4.6 Article

Dexmedetomidine administration during brain tumour resection for prevention of postoperative delirium: a randomised trial

Journal

BRITISH JOURNAL OF ANAESTHESIA
Volume 130, Issue 2, Pages E307-E316

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.bja.2022.10.041

Keywords

brain tumour resection; confusion assessment method; delirium; dexmedetomidine; randomised trial

Categories

Ask authors/readers for more resources

This study aimed to investigate whether dexmedetomidine administration during intracerebral tumour resection could reduce the incidence of postoperative delirium. The results showed a significant reduction in the incidence of delirium during the initial 5 postoperative days in the dexmedetomidine group compared to the placebo group. Dexmedetomidine also improved postoperative pain scores with movement, and recovery and sleep quality. Therefore, the prophylactic use of dexmedetomidine during surgery can effectively reduce postoperative delirium in patients undergoing elective brain tumour resection.
Background: Delirium is common, especially after neurosurgery. Dexmedetomidine might reduce delirium by improving postoperative analgesia and sleep quality. We tested the primary hypothesis that dexmedetomidine administration during intracerebral tumour resection reduces the incidence of postoperative delirium.Methods: This randomised, double-blind, placebo-controlled trial was conducted in two tertiary-care hospitals in Beijing. We randomised 260 qualifying patients to either dexmedetomidine (n=130) or placebo (n=130). Subjects assigned to dexmedetomidine were given a loading dose of 0.6 mg kg -1 followed by continuous infusion at 0.4 mg kg -1 h-1 until dural closure; subjects in the placebo group were given comparable volumes of normal saline. The primary outcome was the incidence of delirium, which was assessed with the Confusion Assessment Method twice daily during the initial 5 postoperative days.Results: The average (standard deviation) age of participating patients was 45 (12) yr, duration of surgery was 4.2 (1.5) h, and patients assigned to dexmedetomidine were given an average of 126 (45) mg of dexmedetomidine. There was less delirium during the initial 5 postoperative days in patients assigned to dexmedetomidine (22%, 28 of 130 patients) than in those given placebo (46%, 60 of 130 patients) with a risk ratio of 0.51 (95% confidence interval: 0.36-0.74, P<0.001). Postoperative pain scores with movement, and recovery and sleep quality were improved by dexmedetomidine (P<0.001). The incidence of safety outcomes was similar in each group.Conclusions: Prophylactic intraoperative dexmedetomidine infusion reduced by half the incidence of delirium during the initial 5 postoperative days in patients recovering from elective brain tumour resection.Clinical trial registration: NCT04674241.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available