Department of Emergency Medicine, University of Kentucky College of Medicine, Lexington, KY, USA.
Department of Emergency Medicine, University of Kentucky Hospital, Lexington, KY, USA.
Am J Case Rep. 2020 Jul 8;21:e923464. doi: 10.12659/AJCR.923464.
BACKGROUND Brugada phenocopies (BrP) are clinical and electrocardiographic (ECG) entities elicited by reversible medical conditions speculated to have pathogenesis rooted in ion current imbalances or conduction delays within the myocardial wall. During an inciting pathologic condition, it produces ECG patterns identical to those of congenitally-acquired Brugada syndrome and subsequently returns to normal ECG patterns upon resolution of the medical condition. This case report describes a 26-year-old man presenting to the Emergency Department (ED) for suspected heroin overdose with a rare ECG consistent with BrP secondary to acute hyperkalemia. CASE REPORT A 26-year-old man with a history of substance abuse and a seizure disorder presented to the ED for acute encephalopathy secondary to a heroin overdose complicated by severe rhabdomyolysis and acute renal failure. Laboratory investigations showed acute hyperkalemia (potassium of 7.2 mmol/L) in addition to an elevated creatine kinase, severe transaminitis, and elevated creatinine. His ECG on admission revealed Brugada-like changes in leads V1-V2, with subsequent resolution upon bicarbonate administration and normalization of potassium. After initial stabilization, the patient was admitted to the Intensive Care Unit (ICU). His rhabdomyolysis and acute kidney injury improved after copious rehydration. He was found to have community-acquired pneumonia, with a negative infectious disease workup, that improved with antibiotics. Upon resolution of his hypoxemic respiratory failure and improvement in mentation, he was discharged from the hospital. CONCLUSIONS Our case report adds to the growing literature on BrP and highlights the importance of recognizing its characteristic ECG pattern as a unique presentation of a common electrolyte derangement.
Brugada 表型(BrP)是由可逆的医学病症引起的临床和心电图(ECG)表现,推测其发病机制与心肌壁内离子电流失衡或传导延迟有关。在诱发病理状态下,它产生与先天性获得性 Brugada 综合征相同的 ECG 模式,随后在医学病症解决后恢复正常 ECG 模式。本病例报告描述了一名 26 岁男性,因疑似海洛因过量就诊于急诊部(ED),其罕见的 ECG 表现符合继发于急性高钾血症的 BrP。
一名 26 岁男性,有药物滥用和癫痫病史,因海洛因过量导致急性脑病就诊于 ED,伴有严重横纹肌溶解症和急性肾衰竭。实验室检查显示急性高钾血症(血钾 7.2mmol/L),此外还伴有肌酸激酶升高、严重肝功能异常和肌酐升高。他入院时的心电图显示 V1-V2 导联 Brugada 样改变,随后给予碳酸氢钠治疗和血钾正常化后得到缓解。初始稳定后,患者被收入重症监护病房(ICU)。横纹肌溶解症和急性肾损伤在大量补液后得到改善。他被发现患有社区获得性肺炎,传染病检查结果为阴性,经抗生素治疗后得到改善。在低氧性呼吸衰竭得到解决并精神状态改善后,他从医院出院。
我们的病例报告增加了关于 BrP 的不断增长的文献,并强调了识别其特征性 ECG 模式作为常见电解质紊乱的独特表现的重要性。