Impella in Cardiogenic Shock Registry

Shock, Cardiogenic Clinical Trial

— Impella  

Official title:

Impella Left or Right Ventricular Support in Cardiogenic Shock

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06007963
• Other study ID #: 62048
• Status: Recruiting
• Start date: January 29, 2021
• Est. completion date: January 1, 2024

Study information

• Verified date: December 2022
• Source: Universitaire Ziekenhuizen KU Leuven
• Contact: Tom Adriaenssens, MD PhD
• Phone: 016/341392
• Email: tom.adriaenssens[@]uzleuven.be
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The purpose of the study is to evaluate the safety, efficacy and clinical usefulness of a mechanical support strategy with the impella device.

Description:

In the last two decades mortality from acute coronary syndromes has decreased dramatically thanks to aggressive use of coronary revascularization techniques. In cardiogenic shock however, a dramatique decrease in mortality since the introduction of primary PCI has not been seen, probably because restoring only coronary flow does not necessary imply restoration of whole body organ perfusion as long as the heart has not recuperated. To restore perfusion there are currently two options: catecholamine drugs (that can increase native cardiac output but at the price of increased oxygen consumption by the myocardium) or mechanical cardiac support (which provides artificial blood flow to the body, but depending on the device increases or decreases myocardial oxygen consumption). The dose of catecholamines used in cardiogenic shock patients is linearly correlated with worse outcome, suggesting a negative effect. Several mechanical cardiac support devices have been developed, but only some can be placed percutaneously and are available in Belgium.

The intra-aortic balloon pump, which was the first and remains the least invasive device, failed to show any mortality benefit in cardiogenic shock. A possible explanation could be the fact that this device device aims at restoring coronary rather than organ perfusion, since the increase in cardiac output after starting the balloon pump is very limited. Extracorporeal membrane oxygenation (ECMO) is an alternative to support organ perfusion, that provides the highest blood flow, but tends to increase cardiac work because it increases afterload. ECMO is also the most invasive percutaneous device since this requires two large bore access catheters to the patients' circulation and the blood flows through a bigger circuit, making it more prone to coagulation defects. The left side Impella device is a micro-axial continuous flow pump which sucks blood from the left ventricle towards the ascending aorta with the goal of increasing blood flow to the body while at the same time unloading the heart. This device only requires one access site (mostly smaller caliber as well). There is extensive experience with the left sided Impella device; its safety and efficacy have already been demonstrated in the past. The first results of the recent 'Detroit Cardiogenic Shock Initiative', aiming at early institution of mechanical support with the Impella device, already showed a significant decrease in mortality in participating centers. The Impella RP device is one of the only percutaneous devices that provide high flow support to the right ventricle by pushing blood from the inferior vena cava to the pulmonary artery. In the FDA approval study safety was demonstrated and outcomes where significantly better with the devices compared to historical controls.

An evolution to an earlier and as minimally invasive as possible strategy for mechanical support in cardiogenic shock is seen as well in the UZ Leuven cardiac intensive care unit. With an expierience of more than 20 years with the impella device in UZ Leuven (among the first to use the earlier versions of the device) this device was chosen as the first step to support the heart (in case of failure of one ventricle without need for additional oxygenation), with ECMO in second line since it is more invasive but delivers biventricular support with capability of higher flows. There are no high quality randomized controlled trials that compare one mechanical support strategy to another (except for one study in which almost 90% of patients were included after cardiac arrest, mostly dying from withdrawal of therapy). To improve quality, it seems key to measure outcomes and analyze these results as thoroughly as possible. For this reason, a prospective registry for all cardiogenic shock patients in the cardiac ICU, treated with the Impella device, is started.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: January 1, 2024
• Est. primary completion date: January 1, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• • Patients admitted for cardiogenic shock (defined as SBP <90 mmHg without vasopressors/inotropics or elevated serum lactate).

AND

• Treatment with Impella device

Exclusion Criteria:

• None

Related Conditions & MeSH terms

• Shock
• Shock, Cardiogenic

Intervention

Procedure:
• Treatment with impella device.
Impella percutaneous mechanical supported patients will be included after revision to support.

Locations

Country	Name	City	State
Belgium	University Hospitals Leuven, Gasthuisberg	Leuven

Sponsors (1)

Lead Sponsor	Collaborator
Universitaire Ziekenhuizen KU Leuven

Country where clinical trial is conducted

Belgium, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Mortality	Description: mortality: as assessed via patient file, contact with patient, general physician or family memeber	30 day and 1 year
Secondary	Myocardial recovery	myocardial recovery: assesses as the difference between echocardiographic left ventricular ejection fracton assessment (baseline versus follow-up time point)	30 dat and 1 year