Remimazolam: A Novel Option for Procedural Sedation in High Risk Patients.

J Pharm Pract

501438Sacred Heart University, College of Health Professions, Fairfield, CT, USA.

Published: February 2023

AI Article Synopsis

  • The drug review evaluates remimazolam, a newly approved benzodiazepine, focusing on its safety and effectiveness in comparison to midazolam.
  • Remimazolam offers faster onset and recovery times, has no significant drug-drug interactions, but may require dose adjustments for certain patients, including the elderly and those with severe liver issues.
  • Despite its advantages, remimazolam is more expensive than existing options, necessitating a review of its costs versus benefits in clinical settings.

Article Abstract

Purpose: The purpose of this drug review was to explore the safety and efficacy of the newly approved benzodiazepine, remimazolam, in order to evaluate its place in therapy.

Summary: Remimazolam has a faster onset of action and recovery time than midazolam when given as single IV doses. Additionally, it has no known CYP450 interactions that would contribute to drug-drug interactions. Patients with severe hepatic impairment may require dose titration as well as the elderly who should be closely monitored. Although remimazolam vials should be protected from light and must be reconstituted immediately before use, the reconstituted vial may be stored for later use at room temperature for up to 8 hours. Remimazolam is more expensive than current options used in practice, as such individual institutional formulary and provider preference will require review to see if its advantages are worth the additional cost and to determine its place in therapy.

Conclusion: Remimazolam is a novel option when choosing a benzodiazepine for procedural sedation that has pharmacokinetic and pharmacodynamic advantages when compared to other commonly prescribed sedatives. Remimazolam has proved superior to midazolam when analyzing drug-drug interactions, onset, and time to alertness. Remimazolam also has a shorter elimination half-life and decreased volume of distribution when compared to midazolam.

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Source
http://dx.doi.org/10.1177/08971900211027303DOI Listing

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