Title
Clonidine in patients undergoing noncardiac surgery
Date Issued
01 January 2014
Access level
open access
Resource Type
journal article
Author(s)
Devereaux P.J.
Sessler D.I.
Leslie K.
Kurz A.
Mrkobrada M.
Alonso-Coello P.
Villar J.C.
Sigamani A.
Biccard B.M.
Meyhoff C.S.
Parlow J.L.
Guyatt G.
Robinson A.
Garg A.X.
Rodseth R.N.
Botto F.
Lurati Buse G.
Xavier D.
Chan M.T.V.
Tiboni M.
Cook D.
Kumar P.A.
Forget P.
Fleischmann E.
Amir M.
Eikelboom J.
Mizera R.
Torres D.
Wang C.Y.
VanHelder T.
Paniagua P.
Berwanger O.
Srinathan S.
Graham M.
Pasin L.
Le Manach Y.
Gao P.
Pogue J.
Whitlock R.
Lamy A.
Kearon C.
Chow C.
Pettit S.
Chrolavicius S.
Yusuf S.
Publisher(s)
Massachussetts Medical Society
Abstract
BACKGROUND: Marked activation of the sympathetic nervous system occurs during and after non-cardiac 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. Copyright © 2014 Massachusetts Medical Society.
Start page
1504
End page
1513
Volume
370
Issue
16
Language
English
OCDE Knowledge area
Sistema cardiaco, Sistema cardiovascular
Scopus EID
2-s2.0-84898670781
PubMed ID
Source
New England Journal of Medicine
ISSN of the container
00284793
Sources of information: Directorio de Producción Científica Scopus