Functional Outcomes of Patella Fractures Treated With Anterior Plate Osteosynthesis at One Year.

OBJECTIVES: To evaluate the functional outcomes of patients with displaced patellar fractures treated with anterior plate constructs. DESIGN: Prospective cohort and retrospective clinical and radiographic assessment. SETTING: Level I Trauma Center. PATIENTS/PARTICIPANTS: Between 2014 and 2018, 18 patients who underwent operative intervention for an isolated, displaced patella fracture (OTA/AO 34C1-3) with a minimum of 1-year follow-up agreed to participate in the study. The mean follow-up was 19.5 ± 6.0 months. INTERVENTION: Patients were treated with 2.4 or 2.7-mm plates and supplemental screws or cerclage wires. MAIN OUTCOME MEASUREMENTS: Patients were evaluated with the Short Form-36 Survey and the Knee Injury and Osteoarthritis Outcome Scores and asked about symptomatic implants. The range of motion was assessed by goniometer. RESULTS: The cohort had no wound complications, infections, nonunion, loss of reduction, or implant failure. Active knee flexion was 131 ± 7 degrees. Five patients (28%) endorsed implant irritation. Only one patient (5.5%) underwent implant removal, which consisted of transverse screw removal alone. Twelve of the 14 patients (86%), who were previously employed, returned to work at 10 ± 7 weeks. All Knee Injury and Osteoarthritis Outcome Scores subscale scores and the Short Form-36 Survey scores for physical functioning, limitations due to physical health, limitations due to mental health, and social functioning were significantly lower than reference population norms (P < 0.05). CONCLUSIONS: Anterior plating provides reliable fixation for displaced patellar fractures and results in a low incidence of implant irritation. However, patients who had anterior fixation for displaced patella fractures continue to exhibit functional deficits at 1-year postoperatively. LEVEL OF EVIDENCE: Therapeutic Level IV. See Instructions for Authors for a complete description of levels of evidence.

Implant Failure Rates and Cost Analysis of Contoured Locking Versus Conventional Plate Fixation of Distal Fibula Fractures.

The authors analyzed 330 consecutive Weber B distal fibula fractures that occurred during a 3-year period and were treated with either a contoured locking plate or a conventional one-third tubular plate to compare the cost and failure rates of the 2 constructs. The primary outcomes were failure of the distal fibular implant and loss of reduction. Secondary outcomes were surgical wound infection requiring surgical debridement and/or removal of the fibular implant, and removal of the fibular plate for persistent implant-related symptoms. No failure of the fibular plates or distal fibular fixation occurred in either group. A total of 5 patients required surgical revision of syndesmotic fixation within 4 weeks of the index surgery. Of these patients, 1 was in the contoured locking plate group and 4 were in the one-third tubular plate group (P=.610). The rate of deep infection requiring surgical debridement and/or implant removal was 6.2% in the contoured locking plate group and 1.4% in the one-third tubular plate group (P=.017). The rate of lateral implant removal for either infection or symptomatic implant was 9.3% in the contoured locking plate group and 2.3% in the one-third tubular plate group (P=.005). A typical contoured locking plate construct costs $800 more than a comparable one-third tubular plate construct. Based on a calculated estimate of 60,000 locking plates used annually in the United States, this difference translates to a potential avoided annual cost of $50 million nationally. This study demonstrates that it is possible to treat Weber B distal fibula fractures with one-third tubular plates at a substantially lower cost than that of contoured locking plates without increasing complications. [Orthopedics. 2017; 40(6):e1024-e1029.].

Complications following tension-band fixation of patellar fractures with cannulated screws compared with Kirschner wires.

BACKGROUND: Displaced patellar fractures are commonly stabilized with a modified anterior tension-band construct. The goal of the current study was to compare the incidence of complications after tension-band fixation of the patella with Kirschner wires as compared with cannulated screws. METHODS: We performed a retrospective cohort study of consecutive, surgically treated patellar fractures. Patients were divided into two cohorts: fractures fixed with use of Kirschner wires and fractures fixed with use of cannulated screws. The primary outcome measure was early loss of fixation that necessitated revision surgery. Secondary outcomes included early postoperative infection and the need for implant removal. RESULTS: Four hundred and forty-eight patellar fractures were studied. Kirschner wires were used for fixation in 315 (70%), and cannulated screws were used for fixation in 133 (30%). The incidence of fixation failure was 3.5% in the Kirschner-wire group and 7.5% in the screw group (p = 0.065). A postoperative infection occurred in 4.4% of patients in the Kirschner-wire group and 1.5% of patients in the screw group (p = 0.17). One hundred sixteen (37%) patients in the Kirschner-wire group and 30 (23%) in the screw group underwent elective implant removal (p = 0.003). After adjusting for confounding variables, a trend toward increased incidence of fixation failure with screws as compared with Kirschner wires was present (p = 0.083). Patients treated with Kirschner wires were twice as likely to undergo implant removal compared with those treated with screws (p = 0.002). CONCLUSIONS: Serious complications are uncommon following treatment of patellar fractures with a modified tension-band technique, with use of either Kirschner wires or cannulated screws. In both groups the rate of fixation failure was low, as was the rate of postoperative infection. Symptomatic implants, the most common complication observed, were twice as frequent in patients treated with Kirschner wires.

Reverse achilles tendon allograft technique for anterior cruciate ligament reconstruction.

Because of the increasing popularity of allograft anterior cruciate ligament (ACL) reconstructions, the technical difficulties with posterior bone loss in revision ACL surgery, and the limited supply of bone-patellar tendon-bone donor grafts, we have developed a technique using a reversed Achilles tendon allograft to reconstruct the ACL-deficient knee. This technique allows for bony tibial fixation with an interference screw by rotating the graft 180 degrees and optimizing soft-tissue fixation at the femur with an EndoButton CL (Smith & Nephew, Andover, MA). Short-term follow-up (average, 26.4 weeks) of 10 patients undergoing the reversed Achilles technique has shown excellent results, with Lysholm scores between 91 and 100 and 84 and 90 in 8 of 10 and 2 of 10 patients, respectively. Objective stability assessments, including the Lachman test, anterior drawer, and pivot-shift tests, were also encouraging. Reverse Achilles tendon allografts can be excellent alternatives for ACL reconstruction when bone-patellar tendon-bone grafts are not indicated.

Preliminary results of tibial bone transports with pulsed low intensity ultrasound (Exogen).

OBJECTIVE: This study assessed whether the use of noninvasive, pulsed low intensity ultrasound (Exogen) reduced external fixation time for bone transport patients with large, segmental tibial defects. DESIGN: This was a prospective study compared to a previously treated control group. SETTING: All surgeries and postoperative care were done at the senior author's hospital facilities. PATIENTS/PARTICIPANTS: Eight patients with large tibial segmental defects, acute or chronic, were studied. All patients were male, mean age 34 years (range 18-50). INTERVENTION: All patients were treated with a single-level bone transport. Bone transports started 5 to 10 days after a metaphyseal corticotomy and progressed with one-quarter millimeter advancement 2 to 4 times per day. Exogen was applied to the regenerate site in the second postoperative week and to the docking site after docking was complete. The treatment was used for 20 minutes daily at each site. The patients were followed weekly for the first 4 weeks. They were then followed bimonthly for 2 months and then monthly until consolidation had occurred. MAIN OUTCOME MEASURES: The 2 main outcome measures used were the external fixation time measured in months and the external fixation index (time in the frame per cm of bone transported) measured in months per cm. RESULTS: The mean follow-up from frame removal to the time of the last clinic visit was 12.4 months (range 4-32). The mean external fixation time was 13.91. The mean external fixation index was 1.34 months per cm transported for the Exogen group and 2.02 months per cm for the control group. Although not statistically significant because of small numbers, the external fixation index was reduced by 17.21%. CONCLUSION: These data further confirm already published data on the acceleration of fracture healing by low intensity pulsed ultrasound and, in our case, regenerate consolidation. Shorter treatment periods reduce complications and expenses and return patients back to regular activities more quickly.