Total Ankle Arthroplasty


Although many orthopaedic surgeons abandoned ankle arthroplasty because of high failure and complication rates, the continued search for alternatives to ankle arthrodesis for ankle arthritis has led to a renewal of interest. The development of contemporary designs more biomechanically compatible with the anatomy and kinematics of the ankle, improved techniques and instrumentation, and the introduction of biologic ingrowth for component fixation have led to a profusion of studies evaluating the design, technique, and outcomes of total ankle arthroplasty (TAA). The results of these studies have spurred an increase in the use of TAA as an alternative to traditional ankle arthrodesis for a number of conditions. As surgeons become more experienced with the technique, the frequency of TAA has increased dramatically over the past decade, particularly in patients with posttraumatic arthritis and osteoarthritis.

Development of Total Ankle Arthroplasty Systems

Since the first report of TAA in the 1970s, many TAA systems have been introduced. The first-generation, cemented, constrained designs were very stable but required extensive bony resection for implantation and frequently failed because of loosening, subsidence, and extensive osteolysis. Second-generation, less constrained implants required less bone resection and did not require cement fixation; because shear forces and torsion at the bone-prosthesis were reduced, loosening was less frequent. However, increased polyethylene wear and failure compromised the stability of the components, often leading to painful impingement and subluxation or complete dislocation of the components. Contemporary, third-generation, semi-constrained total ankle systems consist of three components: a metallic baseplate that is fixed to the tibia, a domed or condylar-shaped metallic component that resurfaces the talus, and an ultrahigh-molecular-weight polyethylene bearing surface interposed between the tibial and talar components. Systems in which the polyethylene component is locked into the baseplate are often referred to as “two-piece” or “fixed-bearing” designs, whereas those with the polyethylene component not attached to the baseplate are called “three-piece” or mobile or meniscal bearing systems. Currently, there are over 50 different TAA systems in use worldwide, most of which have not been approved for use by the US Food and Drug Administration (FDA). There is no convincing evidence of the clear superiority of one design over another among the currently available systems; choice of a prosthesis depends on individual patient factors, institutional factors, and the surgeon’s training and experience.

Design Rationale

The development of an implant system that mimics the normal anatomy and biomechanics of the ankle and achieves success rates similar to those of hip and knee arthroplasty has been hampered by several anatomic features of the ankle joint: (1) the ankle has significantly less contact area between joint surfaces than the hip or knee; (2) the ankle experiences 5.5 times body weight with normal ambulation, compared with three times body weight at the knee; and (3) the articular cartilage surface of the ankle is uniformly thinner than that of the knee.

The biomechanical concepts that have resulted in the most recent generation of ankle arthroplasties are somewhat beyond the scope of a surgical-oriented textbook; however, the number and variety of implants on the market demand a familiarity of basic principles of component design.

The design of TAA systems continues to evolve as we learn more about the modes of failure from longer-term studies. First-generation implants had high rates of osteolysis, implant loosening, tibial and talar bone loss, and wound complications. Second-generation designs used porous metal-backed surfaces to improve osseous integration; replaced the tibiotalar, talofibular, and medial-malleolar-talar articulations; and/or improved stability by fusing the syndesmosis. Complications related to nonunion of the syndesmosis, polyethylene wear, and migration and impingement of the implants led to a number of modifications in third- and fourth-generation designs: less bone resection, more bony ingrowth, retention of ligamentous support, and anatomic balancing.

Fixed-Bearing VersusMobile-Bearing Designs

Most modern implants fall into two basic groups: those with a mobile polyethylene component that has the ability, at least in theory, to move under the tibial component to adapt to changes in joint forces ( Fig. 10.1A ) and those with the polyethylene component fixed rigidly to the tibial component ( Fig. 10.1B ). Mobile-bearing designs are used most commonly in Europe and have a long history of outcomes from which they can be evaluated. Another theoretical advantage of these designs is the “forgiveness” of the implant, which allows small variances in alignment to be compensated for by a reorientation of the prosthesis to accommodate the joint forces. The ability of the polyethylene component to move should, in theory, keep the articulation between the talar component and the polyethylene component more congruent and less likely to lead to edge load and advanced wear. In experienced hands, however, there is a question of how much the polyethylene component actually moves under the tibia. Barg et al. found very little anteroposterior movement of the talar component under the tibia in follow-up radiographs of a three-component, mobile-bearing design. They noted that the prosthesis functioned largely like a fixed-bearing design, but with a possible advantage of allowing an individualized position of the polyethylene insert in response to individual soft-tissue loads produced by different ankle joint configurations. Aside from the STAR ankle implants ( Fig. 10.2 ), implants approved for use in the United States are fixed-bearing designs.

FIGURE 10.1, A, Mobile-bearing, three-component total ankle replacement; polyethylene is independent of tibial component. B, Fixed-bearing, two-component ankle replacement; polyethylene is fixed to tibial component.

FIGURE 10.2, A and B, STAR arthroplasty in patient with good bone quality and minimal deformity.

Proponents of fixed-bearing designs suggest that the normal ankle joint, as opposed to the knee, has a more stable central axis of motion and less need for an additional degree of freedom of motion. Backside polyethylene wear against the tibial component is a major concern with mobile-bearing designs and less with fixed designs. Attention to detail in the proper alignment of the prosthesis along the mechanical axis of the limb has been suggested to prevent excessive wear.

A multicenter study by Gaudot et al. comparing fixed-bearing with mobile-bearing implants found no significant differences in accuracy of positioning, clinical and radiographic mobility, or morbidity. In a more recent randomized trial, Queen et al. also found no clinically meaningful differences in outcomes between the two implant types when examining gait mechanics and pain at 1-year follow-up. The most recent American Orthopaedic Foot and Ankle Society (AOFAS) scores were higher for patients with fixed-bearing implants than for those with mobile-bearing implants, and radiolucent lines and subchondral cysts were less frequent. In contrast, Currier et al. analyzed 70 retrieved ankle implants, most commonly for loosening and polyethylene fracture. Loosening occurred more frequently in fixed-bearing designs than in mobile-bearing designs. Lundeen et al. in a study of patients with a third-generation mobile-bearing TAA concluded that the multiplanar articulation in mobile-bearing TAA may reduce excessively high peak pressures during tibial and talar motion, which may have a positive effect on gait pattern, polyethylene wear, and implant longevity.

Alignment

Currently available implant systems are designed to be placed along the mechanical axis of the limb and depend on satisfactory alignment above and below the ankle joint. The most common method of obtaining correct alignment is an external alignment jig, using intraoperative fluoroscopy to judge the alignment. At least one system uses an intramedullary alignment rod ( Fig. 10.3 ). One innovation is a tomography-produced customized cutting jig, such as those available for knee arthroplasty. Patient-specific instrumentation has been successfully used in arthroplasty of other joints (e.g., knee, shoulder, hip), but has rarely been described in TAA. Cadaver and clinical studies have shown this instrumentation to provide accuracy and reproducibility among multiple surgeons, implants, and facilities. Hamid et al. did not find a difference in postoperative alignment with patient-specific instrumentation or standard referencing; however, use of patient-specific instrumentation significantly decreased operative time and, thus, costs. Another fairly recent system uses a lateral approach to more accurately reproduce the center of rotation of the ankle and minimize bone resection ( Fig. 10.4 ).

FIGURE 10.3, A and B, INBONE II ankle arthroplasty.

FIGURE 10.4, A and B, Trabecular metal total ankle (Zimmer, Warsaw, IN).

Ingrowth Versus Cement Fixation

In the United States, FDA-approved designs, except for the fourth-generation STAR ankle and the Hintermann Series2, are approved for use with cement and, although they are often porous coated similar to the cement-less implants of the hip or knee, implantation of the components without cement is considered off-label use. There are few reports comparing the use of cement with ingrowth fixation in the literature, and at this time, there does not appear to be a consensus on the issue.

Metaphyseal Fixation

Distribution of the forces over as broad an area as possible is one goal of implant design. Tibial components should, if possible, rest flush on the cut surface of the metaphysis of the tibia and engage the anterior and posterior cortices without significant overhang. The use of stems of some type to help with the stability of the implant and broaden the weight-bearing surface seems prudent. Some designs have stems that are placed through a cut-out notch in the anterior cortex, and others are driven into the metaphysis in an intramedullary fashion. Changes in the geometry and depth of resection of the tibia and talus have been suggested to decrease aseptic component loosening. In a biomechanical study, standard flat-cut resections were compared to subject-specific, anatomic radius-based (round) resections to determine their effect on bony support. Statistically significant decreases in bony support for both the talus (8% to 19%) and tibia (8% to 46%) were seen with flat-cut resections. The authors concluded that biomechanical characteristics of TAA affected by bony support of the prostheses, including implant stability and resistance to subsidence, may be improved with round resections compared to flat-cut resections.

Talar Component Design

Because the talar component is subjected to high forces during normal gait, talar components that cover the entire surface of the talus might have the advantage of better distribution of these forces and smaller chance of subsidence into the body of the talus. Balanced against this is the concern for wear or impingement in the medial and lateral ankle gutters. Fukuda et al. demonstrated that a talar component placed in a malrotated position had poor contact characteristics at the extremes of ankle motion, causing concern for increased polyethylene wear or talar component loosening. Evaluating the contact pressures with the Agility total ankle design, Nicholson et al. found pressures higher than those recommended for the talar component–polyethylene articulation. Although this design has been modified since this study in 2004, the findings demonstrate the issue of talar component design regarding contact pressure and potential wear.

Polyethylene Wear

Wear debris of polyethylene within joint replacement systems has been shown to result in clinical complications, including osteolysis and component loosening. Highly cross-linked polyethylene (HXPE) was introduced to avoid these complications and has been shown to result in improved wear performance in total hip, knee, and shoulder implants. In a biomechanical study of bicondylar, fixed-bearing total ankle implants with either conventional polyethylene or HXPE, Bischoff et al. found that HXPE samples exhibited a wear rate reduction of 74% compared with conventional polyethylene articulating on metal. The extent to which these laboratory findings affect clinical outcomes has not been determined, and clinical outcomes studies are needed to clarify the benefits of HXPE in TAA implants.

Preoperative Evaluation

A thorough understanding of the patient’s medical history and review of systems are important in the decision-making process and the consideration of the patient for TAA. Systemic diseases such as diabetes, inflammatory arthritis, chronic obstructive pulmonary disease, and peripheral vascular or heart disease may adversely affect the outcome and healing of the incision. Conditions such as sleep apnea, malnutrition, vitamin D deficiency, and depression are associated with decreased functional outcomes and poor results. We do not perform elective TAA in active smokers. It must be clear that the ankle joint is indeed the cause of the patient’s primary complaint. Many patients have adjacent joint disease that might also need to be treated before or at the time of surgery. Selective injections of lidocaine are helpful in accurately identifying the painful pathologic process. A complete assessment of the limb is important. A lumbar spine pathologic process with sciatica and radicular lower extremity pain or degenerative disease of the hip or knee may cause a change in the management plan. Patients with combined knee and ankle arthritis and deformity often are best managed by correction of the knee deformity first, followed by the ankle replacement.

A thorough evaluation of the neurovascular status of the limb is essential, and any concerns should prompt a formal vascular evaluation. The patient’s gait should be evaluated for limp, and any alterations of knee or hip motion to compensate for the arthritic ankle and limb-length difference should be assessed. The standing evaluation is important for clinical assessment of ankle and hindfoot alignment. Is there a supramalleolar deformity that must be corrected? Is the hindfoot well aligned, or is there a component of varus or valgus? Clinical assessment of the gastrocsoleus complex and the Achilles tendon is important. The Silfverskiöld test for selective gastrocnemius tightness might reveal a contracture that is independent of ankle range of motion and that must be released intraoperatively. Coetzee and Castro demonstrated the inability to distinguish true range of motion of the tibiotalar joint on clinical examination and proposed a radiographic evaluation of the range of motion preoperatively. Nonetheless, an idea of sagittal plane range of motion is important. Overall hindfoot motion is important as well. A stiff, arthritic hindfoot might be the difference between choosing arthroplasty or arthrodesis. Strength testing of the leg motor groups should not reveal major deficits that would impair the outcome. The anterior skin should be stable and without lesions that would impair the healing of the surgical incision.

At a minimum, standing radiographs of the ankle in anteroposterior, lateral, and mortise views should be obtained. Any suspicion of proximal limb malalignment should be evaluated with standing lower extremity films. Because an accurate assessment of the alignment of the hindfoot is not possible with standing films of the ankle, Frigg et al. described a hindfoot alignment view ( Fig. 10.5 ) that gives a better appreciation of overall alignment and helps to determine if an adjunctive procedure is needed to improve the alignment of the foot distal to the ankle joint.

FIGURE 10.5, A and B, Hindfoot alignment view of right total ankle replacement. FTGA , Frontal tibial ground angle; HAVA , hindfoot alignment view angle; HAVD , hindfoot alignment view distance; LHA , lateral heel angle; white line, reconstruction of ankle joint based on length of medial malleolus.

Although coronal plane deformities usually are the focus of radiographic evaluation before TAA, sagittal plane deformities have been shown to alter the mechanics and joint reaction forces more than coronal plane deformities. Several methods for evaluating the lateral position of the talus on radiographs have been described. Veljkovic et al. described a sagittal talar position measurement that they named the lateral tibial station (LTS); the LTS defines the center of rotation of the talus as related to the anatomic tibial axis. In a study of 82 ankles, they showed that this measurement can be reliably obtained on preoperative weight-bearing lateral radiographs; the mean LTS measurement was 1.7 mm (normal range, 0.8076 to 3.1496 mm). The value of the LTS in evaluating ankle pathology remains to be established.

Radiographic evaluation should include assessment of the quality of the bone stock, coronal plane alignment of the ankle with supramalleolar deformities or joint incongruencies, the presence of osteophytes requiring removal, adjacent joint arthritis or malalignment that requires correction, calcaneal pitch angle as a predictor of gastrocsoleus contracture, and the presence of major cysts or defects that will need grafting.

The effect of bone mineral density (BMD) on outcomes of TAA has not been clearly delineated. Dual-energy x-ray absorptiometry (DEXA) scanning generally is not obtained to evaluate BMD before TAA because of the additional time and costs involved. CT scans are, however, often obtained before TAA, and Hounsfield units measured on CT have been shown to correlate well with DEXA T-scores. In a study of 198 ankles, BMD (Hounsfield units) was measured on preoperative CT scans and compared to outcomes at 2.4-year follow-up. After controlling for age, gender, and BMI, only tibial Hounsfield units of less than 200 were significantly associated with periprosthetic fracture. Prophylactic internal fixation of the medial malleolus may be considered for patients with tibial Hounsfield units of less than 200 as measured on CT scans. Severe osteoporosis often is listed as a contraindication to TAA, but newer implant designs and surgical techniques (e.g., noncemented fixation and patient-specific implants) have overcome some of the problems of TAA in osteoporotic bone, and outcomes have improved, especially in older, more sedentary patients with osteoporosis. DEXA scanning or BMD evaluation on CT scans is indicated in patients at risk for osteoporosis.

Indications

Although degenerative, inflammatory, and posttraumatic arthritic conditions of the ankle are the primary indications for TAA, there is little clinical evidence on which to base more specific indications and contraindications. The ideal candidate for ankle arthroplasty has been described as an older, thin, low-demand individual with minimal deformity and retained ankle range of motion. These descriptions, however, are vague and controversial. Some have defined “young” as younger than 50 years of age and “thin” as weighing less than 200 lb, but there is no clinical evidence to support these classifications. Commonly cited contraindications to TAA include age younger than 50 years, history of poor patient compliance, heavy industrial labor, heavy smoking, uncontrolled diabetes with neuropathy, significant ankle instability, angular deformity of more than 10 to 15 degrees, vascular insufficiency, obesity (over 250 lb), significant bone loss, osteonecrosis, and active or previous infection. More recently, however, a number of these contraindications have been questioned. Demetracopoulos et al. reviewed outcomes in 395 consecutive patients according to age (younger than 55, 55 to 70, and older than 70 years of age) and found no differences in pain relief or physical outcomes or in the incidences of wound complications, reoperations, or revisions. Tenebaum et al. compared clinical and gait outcomes in patients older than 70 years to those in patients between 50 and 60 years of age; improvements were equivalent in the two groups. Good results have been reported in both obese patients and diabetic patients (see sections on Obesity and Diabetes), as well as those with angular deformities of more than 20 degrees (see section on Deformity Correction).

Because TAA is generally considered a “motion-sparing” procedure rather than a “motion-producing” procedure, its use in individuals with ankle stiffness has been limited; however, Brodsky et al. compared outcomes to preoperative range of motion and found that, although a low preoperative range of motion was predictive of overall lower physical function, patients with stiff ankles had clinically greater improvements in function. These findings suggest that TAA can offer clinically meaningful improvements in gait function and should be considered for patients with end-stage tibiotalar arthritis, even with limited sagittal range of motion.

Reports are variable concerning the outcomes of TAA in arthritis of different etiologies; most studies, however, have not found etiology to significantly affect implant survival. Bennett et al. reviewed the outcomes of 173 TAAs of differing etiologies (osteoarthritis, rheumatoid arthritis, pilon fracture, ankle fracture, and posttraumatic arthritis without previous fracture) and found no major differences in any of the reported outcomes at 2-year follow-up. Whatever the etiology of the arthritis, severe involvement does not necessarily portend a poor result. In a group of 124 patients, Chambers et al. found no differences in Short-Form 36 (SF-36) scores regardless of Kellgren-Lawrence grade of arthritis severity. Those with the most severe arthritis (Kellgren-Lawrence grade 4) had the most improvement in all domains of the Foot and Ankle Outcome Score and were more satisfied (91%) with their outcomes than all other groups (50%); 94% of patients with severe arthritis thought their quality of life had been improved compared to 47% in those with severity grades of less than 4. Although radiographic severity is an important factor that should be considered, it does not appear to contradict TAA.

Total Ankle Arthroplasty or Ankle Arthrodesis for Ankle Arthritis

Ankle arthrodesis (see Chapter 11 ) has long been the gold standard for the surgical treatment of moderate to severe ankle arthritis. It is, therefore, reasonable to ask if there is a compelling reason to pursue TAA as a treatment option for patients with ankle arthritis. Although the patient satisfaction rate after ankle arthrodesis is fairly high, there are certainly circumstances in which arthrodesis might not be the best procedure, including preexisting subtalar or other hindfoot arthritis, contralateral hindfoot or ankle arthritis, and hip or knee impairment such that motion through the ankle joint may be beneficial to the overall limb and patient function.

No level I studies have directly compared the two procedures, and reports in the literature are contradictory ( Table 10.1 ). The most recent reports seem to favor TAA with the latest-generation implants over arthrodesis, citing better functional outcomes, fewer complications, and better patient satisfaction. Some gait studies have noted no difference in gait patterns after arthroplasty and arthrodesis, whereas others report more nearly normal gait and better walking on uneven surfaces after arthroplasty; gait appears to be improved by either procedure. Daniels et al. compared intermediate outcomes (mean 5.5-year follow-up) of arthrodesis (107 patients) and arthroplasty (281 patients) in a diverse cohort of patients and found comparable clinical outcomes; however, rates of reoperation and major complications were higher after ankle arthroplasty. Norvell et al. found that ankle-specific adverse events were infrequent and only weakly associated with operative procedure. Careful patient selection is mandatory for the success of either of these procedures in the treatment of ankle arthritis.

TABLE 10.1
Reported Outcomes of Ankle Arthroplasty Compared With Ankle Arthrodesis
Study Patients Follow-Up Results
SooHoo et al. (2007) 4705 arthrodesis
480 TAA
5 years Higher risk of complications in arthroplasty group but less frequent subtalar joint arthritis requiring fusion
Haddad et al. (2007) 852 arthroplasty
1262 arthrodesis
Literature review Intermediate outcomes of arthroplasty and arthrodesis roughly equivalent
Saltzman et al. (2009) 224 patients 2 years Arthroplasty group had better function and equivalent pain relief as ankles treated with arthrodesis
Slobogean et al. (2010) 107 patients 1 years Significant improvements on preference-based quality of life measures in both; no significant differences
Schuh et al. (2011) 41 patients 3 years No significant differences in activity levels, participation in sports scores, or UCLA and AOFAS scores
Krause et al. (2011) 161 patients 3 years Significantly higher complication rate with arthroplasty (54%) than with arthrodesis (26%)
Flavin et al. (2013) 28 patients Gait study Arthroplasty produced a more symmetric vertical ground reaction force curve, which was closer to that of the controls that the curve of the arthrodesis group
Daniels et al. (2014) 388 patients 5.5 years Intermediate-term clinical outcomes comparable; rates of reoperation and major complications higher after arthroplasty
Jiang et al. (2015) 12,250 arthrodesis
3002 arthroplasty
N/A Arthroplasty independently associated with lower risk of blood transfusion, nonhome discharge, and overall complication rate; however, no significant difference in risk for the majority of medical perioperative complications
Jastifer et al. (2015) 77 patients 2 years (gait study) Both had improved walking performance on uneven surfaces; arthroplasty patients had higher scores walking up stairs, down stairs, and uphill
Pedowitz et al. (2016) 47 arthroplasty
27 arthrodesis
Minimum 2 years TAA preserves more anatomic movement, has better pain relief, and better patient-reported function
Stavrakis and SooHoo (2016) 1280 arthroplasty
8491 arthrodesis
Short-term complication rates low for both procedures; lower rates of readmission and periprosthetic joint/wound infection with TAA
DiGiovanni and Guss (2017) 273 3 years Improvements in MFA and SF-36 scores significantly better with arthroplasty
Odum et al. (2017) 1574 arthroplasty
1574 arthrodesis
Data from NIS Arthrodesis associated with a 1.8 times higher risk of a major complication, but a 29% lower risk of a minor complication
Kim et al. (2017) Meta-analysis TAA 6-67 monthsAA 6-62 months Similar clinical outcomes; frequency of re-operation and major surgical complications significantly increased with TAA
Norvell et al. (2018) 494 Ankle-specific adverse events were infrequent and only weakly associated with operative procedure
AOFAS , American Orthopaedic Foot and Ankle Society; MFA, Musculoskeletal Function Assessment; N/A , not applicable; NIS , Nationwide Inpatient Sample; SF-36, Short-Form 36; TAA , total ankle arthroplasty; UCLA , University of California, Los Angeles.

Outpatient Total Ankle Arthroplasty

The success of outpatient total hip, knee, and shoulder arthroplasty, with no compromise of safety, satisfaction, or results, has prompted many surgeons to move TAA to an ambulatory surgical center. Although there are relatively few reports of the outcomes of this procedure, available reports cite good outcomes with few complications, in addition to cost savings and patient satisfaction. Two reviews of complications in outpatient TAA reported overall complication rates of 5% and 15%; most complications were minor, and readmissions and reoperation were infrequent. In a comparison of outpatient and inpatient TAA, Gonzales et al. found a 13% cost savings in the outpatient group, with a low complication rate and high patient satisfaction. The most important aspect of outpatient TAA, as with any outpatient arthroplasty, is careful patient selection. An algorithm developed by our surgeons for selecting patients for outpatient total joint arthroplasty is a helpful guide ( Fig. 10.6 ). There is limited evidence to determine specific patient factors that may preclude outpatient TAA surgery; however, experience in arthroplasty of the foot and ankle and other joints has identified various patient factors that are associated with perioperative complications and a longer length of hospital stay, such as elevated HbA1c level, obesity, hypoalbuminemia, age greater than 64, increased operating room time, American Society of Anesthesiologists (ASA) score of 2 or higher, and presence of comorbidities. Taylor and Parekh formulated a detailed algorithm specifically for outpatient TAA based on a number of patient and procedure characteristics ( Fig. 10.7 ).

FIGURE 10.6, Algorithm for patient selection for outpatient total joint procedures. BMI, Body mass index; CAD, coronary artery disease; CHF, congestive heart failure; COPD, chronic obstructive pulmonary disease; DVT, deep vein thrombosis; HTN, hypertension; ICD, implantable cardiac defibrillator; OSA, obstructive sleep apnea; PE, pulmonary embolism; PTCA, percutaneous transluminal coronary angioplasty; TJA, total joint arthroplasty.

FIGURE 10.7, Algorithm for selection of patients for outpatient ambulatory total ankle arthroplasty. BMI, Body mass index; TAA , Total ankle arthroplasty.

In addition to selecting appropriate patients, appropriate use of a multimodal perioperative and postoperative pain management protocol is essential. The choice of pain management protocols has shifted away from oral and intravenous administration of narcotics to peripheral nerve blocks and indwelling catheters as better options. Continuous popliteal sciatic nerve block is commonly used for major foot and ankle reconstructions. Liposomal bupivacaine (Exparel; Pacira Pharmaceuticals, Parsippany, NJ) administered as a periarticular injection has been shown to have marked benefits in postoperative pain control. Mulligan et al. compared liposomal bupivacaine to popliteal sciatic nerve block for TAA and found no significant differences between the groups with regard to complications, emergency department visits, readmissions, reoperations, visual analog scale (VAS) pain score, and narcotic use.

The management of perioperative blood loss, especially postoperative hemarthrosis, is another modifiable factor affecting patient recovery, complication rates, and costs. Tranexamic acid (TXA) has been shown to be effective for reducing perioperative blood loss with arthroplasty of other joints, but little information is available for determining its effectiveness in TAA. Nodzo et al. described 50 patients with uncemented TAA, 25 of whom received TXA and 25 who did not. Drain output and change in preoperative to postoperative hemoglobin levels were significantly less and the overall wound complication rate was lower in patients who received TXA. We do not routinely use TXA for TAA.

Total Ankle Arthroplasty

Technique 10.1

Patient Positioning

  • Most systems require an anterior approach to the ankle. Place the patient supine on the operating table with the foot near the end of the table. Place a small bump or lift under the ipsilateral hip to help place the ankle straight and avoid the tendency of the leg to externally rotate.

  • After induction of general anesthesia, apply and inflate a thigh tourniquet to control bleeding and improve visualization.

Approach

  • Any significant deformity above or below the ankle joint must be corrected before placement of the total ankle implants (see Technique 10.2).

  • The approach is determined by the prosthesis design, and the reader is referred to the specific implant chosen; however, most systems require an anterior approach to the ankle.

  • Make an incision from about 10 cm proximal to the ankle joint on the lateral side of the anterior tibial tendon, over the flexor hallucis tendon. This incision is medial to the most medial major branch of the superficial peroneal nerve, the dorsal medial cutaneous nerve. Often a very small medial branch of this nerve crosses the incision just distal to the ankle joint and must be incised for exposure. The patient should be warned before surgery that a small area of numbness may be present just medial to the incision.

  • Open the flexor hallucis longus sheath and retract the tendon medially. Retract the neurovascular bundle containing the anterior tibial artery, vein, and deep peroneal nerve laterally with the extensor digitorum longus tendons.

  • Make a straight incision in line with the skin incision in the ankle capsule and reflect the capsule medially until the medial ankle gutter is exposed and laterally until the lateral gutter is exposed.

  • Expose the dorsal talonavicular joint and remove any anterior, medial, or lateral osteophytes. If better exposure of the joint line is needed, use an osteotome to perform a more aggressive removal of the anterior osteophytes.

  • Prepare the bone for implant insertion according to the technique guide specific for the implant selected. Take care to place the implant in proper alignment in all planes for sufficient bone coverage of the prosthesis and for proper tensioning of the soft tissues and ligamentous support after final implantation. There should be a balance between choosing a thicker polyethylene insert (better for wear characteristics) and excessive bone resection and joint motion and stability.

  • Close the capsule over the prosthesis and insert a closed suction drain; close the superior extensor retinaculum over the flexor hallucis longus sheath and close the skin in layers.

  • A popliteal block is routinely used for postoperative analgesia.

Postoperative Care

At our institution, patients are typically kept overnight in the hospital and are seen by a physical therapist the following day for instruction in gait training with touch-down weight bearing. Patients with outpatient TAA have physical therapy instruction before surgery and carry out learned exercises at home. Therapy with antibiotics, binasal cannula oxygen, and deep venous thrombosis (DVT) prophylaxis with low-molecular-weight heparin is the normal postoperative protocol, although this is not typically continued after discharge unless the patient has risk factors for DVT; one aspirin daily after discharge may be beneficial. Different implants have different recommendations for postoperative care, but we typically delay weight bearing for 4 to 6 weeks and begin active ankle motion once the incision is healed, typically 2 weeks after surgery. Gradual progressive weight bearing, calf strengthening, proprioceptive training, and range-of-motion exercises are started at 4 to 6 weeks, with the ankle protected in a prefabricated walking boot. A light ankle brace is applied at 8 to 10 weeks, and full activities are allowed at 3 months, or when the calf muscles are fully rehabilitated. No restrictions are placed on the patients’ activities or sports programs, but they are encouraged to avoid impact exercises for conditioning.

Considerations for Adjunctive Procedures

Deformity Correction

Osteoarthritic ankles considered for arthroplasty should have minimal periarticular deformity, or this deformity should be correctable with osteotomy or arthrodesis.

Determination of the site of the deformity is mandatory. Bonasia et al. characterized deformities as varus or valgus, incongruent or congruent ( Table 10.2 ). In the valgus ankle and hindfoot, the following procedures should be considered: medial displacement osteotomy of the calcaneus (see Technique 83.7 ), Cotton osteotomy of the medial cuneiform or selective arthrodesis of the medial midfoot (see Techniques 83.8 and 85.5 ), subtalar arthrodesis with or without talonavicular arthrodesis (see Technique 85.6 ), posterior tibial tendon reconstruction with tendon transfer (see Technique 83.2 ), and closing wedge osteotomy of the distal tibia (see Technique 58.10 ). Demetracopoulos et al. evaluated 80 patients with preoperative valgus deformities of at least 10 degrees (average of 15 degrees). After TAA, the average postoperative deformity was 1.2 degrees, with significant improvements in VAS, SF-36, American Orthopaedic Foot and Ankle Society (AOFAS), and Short Musculoskeletal Function Assessment (SMFA) scores. The authors concluded that correction of coronal alignment could be obtained and maintained in patients with moderate-to-severe preoperative valgus malalignment. Lee et al. compared intermediate and long-term outcomes of TAA in 144 ankles with preoperative varus, valgus, or neutral alignment. Outcomes similar to those in ankles with neutral alignment were obtained in ankles with varus or valgus malalignment of up to 20 degrees when neutral alignment was achieved with TAA.

TABLE 10.2
Ankle Joint Pathologies That Include Distal Tibial Articular Surface Malalignment, Talar Tilt due to Ligamentous Instability, or Both
Modified from Bonasia DE, Dettoni F, Femino JE, et al: Total ankle replacement: When, why, and how?, Iowa Orthop J 30:119–130, 2010.
Deformity Type Abnormal Angles
Varus tibial deformity-congruent joint Increased LDTA, CORA at the level of tibial articular surface, normal tibial-talar angle
Valgus tibial deformity-congruent joint Increased LDTA, CORA at the level of tibial articular surface, normal tibial-talar angle
Varus tibial deformity-incongruent joint Decreased LDTA, CORA at the level of tibial articular surface, tibial-talar angle >10 degrees
Valgus tibial deformity-incongruent joint Increased LDTA, CORA at the level of tibial articular surface, tibial-talar angle >10 degrees
Incongruent joint Normal LDTA, tibial-talar angle >10 degrees
ADTA , Anterior distal tibial angle, sagittal plane—increased ADTA represents recurvatum deformity; CORA , center of rotation of angulation, at or proximal to joint line; LDTA , lateral distal tibial angle, coronal plane—decreased LDTA represents varus deformity; T-T angle—angle formed by tibial and talar articular surfaces: >10 degrees = incongruent joint.

For the varus ankle, procedures to consider include deltoid ligament release or sliding osteotomy of the medial malleolus, opening wedge osteotomy of the distal tibia (see Technique 11.1 ), Dwyer closing wedge osteotomy of the calcaneus (see Technique 87-11 ), dorsiflexion osteotomy of the first metatarsal (see Technique 84-19 ), and subtalar, double, or triple arthrodesis (see Chapter 85 ).

Varus deformity of the distal tibia above the level of the joint is best treated with supramalleolar osteotomy. Varus deformity of the tibial plafond at the joint from erosion of the medial malleolus or medial subchondral bone can be corrected by accurate placement of the tibial cut. Joo and Lee reported satisfactory clinical and radiographic outcomes in patients with moderate and severe varus deformities similar to those in patients with neutral alignment when postoperative neutral alignment was obtained, and special care was taken to correct causes of the varus malalignment with additional procedures.

For the varus unstable ankle with deformity below the level of the joint, sometimes an osteotomy of the hindfoot is required ( Fig. 10.8 ). If instability persists intraoperatively, a lateral ligament reconstruction should be done. Judicious release of the deltoid ligament, especially the deep deltoid ligament, may be wise in this setting. To avoid devascularization of the talus by injury to the deltoid branch of the posterior tibial artery, a sliding osteotomy of the medial malleolus has been described, with or without fixation. Reddy et al. reported correction of coronal plane deformity without osteotomy in ankles with an average of 18 degrees of varus. Deltoid release was necessary for all ankles with more than 18 degrees of varus deformity, and all ankles with more than 25 degrees of varus developed recurrent deformity. Hobson et al. suggested that TAA could be safely done with up to 30 degrees of coronal plane deformity. In their short-term follow-up of 103 patients with severe varus deformities, Sung et al. found that those with more than 20 degrees of varus deformity had outcomes similar to those with varus deformities of less than 20 degrees, with no significant differences in postoperative complications or implant failures. Adjunctive procedures, such as osteotomy, ligament release or lengthening, and tendon transfers, were done as needed. In the comparison study of Lee et al., adjunctive procedures were required in 71% of ankles with varus deformities, in 56% of those with valgus deformities, and in 39% of those with neutral alignment. Percutaneous Achilles tendon lengthening and release of the medial deltoid ligament were the most frequently done concomitant procedures; calcaneal osteotomy was done in five ankles (three in the varus group and two in the valgus group).

FIGURE 10.8, A and B, Calcaneal osteotomy and midfoot arthrodeses were required to correct pes planus deformity before total ankle arthroplasty.

Tan and Myerson divided varus ankle deformities into anatomic levels and described procedures for correction at each level. For extraarticular deformity above the ankle joint, they recommended a medial opening wedge osteotomy or, for severe ankle arthritis, a dome osteotomy. With a medial opening wedge osteotomy, they recommended a staged procedure in which total ankle replacement is done later. The dome osteotomy is useful for multiplanar supramalleolar deformity and can usually be done simultaneously with replacement ( Fig. 10.9 ). For deformity at the level of the ankle joint and a congruent joint, a “neutralizing” distal tibial cut may be all that is needed for realignment. A wedge of the distal tibia is removed with minimal bone resection at the eroded medial plafond and a larger resection at the lateral plafond. For a severely tilted talus, additional procedures are required, including the removal of osteophytes from the lateral gutter and a lateral ankle stabilization procedure. Medial-side releases of the deltoid and posterior tibial tendon have been described, but Tan and Myerson recommended a lengthening medial malleolar osteotomy, as described by Doets et al. ( Fig. 10.10 ), rather than soft-tissue releases, because it allows controlled lengthening of the medial side of the ankle and provides reliable bony healing. With more severe varus tilt of the talus with a markedly dysplastic medial malleolus and incongruent joint, a useful alternative osteotomy is the medial tibial plafondplasty, which is done as a separate, staged procedure before ankle replacement. Residual heel varus that remains after component implantation can be corrected with a lateralizing calcaneal osteotomy. Combined deformities are generally best treated with correction of the deformities, followed by a staged ankle arthroplasty. Supramalleolar deformities are corrected first, followed by correction of hindfoot and forefoot varus and any ligamentous reconstruction needed.

FIGURE 10.9, Dome osteotomy and ankle replacement done at the same time. A , Osteotomy is marked with electrocautery and completed. B , Osteotomy is then stabilized with an anterior plate placed superior to the tibial component. C , Total ankle components are then implanted in the usual fashion.

FIGURE 10.10, Medial malleolar lengthening osteotomy. A, Ankle with incongruent varus deformity. B , After implantation of a mobile-bearing prosthesis and correction of the deformity by medial malleolar osteotomy.

Dome Osteotomy for Correction of Varus Deformity Above the Ankle Deformity

Technique 10.2

(Tan and Myerson)

  • Make an anterior midline incision, which also will be used for implantation of the total ankle prosthesis.

  • Use cautery to carefully mark out the planned dome osteotomy, placing the center of the radius of curvature of the dome at the center of rotation of angulation.

  • Make sure the cut will allow adequate room for the tibial prosthesis and its stem after internal fixation of the osteotomy.

  • Drill multiple bicortical holes along the planned osteotomy and connect them with an osteotome to complete the osteotomy ( Fig. 10.11A ).

    FIGURE 10.11, Intraoperative fluoroscopy views of medial malleolar osteotomy. A , Plane of the osteotomy is planned with a Kirschner wire and completed. B , Next, it is provisionally fixed with cannulated wires. C , The wires are replaced with cannulated screws after the prosthesis is implanted. SEE TECHNIQUE 10.2 .

  • Manipulate the distal fragment in the coronal and sagittal planes to correct the deformity.

  • Stabilize the osteotomy with an anterior plate and screws ( Fig. 10.11B, C ).

  • Proceed with TAA in the usual fashion

  • Inflate the tourniquet after the arthrotomy and before preparation of the osseous surfaces.

Medial Tibial Plafondplasty for Varus Deformity at the Ankle Joint

Technique 10.3

(Tan and Myerson)

  • Make a medial incision along the subcutaneous border of the tibia.

  • Insert a guide pin in the medial tibia, aimed to exit at a point in the plafond just medial to the midpoint where the articular erosion ends. This acts as a guide for the planned osteotomy.

  • Under fluoroscopic guidance, insert three additional Kirschner wires parallel to and 6 mm above the joint line in the subchondral bone of the distal tibia. These wires prevent violation of the articular surface by the oscillating saw used to make the osteotomy.

  • Use an oscillating saw to make the osteotomy to the level of the three Kirschner wires and insert a broad osteotome to hinge open the osteotomy.

  • Hinge the medial malleolar fragment downward to restore a more normal morphology of the ankle mortise.

  • Debride the lateral gutter to facilitate realignment and to obtain lateral-sided stability, which may require an additional lateral-sided reconstruction.

  • Hold the osteotomy open with a lamina spreader and pack it tightly with bone graft.

  • Fix the osteotomy with a plate and screws.

Ligament Considerations

Ligament stability is also imperative for optimal outcome, especially with less constrained designs. Some stability can be obtained intraoperatively by proper selection of implant and polyethylene thickness, but occasionally collateral ligament reconstruction should be done.

Techniques for the reconstruction of a chronically unstable ankle are discussed in Chapter 90 . Coetzee, however, reported that the usual “anatomic” lateral ligament reconstruction techniques were not satisfactory with TAA. He described a simple, nonanatomic reconstruction to provide a strong checkrein against inversion and to limit anterior translation of the ankle (Technique 10.4).

Medial reconstruction of the deltoid ligament with TAA is uncommon, but sometimes necessary, in late-stage posterior tibial tendon insufficiency (see Chapter 83 ). Correction of hindfoot valgus with osteotomy and/or arthrodesis may provide enough mechanical support to allow stability of the ankle prosthesis. Reconstruction of the deltoid ligament in this setting is an advanced procedure, and complications are not uncommon. Arthrodesis of the ankle may be advisable.

Reconstruction of Lateral Ankle Ligaments for Chronic Instability as an Adjunct to Total Ankle Arthroplasty

Technique 10.4

(Coetzee)

  • After implantation of the ankle components, perform a modified Broström reconstruction of the lateral ligaments (see Technique 90.2 ).

  • Make a separate incision to expose the lateral side of the ankle and the peroneal tendons. Harvest one half of the peroneus brevis tendon. If the tendon has signs of a pathologic process or a tear, harvest the entire tendon to ensure maximal strength. Leave the distal attachment intact and harvest the tendon as far proximal as possible.

  • Route the peroneus brevis tendon over the modified Broström repair from the lateral side of the ankle to the anterolateral tibia.

  • Secure the tendon under adequate tension to the tibia with a staple.

  • Test the stability of the ankle to be sure that equal medial and lateral joint movements are possible.

Often, patients with arthritis of the ankle have a concomitant contracture of the triceps surae and may benefit from a lengthening procedure. Assessment of a contracture may be difficult in a stiff, arthritic ankle, but should be attempted after placement of the components. To regain ankle extension, either a smaller polyethylene component can be used, or a lengthening procedure can be done. Most patients with a significant contracture require a gastrocnemius recession (Vulpius) rather than a triple hemi-section; however, Queen et al. found equivalent outcomes with the two procedures. Patients with either lengthening procedure had better outcomes than those with TAA alone.

Special Circumstances

Inflammatory Arthritis

Patients with rheumatoid arthritis commonly have involvement of the foot and ankle, with severe pain and functional limitations. Arthrodesis has been the standard procedure for these patients, but more recently arthroplasty is being chosen because of the ability to preserve motion and decrease stress on the midfoot and subtalar joints. Early results of TAA in these patients were disappointing, with high complication rates and component loosening in as many as 75%. More recent studies, with the use of newer techniques and implants, report better outcomes. Kraal et al. had a cumulative incidence of failure at 15 years of 20% in 76 rheumatoid patients with mobile-bearing total ankle replacement. Pedersen et al. found similar outcomes in 50 patients with rheumatoid arthritis compared with a matched cohort of 50 patients with noninflammatory arthritis, although the noninflammatory arthritis group reported better function at final follow-up. Revision rates were 12% in the rheumatoid arthritis group and 10% in the noninflammatory arthritis group. Other studies have documented reliable pain relief and good functional results with uncemented prostheses and cemented two-piece and three-piece implants in patients with rheumatoid arthritis.

Obesity

Obesity (body mass index [BMI] >30) is a growing problem that affects all types of orthopaedic surgery, including total joint replacement. Many patients with arthritis of the ankle are sedentary and obese, and this poses a dilemma for the surgeon, who must weigh the possibility of providing significant pain relief against the likelihood of implant failure caused by increased stress on the implant from extra weight. Outcomes of TAA in obese and morbidly obese (BMI >40) patients reported in the literature are varied. Schipper et al. compared outcomes in obese and nonobese patients and found that obese patients had an increased long-term risk of implant failure and a significantly decreased 5-year implant survivorship, whereas Bouchard et al. found no significant difference in the proportion of complications or revisions in a similar comparison study. Barg et al. also reported comparable survivorship (93% at 6 years), as well as significant pain relief and functional improvement in obese patients. In a series of 455 patients, including 266 with BMI of less than 30 (control), 116 with a BMI between 30 and 35, and 73 with a BMI of over 35, Gross et al. found no difference in complication, infection, or failure rates. Although obese patients had lower functional outcome scores, they did have significant functional and pain improvements after TAA. Although we have no definitive upper limit on weight for this procedure, a BMI over 40 is a reason for caution and careful patient counseling. Morbidly obese patients are strongly encouraged to use a bracing system to provide a measure of pain relief while they actively work on weight loss.

Diabetes

Perhaps no other medical condition affects decision making in foot and ankle surgery as much as diabetes. It has been shown to be a factor contributing to complications, particularly infection, after a variety of orthopaedic procedures. In their review of a national database, Schipper et al. found that diabetes was independently associated with a significantly increased risk of perioperative complications, nonhome discharge, and length of hospital stay after TAA and ankle arthrodesis. Gross et al., however, compared outcomes of TAA in 50 patients with diabetes with those in 55 patients without diabetes and found no significant differences in secondary operations, revisions, or failure rates. Although patients with diabetes were heavier and had worse ASA preoperative grades, they did not have significantly different rates of complications or infections, and all had pain relief and improved function. Findings that support the use of TAA in diabetic patients include hemoglobin A1C consistently less than seven, no evidence of peripheral neuropathy, normal vascular status, normal weight (or at least not morbid obesity), and no other target organ disease (retinopathy or nephropathy).

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