Extract
Numerous publications clearly support the conclusion that, overall, total
knee arthroplasty is successful. The definitive improvement in quality of
life, in combination with the aging of the population, has led to an
increasing demand for total knee arthroplasty. While cruciate-retaining and
posterior-stabilized devices will perform well for the vast majority of
patients presenting as candidates for primary total knee arthroplasty, the
orthopaedic surgeon occasionally encounters cases of advanced severity
(Figs. 1-A and
1-B)1-4.
Complex presentations range from higher degrees of ligamentous incompetency to
severe restriction of the range of motion with substantial flexion contracture
to posttraumatic arthritis and to post-osteotomy deformity of either the
distal part of the femur or the proximal part of the tibia. The challenge
confronting the reconstructive surgeon is to obtain a well-balanced
flexion-extension gap with balanced collateral ligaments. This is frequently
best accomplished with a modular system that offers a continuum of constraint
(Fig. 2). Modularity allows
intraoperative customization; namely, the use of stems, wedges, and augments.
Frequently these difficult primary arthroplasties require the use of
posterior-stabilized constrained
implants1,5-16.
Numerous publications clearly support the conclusion that, overall, total
knee arthroplasty is successful. The definitive improvement in quality of
life, in combination with the aging of the population, has led to an
increasing demand for total knee arthroplasty. While cruciate-retaining and
posterior-stabilized devices will perform well for the vast majority of
patients presenting as candidates for primary total knee arthroplasty, the
orthopaedic surgeon occasionally encounters cases of advanced severity
(Figs. 1-A and
1-B)1-4.
Complex presentations range from higher degrees of ligamentous incompetency to
severe restriction of the range of motion with substantial flexion contracture
to posttraumatic arthritis and to post-osteotomy deformity of either the
distal part of the femur or the proximal part of the tibia. The challenge
confronting the reconstructive surgeon is to obtain a well-balanced
flexion-extension gap with balanced collateral ligaments. This is frequently
best accomplished with a modular system that offers a continuum of constraint
(Fig. 2). Modularity allows
intraoperative customization; namely, the use of stems, wedges, and augments.
Frequently these difficult primary arthroplasties require the use of
posterior-stabilized constrained
implants1,5-16.
We previously reported the early clinical results and failure mechanisms in
a large series of 395 patients who had undergone a total of 421 consecutive
difficult primary and revision total knee arthroplasties performed with a
modular posterior-stabilized constrained
device12. At the
time of the review, 102 patients (107 knees) had died; the outcomes in these
patients were known, and the deaths were unrelated to the index arthroplasty.
The duration of follow-up of the living patients averaged five years. The
average Knee Society clinical score improved from 48 of a possible 100 points
preoperatively to 79 points at the most recent evaluation, whereas the average
range of motion improved from 91° to 101°. Overall survivorship, with
partial or complete revision for any reason (septic or aseptic) as the end
point, was 89%. Survivorship with aseptic revision as the end point was 94%.
Revision due to infection was required in twenty-three knees (5%). Of these
infections, nine were recurrent in a group of ninety knees that had undergone
reimplantation after removal of the original prosthesis because of infection
and fourteen developed in the 331 knees without a previous history of
infection. There were twenty-four partial or complete aseptic revisions (6%),
with six done because of arthrofibrosis, five done because of aseptic
loosening, four related to the extensor mechanism, three done because of
instability, three done because of periprosthetic fracture, two done because
of soft-tissue impingement, and one related to a malignant tumor.
The use of antibiotic-impregnated cement has been shown to significantly
reduce the prevalence of deep infection after primary total knee arthroplasty
(p = 0.0238)17. We
currently use and recommend the use of antibiotic-impregnated cement for all
difficult primary and revision arthroplasties. Because implant fixation and
prosthetic stability can be achieved and the extensor mechanism can be managed
correctly, substantial improvements in terms of pain relief, function, and the
range of motion can be expected with the use of a modular posterior-stabilized
constrained knee system. Wear and failure due to the modularity of the
prosthesis are not among the common failure mechanisms.
While the need for a varus/valgus constrained condylar device is fairly
common in revision total knee arthroplasty, its use in primary arthroplasty is
rare (Fig. 3). Constrained
condylar prostheses are nonlinked devices that offer substantial varus/valgus
constraint by virtue of an enlarged, extended tibial spine that fits within
the intercondylar notch of the femoral component. This configuration generally
allows a degree or two of varus/valgus laxity and a degree or two of rotation.
This is distinctly different from a posterior-stabilized device, which
provides no varus/valgus stability and no rotational constraint. A
posterior-stabilized constrained articulation, rather than a
posterior-stabilized articulation, is selected when the medial or lateral
collateral ligament is compromised (Fig.
4).
We conducted a retrospective review of one surgeon's (A.V.L. Jr.) ten-year
experience with a single design of modular posterior-stabilized constrained
total knee arthroplasty; our purpose was to evaluate its application as a
primary procedure and to evaluate the midterm outcomes of treatment of these
difficult cases. The device utilized in the current study was the Maxim
Posterior-Stabilized Constrained implant
(Fig. 5), which is one of three
major categories of knee implants within the Maxim Complete Knee System
(Biomet Orthopaedics, Warsaw, Indiana). This device has a modular design that
allows incorporation of stems of varying degrees of width and length. Augments
with which to address deficiency of the distal part of the femur or proximal
part of the tibia are also available. Posterior-stabilized and
posterior-stabilized constrained polyethylene articulations are available.
Selection of the posterior-stabilized rather than the posterior-stabilized
constrained implant is based on the final intraoperative assessment of coronal
stability in flexion and extension. Of the primary total knee arthroplasties
performed by the senior author (A.V.L. Jr.) from 1988 through 2006, a
posterior-stabilized constrained-type device was used in only 1.3% of the
knees and further constraint—that is, a rotating hinge device—was
used in 0.5% (Fig. 3).
While still available for use today, the Maxim System has evolved into the
Vanguard Complete Knee System (Biomet)
(Figs. 6-A through 6-H). The
most important differences in the Vanguard System, compared with the Maxim
System, include extension and broadening of the anterior flange to facilitate
earlier nonconstrained capture of the patella, 2 mm of lateralization of the
trochlear groove, anatomical angulation of the trochlear groove at 6.5° of
valgus, a swept-back patellofemoral articulation as a result of a more
aggressive anterior chamfer resection, greater extension of the trochlear
articulation into the tibiofemoral articulation to minimize patellar
crepitation and clunk syndrome, an increase in posterior condylar thickness of
1 mm to provide a greater area of contact with deep flexion, broadening of the
posterior aspects of the femoral condyles (also to provide a greater area of
contact in deep flexion), a gradual increase in the lengths of the posterior
aspects of the femoral condyles proportional to size, variation of
intercondylar resection (with the resection narrower for smaller sizes than
for larger sizes) to facilitate greater preservation of the medial and lateral
femoral condyles, a tighter fit of the tibial spine within the intercondylar
space to facilitate a greater degree of stability, and a cam extension to
provide greater hop height for increased protection against dislocation.
Having successfully used the Maxim Posterior-Stabilized Constrained implant,
we have transitioned to the Vanguard Super-Stabilized Knee (SSK) constrained
implant.
A retrospective review of difficult primary total knee arthroplasties
performed by one surgeon (A.V.L. Jr.) between July 1992 and December 2003
identified fifty-three patients with sixty-one involved knees in which a
single modular posterior-stabilized constrained design had been implanted.
These cases were associated with complex ligamentous deficiency and severe
osseous deformity and represent an extremely small percentage of the primary
total knee arthroplasties performed during that time period. All of the
operations were performed through a standard median parapatellar incision, and
metaphyseal cemented fixation was utilized for all components. Preoperative
and postoperative Hospital for Special Surgery (HSS) scores (used until 1997)
or Knee Society (KS) scores (used from March 1997) were analyzed, as was the
range of motion and the need for subsequent surgical or other procedures.
There were thirteen male and forty female patients. The presenting
diagnosis was osteoarthritis in twenty-seven knees (44%), rheumatoid arthritis
in fifteen (25%), posttraumatic arthritis in eight (13%), and a failed open
reduction and internal fixation of a fracture in eleven (18%). The average age
(and standard deviation) at the time of surgery was 63.8 ± 13.8 years
(range, twenty-four to eighty-eight years). The average height was 163 cm (64
in), the average weight was 76 kg (168 lb), and the average body mass index
was 29.2 ± 6.4 kg/m2 (range, 21.0 to 50.4
kg/m2).
At the time of follow-up, sixteen patients (eighteen knees) had died; all
of the deaths were unrelated to the total knee arthroplasty, and the outcomes
of all of the arthroplasties were known. The duration of follow-up of the
surviving patients averaged 5.6 years, with a maximum of 13.4 years. The range
of motion improved from an average of 89° preoperatively to an average of
103° at the most recent evaluation. The average HSS score (0 to 100
possible points) improved from 49.6 points preoperatively to 76.7 points
postoperatively, the average KS clinical score (0 to 100 possible points)
improved from 35 to 86.1 points, and the average KS function score (—20
to 100 possible points) improved from 35.2 to 48.4 points
(Fig. 7). Eight knees (13%)
required manipulation because of postoperative arthrofibrosis. Revision (of
any component part) was performed in seven knees (11%)
(Fig. 8). Three revisions (5%)
were done (at two, twenty-seven, and seventy-seven months) because of deep
infection; two of these revisions consisted of radical débridement and
two-stage reimplantation, and one was a fusion. There were four aseptic
revisions: two (3%) were done (at twenty-nine and forty-months) because of
complications related to the extensor mechanism, one (2%) was done (at
ninety-five months) because of instability, and one was done (at twenty
months) because of a periprosthetic fracture. The revisions due to the
extensor mechanism complications consisted of a patellectomy in one knee and a
change of the tibial polyethylene insert in the other. All other revisions
included a full exchange of the component. There were no revisions due to
aseptic loosening (Figs. 9-A, 9-B, 9-C,
9-D, 10-A, 10-B, 10-C,
10-D, 11-A, 11-B, 11-C, 11-D,
11-E, 12-A, 12-B, 12-C, and
12-D).
Over the last twenty-five years, multiple reports of both poor and
excellent outcomes following complex total knee arthroplasty have been
published. It appears, on the basis of a review of the literature and the
current study, that the possible concerns about the increased constraint and
modularity necessary to obtain appropriate stability, adequate fixation, and
reestablishment of the joint line are not
warranted14,15.
Instead, the more common failure mechanisms and reasons for early failures
with this modular constrained design of total knee arthroplasty are infection,
problems related to the extensor mechanism, and recurrent instability. No
cases of aseptic loosening were identified in this series of difficult primary
arthroplasties.
Complex primary total knee arthroplasties with constrained condylar devices
have had good results in other series. Sprenger and Doerzbacher, in a study of
fifty-four primary total knee arthroplasties with use of the GSB-II
(Gschwend-Scheier-Bahler-II) implant (Sulzer Medica), noted ten and
eighteen-year cumulative life-table survival rates of 95.7% and 88.1%, with
removal of the prosthesis or infection as the end
point18. In a
series of forty-four primary total knee arthroplasties done with a constrained
condylar device in thirty-seven elderly patients with an average of 17.6°
of valgus deformity, Easley et al. reported no failures, loosening, or
instability after an average duration of follow-up of 7.8
years7.
Font-Rodriguez et al. noted a seven-year success rate of 98% after sixty-four
primary constrained condylar total knee
arthroplasties8. In
a recent study by Anderson et al., of seventy primary total knee
arthroplasties done with constrained condylar implants without stems in
sixty-one patients, no radiographic evidence of loosening or wear was seen at
an average of 44.5 months
postoperatively19.
Lachiewicz and Soileau recently reported that, of fifty-four knees (forty-four
patients) treated with a primary total knee arthroplasty with a constrained
prosthesis and followed for a mean of nine years, two knees required revision
because of aseptic loosening (of the tibial component in one and of the
femoral component in the other); the survival rate was 96% at ten
years11.
The management of instability and the achievement of a functional range of
motion depend on both adequate restoration of the joint line and avoidance of
flexion instability or patella
baja1,2,12,20.
Patellar instability and complications related to the extensor mechanism can
be avoided by ensuring correct rotation of the femoral and tibial implants and
by following an algorithm for
reconstruction21.
We have addressed the issue of recurrent instability by using the Vanguard
Complete Knee System, which is a direct descendent of the Maxim Complete Knee
System. Enhanced stability is afforded by increased tolerances of the tibial
spine within the intercondylar housing of the femoral component. This system
also addresses patellar issues and extensor mechanism-related complications
with several design features, including an extended anterior flange to
facilitate early capture of the patella within the trochlear groove, a
lateralized trochlear groove, a swept-back femoral component facilitated by a
tapered anterior chamfer resection, and an extended trochlear groove.
In this series, septic failure was a major factor affecting the early
results of complex primary total knee arthroplasty. With recent reports in the
literature suggesting that the use of antibiotic-impregnated cement
significantly reduces the prevalence of deep infection following primary total
knee arthroplasty (p =
0.0238)17, we
currently use such cement for all difficult primary and revision total knee
arthroplasties.
Because implant fixation and prosthetic stability can be achieved and the
extensor mechanism can be managed correctly, substantial improvements in terms
of pain relief, function, and the range of motion can be expected with use of
a modular posterior-stabilized constrained knee system. Wear and failure due
to modularity of the prosthesis have not been among the failure mechanisms.
?
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