Abstract

PurposePrognosis of patients presenting with INTERMACS 1 critical cardiogenic shock is generally poor. The aim of our study was to investigate the results of CentriMag™ extracorporeal short-term mechanical circulatory support as a bridge to decision in patients presenting with critical cardiogenic shock in our unit.MethodsWe retrospectively analysed 63 consecutive patients from January 2005 to June 2017, who were treated with a CentriMag™ device at our institution as a bridge to decision. Patients requiring extracorporeal support for post-cardiotomy shock and for primary graft dysfunction after heart transplantation were excluded.ResultsPatients’ median age was 44 years (IQR 31–52, range 15.4–62.0) and 42 (67%) were male. Primary diagnosis at presentation was ischaemic cardiomyopathy (n = 24; 38.1%), viral myocarditis (n = 19; 30.2%), idiopathic dilated cardiomyopathy (n = 8; 12.7%), and others (n = 12; 19%). The median duration of support was 25 (IQR 9.5–56) days. A total of 7 (11%) patients were supported with peripheral veno-arterial (VA) extra corporeal membrane oxygenation (ECMO), 6 (9%) with central VA ECMO, 8 (13%) with left ventricular assist device (LVAD), 17 (27%) with biventricular assist device (BiVAD), and 25 (40%) with ECMO and then converted to BiVAD. Overall, 22 (34.9%) patients died while on CentriMag™ mechanical circulatory support. Complications included bleeding requiring reoperation/intervention in 24 (38%), renal failure requiring dialysis in 29 (46%), bacterial infections in 23 (37%), fungal infections in 15 (24%), critical limb ischaemia in 6 (10%), and stroke in 8 (13%). The overall survival to successful explant from CentriMag™ was 65.1% (n = 41) and survival to hospital discharge was 58.7% (n = 37). Of these, 10 (16%) had cardiac recovery and were successfully explanted, 20 (32%) were bridged to heart transplantation, 11 (17%) were bridged to long-term left ventricular assist device, 3 (4.7%) were later on transplanted, and 1 (1.6%) recovered to decommissioning. The 1-, 5-, and 10-year survival rates were 55%, 46%, and 23% respectively.ConclusionOur results demonstrate an excellent outcome with the use of the CentriMag™ device in this seriously ill population. Despite requiring multiple procedures, over 58% of patients were discharged from hospital with 5-year survival of 46%.

Highlights

  • Refractory heart failure despite maximal medical therapy carries a poor prognosis

  • These patients have been supported with a variety of mechanical options, including intra-aortic balloon pump (IABP), percutaneous devices like Impella®, extra corporeal life support (ECLS) with CentriMagTM, and implantation of durable devices like HeartMate 3TM

  • We retrospectively analysed 63 consecutive patients from January 2005 to June 2017, who were treated with a CentriMagTM device (Abbott Laboratories, Abbott Park, IL) at our institution as a ‘bridge to decision’ which means these patients had multi-organ dysfunction at presentation due to low cardiac output and were not suitable directly for transplantation/durable left ventricular assist device (LVAD)

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Summary

Introduction

Refractory heart failure despite maximal medical therapy carries a poor prognosis These patients often present acutely with no time for full assessment for heart transplantation. Even the cause of heart failure is unclear at presentation These patients have been supported with a variety of mechanical options, including intra-aortic balloon pump (IABP), percutaneous devices like Impella®, extra corporeal life support (ECLS) with CentriMagTM, and implantation of durable devices like HeartMate 3TM. These mechanical device strategies allow time to stabilise the haemodynamics in these very sick patients, to perform the S266. This strategy as bridge to decision is deemed cost effective and funded via the National Health Service (NHS) in UK

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