MortalitY in candIAc surgery (MYRIAD): A randomizeD controlled trial of volatile anesthetics. Rationale and design
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F17%3A10364154" target="_blank" >RIV/00216208:11110/17:10364154 - isvavai.cz</a>
Alternative codes found
RIV/00064165:_____/17:10364154
Result on the web
<a href="http://dx.doi.org/10.1016/j.cct.2017.05.011" target="_blank" >http://dx.doi.org/10.1016/j.cct.2017.05.011</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.cct.2017.05.011" target="_blank" >10.1016/j.cct.2017.05.011</a>
Alternative languages
Result language
angličtina
Original language name
MortalitY in candIAc surgery (MYRIAD): A randomizeD controlled trial of volatile anesthetics. Rationale and design
Original language description
Objective: There is initial evidence that the use of volatile anesthetics can reduce the postoperative release of cardiac troponin I, the need for inotropic support, and the number of patients requiring prolonged hospitalization following coronary artery bypass graft (CABG) surgery. Nevertheless, small randomized controlled trials have failed to demonstrate a survival advantage. Thus, whether volatile anesthetics improve the postoperative outcome of cardiac surgical patients remains uncertain. An adequately powered randomized controlled trial appears desirable. Design: Single blinded, international, multicenter randomized controlled trial with 1:1 allocation ratio. Setting: Tertiary and University hospitals. Interventions: Patients (n = 10,600) undergoing coronary artery bypass graft will be randomized to receive either volatile anesthetic as part of the anesthetic plan, or total intravenous anesthesia. Measurements and main results: The primary end point of the study will be one-year mortality (any cause). Secondary endpoints will be 30-day mortality; 30-day death or non-fatal myocardial infarction (composite endpoint); cardiac mortality at 30 day and at one year; incidence of hospital re-admission during the one year follow-up period and duration of intensive care unit, and hospital stay. The sample size is based on the hypothesis that volatile anesthetics will reduce 1-year unadjusted mortality from 3% to 2%, using a two-sided alpha error of 0.05, and a power of 0.9. Conclusions: The trial will determine whether the simple intervention of adding a volatile anesthetic, an intervention that can be implemented by all anesthesiologists, can improve one-year survival in patients undergoing coronary artery bypass graft surgery.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
30223 - Anaesthesiology
Result continuities
Project
—
Continuities
V - Vyzkumna aktivita podporovana z jinych verejnych zdroju
Others
Publication year
2017
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Contemporary Clinical Trials
ISSN
1551-7144
e-ISSN
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Volume of the periodical
59
Issue of the periodical within the volume
August
Country of publishing house
US - UNITED STATES
Number of pages
6
Pages from-to
38-43
UT code for WoS article
000405157600005
EID of the result in the Scopus database
2-s2.0-85019761836