Publication:
Massive and Irreparable Rotator Cuff Tears

dc.contributor.authorBilgin, Emre
dc.contributor.authorKapıcıoğlu, Mehmet
dc.contributor.authorBilsel, İsmail Kerem
dc.contributor.institutionauthorKAPICIOĞLU, MEHMET
dc.contributor.institutionauthorBİLSEL, İSMAIL KEREM
dc.date.accessioned2020-08-31T20:59:23Z
dc.date.available2020-08-31T20:59:23Z
dc.date.issued2020-01-01T00:00:00Z
dc.description.abstractRotator cuff (RC) tears are a considerable reason of shoulder disability in both the young and elderly population. Although instrumentation methods and surgical techniques have been improving, the failure rates remain still high after tendon repairs attributed to large tear size, increased age, poor tendon quality and fatty infiltration of the RC muscle.To enhance the healing potential of RC and improve outcomes after repair, various augmentation methods have been introduced over the past two decades. Growth factors, stem cell therapies and scaffolds are the main augmentation approaches. The aim of these procedures is to enhance the healing potential of the repair construct and, simultaneously, help the restoration of the native tendon-to-bone interface.This chapter will focus on scaffold devices and their role in the augmentation of RC repair. The biomechanical properties of the scaffolds, their efficacy, outcomes and complications based on both preclinical and clinical studies are discussed. An overview of the future trends in scaffold augmentation for RC surgery is presented in light of the current literature.
dc.identifier.citationBilgin E., Kapıcıoğlu M., Bilsel İ. K. , Biological Augmentation in Rotator Cuff Repair: Scaffolds, -Massive and Irreparable Rotator Cuff Tears -, Nuno Sampaio GomesLadislav KovačičFrank MartetschlägerGiuseppe Milano, Editör, Springer, London/Berlin , Berlin, ss.55-66, 2020
dc.identifier.urihttp://hdl.handle.net/20.500.12645/18479
dc.language.isoen
dc.titleMassive and Irreparable Rotator Cuff Tears
dc.typeBook Chapter
dspace.entity.typePublication
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local.publication.isinternational1
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relation.isAuthorOfPublication.latestForDiscoverydb1859ad-a3b3-4299-8b42-89a62b377d7d
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