Thursday, October 1, 2020

Trabecular metal-backed glenoid components in total shoulder arthroplasty: what is their value?

 Modern trabecular metal-backed glenoid components in total shoulder arthroplasty: What is the evidence?

These authors queried the US National Library of Medicine (PubMed/MEDLINE), the Cochrane Database of Systematic Reviews and EMBASE for publications from January 1980 to October 2019 utilizing keywords pertinent to total shoulder arthroplasty, trabecular metal, and clinical outcomes.


They found seven articles to include in their analysis (322 operated shoulders, mean follow-up range: 2–4 years).


The survival rate of modern trabecular metal-backed glenoid components was 96% (309 out of 322 cases) at 43 months mean follow-up, while the rate of aseptic loosening was 0.3% (1 out of 322 cases).  


Fracture of the glenoid component occurred in six cases (overall rate 1.9% of the patients’ cohort), five of which required revision surgery. Among those, there were two cases of intra-operative periprosthetic fractures.

 

Six cases (1.9% of the patients of this review) of instability were found postoperatively, but only one of them required surgery.


Twenty-five cases (7.8% of the patient of this review) of complications not requiring reoperation were noted. Heterotopic ossification was the most common among them (9 out of 322 cases; 2.8%).


There were eight patients with osteopenia behind the glenoid plate and pegs, suggestive of stress shielding of the glenoid bone stock.


There were 35 cases (10.9%) with glenoid component radiolucency (one of them required revision), and 37 cases (11.5%) of metal debris formation, with four of them undergoing revision.


These authors concluded that there was "low quality evidence to show that the use of modern trabecular metal-backed glenoid components in total shoulder arthroplasty may be safe and effective at short-term follow-up. However, this analysis showed alarmingly high rates of both radiolucency of the glenoid component and metal debris formation which raise concern for potential failure of this glenoid component in the long term. Therefore, we feel that modern trabecular metal-backed glenoid components should be still used with caution as part of a structured surveillance or research program until we know if there is a detriment to the prosthesis in the medium to long term."


Here is a related post on an article entitled, Outcomes of Trabecular Metal–backed glenoid components in anatomic total shoulder arthroplasty 


These authors state that "the current design of the Trabecular Metal–backed glenoid component (Zimmer) was released in 2009. Although over 10,000 of these glenoid components have been implanted worldwide, evidence on either the intermediate- or long-term survival of Trabecular Metal–backed glenoid components in anatomic TSA is very limited."

After a Class 2 recall in 2005 because of concern for fracture at the junction of the base and the trabecular metal keel (see this link), this component was cleared by the FDA (see this link) based on its being substantially equivalent to the predicate recalled devices.



The authors investigated implant survival and two year (average 41 month) clinical outcomes for 36 of 47 patients who received a Trabecular Metal–backed glenoid component (see this link) during primary anatomic total shoulder arthroplasty performed by an individual surgeon.

Three patients showed signs of osteolysis, 4 had radiographic evidence of metal debris, and 1 patient had a catastrophic failure after a fall. Of the 47 TSAs, 5 (11%) were revised to a reverse TSA for subscapularis failure and pain. The authors concluded that Trabecular Metal–backed glenoids had a 25% rate of radiographic metal debris and osteolysis at a minimum 2-year follow-up in this series with one catastrophic failure.









This publication on failures of metal backed glenoids is consistent with a prior post, reproduced below

Early Debris Formation with a Porous Tantalum Glenoid Component: Radiographic Analysis with 2-Year Minimum Follow-up.

These authors point out that a first-generation porous tantalum glenoid component previously demonstrated failure, usually preceded by the appearance of intra-articular metallic debris. An example of component dissociation with this first-generation component is shown here.



After redesign, the component was reintroduced in 2009.



The authors reviewed 68 patients receiving a Trabecular Metal porous tantalum glenoid component (73 components; 5 patients underwent staged bilateral procedures) inserted without polymethylmethacrylate cement (representing off-label usage in the U.S.).

Sixty-six (90%) of the 73 components were evaluated at a minimum of 2 years of follow-up (mean radiographic follow-up of 50.8 months; range, 24 to 68 months). Of these, 92.4% demonstrated minimal or no glenoid radiolucency. Overall, the prevalence of metallic tantalum debris formation was 44% (29 of 66). Sequential radiograph review demonstrated that the incidence of metallic debris formation increased for each year of follow-up, with radiographs from 2, 3, 4, and ≥5 years of follow-up demonstrating a metallic debris incidence of 23%, 36%, 49%, and 52%, respectively.


The severity of metallic debris formation also increased with follow-up duration.


Here's an example of Grade 1, debris noted at the bone-metal interface;

of Grade 2, debris visible in soft tissues intra-articularly;

of Grade 3, visible but incomplete cracking or fracturing of the metal component;

                                      

They concluded that the development of metallic debris, increasing in both overall incidence and degree of severity over time, raises concern for potential failure of this glenoid component.

Comment: Metal backed glenoid components continue to manifest problems not present with all-polyethylene components. They demonstrate an increased rate of revision because of loosening, front side and back side polyethylene wear, component dissociation, fracture, instability, and cuff failure (possibility related to the increased thickness of the components) - see this link and the figure below.




 If an arthroplasty with bone ingrowth components requires revision because of infection, cuff failure or instability, removal of the components can result in substantial problems with bone integrity. Such bone damage may compromise secure fixation of a reverse total shoulder glenoid component.

This article presents another issue with metal-backed glenoid components, that of metallic debris, that appears to increase in rate and severity with time after implantation. The mechanism for this debris formation is unclear, but it could be that micromotion of the component pulls the porous trabeculated metal apart.

It can be seen from the list of Young's moduli below (in GPa), that the elastic modulus of polyethylene is closest to that of cortical and cancellous bone:
Cancellous Bone 0.4
Ultra high molecular weight polyethylene 0.5
PMMA bone cement 2
Cortical Bone 8
Titanium 112
Tantalum 186
Cobalt chrome 200.

The Young's modulus of a porous material can be modified by changing the degree of porosity. This is demonstrated in a recent article regarding porous tanalum (see this link). Here is the abstract:


"Relatively high cost of manufacturing and inability to produce modular all tantalum implants has limited its widespread acceptance, in spite of its excellent in vitro and in vivo biocompatibility. In this article, we report how to process Ta to create net shape porous structures with varying porosity using Laser Engineered Net Shaping (LENS™) for the first time. Porous Ta samples with relative densities between 45 to 73% have been successfully fabricated and characterized for their mechanical properties. In vitro cell materials interactions, using human osteoblast cell line hFOB, have been accessed on these porous Ta structures and compared with porous Ti control samples. The results show that the Young’s modulus of porous Ta can be tailored between 1.5 to 20 GPa by changing the pore volume fraction between 27 and 55%. In vitro biocompatibility in terms of MTT assay and immunochemistry study showed excellent cellular adherence, growth and differentitation with abundant extracellular matrix formation on porous Ta structures compared to porous Ti control. These results indicate that porous Ta structures can promote enhanced/early biological fixation. The enhanced in vitro cell-materials interactions on porous Ta surface are attributed to chemistry and its high wettability and surface energy relative to porous Ti. Our results show that these laser processed porous Ta structures can find numerous applications, particularly among older patients, for metallic implants because of their excellent bioactivity."

Nevertheless, based on the evidence available, metal backed glenoids may not offer to the patient advantages over an all polyethylene component as discussed below.

Radiographic and clinical outcomes of total shoulder arthroplasty with an all-polyethylene pegged bone ingrowth glenoid component: prospective short- to medium-term follow-up.

These authors reviewed 80 total shoulders using an all polyethylene glenoid component.  The glenoid was reamed minimally to preserve subchondral bone, which was given priority above correcting retroversion.

1 of 80 shoulders was revised for aseptic glenoid loosening.  81.6% had a radiolucency grade of 0 or 1. Nearly 90% had a glenoid seating grade of A or B. Grade 2 or 3 bone around the central peg was seen in 88.2%. 

No statistical association existed between Walch glenoid types and radiolucency grades, bone grades around the central peg, perfect radiolucency grade, seating grade, and grade 3 bone around the central peg. 

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