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CryoLife annuncia il primo impianto europeo di HeRO Graft
Date:7/31/2013

essor Heye per avere eseguito la procedura.  Nel corso della parte rimanente dell'anno formeremo altri medici all'esecuzione della procedura, in modo da sostenere un lancio più ampio in Europa agli inizi del 2014.  Continuiamo a credere che HeRO Graft rappresenti un'opportunità significativa in grado di fornire un'opzione migliore per l'accesso alla dialisi per i pazienti affetti da malattia renale allo stadio terminale e che favorirà la crescita della Società."

Informazioni su HeRO GraftThe HeRO Graft ha ricevuto l'approvazione iniziale FDA 510(k) nel 2008 e l'approvazione iniziale per il marchio CE nel 2011.  È indicato per pazienti ESRD catetere-dipendenti sottoposti a emodialisi a lungo termine e che hanno esaurito ogni altra opzione di accesso, quali le fistole e gli innesti AV (AVF e AVG). Prima dell'introduzione di HeRO Graft, l'unica opzione a disposizione di questi pazienti era l'accesso con cateteri da dialisi tunnellizzati ipodermici (TDC), che hanno un costo maggiore, percentuali di infezione più elevate, limitano lo stile di vita dei pazienti, e favoriscono la stenosi di vena centrale, o il restringimento.  HeRO Graft supera i limiti dei TDC poiché si tratta di un innesto completamente sottocutaneo che funziona come un innesto di accesso regolare nel corso della dialisi e fornisce un flusso sanguigno superiore e una riduzione del 69 percento della batteriemia (batteri nel sangue) rispetto ai TDC. HeRO Graft è l'unica soluzione AV di accesso sottocutaneo che ha dimostrato di essere in grado di mantenere l'accesso a lungo termine per i pazienti in emodialisi con stenosi della vena centrale.

HeRO Graft è stato impiantato in oltre 6.000 pazienti alla data odierna ed è supportato da quasi 130 studi clinici e presentazioni pubblicate.  Il prodotto ha definito percentuali di rimborso negli USA con codici di rimbor
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SOURCE CryoLife, Inc.
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