Abstract
Background Unilateral fractures involving complete separation of the lateral mass from the vertebra and lamina (floating lateral mass fractures) are a unique subset of cervical spine fractures. These injuries are at significant risk for displacement without operative fixation. Posterior fixation has proven to facilitate adequate fusion. However, there are few data supporting the clinical success of single-level anterior fixation.
Methods Biomechanical evaluation of floating lateral mass fractures and a consecutive case series of patients with rotationally unstable floating lateral mass fractures treated with anterior fixation using an integrated cage-screw device with anterior plating (ICSD) was performed. The study comprised 7 fresh human cadaver cervical spines (C2-C7), and 11 patients with floating lateral mass fractures. Segmental flexibility testing evaluating axial rotation, flexion/extension, and lateral bending was performed in a cadaveric model after 2 types of single-level anterior fixation and 1 type of 2-level posterior fixation. Eleven patients with a floating lateral mass fracture of the cervical spine underwent anterior fixation with an ICSD. Radiographs and clinical outcomes were retrospectively reviewed.
Results Compared with the intact condition, posterior instrumentation significantly (P < .05) reduced range of motion (ROM) in all 3 planes; anterior fixation with cervical plate and interbody spacer significantly reduced ROM in lateral bending only; and the ICSD significantly reduced ROM in flexion/extension and lateral bending. In the clinical arm, there were no long-term complications, subsidence >2 mm, failure of fixation, reoperation, pseudoarthrosis, or listhesis at final follow-up.
Conclusions The addition of 2 screws placed through a cervical cage can improve anterior fixation in a human cadaveric model of floating lateral mass fractures. Early clinical results demonstrate a low complication rate and a high rate of healing with single-level anterior fixation using this technique.
- floating lateral mass fracture ,
- cervical fracture ,
- anterior cervical fusion ,
- posterior cervical fusion
INTRODUCTION
Unilateral fractures involving complete separation of the lateral mass from the vertebra and lamina (previously described as lateral mass fracture-separation, floating facet fractures, floating lateral mass, and unilateral lateral mass-facet fracture) are a unique subset of cervical spine fractures.1,2 The leading cause of these injuries is motor vehicle collisions,3,4 but the exact mechanism of injury has not been clearly established. These fractures often present with minimal displacement; however, there is nearly uniform consensus in the literature that these injuries are rotationally unstable.1,2,4–9 Multiple authors have reported failure to maintain alignment when these fractures are treated in a cervical orthosis, with displacement rates up to 100%.1–14 Because of this risk, these fractures are now routinely treated with operative fixation at level 1 trauma centers.1–3,5–7,11,13–17
Floating lateral mass injuries in the cervical spine have historically been treated by posterior instrumentation (PI) and fusion of at least 3 vertebrae (2 motion segments), with good results.16 These injuries have also been successfully treated via anterior fixation with cervical plate and interbody spacer (SP),7 although failures have been reported with anterior fixation of only 1 motion segment.1,2 Recently, the authors have treated floating lateral mass fractures with anterior fixation of a single motion segment using a novel integrated cage-screw device in addition to standard anterior plating. Although many surgeons often use an anterior technique to address these fractures, there is a need for studies addressing the efficacy of these techniques. To our knowledge, no previous studies exist evaluating the kinematics of floating lateral mass injuries, or relevant fixation methods. The aims of this study were 2-fold. The first was to determine whether fixation can be improved by using an anterior approach with an integrated cage-screw device and anterior plating in a human cadaveric model of floating lateral mass fractures. The second was to present a case series of patients who had received this type of fixation and to determine the rate of loss of fixation and surgical complications.
MATERIALS AND METHODS
Specimen Preparation
Seven fresh human cadaver cervical spines (C2-C7) were used. The specimens were harvested from 4 female and 3 male cadavers (mean age, 59 ± 6 years) and stored at −20°C prior to thawing. The spines had been radiographed previously in the anteroposterior and lateral planes to ensure the absence of fractures, deformities, and any metastatic disease. The spines were carefully denuded of paravertebral musculature while the spinal ligaments, joints, and disc spaces were preserved. Each spine was potted proximally at C2 and distally at C7 in a 3:1 mixture of Bondo auto body filler (Bondo MarHyde Corp, Atlanta, Georgia) and fiberglass resin (Home-Solution All Purpose Bondo MarHyde). Plexiglas markers, each having 3 infrared light-emitting diodes, were secured rigidly to the anterior aspect of C2, C3, C4, C5, C6, and C7 vertebral bodies using bone screws to track its motion with an Optotrak Certus (NDI Inc., Waterloo, Ontario, Canada) motion analysis system. The location of the markers (denoting a rigid body) was approximately aligned sagittally along the curvature of the spine. The Optotrak Certus software was able to superimpose the coordinate systems of 2 adjacent vertebral bodies in order to inferentially determine the relative Eulerian rotations in each of the 3 planes.
Flexibility Testing
The specimen was fixed to the load frame of a 6 degree of freedom spine simulator, and a pure moment was applied to the C2 vertebra through servomotors.18,19 The specimen was maintained moist throughout the test by spraying it with 0.9% saline. All tests were carried out at room temperature of 25°C. Each of the test constructs was subjected to 3 load-unload cycles in each of the physiologic planes generating flexion-extension, right-left lateral bending and right-left axial rotation load displacement curves. This was achieved by programming the motors to apply continuous moments in each physiologic plane. A typical load-unload cycle in the sagittal plane comprised neutral → full flexion → full extension → neutral (3 times). Data from the third cycle were considered for analysis. The design of the load frame enabled unconstrained motion of the spine in response to an applied load. There was no compressive preload applied on the specimen. A load control protocol was used to apply a maximum moment of ±1.5 N/m at a rate of 1°/sec.18–20 This describes the specified rate of motor movement in order to achieve the load limit of 1.5 N/m. The 3-dimensional intervertebral rotation was obtained from the Optotrak Certus data files in the form of Euler angles (°) about the x-, y-, and z-axes: +Rx/−Rx, +Ry/−Ry, and +Rz/−Rz denoting flexion-extension, right-left axial rotation, and right-left lateral bending range of motion (ROM), respectively. The Euler sequence used in this study was xzy.
Study Design
Each of the 7 spines was initially tested in the intact state. Following intact testing, a right-sided floating lateral mass fracture was created at the C5-C6 level. The injury model was designed to mimic a high-grade floating lateral mass pattern. This was achieved by first cleaning the specimen of the residual muscles while preserving the discoligamentous elements of the functional spinal unit. The laminofacet junction and pedicle on the right at C5 were then identified and these structures transected. The lateral mass was allowed to remain—floating in place, secured by the intact facet capsules. The interspinous ligament, supraspinous ligament, and the right side of the anterior longitudinal ligament with adjacent annulus were carefully dissected out of the specimen to simulate the fractured state. Paraspinal musculature had been removed previously. Testing was then repeated under the same loading conditions as for the intact state. After testing of the injured state, the following fixation constructs were tested in sequential order: 1) PI, with posterior lateral mass fixation and rods at C4-C6 (screws at C4, C5, and C6 on the left side, and at C4 and C6 on the right side), with a cross connector at C5-C6; 2) spacer and anterior cervical plate (SP), a radiolucent interbody spacer with an anterior cervical plate at C5-C6; and 3) novel anterior fixation technique (ICSD), with an integrated spacer-plate and anterior cervical plate at C5-C6. Titanium polyaxial screws (3.5 mm in diameter and 14 mm in depth) from the ELLIPSE Occipito-Cervico-Thoracic Stabilization System (Globus Medical Inc., Audubon, Pennsylvania) were placed into the lateral masses at C4, C5, and C6 levels and connected by 3.5-mm–diameter titanium rods and a cross connector at C5-C6. After testing the PI construct, discectomy was carried out at the C5-C6 level in order to place the interbody constructs. The PROVIDENCE Anterior Cervical Plate (Globus Medical Inc.) and COLONIAL Spacer (Globus Medical Inc.) were used as the anterior cervical plate and interbody spacer respectively. COALITION ACDF (Globus Medical Inc.) was used as the integrated spacer-plate device. All the implants were properly sized, and the implantation was carried out as recommended by the respective surgical technique. Subsequent to intact testing, the instrumented constructs were subjected to the same load control protocol for flexibility testing as described above.
Laboratory Data Analysis
ROM data were normalized to intact (100%). Statistical analysis was performed on raw data. Comparison of data was performed using repeated-measures analysis of variance for independent samples followed by Tukey post hoc analysis for multiple comparison procedures.21,22 Significance was accepted at P ≤ .05.
Clinical Data
After approval was obtained from our Institutional Review Board, all Level I and II Trauma Team Activations (n = 2292) seen from January 2008 to June 2011 were included from a prospective trauma database. A total of 194 patients (8%) had a cervical spine fracture, and 12 of these patients had rotationally unstable fractures of the lateral mass and underwent fixation (6% of fractures). Of these patients, 1 was excluded after being lost to follow-up at 56 days, leaving a total sample size of n = 11. The level of injury was confirmed with upright radiographs. Specifically, any spinal level with listhesis on a lateral radiograph of the cervical spine was identified as unstable. Patients with unstable fractures were treated with an integrated cage-screw device with anterior plating. Clinical and radiographic follow-up was then carried out. Metrics used were fusion grade,23 lordosis, range of motion, presence of subsidence >2 mm, and any postoperative complications.
RESULTS
Flexion-Extension
The injured condition had a significantly higher ROM (245% ± 100%, P < .05) compared with intact condition (100%). All instrumented constructs (PI, SP, and ICSD) significantly (P < .05) reduced ROM (11% ± 5%, 31% ± 22%, and 18% ± 9%, respectively) compared with injured condition ROM (245% ± 100%). The PI (11% ± 5%) and ICSD (18% ± 9%) constructs significantly reduced ROM compared with the intact condition (100%). The SP (31% ± 22%) construct reduced ROM compared with the intact condition (100%); however, no statistical significance was achieved.
Lateral Bending
All instrumented constructs (PI, SP, and ICSD) significantly (P < .05) reduced ROM (7% ± 6%, 51% ± 46%, and 27% ± 15%, respectively) compared with the injured (195% ± 76%) and the intact (100%) conditions. The injured (195% ± 76%) condition had a higher ROM compared with the intact (100%) condition; however, no statistical significance was achieved.
Axial Rotation
The injured condition had significantly higher ROM (P < .05) with axial rotation (211% ± 69%) compared with the intact condition (100%). The PI (13% ± 8%) construct, the stiffest of the 3 constructs, significantly (P < .05) reduced ROM compared with the intact (100%) condition. The SP (71% ± 40%) and ICSD (48% ± 26%) constructs reduced ROM compared with the intact condition, without statistical significance. All instrumented constructs significantly (P < .05) reduced ROM compared with the injured condition. Range of motion results are summarized in Figure 1.
Clinical Results
Eleven patients (average age, 34 years; range, 15-80 years; median age, 36 years) with unilateral floating lateral mass fractures of the cervical spine were treated with the ICSD. Of the 11 patients, 4 smoked tobacco. Instrumentation was performed at the level of listhesis demonstrated on upright radiographs obtained either acutely or at the time of follow-up after initial treatment in a cervical collar. This included 1 fracture at C4-C5, 5 fractures at C5-C6, 3 fractures at C6-C7, and 2 fractures at both C5-C6 and C6-C7. Average clinical follow-up was just under 1 year (347 days; range, 80–920 days; median, 328 days), whereas average radiographic follow-up was almost 18 months (509 days; range, 80–1399 days; median, 338 days). Fusion grade was identified as described previously by Carter et al.23 (Table 1). The results are as follows: 8 patients had a fusion grade of 1, and 2 patients had a fusion grade of 2. Of the 4 patients who smoked tobacco, 3 had a fusion grade of 1 and 1 had a fusion grade of 2. In the nonsmokers, 5 had a fusion grade of 1 and 1 had a fusion grade of 2. The average lordosis was 4.08° (range, 1°–6.3°; SD, 1.87°). Of the 11 patients, 8 were found to have <2° of motion at the level of fixation. ROM was not determined in 2 patients because of a lack of radiographic follow-up. Fusion grade, lordosis, and ROM were not determined in 1 patient because of poor radiographic quality secondary to body habitus. The only complication reported was dysphagia in 1 patient, which quickly resolved. Subsidence >2 mm was not found in any patient. At final follow-up, there were no instances of failure of fixation, reoperation, pseudoarthrosis, or significant adjacent segment listhesis. These results are summarized in Table 2.
DISCUSSION
Cervical spine injuries are a common injury in the polytraumatized patient (5.37%),24 occurring in 11.2% of motorcycle collisions and 14.1% of motor vehicle collisions.25 A subset of cervical spine fractures, floating lateral mass fractures, are rotational injuries that require operative fixation to prevent displacement. Previously, fixation was achieved most reliably through posterior instrumentation and fusion. This approach provides excellent stability; however, the logistics of prone positioning can be problematic, especially in patients with extremity fractures (up to 10% of patients with cervical spine fractures26). Additionally, infection rates are higher in the posterior approach compared with an anterior approach.15 Treatment in the supine position decreases operative time and limits the risk of hemodynamic instability and the possibility of neurologic progression associated with prone positioning.27 Because of these advantages, many surgeons routinely treat these patients with anterior fixation of 1 or 2 motion segments. However, significant failure rates (80%–83%) have been reported with single-level anterior instrumentation and fusion in these injuries.1,2 In an attempt to avoid this complication our treatment protocol includes obtaining upright radiographs of the cervical spine to aid in determining the level(s) of rotational instability. Our clinical results suggest that while floating lateral mass fractures are, by definition, a 2-level injury, they commonly result in clinically significant instability at only 1 level. This is demonstrated by the presence of listhesis at only 1 level on upright radiographs. We saw no adjacent segment instability or instrumentation failure with this approach (Figures 2 and 3). It should be noted however, that like the patients in the study by Lee et al.,1 these patients did not have severe neurologic deficits, and their injuries did not preclude rapid mobilization in a cervical orthosis. This facilitated upright radiographs, which determined the level of operative fixation. Furthermore, patients in whom an anatomic reduction cannot be obtained should not be considered for single-level anterior fixation of any type. As Lee et al.1 point out, “horizontalization” of the lateral mass occurs either acutely or gradually as a patient is mobilized. If this rotation of the lateral mass inferiorly in the sagittal plane is not reduced anatomically, or if ligamentous injury is seen at the adjacent segment by magnetic resonance imaging, 2-segment anterior or posterior fixation is required. Additionally, patients with highly displaced fracture patterns that suggest 360-degree ligamentous disruption or fractures involving the vertebral body endplates should not be considered for single-level anterior fixation of any type. Failure to recognize these fracture characteristics may lead to increased rates of fixation failure, pseudoarthrosis, or kyphosis.
In our biomechanical testing, all 3 instrumentation techniques significantly stabilized the cervical spine compared with the injured state (simulated unilateral floating lateral mass fracture). The novel technique using the integrated cage-screw device significantly (P = .05) increased segmental stability in 2 of the 3 testing modes (flexion-extension and lateral bending) compared with the intact state, whereas the more traditional interbody spacer and an anterior plate construct increased stability in only 1 testing mode (lateral bending). Posterior segmental instrumentation improves segmental stability in all 3 planes of motion. However, this technique requires an additional level of fixation, as well as more difficulty with positioning and a more morbid surgical approach.15 In our series, 11 patients with a cervical floating lateral mass injury were treated with single-level anterior fixation with an integrated cage-screw device. Average clinical and radiographic follow-up was less than 1 year, and no loss of fixation, adjacent segment instability, or reoperation occurred. Fusion grade and re-creation of segmental lordosis were adequate in all patients. It should be noted that all patients received an integrated cage-screw device, as well as an anterior plate and screw construct. The integrated cage-screw device was not used in isolation, and this type of construct is not recommended for significant instability when used as a “stand-alone.”
Our study does have limitations. Because of the rarity of floating lateral mass injuries, the sample size of only 11 patients in the case series is quite small. Regarding the biomechanical portion of the study, it is a load-controlled, segmental flexibility study using cadaver models in which bone, disc and ligamentous cuts were made in a controlled setting and the skin and musculature have been removed. Thus, this model characterizes only acute stability and does not allow any comments to be made regarding longer-term stability (eg, testing after cyclical load). Although the floating lateral mass injury was re-created as accurately as possible, the lack of these soft tissues and the sharp nature of the osteotomies are admittedly different than the mechanism that is required to produce such injuries in vivo.
CONCLUSION
In the treatment of unilateral floating lateral mass fractures, posterior instrumentation and fusion provides the most stable fixation. However, our findings suggest that the addition of 2 screws through a cervical cage-screw device can improve anterior fixation in a human cadaveric model of floating lateral mass fractures. Early clinical results show a low complication rate and a high rate of healing with this technique.
Footnotes
Disclosures and COI: This study was approved by the Baylor Scott & White Health Institutional Review Board. CC reports travel support and provision for writing assistance, medicines, equipment, or administrative support, as well as consulting, royalties, and research support from Globus; research support from Pfizer; and consulting for LinkSpine. AMM reports employment and stock/stock options at Globus Medical Inc. PJT reports consultancy for Globus Medical Inc. and Spinology, grants from Globus Medical Inc., and royalties from Globus Medical Inc. MR reports travel support from Globus Medical Inc., royalties from Spinesmith, speaking and/or teaching arrangements with Medtronic, and research support from K2M. MM reports research support from Globus Medical Inc. SC reports stock ownership and research support from Globus Medical Inc. SK reports employment at Globus Medical Inc. NBH, DMG, and VAZ report no conflicts.
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