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| ID | Type | Description | Link |
|---|---|---|---|
| 2024-A00253-44 | Registry Identifier | IDRCB |
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Cardiogenic shock is a life-threatening condition characterized by inadequate cardiac output, leading to organ hypoperfusion and high mortality. Maintaining mean arterial pressure (MAP) is crucial, but standard targets may be insufficient due to venous congestion. Central venous pressure (CVP) can help assess effective perfusion pressure. This study investigates whether a personalized MAP target adjusted by CVP improves organ function and survival compared to standard MAP management.
Cardiogenic shock is a severe and life-threatening condition. Its prognosis remains very poor with a high mortality rate (up to 50% in clinical series) despite recent therapeutic advances. Current recommendations suggest the use of inotropes and vasopressors to maintain tissue perfusion and prevent organ failure.
During cardiogenic shock, the mean arterial pressure (MAP) level is associated with survival. A post hoc analysis of a recent randomized trial found increased mortality among patients in cardiogenic shock whose average MAP was <70 mmHg during the first 36 hours after randomization, compared to patients with MAP ≥70 mmHg (58% vs. 29%, p<0.01). Another observational study found higher mortality among patients with a mean MAP <65 mmHg during the first 24 hours of shock compared to those with MAP ≥65 mmHg (57% vs. 28%, p<0.001). In this study, the incidence of renal failure was also inversely associated with MAP level. The optimal MAP target remains unknown during cardiogenic shock.
Due to the characteristic venous congestion, the effective perfusion pressure may be very low during cardiogenic shock despite MAP being within the usual target (65 mmHg). Furthermore, increased central venous pressure (CVP) is associated with higher mortality during cardiogenic shock. Considering venous congestion by measuring or estimating CVP is necessary to assess the effective perfusion pressure (MAP minus CVP) in order to protect against organ dysfunction. In this perspective, the MAP target should be increased by the value of the CVP.
The investigators hypothesize that personalizing the MAP target (to achieve an effective perfusion pressure of 65 mmHg) improves organ perfusion and survival during cardiogenic shock compared to the usual MAP target of 65 mmHg.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Personalized MAP | Experimental |
| |
| Standard MAP | Active Comparator |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Personalized MAP | Other | Patients receive blood pressure management targeting a personalized MAP ranging from 65 mmHg + CVP to 75 mmHg + CVP, without exceeding 90 mmHg.CVP is measured via a central venous catheter positioned in the superior vena cava. After 48 hours, if tissue perfusion is restored, the MAP target may be reduced to 65-70 mmHg. |
| Measure | Description | Time Frame |
|---|---|---|
| The primary endpoint will be a composite of mortality, use of cardiac mechanical circulatory support, and severe renal failure. | 7 days and 28 days after randomization |
| Measure | Description | Time Frame |
|---|---|---|
| Mortality in the intensive care unit (ICU), and in hospital | 28 days and 90 days after randomization | |
| Length of stay in the ICU and in the hospital | 28 days and 90 days after randomization | |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Armand MEKONTSO DESSAP, MD | Contact | + 33 1 45 17 85 06 | armand.dessap@aphp.fr |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| CHU d'Amiens-Picardie | Not yet recruiting | Amiens | 80000 | France |
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| ID | Term |
|---|---|
| D012770 | Shock, Cardiogenic |
| ID | Term |
|---|---|
| D009203 | Myocardial Infarction |
| D017202 | Myocardial Ischemia |
| D006331 | Heart Diseases |
| D002318 | Cardiovascular Diseases |
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| Standard MAP | Other | Patients receive blood pressure management aiming for a standard MAP target of 65-70 mmHg, according to international guidelines for cardiogenic shock management. |
|
| Proportion of patients requiring cardiac mechanical circulatory support |
| 28 days after randomization |
| Proportion of patients requiring renal replacement therapy | 28 days after randomization |
| Proportion of patients with severe acute kidney injury (stage 2 and stage 3 according to KDIGO AKI classification) | Defined as stage 2 or stage 3 according to the Kidney Disease: Improving Global Outcomes (KDIGO) Acute Kidney Injury classification | 7 days after randomization |
| Duration of inotrope and vasopressor support | 28 days after randomization |
| Use of mechanical ventilation | 28 days after randomization |
| Number of ventilator-free days | 28 days after randomization |
| Evolution of the vasoactive inotropic score (VIS) | The clinical outcome is defined based on the Vasoactive Inotropic Score (VIS), according to published standard references | 5 days after randomization |
| Evolution of lactate levels | 5 days after randomization |
| Evaluation of mottling score | 5 days after randomisation |
| Evaluation of capillary refill time | 5 days after randomization |
| Evaluation of Sequential Organ Failure Assessment (SOFA) score | The clinical outcome is defined based on the Sequential Organ Failure Assessment (SOFA) score, according to published standard references | 5 days after randomization |
| Proportion of patients with sustained ventricular and/or supraventricular arrhythmias | 5 days after randomization |
| Proportion of patients with stroke, non-cerebral ischemia, new or recurrent myocardial infarction | 28 days after randomization |
| Proportion of patients with major bleeding, defined according to the ISTH classification | Defined according to the International Society on Thrombosis and Haemostasis (ISTH) classification. | 28 days after randomization |
| Net clinical benefit at D28 (survival without thrombotic event or major bleeding). | 28 days after randomization |
| Proportion of patients receiving new specific treatments after randomization during hospital stay | 28 days after randomization |
| Hôpital Henri Mondor | Not yet recruiting | Créteil | 94010 | France |
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| Hôpital Privé Jacques Cartier | Not yet recruiting | Massy | 91300 | France |
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| CMC Ambroise Paré - Hartmann | Recruiting | Neuilly-sur-Seine | 92200 | France |
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| CHU d'Orléans | Not yet recruiting | Orléans | 45100 | France |
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| Hôpital Lariboisière | Not yet recruiting | Paris | 75010 | France |
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| Hôpital Cochin | Not yet recruiting | Paris | 75014 | France |
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| Clinique NCT + /Saint-Gatien | Not yet recruiting | Saint-Cyr-sur-Loire | 37540 | France |
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| Centre Cardiologique du Nord | Not yet recruiting | Saint-Denis | 93200 | France |
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| CHRU de Strasbourg | Not yet recruiting | Strasbourg | 67000 | France |
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| CHU de Toulouse | Not yet recruiting | Toulouse | 31000 | France |
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| D014652 |
| Vascular Diseases |
| D007238 | Infarction |
| D007511 | Ischemia |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D009336 | Necrosis |
| D012769 | Shock |