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Wear rates of retentive versus nonretentive reverse total shoulder arthroplasty liners in an in vitro wear simulation

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Although short-term outcomes of reverse total shoulder arthroplasty (rTSA) remain promising, the most commonly cited complication remains prosthetic instability. A retentive rTSA liner is commonly used to increase system constraint; however, no studies have evaluated the rate of polyethylene wear. Our hypothesis was that more constrained retentive liners would have higher wear rates than nonretentive liners. Six nonretentive and six retentive rTSA non-cross-linked polyethylene liners were subjected to 4.5 million cycles of alternating cycles of abduction-adduction and flexion-extension motion loading profiles. The rTSA liners were assessed for gravimetric wear loss, 3-dimensional volumetric loss by novel micro-computed tomography analysis, and particulate wear debris analysis. Volumetric wear rates were significant at 7 specific time points (1.0, 2.0, 2.5, 3.25, 3.75, 4.0, and 4.5 million cycles) throughout testing between nonretentive and retentive liners; however, overall mean volumetric wear rate was not statistically significant (P = .076). Total volume loss between liner test groups was found to be significant starting after 3.5 million cycles of testing. Maximum and mean surface deviations were found to be larger for retentive liners vs. nonretentive liners by micro-computed tomography analysis across the entire articulation surface. Retentive liners undergo significantly greater volume loss and greater surface deviation compared with nonretentive liners, most notably at later time points representing extended implantation times. Additional stability afforded by retentive liners should be balanced against the potential for increased wear and potential for subsequent polyethylene wear-induced aseptic loosening. Copyright © 2015 Journal of Shoulder and Elbow Surgery Board of Trustees. Published by Elsevier Inc. All rights reserved.
Content may be subject to copyright.
Wear rates of retentive versus nonretentive
reverse total shoulder arthroplasty liners in an
in vitro wear simulation
Shannon Carpenter, MD
a
, Daphne Pinkas, MD
a
, Michael D. Newton, BS
b
,
Michael D. Kurdziel, MS
b,c
, Kevin C. Baker, PhD
b,c
, J. Michael Wiater, MD
a,c,
*
a
Department of Orthopaedic Surgery, Beaumont Health System, Royal Oak, MI, USA
b
Department of Orthopaedic Research, Beaumont Health System, Royal Oak, MI, USA
c
Department of Surgery, Oakland University William Beaumont School of Medicine, Rochester, MI, USA
Background: Although short-term outcomes of reverse total shoulder arthroplasty (rTSA) remain promising,
the most commonly cited complication remains prosthetic instability. A retentive rTSA liner is commonly
used to increase system constraint; however, no studies have evaluated the rate of polyethylene wear. Our hy-
pothesis was that more constrained retentive liners would have higher wear rates than nonretentive liners.
Methods: Six nonretentive and six retentive rTSA non-cross-linked polyethylene liners were subjected to
4.5 million cycles of alternating cycles of abduction-adduction and flexion-extension motion loading pro-
files. The rTSA liners were assessed for gravimetric wear loss, 3-dimensional volumetric loss by novel
micro-computed tomography analysis, and particulate wear debris analysis.
Results: Volumetric wear rates were significant at 7 specific time points (1.0, 2.0, 2.5, 3.25, 3.75, 4.0, and
4.5 million cycles) throughout testing between nonretentive and retentive liners; however, overall mean
volumetric wear rate was not statistically significant (P¼.076). Total volume loss between liner test
groups was found to be significant starting after 3.5 million cycles of testing. Maximum and mean surface
deviations were found to be larger for retentive liners vs. nonretentive liners by micro-computed tomog-
raphy analysis across the entire articulation surface.
Discussion and conclusion: Retentive liners undergo significantly greater volume loss and greater surface
deviation compared with nonretentive liners, most notably at later time points representing extended im-
plantation times. Additional stability afforded by retentive liners should be balanced against the potential
for increased wear and potential for subsequent polyethylene wear-induced aseptic loosening.
Level of evidence: Basic Science Study, Biomechanics.
Ó2015 Journal of Shoulder and Elbow Surgery Board of Trustees.
Keywords: Retentive humeral liners; reverse total shoulder arthroplasty; wear particle analysis; in vitro
wear simulation; micro-CT surface deviation analysis
Product support for this study was provided by Zimmer (Warsaw, IN,
USA). Funding was provided by OMeGA Medical Grants Association
(#000605) and the Orthopaedic Research and Education Foundation (#11-
105) fellowship research grants. These entities were not involved in the
study design or collection, analysis, or interpretation of data; in the writing
of the report; or in the decision to submit the article for publication.
Institutional Review Board approval is not applicable: Basic Science
Study, Biomechanics.
*Reprint requests: J. Michael Wiater, MD, Beaumont Health, Depart-
ment of Orthopaedic Surgery, Division of Shoulder and Elbow Surgery,
3535 W 13 Mile Rd, Ste 744, Royal Oak, MI 48073 USA.
E-mail address: mwiater@beaumont.edu (J.M. Wiater).
J Shoulder Elbow Surg (2015) 24, 1372-1379
www.elsevier.com/locate/ymse
1058-2746/$ - see front matter Ó2015 Journal of Shoulder and Elbow Surgery Board of Trustees.
http://dx.doi.org/10.1016/j.jse.2015.02.016
The reverse total shoulder arthroplasty (rTSA) was
originally designed to treat elderly patients with rotator cuff
arthrosis.
4
Since Food and Drug Administration approval in
2003, the indications for rTSA have expanded significantly,
and although promising short-term clinical outcomes have
been described for rTSA, a high complication rate persists,
ranging from 0% to 68% in the literature.
8,9,41
The most
common complications include neurologic injury, intra-
operative periprosthetic fracture, hematoma, infection,
scapular notching, prosthesis loosening and failure, post-
operative stiffness, and prosthetic instability.
3,4,13,16,28,34
Prosthetic instability is the most frequently cited compli-
cation, representing nearly a third of all complications with
an incidence of 0% to 8% in recent studies.
7,16,40
Factors
thought to contribute to rTSA postoperative instability
include distortion of the osseous and soft tissue anatomy by
prior trauma, inadequate soft tissue tensioning, component
malposition, and inappropriate ratio between the central
depth and the diameter of the concave polyethylene
component.
4,14,17,26
One method to improve prosthetic stability is to increase
the system constraint by using a retentive polyethylene
liner. A retentive liner has a slightly deeper concavity and
higher peripheral rim than standard liners, increasing the
humeral socket depth and providing greater congruency
between the liner and the glenosphere. A recent biome-
chanical study by Clouthier et al
11
showed that increased
humeral liner depth enhanced prosthetic stability in all
loading profiles except inferior loading. Gutierrez et al
17
previously looked directly at the hierarchy of stability
factors in rTSA and found that the humeral socket depth
was one of the most important factors, second only to joint
compressive force.
However, the stability of the retentive liner must be
weighed against the risk of potential decrease in range of
motion, leading to possible impingement and increased
scapular notching.
18
In addition, the increased constraint
may escalate polyethylene wear, which could lead to
osteolysis, component loosening, and subsequent
failure.
12,15,27,32,38
To date, no studies have quantified the
wear rate of retentive vs. standard polyethylene liners. The
purpose of this study was to examine and to compare the
wear rates of both retentive and nonretentive polyethylene
liners in an in vitro rTSA model. We hypothesized that
retentive liners, with their increased constraint and articu-
lating surface area, would have an increased rate of poly-
ethylene wear compared with standard nonretentive liners.
Materials and methods
Test groups
Commercially available components (Zimmer Inc., Warsaw, IN,
USA) were used for wear simulation testing. Nonretentive liners
(N ¼6; Trabecular Metal Reverse Shoulder System, 7elevated
rim, 36-mm diameter, þ0-mm thickness) and retentive liners
(N ¼6; Trabecular Metal Reverse Shoulder System, 12elevated
rim, 36-mm diameter, þ0-mm thickness) were subjected to an
in vitro wear simulation protocol matched against 36-mm gleno-
spheres (Fig. 1). All polyethylene liners were non-cross-linked.
Liner components were press-fit into simulator testing fixtures.
In vitro wear simulation protocol and measurement
of wear
With use of a previously developed protocol from our institu-
tion,
31,39
a 12-station hip wear simulator (MTS Bionix, Eden
Prairie, MN, USA) was converted to an rTSA simulator by
modification of the test fixtures, loading profiles, and testing
protocol. A total of 4.5 million cycles of testing were completed,
alternating simulated abduction-adduction and flexion-extension
motion profiles every 250,000 cycles. The abduction-adduction
loading profile simulated 0to 46of arm swing (20-618 N,
90% body weight), and the flexion-extension loading profile
subjected liners to 44to 90of arm swing (20-927 N, 135% body
weight).
Individual components remained immersed in defined bovine
calf serum (21 g protein/L) containing 0.2% sodium azide,
7.0 10
3
g/mL ethylenediaminetetraacetic acid (Ricca Chemi-
cal, Arlington, TX, USA), and deionized water at all times during
testing. Before wear simulation testing, all liners were presoaked
in lubrication fluid to account for fluid adsorption that occurs
during initial liner immersion. One additional liner per group
served as a load-soak control throughout testing to account for
fluid variations during testing. These liners were subjected to axial
loads but no dynamic rotation.
At each 250,000-cycle interval, liners were removed from
testing fixtures, cleaned, and dried with compressed nitrogen gas
according to ISO Standard 14242-2. Liners were then measured
on a precision mass balance (A-200DS; Fisher Scientific, Pitts-
burgh, PA, USA) for determination of mass loss at each interval.
Mass loss was then converted to volume loss using the known
density of ultrahigh-molecular-weight polyethylene (UHMWPE;
0.933 g/cm
3
). Wear was then quantified and reported as volu-
metric wear rate (mm
3
/million cycle [MC]) and total volume loss
(mm
3
) for the duration of the simulation.
Wear particle characterization
Wear particles were isolated from test serum to characterize par-
ticle morphology. Serum samples were selected randomly from 3
nonretentive and 3 retentive testing stations at 4 different time
points throughout testing. The time points were the first and final
abduction-adduction and flexion-extension time points (after
abduction-adduction at 250,000 and 4,250,000 cycles, and after
flexion-extension at 500,000 and 4,500,000 cycles). Each serum
sample was thawed for overnight digestion in 5.0 M NaOH at
37C with constant stirring to digest proteins and filtered through
a 0.2-mm polycarbonate filter.
Filters were sputtered with Au-Pd and subjected to environ-
mental scanning electron microscopy (Quanta FEG40; FEI,
Hillsboro, OR, USA). Ten images of 10,000magnification were
taken from random locations from each filter and analyzed with a
custom MATLAB program (MathWorks, Natick, MA, USA),
rTSA wear simulation of retentive liners 1373
based on a previously described protocol.
31,39
Particles were
characterized by equivalent circle diameter ((4*Area/p)
1/2
), aspect
ratio (d
max
/d
min
), and roundness ((4*Area)/(p*d
max2
)).
Micro-CT surface deviation
Three-dimensional surface deviations between nonretentive and
retentive liners and their respective soak controls were compared
by a micro–computed tomography (micro-CT) technique adapted
from previously described techniques for wear quantification in
the total hip, knee, and disk arthroplasties.
6,21,22,35-37
After
completion of the simulation, each liner was scanned individually
with 45 mm isotropic voxel resolution, 55 kVp, and 450 mA on an
eXplore Locus RS micro-CT scanner (GE Healthcare Pre-Clinical
Imaging, London, ON, Canada) and reconstructed at full resolu-
tion. Three-dimensional meshes were isolated from the recon-
structed scans using DeVIDE software.
5,24,25,29
Briefly, scans were
filtered using median filtering and thresholded to isolate the liner.
The isolated 3-dimensional mask was then meshed using an iso-
surface generator, simplified using quadratic edge collapse deci-
mation, and exported in stereolithography file format.
Liner meshes were then analyzed using open-source MeshLab
software (http://meshlab.sourceforge.net).
10
Liners were pre-
processed using Poisson surface reconstruction to ensure a water-
tight surface, and each worn liner was coaligned with a
corresponding unworn liner using an iterated closest point algo-
rithm. The surface deviation between the worn and control liner
mesh surfaces was calculated at each point on the mesh. These
measurements were used to generate surface deviation maps for
each worn liner. Surface deviation measured with this technique
represents the volume change in response to both material creep and
material loss due to wear at the conclusion of the wear simulation.
Cross-sectional analysis
To quantify regional surface deviation of the worn bearing sur-
faces, a cross-sectional analysis based on a previously published
technique was performed.
35
Micro-CT cross sections were taken
from worn and control liners at 0,45
,90
, and 135, with
0defined as the most inferior pole of the liner and 180at the
peripheral rim. To standardize alignment between liners, the flat
backside of the liner was used as a reference plane, and the center
of rotation was defined as the geometric center of the liner’s 3-
dimensional mesh.
Each pair of cross sections was imported into MATLAB. The
bearing surface was manually selected, and 200 evenly spaced
points were selected from the control surface. Each cross section
was divided into 2 subsets by the center of rotation, yielding a
total of 8 angles at which measurements were taken (Fig. 1). The
Euclidean distance between the worn and control surface, normal
to the control surface, was calculated for each point, and the mean
distance at each angle was measured.
Statistical analysis
All statistical analyses were performed with SPSS Statistical
Software (version 22; IBM SPSS Statistics, Chicago, IL, USA).
Direct comparisons between particle characteristics and surface
deviations were made by the Student ttest with significance set at
P<.05. Volumetric wear rates were compared by a 2-way anal-
ysis of variance with 2 factors: liner type (nonretentive vs.
retentive) and motion profile (abduction-adduction vs. flexion-
extension), with significance set at P<.05 for variables volu-
metric wear rate and total volume loss.
Results
Gravimetric measurement of wear
All 12 stations completed 4.5 million cycles of wear
simulation testing successfully. Volumetric wear rates be-
tween test groups are shown in Figure 2. In taking all time
points into consideration, no significant difference in mean
volumetric wear rates (mm
3
/MC) was found between
nonretentive and retentive liners (88.1 19.1 vs.
96.8 21.9 mm
3
/MC; P¼.076). In examining wear rates
at specific time points in the test (1.0, 2.0, 2.5, 3.25, 3.75,
4.0, and 4.5 million cycles), retentive liners had signifi-
cantly greater wear rates compared with nonretentive liners
(P<.05).
Differences in volumetric wear rate between motion
profiles were observed (Fig. 2,B). The flexion-extension
loading profile exhibited significantly greater volumetric
wear rates than the abduction-adduction loading profile
for both nonretentive (102.4 15.2 vs. 73.8 9.1 mm
3
/
MC; P<.001) and retentive liners (113.1 15.8 vs.
80.4 13.1 mm
3
/MC; P<.001). Within each loading
profile, a significant difference in volumetric wear rate
was found between nonretentive and retentive liners in
both abduction-adduction (73.8 9.1 vs. 80.4
13.1 mm
3
/MC; P¼.011) and flexion-extension loading
profiles (102.4 15.2 vs. 113.1 15.8 mm
3
/MC;
P<.001).
No significant difference in total volume loss was noted
up to 3.5 million cycles of simulation; however, at 3.75
million cycles and after, a significant difference between
liner types was noted. At 4.5 million cycles, retentive
liners had significantly greater total volume loss compared
with nonretentive liners (435.5 30.4 mm
3
vs.
396.4 25.7 mm
3
;P¼.037).
Wear particle analysis
A total of 14,138 wear particles from nonretentive liners
and 12,526 from retentive liners were isolated from envi-
ronmental scanning electron microscopy images for char-
acterization. Wear particles isolated from retentive liners
were larger, with a significantly larger equivalent circle
diameter (0.25 0.14 vs. 0.25 0.12; P¼.023) compared
with nonretentive liners. Retentive liners were also more
fibrillar (less round), with significantly lower aspect ratio
(2.82 1.59 vs. 2.92 1.66; P<.001) and higher
roundness (0.32 0.18 vs. 0.31 0.18; P<.001),
compared with nonretentive liners.
1374 S. Carpenter et al.
Micro-CT surface deviation and cross-sectional
analysis
Three-dimensional surface deviation maps created from
micro-CT scans demonstrate increased penetration of the
glenosphere into retentive liners compared with non-
retentive (Fig. 3). The maximum deviation of retentive
liners (0.69 0.03 mm) was significantly higher than that
of nonretentive liners (0.56 0.06 mm; P<.001). Qual-
itatively, 2 distinct wear scars can be seen on the bearing
surfaces of each liner.
Mean surface deviations obtained from cross-sectional
analysis are shown in Figure 4. Elevated surface de-
viations were observed at 135, 180, and 225,withthe
highest deviations occurring at 180(nonretentive,
0.320 0.067 mm; retentive, 0.549 0.036 mm), cor-
responding to the medial side of the bearing surface.
Surface deviations for both nonretentive and retentive
liners at 180were significantly higher than all other an-
gles, and deviations for retentive liners at 135and 225
were significantly higher compared with those at 0,45
,
90, 270, and 315.
Comparison of gravimetric and mesh volumes
The average post-simulation volumes of nonretentive and
retentive liners, determined gravimetrically, were
6634 34 mm
3
and 7376 38 mm
3
, respectively, whereas
the average volumes of the liners determined from the
meshes isolated from micro-CT were 6600 64 mm
3
and
7313 52 mm
3
, respectively. This yielded an average
percentage difference between gravimetric and mesh vol-
umes of 0.98% and 1.06% for nonretentive and retentive
liners, respectively, showing strong agreement between the
2 measurement techniques.
Discussion
Retentive liners are indicated in rTSA for the reduction of
postoperative instability. They add stability by increasing
rTSA system constraint and have generally been associated
with positive clinical outcomes. However, because of the
relatively recent introduction of this rTSA system, there are
few data available comparing the wear performance of
Figure 2 (A) Volumetric wear rates of retentive and nonretentive rTSA UHMWPE liners subjected to 4.5 million cycles of wear
simulation testing alternating abduction-adduction and flexion-extension motion profiles every 250,000 cycles. (B) Volumetric wear rates
were then examined as function of motion loading profile and liner type. (C) Total volume loss for liner type throughout the entire 4.5
million cycles of testing. *Statistical significance between retentive and nonretentive test groups (P<.05).
Figure 1 Profile of nonretentive and retentive humeral liners (left) used in this simulation. The extended medial lip of the retentive liners
can be appreciated. Cross sections used for surface deviation analysis of worn liners (right). Sections were taken at 0,45
,90
, and 135,
and the bearing surface of each cross section was split into 2 subsets at the center of rotation, yielding 8 angles total from which mea-
surements were taken.
rTSA wear simulation of retentive liners 1375
retentive and nonretentive rTSA liners. A significantly
higher incidence of heterotopic ossification and a trend
toward increased scapular notching have been reported in
retentive trabecular metal reverse shoulder systems.
20
Although component loosening has been cited as a major
reason for revision of rTSA components,
15
no clinical or
biomechanical data are currently available for the effect of
retentive liners on the wear rate or incidence of component
loosening in rTSA. In the setting of total hip arthroplasty,
fully constrained acetabular liners are generally associated
with increased rates of polyethylene wear and subsequent
aseptic loosening due to the increased constraint of the
system.
1,2,23
However, whether this trend applies to reten-
tive liners in rTSA is unclear, as retentive liners add a de-
gree of constraint to the system but are not fully
constraining.
During the course of this simulation, retentive liners
experienced greater total volume loss than nonretentive
liners, with the difference increasing gradually and
becoming statistically significant after 3.5 million cycles of
wear testing. The wear rates of both liner types increased
during the initial bedding-in phase; however, significant
increases in the wear rates of retentive liners at later time
points in the simulation suggest that the wear rates of
retentive liners increased at a greater rate during this initial
phase. This may be due in part to the increased contact area
of retentive liners with the glenosphere, resulting in a
greater wear footprint.
Particles from retentive liners were significantly larger
and more fibrillar than those from nonretentive liners. In
general, more fibrillar particles are thought to elicit a
greater inflammatory response from macrophages.
33
Figure 3 Representative surface deviation color maps of worn nonretentive and retentive liners compared with their respective controls
after completion of the wear simulation. The bearing surface is outlined by a dotted white line. Larger surface deviations can be seen in
retentive liners compared with nonretentive. In both groups, increased wear was seen on the medial aspect of the bearing surface. Scar lines
can be seen across the liner bearing surfaces. These are presumably caused by the motion profile arcs used in the simulation.
Figure 4 Cross-sectional analysis of worn liners compared against soak controls. (A) Mean surface deviation of a cross-sectional analysis
of worn nonretentive and retentive liners. Surface deviations at 180were significantly higher than all other angles for both the nonretentive
and retentive liners, and deviations at 135and 225were significantly higher than those at 0,45
,90
, 270, and 315for retentive liners.
(B) Whisker plots of nonretentive and retentive liners at 0/180showing surface deviation of the worn bearing surface from the control.
Mean surface deviation is more severe at 180than at 0, demonstrating that more wear occurred medially on the bearing surface.
*Significant difference between nonretentive and retentive liners at P>.001.
1376 S. Carpenter et al.
However, whereas the differences in particle morphology
were statistically significant, the actual differences are
small and unlikely to have a clinically relevant impact. The
slight changes in particle morphology can most likely be
attributed to the differences in constraint and contact area
between the 2 liners, with the statistical significance being
largely driven by the large sample sizes (14,138 and 12,526
particles for nonretentive and retentive liners, respectively).
The measurements of particle morphology from this study
were comparable to previous rTSA simulations.
31,39
The techniques described for mapping and quantifying
the surface deviation of worn liners were adapted from
previously described techniques for measuring wear on
polyethylene liners from total hip, total knee, and total disk
replacements.
6,21,35-37
Surface deviations were found to be
globally higher on retentive liners compared with non-
retentive liners. This was further supported by significantly
greater maximum and mean surface deviation of the
retentive liners at all angles during cross-sectional analysis.
These findings support the hypothesis that the observed
differences in volumetric wear cannot be attributed solely
to increased surface area and that the increased wear and
wear rates of retentive liners can be attributed to increased
constraint and surface area.
Cross-sectional analysis of the surface deviation maps
showed the most prominent wear along the 180axis to-
ward the prominent ridge. This trend was common for both
nonretentive and retentive liners. In addition, on most of the
worn components, scar lines along distinct arcs can be
noted crossing the bearing surface. We believe these to be
the result of the 2 distinct motion profiles used in the study
and the focal point of the wear for each profile.
To the authors’ knowledge, this is the first report of a
micro-CT–based technique to characterize UHMWPE wear
in the setting of rTSA and in conjunction with gravimetric
wear analysis. The high agreement between the mesh vol-
umes with the volumes calculated from the final gravi-
metric weights of the liners and the known density of
UHMWPE indicates that the isolation scheme was able to
accurately isolate the liners from micro-CT scans.
Continued research is under way to apply this technique to
retrieved rTSA liners from our institution’s implant
retrieval library to further understand the rate of UHMWPE
wear in vivo. Micro-CT wear mapping of retrieved devices
and correlation with clinical outcomes will help establish
clinically relevant wear rates. Further comparison of clin-
ical results to those from rTSA wear simulations will pro-
vide a vital tool to evaluate and to validate the motion
profiles used for this and other rTSA simulations and to
contextualize the results of previous and future wear sim-
ulations in terms of their potential clinical relevance.
Previous rTSA wear simulations have characterized the
effect of the presence of a hole at the pole of the gleno-
sphere articulating surface, cross-linked polyethylene hu-
meral liners, and inverted bearing materials on rTSA wear
properties.
19,31,39
This simulation adds to a growing body
of knowledge about the effect of device design parameters
on wear rates in rTSA and more broadly the effects of
device design on component wear in joint replacement. The
limitations of this study include the in vitro nature of the
simulation, the use of only 1 model of rTSA component,
and the use of only a single end point for micro-CT anal-
ysis. Continued clinical evaluation of retentive liner device
performance is warranted for complete evaluation of this
device. The main objective of this simulation was to
compare the relative wear rates of retentive and non-
retentive rTSA liners using an established in vitro wear
simulation protocol.
31,39
The increased wear observed in
retentive liners is consistent with existing literature on fully
constrained liners in total hip arthroplasty and suggests that
the added constraint of retentive liners significantly in-
creases wear volume at later time points, potentially
increasing the incidence of polyethylene wear-induced
aseptic loosening during extended implantation periods;
however, this was not evaluated in the current study.
Future research linking wear rates to clinical outcomes
of rTSA systems will help clarify this finding. Only 1
model of humeral liner was tested in this study. Thus,
whereas the trends observed in this study are generalizable
to other retentive rTSA models, which are all character-
ized by a deeper concavity to engage the glenosphere
compared with standard liners, the absolute wear rates
calculated in this study should not be assumed to be
consistent for other models. The micro-CT–based tech-
nique described in this study was performed only after
completion of the simulation. Whereas comparison of
worn to control samples was a valid and repeatable
method of measurement,
30,35
pre-simulation and mid-
simulation scans could be used in future studies to track
the progression of wear within each liner and to account
for the effects of creep deformation.
Conclusion
The results of this in vitro wear simulation indicate that
retentive liners undergo significantly greater volume loss
than nonretentive liners at later time points representing
extended implantation times. The additional stability
afforded by retentive liners should be balanced against
the potential for increased wear and subsequent aseptic
loosening. Surgeons should be aware of this potential
complication when selecting implants during rTSA.
Acknowledgment
The authors acknowledge Basma Khoury, MS, who
facilitated micro-CT scanning of rTSA liners (MicroCT
Core, University of Michigan, Ann Arbor, MI, USA).
rTSA wear simulation of retentive liners 1377
Disclaimer
J. Michael Wiater receives consulting fees from Zimmer,
Synthes Inc., and Tornier Inc.; receives research support
as principal investigator from Zimmer and Tornier Inc.;
and has received payment for presentations and speaking
engagements from Zimmer Inc. All the other authors,
their immediate families, and any research foundations
with which they are affiliated have not received any
financial payments or other benefits from any commer-
cial entity related to the subject of this article.
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rTSA wear simulation of retentive liners 1379
... In the case of prosthetic joint instability, the use of a more constrained or retentive inlay is suggested [106,107]. While retentive inlays contribute to a higher stability, several studies have showed that the risk of increased polyethylene wear and aseptic loosening is increased due to higher shear forces on the articulating partners [106,107]. ...
... In the case of prosthetic joint instability, the use of a more constrained or retentive inlay is suggested [106,107]. While retentive inlays contribute to a higher stability, several studies have showed that the risk of increased polyethylene wear and aseptic loosening is increased due to higher shear forces on the articulating partners [106,107]. Moreover, Mueller et al. reported a significantly greater incidence of polyethylene wear and rim damage of the humeral components in the case of scapular notching [108]. ...
Article
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Purpose of review: The purpose of this review is to summarize recent literature regarding the latest design modifications and biomechanical evolutions of reverse total shoulder arthroplasty and their impact on postoperative outcomes. Recent findings: Over the past decade, worldwide implantation rates of reverse total shoulder arthroplasty have drastically increased for various shoulder pathologies. While Paul Grammont's design principles first published in 1985 for reverse total shoulder arthroplasty remained unchanged, several adjustments were made to address postoperative clinical and biomechanical challenges such as implant glenoid loosening, scapular notching, or limited range of motion in order to maximize functional outcomes and increase the longevity of reverse total shoulder arthroplasty. However, the adequate and stable fixation of prosthetic components can be challenging, especially in massive osteoarthritis with concomitant bone loss. To overcome such issues, surgical navigation and patient-specific instruments may be a viable tool to improve accurate prosthetic component positioning. Nevertheless, larger clinical series on the accuracy and possible complications of this novel technique are still missing. Keywords: reverse total shoulder arthroplasty; biomechanics; implant design; patient-specific instruments; computer navigation
... The authors suggest that constrained liners offer a potential for increased wear and subsequent aseptic loosening which must be considered during intraoperative decision-making upon prosthesis stability. 2 While the present study found favorable 2-year postoperative outcomes and a very low complication rate, future studies will need to study the long-term complications associated with constrained liner use, as it would not be expected to see high rates of polyethylene wear at such an early time point. ...
Article
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Background Prosthetic instability is one of the most common short term complications following reverse total shoulder arthroplasty (RTSA). Numerous strategies exist to attempt to mitigate this complication, including utilization of constrained polyethylene humeral liners. A concern of constrained humeral liners is that they may come at the expense of restricted rotational range of motion (ROM). The purpose of the current study is to compare range of ROM and patient-reported outcomes (PROs), and satisfaction among matched cohorts using constrained versus unconstrained liners after RTSA. Methods A multi-center shoulder arthroplasty registry was retrospectively reviewed to identify patients with two-year clinical follow-up after RTSA with constrained liners used at the surgeon’s discretion. All patients had the same inlay humeral prosthesis with a 135° neck shaft angle. This study cohort was matched 1:2 to control patients who underwent RTSA with standard liners based on age, sex, total glenoid-sided lateralization, glenosphere diameter, and surgery performed on the dominant arm. Improvement in PROs and ROM were compared between groups. Results 22 patients were identified who underwent RTSA with a constrained humeral liner; these were compared to 44 matched patients with standard liners. The groups were found to have no notable differences in demographics, baseline PROs and ROM. At two years postoperatively, both cohorts demonstrated improvements in all PROs without statistically significant differences between the two groups. There were no differences between groups in improvement in any ROM measure, including forward flexion (Constrained: 54o, Standard: 57o, p = 0.771), external rotation at the side (Constrained: 42o, Standard: 41o, p = 0.906) or internal rotation at 90o of abduction (Constrained: 24o, Standard: 20o, p = 0.587). Conclusions For an inlay humeral prosthesis with a 135° neck shaft angle, utilization of a constrained liner for RTSA demonstrates no significant difference in ROM or PROs compared to a well-matched cohort of patients who underwent RTSA with a standard polyethylene humeral liner. This is reassuring data for using constrained liners when there is intraoperative concern for prosthetic instability.
... While single-station shoulder simulators have been developed (summarised in Smith et al., 2015), these clearly lack the capacity for multiple tests in parallel, so other researchers have, understandably, looked to use hip and knee simulators and adapt them to shoulder implant testing. For example, reverse shoulders have been tested in hip simulators (Carpenter et al., 2015;Haider, Sperling, & Throckmorton, 2013;Kohut, Dallmann, & Irlenbusch, 2012;Langohr, Athwal, Johnson, & Medley, 2016;Peers et al., 2015;Vaupel, Baker, Kurdziel, & Wiater, 2012) while total shoulders have been tested in knee simulators (Mummert, Rodriguez, Ghosh, & Bombosch, 2016;Wirth et al., 2009). Here, when the term simulator is used, it is used as a shorthand for 'wear simulator'. ...
Chapter
Shoulder joint replacement is the third most common joint replacement procedure after the knee and the hip. Shoulder joint replacement is, however, showing greater growth than knee or hip replacement. Many different designs are available from hemiarthroplasty through to total shoulder joint replacement. Perhaps remarkably, the most common and most successful shoulder joint replacement is one which inverts the natural geometry of the glenohumeral joint. This is the reverse shoulder prosthesis which, although initially intended as a solution to massive rotator cuff tears, has grown to be used for other clinical indications. There are many different artificial shoulder joint designs and several of these employ novel biomaterials and innovative design ideas. In vitro wear testing of shoulder implants lacks the international standards seen with knee and hip implants, but dedicated shoulder simulators have been developed or others adapted so that designs and materials can be tested prior to in vivo usage.
... [6][7][8][9] The durability of the RSA is related to patient factors, as the quality of bone and factors that are surgeon's responsability. 9 Some well determined factors include preoperative planning, 7,10-14 surgical technique employed, 8,[14][15][16] the remaining functional tendons, 1,17 glenoid bone deformity (GBD), 6,9,10 implant characteristics, 13,[18][19][20] and postoperative management. ...
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Objective To verify whether reverse baseplate positioning without the support of intraoperative three-dimensional technology is within the acceptable parameters in the literature and whether glenoid bone deformity (GBD) compromises this positioning. Methods Sixty-nine reverse shoulder arthroplasties were evaluated with volumetric computed tomography (CT). Two radiologists performed blinded CT scan analysis and evaluated baseplate position within 2mm of the inferior glenoid; the inclination and version of the baseplate in relation to the Friedman line; and upper and lower screw and baseplate metallic peg end point positionings. The patients were divided according to the presence of GBD for statistical analyses. Results The two radiologists concurred reasonably in their interpretations of the following analyzed parameters: baseplate position within 2mm of the inferior glenoid rim (97.1% and 95.7%), baseplate inclination (82.6% and 81.2%), baseplate version (69.6% and 56.5%), the upper screw reaching the base of the coracoid process (71% and 79.7%), the inferior screw remaining inside the scapula (88.4% and 84.1%), and the metallic peg of the baseplate considered intraosseous (88.4% and 72.5%). Conclusion Reverse baseplate positioning without intraoperative three-dimensional technology is within the acceptable parameters of the literature, except for baseplate version and upper screw position. GBD did not interfere with baseplate positioning in reverse shoulder arthroplasty.
Article
Background Anatomic total shoulder arthroplasty (ATSA) and reverse total shoulder arthroplasty (RTSA) reliably alleviate pain and restore shoulder function for a variety of indications. However, these procedures are not well-studied in patients with neurocognitive impairment. Therefore, the purpose of this study was to investigate whether patients with dementia or mild cognitive impairment (MCI) have increased odds of surgical or medical complications following arthroplasty. Methods The PearlDiver database was queried from 2010 through October 2021 to identify a cohort of patients who underwent either ATSA or RTSA and had a minimum 2-year follow-up. Current Procedural Terminology and International Classification of Diseases codes were used to stratify this cohort into three groups: (1) patients with dementia, (2) patients with MCI, and (3) patients with neither condition. Surgical and medical complication rates were compared among these three groups. Results The overall prevalence of neurocognitive impairment among patients undergoing total shoulder arthroplasty was 3.0% in a cohort of 92,022 patients. Patients with dementia had increased odds of sustaining a periprosthetic humerus fracture (odds ratio [OR] = 1.46, P < .001), developing prosthesis instability (OR = 1.72, P < .001), and undergoing revision arthroplasty (OR = 1.55, P = .003) after RTSA compared to patients with normal cognition. ATSA patients with dementia did not have an elevated risk of surgical complications or revision. Conversely, RTSA patients with MCI did not have an elevated risk of complications or revision, although ATSA patients with MCI had greater odds of prosthesis instability (OR = 2.51, P = .008). Additionally, patients with neurocognitive impairment had elevated odds of medical complications compared to patients with normal cognition, including acute myocardial infarction and cerebrovascular accident. Conclusion Compared to patients with normal cognition, RTSA patients with preoperative dementia and ATSA patients with preoperative MCI are at increased risk for surgical complications. Moreover, both ATSA and RTSA patients with either preoperative MCI or dementia are at increased risk for medical complications. As the mean age in the U.S. continues to rise, special attention should be directed towards patients with neurocognitive impairment to minimize postoperative complications aftertotal shoulder arthroplasty, and the risks of this surgery more carefully discussed with patients and their families and caretakers.
Article
Since the 1970s, numerous designs of reverse shoulder arthroplasty (RSA) have been proposed, and in 1994, Grammont came up with the third variation of his Delta Reverse, which facilitated pain relief and recovery of overhead motion in the cuff-deficient arthritic shoulder. These satisfactory results have led to an expansion in the indications including to younger more active patients and also to patients with an intact rotator cuff. However, over time, surgeons have identified adverse effects related to the design of the implant. Thus, the field has seen a push for advances in the design of the different components of the RSA as well as in the positioning of these implants. The objective of this review paper is to a) provide a comprehensive overview of the developments in the design of the components of RSA and to b) identify the best combination of components for RSA in 2022.
Article
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Purpose Metal ion release may cause local and systemic effects and induce hypersensitivity reactions. The aim of our study is first to determine if implant-related hypersensitivity correlates to patient symptoms or not; second, to assess the rate of hypersensitivity and allergies in shoulder arthroplasty. Methods Forty patients with shoulder replacements performed between 2015 and 2017 were studied with minimum 2-year follow-up; no patient had prior metal implants. Each patient underwent radiographic and clinical evaluation using the Constant-Murley Score (CMS), 22 metal and cement haptens patch testing, serum and urine tests to evaluate 12 metals concentration, and a personal occupational medicine interview. Results At follow-up (average 45 ± 10.7 months), the mean CMS was 76 ± 15.9; no clinical complications or radiographic signs of loosening were detected; two nickel sulfate (5%), 1 benzoyl peroxide (2.5%) and 1 potassium dichromate (2.5%) positive findings were found, but all these patients were asymptomatic. There was an increase in serum aluminum, urinary aluminum and urinary chromium levels of 1.74, 3.40 and 1.83 times the baseline, respectively. No significant difference in metal ion concentrations were found when patients were stratified according to gender, date of surgery, type of surgery, and type of implant. Conclusions Shoulder arthroplasty is a source of metal ion release and might act as a sensitizing exposure. However, patch test positivity does not seem to correlate to hypersensitivity cutaneous manifestations or poor clinical results. Laboratory data showed small constant ion release over time, regardless of gender, type of shoulder replacement and implant used. Levels of evidence Level II.
Article
Full-text available
Background and purpose Previous studies on shoulder arthroplasty have usually described small patient populations, and few articles have addressed the survival of shoulder implants. We describe the results of shoulder replacement in the Norwegian population (of 4.7 million) during a 12-year period. Trends in the use of shoulder arthroplasty during the study period were also investigated. Patients and methods 1,531 hemiprostheses (HPs), 69 total shoulder replacements (Neer type TSR), and 225 reversed total shoulder replacement (reversed TSR) operations were reported to the Norwegian Arthroplasty Register between 1994 and 2005. Kaplan-Meier failure curves were drawn up for particular subgroups of patients, and revision rates were calculated using Cox regression analysis. Results The 5- and 10-year failure rates of hemiprostheses were 6% (95% CI: 5–7) and 8% (95% CI: 6–10), and for reversed total shoulder replacements they were 10% (95% CI: 5–15) and 22% (95% CI: 10–33), respectively. For hemiprostheses, the risk of revision for patients who were 70 years or older was half that of those who were younger (RR = 0.47, CI: 0.28–0.77), while the risk of revision was highest for patients with sequelae after fracture compared to those with acute fractures (RR = 3.3, CI: 1.5–7.2). No differences in prosthesis survival were found between the different hemiprosthesis brands. The main reasons for revision of hemiprostheses were pain and luxation. For reversed total prostheses, the risk of revision was less for women than for men (RR = 0.26, CI: 0.11–0.63), and the main cause of revision was aseptic loosening of the glenoid component. During the study period, the incidence of shoulder arthroplasty increased for all diagnostic groups except inflammatory arthritis, for which a decrease was seen. Interpretation We found good results in terms of 5-year prosthesis failure rate, with the use of hemiarthroplasty for patients with inflammatory arthritis, osteoarthritis, and acute fractures. Reversed total shoulder replacement was associated with a rather poor prognosis.
Article
Full-text available
Background Although short-term outcomes of reverse total shoulder arthroplasty have been promising, long-term success may be limited due to device-specific complications, including scapular notching. Scapular notching has been explained primarily as mechanical erosion; however, the generation of wear debris may lead to further biologic changes contributing to the severity of scapular notching. Methods A 12-station hip simulator was converted to a reverse total shoulder arthroplasty wear simulator subjecting conventional and highly cross-linked ultra-high-molecular-weight polyethylene humeral liners to 5 million cycles of alternating abduction-adduction and flexion-extension loading profiles. Results Highly cross-linked polyethylene liners (36.5 ± 10.0 mm3/million cycle) exhibited significantly lower volumetric wear rates compared with conventional polyethylene liners (83.6 ± 20.6 mm3/million cycle; P < .001). The flexion-extension loading profile exhibited significantly higher wear rates for conventional (P < .001) and highly cross-linked polyethylene (P < .001) compared with the abduction-adduction loading profile. Highly cross-linked wear particles had an equivalent circle diameter significantly smaller than wear particles from conventional polyethylene (P < .001). Conclusions Highly cross-linked polyethylene liners significantly reduced polyethylene wear and subsequent particle generation. More favorable wear properties with the use of highly cross-linked polyethylene may lead to increased device longevity and fewer complications but must be weighed against the effect of reduced mechanical properties.
Article
Shoulder arthroplasty (joint replacement) is a viable intervention for individuals with arthritic pathologies that have been refractory to conservative interventions. Although traditional joint replacement procedures have been found efficacious, they are not appropriate for individuals with an irreparable rotator cuff tear. Reverse total shoulder arthroplasty (rtsa) is a complex surgical procedure specifically designed for individuals with advanced arthritis and an irreparable rotator cuff. Owing to the complexity of this procedure, many individuals will have impairments extending well-beyond formal rehabilitation. Thus, the purpose of this article is to provide the necessary information to implement a safe and effective rtsa postrehabilitation program. For a video abstract of this article, see supplemental digital content 1 (see video, http://links.lww.com/scj/a143).
Article
Background: Highly crosslinked polyethylene (XLPE) is believed to demonstrate better wear resistance than conventional polyethylene (CPE) in total hip arthroplasty. Questions/purposes: The purpose of this study was to compare visual damage scores and micro-CT measurements of penetration, a surrogate for wear, between matched retrieved XLPE and CPE acetabular liners. Methods: Thirteen XLPE acetabular liners were matched in terms of implant design (all were of the same design), patient age, sex, liner dimensions, duration of implantation, and reason for revision to a group of CPE liners that were retrieved in the same time period. Penetration resulting from the combination of wear and creep in the two groups of liners was measured with micro-CT. Surface damage was scored by two blinded observers using a surface damage system that considers the seven common damage modes: pitting, scratching, burnishing, abrasions, impingement, embedded debris, and delamination, and wear patterns were documented. Results: There was no difference (p=0.32) in total damage score between the XLPE group (14±4) and the CPE group (15±5). However, there was three times greater penetration (odds ratio, 3.1; confidence interval, 2.3-5.1; p<0.001) in the CPE group (0.18±0.09 mm/year) than in the XLPE group (0.05±0.07 mm/year). There was less volumetric loss in XLPE (82±SD 134 mm3) versus the CPE group (350±SD 342 mm3; p=0.017). Conclusions: XLPE liners undergo less penetration as a result of creep and wear than CPE liners based on quantitative measurements provided by micro-CT, which was not apparent using damage scoring alone. This demonstrates the use of three-dimensional imaging techniques such as micro-CT for quantifying wear in retrieval studies. Clinical relevance: In this study, XLPE had less wear but similar damage scores than CPE, allaying concerns that the beneficial wear properties of XLPE might come with a tradeoff arising from the increased brittleness of that material.
Article
Although instability can occur after reverse total shoulder arthroplasty (RTSA), the risk factors, the treatment, and ultimate fate of the implant in these patients remains poorly understood. Demographics, acute treatment, and the need for revision were evaluated in all patients with RTSAs who sustained a subsequent dislocation within the first 3 months. Standardized outcome scores were collected preoperatively and at the final follow-up. Atraumatic instability occurred in 11 patients (incidence, 2.9%) treated with RTSA early (before 3 months postsurgery). The mean time to dislocation was 3.4 weeks. These patients tended to be previously operated-on (64%), male (82%), overweight (mean body mass index (BMI) of 32.2 kg/m(2), with 82% having a BMI ≥30 kg/m(2)), and without a satisfactory subscapularis repair at initial RTSA (64%). Initial treatment included closed reduction in 9 patients, open reduction in 1, and open reduction with a thicker polyethylene insert in 1. Four experienced recurrent instability requiring a thicker polyethylene insert. Two additional patients were converted to hemiarthroplasty due to persistent instability. Visual analog pain scores (P = .014) and American Shoulder and Elbow Surgeons scores (P = .018) were significantly improved. Simple Shoulder Test scores trended towards improvement (P = .073). Early dislocations of the RTSA prosthesis were uncommon. The most common associated factors were a BMI >30 kg/m(2), male gender, subscapularis deficiency, and previous surgery; in these patients, we now use an abduction orthosis. Closed reduction alone was successful in 4 of the 9 closed reductions (44%). Five of 11 RTSAs (45%) required polyethylene exchange. The RTSA was retained in 82%, 36% with the original implant.
Article
Background: Despite the success of reverse shoulder arthroplasty (RSA) in treating patients with painful pseudoparalytic shoulders, instability is a common complication and currently the factors affecting stability are not well understood. The objective of this study was to investigate a number of factors as well as the interactions between factors to determine how they affect the stability of the prosthesis. These factors included: active arm posture (abduction and abduction plane angles), loading direction, glenosphere diameter and eccentricity, and humeral socket constraint. Methods: Force required to dislocate the joint, determined using a biomechanical shoulder simulator, was used as a measure of stability. A factorial design experiment was implemented to examine the factors and interactions. Results: Actively increasing the abduction angle by 15° leads to a 30% increase in stability and use of an inferior-offset rather than a centered glenosphere improved stability by 17%. Use of a more constrained humeral socket also increased stability; but the effect was dependent on loading direction, with a 88% improvement for superior loading, 66% for posterior, 36% for anterior, and no change for inferior loading. Abduction plane angle and glenosphere diameter had no effect on stability. Conclusion: Increased glenohumeral abduction and the use of an inferior-offset glenosphere were found to increase the stability of RSA. Additionally, use of a more constrained humeral socket increased stability for anterior, posterior, and superior loading. These identified factor effects have the potential to decrease the risk of dislocation following RSA.
Article
Unlabelled: Reverse total shoulder arthroplasty is a treatment option for patients with symptomatic glenohumeral arthritis and a deficient rotator cuff. The reported complication rates vary from 0% to 68%. Given this variation, our purposes were to (1) determine the learning curve for the procedure, (2) identify complications and surgical pitfalls, and (3) compare our results with those of similar published series. We retrospectively reviewed 20 consecutive patients (mean age, 73 years; range, 45-88 years) who had reverse total shoulder arthroplasty by one surgeon, tabulating intraoperative and postoperative complications. Minimum followup was 3 months (average, 9 months; range, 3-21 months). The intraoperative complication rate for the first 10 patients was higher than that for the second 10 patients. There were 33 complications in 15 patients: 11 patients collectively had 22 intraoperative complications and eight patients collectively had 11 postoperative complications. At radiographic followup, 11 patients had scapular notching and nine patients had heterotopic ossification. Our complication rate was higher than published rates. Level of evidence: Level II, prognostic study. See the Guidelines for Authors for a complete description of levels of evidence.
Article
Although early results with reverse total shoulder arthroplasty (rTSA) have been promising, concern exists about the high reported rates of scapular notching and the potential for catastrophic failure of glenoid component fixation. Generation of polyethylene wear debris may also contribute to notching and osteolysis of the scapula. A testing model for polyethylene wear is currently unavailable for reverse shoulder prostheses. The goal of this study was to develop a testing protocol using a commercially available hip simulator. Component design may also influence the generation of polyethylene debris. It is hypothesized that increased polyethylene wear occurs in glenospheres with holes in the articulating surface. Custom fixtures were fabricated to simulate both glenohumeral abduction and flexion on a 12-station hip wear simulator. Loading profiles for both abduction and flexion were alternated every 250,000 cycles for a total of 5 million cycles. Gravimetric analysis of humeral cups throughout the test was used to characterize wear. Lubricant fluid was collected throughout the test and digested for polyethylene particle analysis. Comparisons of volumetric wear rates and total volume loss between glenospheres with and without holes and between flexion and abduction loading profiles showed similar results. Particle analysis displayed fibrillar particles with an equivalent circle diameter of 0.3 ± .1 μm and an aspect ratio of 2.5 ± 1.4. This study represents the first wear simulation and particle characterization of reverse shoulder systems. No significant difference in wear was reported between glenospheres with and without holes.