Vo Kathy T, Horng Howard, Smollin Craig G, Benowitz Neal L
Department of Emergency Medicine, University of California, San Francisco, San Francisco, California; California Poison Control System, San Francisco Division, San Francisco, California.
Department of Laboratory Medicine, University of California, San Francisco, San Francisco, California.
J Emerg Med. 2017 May;52(5):680-683. doi: 10.1016/j.jemermed.2016.11.015. Epub 2016 Dec 12.
Carisoprodol, a centrally acting muscle relaxant with a high abuse potential, has barbiturate-like properties at the GABA-A receptor, leading to central nervous system depression and desired effects. Its tolerance and dependence has been previously demonstrated in an animal model, and withdrawal has been described in several recent case reports. Many cases can be effectively managed with a short course of benzodiazepines or antipsychotic agents. However, abrupt cessation in a patient with a history of long-term and high-dose carisoprodol abuse may result in symptoms that are more difficult for providers to treat.
We present a case of a 34-year-old man with a long history of carisoprodol abuse who was found unresponsive after having ingested 7.5 grams of carisoprodol. He was intubated and admitted to the intensive care unit. He was given propofol, dexmedetomidine, fentanyl, ketamine, lorazepam, midazolam, quetiapine, and haloperidol, some at high-dose infusions, before his agitation and ventilator asynchrony could be controlled. His improvement coincided with the addition of carisoprodol and phenobarbital to his treatment regimen. WHY SHOULD AN EMERGENCY PHYSICIAN BE AWARE OF THIS?: Trends show increasing emergency department presentations for drug-related disorders and treatment. This case highlights an uncommon case of carisoprodol withdrawal that may be encountered by emergency physicians, and demonstrates that benzodiazepines may not be sufficient to suppress severe withdrawal symptoms. Treatment with carisoprodol and phenobarbital provided additional benefit and can be considered in cases of severe carisoprodol withdrawal.
卡立普多是一种具有高度滥用潜力的中枢性肌肉松弛剂,在GABA - A受体上具有类似巴比妥酸盐的特性,可导致中枢神经系统抑制并产生预期效果。此前已在动物模型中证实其耐受性和依赖性,近期也有几例病例报告描述了戒断情况。许多病例可通过短期使用苯二氮䓬类药物或抗精神病药物有效治疗。然而,长期高剂量滥用卡立普多的患者突然停药可能会导致症状,使医疗人员更难治疗。
我们报告一例34岁有长期卡立普多滥用史的男性病例,该患者摄入7.5克卡立普多后被发现无反应。他被插管并收入重症监护病房。在其躁动和呼吸机不同步得到控制之前,给予了丙泊酚、右美托咪定、芬太尼、氯胺酮、劳拉西泮、咪达唑仑、喹硫平和氟哌啶醇,有些是高剂量输注。他的病情好转与在治疗方案中加入卡立普多和苯巴比妥同时发生。
急诊医生为何应了解此事?:趋势显示,与药物相关疾病及治疗的急诊就诊人数在增加。该病例突出了急诊医生可能遇到的罕见的卡立普多戒断病例,并表明苯二氮䓬类药物可能不足以抑制严重的戒断症状。卡立普多和苯巴比妥治疗提供了额外益处,在严重卡立普多戒断病例中可考虑使用。