Friday, April 22, 2011

Posted on the ORTHOSuperSite April 18, 2011
‘Encouraging’ intermediate results seen with meniscal allograft transplantation

SAN FRANCISCO — A minimum 7-year follow-up revealed a high mean satisfaction score among patients who underwent meniscal allograft transplantation.

Brian J. Cole, MD, MBA, presented his group’s findings at the 2011 Annual Meeting of the Arthroscopy Association of North America.

Cole also reported that the procedure could reduce pain, increase range of motion and improve joint function in the long term.

Retrospective review

Brian J. Cole, MD, MBA
Brian J. Cole

Cole and his colleagues retrospectively reviewed prospectively collected data on patients who were meniscus deficient and underwent meniscal allograft transplantation at a single center between Nov. 1997 and July 2002. The patients had a minimum follow-up of 7 years.

The investigators compared preoperative subjective data and findings from physical examinations to follow-up findings. They assessed bone plug/bridge healing and joint space integrity through radiographic evaluation when images were available. They also evaluated patients using SF-12 physical and mental, Lysholm, IKDC and KOOS scores. Patients were also asked to rate their overall satisfaction with the procedure and relate whether they would undergo the surgery on their contralateral knee given similar circumstances.

Improved scores

In all, 22 patients with a mean follow-up of 8.49 years were included in the study. The cohort showed statistically significant improvements in postoperative subjective scores, with a mean postoperative satisfaction rate of 8.8 out of 10. Furthermore, nearly 91% of patients asserted they would, given similar circumstances, undergo the surgery on their contralateral knee. Investigators also found that the patients sustained measured improvements through 2-, 4-, and 7-year postoperative follow-ups.

Meniscal allograft transplantation improved upon preoperative scores whether the procedure was performed concomitantly or in isolation. A comparison of patients over a body mass index of 25kg/m2with those under that mark showed no differences in outcomes. Minimal patellofemoral joint tenderness and effusion were found on follow-up, Cole reported, and patients displayed a near-normal range of motion. Radiographic evaluations, he added, displayed successful bony integration of the bone plugs/bridge from the allograft meniscus.

Though the results were “encouraging,” Cole said further research is necessary to understand the efficacy of allograft meniscus transplantation in preventing the advance of osteoarthritis and maintaining higher levels of function.

“Certainly we can improve this study with a larger cohort, and we are doing that as we speak,” Cole concluded. “Combined vs. isolated procedures really have to be looked at as a breakout to give us a little more insight into why patients are achieving benefits. Obviously, we want to continue to achieve longer follow-up to see when these things will finally break down and fail, because ultimately they will do so.”

For further information: http://www.orthosupersite.com/view.aspx?rid=82750

Posted on the ORTHOSuperSite April 19, 2011

Study identifies predictors of failure after ACL reconstruction in young athletes

SAN FRANCISCO — Investigators from Pittsburgh have found a 13% failure rate after anatomic ACL reconstruction using allograft in young athletes.

The findings, which were presented by Carola Francisca Van Eck, MD, at the 2011 Annual Meeting of the Arthroscopy Association of North America, noted that failure could be associated with a younger patient age, an earlier return to sport and a heavier body weight.

“The purpose of this specific study was to determine the failure rate after anatomic single- and double-bundle ACL reconstruction with allograft and to identify factors associated with failure,” Van Eck said.

A prospective cohort study

The investigators performed a prospective cohort study involving 206 patients who underwent a total of 38 single- and 168 double-bundle ACL reconstructions with allograft between Jan. 2007 and Dec. 2009. Eighty percent of patients had at least 9 months follow-up. The patients had an average age of 24 years and an average body mass index of 24.5. The average return to competition after reconstruction was 263 days.

For the study, the authors defined failure as a subjective episode of instability, clinical examination revealing abnormal laxity, and/or an MRI or arthroscopic diagnosis of rupture or the absence of the ACL graft.

Overall, 13% of patients had graft failure. On average, patients in the double-bundle group who had a failure were younger (19 years vs. 25 years old) and had returned to competition earlier (222 days vs. 267 days). Four patients (11%) in the single-bundle group failed, Van Eck added. These patients were younger (19 years vs. 24 years old) and heavier (83 kg vs. 65 kg).

Longer to heal

“When we looked at our time to failure, we noticed that 48% of the subjects who failed did so before the 9-month mark, when we cleared them to return to sports, and an additional 44% in the first 9 months after returning to sports,” Van Eck said.

Van Eck noted that modifications in postoperative rehabilitation may be necessary in conjunction with modifications in return-to-sport protocol when dealing with patients who have had an anatomic ACL reconstruction.

“The relatively high observed failure rate in our study might be due to the exclusive use of allograft,” she concluded. “Allograft-reconstructed ACL may take longer to heal than when autograft is used. This means that we may need to evaluate graft healing — for example, using MRI — or we may need to enhance healing using tools such as fibrin clot or [platelet-rich plasma].”

For further information: http://www.orthosupersite.com/view.aspx?rid=82804

Posted on the ORTHOSuperSite April 15, 2011

No benefit of platelet-rich plasma found for rotator cuff healing

SAN FRANCISCO — Using autologous platelet-rich plasma at the time of rotator cuff repair fails to have a significant positive impact on healing time as determined by ultrasound observation, according to a study presented here.

The findings were presented by Don A. Buford, MD, at the 2011 Annual Meeting of the Arthroscopy Association of North America.

Buford and colleagues concluded that the addition of platelet-rich plasma (PRP) administered in a single dose at the time of rotator cuff repair using a single-row triple-loaded suture anchor showed no benefit in healing tears measuring up to 3 cm.

Prospective study

Don A. Buford, MD
Don A. Buford

The investigators performed a prospective study involving 100 patients with 3 cm tears in length or smaller who were allocated into two groups. The first group received 5 to 6cc of PRP at the tendon-bone interface at the conclusion of repair. The PRP, in this case, was autologous and prepared with a commercially-available kit. The second cohort of 50 patients did not receive PRP during treatment.

All tears involved either the supraspinatus tendon only or the supraspinatus and infraspinatus tendons, and all were repaired with at least one triple-loaded metal suture anchor. The study noted that if the tear pattern warranted further treatment, additional suture anchors and/or side-to-side sutures were also used.

Postoperative evaluations occurred in-office and consisted of shoulder ultrasound at 6 weeks, 3 months and 6 months.

“Our primary criteria, because there really is not anything in the literature to guide us, was restoration of the rotator cuff footprint lateral to our suture anchor line,” Buford said. “We wanted to see normal ultrasound signal in the tissue and no significant fluid in the subacromial bursa.”

No significant difference

Buford reported 48 of the 50 patients who received PRP went on to experience normal tendon healing with a mean duration of 16.5 weeks. Forty-seven of the patients who did not receive PRP went on to experience normal tendon healing with a mean duration of 14.5 weeks. These results were found through ANOVA statistical analysis and Tukey Value findings to be statistically insignificant, Buford noted.

“We did not find a statistically significant difference in rotator cuff healing with the addition of PRP and, in fact, our trend was actually toward more rapid healing without the addition of PRP, which is something we had not really considered," Buford said. "It may warrant further investigation.”

Buford added he would like to perform further studies for the purpose of finding a cohort that would benefit from the use of PRP.

For further information: http://www.orthosupersite.com/view.aspx?rid=82676

Nanofibrous hollow microspheres self-assembled from star-shaped polymers as injectable cell carriers for knee repair

Nature Materials
10,
398–406
(2011)
doi:10.1038/nmat2999
Received
Accepted
Published online
http://www.nature.com/nmat/journal/v10/n5/abs/nmat2999.html

Thursday, April 7, 2011

Posted on the ORTHOSuperSite March 10, 2011
Better results seen with hamstring autografts than patellar tendon grafts 15 years after ACL reconstruction

SAN DIEGO — Patients who underwent ACL reconstruction with patellar tendon autograft displayed significantly worse outcomes at 15 years postoperative than those reconstructed with four-strandhamstring tendon, according to results of a study presented here.

Leo A. Pinczewski, MBBS, FRACS, presented the findings at the 2011 American Orthopaedic Society for Sports Medicine Specialty Day Meeting.

Pinczewski and colleagues compared the results of 90 consecutive patients with isolated ACL ruptures who underwent hamstring tendon repair with a cohort of 90 patients who had the same injury and underwent patellar tendon repair using the same surgical technique.

The investigators assessed the groups at 2, 5, 7, 10 and 15 years. These assessments included the IKDC Knee Ligament Evaluation, KT-1000, Lysholm Knee Score, kneeling pain, radiographic evaluation and other clinical outcomes.

“After 15 years, significant differences emerge,” Pinczewski said. At the 15-year mark, he noted that patients who received the patellar tendon graft displayed significantly worse outcomes than those who received hamstring tendon repair regarding radiologically-detectable osteoarthritis, motion loss, the single-leg hop test, participation in strenuous activity and kneeling pain.

No significant differences were reported between the groups regarding laxity and overall IKDC grade.

ACL graft rupture occurred in 16% of patients in the hamstring tendon group and 8% of patients in the patellar tendon group. In the study, these ruptures were associated with male patients and non-ideal tunnel position.

Pinczewski also noted that contralateral ACL rupture occurred in more patellar tendon patients than hamstring tendon patients (24% vs. 12%), and these occurrences were associated with patients younger than 18 years old.

For further information: http://www.orthosupersite.com/view.aspx?rid=81404



ORTHOPEDICS March 2011;34(3):186.
Arthroscopic Hip Surgery for the Treatment of Femoroacetabular Impingement
by J.W. Thomas Byrd, MD

In this issue of ORTHOPEDICS, Dr Byrd discusses the importance of patient selection in arthroscopic hip surgery and its use in adolescents and athletes.

In addition to being less invasive, what advantages exist for arthroscopy vs open treatment methods?

The obvious advantage of arthroscopy is that it is less invasive. However, the arthroscopic approach to femoroacetabular impingement is much more than just the technique. Arthroscopy precisely defines the secondary damage that accompanies femoroacetabular impingement and thus is part of the treatment algorithm for determining that bony correction of the impingement is necessary. Many patients may have impingement morphology without impingement pathology. What this means is that many people who have oddly shaped hips pursue long, active lifestyles and never develop problems. Keep in mind that impingement is not a cause of hip pain. Impingement is simply a morphologic condition that predisposes the joint to the secondary damage that then results in the accompanying symptoms.

Is there any single strong predictor of symptoms of femoroacetabular impingement?

Probably the strongest predictor for femoroacetabular impingement is simply maintaining an index of suspicion. When a young adult presents with hip joint pain, the most common lesion is damage to the acetabular labrum. However, it is not normal for the labrum to tear, even in the presence of highly physical activities, and the most likely underlying culprit is a component of femoroacetabular impingement. In dancers and groups where flexibility is a premium, dysplasia may be more common because individuals with dysplasia exhibit more mobility. This mobility may be an advantage, right up to the point that the labrum and other joint structures start to break down.

When is arthroscopy not a good option for the treatment of femoroacetabular impingement?

J.W. Thomas Byrd, MD
J.W. Thomas Byrd

On average, in the hands of a surgeon experienced with arthroscopic management of impingement, most cases can be treated by this method. Having said that, there are many circumstances where the open approach is still clearly the best. Cases that require a concomitant acetabular or proximal femoral osteotomy and some extreme cases of global overcoverage are performed open.

How important is patient selection in the management of femoroacetabular impingement arthroscopically?

Like many operations, patient selection is probably the most important factor in the success of the procedure. First, does the problem require surgery at all, and is it matched for an arthroscopic solution? Second, does the patient have reasonable expectations for the given severity of damage that is being addressed? Ultimately, the success of the procedure is determined by the level of patient satisfaction, and it is important that their expectations can be reasonably met. Lastly, the patient must be ready for the rehabilitation and recovery that is necessary for a successful outcome. I tell patients that surgery is the easy part; I will take care of that for them. It is the rehabilitation and recovery effort on their part that can take 4 months or longer.

What techniques, if any, have been developed to address femoroacetabular impingement and osteoarthritis in athletes?

Numerous techniques have been developed that aid in addressing femoroacetabular impingement and osteoarthritis in athletes. Our clinical assessment skills are getting better, and imaging technology is improving to detect the damage accompanying femoroacetabular impingement. In our experience, >90% of athletes and nonathletes alike already have grade III and grade IV articular damage at the time of arthroscopic intervention. This tells us that we are intervening late in the disease course. Earlier intervention would be preferable, although we have to be cautious about not recommending surgery in asymptomatic individuals. Instruments are available for reshaping the acetabulum and the femoral head to correct the impingement problem. The labrum has been found to have excellent healing capacity, and labral repair techniques have really blossomed. Our biggest challenge remains what to do about the articular surface. Microfracture has been a tried-and-true method, but it is still imperfect. Numerous articular cartilage restorative techniques remain in the works.

Is hip arthroscopy a safe procedure in adolescents with femoroacetabular impingement?

Impingement can first start to manifest itself in adolescence, shortly after skeletal maturity. This is especially true among athletes who are pushing their bodies beyond the diminished physiologic limits imposed by femoroacetabular impingement. Substantial secondary damage is sometimes encountered, even among teenagers. Arthroscopy is just as safe in this population as in mature adults. Of course, numerous precautions are necessary in those who have not yet reached skeletal maturity. The eventual outcome of impingement has usually not been fully determined yet, and any surgery must take into account the risk of altering skeletal growth.

Is there any way to predict the future occurrence of osteoarthritis following hip arthroscopy?

Although no precise statistical data exists, the risk of future osteoarthritis is probably most closely tied to the severity of articular damage at the time of arthroscopic intervention. Thus, earlier detection and intervention still seems preferable once someone’s problem has declared itself.

What is on the horizon for the arthroscopic treatment of femoroacetabular impingement?

The 2 biggest technical challenges with treatment of impingement are the precision with which the bony correction is performed and

knowing exactly what is the right amount of bone to remove. Computer assistance in assessing the morphology of the impingement problem and intraoperative navigation for its correction are on the immediate horizon. Presently, we are forced to make these surgical corrections freehand, and no one knows exactly the precise amount of bone to remove. Computer assistance is close in the future. We do not perform joint replacement surgery without preoperative templates and intraoperative jigs. In the near future, computer assessment will be our templating, and computer navigation will be our intraoperative jigs. It will not be long before we reflect back on these days when we performed this freehand. We are doing okay, but we can and need to do much better.

For further information: http://www.orthosupersite.com/view.aspx?rid=80983

ORTHOPEDICS April 2011;34(4):272.
Ankle Fusion Stability: A Biomechanical Comparison of External Versus Internal Fixation
by Justin R. Hoover, MD; Robert D. Santrock, MD; William C. James, MD

Abstract

This biomechanical study compares bimalleolar external fixation to conventional crossed-screw construct in terms of stability and compression for ankle arthrodesis. The goals of the study were to determine which construct is more stable with bending and torsional forces, and to determine which construct achieves more compression.

Fourth-generation bone composite tibia and talocalcaneal models were made to 50th percentile anatomic specifications. Fourteen ankle fusion constructs were created with bimalleolar external fixators and 14 with crossed-screw constructs. Ultimate bend, torque, and compression testing were completed on the external fixator and crossed-screw constructs using a multidirectional Materials Testing Machine (MTS Systems Corp, Eden Prairie, Minnesota). Ultimate bend testing revealed a statistically significant difference (P=.0022) with the mean peak load to failure for the external fixator constructs of 973.2 N compared to 612.5 N for the crossed-screw constructs. Ultimate torque testing revealed the mean peak torque to failure for the external fixator construct was 80.2 Nm and 28.1 Nm for the crossed-screw construct, also a statistically significant difference (P=.0001). The compression testing yielded no statistically significant difference (P=.9268) between the average failure force of the external fixator construct (81.6 kg) and the crossed-screw construct (81.2 kg).

With increased stiffness in both bending and torsion and comparable compressive strengths, bimalleolar external fixation is an excellent option for tibiotalar ankle arthrodesis.

Ankle arthrodesis has historically been the mainstay of surgical treatment of end-stage ankle arthrosis. Various constructs have been described to create a stable tibiotalar fusion. Open tibiotalar joint preparation with internal crossed-screw fixation is widely used. However, other options are available, and less invasive procedures are particularly useful in patients with a history of infection, poor soft tissue quality, or poor wound-healing capabilities. Open crossed screw construct, plating, intramedullary nail, and external fixation to obtain fusion are described in the literature, and many biomechanical studies have been performed.1-13 The basic premise remains the same: no matter what type of fixation is chosen, stability and compression are needed for successful fusion. It is for this reason that the biomechanical properties of different techniques and constructs continue to be investigated with the goals of improving stability and, in turn, patient outcomes.

In this study, we compared traditional crossed-screw fixation to bimalleolar external fixation in bending, torsion, and compression. Bimalleolar external fixation was originally described by Charnley in 1951.5Since that time, use of these constructs has been relatively limited. Recently, external fixation has gained interest due to the perceived stability. Our hypothesis for this study was that bimalleolar external fixation is superior to crossed-screw technique in bending strength, torsional strength, and compression.

Materials and Methods

Fourth-generation bone composite replicated tibia and talocalcaneal constructs were made to 50th percentile human anatomic specifications.14,15 These constructs have been shown to be comparable to natural bone in terms of their biomechanical properties.14 Each construct was cut precisely to replicate the average human ankle and foot size, therefore giving the appropriate lever arms during mechanical testing. The tibial construct was 40×40×180 mm. The talocalcaneal foot construct block was 40×60×173 mm with a trapezoid talar dome 10 mm in height and a tibiotalar contact surface of 40×25 mm.

A total of 28 constructs were built for mechanical testing. Fourteen external fixation constructs were created using Sidekick Stealth bimalleolar external fixators (Wright Medical Technology, Inc, Arlington, Tennessee). Fourteen conventional crossed-screw fixation constructs were created using 6.5-mm Darco partially threaded cannulated screws (Wright Medical Technology, Inc).

To create the external fixator constructs, four 4.0×300-mm transfixing external fixator pins were inserted in standard fashion in the constructs’ talar neck, calcaneus, and proximal and distal tibia. The talar neck pin was placed 25 mm plantar to the talar dome surface and 15 mm anterior. The calcaneal pin was placed 15 mm proximal to the plantar surface and 15 mm anterior to the posterior aspect of the calcaneal block. The distal tibial pin was placed 30 mm proximal to the construct plafond and 12 mm posterior to the anterior tibial crest. The proximal tibial pin was placed 90 mm proximal to the construct plafond and 20 mm posterior to the anterior tibial crest. The medial and lateral Sidekick Stealth external fixator frames were then placed 32 mm from the medial and lateral edge of the composite bone (Figure 1).

Figure 1: Bimalleolar external fixator constructFigure 2: Bimalleolar external fixator construct
Figure 1: Bimalleolar external fixator construct. Figure 1: Bimalleolar external fixator construct.

The internal fixation crossed-screw constructs were built by predrilling the tibial and talocalcaneal constructs with a 4.4-mm drill bit. This was followed by countersinking the tibial composite bone. Two 6.5×70-mm Darco partially threaded headed screws were placed in standard crossed screw construct from the medial and lateral side of the tibia construct into the talocalcaneal construct (Figure 2).

Ultimate Bend Testing

Four external fixator and 4 crossed-screw constructs were fashioned in the manner outlined above. The tibial component was secured to the base plate box of the multidirectional Materials Testing Machine (MTS machine; MTS Systems Corp, Eden Prairie, Minnesota). The actuator was placed on the plantar surface of the talocalcaneal construct 12.7 mm from the distal end. The MTS machine actuator applied a load at 1 mm per second with data acquisition at 50 Hz until failure. Data was recorded in newtons of force. Failure was defined as a drop in the load (caused by composite fracture, screw pullout, or brace plate fracture).

Ultimate Torque Testing

Four external fixator and 4 crossed-screw constructs were fashioned in the manner outlined above. The tibial component was secured to the base plate box of the multidirectional MTS machine. The actuator was placed on the plantar surface of the talocalcaneal construct in line with the center of the talar dome. The MTS machine actuator applied a load of 1° per second with data acquisition at 25 Hz until failure. Data was recorded in newton-meters. Failure was defined as a drop in the load (caused by composite fracture, screw pullout, or brace plate fracture).

Compression Testing

Six external fixator and 6 crossed-screw constructs were fashioned in the manner outlined above with the exception of placing a 6.35-mm Load Washer Load Cell (Interface, Inc, Scottsdale, Arizona) and a 76.2×76.2×0.8-mm aluminum plate between the tibial and talocalcaneal composite bone (Figure 3). The external fixator talocalcaneal pins were tightened in a static position both medially and laterally. The tibial component was advanced proximally by turning each of the 4 nuts one-quarter turn. Measurements at each one-quarter turn were made in kilograms of force. This was completed until failure. The crossed-screw compression was measured similarly. The crossed screws were set when the underside of the screw head contacted the composite bone material. Once this contact was made, each screw was tightened one-quarter turn, and kilograms of force measurements were made after each one-quarter turn until failure. The number of turns and kilograms of force were recorded. Failure was defined as fracture of the composite bone material in the crossed-screw construct and damage to the articulating bar threads leading to inability to advance the nuts on the medial and lateral braces in the external fixator group.

Figure 3: Compression testing model with transducer
Figure 3: Compression testing model with transducer.

It is to be noted that only 5 external fixator constructs were analyzed, as external fixator sample 1 was loaded without the aluminum plate and therefore was not equivalent to the other constructs and was eliminated from the data. The aluminum plate was necessary to insert because the ring transducer embedded into the composite bone when compressed.

Statistical Analysis

The mean, maximum, minimum, and standard deviations of each parameter at failure were calculated. Student t test was used to compare the external fixation group to the crossed-screw construct group. Statistical significance level was set at P<.05.

Results

The mean peak load to failure for dorsiflexion for the external fixator was 973.2±109.5 N and for the crossed-screw construct was 612.5±89.2 N, which was a statistically significant difference (P=.0022) (Table 1, Figure 4).

Table 1: Ultimate Bend (Dorsiflexion) Peak Load

Figure 4: Peak load
Figure 4: Peak load (n=4).

The mean bending stiffness of the composite tibiotalar joint for each condition is shown in Table 2. The Stealth external fixator yielded a bending stiffness of 34,373±2017 Nm, and the Darco crossed-screw construct was 26,285±1416 Nm, which is a statistically significant difference (P=.0006) (Table 2, Figure 5).

Table 2: Bending Stiffness

Figure 5: Bending stiffness
Figure 5: Bending stiffness (n=4).

Ultimate torque testing revealed the mean peak torque to failure for the external fixator construct was 80.2±11.5 Nm and the crossed-screw construct was 28.1±3.0 Nm. This was a statistically significant difference (P=.0001) (Table 3, Figure 6).

Table 3: Peak Torque

Figure 6: Mean peak torque
Figure 6: Mean peak torque (n=4).

The mean torsional stiffness for the external fixator construct was 3.09±0.10 Nm/degree. The crossed-screw construct mean torsional stiffness was 1.36±1.04 Nm/degree. This was a statistically significant difference using the t test (P=.0324) (Table 4, Figure 7).

Table 4: Torsional (External Rotation) Stiffness

Figure 7: Torsional stiffness
Figure 7: Torsional stiffness (n=4).

Compression testing yielded no statistically significant difference (P=.9268) between the average failure force of the external fixation (81.6 kg) and the crossed screws (81.2 kg). The external fixator failure mode was the nut would not advance further due to damage of the articulating bar threads. Four turns of each nut was the average number of turns to failure. The failure mode for all Darco crossed-screw constructs was fracture of the composite bone. The average number of screw turns was 1.5 turns after the screw was seated (Table 5).

Table 5: Compression Testing

Discussion

Ankle arthrodesis is a valuable procedure for end-stage ankle arthrosis. Multiple techniques have been described, including internal and external fixation. Numerous clinical studies have shown internal crossed screw construct as advantageous due to high rates of fusion, decreased rates of infection, and improved patient comfort.1-13 However, in many cases external fixation may be a more appropriate means of facilitating fusion. Ring external fixators have been shown to be a viable option to establish fusion and is particularly useful in cases of past infection, poor wound-healing capabilities, or decreased bone stock.10 To our knowledge, no study has compared a compression arthrodesis technique using bimalleolar external fixation to crossed screws. Our hypothesis was that bimalleolar external fixation is a more rigid construct with regard to bending strength (dorsiflexion), torsional strength, and compression than crossed screws.

Our results revealed statistically significant differences in both bending forces (P=.0022) and torsional forces (P=.0001), showing that external fixation is more rigid than crossed screws. No statistical significance was seen with regard to compression.

Our study protocol had several limitations, including the use of fourth-generation bone composite, not accounting for subtalar joint involvement, space-occupying use of the load cell ring transducer, effects of musculature and ligaments, and unidirectional force measurements performed on the MTS machine at nonphysiologic rates. Our plans include performing a cadaveric study with multidirectional testing using a bimalleolar external fixator and crossed screws. These anatomic specimens will allow us to take into account the subtalar joint. Additionally, we would like to use less invasive devices to assess compression.

Conclusion

Bimalleolar external fixator is a more rigid construct in both bending and torsion as compared to conventional crossed screws. There was no significant difference between the 2 methods with regard to compression. However, with increased stiffness in both bending and torsion and comparable compressive strengths, a bimalleolar external fixator is an excellent option for tibiotalar ankle arthrodesis in the correct clinical setting. Clinical indications would include patients with a history of infection or poor soft tissue quality.6 In our practice, it is also useful for arthroscopic-assisted ankle fusions due to its minimally invasive nature; it has become our primary mode of fixation for these fusions. Biomechanical testing predicts that it has a low probability of failure due to rigidity of the construct. External fixation was found to be more rigid than a traditional lag-screw technique. These findings may extrapolate into increased fusion rate and earlier or immediate weight bearing in patients undergoing ankle arthrodesis. This would potentially reduce the associated morbidity of extended nonweight bearing while increasing patient satisfaction.

For further information: http://www.orthosupersite.com/view.aspx?rid=81555