# Real‐World Evaluation of Remimazolam for Sedation During Gastrointestinal Endoscopy: Efficacy, Safety, and Risk Factors

**Authors:** Hinako Sakurai, Kurato Miyazaki, Atsushi Nakayama, Motoki Sasaki, Mai Oowada, Misaki Sugawara, Yuki Kubo, Rei Mizobe, Ai Katsumi, Maya Ishizawa, Yuri Imura, Shoma Murata, Daisuke Minezaki, Kentaro Iwata, Anna Tojo, Teppei Masunaga, Kumiko Kirita, Mari Mizutani, Michiko Nishikawa, Yusaku Takatori, Teppei Akimoto, Shintaro Kawasaki, Noriko Matsuura, Hideomi Tomida, Tomohisa Sujino, Kaoru Takabayashi, Kanai Takanori, Naohisa Yahagi, Motohiko Kato

PMC · DOI: 10.1002/jgh3.70351 · JGH Open: An Open Access Journal of Gastroenterology and Hepatology · 2026-02-16

## TL;DR

This study evaluates remimazolam for gastrointestinal endoscopy sedation, finding it safe with a high completion rate but noting hypoxia risks in older patients.

## Contribution

The study provides real-world evidence on remimazolam's efficacy and safety for endoscopic sedation, identifying age as a risk factor for hypoxia.

## Key findings

- Remimazolam achieved a 100% sedation completion rate with minimal serious adverse events.
- Advanced age was identified as a risk factor for hypoxia, but remimazolam dose was not independently linked to hypoxia or hypotension.
- Awakening occurred in 19% of patients, highlighting the need for monitoring during longer procedures.

## Abstract

Remimazolam is a benzodiazepine receptor agonist intravenous anesthetic. This study aimed to evaluate the efficacy and safety of remimazolam for sedation during gastrointestinal endoscopy using real‐world clinical data.

This retrospective observational study included 352 patients who underwent esophagogastroduodenoscopy or colonoscopy sedated with remimazolam between January and February 2024 at our institution. Outcomes included the incidence of awakening during procedures, the sedation completion rate, and the incidence and severity of adverse events. Multivariate logistic regression analyses identified factors associated with hypoxia and hypotension.

Median patient age was 67 years (IQR: 58–74), and 62.2% were male. Median initial and additional doses were 3 (IQR: 2–3 mg) and 1 mg (IQR: 0–2 mg). Awakening occurred in 19.0% of patients. The sedation completion rate was 100%. Adverse events included hypotension (7.8%), hypoxia (13.1%), and bradycardia (4.0%), and no serious adverse events were observed. The only risk factor for hypoxia was advanced age (Odds ratio 1.04, 95% confidence interval: 1.01–1.08, p = 0.03), and the dose of remimazolam itself was not an independent risk factor for either hypoxia or hypotension.

Remimazolam usage for gastrointestinal endoscopic sedation showed a favorable safety profile. Advanced age was associated with an increased risk of hypoxia, suggesting that careful monitoring and individualized sedation protocols are especially necessary for elderly patients. On the other hand, there are still issues regarding the duration of sedation. During long procedures, it is necessary to frequently check the depth of sedation to avoid undersedation.

## Linked entities

- **Chemicals:** remimazolam (PubChem CID 9867812)

## Full-text entities

- **Diseases:** hypersensitivity (MESH:D004342), hepatic disease (MESH:D056486), depression (MESH:D003866), renal disease (MESH:D007674), ASA-PS (MESH:C000719191), cardiovascular disease (MESH:D002318), Hypoxia (MESH:D000860), Bradycardia (MESH:D001919), Hypotension (MESH:D007022), hypoxic (MESH:D002534), respiratory depression (MESH:D012131), respiratory disease (MESH:D012140), pain (MESH:D010146)
- **Chemicals:** Remimazolam (MESH:C522201), benzodiazepine (MESH:D001569), benzodiazepine receptor agonist (-), propofol (MESH:D015742), Flumazenil (MESH:D005442), pethidine (MESH:D008614), oxygen (MESH:D010100), midazolam (MESH:D008874)
- **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/PMC12909598/full.md

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Source: https://tomesphere.com/paper/PMC12909598