# Effect of oliceridine pretreatment on etomidate-induced myoclonus: a prospective, randomized, double-blind, controlled study

**Authors:** Qingqing Sun, Xiaoqian Wang, Ziyuan Chen, Guimin Dong, Xinyuan Shi, Shiyu Yu, Hongyi Xiao, Fanceng Ji

PMC · DOI: 10.3389/fmed.2026.1764143 · Frontiers in Medicine · 2026-03-06

## TL;DR

This study shows that pretreating with oliceridine significantly reduces muscle jerks caused by etomidate during anesthesia, without increasing side effects.

## Contribution

The study introduces oliceridine as a novel pretreatment to mitigate etomidate-induced myoclonus in a controlled clinical trial.

## Key findings

- Oliceridine pretreatment reduced myoclonus incidence by 37.8% compared to normal saline.
- Myoclonus severity was significantly lower in the oliceridine group.
- No significant adverse reactions or hemodynamic changes were observed in the oliceridine group.

## Abstract

Etomidate often induces adverse effects such as myoclonus during anesthesia induction, thereby increasing perioperative risks for patients to some extent. Oliceridine is a novel opioid with fewer opioid-related adverse reactions. This study aims to investigate the effect of oliceridine pretreatment on etomidate-induced myoclonus.

This study is a prospective, randomized, double-blind, controlled study. Patients scheduled for elective surgery under general anesthesia were selected and randomly divided into the oliceridine group (Group O) and the normal saline group (Group C), with 45 patients in each group. Two minutes before etomidate administration, Group O and Group C were given 0.02 mg/kg oliceridine and an equal volume of normal saline, respectively. Primary outcome measure: the incidence of etomidate-induced myoclonus. Secondary outcome measures: the severity of etomidate-induced myoclonus, as well as adverse reactions and hemodynamic changes occurring during the observation period.

The incidence of myoclonus in Group O was significantly lower than that in Group C (13.3% vs. 51.1%, RR = 0.45, 95% confidence interval [95%CI] = 0.310–0.667, p < 0.001). Compared with Group C, the incidence of myoclonus in Group O was reduced by 37.8%. Among the secondary outcomes, the severity of myoclonus in Group O was significantly lower than that in Group C (p < 0.001). The time to loss of consciousness in Group O was shorter than that in Group C (43.24 s ± 6.89 vs. 48.2 s ± 10.34, p = 0.008), and there was a statistically significant difference in the BIS values between the two groups at 2 min after etomidate induction (T2) (44.23 ± 9.38 vs. 53.75 ± 16.54, p = 0.001). In addition, there were no statistically significant differences in adverse reactions or hemodynamic changes between the two groups during the observation period.

Pretreatment with oliceridine can significantly reduce the incidence of etomidate-induced myoclonus. Therefore, oliceridine can be used as a new pretreatment strategy when etomidate is employed for anesthetic induction.

https://www.chictr.org.cn/searchproj.html, identifier ChiCTR2500108944.

## Linked entities

- **Chemicals:** oliceridine (PubChem CID 66553195), etomidate (PubChem CID 36339), normal saline (PubChem CID 5234)

## Full-text entities

- **Diseases:** myoclonus (MESH:D009207), loss of consciousness (MESH:D014474)
- **Chemicals:** Oliceridine (MESH:C586842), Etomidate (MESH:D005045)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

26 references — full list in the complete paper: https://tomesphere.com/paper/PMC13002601/full.md

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Source: https://tomesphere.com/paper/PMC13002601