A rare case of atropine-resistant bradycardia following sugammadex administration

• Main Authors: Takayuki Yoshida, Chisato Sumi, Takeo Uba, Haruka Miyata, Takeshi Umegaki, Takahiko Kamibayashi
• Format: Article
• Language: English
• Published: SpringerOpen 2020-03-01
• Series: JA Clinical Reports
• Subjects: Sugammadex; Bradycardia; Cardiac arrest; Anaphylaxis; Coronary vasospasm; Kounis syndrome
• Online Access: http://link.springer.com/article/10.1186/s40981-020-00326-7

Abstract Background Profound bradycardia caused by sugammadex has been reported, although its mechanism is unclear. Herein, we suggest a possible culprit for this phenomenon. Case presentation A 50-year-old woman without comorbidity except mild obesity underwent a transabdominal hysterectomy and right salpingo-oophorectomy. After surgery, sugammadex 200 mg was intravenously administered. Approximately 4 min later, her heart rate decreased to 36 bpm accompanied by hypotension (41/20 mmHg) and ST depression in limb lead electrocardiogram (ECG). Atropine 0.5 mg was injected intravenously without improving the hemodynamics. Intravenous adrenaline 0.5 mg was added despite the lack of signs suggesting allergic reactions. Her heart rate and blood pressure quickly recovered and remained stable thereafter, although 12-lead ECG taken 1 h later still showed ST depression. Conclusions In this case, the significant bradycardia appeared attributable to coronary vasospasm (Kounis syndrome) induced by sugammadex, considering the ECG findings and high incidence of anaphylaxis due to sugammadex.