Multicentre comparison of various microaxial pump devices as a bridge to durable assist device implantation
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články, multicentrická studie, srovnávací studie
PubMed
40181705
PubMed Central
PMC12287827
DOI
10.1002/ehf2.15282
Knihovny.cz E-zdroje
- Klíčová slova
- Cardiogenic shock, Durable mechanical circulatory support, Impella, Left heart failure, Microaxial flow pump,
- MeSH
- design vybavení MeSH
- funkce levé komory srdeční * fyziologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- následné studie MeSH
- podpůrné srdeční systémy * MeSH
- protézy - design MeSH
- retrospektivní studie MeSH
- senioři MeSH
- srdeční selhání * chirurgie patofyziologie MeSH
- výsledek terapie MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
- srovnávací studie MeSH
AIMS: Patients 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 RESULTS: A 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). CONCLUSIONS: High-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.
Deparment of Cardiac Surgery IRCCS Bologna St Orsola University Hospital Bologna Italy
Department of Anesthesia and Intensive Care IRCCS San Raffaele Scientific Institute Milan Italy
Department of Cardiac Surgery Heidelberg University Hospital Heidelberg Germany
Department of Cardiac Surgery Leipzig Heart Center Leipzig Germany
Department of Cardiac Surgery Schüchtermann Clinic Bad Rothenfelde Germany
Department of Cardiac Surgery University Hospitals Leuven Leuven Belgium
Department of Cardiac Surgery University of Essen Essen Germany
Department of Cardiology University Medical Center Utrecht Utrecht Netherlands
Department of Cardiothoracic and Vascular Surgery Deutsches Herzzentrum der Charité Berlin Germany
Department of Cardiothoracic Surgery Jena University Hospital Jena Germany
Department of Cardiothoracic Surgery Rigshospitalet Copenhagen Denmark
Department of Cardiothoracic Surgery University Hospital Cologne Cologne Germany
Department of Cardiothoracic Surgery University Hospital RTWH Aachen Aachen Germany
Department of Cardiovascular Surgery Charité Universitätsmedizin Berlin Berlin Germany
Department of Cardiovascular Surgery University Heart Center Hamburg Hamburg Germany
Department of Cardiovascular Surgery University Hospital Duesseldorf Duesseldorf Germany
Department of Cardiovascular Surgery University Hospital Schleswig Holstein Kiel Germany
Department of Surgery Division of Cardiac Surgery Medical University of Vienna Vienna Austria
Department of Surgical Sciences University of Turin Turin Italy
DZHK partner site Berlin Berlin Germany
Heart and Diabetes Center North Rhine Westphalia Bad Oeynhausen Germany
Institute of Clinical and Experimental Medicine Prague Czech Republic
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