Prognosis of Patients With Mixed Cardiogenic-Vasoplegic Shock

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCentre Hospitalier Universitaire, Amiens

About this trial

Mixed cardiogenic-vasoplegic shock (M-CS) represents a distinct and severe phenotype of cardiogenic shock characterized by concomitant myocardial dysfunction and inappropriate systemic vasodilation. Despite its clinical relevance, the epidemiology, management, and outcomes of M-CS remain poorly defined.

This retrospective, multicenter, observational registry aims to evaluate the clinical outcomes and prognostic factors associated with mixed cardiogenic-vasoplegic shock. The study will analyze clinical, biological, and invasive hemodynamic data routinely collected during patient management for M-CS.

All included patients will have been admitted for cardiogenic shock, with or without vasoplegia, defined by low cardiac output and, when present, decreased systemic vascular resistance despite adequate filling pressures requiring vasopressor support.

The primary objective is to describe mortality and organ failure rates, while secondary analyses will identify determinants of adverse outcomes and potential phenotypic subgroups.

The PROMIX registry will be conducted across three French university hospitals (CHU Amiens-Picardie, CHU Dijon-Bourgogne, and CHU Rouen-Normandie).

This study is non-interventional, involving only data obtained as part of routine critical care, and will provide the first multicenter overview of this complex and underrecognized form of cardiogenic shock.

Eligibility criteria

Qualifiers

Adult patient (>18 years old)

Admitted to an intensive care unit for cardiogenic shock, at least SCAI stage C

No opposition to data use

Disqualifiers

Missing key data, particularly regarding vasopressor doses and outcomes.

Pregnant women

Anaphylactic shock,

Isolated hemorrhagic shock,

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

2,500 Participants
are grouped into 2 trial groups

Sponsors and collaborators

Centre Hospitalier Universitaire, Amiens

Lead sponsor

Centre Hospitalier Universitaire Dijon

Collaborator

University Hospital, Rouen

Collaborator