Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/113558
Citations
Scopus Web of Science® Altmetric
?
?
Type: Journal article
Title: Clonidine in patients undergoing noncardiac surgery
Author: Devereaux, P.
Sessler, D.
Leslie, K.
Kurz, A.
Mrkobrada, M.
Alonso-Coello, P.
Villar, J.
Sigamani, A.
Biccard, B.
Meyhoff, C.
Parlow, J.
Guyatt, G.
Robinson, A.
Garg, A.
Rodseth, R.
Botto, F.
Buse, G.L.
Xavier, D.
Chan, M.
Tiboni, M.
et al.
Citation: New England Journal of Medicine, 2014; 370(16):1504-1513
Publisher: Massachusetts Medical Society
Issue Date: 2014
ISSN: 0028-4793
1533-4406
Statement of
Responsibility: 
P.J. Devereaux, D.I. Sessler, K. Leslie, A. Kurz, M. Mrkobrada, P. Alonso-Coello, J.C. Villar, A. Sigamani, B.M. Biccard, C.S. Meyhoff, J.L. Parlow, G. Guyatt, A. Robinson, A.X. Garg, R.N. Rodseth, F. Botto, G. Lurati Buse, D. Xavier, M.T.V. Chan, M. Tiboni, D. Cook, P.A. Kumar, P. Forget, G. Malaga, E. Fleischmann, M. Amir, J. Eikelboom, R. Mizera, D. Torres, C.Y. Wang, T. VanHelder, P. Paniagua, O. Berwanger, S. Srinathan, M. Graham, L. Pasin, Y. Le Manach, P. Gao, J. Pogue, R. Whitlock, A. Lamy, C. Kearon, C. Chow, S. Pettit, S. Chrolavicius, and S. Yusuf, for the POISE-2 Investigators*
Abstract: Background: Marked activation of the sympathetic nervous system occurs during and after noncardiac surgery. Low-dose clonidine, which blunts central sympathetic outflow, may prevent perioperative myocardial infarction and death without inducing hemodynamic instability. Methods: We performed a blinded, randomized trial with a 2-by-2 factorial design to allow separate evaluation of low-dose clonidine versus placebo and low-dose aspirin versus placebo in patients with, or at risk for, atherosclerotic disease who were undergoing noncardiac surgery. A total of 10,010 patients at 135 centers in 23 countries were enrolled. For the comparison of clonidine with placebo, patients were randomly assigned to receive clonidine (0.2 mg per day) or placebo just before surgery, with the study drug continued until 72 hours after surgery. The primary outcome was a composite of death or nonfatal myocardial infarction at 30 days. Results: Clonidine, as compared with placebo, did not reduce the number of primary-outcome events (367 and 339, respectively; hazard ratio with clonidine, 1.08; 95% confidence interval [CI], 0.93 to 1.26; P=0.29). Myocardial infarction occurred in 329 patients (6.6%) assigned to clonidine and in 295 patients (5.9%) assigned to placebo (hazard ratio, 1.11; 95% CI, 0.95 to 1.30; P=0.18). Significantly more patients in the clonidine group than in the placebo group had clinically important hypotension (2385 patients [47.6%] vs. 1854 patients [37.1%]; hazard ratio 1.32; 95% CI, 1.24 to 1.40; P<0.001). Clonidine, as compared with placebo, was associated with an increased rate of nonfatal cardiac arrest (0.3% [16 patients] vs. 0.1% [5 patients]; hazard ratio, 3.20; 95% CI, 1.17 to 8.73; P=0.02). Conclusions: Administration of low-dose clonidine in patients undergoing noncardiac surgery did not reduce the rate of the composite outcome of death or nonfatal myocardial infarction; it did, however, increase the risk of clinically important hypotension and nonfatal cardiac arrest.
Keywords: Post-operative complications
Rights: Copyright © 2014 Massachusetts Medical Society. All rights reserved.
DOI: 10.1056/NEJMoa1401106
Grant ID: NHMRC
Published version: http://dx.doi.org/10.1056/nejmoa1401106
Appears in Collections:Aurora harvest 8
Medicine publications

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.