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Randomized Controlled Trial
. 2017 Aug 16;152(8):e171505.
doi: 10.1001/jamasurg.2017.1505. Epub 2017 Aug 16.

Intraoperative Infusion of Dexmedetomidine for Prevention of Postoperative Delirium and Cognitive Dysfunction in Elderly Patients Undergoing Major Elective Noncardiac Surgery: A Randomized Clinical Trial

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Randomized Controlled Trial

Intraoperative Infusion of Dexmedetomidine for Prevention of Postoperative Delirium and Cognitive Dysfunction in Elderly Patients Undergoing Major Elective Noncardiac Surgery: A Randomized Clinical Trial

Stacie Deiner et al. JAMA Surg. .
Free PMC article

Abstract

Importance: Postoperative delirium occurs in 10% to 60% of elderly patients having major surgery and is associated with longer hospital stays, increased hospital costs, and 1-year mortality. Emerging literature suggests that dexmedetomidine sedation in critical care units is associated with reduced incidence of delirium. However, intraoperative use of dexmedetomidine for prevention of delirium has not been well studied.

Objective: To evaluate whether an intraoperative infusion of dexmedetomidine reduces postoperative delirium.

Design, setting, and participants: This study was a multicenter, double-blind, randomized, placebo-controlled trial that randomly assigned patients to dexmedetomidine or saline placebo infused during surgery and for 2 hours in the recovery room. Patients were assessed daily for postoperative delirium (primary outcome) and secondarily for postoperative cognitive decline. Participants were elderly (>68 years) patients undergoing major elective noncardiac surgery. The study dates were February 2008 to May 2014.

Interventions: Dexmedetomidine infusion (0.5 µg/kg/h) during surgery and up to 2 hours in the recovery room.

Main outcomes and measures: The primary hypothesis tested was that intraoperative dexmedetomidine administration would reduce postoperative delirium. Secondarily, the study examined the correlation between dexmedetomidine use and postoperative cognitive change.

Results: In total, 404 patients were randomized; 390 completed in-hospital delirium assessments (median [interquartile range] age, 74.0 [71.0-78.0] years; 51.3% [200 of 390] female). There was no difference in postoperative delirium between the dexmedetomidine and placebo groups (12.2% [23 of 189] vs 11.4% [23 of 201], P = .94). After adjustment for age and educational level, there was no difference in the postoperative cognitive performance between treatment groups at 3 months and 6 months. Adverse events were comparably distributed in the treatment groups.

Conclusions and relevance: Intraoperative dexmedetomidine does not prevent postoperative delirium. The reduction in delirium previously demonstrated in numerous surgical intensive care unit studies was not observed, which underscores the importance of timing when administering the drug to prevent delirium.

Trial registration: clinicaltrials.gov Identifier NCT00561678.

Conflict of interest statement

Conflict of Interest Disclosures: None of the authors reported having a conflict of interest related to the outcomes of this study. Dr Deiner reported receiving product support (processed electroencephalogram and oximetry monitors and sensors) from Covidien and CASMED; however, no funds were received for the conduct of the present study.

Figures

Figure.
Figure.. CONSORT Diagram
CONSORT indicates Consolidated Standards of Reporting Trials.

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