Postoperative residual neuromuscular blockade after reversal based on a qualitative peripheral nerve stimulator response

医学 苏伽马德克斯 神经肌肉阻滞 麻醉 新斯的明 不利影响 入射(几何) 神经肌肉监测 Pacu公司 封锁 外科 异丙酚 罗库溴铵 内科学 受体 物理 光学
作者
Yea-Ji Lee,Ah‐Young Oh,Bon-Woo Koo,Jiwon Han,Jae-Hee Park,Jung-Pyo Hong,Kwang‐Suk Seo
出处
期刊:European Journal of Anaesthesiology [Lippincott Williams & Wilkins]
卷期号:37 (3): 196-202 被引量:13
标识
DOI:10.1097/eja.0000000000001157
摘要

Incomplete recovery of neuromuscular blockade is a common postoperative adverse event in the postanaesthesia care unit.We examined and compared the incidence of residual neuromuscular blockade when the recommended dose of neostigmine or sugammadex was administered according to a qualitative nerve stimulator response.A randomised controlled trial.A tertiary care hospital in South Korea from September 2017 to November 2017.Eighty patients aged between 18 and 69 years were included in this study. All were patients scheduled to undergo elective laparoscopic cholecystectomy and who had an American Society of Anaesthesiologists physical status of one or two were eligible.Patients were allocated randomly to receive neostigmine or sugammadex at the end of surgery. The doses of the reversal agents were based on the response to peripheral nerve stimulation, which was discontinued after administration of the reversal agent.The primary outcome was the incidence of postoperative residual neuromuscular blockade. The secondary outcomes were the incidences of symptoms or signs of residual neuromuscular blockade such as hypoxaemia, inability to maintain head-lift for 5 s and diplopia.The incidence of residual neuromuscular blockade on arrival in the recovery room was 44.4% in the neostigmine group and 0% in the sugammadex group (P < 0.0001, relative risk = 1.80, 95% confidence interval 1.36 to 2.41). The incidences of adverse events in the recovery room were low and comparable between the groups.The incidence of residual neuromuscular blockade on arrival in the recovery room was significantly higher in the neostigmine group than that in the sugammadex group. However, the incidence of adverse events was similar in the neostigmine and sugammadex groups.ClinicalTrials.gov identifier: NCT03292965.

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