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240722s2024 xx |||||o 00| ||eng c |
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|a 10.1016/j.jseint.2024.04.008
|2 doi
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|a pubmed24n1479.xml
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|a eng
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| 100 |
1 |
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|a Wallace, Andrew L
|e verfasserin
|4 aut
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| 245 |
1 |
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|a Safety and efficacy of second-generation all-suture anchors in labral tear arthroscopic repairs
|b prospective, multicenter, 1-year follow-up study
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|c 2024
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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| 338 |
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|a ƒa Online-Ressource
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|2 rdacarrier
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|a Date Revised 23.07.2024
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|a published: Electronic-eCollection
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|a Citation Status PubMed-not-MEDLINE
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|a © 2024 The Author(s).
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|a Background: This study's primary aim was to assess the safety and performance of second-generation all-soft suture anchors following arthroscopic labral tear repair
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|a Methods: This prospective, multicenter study was conducted by 6 surgeons at 6 sites in Europe and the United States between November 2018 and August 2020. Patients who required shoulder arthroscopic repair, for a range of labral injuries, were treated with a second-generation all-soft suture anchor. The primary outcome was clinical success rate (percentage of patients without signs of failure and/or reintervention) at 6 months. Secondary outcomes included clinical success rate at 12 months, intraoperative anchor deployment success rate, and patient-reported outcomes (PROs) at 6 and 12 months, including visual analog scale (VAS) pain assessment, VAS satisfaction assessment, EQ-5D-5L Index Score, EQ-5D-5L VAS Health Score, Rowe Shoulder Score for Instability, American Shoulder and Elbow Surgeons score, and Constant-Murley Shoulder Score. Serious adverse events and serious adverse device effects were collected throughout the study
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|a Results: Forty-one patients were enrolled (mean age, 28.2 years; 87.8% male, 12.2% female). Clinical success was achieved in 27/28 and 31/32 patients at 6 months and 12 months, respectively. Anchor deployment had a 100% success rate. Significant improvements over baseline were reported for all PROs except Constant-Murley Shoulder (6 months) and VAS Satisfaction Score (12 months). One patient experienced 1 serious adverse event and 1 patient experienced 1 serious adverse device effect
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|a Conclusion: Second-generation all-soft suture anchors used in this study demonstrated a high clinical success rate, a favorable safety profile, and patients exhibited significant improvement in PROs
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|a Journal Article
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|a All-soft suture anchor
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|a Arthroscopic repair
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4 |
|a Glenoid labrum
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4 |
|a Labral tear
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| 650 |
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4 |
|a Shoulder instability
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| 650 |
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4 |
|a Shoulder repair
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| 700 |
1 |
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|a Calvo, Emilio
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Ardèvol Cuesta, Jordi
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Lanzetti, Riccardo
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Luengo-Alonso, Gonzalo
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Rokito, Andrew S
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Spencer, Edwin E
|c Jr
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Spoliti, Marco
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|4 aut
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