AI Article Synopsis

  • A large central ingrowth peg was studied as a way to reduce glenoid loosening in total shoulder arthroplasty (TSA), but issues arise when bone ingrowth doesn’t happen, leading to more complications in revisions.
  • A retrospective case series analyzed 49 TSA-to-reverse TSA revisions from 2014 to 2022, comparing outcomes between patients with central ingrowth pegs and those with noningrowth components based on various metrics.
  • Findings showed that patients with central ingrowth pegs had a shorter time to revision and a lower need for structural allografts compared to non-ingrowth, prompting further investigation into the causes of glenoid failure related to component design and revision timing.

Article Abstract

Background: One innovation to reduce glenoid loosening in total shoulder arthroplasty (TSA) is a large, central ingrowth peg. However, when bone ingrowth fails to occur, there is often increased bone loss surrounding the central peg which may increase complexity of subsequent revisions. Our goal was to compare outcomes between central ingrowth pegs and noningrowth pegged glenoid components during revision to reverse total shoulder arthroplasty.

Methods: In a comparative retrospective case series, all patients who underwent TSA-to-reverse TSA revision between 2014 and 2022 were reviewed. Demographic varibles as well as clinical and radiographic outcomes were collected. Ingrowth central peg and noningrowth pegged glenoid groups were compared using -test, Mann-Whitney U, Chi-Square, or Fisher's exact tests where indicated.

Results: Overall, 49 patients were included: 27 underwent revision from noningrowth and 22 from central ingrowth components. Females more commonly had noningrowth components (74% vs. 45%,  = .04) and preoperative external rotation was higher in central ingrowth components ( = .02). Time to revision was significantly earlier in central ingrowth components (2.4 vs. 7.5 years,  = .01). Structural glenoid allografting was required more with noningrowth components (30% vs. 5%,  = .03) and time to revision in patients ultimately requiring allograft reconstruction was significantly later (9.96 vs. 3.68 years,  = .03).

Conclusion: Central ingrowth pegs on glenoid components were associated with decreased need for structural allograft reconstruction during revision; however, time to revision was earlier in these components. Further research should focus on whether glenoid failure is due to glenoid component design, time to revision, or both.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10328762PMC
http://dx.doi.org/10.1016/j.jseint.2023.03.009DOI Listing

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