Chronic ruptures of the quadriceps tendon after total knee arthroplasty (TKA) are rare but are a devastating complication. The objective of this study was to validate the use of fresh frozen total fresh quadriceps tendon allografts for quadriceps tendon reconstruction. The hypothesis of this work was that the graft was functional in more than 67% of cases, a higher percentage than the results of conventional treatments. We designed a continuous monocentric retrospective study of all patients operated on between 2009 and 2017 for a chronic rupture of the quadriceps tendon after TKA by quadriceps allograft reconstruction. The usual demographic and perioperative data and the rehabilitation protocols followed were collected. Initial and final radiographs were analyzed to measure patellar height variation. The main criterion was the possibility of achieving an active extension of the knee with a quadriceps contraction force greater than or equal to 3/5 or the possibility of lifting the heel off the ground in a sitting position.Introduction
Material – methods
Peri-prosthetic fungal infection is generally considered more difficult to cure than a bacterial infection. Two-stage exchange is considered the gold standard of surgical treatment. A recent study, however, reported a favorable outcome after one stage exchange in selected cases where the fungus was identified prior to surgery. The routine one stage exchange policy for bacterial peri-prosthetic infection involves the risk of identifying a fungal infection mimicking bacterial infection solely on intraoperative samples, i.e. after reimplantation, realizing actually a one stage exchange for fungal infection without pre-operative identification of the responsible fungus, which is considered to have a poor prognosis. We report two such cases of prosthetic hip and knee fungal infection. Despite this negative characteristic, no recurrence of the fungal infection was observed. CASE N°1: A 78 year old patient was referred for loosening of a chronically infected total hip arthroplasty (Staphylococcus aureus and Streptococcus dysgalactiae). One stage exchange was performed. Intraoperative bacterial cultures remained sterile. Two fungal cultures were positive for Candida albicans. Antifungal treatment was initiated for three months. No infection recurrence was observed at three year follow up. CASE N° 2: A 53-year-old patient was referred for loosening of a chronically infected total knee prosthesis (Staphylococcus aureus methicillin susceptible, Klebsiella pneumoniae and Staphylococcus epidermidis). One stage exchange was performed. Intraoperative bacterial cultures remained sterile. Five fungal cultures were positive for Candida albicans. Antifungal treatment was initiated for three months. No infection recurrence was observed at two-year follow-up. This experience suggests that eradication of fungal infection of a total hip or knee arthroplasty may be possible after one stage exchange even in cases where the diagnosis of fungal infection was not known before surgery, when the fungus was not identified and its antifungal susceptibility has not been evaluated before surgery. It is however not possible to propose this strategy as a routine procedure.INTRODUCTION
DISCUSSION
We are using a non image based navigation system on a routine basis for unicompartmental knee replacement (UKR). We prospectively studied 60 patients who underwent navigated minimally invasive UKR for primary medial osteoarthritis at our hospital between October 2005 and October 2006. We established a navigated control group of 60 patients who underwent conventional implantation of a UKA at our hospital between April 2004 and September 2005. There were 42 male and 78 female patients with a mean age of 65 years (range, 44–87 years). There were no differences in all preoperative parameters between the two groups. The accuracy of implant positioning was determined using predischarge standard anteroposterior and lateral radiographs. The following angles were measured: femorotibial angle, coronal and sagittal orientation of the femoral component, coronal and sagittal orientation of the tibial component. When the measured angle was in the expected range, one point was given. The accuracy was defined as the sum of the points given for each angle, with a maximum of five points (all items fulfilled) and a minimum of 0 point (no item fulfilled). Our primary criterion was the radiographic accuracy index on the postoperative radiograph evaluation. All other items were studied as secondary criteria. The mean accuracy index was similar in the two groups: 4.1 ± 0.8 in the study group and 4.2 ± 1.2 in the control group. 36 patients (60%) in the control group and 37 patients (62%) in the study group had the maximum accuracy index of five points. All measured angles were similar in the two groups. There were no differences between the percentages of patients in the two groups achieving the desired implant positions. Mean operating time was similar in the two groups. There were no intraoperative complications in either group. The groups had similar major postoperative complication rates during hospital stay (3% for both). The used navigation system is based on an anatomic and kinematic analysis of the knee joint during the implantation. The modification of the existing software for minimal invasive approach has been successful. It enhances the quality of implantation of the prosthetic components and avoids the inconvenient of a smaller incision with potential less optimal visualization of the intra-articular reference points. However, all centers observed a significant learning curve of the procedure, with a significant additional operative time during the first implantations. The postoperative rehabilitation was actually easier and faster, despite the additional percutaneous fixation of the navigation device. This system has the potential to allow the combination of the high accuracy of a navigation system and the low invasiveness of a small skin incision and joint opening.
Revision total knee replacement (TKR) is a challenging procedure, especially because most of the standard bony and ligamentous landmarks used during primary TKR are lost due to the index implantation. However, as for primary TKR, restoration of the joint line, adequate limb axis correction and ligamentous stability are considered critical for the short- and long- term outcome of revision TKR. There is no available data about the range of tolerable leg alignment after revision TKR. However, it is logical to assume that the same range than after primary TKR might be accepted, that is ± 3° off the neutral alignment. One might also assume that the conventional instruments, which rely on visual or anatomical alignments or intra- or extra-medullary rods, are associated with significant higher variation of the leg axis correction, especially in cases with significant bone loss which prevents to control the exact location of the usual, relevant landmarks. Navigation system might address this issue. We used an image-free system (ORTHOPILOT TM, AESCULAP, FRG) for routine implantation of primary TKR. The standard software was used for revision TKR. Registration of anatomic and cinematic data was performed with the index implant left in place. The components were then removed. New bone cuts as necessary were performed under the control of the navigation system. The size of the implants and their thickness was chosen after simulation of the residual laxities, and ligament balance was adapted to the simulation results. The system did not allow navigation for intra-medullary stem extensions and any bone filling which may have been required. This technique was used for 54 patients. The accuracy of implantation was assessed by measuring following angles on the post-operative long-leg radiographs: mechanical femoro-tibial angle (normal = 0°, varus deformation was described with a positive angle); coronal orientation of the femoral component in comparison to the mechanical femoral axis (normal = 90°, varus deformation was described with an angle <
90°); coronal orientation of the tibial component in comparison to the mechanical tibial axis (normal = 90°, varus deformation was described with an angle <
90°); sagittal orientation of the tibial component in comparison to the proximal posterior tibial cortex (normal = 90°, flexion deformation was described with angle <
90°). Individual analysis was performed as follows: one point was given for each fulfilled item, giving a maximal accuracy note of 4 points. Prosthesis implantation was considered as satisfactory when the accuracy note was 4 (all fulfilled items). The rate of globally satisfactory implanted prostheses and the rate of prostheses implanted within the desired range for each criterion were recorded. Limb alignment was restored in 88%. The coronal orientation of the femoral component was acceptable in 92% of the cases. The coronal orientation of the tibial component was acceptable in 89% of the cases. The sagittal orientation of the tibial component was acceptable in 87% of the cases. Overall, 78% of the implants were oriented satisfactorily for the four criteria. The navigation system enables reaching the implantation objectives for implant position and ligament balance in the large majority of cases, with a rate similar to that obtained for primary TKA. The navigation system is a useful aid for these often difficult operations, where the visual information is often misleading.
Navigation systems are able to measure very accurately the movement of bones, and consequently the knee laxity, which is a movement of the tibia under the femur. These systems might help measuring the knee laxity during the implantation of a total (TKR) or a unicompartmental (UKR) knee replacement. 20 patients operated on for TKR (13 cases) or UKR (7 cases) because of primary varus osteoarthritis have been analyzed. Pre-operative examination involved varus and valgus stress X-rays at 0 and 90° of knee flexion. The intra-operative medial and lateral laxity was measured with the navigation system at the beginning of the procedure and after prosthetic implantation. Varus and valgus stress X-rays were repeated after 6 weeks. X-ray and navigated measurements before and after knee replacement were compared with a paired Wilcoxon test at a 0.05 level of significance. The mean pre-operative medial laxity in extension was 2.3° (SD 2.3°). The mean pre-operative lateral laxity in extension was 5.6° (SD 5.1°). The mean pre-operative medial laxity in flexion was 2.2° (SD 1.9°). The mean pre-operative lateral laxity in flexion was 6.7° (SD 6.0°). The mean intra-operative medial laxity in extension at the beginning of the procedure was 3.6° (SD 1.7°). The mean intra-operative lateral laxity in extension at the beginning of the procedure was 3.0° (SD 1.3°). The mean intra-operative medial laxity in flexion at the beginning of the procedure was 1.9° (SD 2.6°). The mean intra-operative lateral laxity in flexion at the beginning of the procedure was 3.5° (SD 2.7°). The mean intra-operative medial laxity in extension after implantation was 2.1° (SD 0.9°). The mean intra-operative lateral laxity in extension after implantation was 1.9° (SD 1.1°). The mean intra-operative medial laxity in flexion after implantation was 1.9° (SD 2.5°). The mean intra-operative lateral laxity in flexion after implantation was 3.0° (SD 2.8°). The mean post-operative medial laxity in extension was 2.4° (SD 1.1°). The mean post-operative lateral laxity in extension was 2.0° (SD 1.7°). The mean post-operative medial laxity in flexion was 4.4° (SD 3.3°). The mean post-operative lateral laxity in flexion was 4.7° (SD 3.2°). There was a significant difference between navigated and radiographic measurements for the pre-operative medial laxity in extension (mean = 1.4° – p = 0.005), the pre-operative lateral laxity in extension (mean = 2.6° – p = 0.01), the pre-operative lateral laxity in flexion (mean = 3.3° – p = 0.005). There was no significant difference between navigated and radiographic measurements for the pre-operative medial laxity in flexion (mean = 0.3° – p = 0.63). There was a significant difference between navigated and radiographic measurements for the postoperative medial laxity in flexion (mean = 2.5° – p = 0.004). There was no significant difference between navigated and radiographic measurements for the postoperative medial laxity in extension (mean = 0.3° – p = 0.30), the post-operative lateral laxity in extension (mean = 0.2° – p = 0.76), the post-operative lateral laxity in flexion (mean = 1.7° – p = 0.06). These differences were less than 2 degrees in most of the cases, and then considered as clinically irrelevant. The navigation system used allowed measuring the medial and lateral laxity before and after TKR. This measurement was significantly different from the radiographic measurement by stress X-rays for pre-operative laxity, but not statistically different from the radiographic measurement by stress X-rays for post-operative laxity. The differences were mostly considered as clinically irrelevant. The navigated measurement of the knee laxity can be considered as accurate. The navigated measurement is valuable information for balancing the knee during TKR. The reproducibility of this balancing might be improved due to a more objective assessment.
Revision TKR is a challenging procedure, especially because most of the standard bony and ligamentous landmarks are lost due to the primary implantation. However, as for primary TKR, restoration of the joint line, adequate limb axis correction and ligamentous stability are considered critical for the short- and long-term outcome of revision TKR. There is no available data about the range of tolerable leg alignment after revision TKR. However, it is logical to assume that the same range than after primary TKR might be accepted, that is ± 3° off the neutral alignment. One might also assume that the conventional instruments, which rely on visual or anatomical alignments or intra- or extramedullary rods, are associated with significant higher variation of the leg axis correction. We used an image-free system (ORTHOPILOT TM, AESCULAP, FRG) for routine implantation of primary TKA. The standard software was used for revision TKA. Registration of anatomic and kinematic data was performed with the index implant left in place. The components were then removed. New bone cuts as necessary were performed under the control of the navigation system. The size of the implants and their thickness was chosen after simulation of the residual laxities, and ligament balance was adapted to the simulation results. The system did not allow navigation for centromedullary stem extension and any bone filling which may have been required. This technique was used for 54 patients. The accuracy of implantation was assessed by measuring the limb alignment and orientation of the implants on the post-operative radiographs. Limb alignment was restored in 88%. The coronal orientation of the femoral component was acceptable in 92% of the cases. The coronal orientation of the tibial component was acceptable in 89% of the cases. The sagittal orientation of the tibial component was acceptable in 87% of the cases. Overall, 78% of the implants were oriented satisfactorily for the five criteria. The navigation system enables reaching the implantation objectives for implant position and ligament balance in the large majority of cases, with a rate similar to that obtained for primary TKA. The navigation system is a useful aid for these often difficult operations, where the visual information is often misleading. The navigation system used enables facilitated revision TKA.
Anterior cruciate ligament (ACL) reconstruction allows overall good results, but there is still a significant rate of failure. It is well accepted that the main reason for ACL reconstruction failure is a misplacement of tibial or femoral tunnels. Conventional techniques rely mainly on surgical skill for intra-operative tunnel placement. It has been demonstrated that, even by experienced surgeons, there was a significant variation in the accuracy of tunnel placement with conventional techniques. Navigation systems might enhance the accuracy of ACL replacement. 10 cadaver knees with intact soft-tissue and without any intra-articular abnormalities were studied. We used a non image based navigation system (OrthoPilot ®, Aesculap, Tuttlingen, FRG). Localizers were fixed on bicortical screws on the distal femur and on the proximal tibia. Both kinematic and anatomic registration of the knee joint were performed by moving the knee joint in flexion-extension and palpating relevant intra- and extra-articular landmarks with a navigated stylus. The most anterior, posterior, medial and lateral point of both tibial and femoral attachment of the ACL were marked with metallic pins. The navigated stylus was positioned on these points, and the system recorded its position in comparison to the bone contours. Subsequently, we performed conventional plain AP and lateral X-rays and a CT-scan, and measured the position of the pins in comparison to the bone contours. Finally, all measurements were made again with a caliper after disarticulating the knee joint. We calculated the center of the footprint as the mid-point between the four pins of both tibial and femoral attachment for each measurement technique. All measurements were expressed as percentages of the bone size to compensate for the different sizes. There were no significant difference in the paired measurements of the location of the ACL footprints on both femur and tibia between anatomic, radiographic, CT-scan and navigated measurements. There was a significant correlation between the paired measurements of the location of the ACL footprints on both femur and tibia with either measurement techniques. Anatomic measurement is the gold standard experimental technique for the positioning of the ACL foot-print, and CT-scan measurement is currently the gold standard technique in clinical situation. According to this reference, the position of ACL attachments on the tibia and on the femur can be accurately defined by the navigation system. Intra-operative measurement of the location of the bone tunnels during ACL replacement with this navigation system should be accurate as well.
Unicompartmental knee replacement (UKR) is accepted as a valuable treatment for isolated medial knee osteoarthritis. Minimal invasive implantation might be associated with an earlier hospital discharge and a faster rehabilitation. However these techniques might decrease the accuracy of implantation, and it seems logical to combine minimal invasive techniques with navigation systems to address this issue. The authors are using a non image based navigation system (ORTHOPILOT ™, AESCULAP, FRG) on a routine basis for UKR. We prospectively studied 60 patients who underwent navigated minimally invasive UKR for primary medial osteoarthritis at our hospital between October 2005 and October 2006. We established a navigated control group of 60 patients who underwent conventional implantation of a UKA at our hospital between April 2004 and September 2005. There were 42 male and 78 female patients with a mean age of 65 years (range, 44–87 years). There were no differences in all preoperative parameters between the two groups. The accuracy of implant positioning was determined using predischarge standard anteroposterior and lateral radiographs. The following angles were measured: femorotibial angle, coronal and sagittal orientation of the femoral component, coronal and sagittal orientation of the tibial component. When the measured angle was in the expected range, one point was given. The accuracy was defined as the sum of the points given for each angle, with a maximum of five points (all items fulfilled) and a minimum of 0 point (no item fulfilled). Our primary criterion was the radiographic accuracy index on the postoperative radiograph evaluation. All other items were studied as secondary criteria. The mean accuracy index was similar in the two groups: 4.1 ± 0.8 in the study group and 4.2 ± 1.2 in the control group. 36 patients (60%) in the control group and 37 patients (62%) in the study group had the maximum accuracy index of five points. All measured angles were similar in the two groups. There were no differences between the percentages of patients in the two groups achieving the desired implant positions. Mean operating time was similar in the two groups. There were no intraoperative complications in either group. The groups had similar major postoperative complication rates during hospital stay (3% for both). The used navigation system is based on an anatomic and kinematic analysis of the knee joint during the implantation. The modification of the existing software for minimal invasive approach has been successful. It enhances the quality of implantation of the prosthetic components and avoids the inconvenient of a smaller incision with potential less optimal visualization of the intra-articular reference points. However, all centers observed a significant learning curve of the procedure, with a significant additional operative time during the first implantations. The postoperative rehabilitation was actually easier and faster, despite the additional percutaneous fixation of the navigation device. This system has the potential to allow the combination of the high accuracy of a navigation system and the low invasiveness of a small skin incision and joint opening.
There was no significant difference in the pre-operative data between both groups. The post-operative coronal group A and 17 cases in group B. The prosthesis was optimally implanted in 17 cases in group A and 18 cases in group B. No difference was statistically significant.