Total intravenous anesthesia induced and maintained by a combination of remimazolam and remifentanil without a neuromuscular blocking agent: a prospective, observational pilot study

• Published in: BMC anesthesiology 2022-07, Vol.22 (1), p.1-237, Article 237
• Main Authors: Park, Insun, Cho, Mincheul, Nam, Sun Woo, Hwang, Jung-Won, Do, Sang-Hwan, Na, Hyo-Seok
• Format: Article
• Language: English
• Subjects: Anesthesia; Benzodiazepines; Cardiac arrhythmia; General anesthesia; Hypertension; Hypotension; Hysteroscopy; Intravenous administration; Medical research; Medicine, Experimental; Midazolam; Neuromuscular blockade; Normal distribution; Patients; Remifentanil; Remimazolam; Respiratory tract; Surgery
• ISSN: 1471-2253; 1471-2253
• DOI: 10.1186/s12871-022-01779-2

Background A novel short-acting benzodiazepine, Remimazolam, has recently been approved for general anesthesia and sedation. Hence, we investigated the feasibility and safety of remimazolam during the induction and maintenance of general anesthesia without using a neuromuscular blocking agent (NMBA) in patients undergoing hysteroscopic surgery. Methods This prospective observational study included 38 patients undergoing hysteroscopic surgery. Remimazolam and remifentanil were the main anesthetic agents without an NMBA, and a supraglottic airway was inserted to protect the airway. The induction time, amount of each anesthetic agent used during anesthesia, intraoperative bispectral index (BIS) hemodynamic parameters, and recovery profiles were measured. Results General anesthesia was successfully administered to 37 patients using remimazolam and remifentanil without NMBA. The induction doses of remimazolam and remifentanil were 0.4 mg/kg (interquartile range [IQR] 0.34-0.47 mg/kg) and 1.07 [mu]g/kg (IQR, 0.90-1.29 [mu]g/kg), respectively. Additionally, the maintenance doses of remimazolam and remifentanil were 1.14 mg/kg/h (IQR, 0.88-1.55 mg/kg/h) and 0.06 [mu]g/kg/min (IQR, 0.04-0.08 [mu]g/kg/min), respectively. Intraoperative BIS values had risen temporarily > 60 in eight patients (21.6%) despite administration of 2 mg/kg/h of remimazolam; thus, they were treated with supplementary midazolam. The median recovery time was 7 min (IQR, 5-8 min) after 40 min (IQR, 40.0-57.5 min) of total mean anesthesia time. There was no correlation between the infusion dose of remimazolam and recovery profiles, such as recovery time, final BIS of anesthesia, modified observer assessment of alertness/sedation (OAA/S) scale or post-anesthesia recovery (PAR) score when arriving at the PACU, and length of stay in the PACU (all P > 0.05). Conclusion Remimazolam can be combined with remifentanil without an NMBA in female patients who undergo hysteroscopic surgery, during which a supraglottic airway is a feasible method to protect the airway. Trial registration The study protocol was registered at ClinicalTrials.gov (NCT05025410) on 27/08/2021. Keywords: General anesthesia, Hysteroscopy, Neuromuscular blockade, Remimazolam, Remifentanil