
AbstractAimsPatients with acute decompensated advanced heart failure requiring left ventricular assist device (LVAD) implantation often experience progressive cardiac function deterioration, negatively impacting surgical outcomes. This study aimed to assess the efficacy of different microaxial flow pump (mAFP) support devices (Impella®) in achieving optimal left ventricular unloading for preconditioning and facilitating definitive treatment in this high‐risk patient cohort.Methods and resultsA retrospective analysis was conducted across 19 high‐volume European centres. The study population included patients transitioning from temporary to durable circulatory support over a 7.5‐year period, with a median follow‐up of 1 year. Patients were categorized based on mAFP support capacity: those receiving high‐flow support (>5 L/min, ‘5+’) and those with lower‐flow support (3.5 L/min, ‘CP’). Patients who were initially treated with CP but subsequently upgraded to 5+ support were classified in the 5+ group. Demographic and clinical characteristics, mobilization, right heart function, and organ dysfunction outcomes were analysed. A total of 339 patients received preoperative mAFP support prior to LVAD implantation. The 5+ group comprised 247 patients (73%), including 38 patients who were upgraded from CP, while the CP group included 92 patients (27%). Baseline demographic and clinical characteristics were comparable between groups, except for mobilization status, which showed significant differences (P < 0.001). Patients in the 5+ group achieved higher rates of full and partial mobilization compared to the CP group. Extracorporeal life support (ECLS) was more frequently required in the CP group than in the 5+ group (40.5% vs. 33.8%; P < 0.001). Additionally, right ventricular assist device (RVAD) implantation was significantly more common in the CP group (29.2% vs. 18.2%; P = 0.026). Patients in the 5+ group demonstrated greater reductions in both vasoactive inotropic scores (P = 0.006) and inotropic scores (P = 0.008). Furthermore, liver dysfunction (P = 0.016), renal failure (P = 0.041), and the need for dialysis (P = 0.013) were significantly more prevalent in the CP group. There were no significant differences between the two groups in terms of LVAD operative duration (P = 0.637) or cardiopulmonary bypass time (P = 0.408).ConclusionsHigh‐flow mAFP devices (+5) provided superior haemodynamic support, enhanced left ventricular unloading, and reduced dependence on catecholamines compared to lower‐flow CP devices. These improvements were associated with lower rates of right ventricular failure, renal dysfunction, and liver injury. However, no statistically significant difference was observed between mAFP groups regarding 30‐day mortality rates.
Male, Cardiac & Cardiovascular Systems, 610 Medizin, Prosthesis Design, Impella, Ventricular Function, Left, TEMPORARY, 610 Medical sciences, Humans, Diseases of the circulatory (Cardiovascular) system, 1102 Cardiorespiratory Medicine and Haematology, Cardiogenic shock, Retrospective Studies, Aged, Heart Failure, Science & Technology, Left heart failure, MECHANICAL CIRCULATORY SUPPORT, Equipment Design, Middle Aged, Durable mechanical circulatory support, Treatment Outcome, Microaxial flow pump, RC666-701, Cardiovascular System & Cardiology, Female, Original Article, Heart-Assist Devices, ADVERSE EVENTS, 3201 Cardiovascular medicine and haematology, Life Sciences & Biomedicine, Follow-Up Studies
Male, Cardiac & Cardiovascular Systems, 610 Medizin, Prosthesis Design, Impella, Ventricular Function, Left, TEMPORARY, 610 Medical sciences, Humans, Diseases of the circulatory (Cardiovascular) system, 1102 Cardiorespiratory Medicine and Haematology, Cardiogenic shock, Retrospective Studies, Aged, Heart Failure, Science & Technology, Left heart failure, MECHANICAL CIRCULATORY SUPPORT, Equipment Design, Middle Aged, Durable mechanical circulatory support, Treatment Outcome, Microaxial flow pump, RC666-701, Cardiovascular System & Cardiology, Female, Original Article, Heart-Assist Devices, ADVERSE EVENTS, 3201 Cardiovascular medicine and haematology, Life Sciences & Biomedicine, Follow-Up Studies
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