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SI-BONE, Inc. annuncia il raggiungimento di 25.000 impianti iFuse
Date:9/10/2013

re che prosegue dai 12 ai 24 mesi con 82% e 100% di soddisfazione dei risultati chirurgici.(3),(4)  Di fatto, iFuse Implant System è l'unico dispositivo utilizzato in fusioni dell'articolazione sacroiliare a ridotta invasività per il quale siano stati pubblicati dati sull'efficacia e sulla sicurezza clinica con revisione da parte di terzi. 

"Venticinquemila impianti in poco più di quattro anni sono un risultato significativo ed è gratificante sapere che i nostri sforzi hanno aiutato così tanti pazienti.  I chirurghi, oltre ad altri professionisti del settore sanitario, hanno ora a disposizione una interessante alternativa per curare le rotture dell'articolazione sacroiliaca e la sacroileite degenerativa con diagnosi di dolore dell'articolazione sacroiliaca," ha dichiarato Jeffrey Dunn, Presidente e Amministratore Delegato di SI-BONE.

Il dott. Peter Whang, Professore Associato del Reparto di Ortopedia e Riabilitazione presso la Yale University School of Medicine, ha affermato, "l'articolazione sacroiliaca è diventata una fonte sempre più accettata di dolore del dorso inferiore e va sempre presa in considerazione nelle diagnosi differenziali.  Con questi pazienti è di importanza critica identificare in modo preciso l'origine del dolore e definendo una diagnosi corretta del dolore mediato dall'articolazione sacroiliare, potrebbe essere possibile evitare procedure non necessarie e in definitiva migliorare i risultati chirurgici.  In questa popolazione scelta, sta aumentando il corpus dell'esperienza clinica e della letteratura pubblicata che dimostra come la fusione dell'articolazione sacroiliare con ridotta invasività sia sicura ed efficace nell'alleviare i sintomi del dolore assiale del dorso inferiore."

Il dott. Gunnar Andersson, membro del Consiglio di Amministrazione della International So
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SOURCE SI-BONE, Inc.
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Related medicine technology :

1. SI-BONE, Inc. Announces Spring Society Meeting Attendance
2. SI-BONE, Inc. Announces Publication of Postmarket Surveillance Safety Data on First 5,319 Patients Treated with iFuse Implant System
3. SI-BONE, Inc. annuncia la pubblicazione dei dati sulla sicurezza della sorveglianza post-commercializzazione per i primi 5.319 pazienti trattati con il sistema di impianto iFuse Implant System
4. SI-BONE, Inc. Announces 25,000 iFuse Implant Milestone
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6. Nonin Medical annuncia lo spostamento del Centro Assistenza Clienti dalla Svezia ai Paesi Bassi
7. CryoLife annuncia il primo impianto europeo di HeRO Graft
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