Efficacy and safety of adamgammadex for reversing rocuronium‐induced deep neuromuscular blockade: A multicenter, randomized, phase IIb study

Author:

Zhao Yanhua1,Chen Sifan1,Xie Wenqin2,Zhang Xiaoqing3,Chen Guozhong4,Ji Fuhai5,Wang Dongxin6,Qi Youmao7,Jie Qing7,Su Diansan1,Yu Weifeng1

Affiliation:

1. Department of Anesthesiology, Ren Ji Hospital Shanghai Jiao Tong University School of Medicine Shanghai China

2. Department of Anesthesiology Quanzhou First Hospital Affiliated to Fujian Medical University Quanzhou China

3. Department of Anesthesiology Tongji Hospital of Tongji University Shanghai China

4. Department of Anesthesiology The 900 Hospital of the Chinese People's Liberation Army Joint Logistic Support Force Fuzhou China

5. Department of Anesthesiology The First Affiliated Hospital of Soochow University Suzhou China

6. Department of Anesthesiology Peking University First Hosptial Beijing China

7. Hangzhou Adamerck Pharmlabs Inc Hangzhou China

Abstract

AbstractThe rapid reversal of deep neuromuscular blockade (NMB) is important but remains challenging. This study aimed to evaluate the efficacy and safety of adamgammadex versus sugammadex in reversing deep rocuronium‐induced NMB. This multicenter, randomized, phase IIb study included 80 patients aged 18–64 years, American Society of Anesthesiologists (ASA) grade 1–2, undergoing elective surgery under general anesthesia with rocuronium. Patients were randomized to the adamgammadex 7, 8, and 9 mg/kg group or the sugammadex 4 mg/kg group. The primary efficacy variable was the time to recovery of train‐of‐four ratio (TOFr) to 0.9. The secondary efficacy variables were the time to recovery of TOFr to 0.7, antagonistic success rate of the recovery of TOFr to 0.9 within 5 min, and incidence rate of recurarization within 30 min after drug administration. The explorative efficacy variable was the time to recovery of the corrected TOFr to 0.9 (actual/baseline TOF ratio). Adamgammadex 7, 8, and 9 mg/kg and sugammadex 4 mg/kg groups did not significantly differ in all efficacy variables. Importantly, adamgammadex 9 mg/kg permitted reversal within a geometric mean of 2.9 min. According to the safety profile, adamgammadex achieved good tolerance and low incidence of drug‐related adverse events compared with the 4 mg/kg sugammadex. Adamgammadex 7, 8, and 9 mg/kg facilitated rapid reversal of deep rocuronium‐induced NMB and had good tolerance and low incidence of drug‐related adverse events. Therefore, adamgammadex is a potential and promising alternative to sugammadex.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Pharmacology, Toxicology and Pharmaceutics,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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