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Posterior Stabilized
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Total Knee Arthroplasty
MusaB.Zaid andThomasP.Vail
Contents
28.1 Introduction – 318
28.2 Case Example – 318
28.3 Surgical Technique – 318
28.3.1 Positioning – 318
28.3.2 Exposure – 319
28.3.3 Distal Femoral Preparation – 319
28.3.4 Tibial Preparation – 320
28.3.5 Extension Gap Balancing – 321
28.3.6 Femoral Sizing andRotation – 322
28.3.7 Patellar Preparation – 323
28.3.8
Trialing andTibial Sizing – 323
28.3.9 Cementation andFinal Component Placement – 323
28.3.10 Closure – 324
317
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28.4 Literature Review – 324
References – 325
© The Author(s), under exclusive license to Springer-Verlag GmbH, DE, part of Springer Nature 2022 E. Hansen, K.-D. Kühn (eds.), Essentials of Cemented Knee Arthroplasty,
https://doi.org/10.1007/978-3-662-63113-3_28
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M. B. Zaid and T. P. Vail
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28.1 Introduction
The decision to utilize a cruciate-retaining versus a pos­terior stabilized total knee arthroplasty continues to be an area of debate as one technique has not separated itself from the other in achieving optimized pain relief and functional outcome. While current literature sug­gests that posterior stabilized knee arthroplasty may provide increased postoperative range of motion, there is minimal difference in rates of aseptic loosening or patient-reported outcomes when compared to cruciate­retaining total knee arthroplasty. The purpose of this chapter is to highlight the surgical technique of per­forming a cemented posterior stabilized total knee arthroplasty as well as to briey discuss the kinematic considerations of a posterior stabilized knee arthro­plasty and explore some of the recent literature examin­ing functional and patient-related outcomes between cruciate-retaining and posterior stabilized implant designs.
28.2 Case Example
On examination, her body mass index is 26 kg/m3. She walks with an antalgic gait, valgus thrust. She has full painless passive and active range of motion of her bilateral hips with no pain on active straight leg raise. Examination of her knees is signicant for mild medial and lateral joint line tenderness and no effusion. The patient has bilateral, left greater than right, valgus knee alignment with a symmetrical range of motion of 0–130°. She is stable to anterior–posterior stress exam and her valgus deformity is passively correctable with solid endpoints on collateral ligament testing. She is neurovascularly intact.
Anterior–posterior, sunrise, lateral, and Rosenberg view radiographs of the bilateral knees demonstrate val­gus alignment with bone-on-bone lateral joint space narrowing and associated subchondral sclerosis (. Fig.28.1).
Given the severity of the patient’s symptoms, the associated limitation of her activities, and impact on her quality of life, staged bilateral total knee arthroplasty is recommended. As her left knee is more symptomatic, the patient elects to have a left total knee arthroplasty rst. Postoperative results are shown in .
Fig.28.2.
A 75-year-old female with a past medical history of hypertension has been followed in the arthroplasty clinic with bilateral, left greater than right, knee pain that has progressively worsened over the last year. She describes activity-related, dull-aching pain located in her anterior knees that gets worse with using stairs, prolonged stand­ing, and walking. Additionally, she has noticed increased bowing of her knees. The patient currently can ambulate greater than six blocks and does not use any assistive devices. She has previously attempted oral anti­inammatories and intra-articular cortisone injections experiencing mild relief of her symptoms. Her review of systems is notable for joint pain; she denies back pain or other signicant joint symptoms.
28.3 Surgical Technique
28.3.1 Positioning
The patient is placed supine on a standard operating room Table. A well-padded, high-thigh tourniquet is placed on the operative extremity and is only inated during nal component cementation. The operative extremity is prepped and draped in the usual sterile fash­ion and then placed in a knee positioning device and secured. The ankle is left free to allow for visualization of the malleoli during placement of the extramedullary tibial alignment guide.
. Fig. 28.1 Preoperative radiographs demonstrating valgus alignment with medial-sided bone-on-bone arthritis and osteophyte formation
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. Fig. 28.2 Postoperative radiographs demonstrating a well-sized, well-xed, cemented posterior stabilized total knee arthroplasty
28.3.2 Exposure
With the knee in a 40–45° exed position, a curved medial peripatellar skin incision, avoiding the tibial tubercle and other bony prominences, is used. A capsu­lar incision is then performed starting distally using a knife, proceeding from the medial one-third of the tibial tubercle, incorporating the medial 6–8 mm of the infrapatellar ligament, creating a cuff of tissue around the medial aspect of the patella, and then proceeding proximally in the medial 6–8mm of the quadriceps ten­don to a distance of about one patella diameter above the superior pole of the patella. The patella is then reected laterally and the fat pad is excised.
An “internal release of the patella” is performed by elevating the capsular attachment to the patella along the lateral patellar border at the osteochondral junction. The lateral patellofemoral ligament is divided sharply. A limited synovectomy is performed (this can be more extensive if there is extensive synovitis or synovial thick­ening). Exposure in standard varus or valgus knee with
a correctable deformity (as opposed to a more severe, xed deformity required a greater release of contrac­ture) includes minimal elevation of the deep MCL to allow visualization of the proximal tibia sufcient to perform a proximal tibial resection.
Once this standard exposure is completed, the knee is exed with the patella subluxated to the lateral gutter. This allows sufcient visualization of the distal femur and proximal tibia to begin the bone resection and assessment of the exion and extension gaps.
28.3.3 Distal Femoral Preparation
The knee is brought into exion and a rongeur is used to remove any osteophytes that may be present along the articular cartilage edges sufciently large to interfere with the assessment of the joint line using the distal fem­oral resection guide. For intramedullary guidance of the distal femoral cut, the diaphysis of the distal femur is then opened above the notch toward its medial border at
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. Fig. 28.3 Intraoperative photograph demonstrating exposure of
the distal femur as well as marking the start site for the intramedul­lary alignment guide located 7–10mm anterior and just medial to the femoral origin of the posterior cruciate ligament
a location 7–10mm anterior and just medial to the fem­oral origin of the posterior cruciate ligament (. Fig. 28.3). The intramedullary alignment rod is inserted into the distal femur with the attached distal femoral cutting block preset at the desired valgus angle relative to the anatomic axis. This desired angle can be determined with preoperative imaging. The resection level is set such that the resected bone matches the thick­ness of the prosthesis, thereby preserving the joint line. Once positioned, the cutting jig is secured with pins allowing removal of the alignment rod and creation of the distal femoral using an oscillating saw through the jig (. Fig.28.4).
> Care should be taken to assure that the cutting instru-
ment does not deviate off of sclerotic bone thereby moving the cut off of the desired angle.
. Fig. 28.4 Intraoperative photograph demonstrating placement
of the distal femoral cutting guide followed by removal of the intra­medullary alignment guide. Note the entry position of the intramed­ullary guide just above the notch and slightly medial to the mid-line. An oscillating saw is used to make this cut through the guide
28.3.4 Tibial Preparation
Following distal femur preparation, the knee is brought into 90° of exion to prepare the proximal tibia. While it is possible to create both the distal femoral and proxi­mal tibial cuts with navigation or custom blocks, most often an extramedullary tibial guide is used. Likewise, it is also acceptable to make the proximal tibial cut rst, and the distal femoral cut next, using the proximal tibia to guide the femoral cut. In either workow, the extra­medullary guide is secured to the leg via pins at the joint line and clamps that reach around the tibial at or above the lateral and medial malleoli. The position of the jig proximally sets the relationship of the proximal tibial cut to the mechanical and anatomic axes. Some surgeons prefer a predetermined proximal tibial angle, others use
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. Fig. 28.5 Intraoperative photograph demonstrating placement
of the extramedullary tibial alignment guide. The resection stylus is placed on the tibial plateau to set the proper level of proximal tibial bone resection. The amount of resection correlates with the com­bined thickness of the metal prosthetic tray and tibial insert
surface anatomy such as the intermalleolar position dis­tally and the medial third of the tibial tubercle proxi­mally, and others choose to make the proximal tibial cut perpendicular to the mechanical axis.
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> With any of those choices, it is assumed that the sur-
geon accounts for the variability in individual anat­omy and preexisting deformity to achieve the desired outcome.
When performing a posterior stabilized knee replace­ment, to accommodate the articular design of the pros­thesis, the posterior slope is typically set to 5° or less. The desired varus and valgus alignment of the extra­medullary tibial guide can be checked using a drop rod from anterior portion of the alignment guide and adjusted relative to surface landmarks on the tibia such as the tibial crest or the malleoli. While not critical at this stage, rotation of the proximal tibial cutting block is set by aligning the central mark on the cutting block with the medial third of the tibial tubercle. To the extent that any slope is incorporated into the cut, the rotation does become important as rotation of the cutting block that has a greater anterior than posterior resection can translate into varus or valgus if rotation is off of the midline.
Finally, the resection stylus is placed on the tibial
plateau to set the proper level of bone resection
Fig. 28.5). Depending upon the point of reference,
(. the resection level can vary, with less bone being removed if the point of reference is from a decient area, and bone resection commensurate with the implant thick­ness if the point of reference is taken from the healthy joint line. The proximal tibia cut is then made using an oscillating saw.
. Fig. 28.6 Intraoperative photograph demonstrating a balanced
or rectangular extension gap
> Great care should be taken to protect the collaterals,
and to feel the posterior cortex, moving slowly with
the saw as the posterior vascular structures, collater-
als, and capsule are at particular risk when making
the tibial cut.
28.3.5 Extension Gap Balancing
After the distal femur and proximal tibia cuts have been made, the extension gap is checked. The leg is brought into a full extension and a spacer block is inserted to evaluate the balance of the extension gap. Ideally, the extension gap is close to being rectangular rather than trapezoidal (. Fig. 28.6). There should be no signicant medial to lateral laxity, or differences of >2 mm, when the spacer block is placed and ligament balance is assessed.
> This is a very subjective step in the procedure, as there
is no dened magnitude of varus or valgus stress that
should be applied when assessing the extension gap
balance.
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However, if the surgeon determines that the extension gap is not acceptably balanced, then some soft tissue releases may be needed (assuming that the desired resec­tion angle of the distal femoral and proximal tibial cuts has been achieved). Typically for a valgus knee, the lat­eral capsule at the joint line can be elevated off of the tibia, followed by elevation of the iliotibial band inser­tion just above Gerdy’s tubercle, and nally if needed the popliteobular ligament (capsule complex below the popliteus). For a varus knee, the medial capsule, the pos­teromedial corner, and the supercial medial collateral can be released in sequence to achieve balance in the extension gap.
28.3.6 Femoral Sizing andRotation
Once optimal extension gap balance has been achieved, one can proceed with femoral sizing and nishing. This step can be done either using a measured resection method or a gap balance method. Some surgeons using a measured resection technique prefer to start with the distal femoral cut and then nish the femoral prepara­tion using the epicondylar axis or Whiteside’s line to set rotation, balancing ligaments at the end after all of the desired femoral and tibial cuts are made. In the gap­balancing workow, the releases are performed at the outset once the extension gap cuts have been made.
The femoral nishing, which included the anterior, posterior, and chamfer cuts, is then made using the tibial cut and the ligament tension to set the rotation. For the gap-balancing workow, the knee is brought into 90° of exion and the femur size is determined. The femoral component rotation is then set using a ligament­tensioning device or a spacer block that sits on the tibia and is used as a reference for setting femoral component rotation (.
Fig. 28.7). At this step, a varus and valgus
force can be applied to check for symmetry and lift off of the jig from the proximal tibia to assess the exion gap balance. Adjustments can be made in the size of the femoral component, the thickness of the polyethylene insert, or the rotation of the femoral component before the cuts are made to set the rotation.
. Fig. 28.7 Intraoperative photograph demonstrating distal femo-
ral sizing. Subsequent to sizing, the rotational position of the distal femoral component is established using a ligament-tensioning device in a gap-balancing workow. This can be accomplished with a lam­ina spreader, an electronic tensiometer, or a specially designed instru­ment. In this example, the intramedullary rod serves as the pivot point, allowing balancing of the medial and lateral exion gaps as the ligaments are tensioned by the instrument. Once the optimal rotation and size are established, the femoral cutting guide is pinned in place and removed
. Fig. 28.8 Intraoperative photograph of the notch cut being per-
formed. The medial–lateral position of the notch cut determines the ultimate medial–lateral position of the implant. It should be placed as far lateral as possible without lateral overhang to facilitate patella tracking
> Ideally, the extension and exion gaps should be close
to equal; if the exion space is too large, upsizing the
femoral component should be considered. If the ex-
ion space is too small, the femoral component can be
downsized.
Once the optimal rotation and size are established, the femoral cutting guide is pinned in place and removed (. Fig. 28.7). Retractors are placed to protect soft tis­sues, and an oscillating saw is then used to cut the ante­rior, anterior chamfer, posterior, and posterior chamfer
cuts at the distal femur. The notch cut is then completed
Fig.28.8). The medial–lateral position of the notch
(. cut determines the ultimate medial–lateral position of the implant. It should be placed as far lateral as possible without lateral overhang to facilitate patella tracking. Next, a lamina spreader can be used to distract the ex­ion gap to gain visualization of the posterior femoral condyles to remove residual osteophytes. Trial implants can now be inserted and overall balance, t, and range of motion rechecked.
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. Fig. 28.9 Intraoperative photograph showing tibial sizing. The
tibia is sized by selecting a tibial baseplate that maximizes tibial cov­erage without overhang. Rotation of the implant is set using ana­tomic landmarks such as the tibial tubercle and ankle joint
28.3.7 Patellar Preparation
The patella is sized and the cutting guide is set according to the available patellar bone. Generally, the patella is cut at its osteochondral border, noting that the lateral facet is generally longer, thinner, and less steep than the medial facet of the patella.
28.3.8 Trialing andTibial Sizing
With the trial femoral component impacted onto the femur and the tibial trial in place, a visual check should be performed to ensure that the distal femur cuts are appropriate, tting into the femoral trial. The tibia is sized by selecting a tibial baseplate that maximizes tibial coverage without overhang (. Fig. 28.9). Tibial com­ponent rotation can be assessed before nalizing the preparation by putting the trial construct through a range of motion and marking the tibial component rotation at the joint line. If the knee is stable and well balanced, and the desired tibial component rotation is established, then the nal tibial preparation is performed using the drill and punch method.
28.3.9 Cementation andFinal Component
Placement
The tourniquet is inated and a pulse lavage is used to prepare all the bony surfaces which are subsequently patted dry. First, the tibial component is cemented into place. Cement is placed and nger-packed (some sur­geons use a cement gun) along the proximal tibial sur­face and the keel hole as well as on the tibial baseplate (. Figs. 28.10 and 28.11). Cement is placed onto the
. Fig. 28.10 Intraoperative photograph demonstrating nger-
packed cement along the proximal tibial surface. Cement is also placed along the distal femur prior to placement of the femoral com­ponent (not shown). Keeping blood and fat out of the interface between the implant and the cement is important for optimal implant xation
. Fig. 28.11 Cement is placed onto the dry implant coating the
cement-facing surface of the tibia (shown) and femur
dry implant coating the cement-facing surface of the tibia and femur. Similarly, cement is placed on the ante­rior and distal femoral cuts, and a small amount of cement is placed on the posterior anges of the implant. The components are then placed and impacted. Excess cement is removed. A trial liner is placed and the knee is brought into extension.
> It is important to keep the knee very still and properly
aligned while the cement cures. Movement of the knee while the cement is in a plastic phase can lead to bone–cement or implant–cement radiolucency and suboptimal cement mantle.
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The patellar component is cemented in place after the tibia and femur. The knee is once again checked for a stable range of motion once the cement is allowed to fully harden. The tourniquet is deated and the polyeth­ylene liner is placed.
28.3.10 Closure
The knee capsule is closed anatomically using monola­ment absorbable suture on the deep layers, and either nylon suture, stables, or a running subcuticular closure on the skin. The wound is dressed with a sterile dressing.
28.4 Literature Review
Introduction
z
For the primary total knee arthroplasty, numerous pros­thesis designs exist with the two most common being the cruciate-retaining (CR) and posterior stabilized (PS). While the cruciate-retaining implant design relies on the patient’s native posterior cruciate ligament to allow for femoral rollback during deep exion, the posterior sta­bilized design utilizes a central post on the tibial poly­ethylene insert which engages with a transverse cam located on the femoral component between the condyles (. Fig. 28.12). In the PS design, during deep exion, the cam and post engage, which in theory limits the degree of anterior femoral translation and leads to sub­sequent femoral rollback allowing increased knee ex­ion (Insall etal. 1982).
The rst iteration of the posterior stabilized design was introduced in 1978 by Insall and Burstein and con­sisted of an all-polyethylene tibial component. Since that time, the PS design has undergone a variety of changes to improve kinematics and durability (Insall and Clarke 1993).
> The posterior stabilized total knee arthroplasty is a
popular implant design with numerous studies dem-
onstrating excellent range of motion, survivorship,
and functional outcomes.
Range of Motion
z
It has been hypothesized that replacing the native poste­rior cruciate ligament with a cam and post can improve the range of motion through mechanical enforcement of femoral rollback (Pagnano etal. 1998; Bercik etal.
2013). Numerous studies have demonstrated the ability
to obtain excellent range of motion with a posterior sta­bilized knee. In a prospective cohort of over 240 knees, Hirsch et al. compared range of motion between posterior- stabilized, cruciate-retaining, and cruciate­sacricing knees and found that posterior stabilized
. Fig. 28.12 The posterior stabilized total knee implant utilizes a
central post (*) on the tibial polyethylene insert which engages with a transverse cam located on the femoral component between the condyles
knees obtained signicantly increased range of motion as compared to cruciate-retaining knees (112° vs. 104°) (Hirsch etal. 1994). This nding of improved range of motion compared to cruciate-retaining implants has been reproduced in numerous studies (Maruyama etal.
2004; Yoshiya etal. 2005; Catani etal. 2004) including a
recent meta-analysis by Bercik et al. which concluded that PS knees had on average an increase of 3.33° of range of motion as compared to CR knees (Bercik etal.
2013). In addition to improved overall range of motion,
numerous studies have found that posterior stabilized knees may provide increase exion as compared to cruciate- retaining knees. Similar to range of motion, the recent meta-analysis by Bercik etal. showed that patients were able to obtain signicantly more exion in poste­rior stabilized knees as compared to cruciate-retaining knees (Bercik etal. 2013).
Loosening and Survivorship
z
Although early on it was hypothesized that retaining the native posterior cruciate ligament could mitigate aseptic loosening by resisting shear forces at the bone–implant interface (Pagnano et al. 1998), early biomechanical testing of posterior stabilized knees demonstrated that articulation of the post-and-cam mechanism on a PS
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knee led to compressive rather than shear forces at the proximal tibia (Insall etal. 1982). These biomechanical ndings support today’s clinical results.
In a long-term prospective cohort study of 55 young patients (<60years at index surgery) undergoing a pos­terior stabilized knee arthroplasty, Meftah etal. experi­enced no cases of aseptic loosening at an average follow-up of 12.3 years (range 11–13) (Meftah et al.
2015). Additionally, the posterior stabilized implants
had excellent survivorship of 98% at nal follow-up (Meftah et al. 2015). Even at 15-year follow-up, Lachiewicz etal. experienced an aseptic loosening rate of <1% and survivorship of 96.8% for a cohort of patients who underwent a modular posterior stabilized knee arthroplasty.
> These results suggest that posterior stabilized knees
may not be at an increased risk for aseptic loosening
and have excellent survivorship.
Functional Outcomes
z
Patient-reported outcomes following posterior stabi­lized knee arthroplasty are similar to those of cruciate­retaining knee replacements as demonstrated by numerous randomized trials. In a recent randomized controlled trial comparing PS to CR knees, Scott etal. found no signicant difference in Knee Society pain, function, and motion scores at a minimum follow-up of 2 years in a cohort of 111 patients (Scott and Smith
2014). Similarly, Maruyama etal. found no signicant
difference in postoperative knee scores at an average follow-up of 31.7months in a prospective randomized comparison of patients undergoing posterior stabilized versus cruciate-retaining total knee arthroplasty (Maruyama etal. 2004). Additionally, a meta-analysis of randomized trials comparing posterior stabilized and cruciate-retaining implants failed to demonstrate a sig­nicant difference in functional outcomes and postop­erative Knee Society pain scores at 2- and 5-year average follow-up (Li etal. 2014).
Kinematics and Gait
z
As previously discussed, it is theorized that the cam­and- post mechanism on a posterior stabilized knee rec­reates native femoral rollback and allows for increased knee exion. Numerous studies have compared the kine­matics of cruciate-retaining and posterior stabilized implants. While initially it was thought that retaining the PCL would allow for predictable femoral rollback that mimicked native knee kinematics, this has failed to be proven. Dennis et al. demonstrated the concept of “paradoxical anterior femoral translation” where abnor­mal anterior femoral translation upon the tibia can occur in cruciate-retaining implants (Dennis etal. 1996).
This abnormal femoral motion can theoretically lead to increased tibial polyethylene wear and shear forces. Unlike CR implant designs, posterior stabilized total knee implants have been shown to restore physiological femoral rollback. Using in vivo uoroscopy, Fantozzi et al. have demonstrated that posterior stabilized implants successfully recreate physiological femoral roll­back during activities of daily living such as walking, going from sitting to standing posture, and during stair climbing (Fantozzi etal. 2006).
Take-Home Messages
5 Posterior stabilized total knee implants uti-
lize a cam-and-post mechanism to recreate native femoral rollback.
5 Posterior stabilized total knee implants
have demonstrated excellent 10- and 15-year survivorship with low rates of aseptic loos­ening.
5 Posterior stabilized implants may offer
slightly more increased exion as compared to cruciate- retaining implants.
5 Functional outcomes following posterior
stabilized knee replacement are comparable to cruciate- retaining implants.
5 Joint kinematics may be more closely
restored with a posterior stabilized implant as compared to a cruciate-retaining implant.
5 Keeping blood and fat out of the interface
between the implant and the cement is important for optimal implant xation.
References
Bercik MJ, Joshi A, Parvizi J (2013) Posterior cruciate-retaining ver-
sus posterior-stabilized total knee arthroplasty: a meta-analysis. J Arthroplasty 28:439–444
Catani F, Leardini A, Ensini A et al (2004) The stability of the
cemented tibial component of total knee arthroplasty. J Arthroplasty 19:775–782
Dennis DA, Komistek RD, Hoff WA, Gabriel SM (1996) In vivo
knee kinematics derived using an inverse perspective technique. Clin Orthop Relat Res 331:107–117
Fantozzi S, Catani F, Ensini A, Leardini A, Giannini S (2006)
Femoral rollback of cruciate-retaining and posterior-stabilized total knee replacements: in vivo uoroscopic analysis during activities of daily living. J Orthop Res 24:2222–2229
Hirsch HS, Lotke PA, Morrison LD (1994) The posterior cruciate
ligament in total knee surgery. Save, sacrice, or substitute? Clin Orthop Relat Res 309:64–68
Insall JN, Clarke HD (1993) Historic development, classication,
and characteristics of knee prostheses. In: Insall & Scott surgery of the knee, 6th edn, pp1375–1404.e6
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Insall J, Lachiewicz P, Burstein A (1982) The posterior stabilized
condylar prosthesis: a modication of the total condylar design.
Two to four-year clinical experience. J Bone Joint Surg Am
64:1317–1323 Li N, Tan Y, Deng Y, Chen L (2014) Posterior cruciate-retaining ver-
sus posterior stabilized total knee arthroplasty: a meta-analysis
of randomized controlled trials. Knee Surg Sports Traumatol
Arthrosc 22:556–564 Maruyama S, Yoshiya S, Matsui N, Kuroda R, Kurosaka M (2004)
Functional comparison of posterior cruciate-retaining versus
posterior stabilized total knee arthroplasty. J Arthroplasty
19:349–353 Meftah M, White PB, Ranawat AS, Ranawat CS (2015) Long-term
results of total knee arthroplasty in young and active patients
with posterior stabilized design. Knee 23:318–321
Pagnano MW, Cushner FD, Scott WN (1998) Role of the posterior
cruciate ligament in total knee arthroplasty. J Am Acad Orthop Surg 6:176–187
Scott D, Smith R (2014) A prospective, randomized comparison of
posterior stabilized versus cruciate-substituting total knee arthroplasty: a preliminary report with minimum 2-year results. J Arthroplasty 29:179–181
Yoshiya S, Matsui N, Komistek RD, Dennis DA, Mahfouz M,
Kurosaka M (2005) In vivo kinematic comparison of posterior cruciate- retaining and posterior stabilized total knee arthroplas­ties under passive and weight-bearing conditions. J Arthroplasty 20:777–783
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