Effective remimazolam loading dose for adequate sedation in regional anesthesia
Purpose Remimazolam is a novel ultrashort-acting sedative considered appropriate for continuous infusion during surgical procedures. Nevertheless, information regarding its loading dose for sedation during surgery is limited. We aimed to determine the 90% effective dose (ED 90 ) of the remimazolam l...
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Veröffentlicht in: | Canadian journal of anesthesia 2024-06, Vol.71 (6), p.818-825 |
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Sprache: | eng |
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Zusammenfassung: | Purpose
Remimazolam is a novel ultrashort-acting sedative considered appropriate for continuous infusion during surgical procedures. Nevertheless, information regarding its loading dose for sedation during surgery is limited. We aimed to determine the 90% effective dose (ED
90
) of the remimazolam loading dose for sedation in patients undergoing limb surgery under regional anesthesia.
Methods
We included 50 patients aged 19–80 yr undergoing limb surgery under regional anesthesia. After regional anesthesia, remimazolam besylate was administered at the assigned dose. For ten minutes after the initiation of loading, the level of sedation was evaluated using the Modified Observer’s Assessment of Alertness/Sedation (MOAA/S) scale. The primary outcome was the ED
90
based on whether patients reached a MOAA/S score of ≤ 3 points (loss of response to verbal command) within ten minutes. The secondary outcomes were the ED
50
and the estimated effect site and plasma concentration at the time of achieving successful sedation.
Results
In total, 49 patients were included in the final analysis, and adequate sedation with the assigned loading dose was successful in 42 patients. The log-logistic function showed that the ED
90
and ED
50
were 0.617 mg·kg
−1
·hr
−1
(95% confidence interval [CI], 0.511 to 0.722; 98% CI, 0.492 to 0.741) and 0.438 mg·kg
−1
·hr
−1
(95% CI, 0.335 to 0.541; 98% CI, 0.315 to 0.560), respectively.
Conclusion
The ED
90
of the remimazolam loading dose to achieve adequate sedation in patients undergoing limb surgery under regional anesthesia was 0.617 mg·kg
−1
·hr
−1
(95% CI, 0.511 to 0.722; 98% CI, 0.492 to 0.741).
Study registration
ClinicalTrials.gov (NCT05340335); first posted 22 April 2022. |
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ISSN: | 0832-610X 1496-8975 1496-8975 |
DOI: | 10.1007/s12630-024-02698-1 |