Aims

The aim of this meta-analysis was to determine the pooled incidence of postoperative urinary retention (POUR) following total hip and knee arthroplasty (total joint replacement (TJR)) and to evaluate the risk factors and complications associated with POUR.

Aims

Despite numerous studies focusing on periprosthetic joint infections (PJIs), there are no robust data on the risk factors and timing of metachronous infections. Metachronous PJIs are PJIs that can arise in the same or other artificial joints after a period of time, in patients who have previously had PJI.

Aims

Despite numerous studies on periprosthetic joint infections (PJI), there are no robust data on the risk factors and timing of metachronous infections. This study was performed to answer the following questions: 1) Is there any difference of manifestation time of metachronous PJIs between different localizations of multiple artificial joints? 2) Can we identify any specific risk factor for metachronous PJIs for different localizations of multiple artificial joints?

Aim

The prevalence of unexpected positive cultures (UPC) in aseptic revision surgery of the joint with a prior septic revision procedure in the same joint remain unknown. The purpose of this study was to determine the prevalence of UPC in aseptic revisions performed in patients with a previous septic revision in the same joint. As secondary outcome measure, we explore possible risk factors associated with UPC and the re-revision rates.

Aims

The outcome of repeat septic revision after a failed one-stage exchange for periprosthetic joint infection (PJI) in total knee arthroplasty (TKA) remains unknown. The aim of this study was to report the infection-free and all-cause revision-free survival of repeat septic revision after a failed one-stage exchange, and to determine whether the Musculoskeletal Infection Society (MSIS) stage is associated with subsequent infection-related failure.

Aims

One-stage exchange for periprosthetic joint infection (PJI) in total hip arthroplasty (THA) is gaining popularity. The outcome for a repeat one-stage revision THA after a failed one-stage exchange for infection remains unknown. The aim of this study was to report the infection-free and all-cause revision-free survival of repeat one-stage exchange, and to investigate the association between the Musculoskeletal Infection Society (MSIS) staging system and further infection-related failure.

Aims

One-stage revision hip arthroplasty for periprosthetic joint infection (PJI) has several advantages; however, resection of the proximal femur might be necessary to achieve higher success rates. We investigated the risk factors for resection and re-revisions, and assessed complications and subsequent re-revisions.

Arthrofibrosis is a relatively frequent complication after total knee arthroplasty. Although stiffness after total hip arthroplasty (THA), because of formation of heterotopic ossification or other causes, is not uncommon, to the authors’ best knowledge, arthrofibrosis after THA has not been described. The aim of this study is to describe the arthrofibrosis of the hip after primary total hip arthroplasty using an established clinical and histological classification of arthrofibrosis.

We retrospectively examined all patients who were histologically confirmed to have arthrofibrosis after primary THA during revision surgery by examination of tissue samples in our clinic. Arthrofibrosis was diagnosed according to the histopathological SLIM-consensus classification, which defines seven different SLIM types of the periimplant synovial membrane. The SLIM type V determines the diagnosis of endoprosthesis-associated arthrofibrosis.

The study population consists of 66 patients who were revised due to arthrofibrosis after primary THA. All patients had a limitation in range of motion prior to revision with a mean flexion of 90° (range from 40 to 125), mean internal rotation of 10° (range from 0 to 40) and mean external rotation of 20° (range from 0 to 50). All patients had histological SLIM type V arthrofibrosis, corresponding to endoprosthesis-associated arthrofibrosis. Histological examination revealed that seven patients (10.6%) had particle-induced and 59 patients (89.4%) had non-particle-induced arthrofibrosis.

This is the first decription of endoprosthetic-associated arthrofibrosis after primary THA on the basis of a well-established histological classification. Our study results could enable new therapeutic and diagnostic opportunities in patients with such an arthrofibrosis. Surgeons should keep arthrofibrosis as a possible cause for stiffness and pain after primary total hip arthroplasty in mind. Level of evidence Diagnostic study, Level of Evidence IV

Thorsten Gehrke and Lara Althaus contributed equally to the writing of this manuscript.

Introduction

Despite several preventive strategies, periprosthetic joint infection (PJI) following total joint arthroplasty (TJA) is still a devastating complication. Early diagnosis and appropriate treatment are crucial to achieve successful infection control, but challenging since there is no test with 100% sensitivity and 100%. Therefore, several national and international guidelines include synovial analysis of joint aspirates as important diagnostic criteria, but cut-off levels for synovial cell count (CC) and polymorphonuclear (granulocyte) percentage (PMN%) are still debatable. The current investigation was performed to analyze the overall accuracy and optimal cut-off of synovial CC and PMN% following total knee (TKA) and total hip arthroplasty (THA).

The presence of obesity has negative influence on the progress of osteoarthritis and increases the risk of undergoing a primary THA at an earlier age. However, the correlation of BMI and the risk for postoperative complications, revision surgery and infection rate is still controversial. In the largest cohort to this date, we used the German insurance claims database to evaluate the correlation of BMI and the risk of postoperative complications, mortality and revision rates following primary THA.

Using nationwide billing data of the German health-care insurance for inpatient hospital treatment, we identified patients over the age of 20 years who had undergone either THA or short-stem THA between January 2012 and December 2014. BMI was classified into four groups (< 30 kg/m², 30 to 34.9 kg/m², 35 to 39.9 kg/m², > 40 kg/m²). In all patients, the 90-day complication, mortality and revision rates were calculated. Furthermore, all complications and revisions were determined at a latest follow-up of 1 year. We used multivariable logistic regression to model the odds of complications as a function of BMI groups. Adjusted odds ratios (OR) and 95% confidence intervals (CI) were calculated.

A total of 131,576 total hip arthroplasties in 124,368 patients were included for final analysis. BMI had a significant effect on risk adjusted 1-year overall complications, 1-year revision surgery and 90-day surgical complications. The adjusted odd ratios increased significantly with BMI category. Especially morbidly obese patients with a BMI >40 kg/m² had a threefold higher risk for deep infection and a two-fold higher risk for the overall complication and revision rates as compared to patients with a BMI <30 kg/m².

Obesity plays an important role in patients undergoing primary THA, especially patients with a BMI beyond 40 kg/m² have a markedly higher risk for revision surgery and overall complication rates. This study aims to increase awareness among physicians in order to improve risk stratifications and to better educate patients with regard to obesity and postoperative expectations prior to undergoing elective total hip arthroplasty.

Aim

Alpha-defensin was recently introduced as a new biomarker having a very high accuracy to rule out periprosthetic joint infection (PJI). A new rapid lateral flow version of the Alpha-defensin test was developed and introduced to detect high levels of Alpha-defensin in synovial fluid quickly and with ease. We conducted a single-centre prospective clinical study to compare the results of the Alpha-defensin rapid test* against the conventional diagnostics according to MSIS criteria.

Introduction

High tibial osteotomy (HTO) is a commonly used surgical technique for treating moderate osteoarthritis (OA) of the medial compartment of the knee by shifting the center of force towards the lateral compartment. The amount of alignment correction to be performed is usually calculated prior to surgery and it's based on the patient's lower limb alignment using long-leg radiographs. While the procedure is generally effective at relieving symptoms, an accurate estimation of change in intraarticular contact pressures and contact surface area has not been developed. Using electromyography (EMG), Meyer et al. attempted to predict intraarticular contact pressures during gait patterns in a patient who had received a cruciate retaining force-measuring tibial prosthesis. Lundberg et al. used data from the Third Grand Challenge Competition to improve contact force predictions in total knee replacement. Mina et al. performed high tibial osteotomy on eight human cadaveric knees with osteochondral defects in the medial compartment. They determined that complete unloading of the medial compartment occurred at between 6° and 10° of valgus, and that contact pressure was similarly distributed between the medial and lateral compartments at alignments of 0° to 4° of valgus. In the current study, we hypothesised that it would be possible to predict the change in intra-articular pressures based on extra-articular data acquisition.

Knee arthrodesis is a potential salvage procedure for limb preservation after failure of total knee arthroplasty (TKA) due to infection. In this study, we evaluated the outcome of single-stage knee arthrodesis using an intramedullary cemented coupled nail without bone-on-bone fusion after failed and infected TKA with extensor mechanism deficiency. Between 2002 and 2012, 27 patients (ten female, 17 male; mean age 68.8 years; 52 to 87) were treated with septic single-stage exchange. Mean follow-up duration was 67.1months (24 to 143, n = 27) (minimum follow-up 24 months) and for patients with a minimum follow-up of five years 104.9 (65 to 143,; n = 13). A subjective patient evaluation (Short Form (SF)-36) was obtained, in addition to the Visual Analogue Scale (VAS). The mean VAS score was 1.44 (SD 1.48). At final follow-up, four patients had recurrent infections after arthrodesis (14.8%). Of these, three patients were treated with a one-stage arthrodesis nail exchange; one of the three patients had an aseptic loosening with a third single-stage exchange, and one patient underwent knee amputation for uncontrolled sepsis at 108 months. All patients, including the amputee, indicated that they would choose arthrodesis again. Data indicate that a single-stage knee arthrodesis offers an acceptable salvage procedure after failed and infected TKA.

Cite this article: Bone Joint J 2015;97-B:649–53.

Injuries to the posterior cruciate ligament (PCL) and the posterolateral corner (PLC) of the knee remain a challenging orthopaedic problem. Studies evaluating PCL and PLC reconstruction have failed to demonstrate a strong correlation between the degree of knee laxity as measured by uniplanar testing and subjective outcome or patient satisfaction. The effect that changing the magnitude of posterior tibial slope has on multiplanar, rotational stability of the PCL-deficient knee has yet to be determined. We aimed to evaluate the effect that changes in posterior tibial slope would have on static and dynamic stability of the PCL-PLC deficient knee.

Ten knees were used for this study. Navigated posterior drawer and standardised reverse mechanised pivot shift maneuvers were performed in the intact knee and after sectioning the PCL, the lateral collateral ligament (LCL), the popliteofibular ligament (PFL) and the popliteus muscle tendon (POP). Navigated high tibial osteotomy (HTO) was performed to obtain the desired change in tibial plateau slope (+5® or −5® from native slope). We then repeated the posterior drawer and the reverse mechanised pivot shift test for each of the two altered slope conditions.

Mean posterior tibial translation during the posterior drawer in the intact knee was 1.4 mm (SD = 0.48 mm). In the PCL-PLC deficient knee, posterior tibial translation increased to 18 mm (SD = 5.7 mm) (P < 0.001). Increasing the amount of posterior tibial slope by 5® reduced posterior tibial translation to 12 mm (SD = 4.7 mm) (P < 0.01). Decreasing the amount of posterior slope by 5® compared to the native knee, increased posterior tibial translation to 21 mm (SD = 6.8 mm) (P < 0.01). There was a significant negative correlation between the magnitude of tibial plateau slope and the magnitude of the reverse pivot shift (R2 = 0.71; P < 0.0001).

Mean posterior tibial translation during the reverse mechanised pivot shift test in the intact knee was 7.8 mm (SD = 2.8 mm). In the PCL-PLC deficient knee, posterior tibial translation increased to 26 mm (SD = 5.6 mm) (P < 0.001). Increasing the amount of posterior tibial slope by 5® reduced posterior tibial translation to 21 mm (SD = 6.7 mm) (P < 0.01). Decreasing the amount of posterior slope by 5® compared to the native knee, increased posterior tibial translation to 34 mm (SD = 8.2 mm) (P < 0.01). There was a significant negative correlation between the magnitude of tibial plateau slope and the magnitude of the reverse pivot shift (R2 = 0.72; P < 0.0001).

Decreasing the magnitude of posterior slope of the tibial plateau resulted in an increase in the magnitude of posterior tibial translation during the posterior drawer and the reverse mechanised pivot shift test in the PCL-PLC deficient knee. Conversely, increasing the slope of the tibial plateau reduced the amount of posterior tibial translation during the posterior drawer and the reverse mechanised pivot shift test. However, the effect of the increase in slope was not sufficient to reduce posterior tibial translation to levels similar to those of the intact knee.

Accurate and reliable registration of the ankle center is a necessary requirement in computer-assisted TKR. There is debate among surgeons over which registration procedure more accurately reflects the true center of the ankle joint. The aim of this study was to compare two different ankle registration landmarks on radiographs and determine how much they differed from the anatomic center of the talus in the frontal plane. Specifically, we asked what the average deviation in tibial mechanical axis registration would be when registering the ankle center using: A) the extreme medial and lateral points; and B) the most distal points, of the respective malleoli. A second question was whether or not BMI had any significant effect on mechanical axis registration error.

We reviewed the preoperative hip-to-ankle radiographs of 40 patients who underwent navigated TKR at our institution. The patient cohort was composed of 32 females and 7 males, with a mean age of 69 years (range, 45–84 years) and a mean BMI of 29.9 (range, 14.7–43.3). All radiographs were stored in and reviewed using PACS.

No clinically significant divergence from the anatomic center of the ankle was seen when using the Extremes Midpoint technique (mean divergence = 0.2® lateral; SD = 0.5®; 95% CI = −0.3®, −0.1®) or the Distal Midpoint technique (mean divergence = 0.2® lateral; SD = 0.6®; 95% CI = −0.39®, 0®). The mean difference between both techniques was 0.02® (SD = 0.3®; 95% CI = −0.1®, 0.1®; P = 0.68). BMI had no significant effect on the divergence from the true ankle center for either the Extremes Midpoint (R² = 0.002; P = 0.78) or the Distal Midpoint techniques (R² = 0.004; P = 0.90).(Figure 2)

The center of the ankle, as determined by using the Extremes Midpoint technique, lied 1.1 mm (SD = 2.6 mm; 95% CI = −1.9 mm to −0.3 mm) from the anatomic axis of the tibia. When determined using the Distal Midpoint technique, the center of the ankle lied 1.7 mm (SD = 2.3 mm; 95% CI = −2.5 mm to −0.98 mm) from the anatomic axis. Although statistically significant (P = 0.028), this difference was not clinically relevant (<3 mm). BMI had no significant effect on these differences (R² = 0.07; P = 0.11; R² = 0.02, P = 0.38).(Figure 3)

There is no significant difference between ankle registration using the Extremes Midpoint or the Distal Midpoint techniques and the anatomic center of the ankle. Patients' BMI does not seem to affect the registration of the ankle center with either technique.

Background: Navigation allows for determination of the mechanical axis of the lower extremity. We evaluated the intra- and inter-observer reliability with an image-free navigation system and determined the accuracy of the navigation system to monitor changes in lower limb alignment as compared to alignment measured with a novel 3D CT method.

Methods: A total of 13 cadaver legs were used to evaluate the intra- and inter-observer registration reliability by three observers. Navigated HTOs were then performed on all legs and pre/postoperative values of the varus-valgus angles were recorded. Data were compared to equivalent measures obtained by 3D CT using intra-class correlation coefficients (ICCs).

Results: The ICCs for intra-observer varus-valgus reliability ranged from 0.756 to 0.922, inter-observer reliability was 0.644. ICCs for navigation-CT comparison were 0.784 for varus-valgus angle (pre-op), 0.846 (postop) and 0.873 (delta). Maximum differences in navigation-CT measurements in varus-valgus angle (delta) were 4.5° for all trials. There was poor reliability and accuracy in the axial plane (tibial rotation) as well as fair reliability and accuracy in the sagittal plane (tibial slope).

Conclusion: Image-free navigation is reliable for dynamic monitoring of coronal leg alignment but shows relevant limitations in determination of sagittal and axial plane alignment.

Background: Correct ligament balance is a critical factor in both cruciate retaining and substituting total knee arthroplasty (TKA). Due to a lack in current tools, however, little data exists on gap kinematics with the patella is in its anatomical position and with the ligaments tensed. The objective of this study was to quantify the effects of the patellar position and PCL resection on gap kinematics when constant tension is applied to the medial and lateral compartments.

Methods: A novel computer-controlled tensioner was used to measure the medial and lateral gaps in 10 normal knee specimens throughout a full range of motion. Gaps were measured medially and laterally using constant applied forces of 50N, 75N and 100N per side. Gap data were acquired at 0°, 30°, 60°, 90°, 120° of flexion. The test was performed with the patella everted and reduced, and with the PCL intact and resected.

Results: At 90° of flexion:

the mean medial gap was 1.5–2.5mm smaller than the mean lateral gap for all scenarios and forces tested (p< 0.05);

During knee flexion from 30° to 90°, the PCL tended to squeeze the medial compartment by 1–2mm (p< 0.05). Increasing the force from 50N to 100N per side resulted in a mean gap increase of 0.5mm throughout the range of flexion.

Conclusions: Measurement of gap kinematics with a computer-controlled tensioner and a completely reduced patella is feasible. Everting the patella and resecting the PCL both have significant effects on flexion gap balance and symmetry. Knees which are balanced with the patella everted may be post-operatively 1–3mm more lax in flexion than planned. Retaining the PCL may result in asymmetric tightening of the medial gap from 30° to 90°.

Introduction: Intraoperative visualisation of anatomic joint line reduction and hardware placement is techniqually demanding, twodimensional c-arm imaging do not always allow acute decision making about remaining articular steps and hardware misplacement. Postoperatively identification of these failures may need extensive revison surgery and is costly. The new mobile Iso-C3D imaging device provides intraoperative multiplanar reconstructions, consequently immediate decision making becomes possible.

Materials and Methods: 250 different joint fractures were intraoperatively scanned with the Iso-C3D (ankle fractures; forefoot, calcaneus; pilon tibiale; tibia plateaus; wrists; spine; pelvic fractures). Multiplanar reconstructions were obtained from 100 fluoroscopic images the Iso-C-3D provides during one automatic scan protocol. Decisions about remaining articular steps and implant misplacements were compared with the knowledge of conventional c-arm images which were done before. If necessary directly intraoperative corrections were performed.

Results: In 43 clinical cases (17%) a direct intraoperative correction resulted in implant change (8%) or correction of reduction (9%), caused by articular steps > 2mm, screw or k-wire misplacement. In all those cases conventional c-arm images did not reveal the significant step or misplacement, correction decision were all based on the Iso-C3D imaging in those cases. In other (9%) significant steps or misplacements were identified in c-arm images and confirmed with the Iso-C3D images.

Discussion: With the new intraoperative three dimensional imaging device a direct introperative idenfication of remaining intraarticular steps and implant misplacements becomes possible. Missed steps and misplacements can be avoided and reduction of operative revison rates might result.

Introduction: Image based navigation is able to increase precision and reduce intraoperative radiation time in drilling procedures in orthopeadic trauma indications. Due to specific anatomic conditions and necessary adequate fluoroscopic visualizing, specific indications need intraoperative 3-D fluoroscopy based navigation modalities. This kind of navigation has already been successfully used in several orthopaedic interventions. The complex anatomic structure of the scaphoid, the suggested minimal invasiveness and misplacement rates of the screws make 2-D based fluoroscopic navigation impossible. Missing options for a stable reference marker fixation at the scaphoid or carpus did not allow an intraoperative registration for the navigation. We report about the development of an adequate non invasive fixation technique of the reference marker for navigated interventions and the first implementation of 3-D fluoroscopy based scaphoid screws.

Materials and method: Fixation of the reference marker was achieved by immobilisation of the complete hand and forearm in maximum dorsal extension of the wrist. We used a completely new developed radiolucent hand fixation device (HFD) fixed nonivasively to the carpus and a conventional navigation system (Brainlab, Germany) in combination with 3-D fluoroscopic imaging (Iso-C, Siemens, Germany).

Tests were done on 10 intact specimen and the process included the initial drilling and final placement of an osteosynthetic screw. Postoperative placement was controlled with a 3-D scan. Results concerning a defined optimal screw positioning and drill failures attempts were done by another independent surgeon.

Results: All 3-D scans were done without complications. The multiplanar reconstructions allowed a proper visualisation of the scaphoid in all cases. No additional movement of the fixed extremity occurred during the operation. No registration failures were detected. An optimally defined screw placement in the scaphoid was achieved in 9 cases. Two repeated drill attempts were necessary in one case, another case needed three drill attempts. The scaphoid was never perforated.

Discussion: Our development of a new immobilizing device for the complete hand and forearm allows proper use of 3-D fluoroscopy based navigation at the scaphoid including a placement of an osteosynthetic screw. Further movements of the hand or fingers are intraoperatively only possible after the definite drill placement has been performed.

The 3-D imaging modality allows a direct control of the reduction and screw placement intraoperatively. Our tests did not include simulated fracture conditions, a general use of our new technique can now only be implemented to non displaced fracture types, while clinical and further laboratory tests have to improve our findings for all types of scaphoid fractures.

Introduction: The main purpose of this study was to analyze the accuracy of conventional versus navigated open wedge corrective osteotomies of the proximal tibia. Furthermore, the intraoperative radiation dosage and the time of the operative procedure of both groups were compared.

Methods: 20 legs of 11 fresh cadaver (9 male, 2 female, age 35–71 years) were randomly assigned to conventional open wedge high tibial osteotomy (HTO) (n=10) or navigated open wedge HTO (n=10). Two legs had to be excluded because of pre-existing knee injuries. The aim of all corrective operations was to align the mechanical axis to pass through 80% of the tibial plateau (80% Fujisawa line), regardless of the preexisting alignment. The intraoperative mechanical axis was evaluated either by the cable technique for conventional HTO, or by a navigation module for navigated HTO (Medivision, Oberdorf/Switzerland). An angle fixed implant with interlocking screws (Tomofix, Mathys, Bettlach/Switzerland) was used to minimize postoperative loss of correction. Postoperatively, CT-scans were performed and the Fujisawaline and MPTA measured with a computer software for deformity analysis (Med-iCAD) The main outcome parameter was the accuracy of the correction, which was measured by the Fujisawa line. Secondary outcome parameters were the intraoperative radiation measured by the dose area product and the time of the operative procedure. For statistical analysis the standard deviation (S.D.) was calculated and the paired t-test applied.

Results: After conventional HTO, the mechanical axis was intersecting the Fujisawa line at 72.1% of the tibial plateau (range 60.4–82.4%, S.D. 7.2%). In contrast, after navigated HTO the tibia plateau was passed through 79.7% (range 75.5–85.8%, S.D. 3.3%). Thus, the accuracy of the correction was significantly higher after navigated HTO (p=0.020). In addition, the standard deviation of the corrections was significantly lower after navigated HTO (p=0.012). The medial proximal tibia angle (MPTA) increased 7.9° (range: 4.7–12.1°) after conventional HTO and 9.1° (range: 4.6–12.6°) after navigated HTO. The average dose area products of the conventional HTO (49.5 cGy/cm2, range 36.0–81.2 cGy/cm2) and navigated HTO (42.8 cGy/cm2, range 28.3–58.1 cGy/cm2) were comparable (p=0.231). However, navigated HTO elongated the operation time significantly (navigated HTO: 82 min, range 55–98 min; conventional HTO: 59 min, range 47–73 min) (p< 0.001).

Conclusion: Continuous three-dimensional imaging of the axis and of intraoperative tools with the a navigation module significantly improves the accuracy of open wedge osteotomies of the proximal tibia. Prospective clinical studies will show whether the results of this cadaver study can be transferred to the regular clinical use.

In computer assisted orthopaedic surgery, rigid fixation of the Reference Marker (RM) system is essential for reliable computer guidance. A minimum shift of the RM can lead to substantial registration errors and inaccuracies in the navigation process. Various types of RM systems are available but there is little information regarding the relative stabilities of these systems. The aim of this study was to test the rotational stability of three commonly used RM systems.

One hundred and thirty Synbones and 15 cadavers were used to test the rotational stability of three different RM systems (Schanz’ screw, Brain-Lab MIRA and Stryker adjustment system). Using a specially developed testing device, the peak torque sustained by each RM system was assessed in various anatomical sites.

Comparison of means for Synbone showed that the BrainLab MIRATM system was the most stable (mean peak torque 5.60+/− 1.21 Nm) followed by the Stryker systemTM (2.53+/− 0.53 Nm) and the Schanz screw(0.77+/− 0.39 Nm)(p< 0.01). The order of stability in relation to anatomical site was femoral shaft, distal femur, tibial shaft, proximal tibia, anterior superior iliac spine, iliac crest and talus. Results from the cadaver experiments showed similar results. Bi-cortical fixation was superior to mono-cortical fixation in the femur(p< 0.01) but not the tibia(p=0.22).

The RM system is the vital link between bone and computer and as such the stability of the RM is paramount to the accuracy of the navigation process. In choosing RM systems for computer navigated surgery surgeons should be aware of their relative stability. Anatomical site of RM placement also affect the stability. Mono-cortical fixation is generally less stable than bi-cortical.

The aim of this pilot study was to evaluate the accuracy of two different methods of navigated retrograde drilling of talar lesions. Artificial osteochondral talar lesions were created in 14 cadaver lower limbs. Two methods of navigated drilling were evaluated by one examiner. Navigated Iso-C^3D was used in seven cadavers and 2D fluoroscopy-based navigation in the remaining seven. Of 14 talar lesions, 12 were successfully targeted by navigated drilling. In both cases of inaccurate targeting the 2D fluoroscopy-based navigation was used, missing lesions by 3 mm and 5 mm, respectively. The mean radiation time was increased using Iso-C^3D navigation (23 s; 22 to 24) compared with 2D fluoroscopy-based navigation (14 s, 11 to 17).

Tibial rotation and translation provide important stability parameters after ACL reconstruction. An accurate tool for a combined pre- intra- and postoperative stability measurement is not in clinical use so far. Navigation of the drill canals for the ACL placement and evaluation of possible impingement problems has been introduced for some years already, while measurement of the tibial translation and rotation is only available for a short time and only available for a few navigation modules. Navigation provides an accuracy of 1mm/1°, therefore navigated measurement of tibial rotation and translation were evaluated in this study with a new developed mechanical device and directly compared to conventional measurement techniques.

Accuracy of navigation was compared with the KT1000 for the anterior-posterior (AP) translation and to a new developed goniometer tool concerning the rotational range of motion. Comparative tests included plastic whole leg models and specimens. Tests were repeated with intact and dissected ACL′s. A conventional navigation system (Vector Vision, Brainlab, Germany) was used in all cases. This included software developed for fluoroscopy based navigated ACL reconstruction. The following knee kinematics were detectable with the navigation system: Flexion/Extension degrees of the knee joint (°); AP translation of the tibia in relation to the femur (mm); Axial tibial rotation relative to the femur (°).

Validation of Navigation: first neutral tibial rotation was defined and marked in the knee joint in neutral position. All rotational measurements were done with a new developed goniometer tool and compared to the navigated technique. Then the knee was rotated externally until 45° (maximum) and internally 45° (maximum), by single 2.5° steps. These measurements were repeated in 0°, 30°, 60° and 80° knee flexion. All tests were repeated three times and performed by 3 different observers. A total of 1296 measurements were done. Measurements of the tibial translation were compared with the KT 1000 for the specimen testing.

Results revealed: accurate navigated measurement of tibial rotation in plastic and specimen models; variation of absolute AP translation values between KT1000 and navigation; variation of the AP translation corresponding to the ACL condition; increased range of total tibial rotation after dissecting the ACL compared to the intact ligament.

Restoration of the rotational stability and limiting of the AP translation is necessary to provide normal knee kinematics after ACL reconstructions. Intraoperative measurements of these stability parameters are demanding and so far not established with navigation systems or conventionally. As our results show, navigation offers an accurate technique for measurement of the AP translation and rotation of the knee with intact and dissected ACL’s under laboratory conditions. General use in the evaluation of a successful ACL reconstruction becomes possible intraoperative and might be reproducible for further measurements. Clinical studies are needed to improve our results.

Anatomic reduction and appropriate implant placement is essential for optimal treatment of intraarticular tibial plateau fractures. Standard intraoperative fluoroscopy provides limited visualization of the reduction and hardware placement compared with pre- or postoperative 3-D imaging modalities. As such, post-operative computer tomography (CT) has become a common procedure to evaluate the quality of the reduction and fixation. The Iso-C3D provides 3-D intraoperatively imaging to dynamically assess the surgical reduction and fixation at different anatomic regions. We report on our first 19 clinical tibial plateau fractures scanned intra-operatively with the Iso-C 3D.

Between January and November 2003, 19 intraarticular tibia plateau fractures were scanned intraoperatively with the Iso-C3D (Siemens, Germany). No formal selection criteria were utilised except for the presence of a tibial plateau fracture. Operative procedures included 14 cases of open reduction internal fixation and 5 cases of internal fixation with arthroscopic assisted reduction.

Imaging Technique: All patients were positioned on full-carbon tables for the operative procedure. After initial operative reduction and fixation, conventional two-dimensional fluoroscopic imaging was performed using standard AP and lateral projections. These images were evaluated by the operating surgeon; if the reduction and fixation was judged to be appropriate, Iso-C3D imaging was initiated

In 21% (n=4) of all cases an immediate revision of the operative procedure was performed after Iso-C3D imaging. These revisions were not deemed necessary with conventional fluoroscopy alone. In two cases, significant intra-articular incongruencies (greater than two millimetres) were noted. Additionally, in two cases, implant mal-position was detected. All patients had a postoperative CT scan. All CT scans confirmed the intraoperative Iso-C imaging, no further additional articular incongruencies or malpositioned implants were identified. When compared to conventional C-arm images, the Iso-C 3D scans demonstrated improved ability to identify the articular malreduction and implant mal-position in all cases.

We have demonstrated that the Iso-C3D provides reliable intraoperative evaluation of reduction and hardware placement compared to traditional CT scans for tibial plateau fractures. In addition, clinically relevant intra-operative information was gained with its use in this study. In four (21%) cases, the operative treatment was modified due to the use of the multiplanar imaging modality. On average, 10 minutes of additional operative time was required for the use of Iso-C3D scanning and the evaluation of the images. Further prospective clinical studies are needed to improve our findings.