# Low-dose mivacurium facilitates laryngeal mask airway insertion in patients undergoing hysteroscopic surgery: a prospective, single-center, double-blind randomized controlled trial

**Authors:** Yingchao Guan, Lizhen Wu, Haochen Wang, Conghui Wang, Yusong Lin, Minghong Ju, Xiaojing Cong, Wen He, Xiaodong Wang

PMC · DOI: 10.3389/fphar.2025.1700175 · 2025-10-17

## TL;DR

Low-dose mivacurium helps insert a laryngeal mask airway more easily during hysteroscopic surgery and reduces side effects like sore throat and nausea.

## Contribution

This study is the first to demonstrate that low-dose mivacurium improves laryngeal mask airway insertion and reduces anesthetic use and postoperative discomfort.

## Key findings

- Mivacurium reduced swallowing, coughing, and pharyngeal spasm during laryngeal mask airway insertion.
- Mivacurium increased first-attempt success and reduced insertion time and propofol use.
- Mivacurium lowered postoperative sore throat and nausea compared to the control group.

## Abstract

To explore whether the application of mivacurium can facilitate laryngeal mask airway (LMA) insertion and benefit patients.

A total of 167 patients undergoing hysteroscopy were randomly divided into mivacurium (group M) and control (group C) groups. The anesthesia induction scheme was mivacurium + sufentanil + propofol in group M, whereas mivacurium was replaced with saline in group C. The main outcome was the LMA insertion condition Secondary outcomes included attempts and elapsed time of LMA insertion, intraoperative anesthetic consumption, perioperative hemodynamics, postoperative sore throat (POST), nausea, vomiting, dizziness, and agitation.

There was no difference in the baseline data (p > 0.05). There was no significant difference in mouth opening; however, the incidence of swallowing, coughing, body movement, and pharyngeal spasm in group M was lower (p < 0.001), and the proportion of no resistance during LMA insertion was higher (80.5% vs. 21.2%, p < 0.001). The success rate of first-attempt LMA insertion in group M was higher (98.8% vs. 48.2%, p < 0.001), the elapsed time was shorter (16.9 (9.0) vs. 73.0 (91.5) s, p < 0.001), and fewer patients needed additional propofol (1.2% vs. 54.1%, p < 0.001). Blood staining on the LMA surface showed no significant difference, but the postoperative pharyngeal pain score in group M was lower (1.0 (1.0) vs. 2.0 (1.0), p < 0.001). Intraoperative propofol and remifentanil consumption, postoperative dizziness and nausea were lower in group M.

Mivacurium facilitates LMA insertion and reduce intraoperative anesthetic consumption and adverse reactions, such as POST, nausea, and dizziness,so as to benefit the patient.

clinicaltrials.gov, identifier ChiCTR2500101122.

## Linked entities

- **Chemicals:** mivacurium (PubChem CID 5281042), sufentanil (PubChem CID 41693), propofol (PubChem CID 4943), remifentanil (PubChem CID 60815)

## Full-text entities

- **Diseases:** agitation (MESH:D011595), postoperative (MESH:D019106), vomiting (MESH:D014839), nausea (MESH:D009325), POST (MESH:D010612), dizziness (MESH:D004244)
- **Chemicals:** Mivacurium (MESH:D000077590), propofol (MESH:D015742), remifentanil (MESH:D000077208), sufentanil (MESH:D017409)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12575122/full.md

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Source: https://tomesphere.com/paper/PMC12575122