Intra-aortic Balloon Pump for Acute-on-Chronic Heart Failure Complicated by Cardiogenic Shock
- PMID: 34774745
- DOI: 10.1016/j.cardfail.2021.11.009
Intra-aortic Balloon Pump for Acute-on-Chronic Heart Failure Complicated by Cardiogenic Shock
Abstract
The intra-aortic balloon pump (IABP) is widely implanted as temporary mechanical circulatory support for cardiogenic shock (CS). However, its use is declining following the results of the IABP-SHOCK II trial, which failed to show a clinical benefit of the IABP in acute coronary syndrome (ACS)-related CS. Acute-on-chronic heart failure has become an increasingly recognized, distinct cause of CS (HF-CS). The pathophysiology of HF-CS differs from that of ACS-CS because it typically represents the progression from a state of congestion (with relatively preserved cardiac output) to a low-output state with hypoperfusion. The IABP is a volume-displacement pump that promotes forward flow from a high-capacitance reservoir to low-capacitance vessels, improving peripheral perfusion and decreasing left ventricular afterload in the setting of high filling pressures. The IABP can improve ventricular-vascular coupling and, therefore, myocardial energetics. Additionally, many patients with HF-CS are candidates for cardiac replacement therapies (left ventricular assist device or heart transplantation) and, therefore, may benefit from a bridge strategy that stabilizes the hemodynamics and end-organ function in preparation for more durable therapies. Notably, the new United Network for Organ Sharing donor heart allocation system has recently prioritized patients on IABP support. This review describes the role of IABP in the treatment of HF-CS. It also briefly discusses new strategies for vascular access as well as fully implantable versions for longer duration of support.
Keywords: acute on chronic heart failure; cardiogenic shock; intra-aortic balloon pump.
Copyright © 2021 Elsevier Inc. All rights reserved.
Conflict of interest statement
Conflicts of Interest Dr. Colombo reports consultant fees and other from Abbott outside the submitted work. Dr Morici reports lecture fees from Pfizer/Bristol-Myers Squibb and grant research from Getinge Global USA. Dr. Kapur receives speaking/consulting honoraria and instutional research support from Abbott, Abiomed, Boston Scientific, Edwards, Getinge, Medtronic, LivaNova, MD Start, Precardia, and Zoll. Dr. Garan reports consulting fees from Abiomed and NuPulseCV and has received research support from Abbott and Verantos. The other authors have no conflict of interest to disclose.
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