We evaluated the efficacy of using the expandable nail for treating non-union and malunion of the tibial and femoral shafts. Records of 20 patients were retrospectively reviewed: 12 had femoral non-union, 7 had tibial non-union, and one had tibial malunion. The bones underwent reaming and the largest possible nail sizes were inserted during reoperation. The mean age of the patients was 35 years (26-49) in the tibia group and 53 years (23-85) in the femur group. The fractures were defined according to AO/OTA classification and divided between open and closed. The initial treatment was 6 interlocking intramedullary nails and 2 external fixation in the tibia group, and 6 interlocking intramedullary nails, 3 plates and screws and 2 proximal femoral nails in the femoral group. The respective intervals between the original trauma and re-operation were 12 months and 15 months and the respective operation times were 59 minutes (35-70) and 68 minutes (20-120). All fractures healed satisfactorily without the need for an additional procedure. Healing time was 26 weeks (6-52) and 14 weeks (6-26) in the tibia and femur group, respectively. Limb shortenings of 10cm and 4cm were recorded in one patient each in the tibia group and of 3cm in one patient in the femur group. Using the expandable nail system permitted us to ream the bone and expand the nail to its maximal diameter, i.e. up to 16mm in the tibia and 19mm in the femur. We believe that using a bigger nail diameter contributes to better stabilisation of the fracture and promotes better and faster bone healing. Based on our experience, we recommend the use of the expandable nail system to treat tibia and femur shaft non-unions and malunions.
We evaluated the efficacy of using the expandable nail for treating non-union and malunion of the tibial and femoral shafts. Records of 20 patients were retrospectively reviewed: 12 had femoral non-union, 7 had tibial non-union, and one had tibial malunion. The bones underwent reaming and the largest possible nail sizes were inserted during reoperation. The mean age of the patients was 35 years (26–49) and in the tibia group and 53 years (23–85) in the femur group. The fractures were defined according to AO/OTA classification and divided between open and closed. The initial treatment was 6 interlocking intramedullary nails and 2 external fixation in the tibia group, and 6 interlocking intramedullary nails, 3 plates and screws and 2 proximal femoral nails in the femoral group. The respective intervals between the original trauma and re-operation were 12 months and 15 months and the respective operation times were 59 minutes (35–70) and 68 minutes (20–120). All fractures healed satisfactorily without the need of an additional procedure. Healing time was 26 weeks (6– 52) and 14 weeks (6–26) in the tibia and femur group, respectively. Limb shortenings of 10 cm and 4 cm were recorded in one patient each in the tibia group and of 3 cm in one patient in the femur group. Using the expandable nail system permitted us to ream the bone and expand the nail to its maximal diameter, i.e., up to 16 mm in the tibia and 19 mm in the femur. We believe that using a bigger nail diameter contributes to better stabilization of the fracture and promotes better and faster bone healing. Based on our experience, we recommend the use of the expandable nail system to treat tibia and femur shaft non-unions and malunions.
Medial transfer of the tibial Tuberosity remains the treatment of choice for skeletally mature patients with patellar malalignment (recurrent dislocation, subluxation with or without patellar tilt). As many patients with patellar malalignment have patellar articular cartilage lesion or patella alta, anteriorisation and distalisation of the tibial tuberosity is advised.
All operations were done either by selective epidural anesthesia (only sensory and not motor) or general anesthesia without muscle relaxant using quadriceps muscle stimulation. The mean tibial tuberosity medialisation, anteriorisation and distalisation was 1.4 cm (0–2.5 cm) 0.4cm (0–1.1cm) and 0.87cm (0–1.2cm) respectively.
84% of the patients stated they would have the operation again. All patients had full active range of motion on both knees without extension lag. At the final evaluation visit the Lisholm and Karlsson scores were good and excellent in 72% and 72.5%, 18.8% and 23.5% had fair results and only 8.7% and 4.4% had poor results respectively. The poor results correlated well with the degree of the patella cartilage damage found during surgery, poor selection of patients and extreme ligamentous laxity. There were two complications: one non-union of the tibial tuberosity treated successfully with bone grafting and one non displaced fracture bellow the osteotomy, treated conservatively. Both had excellent results.
All the radiographic and clinical evaluations were completed both before THR surgery and 3 months following the surgery during routine follow up.
TOH was first described by Curtis and Kinkade in 1959, in women in the 3rd trimester of pregnancy. Later the disease was described in middle-aged males (4th-6th decade). Very rare occurrence was described in children and in females not connected to pregnancy. Thirty-six patients with sudden hip pain with normal radiographs but increase uptake on bone scan and bone marrow edema in the head and neck on MRI were investigated by the senior author. Two patients (age 16 and 18) had Osteoid osteoma in the neck and two elderly patients (72 female and 75 male) had stress fracture in the neck were excluded from the study. The rest, 32 patients (28 males and 4 females – not connected to pregnancy) are the study group. Three male patients had bilateral involvement 1 to 3 years apart. The initial symptoms were pain, limping with minimal or no restriction in range of motion. All patients had plain radiographs, bone scan and MRI. Bone scan was positive in all and MRI showed bone edema in the neck and head in all. All patients were initially treated by non-weight bearing for six weeks followed by additional MRI every 6 weeks till the bone edema and symptoms subsided. In all patients the third MRI showed improvement in bone edema and were allowed to weight bear. None of the patients showed progression from TOH to AVN even in 7 patients with Crescent lines on T-1 images. The mean F.U. was 51 months (4 to 131 months). Five patients still complained of mild pain in the affected hip, all with the exception of one had full range of motion. None of the patients had limping. All the plain radiographs were normal, with no signs of AVN or deformity of the head. In contrast the Dexa measurements of all patients showed decreased bone density in the affected hip compared to the other.
Based on these advantages, as well as its simplicity in use and short surgical technique, we recommend it for treatment of long bone fractures.
We describe our experience of 79 patients with complaints consistent with MP, treated, by the senior author, over a 13-year period.
Initial management consisted of anti inflammatory agents, rest and redaction of aggravating factors. Diagnostic nerve block test was carried out for those who were refractory to the above treatment. All patients who responded to the local anesthetic test were treated with local infiltration of corticosteroids. Surgical intervention was reserved for patients who responded to the lidociane test but were refractory to repeated corticosteroids injections. Patients who failed to respond to the test injection were evaluated by CT-scan of the lumbar spine and by abdominal ultrasound (for female patients only). Follow-up ranged 1–13 years.
In forty-two out of 52 patients (81%) who responded to the nerve block test and received treatment with corticosteroid injections, Long-lasting relief was obtained. Three patients refractory to repeated injections of corticosteroid underwent surgery (neurolysis in one patient and nerve resection in two). CT-scan of the lumbar spine revealed significant spinal stenosis and nerve root compression at the level of L1–3 in 3 out of 6 patients.
All fractures healed at an average time of 9.2 weeks (5–26) and for the open fractures 19 (12–26) weeks. Hardware was removed in 8 cases with no complications. In two cases re-operation was needed. In one early case the nail was fractured and replaced. In the second case the bone was circlaged due to fragmentation around the fracture site and a bigger nail was inserted few days later (wrong smaller nail was inserted previously).
No doubt that revision TKR is a challenging procedure. This procedure may be divided into three steps. First, a careful clinical examination is needed to assess range of motion, stiffness and possible difficulty in exposing and extracting the prosthesis. Second, an examination of joint stability is needed. Finally, radiographs should be evaluated for any bone deficiency that may require bone grafting or special prosthesis. Exposure approaches may change in cases when second stage implantation is performed when an infected total knee replacement exists and when a cement spacer is used. In the cases when the cement spacer is left in place for a longer period of time, stiffness is much more prominent and therefore exposure may be even more difficult. Subvastus and midvastus approaches are not suitable for this kind of revision. Usually in revision of total knee replacement or after cement spacer procedures, a larger exposure with the use of either snip incision, or osteotomy of the tibial tuberosity, or VY exposure is required. There are some cases where one can perform revision total knee without the extra exposure mentioned. In revising total knee replacement, it is imperative that the joint line be restored to its original position. There are a few techniques that can be used to achieve this task by using a few landmarks. They include:
The residue of the menisci. The distance measured from the medial epicondyle to the joint surface. The distance measured from the head of the fibula to the original joint surface. This can be done by comparing the other non-operated knee too. The decision to which kind of prosthesis to use depends on the amount of bone loss and the injury to the surrounding structures and ligaments. One should be prepared for all options during surgery, in other words, using constrain or unconstraint prosthesis in the same patients. This depends solely on the findings during surgery. In our hospital, we have used all the exposure approaches of the knee in revision surgery. We prefer the snip excision in the first stage, and if this is not sufficient then a tibial tuberosity osteotomy is preferred to the VY incision of the quadriceps mechanism. We found that using the meniscal residue is a very useful landmark for the joint line and we use it constantly.
The incidence of comminuted proximal femur fractures is increasing, due to the growing proportion of elderly people in the general population. Severely depleted cancellous bone in the femoral head and neck prevent stable proximal purchase, mandatory for intertrochanteric and subtrochanteric fractures. Osteoporotic bones are associated with high implant failure rates, evidenced by cutout and upward screw penetration of the hip joint. A new method for femoral head fixation is described. The peg consists of a distal end that can expand in diameter from 7.8mm to 10.5mm by using pressurized saline, allowing good abutment into the femoral head. The peg may be connected to a side plate or an intramedullary device for inter or subtrochanteric fractures.
Preliminary positive results indicate that this new method may be suitable for inter or subtrochanteric femoral fracture fixation.
Osteonecrosis (ON) around the knee joint can be spontaneous (primary), without comorbid medical conditions, or secondary. ON is characterized by sudden pain, usually self resolving after six months to a year, night pain, and involving mainly women older than 55 years of age. Twenty seven patients with primary ON were retrospectively reviewed. The patients were evaluated clinically (physical examination and H.S.S. scoring) and radiographically (plain radiographs were done at the beginning and at the end of follow-up and MRI studies). The MRI study included calculations of the area and the volume of the lesion, osteoarthritic changes, bone collapse and meniscal pathologic findings. The majority of the patients, 96% (26/27), complained of sudden pain. Night pain was observed in 46% of the patients. Osteoarthritic changes observed in 60% of the patients and further deterioration (37%) was noted at follow up radiographs. Osteoarthritic changes were more predominant in patients with tibial condyle involvement rather than those with femoral involvement, 61% vs. 43% (p=0.04), respectively. Diagnosis of osteonecrosis by the initial radiographs was more common in patients with femoral involvement (7 femurs vs. 1 tibia). All ON lesions were diagnosed by MRI, from these, 17 meniscal tears (63%) were detected. Several observations were noted in the volumetric analysis: Tibial lesions were larger than femoral lesions (8.1cm3 vs. 3.1cm3, respectively, p=0.026). Women had significantly larger lesions in volume and area than men (area – 5.09cm2 vs 2.05cm2, p=0.01; and volume – 6.6cm3 vs. 1.2cm3, p=0.001). Significant correlation was found between bone collapse and the need for total knee replacement (TKR): 40% collapse in the TKR patients versus 13.6% collapse without TKR (p=0.028). Patients that were diagnosed with collapse at the end of the follow up had a larger area (5.8cm2 vs 3.7cm2) and a lower HSS score (68.5 points vs. 83 points, p=0.02) than those without. A significant correlation was noted between a larger lesion area and lower HSS scoring (p=0.037) at the end of the follow-up. Patients with tibial lesions had more meniscal pathologies involvement, 56.3% vs. 43.8%, however it was not statistically significant (p=0.68). We conclude that MRI study for patients with ON and calculating the area and the volumetric data particularly, is an accurate predictive tool for the natural history of knee ON. The findings presented here may guide us in determining the best possible treatment.
All surgeries were minimally invasive using a single 2–4 cm skin incision.
Between the years 1999 and 2001, approximately 3000 expandable intramedullary nails were used worldwide in various surgical procedures. From this number, 250 of these nails were used for traumatic fractures and are the focus of the study presented here. The subjects consisted of 160 males and 90 females with a mean age of 41 years. Initial radiographs were obtained for all subjects. Additional X-rays and follow-up data were reported for only 75 patients (30%) with follow-up time averaging 18 weeks. Most of the fractures occurred in the midshaft (64%), followed by distal thirds (22%), and then proximal (14%). The group was then divided according to fracture location: humerus, tibial and femur. The nail was used in 92 humerus fractures. Follow-up data was available for 35 patients with a follow-up time averaging 16 weeks. The nail was inserted retrograde in 61% of the patients and antigrade in 39% of the patients. Partial reaming was done in 42% of the cases. Mean operating time was 52 minutes and fluoroscopy time was 3.8 minutes. Anatomical reduction was achieved in 96% of the cases and in 4% of the cases, acceptable reduction was achieved with a varus <
10°. Surgical outcomes included 28 complete bone union, and 7 partial union. Eight nails were removed after complete union was achieved. In addition, the inflatable nail was used for treatment of 114 tibial fractures. In 39% of the cases a partial reaming was done. Average operating time was 39 minutes and fluoroscopy time was 3.4 minutes. All the fractures were reduced anatomically. In 25 patients with mean follow-up of 18 weeks, 14 united completely and 11 united partially. Nine nails were removed after completion of the union. Data on 44 patients with femoral fractures treated by the inflatable nail were also reported. Only 15 patients were available for follow-up with an average of 21 weeks follow-up time. Nail insertion by the antegrade approach was used in 89% of the patients and the retrograde approach was used in 11% of the patients. Partial reaming was done in 44% of the cases. Mean operating time was 60 minutes and fluoroscopy time 7.5 minutes. Anatomical reduction was achieved in all with the exception of two patients with mild valgus deformity (<
10°). By the end of the study period, 8 had complete union, 7 had partial union. In summary, the nail was found to be very effective and safe. The surgeons who performed the surgery reported that surgical and fluoroscopy time were both reduced by half. Reaming was not mandatory and this contributed to the shortened operating time. No complications were encountered during extraction of all the nails after completion of union, even in those patients in whom the nail developed an hour glass configuration according to the size of the medullary canal. It is still too early to conclude if this nail will produce better or equal results to the conventional interlocking nails. Nevertheless, the lack of reaming, locking, and the low contact area of the nail with the medullary canal, may explain the rapid healing observed in some cases.