e21842. doi: 10.1097/MD.0000000000021842.
Despite toxicity and unpredictable adverse effects, ecstasy use has increased in the United States. Onset of hyperpyrexia, rhabdomyolysis, disseminated intravascular coagulation (DIC), among other symptoms, occurs within hours of ingestion. Moreover, patients who experience hyperpyrexia, altered mental status, DIC, and multiorgan failure, rarely survive. This case presents a chronic ecstasy user whose symptoms would have predicted mortality. The report demonstrates a patient who experiences protracted hyperthermia, with delayed rhabdomyolysis and DIC. In addition, his peak creatine kinase (CK) of 409,440 U/L was far greater than the expected 30,000 to 100,000 U/L, being the second largest CK recorded in a survivor.
This case report presents a 20-year-old man who presented to the emergency department after experiencing a severe reaction to ecstasy. He was a chronic user who took his baseline dosage while performing at a music event. He experienced hyperpyrexia immediately (106.5°F) while becoming stiff and unresponsive. Before emergency medical service arrival, his friends placed cold compresses on the patient and rested him in an ice filled bathtub.
Per history from patient's friends and toxicology results, the patient was diagnosed with ecstasy overdose, which evolved to include protracted hyperthermia and delayed rhabdomyolysis.
Due to a Glasgow coma scale score of 5, he was intubated and sedated with a propofol maintenance. Hyperpyrexia resolved (temperature dropped to 99.1°F) after start of propofol maintenance. He was extubated after 24 hours, upon which he experienced hyperthermia (101.4°F at 48 hours), delayed rhabdomyolysis, and DIC (onset at 37 hours). He remained in hyperthermia for 120 hours until carvedilol permanently returned his temperature to baseline. His plasma CK reached a peak of 409,440 U/L at 35 hours.
After primary management with intravenous fluids, the patient returned to baseline health without any consequences and was discharged after 8 days. A follow-up of 3 months postdischarge revealed no complications or disability.
Clinically, the case highlights how physicians should be aware of the unusual time course adverse effects of ecstasy can have. Lastly, as intensity and duration of hyperpyrexia are predictors of mortality, our case indicates maintenance of sedation with propofol and use of oral carvedilol; both are efficacious for temperature reduction in ecstasy toxicity.
尽管摇头丸存在毒性且有不可预测的不良反应,但在美国其使用仍呈上升趋势。服用后数小时内会出现高热、横纹肌溶解、弥散性血管内凝血(DIC)等症状。此外,出现高热、精神状态改变、DIC和多器官功能衰竭的患者很少存活。本病例介绍了一名长期使用摇头丸的患者,其症状本可预示死亡。该报告展示了一名经历持续性高热、延迟性横纹肌溶解和DIC的患者。此外,他的肌酸激酶(CK)峰值为409,440 U/L,远高于预期的30,000至100,000 U/L,是幸存者中记录到的第二高CK值。
本病例报告了一名20岁男性,在对摇头丸产生严重反应后前往急诊科就诊。他是一名长期使用者,在一次音乐活动中服用了其基线剂量的摇头丸。他立即出现高热(106.5°F),同时变得僵硬且无反应。在急救人员到达之前,他的朋友为患者敷上冷敷,并让他躺在装满冰的浴缸中。
根据患者朋友提供的病史和毒理学结果,患者被诊断为摇头丸过量,进而发展为持续性高热和延迟性横纹肌溶解。
由于格拉斯哥昏迷量表评分为5分,他接受了插管并用丙泊酚维持镇静。开始丙泊酚维持治疗后,高热症状得到缓解(体温降至99.1°F)。24小时后他被拔管,拔管后他出现高热(48小时时体温为101.4°F)、延迟性横纹肌溶解和DIC(37小时时出现)。他持续高热120小时,直到卡维地洛使其体温永久恢复至基线水平。他的血浆CK在35小时时达到峰值409,440 U/L。
经过静脉补液的初步治疗后,患者恢复到基线健康状态,没有任何后遗症,并在8天后出院。出院后3个月的随访显示没有并发症或残疾。
临床上,该病例凸显了医生应如何意识到摇头丸可能产生的不寻常的时间进程不良反应。最后,由于高热的强度和持续时间是死亡率的预测指标,我们的病例表明使用丙泊酚维持镇静和口服卡维地洛;两者在治疗摇头丸中毒导致的体温降低方面均有效。