The etiology of the flexion contracture is related to recurrent effusions present in a knee with end-stage degenerative joint disease secondary to the associated inflammatory process. These recurrent effusions cause increased pressure in the knee causing pain and discomfort. Patients will always seek a position of comfort, which is slight flexion. Flexion decreases the painful stimulus by reducing pressure in the knee and relaxing the posterior capsule. Unfortunately, this self-perpetuating process leads to a greater degree of contracture as the disease progresses. Furthermore, patients rarely maintain the knee in full extension. Even during the gait cycle the knee is slightly flexed. As their disease progresses, patients limit their ambulation and are more frequently in a seated position. Patients often report sleeping with a pillow under their knee or in the fetal position. All of these activities increase flexion contracture deformity. Patients with excessive deformity >40 degrees should be counseled regarding procedural complexity and that increasing constraint may be required. Patients are seen preoperatively by a physical therapist and given a pre-arthroplasty conditioning program. Patients with excessive flexion contracture are specifically instructed on stretching techniques, as well as quadriceps rehabilitation exercises.

The focus in the postoperative physiotherapy rehabilitation program continues toward the goal of full extension. Patients are instructed in appropriate stretching regimes. Patients are immobilised for the first 24 hours in full extension with plaster splints, such as with a modified Robert Jones dressing. This dressing is removed on postoperative day one. The patient is then placed in a knee immobiliser and instructed to wear it at bed rest, during ambulation and in the evening, only removing for ROM exercises. In cases of severe flexion deformity >30 degrees, patients are maintained in full extension for 3–4 weeks until ROM is begun. Patients are encouraged to use a knee immobiliser for at least the first 6 weeks postoperatively.

Treating patients with flexion contracture involves a combination of bone resection and soft tissue balance. One must make every effort to preserve both the femoral and tibial joint line. In flexion contracture the common error is to begin by resecting additional distal femur, which may result in joint line elevation and mid-flexion instability. The distal femoral resection should remove that amount of bone being replaced with metal. Attention should be directed at careful and meticulous balance of the soft tissues and release of the contracted posterior capsule with re-establishment of the posterior recess, which will correct the majority of flexion contractures.

Inability to achieve ROM after TKA represents a frustrating complication for both patient and surgeon. Non-operative treatments for the stiff TKA include shoe lift in contralateral limb, stationery bicycle with elevated seat position, extension bracing, topical application of hand-held instruments to areas of soft tissue-dysfunction by a trained physical therapist over several outpatient sessions, and use of a low load stretch device. Manipulation under anesthesia is indicated in patients after TKA having less than 90 degrees ROM after 6 weeks, with no progression or regression in ROM. Other operative treatments range from a downsizing exchange of the polyethylene bearing to revision with a constrained device and low-dose irradiation in cases of severe arthrofibrosis.

The battle of revision TKA is won or lost with safe, effective, and minimally bony-destructive implant removal, protecting all ligamentous stabilisers of the knee and, most importantly, the extensor mechanism. For exposure, incisions should be long and generous to allow adequate access. A standard medial parapatellar capsular arthrotomy is preferred. A synovectomy is performed followed by debridement of all scar tissue, especially in the medial and lateral gutters. All peripatellar scar tissue is excised followed by release of scar tissue within the patellar tendon, allowing for displacement or everting of the patella. As patellar tendon avulsion at any time of knee surgery yields disastrous results, the surgeon should be continuously evaluating the patellar tendon integrity, especially while displacing/everting the patella and bringing the knee into flexion. If displacement/eversion is difficult, consider rectis-snip, V-Y quadricepsplasty, or tibial tubercle osteotomy. The long-held requisite for patellar eversion prior to component removal is inaccurate. In most cases simple lateral patellar subluxation will provide adequate exposure.

If a modular tibial system is involved, removal of the tibial polyethylene will decompress the knee, allowing for easier access to patellar, femoral, and tibial components. For patellar component removal, first identify the border of the patella, then carefully clean and debride the interface, preferably with electrocautery. If the tibial component is cemented all-polyethylene, remove using an oscillating saw at the prosthetic-bone interface. Debride the remaining cement with hand tools, ultrasonic tools, or burrs. Remove the remaining peg using a low-speed burr. If the tibial component is metal-backed, then utilise a thin saw blade or reciprocating saw to negotiate the undersurface of the component between the pegs. If pegs are peripherally located, cut with a diamond disc circular cutting tool. Use a trephine to remove the pegs.

For femoral component removal, identify the prosthetic-bone/prosthetic-cement interface then remove soft tissue from the interface, preferably with electrocautery. Disrupt the interface around all aspects of the component, using any of following: Gigli saw for cementless components only, micro saw, standard oscillating saw, reciprocating saw, a series of thin osteotomes, or ultrasonic equipment. If the femoral component is stemmed, remove the component in two segments using an appropriate screwdriver to remove the screw locking the stem to the component. Remove the femoral component with a retrodriver or femoral component extractor. Debride cement with hand tools or burr, using care to avoid bone fracture. If a stem is present, then remove with the appropriate extraction device. If “mismatch” exists, where femoral (or likewise, tibial) boss is smaller in diameter than the stem, creating a cement block prohibiting stem removal, remove the cement with hand tools or burr. If the stem is cemented, use hand tools, ultrasonic tools, or a burr to debride the cement. Curette and clean the canals.

For tibial component removal, disrupt the prosthetic-cement/prosthetic-bone interface using an oscillating or reciprocating saw. Gently remove the tibial component with a retrodriver or tibial extractor. If stem extensions are utilised, disengage and debride all proximal cement prior to removing the stem. If stem is present, then remove stem with appropriate extraction device. If stem is grit-blasted and well-fixed, create 8mm burr holes 1.5 to 2.5cm distal to tibial tray on medial aspect and a small divot using burr, then drive implant proximally with Anspach punch. Alternatively, a tibial tubercle osteotomy may be performed. If the stem is cemented, use hand tools, ultrasonic tools or burr to debride cement.

According to Webster's Dictionary, efficiency is defined as the capacity to produce desired results with a minimal expenditure of energy, money, time, and materials. For a surgeon performing an operative procedure this would mean “skillfulness in avoiding wasted time and effort.” (www.webster-dictionary.org) The essential ingredient to becoming efficient is to promote a culture of efficiency. There are 10 elements: 1) proactive surgeon perspective; 2) effective utilization of preoperative holding area; 3) preoperative planning / templating; 4) development of preference cards; 5) operating room set-up protocols; 6) operating room team concept; 7) streamlined instrument sets; 8) consistent operative workflow; 9) standardised closure / dressings; and 10) prompt and meticulous room turnover. Efficient performance of an operative procedure requires skillfulness in avoiding wasted time and effort. Perioperative efficiencies are optimised by development of “swing,” “flip,” or “double occupancy” criteria, understanding of timing of when to initiate the anesthetic block for the next case, skin closure routine by physician assistant/nurse practitioner/private scrub, and marking the operative site of your first two patients upon arrival to the hospital or surgery center. Utilise a pro-active approach to prepare case carts the day before surgery. The operating room team turns over their own rooms, with a “clean as you go” mentality. Develop a formalised communication process for patient flow issues, such as real-time push-to-talk group calling phones. Determine in advance the number of instrument sets required for the day's caseload to mitigate flash sterilization and decrease room turnover time. The goal of the surgeon is to be out of the operating room for 5 minutes in between cases before the next incision, utilizing that time to enter orders, communicate with the family, dictate, and mark the operative site of the patient who will follow the one in the case about to start. Implant selection can help if consistent. Everyone must know the instrument trays including surgeon, scrubs, and nurses. Minimise both the number of trays and the redundancy of instrumentation. Templating should be done in advance of the day of surgery. Keep your surgery consistent and always deliver your best product. The workflow for inpatient and outpatient surgeries should be the same: same implant, same approach, and same closure.

The culture of efficiency requires buy-in by all involved in the operative procedure. Every one entering the operating theatre should have proper body coverage – no hair visible, no nose visible. There should be a strict limit to needless activity: minimum opening of doors, no changing of personnel during an operation, and use of intercom/telephone to request equipment. As the surgeon and the team begin to embrace efficiency, surgical times will decrease. Multiple studies have demonstrated that increased surgical time is associated with a higher incidence of infection. This is secondary to time-dependent contamination of the surgical wound and field.

The take home message is to develop and embrace efficiency. Operating room efficiency is the product of multiple factors including preoperative preparation, skilled anesthesia team, motivated operating room staff, choreographed surgery, and well-designed instrumentation. The surgeon is the captain of the ship and the staff follows his or her lead. Your operating room days will flow smoothly. Your operations will proceed with minimal stress. You will spend less time drinking coffee between cases and have more free time at the end of the day. However, most importantly, you will deliver a quality product to your patient.

Total hip arthroplasty (THA) continues moving to the outpatient arena, and may be feasible for some conversion and revision scenarios. Controversy surrounds appropriate patient selection. The purpose of this study is to report complications associated with outpatient revision and conversion THA, and to determine if comorbidities are associated with complications or overnight stay.

From June 2013 through March 2018, 43 patients (44 hips) underwent conversion (n=12) or revision (n=32) THA at a free-standing ambulatory surgery center. Mean patient age was 58.4 years, and 52% of patients were male. Conversion procedures were for failed resurfacing in two, failed hemiarthroplasty in one, and failed fracture fixation with retained hardware in 9. Revision procedures involved head only in one, head and liner in 20, cup and head in 7, stem only in 2, and stem and liner in 2.

Forty-four (93%) were discharged same day without incident, none required transfer to acute facility, and 3 required overnight stay with 2 of these for convenience and only one for a medical reason, urinary retention. Three patients with early superficial infection were successfully treated with oral antibiotics. There were no major complications, readmissions, or subsequent surgeries within 90 days. One or more major comorbidities were present in 17 patients (39%) including 1 valvular disease, 8 arrhythmia, 2 thromboembolism history, 3 obstructive sleep apnea, 6 chronic obstructive pulmonary disease, 2 asthma, 4 frequent urination, and 1 renal disease. The single patient who stayed overnight for a medical reason had no major medical comorbidities.

Outpatient arthroplasty, including revision THA in some scenarios, is safe for many patients. Presence of medical comorbidities was not associated with risk of complications. The paradigm change of patient education, medical optimization, and a multimodal program to mitigate risk of blood loss and reduce need for narcotics facilitates performing arthroplasty safely in an outpatient setting.

The etiology of the flexion contracture is related to recurrent effusions present in a knee with end-stage degenerative joint disease secondary to the associated inflammatory process. These recurrent effusions cause increased pressure in the knee causing pain and discomfort. Patients will always seek a position of comfort, which is slight flexion. Flexion decreases the painful stimulus by reducing pressure in the knee and relaxing the posterior capsule. Unfortunately, this self-perpetuating process leads to a greater degree of contracture as the disease progresses. Furthermore, patients rarely maintain the knee in full extension. Even during the gait cycle the knee is slightly flexed. As their disease progresses, patients limit their ambulation and are more frequently in a seated position. Patients often report sleeping with a pillow under their knee or in the fetal position. All of these activities increase flexion contracture deformity. Patients with excessive deformity >40 degrees should be counseled regarding procedural complexity and that increasing constraint may be required. Patients are seen pre-operatively by a physical therapist and given a pre-arthroplasty conditioning program. Patients with excessive flexion contracture are specifically instructed on stretching techniques, as well as quadriceps rehabilitation exercises.

Avoiding Pitfalls and Complications: Treating patients with flexion contracture involves a combination of bone resection and soft tissue balance. One must make every effort to preserve both the femoral and tibial joint line. In flexion contracture the common error is to begin by resecting additional distal femur, which may result in joint line elevation and mid-flexion instability. The distal femoral resection should remove that amount of bone being replaced with metal. Attention should be directed at careful and meticulous balance of the soft tissues and release of the contracted posterior capsule with re-establishment of the posterior recess, which will correct the majority of flexion contractures.

Residual Flexion Contracture: Inability to achieve ROM after TKA represents a frustrating complication for both patient and surgeon. Non-operative treatments for the stiff TKA include shoe lift in contralateral limb, stationery bicycle with elevated seat position, extension bracing, topical application of hand-held instruments to areas of soft tissue-dysfunction by a trained physical therapist over several outpatient sessions, and use of a low load stretch device. Manipulation under anesthesia is indicated in patients after TKA having less than 90 degrees ROM after 6 weeks, with no progression or regression in ROM. Other operative treatments range from a downsizing exchange of the polyethylene bearing to revision with a constrained device and low-dose irradiation in cases of severe arthrofibrosis.

Introduction

Persistent pain after medial unicompartmental knee arthroplasty (UKA) is a prevailing reason for revision to total knee arthroplasty (TKA). Many of these pathologies can be addressed arthroscopically. The purpose of this study is to examine the outcomes of patients who undergo an arthroscopy for any reason after medial UKA.

The use of short femoral components in primary total hip arthroplasty (THA) represents an attractive option. Advocates tout bone preservation and ease of use in less invasive surgical approaches. In 2006 we adopted the concept and have had experience with over 5,700 short, tapered, titanium, porous plasma-sprayed stems in patients undergoing primary THA. The plasma-sprayed portion of this stem is similar to the longer, standard length TaperLoc stem, with shortening resulting from a 3 cm reduction in length of the distal portion of the implant. However, the proximal aspect maintains the same flat, tapered wedge proximal geometry as the standard stem. During insertion in some femurs it was noted that distal canal fill occurred preferentially to proximal canal fill. This required distal broaching in order to accommodate a larger stem. In an effort to avoid this clinical situation and to improve the gradual off-loading that is the goal of a tapered geometry, the design was modified in 2011 to reduce the profile of the component. Other modifications include a lower caput-collum-diaphyseal (CCD) angle to enhance horizontal offset restoration without increasing leg length, width sizing from 5–18 mm in 1 mm increments, and polished neck flats to increase range of motion. Undoubtedly, porous plasma sprayed tapered titanium stems are successful in primary THA. Short stems can better accommodate proximal-distal femoral mismatch, particularly in hips with a large metaphysis and a narrow diaphysis, hips with an excessively bowed femur, and hips with severe deformity such as that encountered with developmental dysplasia and post-traumatic arthritis. Short stems violate less femoral bone stock, allowing for more favorable conditions should revision surgery become necessary. The concept of a short stem is appealing to patients, who perceive it as less invasive. In addition, short stems facilitate shorter incision surgery and operative approaches such as the muscle-sparing anterior supine intermuscular. Increased canal fill has been associated with distal cortical hypertrophy. Reducing the distal portion of the stem has reduced the incidence of distal canal fill, and allows for placement of a slightly larger implant.

Converting UKA to TKA can be difficult, and specialised techniques are needed. Issues include bone loss, joint line approximation, sizing, and rotation. Determining the complexity of conversion pre-operatively helps predict the need for augmentation, grafting, stems, or constraint.

In a 2009 study from our center, 50 UKA revised to TKA (1997–2007) were reviewed: 9 implants (18%) were modular fixed-bearing, 4 (8%) were metal-backed nonmodular fixed-bearing, 8 (16%) were resurfacing onlay, 10 (20%) were all-polyethylene step-cut, and 19 (38%) were mobile bearing designs; 5 knees (10%) failed due to infection, 5 (10%) due to wear and/or instability, 10 (20%) for pain or progression of arthritis, 8 (16%) for tibial fracture or severe subsidence, and 22 (44%) due to loosening of either one or both components. Insert thickness was no different between implants (P=0.23) or failure modes (P=0.27). Stemmed component use was most frequent with nonmodular components (50%), all-polyethylene step-cut implants (44%), and modular fixed-bearing implants (33%; P=0.40). Stem use was highest in tibial fracture (86%; P=0.002). Augment use was highest among all-polyethylene step-cut implants (all-polyethylene, 56%; metal-backed, 50%; modular fixed-bearing, 33%; P=0.01). Augmentation use was highest in fracture (86%) and infection (67%), with a significant difference noted between failure modes (P=0.003). Failure of nonmodular all-polyethylene step-cut devices was more complex than resurfacing or mobile bearing. Failure mode was predictive of complexity. Reestablishing the joint line, ligamentous balance, and durable fixation are critical to assuring a primary outcome.

In a 2013 multicenter study of 3 institutions including ours, a total of 175 revisions of medial UKA in 168 patients (81 males, 87 females; average age of 66 years) performed from 1995 to 2009 with a minimum of 2-year clinical follow-up were reviewed. The average time from UKA to revision TKA was 71.5 months (range: 2 months to 262 months). The four most common reasons for failure of the UKA were femoral or tibial loosening (55%), progressive arthritis of the lateral or patellofemoral joints (34%), polyethylene failure (4%) and infection (3%). Mean follow-up after revision was 75 months. Nine of 175 knees (4.5%) were subsequently revised at an average of 48 months (range 6 months to 123 months.) The rate of revision was 1.23 revisions per 100 observed component years. The average Knee Society pain and function score increased to 75 and 66, respectively. In the present series, the re-revision rate after revision TKA from UKA was 4.5 % at an average of 75 months or 1.2 revisions per 100 observed component years.

In a current study from our center, 174 patients (180 UKA) underwent revision procedures (1996–2017). Most prevalent indications for revision were aseptic loosening (45%) arthritic progression (17%) and tibial collapse (13%). At 4 years mean follow-up, 5 knees (2.8%) have required re-revision involving any part, which is similar to what we recently reported at 5.5 years in a group of patients who underwent primary TKA (6 of 189; 3.2%), and much lower than what we observed at 6.0 years in a recent report of patients who underwent aseptic revision TKA (35 of 278; 12.6%).

Compared to published individual institution and national registry data, re-revision of a failed UKA is equivalent to revision rates of primary TKA and substantially better than re-revision rates of revision TKA. These data should be used to counsel patients undergoing revision UKA to TKA.

Bi-cruciate-retaining (BCR) total knee arthroplasty (TKA), which retains both the anterior (ACL) and posterior cruciate (PCL) ligaments, serves as an alternative to the traditional TKA procedure. Despite the difficulty of ensuring the structural integrity of the prosthesis, the BCR TKA can yield improved patient outcomes such as range of motion, kinematics, and even the survivorship of the implant. When possible, BCR TKA can and should be considered as a viable option to treat end-stage arthritis of the knee. Reconsidering the frequency of the BCR TKA is necessary for several reasons. Patient outcomes following BCR TKA are similar to outcomes for mobile-bearing UKA. Patients with an intact ACL do better with preservation (UKA or BCR TKA) of the ACL. The corollary is also true that removing an intact ACL at the time of arthroplasty has worse outcomes than traditional TKA in patients with an absent ACL. Reported outcomes of BCR TKA include more normal knee function, excellent prosthetic survivorship, and greater patient satisfaction. The BCR TKA may provide a missing link in the continuum of constraint for primary knee arthroplasty.

Many early BCR designs fell out of favor because of high rates of prosthetic loosening, and because the procedure was more technically demanding than that of highly successful ACL-sacrificing TKA devices. Recently there has been a reemergence of the BCR arthroplasty concept with improvements in design. By retaining both the ACL and PCL, BCR TKA patients show more normal knee function and flexibility due to anterior stability and replication of the physiological tension in the ACL. Modern BCR TKA models have improved upon early designs but are limited in use mainly due to the lack of an optimal prosthesis design and the relative difficulty of the surgical procedure.

Bi-cruciate-retaining TKA is a viable procedure if an appropriate femorotibial gap can be created to mimic physiological tension of the ACL and PCL. In terms of the surgical technique, the procedure begins with femoral preparation to facilitate tibial preparation. Distal femoral resection is performed first taking care to avoid damage to the ACL. Femoral preparation is then completed with a four-in-one guide that incorporates a protector to ensure the ACL is not resected. Good exposure is essential to tibial preparation, which is the critical part of the procedure and involves several steps of setting the depth of resection, and making accurate cuts to protect the tibial eminence island of bone and set tibial component rotation. The medial and lateral tibial cuts must be absolutely parallel. Precise cement technique is required for the tibial baseplate, and care must be taken when trialing the dual bearings.

Normal kinematics are preserved when both the ACL and PCL remain intact. Bi-cruciate-retaining TKA knees have been shown to restore more normal kinematics and have better “feel” than traditional ACL-sacrificing TKA knees. Bilateral TKA patients with designs of both types prefer their BCR TKA to their ACL-sacrificing TKA more often than not. An intact ACL has been shown to be present in 60–80% of arthritic knees, further justifying the consideration to retain both cruciate ligaments during TKA. New materials and refined instrumentation and techniques have helped improve the viability of BCR TKA, which may represent an additional option in the continuum of constraint for knee arthroplasty.

Not all knee surgery cases are created equal is a maxim that holds true for both primary and revision scenarios. Complex cases involve patients presenting with compromised bone and/or soft tissue. For primary knees, these include cases with bony deformity or deficiency, severe malalignment, arthrofibrosis, ligamentous instability or contracture, prior fracture or trauma with or without failed fixation, prior hardware complicating component placement, or compromised extensor mechanism. In revision surgery, complex scenarios include cases compromised by bone loss, deterioration of the soft tissues and resulting instability, periprosthetic fracture, leg length discrepancy, infection, and more recently, hypersensitivity reactions. In this interactive session, a moderator and team of experts will discuss strategies for evaluation and management of a variety of challenging knee case scenarios.

The number one reason to consider large heads in total hip arthroplasty (THA) is for increased stability. Large diameter femoral heads substantially increase stability by virtue of increased range of motion and increased jump distance, which is the amount of displacement required to sublux the head out of the socket. Prevention is the best means for reducing dislocation, with requisites for stability being appropriate component position, restoration of leg length, and restoration of offset.

In a review from our center studying the frequency of dislocation with small diameter femoral heads (≤32 mm) in 1262 patients (1518 hips) who underwent primary THA performed via a direct lateral approach, we observed a dislocation rate of 0.8% (12 of 1518). In a subsequent study of 1748 patients (2020 hips) who underwent primary THA at our center with large diameter heads (mean 43 mm, range 36–60 mm), we observed a substantially lower 0.04% frequency of dislocation (one of 2010) at a mean followup of 2.6 years.

Our findings have been echoed in studies from several other centers. Howie et al. reported a prospective controlled trial of 644 low risk patients undergoing primary or revision THA randomised to receive either a 36 mm or 28 mm metal head articulated on highly crosslinked polyethylene. They observed significantly lower frequency of frequency of dislocation with 36 mm heads both overall (1.3%, 4 of 299 versus 5.4%, 17 of 216 with 28 mm heads, p=0.012) and in primary use (0.8%, 2 of 258 versus 4.4%, 12 of 275 with 28 mm heads, p=0.024), and a similar trend in their smaller groups of revision patients (5%, 2 of 41, versus 12%, 5 of 41 with 28 mm heads, p=0.273).

Lachiewicz and Soileau reported on early and late dislocation with 36- and 40 mm heads in 112 patients (122 hips) at presumed high risk for dislocation who underwent primary THA. Risk factors were age >75 for 80 hips, proximal femur fracture for 18, history of contralateral dislocation for 2, history of alcohol abuse in 2, large acetabulum (>60 mm) in 6, and other reasons in 14. Early dislocation (<1 year) occurred in 4% (5 of 122), all with 36 mm heads. Late dislocation (>5 years) did not occur in any of the 74 patients with followup beyond 5 years.

Stroh et al. compared 225 patients (248 hips) treated with THA using small diameter heads (<36 mm) to 501 patients (559 hips) treated with THA using large diameter heads (≥36 mm). There were no dislocations with large diameter heads compared with 1.8% (10 of 559) with small diameter heads.

Allen et al. studied whether or not large femoral heads improve functional outcome after primary THA via the posterior approach in 726 patients. There were 399 done with small heads (<36 mm), 254 with medium heads (36 mm), and 73 with large heads (>36 mm), analyzed pre-operatively, at 6 months, and at 12 months. The authors could not find a correlation between increasing head size and improved function at one year, but observed that dislocation was reduced with large diameter heads.

Optimization of hip biomechanics via proper surgical technique, component position, and restoration of leg length and offset are mandatory in total hip arthroplasty. Large heads enhance stability by increasing range of motion prior to impingement and enhancing jump stability.

Total hip arthroplasty (THA) performed in patients aged 60 years and younger requires several decades of implant use under increased activity demands. Implant longevity and stable fixation are necessary for 30 or more years. The search for the optimal bearing combination for use in younger, high demand patients presents a challenge for orthopaedic surgeons as they consider the pros and cons of each material and interaction. A recent U.S. study of implant utilization trends that included 174 hospitals and 105,000 THA between 2001 and 2012 found that in 2012 93% of THA were cementless and 35% of THA bearings were ceramic-on-highly crosslinked polyethylene (HXLPE). Another recent article used the Nationwide Inpatient Sample from 2009 to 2012 to study bearing usage trends in 9265 primary THA in patients 30 years old or younger. The researchers observed ceramic-on-polyethylene as the most commonly bearing surface, used in 36% of patients, and which represented an increase from an earlier study of extremely young patients undergoing primary THA between 2006 to 2009, use of so-called hard-on-hard bearings decreased. Benefits of ceramic-on-HXLPE bearings are that unlike metal-on-polyethylene and metal-on-metal combinations, taperosis and adverse reactions to metal debris are non-existent. Ceramic-on-polyethylene is forgiving, it is an extremely low wear couple, it is the current presenter's bearing of choice in high demand patients, and it is a good option in the scenario of revision of failed metal-on-metal or for taperosis. Advantages to bulk ceramics are: extremely hard and scratch resistant to third body wear, not damaged by instruments and repositioning, excellent wettability, extreme low wear against itself with no known pathogenic reaction to ceramic particles, inherently stable with no oxidation or aging effect, no corrosion, safe in terms of metal ion release, no known risk of hypersensitivity or allergy, and no concerns about biological reaction. Biolox® (Ceramtec AG; Plochingen, Germany) ceramics have been available since 1974, with fourth generation Biolox® Delta introduced in 2003. Extensive clinical experience includes over 1630 published studies with over 12 million Biolox® components implanted with almost every available hip system. Two recent meta-analyses studies of randomised controlled trials comparing ceramic-on-ceramic to ceramic-on-polyethylene found significantly higher linear wear in ceramic-on-polyethylene but higher incidences of noise and fracture in ceramic-on-ceramic THA. There were no differences in revision, function, dislocation, osteolysis or loosening. A recent meta-analysis review of randomised controlled trials reporting survivorship of ceramic-on-ceramic, ceramic-on-HXLPE, and metal-on-HXLPE found no difference among bearing surfaces in risk of revision after primary THA in patients younger than 65. Risk ratio for revision was 0.65 (p=0.50) between ceramic-on-ceramic and ceramic-on-HXLPE, and 0.40 (p=0.34) between ceramic-on-ceramic and metal-on-HXLPE. A recent study of ceramic-on-HXLPE bearings for 130 cementless THA in 119 patients younger than 50 years at mean follow-up of 8.3 years (range, 7–9) reported a mean post-operative Harris hip score of 94, UCLA activity score of 8.1, no acetabular revisions, no osteolysis, no head or liner fracture, and 0.022 ± 0.003 mean annual penetration rate of the femoral head. While longer follow-up is necessary, ceramic-on-HXLPE bearings are an attractive option in younger, high demand patients undergoing primary THA.

The number one reason to consider large heads in total hip arthroplasty (THA) is for increased stability. Large diameter femoral heads substantially increase stability by virtue of increased range of motion and increased jump distance, which is the amount of displacement required to sublux the head out of the socket. Prevention is the best means for reducing dislocation, with requisites for stability being appropriate component position, restoration of leg length, and restoration of offset.

In a review from our center studying the frequency of dislocation with small diameter femoral heads (≤32 mm) in 1262 patients (1518 hips) who underwent primary THA performed via a direct lateral approach, we observed a dislocation rate of 0.8% (12 of 1518). In a subsequent study of 1748 patients (2020 hips) who underwent primary THA at our center with large diameter heads (mean 43 mm, range 36–60 mm), we observed a substantially lower 0.04% frequency of dislocation (one of 2010) at a mean followup of 2.6 years.

Our findings have been echoed in studies from several other centers. Howie et al. reported a prospective controlled trial of 644 low risk patients undergoing primary or revision THA randomised to receive either a 36 mm or 28 mm metal head articulated on highly crosslinked polyethylene. They observed significantly lower frequency of frequency of dislocation with 36 mm heads both overall (1.3%, 4 of 299 versus 5.4%, 17 of 216 with 28 mm heads, p=0.012) and in primary use (0.8%, 2 of 258 versus 4.4%, 12 of 275 with 28 mm heads, p=0.024), and a similar trend in their smaller groups of revision patients (5%, 2 of 41 versus 12%, 5 of 41 with 28 mm heads, p=0.273).

Lachiewicz and Soileau reported on early and late dislocation with 36- and 40 mm heads in 112 patients (122 hips) at presumed high risk for dislocation who underwent primary THA. Risk factors were age >75 for 80 hips, proximal femur fracture for 18, history of contralateral dislocation for 2, history of alcohol abuse in 2, large acetabulum (>60 mm) in 6, and other reasons in 14. Early dislocation (<1 year) occurred in 4% (5 of 122), all with 36 mm heads. Late dislocation (>5 years) did not occur in any of the 74 patients with follow up beyond 5 years.

Stroh et al. compared 225 patients (248 hips) treated with THA using small diameter heads (<36 mm) to 501 patients (559 hips) treated with THA using large diameter heads (≥36 mm). There were no dislocations with large diameter heads compared with 1.8% (10 of 559) with small diameter heads.

Allen et al. studied whether or not large femoral heads improve functional outcome after primary THA via the posterior approach in 726 patients. There were 399 done with small heads (<36 mm), 254 with medium heads (36 mm), and 73 with large heads (>36 mm), analyzed preoperatively, at 6 months, and at 12 months. The authors could not find a correlation between increasing head size and improved function at one year, but observed that dislocation was reduced with large diameter heads.

Optimization of hip biomechanics via proper surgical technique, component position, and restoration of leg length and offset are mandatory in total hip arthroplasty. Large heads enhance stability by increasing range of motion prior to impingement and enhancing jump stability.

Patient specific instruments have been developed in response to the conundrum of limited accuracy of intramedullary and extramedullary alignment guides and chaos caused by computer assisted orthopaedic surgery. This technology facilitates preoperative planning by providing the surgeon with a three dimensional (3-D) anatomical reconstruction of the knee, thereby improving the surgeon's understanding of the preoperative pathology. Intramedullary canal penetration of the femur and tibia is unnecessary, and consequently, any potential for fat emboli is eliminated. Component position and alignment are improved with a decrease in the number of outliers. Patient specific instruments utilise detailed magnetic resonance imaging (MRI) or computed tomography (CT) scans of the patient's knee with additional images from the hip and ankle for determination of critical landmarks. From these studies a 3-D model of the patient's knee is created and with integration of rapid prototyping technology, guides are created to apply to the patient's native anatomy to direct the placement of the cutting jigs and ultimately the placement of the components.

The steps in considering utilization of patient specific guides are as follows: 1) the surgeon determines that the patient is a candidate for TKA, 2) an MRI or CT scan is obtained at an approved facility in accordance with a specific protocol, 3) the MRI or CT is forwarded to the manufacturer, 4) the manufacturer creates the 3-D reconstructions, anatomical landmarks are identified, implant size is determined, and ultimately femoral and tibial component implant placement is determined via an algorithm, 4) the surgical plan is executed, 5) the physician reviews and modifies or approves the plan, 6) the guides are then produced via rapid prototyping technology and delivered to the hospital for the surgical procedure.

Guides generated from MRIs are designed to uniquely register on cartilage surface whereas guides produced from CT scans must register on bony anatomy. There are currently two types of guides produced: those which register on the femur and tibia and allow for the placement of pins to accommodate the standard resection blocks; and those produced by some manufacturers which accommodate the saw blade and therefore are a combination of resection and pin guides.

The utilization of patient-specific positioning guides in TKA has several benefits. They facilitate preoperative planning, obviate the need for violation of the intramedullary canals, reduce operating times and improve OR efficiency, decrease instrumentation requirements and thereby reduce potential for perioperative contamination. They are easier to use than computer navigation with no capital equipment purchase and no significant learning curve. Most importantly, patient-specific guides facilitate accurate component position and alignment, which ultimately has been shown to enhance long-term survivorship in total knee arthroplasty.

The surgical approach that is adequate for a primary total hip replacement may need to be modified to achieve a more extensile exposure as required for the revision procedure. A straightforward revision total hip replacement procedure can become quite complex when implant removal is attempted without adequate skill, instrumentation, or exposure. The most commonly used approaches in total hip replacement revision surgery are the transtrochanteric, posterolateral, and anterolateral. Although the effects of these approaches on the long-term clinical survival of the prosthetic composite are not completely clear, surgical approach does affect dislocation rates, trochanteric nonunion rates, and other indicators of clinical success.

Transtrochanteric Approach - Three variations of the transtrochanteric approach exist: A) The classic Charnley trochanteric approach was popularised by virtue of its use in primary total hip arthroplasty (THA) and, therefore, was easily applied to revision THA. This approach allows excellent visualization of the lateral shaft of the femur, thus enhancing implant and cement removal. However, the classic Charnley approach is associated with a high incidence of trochanteric nonunion. Reattachment of the atrophied trochanteric fragment often requires adjunct fixation such as cables, hooks, or bolts. These devices can subsequently break, migrate, or generate particulate debris which, in turn, is capable of producing extensive granuloma. B) The trochanteric slide is accomplished by an anteromedial inclination of the osteotomy, thus providing a more stable interface for reattachment. The trochanteric slide offers the advantage of maintaining muscle continuity. The disadvantage of this technique is decreased visualization of the acetabulum. Adjunct fixation of the trochanter is also required with this approach. C) By creating a 6 cm to 12 cm distal extension to the trochanteric fragment, a large lateral window is developed which enhances both prosthesis and cement removal. Subsequently, trochanteric fixation is enhanced because the extended fragment increases the surface area available for fixation. Because the extended trochanteric osteotomy requires a larger bone resection, proximal femoral bone stock can be compromised. As a result, proximal prosthetic support with a tapered device can force the trochanteric fragment laterally, increasing the likelihood of nonunion. When an extended trochanteric osteotomy is used, the patient's postoperative physical therapy and rehabilitation course should be modified to protect the healing trochanteric fragment.

Posterolateral Surgical Approach is used commonly in revision THA. The technique is popular because it is used widely for endoprosthetic replacement in the treatment of subcapital fractures. Also, the posterolateral approach is quite popular for primary THA. This approach has the advantage of maintaining the integrity of the abductor mechanism. Although femoral exposure is adequate, acetabular exposure can be limited. Also, this approach is associated with an increased incidence of dislocation. Another concern is its close proximity to the sciatic nerve, thus predisposing the patient to the risk of nerve injury.

Anterolateral Surgical Approach has the advantage of improved visualization of the acetabulum and femur without the attending trochanteric complications and proximity to the sciatic nerve. This approach is associated with a low incidence of dislocation. However, the abductor muscle is divided or split and, therefore, abductor dysfunction can occur post-operatively. There also can be an increased incidence of heterotopic ossification, but it avoids the problem of trochanteric nonunion.

Not all total hip arthroplasty cases are created equal is a maxim that holds true for both primary and revision scenarios. Complex cases involve patients presenting with compromised bone and/or soft tissue. For primary cases, these include hips with dysplasia, ankylosis, deformed proximal femora, protrusio acetabuli, prior hip fracture with or without failed fixation, previous bony procedures, or neuromuscular conditions. In revision surgery, complex scenarios include cases compromised by bone loss, deterioration of the soft tissues and resulting in dislocation and instability, peri-prosthetic fracture, leg length discrepancy, infection, and more recently, hypersensitivity reactions. Meticulous surgical technique including component placement is essential. In this interactive session, a moderator and team of experts will discuss strategies for evaluation and management of a variety of challenging hip case scenarios.

When dealing with the patella in total knee arthroplasty (TKA) there are three philosophies. Some advocate resurfacing in all cases, others do not resurface, and a third group selectively resurfaces the patella. The literature does not offer one clear and consistent message on the topic. Treatment of the patella and the ultimate result is multifactorial. Factors include the patient, surgical technique, and implant design. With respect to the patient, inflammatory versus non-inflammatory arthritis, pre-operative presence or absence of anterior knee pain, age, sex, height, weight, and BMI affect results of TKA. Surgical technique steps to enhance the patellofemoral articulation include: 1) Restore the mechanical axis to facilitate patellofemoral tracking. 2) Select the appropriate femoral component size with respect to the AP dimension of the femur. 3) When performing anterior chamfer resection, measure the amount of bone removed in the center of the resection and compare to the prosthesis. Do not overstuff the patellofemoral articulation by taking an inadequate amount of bone. 4) Rotationally align the femur appropriately using a combination of the AP axis, the transepicondylar axis, the posterior condylar axis, and the tibial shaft axis. 5) If faced with whether to medialise or lateralise the femoral component, always lateralise. This will enhance patellofemoral tracking. 6) When resurfacing the patella, only evert the patella after all other bony resections have been performed. Remove peripheral osteophytes and measure the thickness of the patella prior to resection. Make every effort to leave at least 15 mm of bone and never leave less than 13 mm. 7) Resect the patella. The presenter prefers a freehand technique using the insertions of the patellar tendon and quadriceps tendon as a guide, sawing from inferior to superior, then from medial to lateral to ensure a smooth, flat, symmetrical resection. Medialise the patellar component and measure the thickness of reconstruction. 8) When not resurfacing the patella, surgeons generally remove all the peripheral osteophytes, and some perform denervation using electrocautery around the perimeter. 9) Determine appropriate patellofemoral tracking only after the tourniquet is released. 10) Close the knee in flexion so as not to tether the soft tissues about the patella and the extensor. With or without patellar resurfacing, implant design plays in important role in minimizing patellofemoral complications. Newer designs feature a so-called “swept back” femur in which the chamfer resection is deepened, and patellofemoral overstuffing is minimised. Lateralizing the trochlear groove on the anterior flange, orienting it in valgus alignment, and gradually transitioning to midline have improved patellofemoral tracking. Extending the trochlear groove as far as possible into the tibiofemoral articulation has decreased patellofemoral crepitation and patellar clunk in posterior stabilised designs. With respect to the tibial component, providing patellar relief anteriorly in the tibial polyethylene has facilitated range of motion and reduced patellar impingement in deep flexion. On the patella side, the all-polyethylene patella remains the gold standard. While data exist to support all three viewpoints in the treatment of the patella in TKA, it is the presenter's opinion that the overwhelming data support patella resurfacing at the time of primary TKA. It is clear from the literature that the status of the patellofemoral articulation following TKA is multifactorial. Surgical technique and implant design are key to a well-functioning patellofemoral articulation. Pain is the primary reason patients seek to undergo TKA. Since our primary goal is to relieve pain, and there has been a higher incidence of anterior knee pain reported without patellar resurfacing, why not resurface the patella?

Converting UKA to TKA can be difficult, and specialised techniques are needed. Issues include bone loss, joint line approximation, sizing, and rotation. Determining the complexity of conversion pre-operatively helps predict the need for augmentation, grafting, stems, or constraint.

In a 2009 study from our center, 50 UKA revised to TKA (1997–2007) were reviewed: 9 implants (18%) were modular fixed-bearing, 4 (8%) were metal-backed nonmodular fixed-bearing, 8 (16%) were resurfacing onlay, 10 (20%) were all-polyethylene step-cut, and 19 (38%) were mobile bearing designs; 5 knees (10%) failed due to infection, 5 (10%) due to wear and/or instability, 10 (20%) for pain or progression of arthritis, 8 (16%) for tibial fracture or severe subsidence, and 22 (44%) due to loosening of either one or both components. Insert thickness was no different between implants (P=0.23) or failure modes (P=0.27). Stemmed component use was most frequent with nonmodular components (50%), all-polyethylene step-cut implants (44%), and modular fixed-bearing implants (33%; P=0.40). Stem use was highest in tibial fracture (86%; P=0.002). Augment use was highest among all-polyethylene step-cut implants (all-polyethylene, 56%; metal-backed, 50%; modular fixed-bearing, 33%; P=0.01). Augmentation use was highest in fracture (86%) and infection (67%), with a significant difference noted between failure modes (P=0.003). Failure of nonmodular all-polyethylene step-cut devices was more complex than resurfacing or mobile bearing. Failure mode was predictive of complexity. Reestablishing the joint line, ligamentous balance, and durable fixation are critical to assuring a primary outcome.

In a 2013 multicenter study of 3 institutions including ours, a total of 175 revisions of medial UKA in 168 patients (81 males, 87 females; average age of 66 years) performed from 1995 to 2009 with a minimum of 2-year clinical follow-up were reviewed. The average time from UKA to revision TKA was 71.5 months (range 2 months to 262 months). The four most common reasons for failure of the UKA were femoral or tibial loosening (55%), progressive arthritis of the lateral or patellofemoral joints (34%), polyethylene failure (4%) and infection (3%). Mean follow-up after revision was 75 months. Nine of 175 knees (4.5%) were subsequently revised at an average of 48 months (range 6 months to 123 months). The rate of revision was 1.23 revisions per 100 observed component years. The average Knee Society pain and function score increased to 75 and 66, respectively. In the present series, the re-revision rate after revision TKA from UKA was 4.5% at an average of 75 months or 1.2 revisions per 100 observed component years. Compared to published individual institution and national registry data, re-revision of a failed UKA is equivalent to revision rates of primary TKA and substantially better than re-revision rates of revision TKA. These data should be used to counsel patients undergoing revision UKA to TKA.

We perform the direct approach using a standard radiolucent operative table with extender at the foot, and the assistance of fluoroscopy. The patient is positioned supine with the pubic symphysis aligned at the table break. The anterior superior iliac spine (ASIS) and center of the knee are marked, and a line drawn between. The incision commences proximally from two finger breadths distal and two finger breadths lateral to the ASIS, and extends distally 8–10 cm. Using fluoroscopy, the anterior aspect femoral neck is located. The incision is placed over the lateral aspect of the greater trochanter, which avoids the lateral femoral cutaneous nerve. The tensor fascia lata is identified, which has a distinctive purple hue, and dissected free from the intermuscular septum lateral to the sartorius and the rectus muscles. The deep, investing aponeurosis of the tensor fascia lata is split using a tonsil. Just below lie the lateral circumflex vessels, two veins and one artery, which must be either ligated or cauterised. A retractor is placed superior to the femoral neck over top of the superior hip capsule. A blunt, cobra-type retractor is then placed along the inferior femoral neck, deep to the rectus muscle and the rectus tendon. A sharp retractor is then used to peel the rectus off from the anterior capsule and placed over the anterior rim of the acetabulum. An anterior capsulectomy is performed. A saw blade is positioned for femoral neck resection and confirmed with fluoroscopy. After resection, acetabular retractors are placed, the socket is reamed, the cup is placed, and position confirmed with fluoroscopy. Turning to the femoral side, the surgeon palpates underneath and around the tensor, around the lateral aspect of the femur, proximal to the gluteus maximus tendon, and places a bone hook around the proximal femur. Femoral preparation and stem insertion require maneuvering the table and adjusting the patient position. The table is “jack-knifed” by lowering the foot of the table to approximately 45 degrees and placing the bed into approximately 15 degrees of Trendelenburg. The contralateral well leg is placed on the padded Mayo stand. A table-mounted femur elevator is attached to the bed, requiring a change in surgical gloves, and attached to the traction hook around the proximal femur. Gentle retraction is placed on the femur to tension the capsule. As the capsule is released the femur will begin to come up/out of the wound and into view. With increasing gentle retraction via the table-mounted hook, the femur is elevated. Simultaneously, the operative limb is externally rotated and adducted underneath the non-operative leg in a lazy “figure of 4” position by the assistant. The use of a “broach-only” stem design is preferred as direct straight reaming of the femur is difficult in most cases. Fluoroscopic images are obtained to confirm femoral implant positioning, offset, neck and leg length. A standardised rapid recovery hospitalization and rehabilitation protocol is used in all cases.

Not all total hip arthroplasty cases are created equal is a maxim that holds true for both primary and revision scenarios. Complex cases involve patients presenting with compromised bone and/or soft tissue. For primary cases, these include hips with dysplasia, ankylosis, deformed proximal femora, protrusio acetabuli, prior hip fracture with or without failed fixation, previous bony procedures, or neuromuscular conditions. In revision surgery, complex scenarios include cases compromised by bone loss, deterioration of the soft tissues and resulting instability, periprosthetic fracture, leg length discrepancy, infection, and more recently, hypersensitivity reactions. In this interactive session, a moderator and team of experts will discuss strategies for evaluation and management of a variety of challenging hip case scenarios.

Increasing demand for total hip and total knee arthroplasty in an era of economic uncertainty and shrinking budgets has put pressure on surgeons to deliver excellent results and early functional recovery with shorter hospital stays. Patients receiving these operative interventions tend to be younger and more active. Their ultimate source of information is the Internet, which may be compromised by low quality, non-peer reviewed information, or information not at an appropriate reading level for comprehension by lower literacy individuals. Unfortunately, not all patients undergoing total hip and total knee arthroplasty are satisfied with their operative intervention. The most significant etiology of this dissatisfaction is reported to be lack of clarification and alignment of expectations between the surgeon and the patient, which may result from misinformation or lack of understanding by the patient. Furthermore, in the era of rapid recovery, length of stay has significantly decreased from 3–5 days a decade ago, now down to 1–2 days, and in some cases same day surgery. In an effort to mitigate this compromise in communication, we have developed a set of frequently asked questions and responses. These are divided into preoperative questions, perioperative questions, and postoperative questions. These are part of our patient educational materials and provide both office and hospital staff with structured responses to avoid miscommunication and misinformation. We have found it to be imperative that all information provided by the office and hospital have a consistent message.

Introduction:

Patient expectations have escalated over the past several decades with respect to demand for success with total knee arthroplasty (TKA). It is reported that 15% to 20% of TKA recipients are unsatisfied with their result. Dynamic fluoroscopic studies and gait analyses have demonstrated that patients with TKA do not exhibit normal kinematics. On the other hand, patients with partial knee arthroplasty demonstrate more normal kinematics, thought to be secondary to retention of the anterior cruciate ligament (ACL) along with the posterior cruciate ligament (PCL). While not a new concept, bicruciate-retaining designs in TKA that preserve the natural ligament structure of the knee are drawing renewed interest as an option for patients with higher and more complex activity demand. These designs may result in a more natural kinematic feel as perceived by the patient. In a study of 2313 knees in patients undergoing primary knee arthroplasty at our center, the ACL was observed to be intact in 80% and normal in 53%. Bi-cruciate retaining TKA has recently been re-introduced for use in patients with an intact ACL and PCL. As with the introduction of any new technology into orthopaedic surgery, there is a concern regarding learning curve and adverse outcomes. Therefore we review and describe our initial experience with bi-cruciate retaining TKA.

As an increasing number of young, active, large patients are becoming candidates for total hip replacements, there is an increasingly urgent need to identify arthroplasties that will be durable, highly functional and amenable to possible future successful revision. In an era when cemented femoral stems were the primary implant option, the concept of a surface replacement was attractive and, perhaps, appropriate. However, cementless femoral stems of many designs now provide dependable long-term fixation and excellent, near normal function in patients of all ages, sex and level of activity.

However, a number of issues related to cementless stem fixation could be further improved: Optimization of load transfer to proximal femur to minimise fracture risk and maximise bone preservation; Elimination of proximal-distal mismatch concerns, including bowed femurs; Facilitation of femoral stem insertion, especially with MIS THA exposures; Facilitation of revision with implants capable of providing durable fixation for active patients.

The potential benefits of short stem femoral THA implants include: Ease of insertion; Reproducibility of insertion; Avoidance of issues related to proximal-distal anatomic mismatch or variations in proximal femoral diaphyseal anatomy (e.g. femoral bowing); Facilitation of MIS surgical approaches, especially anterior exposures; Optimization of proximal femoral load transfer with consequent maximization of proximal bone preservation.

The purpose of this presentation is to describe the design rationale and characteristics of short (<115mm) uncemented primary THA femoral stem, to evaluate the clinical and radiographic results of short stems and to discuss the possible drawbacks specific to the use of short stems.

Patient expectations have escalated over the past several decades with respect to demand for success with total knee arthroplasty (TKA). It is reported that 15 to 20% of TKA recipients are unsatisfied with their result. Dynamic fluoroscopic studies and gait analyses have demonstrated that patients with TKA do not exhibit normal kinematics. On the other hand, patients with partial knee arthroplasty demonstrate more normal kinematics, thought to be secondary to retention of the anterior cruciate ligament (ACL) along with the posterior cruciate ligament (PCL). While not a new concept, bi-cruciate retaining designs in TKA that preserve the natural ligament structure of the knee are drawing renewed interest as an option for patients with higher and more complex activity demand. These designs may result in a more natural kinematic feel as perceived by the patient. This surgical demonstration will outline patient selection criteria and illustrate the technique for performing ACL- and PCL-preserving, bi-cruciate retaining TKA.

While short stem designs are not a new concept, interest has surged with increasing popularity of less invasive techniques. If the goal of the tapered stem is to load preferentially proximally, why do we need a stem at all? Perhaps the only reason to use a tapered, long stem is to prevent varus; however, studies have shown that varus malalignment of a tapered stem does not affect results. Short stems are easier to insert, especially when using an anterior approach such as the anterior supine intermuscular in which the proximal femur is elevated anteriorly from the wound during stem insertion. Femoral preparation can be accomplished with straightforward broaching of the canal, without use of reamers. Short stems are bone conserving. They violate less femoral bone stock, providing more favorable conditions should a revision be required. However, ease of insertion and bone conservation matter little if not supported by clinical results. Thus, we reviewed our early experience with 2094 patients undergoing 2457 primary THA using short, tapered titanium, porous plasma spray-coated femoral components since January 2006 at our center. The TaperLoc Microplasty stem (Biomet, Warsaw, IN) has been used in 1881 THA, and the TaperLoc Complete Microplasty stem (Biomet) in 576. Patient age averaged 63.6 years. Increased offset was used in 1990 hips (81%). The surgical approach was less invasive direct lateral (LIDL) in 1194 THA (49%), anterior supine intermuscular (ASI) in 1117 (46%), and standard direct lateral (Std) in 146 (6%). Follow-up averaged 20 months. Thirty-five stems (1.4%) have been revised: 15 for infection (12 LIDL, 3 ASI), 1 same day revision for intraoperative femoral shaft perforation (Std), 1 at 3 days for patellar dislocation (LIDL), 2 for early subsidence (1 LIDL, 1 ASI), 13 for periprosthetic femoral fracture (1 Std, 12 ASI), 2 for aseptic loosening (1 LIDL, 1 ASI), and 1 stem well fixed (ASI) removed for loose cup and unable to disarticulate trunnion.

What lessons have we learned? First, we usually require one or two diameter sizes larger with short porous tapered stem versus the standard length version of the same design. The surgeon should be aggressive with sizing, pushing to the largest size possible. Use the broach like a rasp. Drive the component in valgus during insertion. Upon seating the component, do a trial reduction using the shortest available neck length. The component will generally sit slightly prouder than the broach and may require additional effort to seat completely.

Conservation of existing bone stock, compatibility with soft-tissue sparing surgery, more physiologic loading of the proximal femur, and versatility with varying femoral anatomy make the short taper an attractive implant option. The tapered wedge short stem represents the natural evolution of joint arthroplasty to a smaller, less-invasive, and more efficient implant.

Previous studies examined failure mechanisms for revision TKA performed between 1986 and 2000. These studies demonstrated that a majority of failures occurred in the first few years, with a disproportionate amount for infection and implant-associated failure mechanisms. Since these studies were published, efforts have been made to improve implant performance and instruct surgeons towards best practice total knee arthroplasty techniques. Recently our center participated in a multi-center evaluation of revision TKA cases during 2010 and 2011. The purpose was to report a detailed analysis of the failure mechanism and the time to failure to determine whether the failure mechanism of primary TKA has changed over the past 10–15 years. Further, we evaluated the effect of failure mechanism on extent of revision and whether revision surgery was performed at the same location as the index procedure. We identified 844 revisions of failed primary TKA. Aseptic loosening was the predominant mechanism of failure (31.2%), followed by instability (18.7%), infection (16.2%), polyethylene wear (10.0%), arthrofibrosis (6.9%), and malalignment (6.6%). Mean time to failure was 5.9 years (range 10 days to 31 years). 35.3% of all revisions occurred less than 2 years after the index arthroplasty, with 60.2% in the first 5 years. In contrast to previous reports, polyethylene wear is not a leading failure mechanism and rarely presents before 15 years. Implant performance is not a predominant factor of knee failure. Early failure mechanisms are primarily surgeon-dependent.

Two-staged revision including removal of all components is a common approach for treatment of infected THA. However, removal of well-fixed femoral stems can result in bone loss and compromised fixation. An alternative in selected cases is partial two-stage exchange, in which the well-fixed femoral stem is left in situ, only the acetabular component is removed, the joint space is debrided thoroughly, a spacer is placed, IV antibiotics are administered during the interval, and delayed reimplantation is performed.

We recently reported our results using the technique of partial two-stage exchange of infected THA. From 2000 through January 2011 in 19 patients with infected THA treated with partial two-stage exchange including complete acetabular component removal, aggressive soft tissue debridement, retention of the well-fixed femoral stem, placement of an antibiotic-laden cement femoral head on the trunnion of the retained stem, postoperative course of antibiotics, and delayed reimplantation. Indications for this treatment included those patients whose femoral component was determined to be well fixed and its removal would result in significant femoral bone loss and compromise of future fixation. During the study period, this represented 7% (19 of 262) of the patients whom we treated for a chronically infected THA. Minimum follow-up was 2 years (mean, 4 years; range, 2–11 years). None of the 19 patients in this series were lost to followup. We defined failure as recurrence of infection in the same hip or use of long-term suppressive antibiotics.

Two patients (11%), both with prior failure of two-staged treatment of infection, failed secondary to recurrence of infection at an average of 3.3 years. There were no patient deaths within 90 days. Postoperative Harris hip score averaged 68 (range, 31–100).

As 89% of patients in this series were clinically free of infection at a minimum of 2 years, we believe partial two-stage exchange may represent an acceptable option for patients with infected THA when femoral component removal would result in significant bone loss and compromise of reconstruction. Further study is required on this approach.

Background:

Coronal malalignment occurs frequently in total knee arthroplasty (TKA) and reduces implant longevity and function. Designed to improve consistency and efficiency, patient- specific positioning guides (PSPG) generated from preoperative imaging studies represent a paradigm shift from manual instrumentation (MI) and intraoperative computer navigation.

Not all total hip arthroplasty cases are created equal is a maxim that holds true for both primary and revision scenarios. Complex cases involve patients presenting with compromised bone and/or soft tissue. For primary cases, these include hips with dysplasia, ankylosis, deformed proximal femora, protrusio acetabuli, prior hip fracture with or without failed fixation, previous bony procedures, or neuromuscular conditions. In revision surgery, complex scenarios include cases compromised by bone loss, deterioration of the soft tissues and resulting instability, periprosthetic fracture, leg length discrepancy, infection, and more recently, hypersensitivity reactions. In this interactive session, a moderator and team of experts will discuss strategies for evaluation and management of a variety of challenging hip case scenarios

The failure of any joint arthroplasty secondary to infection is devastating to both patient and surgeon. Eradication of infection is the primary treatment objective. Classic teaching has called for removal of all prosthetic components, thorough soft tissue and bone debridement and either immediate or delayed reimplantation with an interim antibiotic polymethylmethacrylate laden spacer. The presence of a residual biofilm on implants is a rationale for component removal. Several sophisticated removal systems have been developed for the acetabulum which facilitate component removal with minimal to no bone loss. However, such systems do not exist for the femoral component. Removal of well-fixed femoral components remains a significant challenge frequently requiring extensive osteotomies which can result in bone loss and compromise of future femoral component fixation. Therefore, it would seem attractive to leave a well fixed femoral component in situ and remove only the acetabular component, perform a thorough debridement, place an antibiotic laden polymethylmethacrylate spacer within the acetabulum and perform a delayed reimplantation. A retrospective analysis of our practice from 2000 to 2010 revealed nineteen patients treated with a partial radical debridement and delayed reimplantation with a minimum of two year follow-up. There were no patient deaths within 90 days. Follow-up averaged 3.9 years. Three patients expired during the study period at an average of 3.5 years post-operative. Two patients, both multiply revised with prior 2-stage treatment of infection, failed secondary to recurrence of infection at an average of 3.3 years. Our results suggest that partial radical debridement represents an acceptable option for patients with infected THA. We have employed this technique when it was deemed that removal of the femoral component would require extensive osteotomy resulting in significant bone loss and compromise of future femoral reconstruction. It has been successful 89% of the time. We are aware that further study is required and we remain cautiously optimistic regarding this treatment modality.

Stiffness after knee arthroplasty is an important complication that the orthopaedic surgeon must be prepared to manage. In some cases, patients have a low-pain threshold or unidentifiable etiologic findings with no clinical indicators of septic or aseptic failure, and no radiographic evidence of mechanical complications. Psychosocial issues are important to consider, such as patient motivation and etiologic findings related to a worker's compensation claim. For patients who fail to achieve satisfactory ROM after TKA with no identifiable cause, treatment options may be categorised as non-surgical and surgical interventions. Non-surgical interventions would be physical therapy and pharmaceutical control for pain management. Surgical interventions include non-invasive options such as manipulation under anesthesia, and invasive options such as arthroscopy and mini-arthrotomy. Manipulation under anesthesia is indicated in the TKA that has less than 90° ROM after six weeks, no progression or regression in ROM. A modified technique has evolved for patients with persistent stiffness after standard-technique manipulation. The modified technique uses epidural anesthesia continued for post-operative analgesia, hospital stay of 1–3 days, CPM for 2–3 days, and daily PT. Continuous epidural infusion with local anesthetic is administered to provide complete analgesia, but allows muscle activation to be maintained during the hospital stay. Although open revision is sometimes required, arthroscopic management may be an effective alternative in certain instances, and also is helpful in diagnosis and treatment of other conditions of the knee that include prosthetic loosening and failure, retained cement, loose bodies, and sub-clinical infections. However, the painful TKA without evidence of significant intra-articular pathologic findings does not always respond well to arthroscopic management. Another option is open arthrotomy, done mainly to excise scar tissue. A synovectomy may be done as well. The polyethylene insert may be removed and an examination of the posterior cruciate ligament (PCL) performed. If the PCL is tight, it can be released and the existing components may be retained. Sometimes the polyethylene liner may be exchanged to a lipped insert to maintain stability. Revision surgery represents another option of treatment that can provide improved results whether manipulation or arthroscopic debridement has been done (14). Revision of one or all components combined with arthrolysis continues to have a role in improvement of ROM and outcomes in the stiff TKA.

Ceramic-on-ceramic alumina bearings (ALX) have demonstrated low wear with minimal biological consequences for almost four decades. An alumina-zirconia composite (BIOLOX-DELTATM) was introduced in 2000 as an alternative ceramic. This contains well-distributed zirconia grains that can undergo some surface phase transformations from tetragonal to monoclinic. We analyzed 5 cases revised at 1–7 years to compare to our simulator wear studies. For the retrieved DELTA bearings, two important questions were

how much tetragonal to monoclinic transformation was there in the zirconia phase and

The retrieval cases were photographed and logged with respect to clinical and revision details. The DELTA balls varied from 22mm to 36mm diameters. These had been mated with liner inserts varying by UHMWPE, BIOLOX-FORTE and BIOLOX-DELTA materials. Bearing features were analyzed for roughness by white-light interferometry, for wear by SEM, for dimensions by CMM and for transfer layers by EDS technique. Surface transformations on DELTA retrievals were mapped by XRD. The four combinations of 36mm diameter BIOLOX-FORTE and BIOLOX-DELTA were studied in a hip simulator, which was run in ‘severe’ micro-separation test mode to 5 million cycles. Wear rates, wear stripes, bearing roughness and wear debris were compared to the retrieval data.

In two DELTA ball cases, there were conspicuous impingement signs, stripe wear and black metallic smears. It is to be noted that the metal transfer sites (EDS) appeared to be from the revision procedures. The retrieved balls run with alumina liners showed monoclinic phase peaking at 32% on the particular surface and internal bore. On the fracture surface of case 1, the monoclinic content had increased to 40%. Various surface roughness indices were assessed on the bearings. The polished articular surfaces averaged roughness (Sa) of the order 3 nm, representing extremely smooth surfaces. The main wear zone was only marginally rougher (5 nm). In contrast the stripe wear zones had roughness of the order 55–140 nm.

In the laboratory, the DELTA bearings provided a 3–6 fold wear reduction compared to FORTE controls. Roughness of stripes increased to maximum 113nm on controls. Roughness of wear stripes showed FORTE with the highest and DELTA with the lowest values. DELTA bearings also revealed much milder wear by SEM imaging. Phase transformations showed peaks at < 30% for both main wear zone and stripe wear sites. It is hypothesized that the concentration of monoclinic phase reached a certain level due to compression contraint imposed by the alumina matrix. With implant wear, additional tetragonal grains of zirconia are exposed and these will also transform to tetragonal. This consistency between laboratory and retrieval studies confirmed the stable nature of the bearings. The BIOLOX-DELTA combination provides optimal potential for a clinically relevant reduction in stripe wear.

With increased use of alternative bearings, surgeons have moved from utilization of 22, 26, 28 and 32mm heads to larger head diameters in total hip arthroplasty (THA). Reported benefits of large heads are enhanced stability secondary to the increased range of motion prior to impingement and the increased jump distance required for subluxation from the acetabulum.

This study evaluates the use of large diameter heads in primary THA comparing the rate of dislocation to a published study from our practice as a historic control.

Between October of 2001 and October 2008, 2015 THA with large heads were performed in 1743 patients. Femoral head sizes ranged from 36 to 60mm, with articulations consisting of metal-on-poly, ceramic-on-poly, and metal-on-metal. Operative approach was 63% less invasive direct lateral, 10% anterior supine intermuscular, and 27% standard direct lateral. In 1999 (Mallory et al., Clin Orthop Relat Res) we reported a low incidence of 12 dislocations (0.8%) in 1518 primary THA done with smaller femoral heads via a standard direct lateral approach. In the current series with large heads, follow-up averaged 22 months. There has been one dislocation requiring revision (0.05%), representing a significant reduction from our earlier report (p=0.0003). Forty additional acetabular components have been revised (2.0%), with eight related to sepsis (0.4%), 23 aseptic loosening (1.1%), six metal sensitivity (0.2%), one pseudotumor (0.05%), one failure of ingrowth (0.05%), and one acute early migration (0.05%).

The use of larger diameter heads has significantly lowered our dislocation rate in primary THA with only one occurrence observed in 2015 cases, for a rate of 0.05% at two years average follow-up.

Lateral retinacular release (LRR) may be necessary to balance the patellofemoral articulation in primary total knee arthroplasty (TKA). However, lateral retinacular release may be associated with an increased risk of patellar necrosis, loosening, perioperative bleeding, and pain.

Additionally, the need for lateral retinacular release may herald a more significant problem with implant positioning, rotation, and balance. The purpose of this study is to report the lateral retinacular release rate with a “patella friendly” femoral TKA design, and to identify if a less invasive approach is associated with reduced need for lateral retinacular release.

A retrospective review of our database identified 4667 primary TKA performed by two surgeons between October 2002 and January 2009. Beginning in 2002, a less invasive approach has been used in over 95% of primary TKA. Also beginning in 2002, the authors began using a new TKA design with a more swept back patellofemoral articulation (Vanguard Complete Knee System; Biomet). During the first two years of the study, the authors also used the Maxim Complete Knee System (Biomet). We previously reported a lateral retinacular release rate associated with the Maxim of 22%. There were 555 Maxim and 4112 Vanguard TKA performed. Lateral retinacular release with Maxim TKA was 12.8% (71/555), significantly less than that previously reported for the same implant design using a standard approach. Lateral retinacular release for Vanguard TKA was 1.8% (72/4112), significantly less than that with the Maxim TKA using either a standard or less invasive approach (p< 0.005).

Implant design, surgical technique, and a less invasive exposure combine to significantly reduce the need for lateral retinacular release in primary TKA.

Surgeons theorize smaller increments in sizing might better address different sized femurs and size differences between genders. This study examines utilisation of intermediate sized components to determine if availability affects outcomes of women and men undergoing total knee arthroplasty (TKA).

We reviewed 1903 consecutive, primary TKA in 1519 patients (64% women) performed with a single implant system. Originally, six femoral sizes were available; four intermediate sizes were added later. The system allows interchange ability of all femoral and tibial sizes and has seven constraint options. Four hundred and five TKA were done prior to intermediate size availability. In women before, 49% were 65mm, 47% 60mm, and 3% 70mm. After, 32% were 62.5mm, 21% 65mm and 8% 67.5mm. In men, 70mm was the most common representing 49% before and 41% after. The 65mm in men dropped from 29% before to 16% after and the 75mm dropped from 21% to 14%. After, 23% were 67.5mm. Minimum follow-up was two years.

When comparing women before versus after, women after had significantly better postoperative Knee Society (KS) pain (p=0.0000), clinical (p=0.003) and function scores (p=0.0000), and improvement in clinical (p=0.0000) and function scores (p=0.0001) while improvement in pain score was similar. Men done after had better postoperative KS pain (p=0.02) and function scores (p=0.002), and improvement in KS clinical (p=0.001) and function (p=0.0002) scores.

Both men and women undergoing TKA after availability of half sizes had better postoperative KS pain, clinical and functional scores, and improvement from preoperative levels compared with men and women before. We conclude a single TKA system with a wide variety of sizing and constraint options can provide consistently excellent results for both men and women undergoing TKA.

Ceramic-on-ceramic bearings (ALX: pure alumina) have been used for human hip joints for almost 40 years. However an alumina matrix composite with zirconia (AMC) was introduced in year 2000 as a high-strength ceramic with almost double the fatigue resistance (AMC = 80.5%ALZ and 18vol% ZrO2). However we have not found any retrieval studies reported for this new ceramic bearing.

Wear maps were generated on three retrieved AMC femoral heads (28 and 36mm diameters) using x-ray diffraction, roughness and SEM imaging techniques. The wear study ran a physiologically appropriate, micro-separation test on 36mm ceramic balls and liners (AMC/ALZ). Wear rates were determined for the four combinations of balls and cups (ALX:AMC) with mapping of main-wear and stripe-wear zones, surface-roughness and analysis of debris morphology. In addition, the zirconia transformation to monoclinic phase was studied in AMC bearings

The retrieval study showed for the first time the wear phenomena occurring on three retrieved AMC femoral heads (at 1, 3, 6 years). Two had been paired with alumina liners and one with a polyethylene liner. Case-1 featured a 36mm ball in an UHMWPE socket, case-2 was an intact 28mm AMC ball and case-3 had a fractured ball from an IDE study. Laser interferometry and SEM were used to image ceramic wear and x-ray diffraction for analysis of transformation in the zirconia phase. Main-wear zones, stripe-wear zones, metal contamination and sites of implant impingement were also characterized. Surface roughness and in-vivo aging were quantified for both non-worn and worn areas. The SEM studies showed well-preserved articular surfaces, some with faint parallel scratches still evident. The latter likely represented the manufacturer’s original polishing marks. Multiple stripe-wear sites were identified with roughness 25–65nm (Sa) whereas polished main-wear zones averaged very low at 2–3nm. Metal impingements sites stained black with transfer of titanium increased roughness up to 140nm. Mildly worn areas of case-2 AMC ball averaged 10% transformation in the zirconia phase (tetragonal to monoclinic). In the stripe-wear zones, the monoclinic phase increased to 30%. The taper-bore and fracture surfaces in case-3 averaged 30% to 40% monoclinic, respectively. The stripe-wear zones and black metal contamination on these retrieved 28mm balls were correlated to multiple impingement sites on the rim of the alumina liners and titanium shells.

The laboratory model produced stripe wear on the ceramic balls and liners. The AlX/AlX controls produced the highest run-in and steady-state wear rates at 6.3 and 2mm3/Mc respectively). In contrast, the AMC/AMC combination produced the lowest wear rates at 0.5 and 0.1 mm3/Mc, respectively). With hybrid ball:cup combinations (AlX:AMC; AMC:AlX) the wear rates were similar and showed a 3-fold reduction compared to controls. In hybrid pairings, the AMC ceramic wore preferentially more than its AlX counterpart, regardless if present as a ball or cup implant. Thus the AMC ball contributed 66% to AMC/AlX total wear whereas the ALZ ball contributed only 33% of the total AlZ/AMC wear.

This study appears to be the first documentation of wear in retrieved AMC bearing surfaces. In general, the AMC surfaces worn in-vivo corresponded well to our in-vitro wear model. The stripe-wear zones in AMC femoral heads had rougher surfaces and higher monoclinic transformation than the main-wear zone. Overall the AMC ceramic appeared more resistant to stripe-wear effects created by the micro-separation and impingement phenomena.

Introduction and Aims: Patellar subluxation is most troublesome and accounts for a number of complications in total knee arthroplasty. The purpose of this study is to report the incidence of need for lateral release before and after tourniquet deflation, and the effect of the tourniquet on proper patellar tracking.

Method: A total of 171 knees in 133 patients were prospectively evaluated for the need for a lateral retinacular release before and after tourniquet deflation. All knees were implanted using the same knee system. An initial group of 99 knees were evaluated with tourniquet inflation while the knee was in flexion. Tourniquet inflation with the knee in flexion versus extension was subsequently assessed in a subset group of 72 knees. The need for lateral release was determined using the rule of ‘no-thumbs’ and rule of ‘full contact’.

Results: A total of 77 knees appeared to need a lateral release before tourniquet deflation. After tourniquet deflation 27 knees required lateral release representing a 65 percent reduction in lateral release. There was no statistically significant difference (p equals 0.5506: Pearson’s chi square) when comparing the flexion/extension groups.

Conclusion: Often, the surgeon evaluates patellar tracking with the tourniquet inflated, not taking into account the effect of tourniquet pressure on the quadriceps muscle. Our findings support the hypothesis that the resulting pressure from the tourniquet impacts patellar tracking. We conclude that if patellar tracking is questionable with the tourniquet inflated, tracking should be re-assessed with the tourniquet deflated before considering a lateral release.

Introduction and Aims: Difficult primary and revision total knee arthroplasty (TKA) with constrained knee systems is becoming more common. Modular systems are critical to success. A review of 457 consecutive cases with a single knee system for difficult primary and revision TKA provides an algorithm for good results.

Method: Between July 1992 and December 2000, 457 consecutive TKA were performed at a single institution using a posterior-stabilised constrained (PSC) system. Ninety-seven cases were primary with ligamentous instability and 360 were revision cases with bone loss and instability. Sixty-two patients died during follow-up, seven were lost to follow-up.

Results: Follow-up averaged 2.5 years. Pre-operative Knee Society (KSS) and Hospital for Special Surgery (HSS) scores averaged 47.3 and 60.0 respectively, and improved to 79.0 and 75.0 (p< 0.001). Range of motion improved significantly (p< 0.001). Incidence of manipulation was 9.4 percent. Infection necessitated debridement in 4.6 percent of cases. Extensor mechanism complications occurred in 2.2 percent. Excision of the patellar component without reinsertion was highest risk. There was a 2.2 percent aseptic loosening rate and 3.0 percent failure for instability.

Conclusion: The authors describe an algorithm for long-term success using a PSC modular knee system based upon critical review of radiographic and clinical outcomes. Methods for achieving stability and fixation affect results. Appropriate augmentation for femoral and tibial deficits re-establishes the joint line and provides excellent range of motion. A step-wise approach to the patella provides durable results. Predictors of success including alignment, the joint line, managing bone loss, fixation, and extensor mechanism are reviewed.

Introduction and Aims: Periprosthetic femur fractures, severe bone loss with loosening, infection and debridements, and non-union can all result in loss of bone stock following total hip (THA) and/or total knee arthroplasty (TKA). In the multiply-operated or osteopenic patient, few options exist when bone is severely compromised. We report results of a total femoral construct to salvage the severely compromised femur.

Method: We retrospectively reviewed 59 consecutive total femurs. Revision THA and/or TKA was performed utilising a custom total femoral construct: a constrained acetabular component, proximal femoral replacement, diaphyseal segment, and rotating hinge knee. Return to ambulation, pain, functional capacity, and subsequent surgery outcomes were measured. All cases involved severe bone loss: 13 aseptic loosening of revision THA and TKA, 24 periprosthetic fractures, five failed non-unions around implants, and 17 cases of multiple debridements for sepsis.

Results: Mean age was 74 years, mean follow-up was 38 months. One peri-operative death occurred. Pain scores improved by 18 points. Average post-operative hip flexion was 90 and knee flexion 93. All but one patient achieved ambulatory capability. Four of 17 septic cases recurred, three successfully treated and one disarticulation. Three other infections occurred in the aseptic and periprosthetic groups, all treated successfully. There were five dislocations, one acetabular revision, and two knee revisions for aseptic loosening.

Conclusion: Total femoral replacement represents a viable salvage procedure for the compromised femur associated with THA and/or TKA. Rapid return to ambulating, relief of pain and improved function can be expected from this, the ultimate revision surgery.

Introduction and Aims: Successful cementless total hip arthroplasty (THA) is well documented, with increasing reports in elderly patients. Concerns exist with respect to the ability to achieve and maintain long-term cementless femoral fixation in this patient population. This study reviews the clinical and radiographic outcomes of a tapered porous femoral component in cementless THA in elderly patients.

Method: Forty-nine hips in 47 patients over 74 years of age underwent primary cementless THA with a tapered stem between April 1996 and April 2000. All femoral heads were sent to pathology. Radiographs, Harris hip scores and clinical data were evaluated. Revision status was known for all hips.

Results: Average age: 79 years, mean follow-up was 46 months. Six patients died during the study (mean 40 months) all THA unrelated. Twenty-two peri-operative variances occurred. There were no dislocations. Three irrigation and drainage procedures were performed, and no revisions. Mean post-operative HHS improved by 33, with 87 percent of patients having no or minimal pain. We identified two cases of stem subsidence to a stable position with no progressive radiolucencies. Mean length of stay was 4.5 days. One patient required intensive care, 52 percent were discharged to home. Metastatic cancer was identified in one femoral head.

Conclusion: Using revision status as an end-point, the success rate was 100 percent. No peri-operative deaths or significant orthopaedic complications were identified. Advanced age and Dorr C anatomy is not a contraindication for tapered cementless THA. The femoral head should routinely be sent to pathology.

Introduction and Aims: With interest in minimally invasive surgery, and smaller incisions for total hip arthroplasty (THA), ways to ensure appropriate alignment are critical. Femoral stem varus has been associated with poorer results. We report the incidence of varus placement of a tapered, proximally plasma-sprayed, titanium femoral component and describe the outcomes of varus at minimum five-year follow-up.

Method: Between 1986 and 1997, 1080 tapered, proximally plasma-sprayed femoral components were implanted in primary cementless THA at one institution. Twenty-six components in 25 patients were placed in five degrees or more of varus. Two patients were lost to follow-up. The need for further surgery was assessed and Harris hip scores evaluated.

Results: Harris hip scores improved an average of 44 points. All femoral components were judged to be osteo-integrated. There was no displacement or progression into further varus, or impending failures. One well-fixed stem was revised at an outside institution for unexplained pain at 2.5 years. Survival with aseptic loosening as an end-point is 100 percent. Overall survival of the femoral component is 96 percent at 10 years average follow-up.

Conclusion: As visualisation decreases with decreasing incision length, a component that is reliably placed into appropriate position is required. Implant position with this component is forgiving. It may be an excellent choice for less-invasive techniques with compromised visualisation. In varus, the stem performs well, with no revisions for aseptic loosening and a 96 percent survival at up to 16 years.

Introduction and Aims: Adequacy of post-operative pain control can effect total knee arthroplasty (TKA) outcomes. We examine the effectiveness of a simple and inexpensive method using long-acting local anesthetic (bupivacaine) with epinephrine and morphine injection on controlling pain, blood loss, and motion in primary TKA.

Method: We retrospectively reviewed 170 patients who underwent 208 primary TKA, by a single surgeon between October 2001 and December 2002. The control group of 75 patients (99 knees) had received no intra-operative injections. The study group of 95 patients (109 knees) had received intra-operative injection of 0.25 percent bupivacane with epinephrine and morphine divided two-thirds soft-tissue injection and one-third intra-articular injection. Bilateral simultaneous TKA in the study group received a divided anaesthetic dose.

Results: The control group required significantly more breakthrough narcotic (85 percent vs 67 percent; p=0.004); and required more narcotic reversal for over-sedation. The study group had significantly higher ROM at discharge 63 degrees vs 52 degrees. Lower ROM at discharge was associated with manipulation (p equals 0.001). The study group required less transfused blood (mean 0.03 vs 0.1 units), and had significantly lower bleeding indices 2.7 vs 3.5.

Conclusion: Preemptive analgesia with intra-articular and soft-tissue injection of long-acting local anesthetic with epinephrine and morphine appears to decrease need for rescue narcotics and reversal agents. The use of the injection also increases ROM at discharge, which reduces the need for manipulation. Lastly, the bleeding index and transfusion requirements are significantly reduced. This inexpensive method is effective in improving the post-operative course of primary TKA.

Introduction: Previously, in vivo kinematic studies have determined the in vivo kinematics of the femur relative to the metal base-plate. These kinematic studies have reported posterior femoral rollback in posterior stabilized (PS) TKA designs, but the actual time of cam/post engagement was not determined. The objective of this present study was to determine, under in vivo conditions, the time of cam/post engagement and the kinematics of the femur relative to the polyethylene insert.

Methods: Femorotibial contact positions for twenty subjects having a PS TKA, implanted by two single surgeons, were analyzed using video fluoroscopy. Ten subjects were implanted with a PS TKA that is designed for early cam/post engagement (PSE) and ten subjects with a PS TKA designed for later cam/post engagement (PSL). Each subject, while under fluoroscopic surveillance, performed a weight-bearing deep knee bend to maximum flexion. Video images were downloaded to a workstation computer and analyzed at ten-degree increments of knee flexion. Femorotibial contact paths for the medial and lateral condyles, axial rotation and condylar lift-off were then determined using a computer automated model-fitting technique.

Results: Subjects implanted with the PSE TKA experienced, on average, the cam engaging the post at 48° (10 to 80°). Subjects having the PSL TKA experienced more consistent results and did experience engagement in deep flexion (Average 75°). Subjects having the PSE TKA experienced, on average, −5.5 mm (1.5 to −9.3) of posterior femoral rollback (PFR), while subjects having the PSL TKA experienced only −2.6 mm (8.5 to −9.0) of PFR. Subjects having the PSE TKA experienced more normal axial rotation patterns. Nine subjects having the PSE TKA experienced condylar lift-off (maximum = 1.9 mm), while only 4/10 having the PSL TKA experienced condylar lift-off (maximum = 2.7 mm).

Discussion: This is the first study to determine the in vivo contact position of the cam/post mechanism. Subjects having a PSE TKA experienced earlier cam/post engagement than subjects having the PSL TKA. Some subjects did not experience any cam/post engagement throughout knee flexion. Subjects having the PSE TKA experienced more PFR and better axial rotation patterns, but subjects having a PSL TKA experienced lesser incidence of condylar lift-off. Results from this study suggest that there may be an advantage to early cam/post engagement, which leads to more normal axial rotation patterns caused by the medial condyle moving in the anterior direction as the lateral condyle rolls in the posterior direction.