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Si, sono un operatore sanitario
Note: Ai sensi e per gli effetti dell’Art. 76 D.P.R. 445/2000 consapevole della responsabilità e delle conseguenze civili e penali previste in caso di dichiarazioni mendaci e/o formazione od uso di atti falsi, nonché in caso di esibizione atti contenenti dati non più corrispondenti a verità e consapevole altresì che qualora emerga la non veridicità del contenuto della presente decadranno i benefici per i quali la stessa è rilasciata confermo di essere un OPERATORE SANITARIO.
I contenuti presenti in questo sito contengono informazioni rivolte agli operatori sanitari, in quanto si riferiscono a prodotti rientranti nella categoria dei dispositivi medici che richiedono l’impiego o l’intervento da parte di professionisti del settore medico-sanitario.
Roller pumps push blood along, creating turbulence that can damage it and create debris by spalling particles from the tubing. Impeller pump blades push through the blood, causing areas of damaging turbulence. Centrifugal pumps, by contrast, promote laminar flow, which improves blood- and air-handling capabilities and decreases blood trauma.
The nonocclusive design of the Bio-Pump™ centrifugal blood pump helps decrease blood trauma associated with extracorporeal circulatory support during cardiopulmonary bypass. It uses the constrained forced-vortex pumping principle, in which a series of smooth-surfaced rotating cones pull the blood into the vortex created by the rotation. As the blood flows toward the pump outlet, the air-handling vortex energy created by the cones transfers to the blood in the form of pressure and velocity.
From early on, the design of centrifugal pumps was found to offer advantages for improved clinical outcomes*.
Both older patients and those undergoing longer procedures are being placed at “an elevated risk of multi-organ dysfunction.”8
Evidence is related to centrifugal blood pumps in general and is not specific to Bio-Pump.
Lynch et al. Centrifugal Blood Pumping for Open Heart Surgery; Minnesota Medicine, 1978; 61:536-537
Wheeldon et al. Vortex Pumping for Routine Cardiac Surgery; Perfusion, 1990; 5(2):135-43
Parault, B, Conrad, S. The Effect of Extracorporeal Circulation Time and Patient Age on Platelet Retention During Cardiopulmonary Bypass: A Comparison of Roller and Centrifugal Pumps; JECT; 1991, 23:34-38
Jakob HG, et al. Routine extracorporeal circulation with acentrifugal or roller pump; ASAIO Trans. 1991 Jul-Sep;37(3):M487-9
Morgan et al. Superiority of centrifugal pump over rollerpump in paediatric cardiac surgery: prospective randomized trial; EJCTS; 1998; 13:526-532
Klein et al. Centrifugal Pumping During Routine Open Heart Surgery; Artificial Organs 1998; 22:326-226
Parolari A, et al. Adult cardiac surgery outcomes: role of the pump type; EJCTS; 2000; 18:575-582
Tomasso et al. Hepatic and renal effects of cardiopulmonary bypass; Best Practice & Research Clinical Anaesthesiology; 2015; 29: 151-161
Caution: Federal Law (USA) restricts the device to sale by or on the order of a physician. For complete listing of indications, contraindications, precautions and warnings, please refer to the Instructions For Use which accompany each product. For distribution only in markets where the Bio-Pump and Bio-Console have been approved.
Bio-Pump, Bio-Console and AffinityTM CP are trademarks of Medtronic, Inc.
Medtronic Italia S.p.A. Società a socio unico soggetta ad attività di direzione e coordinamento da parte di Medtronic PLC.
Cap. soc. € 1.200.487,00 - Codice fiscale, partita IVA e numero di iscrizione al Registro delle Imprese di Milano-Monza-Brianza-Lodi 09238800156 – REA MI – 1275682. Sede Legale e Uffici Via Varesina, 162 Edificio Raimondi - 20156 Milano.