Modelos europeos de telemedicina, como el servicio finlandés Medilux, permiten realizar consultas médicas online mediante un cuestionario clínico, sin acudir a una consulta presencial.

Impella 2.5 improves survival in AMI with cardiogenic shock

Original title: The Use of Impella 2.5 in Severe Refractory Cardiogenic Shock Complicating and Acute Myocardial Infarction. Reference: Frederic Casassus et al. J Interv Cardiol. 2015 Feb;28(1):41-50.

The presence of cardiogenic shock is observed in 7% of patients undergoing acute myocardial infarction (AMI) with ST segment elevation and 2.5% of those with non-ST AMI. In this scenario inotropic have a poor response and the intra-aortic balloon pump (IABP) has been shown in multiple trials to be little or no effective.

22 patients who received the Impella 2.5 device and about to undergoing AMI with refractory cardiogenic shock were analyzed. Angioplasty was performed to culprit vessel and other vessels were treated in accordance with the decision of the surgeon. The involvement of other organs with SOFA and APACHE scores were analyzed prior to implantation of the device.

The average age of the population was 58 years and 40% had cardiopulmonary arrest prior to admission. The SOFA and APACHE scores were 9 and 30 points. All received inotropic; shock start mean time was 7 hours (1.8-19), IABP 54.6%. Angioplasty was successful in 86.4%. Half had cerebral anoxia injury, respiratory failure, and pulmonary edema. The third group showed severe acute deterioration of kidney function (eGFR <30). The Impella device was implanted using femoral approach successfully in all patients. There was a significant immediate improvement of ventricular filling pressures and ventricular function (27 ± 9% versus 43 ± 10%; p <0.0001). Peripheral perfusion improved after 48 hours of support. Impella 2.5 average time was 35.5 hours (21.5-57.8 hours).

Survival at 6 and 12 months was 59.1% and 54.5%. There was no stroke or vascular complications requiring surgery. 

Conclusion

The Impella 2.5 was used as a last alternative in patients who had cardiogenic shock and not responding to conventional treatment. The use of the device was favorable to short and medium term survival.

Editorial comment

This work covered a small population with a high mortality. Inotropic and IABP demonstrated its limited effectiveness. Ventricular assist devices are proving their benefit, giving an improvement in ventricular function, systemic injury and improving survival in the middle term with a low rate of complications related to the device. The development of these devices will help in this scenario.

Courtesy of Carlos Fava MD
Interventional Cardiologist
Buenos Aires – Favaloro Foundation

Carlos Fava

More articles by this author

EuroPCR 2026 | 10-Year Left Main PCI: When Survival Is Similar, Should the Less Invasive Strategy Prevail?

The primary goal of revascularization in left main coronary artery disease (LMCA) is to improve survival. However, debate continues regarding whether, in anatomically suitable...

EuroPCR 2026 | TAVI and Coronary Artery Disease: FFR-Guided PCI Showed Better Outcomes Than an Angiography-Guided Strategy

In patients undergoing TAVI, the concomitant presence of coronary artery disease continues to generate debate: whether coronary lesions should be treated before, during, or...

EuroPCR 2026 | Evolocumab Reduces Cardiovascular Events in Patients With Prior PCI Without Previous Myocardial Infarction: VESALIUS-CV Results

This presentation, delivered by Dr. Brian A. Bergmark and colleagues at EuroPCR 2026, detailed the results of the VESALIUS-CV trial, focusing specifically on the...

EuroPCR 2026 | Is It Safe to Stop Aspirin After One Month in MI Patients Undergoing PCI? TARGET-FIRST Analysis

This is a summary of the post-hoc analysis of the TARGET-FIRST study, presented by Dr. Giuseppe Tarantini at EuroPCR 2026, evaluating early aspirin discontinuation...

LEAVE A REPLY

Please enter your comment!
Please enter your name here

Related Articles

SOLACI Sessionsspot_img
Jornadas Guatemala 2026

Recent Articles

HERA-TAVI: Intra-Annular vs Supra-Annular Valves in TAVI

The HERA-TAVI study is an international multicenter registry that compared the clinical and hemodynamic outcomes of contemporary self-expanding transcatheter heart valves with intra-annular (IA)...

DOUBLE-CHOICE: Lower Pacemaker Implantation Rates with ACURATE neo2 Compared with Evolut in Patients Undergoing TAVI

The DOUBLE-CHOICE trial is a multicenter, randomized, controlled study conducted in Germany to evaluate the performance of next-generation transcatheter heart valves and different anesthesia...

GLUCO-TAVI | Can Glucocorticoids Reduce the Need for Permanent Pacemaker Implantation After TAVI?

Despite the expansion of transcatheter aortic valve implantation (TAVI) indications, cardiac conduction disturbances (CCD) and the need for permanent pacemaker implantation (PPI) remain the...