2014
DOI: 10.1016/j.arth.2014.01.040
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Adverse Clinical Outcomes in a Primary Modular Neck/Stem System

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Cited by 41 publications
(23 citation statements)
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“…Subsequently, a type II voluntary recall was initiated by the manufacturer, Stryker Orthopedics in July 2012 [2]. A similar modular dual taper stem, the ABG II was also recalled at the same time for similar increased risk of revision [11].…”
Section: Discussionmentioning
confidence: 99%
“…Subsequently, a type II voluntary recall was initiated by the manufacturer, Stryker Orthopedics in July 2012 [2]. A similar modular dual taper stem, the ABG II was also recalled at the same time for similar increased risk of revision [11].…”
Section: Discussionmentioning
confidence: 99%
“…However, reports of complications at the neck-stem junction are generating increasing concern [1][2][3][4][5][6]. In addition, registry data indicate higher revision rates compared to standard implants without neck-stem modularity [7].…”
Section: Introductionmentioning
confidence: 99%
“…However, they also have been reported to result in adverse effects, including fretting, corrosion, implant failure, metallic wear debris generation [10, 19, 27, 30, 46], and local tissue reaction [10, 24, 29, 51]. Whether they result in a net improvement to or impairment of reconstructive survivorship remains controversial [8, 13, 14, 34, 50, 52].…”
Section: Introductionmentioning
confidence: 99%