Core set of unfavorable events of shoulder arthroplasty: an international Delphi consensus process

dc.contributor.authorAudigé L., Schwyzer H.
dc.contributor.authorShoulder Arthroplasty Core Event Set (SA CES) Consensus Panel
dc.contributor.authorDurchholz H
dc.contributor.organizationfi=kliininen laitos|en=Department of Clinical Medicine|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.61334543354
dc.converis.publication-id44150229
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/44150229
dc.date.accessioned2022-10-28T12:46:31Z
dc.date.available2022-10-28T12:46:31Z
dc.description.abstract<div><h3>Background</h3><p>Shoulder arthroplasty (SA) complications require standardization of definitions and are not limited to events leading to revision operations. We aimed to define an international consensus core set of clinically relevant unfavorable events of SA to be documented in clinical routine practice and studies.</p></div><div><h3>Methods</h3><p>A Delphi exercise was implemented with an international panel of experienced shoulder surgeons selected by nomination through professional societies. On the basis of a systematic review of terms and definitions and previous experience in establishing an arthroscopic rotator cuff repair core set, an organized list of SA events was developed and reviewed by panel members. After each survey, all comments and suggestions were considered to revise the proposed core set including local event groups, along with definitions, specifications, and timing of occurrence. Consensus was reached with at least two-thirds agreement.</p></div><div><h3>Results</h3><p>Two online surveys were required to reach consensus within a panel involving 96 surgeons. Between 88% and 100% agreement was achieved separately for local event groups including 3 intraoperative (device, osteochondral, and soft tissue) and 9 postoperative event groups. Experts agreed on a documentation period that ranged from 3 to 24 months after SA for 4 event groups (peripheral neurologic, vascular, surgical-site infection, and superficial soft tissue) and that was lifelong until implant revision for other groups (device, osteochondral, shoulder instability, pain, late hematogenous infection, and deep soft tissue).</p></div><div><h3>Conclusion</h3><p>A structured core set of local unfavorable events of SA was developed by international consensus to support the standardization of SA safety reporting. Clinical application and scientific evaluation are needed.</p></div>
dc.format.pagerange2061
dc.format.pagerange2071
dc.identifier.jour-issn1058-2746
dc.identifier.olddbid178872
dc.identifier.oldhandle10024/161966
dc.identifier.urihttps://www.utupub.fi/handle/11111/36519
dc.identifier.urnURN:NBN:fi-fe2021042825820
dc.language.isoen
dc.okm.affiliatedauthorÄärimaa, Ville
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3126 Surgery, anesthesiology, intensive care, radiologyen_GB
dc.okm.discipline3126 Kirurgia, anestesiologia, tehohoito, radiologiafi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherMosby Inc.
dc.relation.doi10.1016/j.jse.2019.07.021
dc.relation.ispartofjournalJournal of Shoulder and Elbow Surgery
dc.relation.issue11
dc.relation.volume28
dc.source.identifierhttps://www.utupub.fi/handle/10024/161966
dc.titleCore set of unfavorable events of shoulder arthroplasty: an international Delphi consensus process
dc.year.issued2019

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