A multicenter, prospective 2-year analysis of the Sidus stem-free shoulder arthroplasty system

Background: The purpose of this multicenter, prospective study was to evaluate the efficacy and safety of a stemless total shoulder arthroplasty compared with a traditional stemmed control. Methods: Ninety-five shoulders were selected for participation in this Food and Drug Administration investigat...

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Main Authors: George S. Athwal, MD, FRCS(C), Ryan J. Krupp, MD, Grant Carlson, BS, Ryan T. Bicknell, MD, MSc, FRCS(C)
Format: Article
Language:English
Published: Elsevier 2020-03-01
Series:JSES International
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2468602619300567
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spelling doaj-fadd2149564746a6933e1907afd7ac842021-03-22T08:43:38ZengElsevierJSES International2666-63832020-03-0141120126A multicenter, prospective 2-year analysis of the Sidus stem-free shoulder arthroplasty systemGeorge S. Athwal, MD, FRCS(C)0Ryan J. Krupp, MD1Grant Carlson, BS2Ryan T. Bicknell, MD, MSc, FRCS(C)3Roth|MacFarlane Hand and Upper Limb Centre, London, ON, Canada; Corresponding author: George S. Athwal, MD, FRCS(C), Roth|MacFarlane Hand and Upper Limb Centre, 268 Grosvenor St, London, ON N6A 4L6, Canada.Norton Orthopaedic Specialists, Louisville, KY, USACampbell University, Buies Creek, NC, USADepartment of Surgery, Queen's University, Kingston General Hospital, Kingston, ON, Canada; Department of Mechanical and Materials Engineering, Queen's University, Kingston General Hospital, Kingston, ON, CanadaBackground: The purpose of this multicenter, prospective study was to evaluate the efficacy and safety of a stemless total shoulder arthroplasty compared with a traditional stemmed control. Methods: Ninety-five shoulders were selected for participation in this Food and Drug Administration investigational device exemption clinical trial and underwent stemless total shoulder arthroplasty. Subjects returned for follow-up at 6 weeks, 6 months, 12 months, and 2 years postoperatively. Outcome measures included pain; range of motion; American Shoulder and Elbow Surgeons, Western Ontario Osteoarthritis of the Shoulder, and Short Form 12 scores; and radiographic review. Baseline data were compared with 2-year follow-up data to determine the rate of composite clinical success compared with the stemmed control. Results: All outcome assessments demonstrated significant improvements (P ≤ .007). The mean American Shoulder and Elbow Surgeons score improved from 20 to 89 (P < .0001), and the mean shoulder pain score decreased from 8.3 ± 1.6 to 0.7 ± 1.5 (P < .0001). The mean Western Ontario Osteoarthritis of the Shoulder score decreased from 1443 ± 256 to 203 ± 267 (P < .0001). On the Short Form 12, the mean physical health score increased from 33 ± 7 to 48 ± 9 (P < .0001) and the mean mental health score increased from 50 ± 13 to 54 ± 8 (P = .007). Mean active forward elevation increased from 97° ± 27° to 143° ± 25° (P < .0001), and mean active external rotation increased from 21° ± 16° to 53° ± 18° (P < .0001). Kaplan-Meier analysis showed an implant survivorship rate of 98% at 2 years. The composite clinical success rate was 87% compared with 85% for the stemmed control. Conclusions: This study showed that a stemless rough-blasted humeral implant with metaphyseal bone fixation provides good clinical and radiographic outcomes and survivorship at 2 years, with outcomes comparable to a traditional stemmed implant.http://www.sciencedirect.com/science/article/pii/S2468602619300567Osteoarthritisstemlesstotal shoulderarthroplastyreplacementcanal sparing
collection DOAJ
language English
format Article
sources DOAJ
author George S. Athwal, MD, FRCS(C)
Ryan J. Krupp, MD
Grant Carlson, BS
Ryan T. Bicknell, MD, MSc, FRCS(C)
spellingShingle George S. Athwal, MD, FRCS(C)
Ryan J. Krupp, MD
Grant Carlson, BS
Ryan T. Bicknell, MD, MSc, FRCS(C)
A multicenter, prospective 2-year analysis of the Sidus stem-free shoulder arthroplasty system
JSES International
Osteoarthritis
stemless
total shoulder
arthroplasty
replacement
canal sparing
author_facet George S. Athwal, MD, FRCS(C)
Ryan J. Krupp, MD
Grant Carlson, BS
Ryan T. Bicknell, MD, MSc, FRCS(C)
author_sort George S. Athwal, MD, FRCS(C)
title A multicenter, prospective 2-year analysis of the Sidus stem-free shoulder arthroplasty system
title_short A multicenter, prospective 2-year analysis of the Sidus stem-free shoulder arthroplasty system
title_full A multicenter, prospective 2-year analysis of the Sidus stem-free shoulder arthroplasty system
title_fullStr A multicenter, prospective 2-year analysis of the Sidus stem-free shoulder arthroplasty system
title_full_unstemmed A multicenter, prospective 2-year analysis of the Sidus stem-free shoulder arthroplasty system
title_sort multicenter, prospective 2-year analysis of the sidus stem-free shoulder arthroplasty system
publisher Elsevier
series JSES International
issn 2666-6383
publishDate 2020-03-01
description Background: The purpose of this multicenter, prospective study was to evaluate the efficacy and safety of a stemless total shoulder arthroplasty compared with a traditional stemmed control. Methods: Ninety-five shoulders were selected for participation in this Food and Drug Administration investigational device exemption clinical trial and underwent stemless total shoulder arthroplasty. Subjects returned for follow-up at 6 weeks, 6 months, 12 months, and 2 years postoperatively. Outcome measures included pain; range of motion; American Shoulder and Elbow Surgeons, Western Ontario Osteoarthritis of the Shoulder, and Short Form 12 scores; and radiographic review. Baseline data were compared with 2-year follow-up data to determine the rate of composite clinical success compared with the stemmed control. Results: All outcome assessments demonstrated significant improvements (P ≤ .007). The mean American Shoulder and Elbow Surgeons score improved from 20 to 89 (P < .0001), and the mean shoulder pain score decreased from 8.3 ± 1.6 to 0.7 ± 1.5 (P < .0001). The mean Western Ontario Osteoarthritis of the Shoulder score decreased from 1443 ± 256 to 203 ± 267 (P < .0001). On the Short Form 12, the mean physical health score increased from 33 ± 7 to 48 ± 9 (P < .0001) and the mean mental health score increased from 50 ± 13 to 54 ± 8 (P = .007). Mean active forward elevation increased from 97° ± 27° to 143° ± 25° (P < .0001), and mean active external rotation increased from 21° ± 16° to 53° ± 18° (P < .0001). Kaplan-Meier analysis showed an implant survivorship rate of 98% at 2 years. The composite clinical success rate was 87% compared with 85% for the stemmed control. Conclusions: This study showed that a stemless rough-blasted humeral implant with metaphyseal bone fixation provides good clinical and radiographic outcomes and survivorship at 2 years, with outcomes comparable to a traditional stemmed implant.
topic Osteoarthritis
stemless
total shoulder
arthroplasty
replacement
canal sparing
url http://www.sciencedirect.com/science/article/pii/S2468602619300567
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