Evidence map›Paper›PMID 40688881›Full record

ReviewCureus2025

Remimazolam as a Novel Anesthetic in Pediatric Procedural Sedation and Anesthesia: A Narrative Review.

Min Zhu, Miaomiao Tang

Abstract readReview
In one paragraph

Review in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Min ZhuDepartment of Anesthesiology, West China Hospital of Sichuan University, Chengdu, CHN.
Miaomiao TangDepartment of Anesthesiology, West China Hospital of Sichuan University, Chengdu, CHN.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As an ultra-short-acting benzodiazepine, remimazolam demonstrates rapid onset, quick offset, and a short half-life. Current evidence suggests that its metabolism is not dependent on hepatic or renal function, and its effects can be reversed by flumazenil, a benzodiazepine antagonist. Ever since its approval for procedural sedation and general anesthesia, it has gained popularity due to its minimal impact on circulation and respiration and reduced incidence of adverse reactions. While the clinical application of remimazolam in adult and elderly patients has been studied and reported extensively, its safety and efficacy in pediatric patients remain unclear. Current evidence suggests its potential clinical value and application prospects in children. This review outlines the pharmacokinetics and pharmacodynamics of remimazolam and summarizes the latest research progress regarding its use in pediatric patients for procedural sedation and anesthetic induction and maintenance. We conducted a literature search using PubMed and the China National Knowledge Infrastructure (CNKI), specifically targeting clinical studies and case reports that evaluated the use of remimazolam for procedural sedation and general anesthesia in pediatric patients. The search strategy incorporated the following keyword combinations: "remimazolam and pediatric anesthesia", "remimazolam and pediatric sedation", "remimazolam and children", and "remimazolam and pediatric patients". In summary, we synthesized existing clinical studies and case reports to provide guidance and insights into the use and research of remimazolam in pediatric patients.

Indexed as

general anesthesianarrative reviewpediatric patientspharmacological characteristicsprocedural sedationremimazolam

Identifiers

PMID40688881
PMCPMC12275966

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.