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18 Anterior Spinal Column Augmentation Techniques
There does seem to be a trend toward early inter­vention showing that patients treated less than 7 weeks after their fracture event do better from a pain standpoint than those treated later [27]. Patients who are hospitalized for pain control do benefit from early vertebral augmentation. This results in shortened hospitalization, fewer read­missions, and lower overall costs [28].

Preoperative Considerations

When planning the procedure, the following fac­tors must be taken into account: the size of the vertebral body, the size of the pedicle, if transpe­dicular or parapedicular approaches will be used, if KP or VP is desired, and if unilateral or bilat­eral needle placement is the chosen technique. A wide vertebral body with a severe compression deformity and wide pedicles may dictate a bilat­eral approach to restore height and ensure there is enough volume of PMMA to reach both sides equally. However, in the smaller vertebral body where fracture height restoration is of less inter­est, a unilateral approach may be sufficient.
Two pedicle approaches are used. Transpedicular is used whenever possible dic­tated by pedicle diameter. In patients with diameters <4 mm, a parapedicular approach may be used. In this technique, the cannula enters the bone, exits along the lateral edge of the pedicle, and reenters the vertebral body. This is possible in the thoracic spine where the rib shields any neurovascular structure. Pedicles
in the high to mid-thoracic spine may be small and severely angled making the parapedicular approach the more viable option. The differing trajectories for transpedicular and parapedicu­lar are shown in Fig. 18.3. Vertebroplasty at our institution is almost always performed from a unilateral approach. Preoperative trajectories should avoid the neuroforamina starting high on the pedicle with a slightly inferior and medial trajectory, planning length, and angles of approach.
Due to longer procedural time, at our institu­tion, kyphoplasty is reserved to single-level defor­mity or disease in younger patients where the level of deformity is believed to cause progression of deformity in the future and where fracture reduction is believed to have a reasonable chance of being accomplished. Vertebroplasty is done over multiple levels due to its speed in older patients where the goal is pain control and main­taining fracture stability without reduction.

Surgical Technique

Vertebroplasty

This procedure is performed under conscious sedation or general anesthesia and should be done in a facility with spine surgery capabilities. Biplanar fluoroscopy is essential and can be done either in the interventional suite or the operating room. It can be done with single C-arm alternat­ing between lateral and AP pictures or by using
Fig. 18.3 Trajectories showing parapedicular and transpedicular approaches
I.K. White et al.
Fig. 18.4 Showing patient positioning with standard C-arm positioning and two C-arms allowing for biplanar fluoros­copy. This same setup can be done in the interventional suite
dual arms which speed the procedure, especially when treating multiple levels.
The patient is positioned prone on a radiolu­cent operating table, and the face and pressure points are padded as well as the elbows and axilla to prevent brachial plexus and ulnar injuries (Fig. 18.4). We have not found a Foley catheter necessary. Although general anesthesia is not necessary, trained personnel should administer the conscious sedation, and vital signs should be continually monitored. The patient is then prepped and draped sterilely.
Based on preoperative images, the parapedic­ular or transpedicular approach is selected. The level of interest is then localized using fluoros­copy, placing the initial mark on the skin just lat­eral to the superior lateral border of the pedicle of interest on the AP image when using transpedic­ular trajectory (Fig. 18.5). When using the para­pedicular trajectory, the skin incision should be made 7–11 cm off of midline to allow for a more medial trajectory. The cranial/caudal trajectory should be the same as transpedicular. The skin is injected with 1% lidocaine with 1:200,000 epi­nephrine or 0.5% Marcaine with 1:200,000 epinephrine down to the pedicle making sure to inject the periosteum. A 2 mm incision is then made either with an 11 blade or 15 blade knife and a No. 11 Jamshidi biopsy needle with trocar in place. Fluoroscopy can be used to plan the
ideal trajectory. If using the transpedicular approach, the needle is advanced to the bone and located at the superior lateral aspect of the pedi­cle. Alternating between AP and lateral views, the course of the needle should follow the trajec­tory of the pedicle with slight triangulation end­ing up in the anterior half of the vertebral body. The needle should be advanced in 1–2 mm incre­ments. When using the transpedicular approach, this is usually done bilaterally as the PMMA has difficulty reaching the contralateral aspect of the body.
When using the parapedicular approach, the cannula is initially located on the transverse pro­cess. The junction of the transverse process and the facet is felt, and the Jamshidi needle is walked inferiorly until it falls off the inferior edge of the transverse process. The entry point is at the lat­eral vertebral body, immediately caudal to the transverse process, and at the lateral junction of the pedicle on the AP fluoroscopy. From this entry point, the goal is to reach the middle of the body on the AP while reaching the anterior half of the vertebral body. It should be noted that the parapedicular approach theoretically increases the patient’s risk for pneumothorax in thoracic cases. The location of the needle for unilateral approaches is important as the amount of cement able to be infused into the body is proportional up to a point in pain reduction, and poor needle
18 Anterior Spinal Column Augmentation Techniques
Fig. 18.5 Choosing entry point on transpedicular and parapedicular trajectories on the AP radiograph. Notice the lateral starting point approximately 7–11 cm off of
placement can reduce the amount of cement that is able to be symmetrically injected [27].
The surgeon should practice safety from excessive radiation by using a clamp or lead gloves to shield their hands. If multiple levels are going to be done, it is preferred to place all needles before cement injections. It used to be common practice before cement injection to inject a small amount of contrast to visualize the venous channels present; however, this practice has not been proven to have clinical utility [29]. Before injecting the bone cement, the operator should check the needle to make sure it is deemed to be in a suitable position. If the needle position is deemed to be non-ideal, there is the option of either replacing the needle or a curved inner can­nula can be used to deliver bone cement through­out the entirety of the vertebral body.
There are several cement products on the mar­ket with differing properties; however, for the majority of cases, PMMA is the bone cement of choice. In commercial kits, it comes as two parts (a methyl-methacrylate polymer powder and a
midline at the level of the pedicle for the parapedicular, whereas the transpedicular is 1 cm off the superolateral border of the pedicle of interest
liquid monomer), and, once mixing occurs, the components begin polymerization. A radio-dense material such as barium is added to aid visualiza­tion. The PMMA is mixed for 3–5 min until it is the consistency of hair conditioner and loaded into a 10 cc syringe. The cement for vertebro­plasty is slightly less thick than that for kypho­plasty, which is more similar to the consistency of toothpaste. During the hardening process, PMMA undergoes an exothermic reaction which may be responsible for some of the pain relief experienced from the procedure. After the cement is deemed to be at the appropriate consistency, the injection tool is connected to the needle. There are a number of devices now available, but
and have an attachment at the base for the needle and for the syringe. The cement is then injected under steady pressure. In the lumbar spine, usu­ally 5–10 cc can be injected safely with decreas­ing amounts for severe fracture patterns and fractures higher in the thoracic spine. During injection, care must be taken not to let cement
I.K. White et al.
Fig. 18.6 After needle is placed, complications can arise with extravasation of cement into large draining veins, along the body into the foramen, into the spinal canal, and out the fracture site into the paravertebral soft tissues
extravasation course beyond the borders of the body. Anteroposterior and lateral images should be taken to assess that the cement remains within the borders of the body. The spinal canal should be critically evaluated as cement extrusion into the spinal canals should be avoided. Complications related to extravasation are shown in Fig. 18.6.
After the cement is injected and the surgeon satisfied with the amount injected and the fluoro­scopic picture, the injection device is removed, and the inner cannula of the Jamshidi needle replaced. This needs to be maintained until the cement has completely hardened as polymeriza­tion causes volume expansion of the PMMA which can back up into the needle. After the PMMA is hardened, the Jamshidi needle is removed by twisting motion, and each incision can be closed with a monofilament suture. The patient should be kept supine for 1–2 h post-op and then discharged home after meeting dis­charge criteria. Neurological examination should be performed before discharge.

Kyphoplasty

Kyphoplasty is a procedure similar to vertebro­plasty with the exception that an inflatable bal­loon tamp is inserted into the vertebral body. The
benefits of this procedure over VP are largely radiographic and theoretical. The major benefit is some height restoration to acute fractures and decreased extravasation of cement due to lower injection pressures and compacted bone around the cavity which was created [30, 31]. Kyphoplasty has been shown to have greater vol­umes of cement injected per level, better short­term pain relief, and better short- and long-term kyphosis angles. Long-term clinical outcomes in terms of pain at 1 year are similar [30, 31]. The downside of kyphoplasty is the longer operative times often necessitating general anesthesia. Recently, the Kyphon device has come “off pat­ent” making the procedure more affordable since generic devices have entered the market reducing costs. Kyphoplasty is often performed bilaterally as this allows for maximal height restoration. In our experience, end plate restoration is more likely to occur in the acute period before frac­tures organize into the chronic phase.
In kyphoplasty, docking of the needle tends to be done in a similar fashion to vertebroplasty done by the bipedicular approach (Fig. 18.7). The kyphoplasty needle should have a mildly triangu­lated trajectory and lie in the posterior half of the vertebral body. The stylet is moved, and a hand drill is used to create a pathway for the balloon. The drill should be stopped 3–6 mm from the
18 Anterior Spinal Column Augmentation Techniques
Fig. 18.7 Balloon-assisted kyphoplasty showing restoration of vertebral body height with packing out of cancellous bone to create cavity and filling with cement under low pressure
most posterior aspect of the anterior cortex of the body, and, at this point, the drill tip should approximate the midline. The drill is then removed, and the balloon tamp is inserted. The markings on the balloon tamp are on the posterior aspect of the balloon, and these markings should be at least 5 mm from the tip of the cannula. The tip of the tamp should not be less than 5 mm from the anterior aspect of the vertebral body to assure that inflation will not be inside the cortical bone.
Once the operator is satisfied with the balloon position, balloons are inflated with contrast under fluoroscopy and with continuous pressure moni­toring. It is important to make sure that balloon tamps do not violate the cortical bone on any sur­face as this will increase the risk of cement extravasation. The balloons should not be inflated to more than 220 psi, which is the maximum rec­ommended pressure. From our experience, stag­gering the balloon inflation helps delineate the level of inflation of each balloon as the contrast can obscure visualization if one is fully inflated on the lateral imaging. This also aids in symmet­ric fracture reduction. Once satisfactory inflation is achieved, balloons are deflated and removed. In the event that the fracture displaces after the balloons are deflated, there is the option to keep one inflated for the injection of the cement. Small
cannulas containing PMMA at the consistency of toothpaste are inserted. It should be noted that this is thicker than the consistency of PMMA used for vertebroplasty. These are injected by hand, taking care to watch for extravasation. Typically cement is injected in small incre­ments bilaterally to allow for better visualization and less fluoroscopy time. Once the surgeon is satisfied with the final images and cement has hardened, the trocars are removed, and the inci­sions can be closed with monofilament suture. Postoperative imaging can be left to the surgeon’s discretion, but oftentimes the patient can be dis­charged the same day.

Kiva

The Kiva implant is a polyetheretherketone (PEEK-Optima) coil deployment system that allows fracture reduction in a controlled manner over a removable Nitinol Osteo guidewire. As the implant is deployed, the coil stacks upon itself adding substance to the body while reducing the fractured end plate. Once the coil is completely deployed, it forms a hollow cylinder ideally with its borders from end plate to end plate. PMMA is injected after the device is deployed to fill the
I.K. White et al.
Fig. 18.8 (a) KIVA device docking needle is placed in a transpedicular trajectory with inner trocar in place. (b) Trocar is removed, and KIVA deployment device is attached. (c) The coil knob is turned to deploy the coil completely. The KIVA device is then deployed over the coil using the knob on the other side. The coil is then
center, containing the PMMA within the walls of the cylinder as shown in Fig.
18.8a–d.
The Kiva implant is deployed through a uni­lateral transpedicular approach. The setup is the same for both vertebroplasty and kyphoplasty, and the procedure can be done under local or general anesthesia. The initial needle is placed in a similar fashion in the anterior half of the verte-
retracted and the device detached, and (d) a polymethylmethacrylate- filled plunger fills the center of the device through holes in the center of the device in a controlled fashion similar to kyphoplasty. The device both restores height and decreases radiographic cement extravasation
bral body. It does not have to reach the midline as with other unilateral approaches. At this point, the stylet for the needle is removed, and the head of the device is inserted near the most anterior part of the vertebral body. The device is then turned medially with the top of the device deploy­ing the coil. Once the coil is deployed, the implant is deployed over the coil slowly increasing the
18 Anterior Spinal Column Augmentation Techniques
anterior vertebral body height. Once the graft is deployed, PMMA is injected through the deploy­ing device through the graft into the center of the cylinder that the graft created. The graft is then detached from the deploying device, and the wound is closed.
The Kiva device was recently compared to kyphoplasty in the KAST trial. The major finding was the Kiva device showed significantly less cement extravasation. This can be explained by the device’s ability to keep the PMMA central. This finding did not result in any difference in clinical outcomes. There was also a decrease in adjacent level fractures but this failed to meet sig­nificance. Overall the trial showed that the Kiva implant is a safe alternative to kyphoplasty.

Using Navigation

In a very select set of instances, visualization of the vertebral column may be obscured in the severely osteoporotic, severely obese, or when vertebral levels are near the diaphragm. In these patients where the landmarks are obscured, plac­ing the needle can be very dangerous. Spinal navigation in these patients should be considered.
A reference arc should be attached to the spi­nous process rostral to the most superior level that needs to be addressed with the camera at the head of the bed. The areas of fracture can be localized with C-arm. The patient is then prepped and draped, and the O-arm is also draped so as to use the biplanar fluoroscopy function of the O-arm. Once acquisition is taken, the O-arm is moved rostral, and the navigated pedicle access needle can be used using three-dimensional navi­gation for either parapedicular or transpedicular trajectories. A Kirschner wire is then placed down the needle into the vertebral body, and the access needle is removed leaving the K-wire in place. If multiple levels are to be done, K-wires should be placed at every level that needs to be addressed. Vertebral augmentation cannulas are then placed over the K-wires, and vertebroplasty is performed under the fluoroscopy function of the O-arm, and, after all levels are completed, a three-dimensional scan can be taken to confirm the location of the cement within the body.
Although this technique is substantially more time consuming, it provides a greater level of safety in those patients with anatomy that one is unable to visualize on plain fluoroscopy.

Illustrative Case

History of Present Illness

This is a case of an 82-year-old female who has a history of osteoporosis confirmed by DEXA scan (T scores <2.5) on calcium supplementa­tion and teriparatide, who sustained an osteopo­rotic compression fracture at T10 3 years prior to vertebroplasty treatment due to intractable pain. She did well after the procedure and returned to her prior functional status until 6 weeks later when, while mopping her floor, the patient felt a pop in her back causing her to lose her breath and fall to the floor in pain. She did not note any numbness, tingling, weakness, or loss of continence.

Physical Examination

Upon initial presentation, she was at her neuro­logic baseline without deficits. She was alert and conversational, oriented x3. She was very tender to palpation over her mid to lower back. All extremities were moving with 5/5 movement with good sensation in all and she did not have any perigenital/anal anesthesia.

Radiographic Evaluation

Her preoperative radiographs are shown in Fig. 18.9a, b showing acute compression frac­tures at T11 and T12.

Initial Management

She was treated with bracing and pain control, and, although she was able to return home, her activity level decreased secondary to pain at her 2- and 6-week appointments. Her standing
I.K. White et al.
Fig. 18.9 (a) AP preoperative radiographs demonstrating compression fractures at T11 and T12. (b) Sagittal radio- graphs demonstrating the same pathology
radiographs looked grossly similar at this appointment showing an intact posterior cortex, but her son reported that she mainly was sitting in her wheelchair without much activity over this time period. It was at this point they decided she would like to undergo vertebroplasty.

Procedure and Outcome

The unilateral parapedicular vertebroplasty was performed under conscious sedation. Fourteen milliliters of PMMA was injected at each level without complication. Trajectories are shown in
18.10a and b. In recovery, she felt immediate
Fig. pain relief. Postoperative radiographs show excellent cement fill without extravasation (Fig. 18.11a, b). At 3 months post-surgery, she has returned to her baseline functional status.

Technical Pearls

• When performing these procedures and espe­cially when doing multiple levels, biplanar fluoroscopy can be used. This can be done in an interventional suite or positioning two C-arms.
• It is always imperative to obtain true AP and lateral images of the targeted vertebrae.
• When doing multiple vertebrae, it should be noted that a single batch of cement should be kept at cool temperatures to slow polym­erization. One batch typically can do three vertebrae, and, at our institution, no more than three levels are ever done at one time due to PMMA toxicity and a higher risk of adverse events. A larger amount of PMMA should be used in kyphoplasty as there should be enough bone cement to fill the cavity created and the surrounding trabecu­lar bone.
• When treating a significantly collapsed verte­bra with kyphoplasty, there are two tech­niques that have been shown to keep the fracture reduced. If there is unilateral col­lapse, the cavity contralateral to the collapse can be filled first, allowing some cement to pack the trabecular bone providing a struc­tural buttress. The second balloon can then be withdrawn.
• The second technique can be used in the set­ting of vertebra plana which re-collapses after balloon withdrawal. One milliliter of PMMA can be injected into the body, and the balloon can be reinserted and inflated allowing cement
18 Anterior Spinal Column Augmentation Techniques
Fig. 18.10 (a) Showing intraoperative parapedicular trajectory in the AP plane reaching the midline. (b) Showing the same in the sagittal plane
Fig. 18.11 (a) Showing postoperative AP radiographs and (b) sagittal radiographs post-augmentation. It should be noted that with vertebroplasty, end plate reduction and deformity correction are no different than preoperative imaging
to harden forming a thin shell of cement. The balloon can then be withdrawn and the rest of the cavity filled with cement.
this procedure involve the initial placement of the trocars and extravasation of bone cement. Placing Jamshidi needles through the neuro-elements can be avoided by obtaining true AP and lateral radiographs, lining up the end plates, pedicles,

Complications and Avoidance

and facet joints. If the image needs to be improved
in the osteoporotic patient, magnification on the Preoperative planning must always focus on the goals of the surgery while preventing complica­tions. The two complications that can arise from
C-arm may be increased, the tube may be brought
closer to the patient, and the respirations may be
held until the Jamshidi needle is placed. As stated
I.K. White et al.
before, the transpedicular approach should start on the superolateral aspect of the pedicle to avoid damage to the nerve roots. The parapedicular approach can be started lateral to the pedicle and medial to the costovertebral joint. It should be noted that the needle on this approach should not be medial to the medial aspect of the pedicle until it reaches the posterior aspect of the vertebral body to once again avoid nerve root injury and damage to the spinal cord. The parapedicular approach is usually done in mid to high thoracic fractures with transpedicular being reserved for low thoracic and lumbar fractures. With these precautions taken, the operator can be certain that the needle is in good position and has not dam­aged any of the neural elements.
The most common complication occurring in both vertebroplasty (VP) and kyphoplasty (KP) is PMMA extravasation that occurs in 11–75% of VP patients and 5–38% of KP patients. These are radiographic leaks and are rarely symptom­atic. Symptomatic leaks were reported in 1.48% of VP patients and 0.06% of the KP patients [30]. This higher leak rate is thought to be caused by the higher pressures that VP cement is injected under, the lower viscosity of the cement, and the ability of kyphoplasty to pack out the bone around the cavity that it creates. The major­ity of these leaks go into the paravertebral soft tissue, but extravasation into the spinal canal can be catastrophic, and having a spine surgeon at the institution available to perform emergent decompression is imperative. In order to avoid this, it is advisable to do this under live fluoros­copy and to confirm an intact posterior cortex when starting out.
Cement extravasation can be minimized first by patient selection, choosing patients with an intact posterior cortex if possible. The needle should be placed in the anterior two-thirds of the vertebral body to allow some room to fill the body without reaching the posterior cortex too early. It is essential to make sure the PMMA is at a consistency thick enough to maintain its integ­rity. When doing a kyphoplasty, the balloon should not be inflated to the point where there is any outpouching through any of the cortical bone so as not to create any breaches. When
deploying the PMMA, it should be done in small increments 0.2–0.5 ml at one time with frequent fluoroscopy. When using the bilateral approach, small amounts of PMMA should be placed alter­nating each side one at a time as on the lateral image large amounts of PMMA on one side can obscure visualization of the contralateral PMMA as it is being deployed. If there is any evidence of breaches in the contrast, the procedure should be stopped immediately. If vertebroplasty is being performed and it is felt that a less than adequate amount of contrast has been deployed, the cannula can be repositioned. Although most cement leaks are clinically inconsequential, if there is a significant leak, the patient must be examined before leaving the operating room, and, in the face of a neurologic deficit, if a deficit is appreciated, emergent decompression should be considered.

Conclusion

Vertebral augmentation is a minimally invasive technique with expanding indications in the fields of oncology, trauma, and metabolic dys­function providing pain relief, deformity correc­tion, and spinal stability with minimal surgical morbidity and, if careful, low complication rates. Surgeon familiarity with these techniques have led to utilization of these materials in hybrid models both in the augmentation of pedicle screw pullout strength and providing anterior stiffness to an unstable spine allowing fewer seg­ments to be fixated. Newer devices are currently being developed that may provide greater defor­mity correction with less chance of cement extravasation.

References

1. Cooper C, Atkinson EJ, O’Fallon WM, Melton LJ 3rd. Incidence of clinically diagnosed vertebral fractures: a population-based study in Rochester, Minnesota, 1985–1989. J Bone Miner Res. 1992;7(2):221–7.
2. Lindsay R, Silverman SL, Cooper C, et al. Risk of new vertebral fracture in the year following a fracture. JAMA. 2001;285(3):320–3.