Key result
VANQUISH Shock registry evaluates 30-day post-discharge survival and 1-year outcomes in cardiogenic shock.
Why the study?
Outcomes in cardiogenic shock remain poor due to major gaps in understanding pathophysiology, patient phenotyping, and challenges conducting adequately powered clinical studies.
Observational
Yes
The VANQUISH Shock registry is designed to prospectively collect detailed longitudinal data on adult patients with cardiogenic shock to improve understanding of pathophysiology, contemporary management, and outcomes.
Enables prospective granular data collection across cardiogenic shock etiologies; leaves open whether biomarkers or machine-learning models will improve risk stratification.
BACKGROUND: Despite efforts to advance therapies in cardiogenic shock (CS), outcomes remain poor. This is likely due to several factors, including major gaps in our understanding of the pathophysiology, phenotyping of patients, and challenges with conducting adequately powered clinical studies. An unmet need exists for a comprehensive multicentre "all-comers" prospective registry to facilitate characterising contemporary presentation, treatment (in a device-agnostic fashion), and short- and intermediate-term outcomes and quality of life (QOL) of CS patients. METHODS: The Multicenter Collaborative to Enhance Biological Understanding, Quality and Outcomes in Cardiogenic Shock (VANQUISH Shock) registry is a prospective observational registry that will study unrestricted adult patients with a primary diagnosis of CS at 4 North American centres with multidisciplinary shock programs. Both acute myocardial infarction (AMI-CS) and acute heart failure (HF-CS) etiologies will be included, and the registry will be device agnostic and widely inclusive. The primary end point will be survival at 30 days after hospital discharge. Secondary outcomes will include in-hospital adverse events and survival to 6 and 12 months. Patients will also undergo neurologic and health-related QOL assessments with the Cerebral Performance Category (CPC) and Short-Form 36 (SF-36) health survey tools before discharge and during follow-up. Serial biospecimens will facilitate biomarker studies. CONCLUSIONS: The VANQUISH Shock registry provides a unique opportunity to study the pathophysiology, contemporary management, clinical course, and outcomes of CS. By capturing detailed and high-quality longitudinal data, the registry will address existing knowledge gaps and serve as a springboard for future mechanistic clinical studies to advance the field.
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Tehrani et al. (2022) conducted an observational in Cardiogenic shock. Multidisciplinary shock team management in cardiogenic shock was evaluated on Survival at 30 days after hospital discharge. The VANQUISH Shock registry is a prospective observational study designed to evaluate 30-day post-discharge survival and 1-year outcomes in adults with cardiogenic shock across 4 North American sites.
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