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27 Lumbar Disc Arthroplasty
369
The rare complication of wear debris reac­tions, such as granuloma or pseudotumor for­mation, is often unpredictable except in patients with known reaction or allergy to any of the materials utilized in the replacement disc. If this information is known, such patients are not candidates for L-TDR [3, 12, 14, 16, 27].
Careful surveillance for thromboembolic events is advisable as these patients are at partic­ularly high risk because of the mobilization of the great vessels. Postoperative DVT chemical pro­phylaxis should be discussed with the access vas­cular surgeon. Infections are rare but if they do occur decompression and fusion procedures with or without removal of the hardware are often indicated.

Conclusion

Lumbar disc replacement surgery continues to evolve based on our expanding knowledge of lumbar segmental biomechanics and results of long-term Level 1 evidence-based clinical trials. Data from recent long-term multicenter pro­spective randomized trials as well as meta-anal­ysis studies reveal superiority to fusion in both clinical and radiographic outcomes. Devices which permit controlled posterior translation of the superior articular facet processes in flexion and also limit the over-distraction of the disc interspace correlate with improved clinical out­comes. Careful patient selection, including facet joint assessment with appropriate imaging and diagnostic pain injections, is recommended especially at the L5-S1 level. Expanded indica­tions include broad-based disc herniations with spinal stenosis, multilevel degenerative disc dis­ease, and hybrid surgical indications. The prin­ciples of lumbar disc replacement surgery include careful patient preoperative evaluation and selection, meticulous and careful spine access, and appropriate implant selection based on vertebral body dimensions. Further assess­ment of endplate morphology needs to be con­sidered to ensure optimal clinical and radiographic outcomes.

References

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2. Carragee EJ, Hannibal M. Diagnostic evalua­tion of low back pain. Orthop Clin North Am. 2004;35(1):7–16.
3. Yue JJ, Lawrence JP. Indications and contraindica­tions for lumbar nonfusion surgery: patient selec­tion. In: Yue JJ, Bertagnoli R, McAfee PC, An HS, editors. Motion preservation surgery of the spine. Philadelphia: Saunders Elsevier; 2008.
4. Boden SD, Davis DO, Dina TS, Patronas NJ, Wiesel SW. Abnormal magnetic-resonance scans of the lumbar spine in asymptomatic subjects. A prospective investigation. J Bone Joint Surg Am. 1990;72(3):403–8.
5. Fernstrom U. Arthroplasty with intercorporal endo­prothesis in herniated disc and in painful disc. Acta Chir Scand Suppl. 1966;357:154–9.
6. Hamby WB, Glaser HT. Replacement of spinal inter­vertebral discs with locally polymerizing methyl methacrylate: experimental study of effects upon tis­sues and report of a small clinical series. J Neurosurg. 1959;16(3):311–3.
7. Buttner-Janz K, Guyer RD, Ohnmeiss DD. Indications for lumbar total disc replacement: selecting the right patient with the right indication for the right total disc. Int J Spine Surg. 2014;8
8. Garcia R Jr, Yue JJ, Blumenthal S, Coric D, Patel VV, Leary SP, et al. Lumbar total disc replacement for discogenic low back pain: two-year outcomes of the activL multicenter randomized controlled IDE clini­cal trial. Spine. 2015;40(24):1873–81.
9. Harrop JS, Youssef JA, Maltenfort M, Vorwald P, Jabbour P, Bono CM, et al. Lumbar adjacent segment degeneration and disease after arthrodesis and total disc arthroplasty. Spine. 2008;33(15):1701–7.
10. Freeman BJ, Davenport J. Total disc replacement in the lumbar spine: a systematic review of the lit­erature. Eur Spine J Off Publ Eur Spine Soc Eur Spinal Deform Soc Eur Sect Cerv Spine Res Soc. 2006;15(Suppl 3):S439–47.
11. Guyer RD, Pettine K, Roh JS, Dimmig TA, Coric D, McAfee PC, et al. Comparison of 2 lumbar total disc replacements: results of a prospective, ran­domized, controlled, multicenter Food and Drug Administration trial with 24-month follow-up. Spine. 2014;39(12):925–31.
12. Coric D, Kim P. Lumbar arthroplasty: Total disk replacement and nucleus replacement technologies. In: Winn HR, editor. Youmans neurological surgery. 6th ed. Philadelphia: Saunders Elsevier; 2011.
13. Gamradt SC, Wang JC. Lumbar disc arthroplasty. Spine J Off J North Am Spine Soc. 2005;5(1):95–103.
14. Nie H, Chen G, Wang X, Zeng J. Comparison of total disc replacement with lumbar fusion: a meta-analysis
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of randomized controlled trials. J Coll Physicians Surg Pak: JCPSP. 2015;25(1):60–7.
15. McAfee PC, Cunningham B, Holsapple G, Adams K, Blumenthal S, Guyer RD, et al. A prospec­tive, randomized, multicenter Food and Drug Administration investigational device exemption study of lumbar total disc replacement with the CHARITE artificial disc versus lumbar fusion: part II: evaluation of radiographic outcomes and corre­lation of surgical technique accuracy with clinical outcomes. Spine. 2005;30(14):1576–83. discussion E388–90
16. Blumenthal S, McAfee PC, Guyer RD, Hochschuler SH, Geisler FH, Holt RT, et al. A prospective, ran­domized, multicenter Food and Drug Administration investigational device exemptions study of lumbar total disc replacement with the CHARITE artificial disc versus lumbar fusion: part I: evaluation of clini­cal outcomes. Spine. 2005;30(14):1565–75. discus­sion E387–91
17. Park SJ, Lee CS, Chung SS, Lee KH, Kim WS, Lee JY. Long-term outcomes following lumbar Total disc replacement using ProDisc-II: average 10-year fol­low- up at a single institute. Spine. 2016;41(11):971–7.
18. Zigler J, Garcia R. ISASS policy statement – lumbar artificial disc. Int J Spine Surg. 2015;9:7.
19. Huang RC, Lim MR, Girardi FP, Cammisa FP Jr. The prevalence of contraindications to total disc replace­ment in a cohort of lumbar surgical patients. Spine. 2004;29(22):2538–41.
20. Hannibal M, Thomas DJ, Low J, Hsu KY, Zucherman J. ProDisc-L total disc replacement: a comparison of
1-level versus 2-level arthroplasty patients with a min­imum 2-year follow-up. Spine. 2007;32(21):2322–6.
21. Andersson GB. Epidemiological features of chronic low-back pain. Lancet (London, England). 1999;354(9178):581–5.
22. Hagen KB, Jamtvedt G, Hilde G, Winnem MF. The updated cochrane review of bed rest for low back pain and sciatica. Spine. 2005;30(5):542–6.
23. Oesch P, Kool J, Hagen KB, Bachmann S. Effectiveness of exercise on work disability in patients with non­acute non-specific low back pain: systematic review and meta-analysis of randomised controlled trials. J Rehabil Med. 2010;42(3):193–205.
24. Borenstein DG, O’Mara JW Jr, Boden SD, Lauerman WC, Jacobson A, Platenberg C, et al. The value of magnetic resonance imaging of the lumbar spine to predict low-back pain in asymptomatic subjects: a seven-year follow-up study. J Bone Joint Surg Am. 2001;83-A(9):1306–11.
25. Carragee EJ, Alamin TF. Discography. A review. Spine JOff J North Am Spine Soc. 2001;1(5):364–72.
26. Derby R, Kim BJ, Lee SH, Chen Y, Seo KS, Aprill C. Comparison of discographic findings in asymp­tomatic subject discs and the negative discs of chronic LBP patients: can discography distinguish asymptom­atic discs among morphologically abnormal discs? Spine JOff J North Am Spine Soc. 2005;5(4):389–94.
27. Yue JK, Chan AK, Winkler EA, Upadhyayula PS, Readdy WJ, Dhall SS. A review and update on the guidelines for the acute management of cervi­cal spinal cord injury – part II. J Neurosurg Sci. 2016;60(3):367–84.

Minimally Invasive Posterior Lumbar Fusion Techniques

Luis M. Tumialán
Abbreviations
ALIF Anterior lumbar interbody fusion AP Anteroposterior MIS Minimally invasive surgery MR Magnetic resonance TLIF Transforaminal lumbar interbody fusion VAS Visual analog scale

Introduction

In 1997, Foley and Smith introduced a parame­dian transmuscular approach to the lumbar spine to perform microdiscectomies through a cylindri­cal access port secured after dilatation of the paraspinal muscles [1]. Building on the familiar­ity of the transmuscular decompression tech­niques, surgeons combined well-established percutaneous techniques for instrumentation of the pedicles. The subsequent development of minimally invasive techniques to accomplish the goals of lumbar fusion followed a logical step-
L.M. Tumialán, MD (*) Department of Neurosurgery, Barrow Neurological Institute, St. Joseph’s Hospital and Medical Center, 350 W. Thomas Rd., Phoenix, AZ 85013, USA
luis.tumialan@barrowbrainandspine.com
e-mail:
28
wise progression from that minimally invasive decompression platform.
From an anatomical standpoint, the parame­dian transmuscular access to the lumbar segment lent itself especially well to transforaminal access to the disc space. In short order, the tenets of interbody fusion established by Cloward [2] were applied to the unilateral transforaminal corridor popularized by Harms and Jeszenszky [2, 3]. As spine surgeons synthesized percutaneous and minimally invasive techniques with experience in traditional midline open surgery, the mini­mally invasive transforaminal lumbar interbody fusion (MIS TLIF) arose as the leading proce­dure for the management of single-level lumbar degenerative disc disease.
Currently, three main approaches to the MIS TLIF reflect the evolution of the procedure: percutaneous microendoscopic, mini-open, and hybrid (percutaneous/mini-open) approaches. The first main approach that arose was instru­mentation of the pedicle by a purely percutane­ous technique with tubular access to the segment for decompression and interbody; this technique was popularized by groups led by Foley and Fessler [4, 5]. The percutaneous instrumentation of the pedicle reconciled the anatomical challenge of attempting to expose pedicle screw entry points through the same incision that also exposes the midline elements. A percutaneous approach spared the patient the lateral exposure needed from a midline approach, which was linked with extensive tis-
© Springer International Publishing AG 2017 L.T. Holly, P.A. Anderson (eds.), Essentials of Spinal Stabilization, DOI 10.1007/978-3-319-59713-3_28
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sue trauma. Instead, the instrumentation of the pedicles was accomplished with direct cannula­tion of the pedicle through a distinct operative site, which was nothing more than a stab inci­sion. With the percutaneous technique, there was no need to widely expose the anatomy, with the resultant disruption of the musculature and consequential decrease in blood flow because of the considerable muscle-retractor interface. The benefit of minimizing the extent of exposure translated into reduced postopera­tive discomfort, shorter hospitalizations, and a lower risk of infection [57].
Refinements to the minimal access ports prompted further evolution of the percutaneous form of the procedure. Instead of four stab inci­sions for the percutaneous pedicle fixation and the incision for the paramedian transmuscular decompression and interbody, an expandable minimal access port secured over the facet allowed for exposure of the entire transforaminal corridor in addition to access to the pedicle screw entry point. In this manner, a hybrid percutane­ous mini-open procedure was described.
However, limitations to the percutaneous pro­cedure prompted surgeons to consider the applica­tion of other minimally invasive techniques and other minimal access ports. The first limitation was the radiation exposure to the surgeon involved in percutaneous instrumentation of the lumbar spine [8]. The recent availability of computer- assisted navigation has minimized this concern. However, as MIS TLIF continues to be used more in an ambulatory surgery setting, it is unlikely that com­puter-assisted navigation will increase in this set­ting given its cost. The second limitation was the inability to perform a posterolateral fusion. While this inability may be of varying importance given the high reliability of interbody fusion, access to the transverse processes also provided access to the facet joint contralateral to the transforaminal approach. Having that access is becoming increas­ingly important to preserve, if not restore, segmen­tal lordosis. In a comparison study of anterior lumbar interbody fusion (ALIF) and TLIF, Hsieh and colleagues [9] demonstrated a two-degree loss of lumbar lordosis and a loss in foraminal height in a TLIF cohort compared to an ALIF cohort.
To address these limitations, surgeons began to explore what has been labeled the mini-open TLIF. With this technique, expandable minimal access ports are used to directly visualize the pedicle screw entry points for instrumentation of the spine, and then that same exposure is simulta­neously used to complete the decompression on one side and the posterolateral fusion and a modi­fied Smith-Petersen osteotomy on the other [10].
The most important element of a minimally invasive procedure is that the result can be equiv­alent to its open counterpart. All surgeons should explore the various technologies available as they proceed through their learning curves to achieve the goals of decompression, stabilization, and successful long-term clinical outcomes. Throughout that process, a thoughtful analysis of the clinical and radiographic outcomes should guide each surgeon to the technique that works best in his or her hands. Among the radiographic criteria that should be scrutinized is the capacity to restore foraminal height and segmental lordosis in the short term and to achieve radiographic union and subsidence of the interbody in the long term. Additionally, an analysis of validated clini­cal outcomes measures should be used to care­fully examine the patient’s return to functional mobility and demonstrate improvements in visual analog scale (VAS) leg and VAS back scores. The thoughtful analysis of those outcomes, both clini­cal and radiographic, will lead surgeons to find the minimally invasive technique that offers the most reliable surgical intervention. In keeping with that spirit of refinement, the technique described in this chapter represents the technique that evolved during the author’s learning curve while perform­ing over 500 MIS TLIFs.

Indications and Patient Selection

The most common indications for the MIS TLIF are single-level and two-level lumbar degenera­tive pathologies that include spondylolisthesis, recurrent disc herniation (third recurrence), recur­rent facet cyst, and advanced degenerative disc disease with radiculopathy [ experience, three-level lumbar degenerative disc
11]. In the author’s
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disease may not be outside the realm of minimally invasive surgery, but it does tend to be outside the realm of the MIS TLIF. A three-level pathology may be best treated with a combination of other surgical approaches, such as transpsoas interbody approaches, minimally invasive decompressions, and percutaneous instrumentation.
The ability to proficiently select patients offers the greatest likelihood of clinical and radio­graphic success. Patients with elevated body mass indices should be encouraged to make every effort to move toward their ideal body mass index before surgery and to continue that trend after surgery. It has been the author’s experience that instituting a core-strengthening program before surgery may further facilitate the weight-loss goal. Concern for osteoporosis in a patient should prompt a bone mineral density study; evidence of osteoporosis should prompt consideration of for­mal treatment for 3–6 months before surgery, but should not alter the decision to proceed with a minimally invasive approach.

Preoperative Considerations

After obtaining a history and performing a physi­cal examination, anteroposterior (AP), lateral, and flexion-extension radiographs, along with magnetic resonance (MR) images, are obtained. The MR image can clearly demonstrate compres­sion of the neural elements, which should corre­late with the patient’s neurological examination and subjective complaints. MR imaging may also adequately demonstrate alignment and allow for grading of spondylolisthesis. Patients may pres­ent with either unilateral symptoms or bilateral symptoms. Unilateral symptoms mandate a transforaminal approach from the symptomatic side. Bilateral symptoms, in the presence of bilat­eral foraminal stenosis, may mandate bilateral facetectomies. In the setting of bilateral facetec­tomies, bilateral access to the disc space may be considered; however, the author’s preference is to perform a unilateral transforaminal interbody. Careful analysis of the T1-weighted parasagittal MR image is critical in assessing the neural fora-
men compromise, which may help in deciding whether facetectomy is needed. In the setting of central stenosis with symptoms of neurogenic claudication, severe foraminal stenosis on one side alone may prompt a transforaminal approach from that side.
Flexion and extension studies are helpful in determining the degree of stability of the seg­ment. Extension studies are particularly helpful in determining how much reduction will be obtainable by positioning (Fig. 28.1).
The AP and lateral radiographs will be predic­tive of the type of imaging that can be obtained with fluoroscopy in surgery. It is valuable to appreciate a severe coronal imbalance before sur­gery, so that necessary adjustments can be made to the fluoroscope and incision. Figure 28.2 illus­trates the capacity to adjust the fluoroscope based on preoperative imaging. In this patient with a severe coronal imbalance to the left, her symp­tomatic side, an AP preoperative radiograph prompted a preoperative AP fluoroscopic image to guide the angle for the fluoroscope and to guide the markings for the incisions.
Any concern for scoliosis on AP or lateral imaging should prompt standing 36-inch scolio­sis films. It is important to recognize that there is an inherent limitation to the amount of lumbar lordosis that may be restored in a single-level MIS TLIF. In the author’s experience, 12 degrees of lordosis is at the upper threshold that can reliably be achieved. Therefore, a significant mismatch in lumbar lordosis and pelvic inci­dence warrants careful consideration of the operative plan.

Surgical Technique

The operative goals of the MIS TLIF include instrumentation of the pedicles, decompression of the neural elements, and restoration of the disc height and segmental lordosis through interbody placement. The operating room, the scrub techni­cian’s back table, and a Mayo stand should all be set up to facilitate the flow of the operation to accomplish these goals. The MIS TLIF, which is
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Fig. 28.1 Grade 1 spondylolisthesis. Standing lateral neutral, flexion, and extension radiographs demonstrating the mobility of Grade 1 spondylolisthesis. (a) Standing neutral radiograph revealing a subtle Grade 1 spondylolis­thesis. (b) Flexion study clearly demonstrating anterior translation of the L4 vertebral body on L5. (c) Extension
performed through two paramedian incisions with instrumentation placed under direct visual­ization of the bony anatomy and minimal fluoros­copy, has a logical progression of three phases: instrumentation phase, decompression phase, and interbody phase. Creating these distinct phases of the operation allows the entire opera­tive team to anticipate and thereby facilitate, if not expedite, each phase of the operation.

Operating Room Setup

The patient is positioned on a Jackson table that has the capacity to rotate, which will facilitate the decompression phase. Positioning the patient on the Jackson table will also optimize the capacity to restore segmental lordosis and minimize blood loss by decreasing intra-abdominal pressure. Hyperextension of the hips will also optimize capturing the maximum lumbar lordosis that can be achieved. An electrophysiologist connects the patient for neuromonitoring. The operating microscope is positioned on the side of the trans­foraminal approach. The fluoroscope is posi­tioned with the image intensifier opposite the side of the microscope. It is the author’s prefer­ence not to obtain fluoroscopic images at this
study demonstrating near anatomical reduction of the L4 vertebral body on L5. The extension study predicts how much reduction can be achieved just by positioning the patient on a Jackson table (Used with permission from Barrow Neurological Institute, Phoenix, Arizona)
point unless there is a significant coronal imbal­ance demonstrated on preoperative AP and lateral radiographs. Instead, the bony landmarks are pal­pated, and the L4–L5 level is approximated on the basis of the anterior superior iliac spine. However, it is commonplace in other institutions to obtain both preoperative AP and lateral fluoro­scopic images before preparing and draping the patient. If the operative level is L3–L4, then the planned incisions are shifted upward; for L5–S1, the incisions are shifted downward. Two inci­sions 28 mm in length and 3.5–4 cm from the midline are marked (3.5 cm for patients with a low body mass index, 4 cm for a high body mass index). The patient is prepared and draped with the fluoroscope draped immediately into the field (Fig. 28.3).

Instrumentation Phase

Step One: Plan and Confirm Incisions At this
point in the operation, because the incisions were planned with palpation of the bony landmarks, the level must be confirmed with fluoroscopy. A spinal needle is passed through the midpoint of the proposed incision and a fluoroscopic image taken. The incision is accordingly adjusted,
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Fig. 28.2 Severe coronal imbalance requiring an L4–L5 MIS TLIF. (a) Anteroposterior (AP) radiograph demon­strating the severe coronal imbalance (image has been flipped to match fluoroscopic images taken at surgery). (b) Preoperative photograph shows a Steinmann pin placed over the operative segment to plan the incisions and adjust the fluoroscope. (c) AP fluoroscope image
Fig. 28.3 Planning and confirmation phase of the MIS TLIF. Photographs of the planning and confirmation phase. (a) Photograph of the two 28-mm proposed inci­sions located 3.5 cm off the midline based on landmarks. (b) Spinal needles are docked onto the facet to confirm the
demonstrating a true lateral despite the coronal imbal­ance. Optimizing visualization of the pedicles with a true lateral facilitates instrumentation. (d) Lateral and (e) AP fluoroscopic images demonstrating placement of the interbody and the pedicle screws (Used with permission from Barrow Neurological Institute, Phoenix, Arizona)
level. (c) Lateral fluoroscopic image confirms the ideal placement of the incision parallel to the disc space (Used with permission from Barrow Neurological Institute, Phoenix, Arizona)
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Fig. 28.4 Securing the minimal access ports. Fluoroscopic images demonstrating the securing of the minimal access ports. (a) Lateral fluoroscopic image dem­onstrating the initial dilator docked onto the L3–L4 facet joint. (b) Subsequent lateral fluoroscopic image with the right-sided expandable minimal access port in position
remarked, and infiltrated with a lidocaine/bupi­vacaine hydrochloride mixture to begin pain con­trol. Two incisions 3.5–4 cm lateral to the midline and 28 mm long are made. Blunt dissection is used to dissect down to the fascia, which is then divided with cautery. The division of the fascia is slightly more medial than the skin incision, which will optimize a trajectory toward the pedicle. At L3–L4 and L4–L5, the fascial opening has to be more generous in the rostral direction to reach rostral pedicle screw entry points. At L5–S1, the fascial opening needs to be more generous in the caudal direction to reach the sacral pedicle screw entry point. Direct palpation of the facet and transverse processes should be easily performed before beginning the dilatation process.
and a dilator in position to begin the process on the left side. After the second minimal access port is secured, exposure of the pedicle screw entry points can begin (Used with permission from Barrow Neurological Institute, Phoenix, Arizona)
not allow for movement in any direction. There is little utility in subsequent fluoroscopic images after confirmation of the initial dilator unless the dilators are dislodged. The length of the retractor blades is determined by the measurements on the outside of the dilator and the expandable minimal access which has been secured in position. If two surgeons are operating, the process is repeated on the contralateral side. If one surgeon is operating, the exposure and the instrumentation is com­pleted on one side before proceeding with the dilatation and exposure of the contralateral side. Upon completion of securing the minimal access ports, the fluoroscope is rolled to the foot of the bed and kept there until the exposure of the pedi­cle screw entry points is completed.
Step Two: Secure Expandable Minimal Access Ports The first dilator is placed over the top of
the facet on one side and confirmed with a fluoro­scopic image. The ideal trajectory of the dilator is parallel to the disc space in the center of the facet (Fig. 28.4). Once the ideal position is captured, the first dilator is anchored into position and sequential dilators placed on top. As the dilators increase in diameter, they will reach a point where they will begin to engulf the entire facet. There is an unmistakable sensation of the final dilator encompassing the entire facet that does
Step Three: Exposure of the Pedicle Screw Entry Points Any desire to open the minimal
access port should be suppressed until the entire facet is exposed. Opening the blades of the mini­mal access port too soon can result in a compro­mised exposure from a wall of muscle collapsing over the anatomy. Under ideal circumstances, a thin veil of muscle is all that resides over the top of the facet; this muscle can be quickly painted away with cauterization. Once the entire facet can be visualized, exposure proceeds onto the inferior lat­eral aspect of the facet where the transverse process
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of the caudal segment will be quickly encountered. At this point, it is reasonable to begin to open the inferior blade of the expandable retractor to further visualize the pedicle screw entry point. Within the first few minutes of exposure, the caudal pedicle screw entry point should come into view.
Following the inferior articular process in the rostral direction will locate the pars interarticu­laris and more rostrally to the pedicle screw entry point. With exposure of the pars interarticularis, a gradual opening of the rostral blade will provide access to the transverse process and the rostral facet. It is essential to prevent any disruption of the facet capsule of the facet located above to mitigate the risk of adjacent segment degenera­tion. The focus for exposure of the rostral pedicle screw entry point should be the transverse pro­cess and the pars interarticularis first with the inferior lateral aspect of the facet last.
Fluoroscopy at this phase is of little utility; rather, it should not be used until the transverse process of the levels to be instrumented can be clearly visualized. The pedicle is reliably at the junction of the midpoint of the transverse process, lateral inferior facet, and pars interarticularis. When all four of these entry points can clearly be visualized, the fluoroscope is rolled back into position. The drill is then used to make a small opening at the junction of these three anatomical landmarks after confirmation with a lateral fluoro­scopic image. A pedicle probe with 15–20 degrees of angulation (at L3 or L4) or 20–25 degrees of angulation (at L5 or S1) is then used to probe into the pedicle with the sagittal trajectory parallel to the superior endplate of the vertebral body.
Probing the pedicle is a purely tactile process. There is an unmistakable sensation of having the tip of the pedicle probe advance as it displaces the cancellous bone within the center of the pedicle. If significant resistance is met, it is likely that a cortical wall has been encountered. Forcing the probe at this point is a recipe for a breach. It is a worthwhile endeavor to remove the probe, evalu­ate the entry point, and consider an AP image. If the probe advances with a converging trajectory, it need not be advanced more than 30 mm. Most pedicle probes are graduated with markings every 5 or 10 mm. If electrophysiological monitoring is
used, the pedicle probe may be stimulated to 20 mA. The generation of a compound motor action potential will mandate careful evaluation of the entry point, an AP image, and identification of the breach with a ball-tipped probe [12]. If no compound motor action potential is generated, the pedicle probe is removed, and the ball-tip probe confirms intact medial, lateral, superior, and inferior walls along with a bottom within the vertebral body. A tap is used to further prepare for the pedicle screw. Typically, the hole for the ped­icle is undertapped by 1 mm (i.e., if the intention is to place a 7.5-mm- diameter screw, then a 6.5­mm tap is used). Knowing the length of the tap is also valuable in determining the length of the screw. Once the threads of the tap have been bur­ied, a lateral fluoroscopic image can determine the ideal length of the pedicle screw to be placed (Fig. 28.5). The process described above is repeated for all pedicle screws. If two surgeons are operating, simultaneous confirmation of the pedicle screw entry points is a strategy to mini­mize fluoroscopy. After all the pedicles have been tapped, all four screws may be secured into posi­tion. More recent pedicle screw configurations allow for either headless screws or lower profile tulip heads, neither one of which interferes with the decompression phase. An alternative is to place guidewires to mark the pedicle screw holes.

Decompression Phase

Step One: Exposure of the Lamina and Pars Interarticularis
the pedicle screws, the fluoroscope is now rolled to the head of the bed and the operating micro­scope placed into position. The base of the spi­nous process is exposed, along with the entire hemilamina extending out to the pars interarticu­laris. When all the bony anatomy can be clearly visualized from pedicle screw to pedicle screw and to the base of the spinous process, drilling of the osteotomy cuts may begin.
Step Two: Osteotomy Cuts
cut is a horizontal osteotomy made just below the rostral pedicle screw (Fig.
After successful placement of
The first osteotomy
28.6). A drill is used to
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Fig. 28.5 Pedicle screw placement sequence. (a) Lateral fluoroscopic image with a drill at the junction of the mid­transverse process, inferior lateral facet, and pars interar­ticularis. (b) Pedicle probe with a converging trajectory of 15–20 degrees parallel to the endplate advances with the unmistakable tactile feel of displacing cancellous bone. (c) After the integrity of the pedicle is ensured with a ball-
thin the bone down to the ligamentum flavum, extending the osteotomy medial into the lamina to the junction of the spinous process. The next osteotomy is a vertical osteotomy cut that under­cuts the base of the spinous process so that the contralateral recess may be reached. Once again, drilling continues until the bone is thinned to the level of the ligamentum flavum. Completion of the osteotomy cuts allows for removal of the infe­rior articular process and lamina. Removal of this large segment of bone provides a large amount of autograft that can be milled and used for graft in the disc space. Access to the superior articular process and caudal lamina allows for an osteot­omy of the superior articular process and the superior aspect of the rostral lamina. The caudal pedicle screw is a guide for the level of the oste-
tipped probe, the pedicle is undertapped. The length of the tap threads determines the ideal length of the screw. (d) In this case, the 5.5-mm tap measured 37.5 mm and a 40-mm-long, 6.5-mm-diameter pedicle screw was placed (Used with permission from Barrow Neurological Institute, Phoenix, Arizona)
otomy of the superior articular facet. Extending the bone work medially and caudally to the pedi­cle screw allows for a generous foraminotomy of the traversing root and the insertion of the liga­mentum flavum for the segment.
Step Three: Resection of the Ligamentum Flavum After bony resection, the ligamentum
flavum may be accessed from insertion point to insertion point. Rotating the operating table away from the surgeon is helpful in accessing the con­tralateral recess. A plane may be developed over the top of the thecal sac with a right-angle ball­tipped probe and a Kerrison punch used to resect the ligamentum flavum. A piecemeal approach is one way to complete the decompression. Another viable alternative is to identify the insertion