Cardiogenic shock is currently the main cause of death after myocardial infarction and 50% of deaths occur within the first 48 hours. To limit the extent of the myocardial necrosis is the primary objective of the treatment in this context. The symptomatic treatment of the ventricular failure alone does not allow a reduction of mortality. The immediate prognosis is not significantly improved by the current standard of care, including early revascularisation and intra-aortic balloon counterpulsation. In order to improve the immediate prognosis, it seems necessary to limit the irreversible myocardial lesions and the systemic inflammatory response induced by an extended myocardial infarction (complement activation, cytokines production, iNOS expression, etc.). These objectives may be reached by a more extended utilization and availability of circulatory assistance methods. The investigators propose to compare, in a randomised multicenter study, two treatments of the myocardial infarction with cardiogenic shock among 44 patients: Standard Treatment versus ECLS-Impella +/- standard treatment. In June 2007, an amendment replaced the device ECMO by the use of Impella intra-thoracic pump. This amendment has been approved by the Ethic Committee on July 7, 2007. In March 2009, a new amendment has been approved by the EC. This amendment allowed to revise the number of patients to enroll (reduced to 44) and this lead us to modify also the primary endpoint : variation of BNP levels between H0 and H24 (H0 defined as the nearest value of BNP level obtained before the randomization).Showing a more important BNP levels decrease in the experimental group compared to standard treatment group, the investigators obtain an indirect argument to show a superior efficacy of the tested strategy.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
19
Percutaneous implantation of Impella pump for a duration of 3 days as a minimum and up to 7 days (recommended)
Brest University Hospital
Brest, France
Caen University Hospital
Caen, France
Clermont-Ferrand University Hospital
Clermont-Ferrand, France
Hôpital de la Croix Rousse
Lyon, France
Hôpital de la Timone
Marseille, France
Paris Sud Cardiovascular Institute
Massy, France
Mulhouse Hospital
Mulhouse, France
Pitié-Salpétrière Hospital
Paris, France
Cochin Hospital
Paris, France
Hôpital Haut-Lévèque
Pessac, France
...and 3 more locations
Variation of BNP levels between H0 and H24 (Ho is defined as the nearest value of BNP level before the randomization).
Time frame: one month
BNP levels measured at H6, H12, H48 and H72.
Time frame: one month
BNP level measured at H48 after assistance weaning.
Time frame: one month
haemoglobin levels
Time frame: one month
lactate levels
Time frame: one month
creatinine levels
Time frame: one month
Mortality at day 30 or Evolution to a refractory cardiogenic shock requiring an intra-thoracic ventricular assistance or an ECMO (ECLS-Impella group) and all types of ventricular assistance (IAPB group) or a cardiac graft within 30 days.
Time frame: one month
Mortality at Day 30, at 6 months, at 1 year.
Time frame: one year
Infarct size at 1 month and 4 months.
Time frame: 4 months
Amines maximal dose
Time frame: one month
Cardiologic treatments outside the hospital
Time frame: one year
Assistance last
Time frame: one month
mechanical ventilation last
Time frame: one month
assistance weaning failure
Time frame: one month
haemorrhagic, ischemic and septic complications.
Time frame: six months
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