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Published in: Canadian Journal of Anesthesia/Journal canadien d'anesthésie 11/2014

Open Access 01-11-2014 | Reports of Original Investigations

A randomized feasibility trial of clonidine to reduce perioperative cardiac risk in patients on chronic beta-blockade: the EPIC study

Authors: Duminda N. Wijeysundera, MD, PhD, Peter T. Choi, MD, Neal H. Badner, MD, Penelope M. Brasher, PhD, George K. Dresser, MD, PhD, Diego H. Delgado, MD, W. Scott Beattie, MD, PhD

Published in: Canadian Journal of Anesthesia/Journal canadien d'anesthésie | Issue 11/2014

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Abstract

Purpose

Clonidine may help prevent cardiac complications in patients undergoing non-cardiac surgery and receiving chronic beta-blocker therapy. We conducted a multicentre pilot randomized trial to estimate recruitment rates for a full-scale trial and to assess the safety and tolerability of combining clonidine with chronic beta-blockade.

Methods

Patients who were at elevated perioperative cardiac risk, receiving chronic beta-blockade, and scheduled for major non-cardiac surgery were recruited in a blinded (participants, clinicians, outcome assessors) placebo-controlled randomized trial at three Canadian hospitals. Participants were randomized to clonidine (0.2 mg oral tablet one hour before surgery, plus 0.2 mg·day−1 transdermal patch placed one hour before surgery and removed four days after surgery or hospital discharge, whichever came first) or matching placebo. Feasibility was evaluated based on recruitment rates, with each centre being required to recruit 50 participants within 12-18 months. Additionally, we reviewed study drug withdrawals and safety outcomes, including clinically significant hypotension or bradycardia.

Results

Eighty-two of the 168 participants were randomized to receive clonidine and 86 to receive placebo. The average time to recruit 50 participants at each centre was 14.3 months. Six patients (7%) withdrew from clonidine, while four (5%) withdrew from placebo. Based on qualitative review, there were no major safety concerns related to clonidine. There was a moderate overall rate of cardiac morbidity, with 18 participants (11%) suffering postoperative myocardial infarction.

Conclusion

This pilot randomized trial confirmed the feasibility, safety, and tolerability of a full-scale trial of oral and transdermal clonidine for reducing the risk of cardiac complications during non-cardiac surgery. This trial was registered at www.clinicaltrials.gov: NCT00335582.
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Footnotes
1
The R Project for Statistical Computing. R. A language and environment for statistical computing. (Available from URL: http://​www.​R-project.​org). Vienna, Austria: R Foundation for Statistical Computing; 2013 (accessed July 2014).
 
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Metadata
Title
A randomized feasibility trial of clonidine to reduce perioperative cardiac risk in patients on chronic beta-blockade: the EPIC study
Authors
Duminda N. Wijeysundera, MD, PhD
Peter T. Choi, MD
Neal H. Badner, MD
Penelope M. Brasher, PhD
George K. Dresser, MD, PhD
Diego H. Delgado, MD
W. Scott Beattie, MD, PhD
Publication date
01-11-2014
Publisher
Springer US
Published in
Canadian Journal of Anesthesia/Journal canadien d'anesthésie / Issue 11/2014
Print ISSN: 0832-610X
Electronic ISSN: 1496-8975
DOI
https://doi.org/10.1007/s12630-014-0226-6

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