Lin Nai-Hui, Su Yu-Jang, Yang Hsiu-Wu, Chen Hsin-Tang
Mackay Memorial Hospital Department of Emergency Medicine No. 92, Sec. 2, Chung Shan N. Rd. Taipei 104 Taiwan.
Mackay Memorial Hospital Department of Emergency Medicine Poison Center New Taipei Taiwan.
J Acute Med. 2019 Dec 1;9(4):189-193. doi: 10.6705/j.jacme.201912_9(4).0005.
Rivastigmine is a non-competitive reversible inhibitor of acetylcholinesterase which is approved as one of the fi rst-line treatment options for Alzheimer's disease. We present the case of a 33-year-old woman with acute cholinergic syndrome secondary to deliberate rivastigmine poisoning. The patient presented at the emergency department (ED) with drowsy consciousness, dizziness, vomiting, diarrhea, sweating, and hypertension (171/103 mmHg). At the scene, an empty bottle of Rivast 120 mL/Bot, containing rivastigmine 2 mg/mL, was found beside the patient. Two hours later, we noted bronchorrhea and persistent salivation along with drowsiness, agitation, fatigue, incontinence, and limbs paralysis. A notably low serum cholinesterase level (651 U/l) was identified. Acute cholinergic syndrome secondary to rivastigmine intoxication was diagnosed. Endotracheal intubation with ventilator support was required due to respiratory failure. Atropine (0.5 mg intravenous injection) was administered. She was subsequently admitted to the intensive care unit for further care. Extubation was performed on the third day. The patient insisted on being discharged on the second day after extubation, and after administration of a total of 11 mg of atropine, no signs of either intermediate syndrome or delayed polyneuropathywere noted. rivastigmine, an acetylcholinesterase inhibitor, can precipitate an acute cholinergic crisis in cases of intoxication. Typical clinical features of cholinergic excess include increased secretions in the airway and oral cavity, miosis, diarrhea, anxiety, twitching, bronchoconstriction, convulsions, confusion, and gastrointestinal and muscular cramps. The treatment for acute cholinergic crisis is administration of atropine alone or in combination with an antidote to the cholinesterase inhibitor (such as pralidoxime). Patients often recover well with atropine supplements and optimal supportive care.
卡巴拉汀是一种非竞争性可逆性乙酰胆碱酯酶抑制剂,被批准作为阿尔茨海默病的一线治疗选择之一。我们报告一例33岁女性因故意服用卡巴拉汀中毒继发急性胆碱能综合征的病例。患者因意识嗜睡、头晕、呕吐、腹泻、出汗和高血压(171/103 mmHg)就诊于急诊科。在现场,患者身旁发现一瓶120 mL装的Rivast空瓶,每毫升含卡巴拉汀2毫克。两小时后,我们注意到患者出现支气管分泌过多和持续流涎,同时伴有嗜睡、烦躁、疲劳、大小便失禁和肢体麻痹。检测发现血清胆碱酯酶水平显著降低(651 U/l)。诊断为卡巴拉汀中毒继发急性胆碱能综合征。因呼吸衰竭,患者需要气管插管并接受呼吸机支持。给予阿托品(静脉注射0.5毫克)。随后患者被收入重症监护病房进一步治疗。第三天进行了拔管。患者在拔管后第二天坚持出院,在总共给予11毫克阿托品后,未发现中间综合征或迟发性多发性神经病的迹象。卡巴拉汀作为一种乙酰胆碱酯酶抑制剂,在中毒情况下可引发急性胆碱能危机。胆碱能亢进的典型临床特征包括气道和口腔分泌物增加、瞳孔缩小、腹泻、焦虑、抽搐、支气管收缩、惊厥、意识模糊以及胃肠道和肌肉痉挛。急性胆碱能危机的治疗方法是单独使用阿托品或与胆碱酯酶抑制剂解毒剂(如解磷定)联合使用。通过补充阿托品和最佳的支持治疗,患者通常恢复良好。