The efficacy and tolerability of norepinephrine and epinephrine in cardiogenic shock after reperfused myocardial infarction will be compared, by following cardiac index evolution as main criteria. The study is a pilot pathophysiological study, randomized, double blind and multicenter.
Cardiogenic shock secondary to myocardial infarction is a frequent pathology in reanimation and is associated with high mortality (50%). Hemodynamic management and notably the choice of vasopressor in cardiogenic shock states secondary to myocardial infarction (cardiac index \< 2.2 l/min/m-2) is not codified. There are two opposite views: a) the first is based on the fact that an hypotensive patient with low cardiac output is primarily in need of an inotropic agent and that, consequently, epinephrine is the molecule of choice (inotropic and vasoconstrictor); b) the second is based on the fact that hypotension also reflects a certain degree of vascular failure and vascular vasoplegia and therefore norepinephrine is the molecule of choice along with, if needed, the eventual addition of dobutamine in order to separately titrate vasoconstriction and inotropism. Study hypotheses: epinephrine could facilitate myocardial function by providing the latter with its preferred substrate (lactate) and thus induce a higher cardiac index along with increased energy expenditure. Norepinephrine is the therapy of choice of hypotensive states; nevertheless its lack of inotropic effect could theoretically exacerbate myocardial failure. Thus, the aim of the study is to compared the efficiency and the tolerability of norepinephrine and epinephrine in cardiogenic shock after reperfused myocardial infarction.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
58
perfusion of commercial epinephrine prepared in syringes in order to obtain a MAP of 65-70 mmHg
perfusion of commercial norepinephrine prepared in syringes in order to obtain a MAP of 65-70 mmHg
Nancy Brabois university hospital
Vandœuvre-lès-Nancy, Meurthe Et Moselle, France
CHU de BESANCON / Hôpital Jean Minjoz
Besançon, France
CHU de DIJON
Dijon, France
CHU de LIMOGES Hôpital Dupuytren
Compared effects of investigated drugs on cardiac index
effectiveness of the treatment assessed by the evolution of cardiac index
Time frame: H0; H2, H4, H6, H12, H24, H48 and H72
pro/anti-inflammatory cytokines
Compared effects of investigated drugs on pro/anti-inflammatory cytokines
Time frame: H0, H24, H48 and H72
BNP
Compared effects of investigated drugs on BNP
Time frame: H0, H24, H48 and H72
Troponin
Compared effects of investigated drugs on Troponin
Time frame: H0, H24, H48 and H72
catecholamine doses
Compared effects of investigated drugs on the catecholamine doses
Time frame: H0, H24, H48 and H72
organ failure (SOFA Score)
Compared effects of investigated drugs on the organ failure
Time frame: H0, H24, H48 and H72
Lactate clearance
Compared effects of investigated drugs on the Lactate clearance
Time frame: H0, H2, H6, H12, H24 and H48
heart rate
Compared effects of investigated drugs on heart rate and the incidence of arrhythmia
Time frame: H0, H2, H4, H6, H12, H24, H48 and H72
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Limoges, France
APHM Hôpital NORD
Marseille, France
Chr Metz Thionville
Metz, France
CH de MULHOUSE
Mulhouse, France
AP-HP-Hôpital Cochin
Paris, France
CHU de STRASBOURG / NHC
Strasbourg, France
CHU Toulouse
Toulouse, France
...and 1 more locations
cardiac power index
Compared effects of investigated drugs on cardiac power
Time frame: H0, H2, H4, H6, H12, H24, H48 and H72.
SVO2
Compared effects of investigated drugs on the SVO2
Time frame: H0, H2, H4, H6, H12, H24, H48 and H72.
cardiac double product
Compared effects of investigated drugs on the cardiac double product
Time frame: H0, H2, H4, H6, H12, H24, H48 and H72.
refractory cardiogenic shock
compared effects of the investigated drugs on the occurrence of refractory cardiogenic shock
Time frame: H0, H2, H4, H6, H12, H24, H48 and H72.