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CHAPTER 26

Spinal Instrumentation Overview in Lumbar Degenerative Disorders: Cages

Kenneth M.C. Cheung and John C.Y. Leong
ROLE OF CAGES IN THE LUMBAR SPINE
Cages are interbody spacers used to bridge or reconstruct the interval between tw o vertebral bodies (1–4). There are many different designs, but in general, they all provide a mechanically strong scaffold inside of which osteoinduc­tive or osteoconductive materials can be placed. Such material maybe autogenous bone graft, allograft, or more recently bone morphogenetic proteins (5–10).
Cages are used in either degenerative conditions of the spine requiring fusion, or as a form of anterior column reconstruction after destruction by tumor, infection, or trauma. This overview concentrates on its application in degenerative spinal conditions, in which cages are either used as an anterior load-sharing device after posterior spinal instrumentation and fusion (1,4,7,11,12); or as a replacement for bone graft after anterior lumbar inter­body fusion (ALIF) (13), sometimes referred to as a “stand-alone” cage.
TYPES OF CAGES
There are no universally accepted classifications for the cages available today. However, they can be broadly divided into different types by their design or material (1).
Three general designs are used, as follows.
Horizontal Cylinders
One example is the Bagby and Kuslich lumbar (BAK/L) interbody fusion cage (Sulzer Spine-Tech, Min­neapolis, MN) (Fig. 26-1). These devices generally are made from titanium. Usually a pair is inserted together b y either the anterior or posterior approach, and by use of either open or minimally invasive techniques (11,13–19).
Vertical Rings
An example is the titanium mesh cage manufactured by DePuy AcroMed (Johnson & Johnson, Raynham, MA), sometimes referred to as the Harms cage (Fig. 26-
2). They are designed to allow the length to be cut as desired; therefore, they can be used to span either a sin­gle disc space or multiple segments of the lumbar spine. Because of the presence of sharp edges, they are usually and more safely inserted via an open technique (20,21).
Open Boxes
An example is the Brantigan carbon cage (Fig. 26-3) (22–24). The bo x es are designed either with conical supe­rior and inferior surfaces for an anatomic f it into the disc space, or as wedges to recreate lumbar lordosis. Some are designed as a single large cage, which requires an open technique for insertion; whereas others involve two smaller rectangular cages, which can be inserted posteri­orly using minimally invasive techniques.
Cage Materials
In general, these are usually made from titanium, carbon, or a carbon composite (polyetheretherketone [PEEK]). Titanium is a mechanically strong and bio-inert material that is magnetic resonance imaging (MRI) com­patible. Therefore, cages made using this material can have relatively thin struts that allow more room for bone graft in its interior. The presence of a metallic shadow on radiographs makes the assessment of bony fusion within the cage difficult. Some surgeons attempt to overcome this by placing bone graft anterior to the cage as well as within it (5). Carbon and PEEK cages are radiolucent and allow for an easier assessment of bone fusion. Addition-
286
FIG. 26-1. Bagby and Kuslich lumbar interbody fusion cage, an example of a threaded horizontal cylinder.
ally, they hav e a Young’s modulus that nearly matches that of cortical bone. This allows the compressive load on the cage to be shared by the bone graft inside the cage and may facilitate a more consistent and rapid bone fusion. Both carbon and PEEK cages are also MRI compatible.
INDICATIONS FOR CAGES
Before the advent of cages, bone grafts such as tricor­tical iliac crest grafts and fibula strut grafts were used very successfully as a form of anterior column support and to promote spinal fusion (25,26). Thus, there are no absolute indications for the use of cages, and the value of cages as an alternative to autogenous bone graft should be judged with the latter as a gold standard. Accordingly, the indication for use of a cage is the same as that for bone graft, namely, anterior column reconstruction and fusion.
Proponents of cages suggest that they may ha v e a num­ber of advantages over conventional bone graft material alone. Such advantages mainly stem from the separation of their mechanical and biological roles and may include:
1. Enhanced mechanical stability
2. Maintenance of intervertebral disc height
3. Avoidance of bone graft donor site morbidity by using alternative osteoconductive and osteoinductive materials inside the cage.
FIG. 26-2. Titanium mesh cage (Harms), an example of a vertical cylinder. End-rings (right side) can be added to the reduce stress concentration at the ends of the cage, and therefore reduce the chance of sinking into the end plate.
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FIG. 26-3. Brantigan carbon cage, an example of an open box design.
Cages are designed to have better mechanical stability than bone graft by virtue of their material and design. Cylindrical cages have a threaded design (Fig. 26-1) and use a screw-in technique for insertion (14,27), whereas box cages have a serrated surface (Fig. 26-3) (13,28). Both help to increase motion segment stiffness and resis­tance to pull-out. It is claimed that this may improve the chance of a successful fusion, although this point remains to be proved scientifically.
Cages may be better at maintaining disc height than bone graft alone. In our long-term follow-up study (mean dura­tion of 14 years) of 67 patients that underwent anterior lum­bar interbody fusion at L4-5 with autologous iliac crest graft (29), we demonstrated that there was an initial dis­traction of the disc space by 34% (4.1 mm) followed by an eventual partial loss of this distraction in 86% of cases despite a successful fusion. The mean preoperative disc space height was 12.1 mm, increased immediately after surgery to 16.2 mm, but settled to 12.6 mm at the latest fol­low-up. The reduction in distraction occurred within the first 3 months after surgery and was correlated with age, but not with recurrence of symptoms, the amount of initial distraction or sex of the individual. L4-5 segmental angula­tion followed a similar trend. The early loss of disc space distraction likely resulted from moulding of the bone graft into the created space, and bone graft softening and resorp­tion during remodeling. Studies have sho wn that restoration of disc space height tightens the posterior ligaments and opens up the intervertebral foramina, thereby indirectly decompressing the neural foramina exiting nerve roots (30). Although this has been used as a justification for using cages, it should be borne in mind that our study showed that the loss of disc space distraction did not correlate with return of the patients’ symptoms, and no long-term clinical study is available to demonstrate that disc space height is maintained with cages. Indeed, there is some evidence in both animal and human studies that disc space reduction and loss of lordosis also occur with threaded cylindrical cages (31,32). Special considerations should be given to patients with reduced bone density because there is a risk of end-plate fracture by the implanted cage, which may result in loss of distraction (29,33).
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Avoidance of donor site morbidity (34,35) is often cited as another reason for using a cage. However, until recently only osteoconductive materials, such as allograft bone and hydroxyapatite b locks, were availab le as replace­ments for autogenous bone. We caution that the use of such materials as the ultimate aim is still to achieve a fusion and autogenous bone graft is still currently the best material for this purpose. There have been several studies examining the use of bone morphogenetic proteins placed inside cages in human patients (8,10). Both stud­ies concluded that recombinant bone morphogenetic pro­tein-2 (rhBMP-2), can effectiv ely achieve a spinal fusion, although the number of patients involved were small, and the follow-up short. Large-scale randomized controlled trials with long-term follow-up are required to prove this definitively.
CHOICE OF CAGES
The ideal cage should rigidly immobilize the spine in all directions, be strong enough to withstand repeated loading, and have a modulus of elasticity close to that of cortical bone. It should also be easy to insert by either an open or minimally in vasive approach, and should be clin­ically effective by randomized controlled trials and long­term follow-up.
It is difficult to advise readers on the optimal choice of cage because of the wide variety of cages currently avail­able, with more likely to come on the market in the future. However, users should be aware of some biome­chanical and clinical considerations with the currently available designs.
One area of concern with the use of cages compared to bone graft is that the stiff struts of the cage stress shield the bone graft placed inside the cage. Because bone heals best under compression, this could result in reduced fusion rates. In a study by Kanayama et al. (37), a calf spine model was used to quantify the stress-shielding effects of 11 lumbar interbody fusion cages by measuring pressure within the cages. This was achieved by injecting the cages with a silicon elastomer before insertion, and intracage pressures were measured using pressure needle transducers. The authors concluded that threaded fusion cages demonstrated significantly lower intracage pres­sures compared with nonthreaded cages and structural allografts. Whether this is clinically relevant is not known, because there are no comparati ve studies e xamin­ing fusion rates among the various types of cages.
The possibility of stress shielding and the presence of motion within the spine segment despite the use of cages raise the question of whether they can be used as stand­alone devices, without supplemental fixation. Because of a lack of clinical studies with long-term follow-up, this question cannot be currently answered. There are cer­tainly advocates who recommend supplemental posterior fixation to improve the chance of fusion (38,42–46). It should be borne in mind that iliac crest bone grafting without instrumentation has been used successfully to perform anterior lumbar interbody fusion with fusion rates for a single level fusion of up to 96% (26,29,47,48). This should be the benchmark against which fusions with cages are compared.
Clinical Considerations
Biomechanical Considerations
In general, studies comparing the stiffness of the spine segment after cage insertion have shown no signif icant differences among the various designs (13,36–38). All are effective at stabilizing the spine, compared with its intact condition, in flexion, axial rotation, and lateral bending. This effectiveness is dependent on their ability to distract the surrounding soft tissues and their contact with the host bone. Hence, the cage needs to be appropri­ately sized for height as well as fit (13,39). Differences within a particular category of cage design may have an effect on mechanical stability. For instance, cages with sharp teeth have higher “pull-out” forces (13), whereas Harms cages without the addition of the end-rings impart only marginally better stability in rotation when com­pared to bone graft (40). All stand-alone cages, however, are less effectiv e in stabilizing the spine in e xtension, and motion between the cage–bone junction is present unless supplemental fixation is used (41). Addition of f ixation, whether anterior or posterior, and by translaminar or pedicle screws, will significantly improve the fusion seg­ment stiffness (3,36,38,42).
Interbody fusion in degenerative disc disease serves a number of purposes. First, by removing the disc it removes a potential source of pain, and by removing her­niated fragments it decompresses the nerve roots. Sec­ond, fusion stabilizes the segment and augments the ante­rior column. Third, restoration of disc space height tightens up the posterior ligaments and opens up the intervertebral foramina, thus indirectly decompressing the nerve roots (30,31). The first two aims can be ade­quately achiev ed by anterior interbody fusion with tricor­tical iliac crest bone graft, whereas a cage may be required for the third aim. However, before a rational choice of fusion devices can be made, surgeons should be aware of the clinical track record of cages.
There are very few reports of long-term results of cages. One of the longest and earliest experiences in the use of interbody spacer was by the senior author in 1994 (49). A titanium mesh interbody spacer was inserted as a stand-alone device without bone grafting in 23 patients with an average follow-up period of 8 years (range, 5 to 12 years). This study demonstrated that bony ingrowth into the titanium mesh occurred in 18 of 23 patients, as shown by lack of a radiolucent line at the bone–implant
CHAPTER 26/SPINAL INSTRUMENTATION OVERVIEW / 289
junction, and was subsequently confirmed in retrieval studies. However, six of these 18 implants failed by a mid-substance disruption of the mesh, with three im­plants developing a crack, and three becoming deformed. In all six patients, movement could be demon­strated between the adjacent vertebral bodies, despite the lack of a radiolucent line. The authors postulated that with the solid metal–bone interface, the mesh became subjected to more stress during flexion and extension, such that if solid bone fusion did not occur, the implant failed in its mid-substance. One of the best ways to demonstrate bone fusion is the presence of anterior bridging bone (Fig. 26-4). This occurred in four of the 23 cases, and when this was seen, no further movement between the adjacent vertebral bodies could be demon­strated on flexion and extension, and no mesh failures occurred.
Based on this experience, the authors feel that one should make the distinction between bone ingrowth into the periphery of the cage, and bone fusion, which extends from one end plate to the other. If the latter does not occur, then the cage may fail in the long term. Thus, in reading the literature on the results of cages, the reader should make this distinction and note the duration of fol­low-up. Any study with less than 5 years of follow-up is very unlikely to see cage failure because of bone ingrowth only and the lack of a solid bone fusion.
One study examined needle biopsies from tissue within radiographically successful intervertebral body fusion cages filled with autograft (6). Five cages were implanted anteriorly, one with additional fixation, and four cages were implanted as part of a posterior lumbar interbody fusion. Five were carbon cages (Brantigan cage), whereas four were titanium mesh (Harms Cage), with a mean postimplantation biopsy duration of 28 months (range, 8 to 72 months). Biopsies were obtained from within the center of the cages and showed small fragments of
FIG. 26-4. Implanted titanium mesh block showing anterior bone bridging and solid fusion.
necrotic bone associated with viable bone and restoration of hematopoietic bone marrow. Numerous cement lines demarcated the edges of previous cycles of remodeling, and the ratio of necrotic to viable bone varied greatly among cases. Small particles of debris were found in four of the five carbon-fiber cages and in one of the four spec­imens from titanium cages, but there was no visible bone resorption or inflammation. It could be interpreted that, despite stress-shielding by the cage, solid bone fusion eventually may occur, although bone grafts contained within these cages are still undergoing remodeling beyond the 3 to 6 months that autograft is normally expected to fuse and remodel.
In 1997, Ray (50) reported his initial results of using a stand-alone threaded cage packed with autogenous bone graft and inserted via a posterior approach. Fusion, as assessed by plain lateral radiographs and lack of move­ment on flexion-extension radiographs, was said to occur in 91%. Lack of movement may result only from bony ingrowth into the superior and inferior faces of the cage for a limited distance. The word “fusion” should be used only if there is evidence of continuous bony ingrowth through the entire extent of the cage. To date, this has not been definitively demonstrated in any study.
Kuslich et al. reported on the 4-year follow-up results of the BAK cage in 25.6% of the original study popula­tion (18). Their overall “fusion rate” was 91.7% and
95.1% at 2 and 4 years, respectively. This was from a combination of anterior and posterior approaches. Whether or not additional instrumentation was used is unknown. The late-occurring complication rate was
13.8%. Complications necessitating a second operation occurred in 8.7%, and reoperations directly related to the device occurred in 3.1%. This study has been criticized for the small number of patients available for follow-up assessment (51,52).
Studies examining the use of other cages have tended to be combined with posterior fixation, and they all report “fusion rates” in the range of 90% to 100% (7,12,20,23,24,53). However, it should be noted that no movement would be detectable on flexion-extension radi­ographs with solid posterior f ixation, thereby hampering fusion assessment. It requires long-term follow-up to demonstrate nonunion from loosening or implant failure (54).
One additional criterion in the choice of cages is the surgeon’s familiarity with the techniques of insertion. Although the majority of the box cages are used in a similar manner to bone graft, the threaded cylindrical cages require a specialized technique of insertion. Atten­tion to detail is important, because complications arising from inadequate distraction of the anulus fibrosus, under sizing of the cages, and dural tears from a poste­rior approach all have been described (55). Additionally, some cages are designed for anterior minimally invasive insertion (15–17,56–58), whereas others are designed for
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use as a PLIF only. These are all important issues to con­sider, and an y sur geon intending to use such cages should be thoroughly familiar with their indications and design considerations.
SUMMARY
Lumbar interbody fusion cages may have some advan­tages over conventional autogenous bone grafting tech­niques. They have the theoretical potential to maintain vertebral distraction, and separate the structural and bio­logical functions of an interbody spacer. With the devel­opment of osteoinductive compounds delivered as a recombinant protein or via gene therapy (59), bone graft harvesting and donor site morbidity theoretically could be avoided altogether. However, techniques of insertion may be demanding and surgeons should be familiar with the design before using a cage of their choice. Finally, one should balance the use of such expensive implants with the low cost and proven effectiveness of autogenous bone graft, which is the gold standard in anterior inter­body reconstruction and fusion to date.
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10. Kleeman TJ, Ahn UM, Talbot-Kleeman A. Laparoscopic anterior lum­bar interbody fusion with rhBMP-2: a prospective study of clinical and radiographic outcomes. Spine 2001;26(24):2751–2756.
11. Hacker RJ. Comparison of interbody fusion approaches for disabling low back pain. Spine 1997;22(6):660–665.
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15. Zucherman JF, Zdeblick TA, Bailey SA, et al. Instrumented lapa­roscopic spinal fusion. Preliminary Results. Spine 1995;20(18): 2029–2034;discussion 2034-2035.
16. McAfee PC, Regan JJ, Geis WP, et al. Minimally invasive anterior retroperitoneal approach to the lumbar spine. Emphasis on the lateral BAK. Spine 1998;23(13):1476–1484.
17. Regan JJ, Aronoff RJ, Ohnmeiss DD, et al. Laparoscopic approach to L4-L5 for interbody fusion using BAK cages: experience in the first 58 cases. Spine 1999;24(20):2171–2174.
18. Kuslich SD, Danielson G, Dowdle JD, et al. Four-year follow-up results of lumbar spine arthrodesis using the Bagby and Kuslich lumbar fusion cage. Spine 2000;25(20):2656–2662.
19. Wong HK, Goh JC, Goh PS. Paired cylindrical interbody cage fit and facetectomy in posterior lumbar interbody fusion in an Asian popula­tion. Spine 2001;26(5):572–577.
20. Lenke LG, Bridwell KH. Mesh cages in idiopathic scoliosis in adoles­cents. Clin Orthop Rel Res 2002;1(394):98–108.
21. Eck KR, Bridwell KH, Ungacta FF, et al. Analysis of titanium mesh cages in adults with minimum two-year follow-up. Spine 2000;25(18): 2407–2415.
22. Brantigan JW, McAfee PC, Cunningham BW, et al. Interbody lumbar fusion using a carbon fiber cage implant versus allograft bone. An investigational study in the Spanish goat. Spine 1994;19(13): 1436–1444.
23. Brantigan JW, Steffee AD, Lewis ML, et al. Lumbar interbody fusion using the Brantigan I/F cage for posterior lumbar interbody fusion and the variable pedicle screw placement system: two-year results from a Food and Drug Administration investigational device exemption clini­cal trial. Spine 2000;25(11):1437–1446.
24. Hashimoto T, Shigenobu K, Kanayama M, et al. Clinical results of sin­gle-level posterior lumbar interbody fusion using the Brantigan I/F car­bon cage filled with a mixture of local morselized bone and bioactive ceramic granules. Spine 2002;27(3):258–262.
25. Leong JC, Chun SY, Grange WJ, et al. Long-term results of lumbar intervertebral disc prolapse. Spine 1983;8(7):793–799.
26. Luk KD , Chow DH, Evans JH, et al. Lumbar spinal mobility after short anterior interbody fusion. Spine 1995;20(7):813–818.
27. Tencer AF, Hampton D, Eddy S. Biomechanical properties of threaded inserts for lumbar interbody spinal fusion. Spine 1995;20(22): 2408–2414.
28. Dietl RH, Krammer M, Kettler A, et al. Pullout test with three lumbar interbody fusion cages. Spine 2002;27(10):1029–1036.
29. Cheung KMC, Zhang YG, Lu DS, et al. Reduction of disc space dis­traction after anterior lumbar interbody fusion with autologous iliac crest graft. Spine 2003;28(13):1385–1389.
30. Chen D, Fay LA, Lok J, et al. Increasing neuroforaminal volume by anterior interbody distraction in degenerative lumbar spine. Spine 1995;20(1):74–79.
31. Sandhu HS, Turner S, Kabo JM, et al. Distractive properties of a threaded interbody fusion device. An in vivo model. Spine 1996;21 (10):1201–1210.
32. Goldstein JA, Macenski MJ, Griffith SL, et al. Lumbar sagittal align­ment after fusion with a threaded interbody cage. Spine 2001;26(10): 1137–1142.
33. Jost B, Cripton PA, Lund T, et al. Compressive strength of interbody cages in the lumbar spine: the effect of cage shape, posterior instru­mentation and bone density. Eur Spine J 1998;7(2):132-141.
34. Cunningham BW, Kanayama M, Parker LM, et al. Osteogenic protein versus autologous interbody arthrodesis in the sheep thoracic spine. A comparative endoscopic study using the Bagby and Kuslich interbody fusion device. Spine 1999;24(6):509–518.
35. Younger EM, Chapman MW. Morbidity at bone graft donor sites. J Orthop Trauma 1989;3(3):192–195.
36. Oxland TR, Hoffer Z, Nydegger T, et al. A comparative biomechanical investigation of anterior lumbar interbody cages: central and bilateral approaches. J Bone Joint Surg 2000;82(3):383–393.
37. Kanayama M, Cunningham BW, Haggerty CJ, et al. In vitro biome­chanical investigation of the stability and stress-shielding effect of lumbar interbody fusion devices. J Neurosurg 2000;93(2 Suppl): 259–265.
38. Lund T, Oxland TR, Jost B, et al. Interbody cage stabilisation in the lumbar spine: biomechanical evaluation of cage design, posterior instrumentation and bone density. J Bone Joint Surg Br 1998;80(2): 351–359.
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39. Goh JC, Wong HK, Thambyah A, et al. Influence of PLIF cage size on lumbar spine stability. Spine 2000;25(1):35–39.
40. Lee SW, Lim TH, You JW, et al. Biomechanical effect of anterior graft­ing devices on the rotational stability of spinal constructs. J Spinal Dis­ord 2000;13(2):150–155.
41. Kim Y. Prediction of mechanical behaviors at interfaces between bone and two interbody cages of lumbar spine segments. Spine 2001;26(13): 1437–1442.
42. Le Huec JC, Liu M, Skalli W, et al. Lumbar lateral interbody cage with plate augmentation: in vitro biomechanical analysis. Eur Spine J 2002;11(2):130–136.
43. Hitchon PW, Goel V, Rogge T, et al. Spinal stability with anterior or pos­terior ray threaded fusion cages. J Neurosurg 2000;93(1 Suppl):102–108.
44. Nydegger T, Oxland TR, Hoffer Z, et al. Does anterolateral cage inser­tion enhance immediate stabilization of the functional spinal unit? A biomechanical investigation. Spine 2001;26(22):2491–2497.
45. Oxland TR, Lund T. Biomechanics of stand-alone cages and cages in combination with posterior fixation: a literature review. Eur Spine J 2000;9(Suppl 1):S95–S101.
46. Rathonyi GC, Oxland TR, Gerich U, et al. The role of supplemental translaminar screws in anterior lumbar interbody fixation: a biome­chanical study. Eur Spine J 1998;7(5):400–407.
47. Inoue S, Watanabe T, Hirose A, et al. Anterior discectomy and inter­body fusion for lumbar disc herniation. A review of 350 cases. Clin Orthop 1984;(183):22–31.
48. Fujimaki A, Crock HV, Bedbrook GM. The results of 150 anterior lum­bar interbody fusion operations performed by two surgeons in Aus­tralia. Clin Orthop 1982;(165):164–167.
49. Leong JC, Chow SP, Yau AC. Titanium-mesh block replacement of the intervertebral disk. Clin Orthop Rel Res 1994;(300):52–63.
50. Ray CD. Threaded titanium cages for lumbar interbody fusions. Spine 1997;22(6):667–679.
51. Lonstein JE. Re: four-year follow-up results of lumbar spine arthrode­sis using Bagby and Kuslich lumbar fusion cage. Spine 2001;26(13): 1506–1508.
52. Winter RB. Re: four-year follow-up results of lumbar spine arthrodesis using Bagby and Kuslich lumbar fusion cage. Spine 2001;26(13): 1507–1508.
53. Janssen ME, Lam C, Beckham R. Outcomes of allogenic cages in ante­rior and posterior lumbar interbody fusion. Eur Spine J 2001;10(Suppl
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54. Tullberg T. Failure of a carbon fiber implant. A case report. Spine 1998;23(16):1804–1806.
55. McAfee PC, Cunningham BW, Lee GA, et al. Revision strategies for salvaging or improving failed cylindrical cages. Spine 1999;24(20): 2147–2153.
56. Mathews HH, Evans MT, Molligan HJ, et al. Laparoscopic discectomy with anterior lumbar interbody fusion. A preliminary review. Spine 1995;20(16):1797–1802.
57. Thalgott JS, Chin AK, Ameriks JA, et al. Minimally invasive 360 degrees instrumented lumbar fusion. Eur Spine J 2000;9(Suppl 1):S51–S16.
58. Heniford BT, Matthews BD, Lieberman IH. Laparoscopic lumbar interbody spinal fusion. Surg Clin North Am 2000;80(5):1487–1500.
59. Chen Y, Cheung KM, Kung HF, et al. In vivo new bone formation by direct transfer of adenoviral-mediated bone morphogenetic protein-4 gene. Biochem Biophys Res Commun 2002;298(1):121–127.
CHAPTER 27

Translaminar Screw Fixation

Dieter Grob
One of the surgical concepts to reduce pain originating from the lumbar spine is to immobilize the involved ver­tebrae. The most natural way to achieve this is to take advantage of the process of bone healing. By preparing the parts to be fixed with decortication and additional placement of bone graft, fusion may be enhanced. The mechanical situation of the spine, with considerable lever arms and multiple segmental centers of motion, implies a relatively low success rate of solid bony bridging.
To improve the fusion rate and reduce the need for rigid and cumbersome external fixation postoperativ ely, internal fixation has been introduced to temporarily immobilize the spine and thus enhance bony calcification. For this purpose Hadra (1) introduced first metallic wires in 1891. Before the era of pedicular screw fixation was introduced in Europe in the early 1960s (2), attempts to stabilize verte­brae posteriorly with screws only were attempted. The use of facet screws was first reported by King (3), whose tech­nique was to immobilize the lumbosacral joints with short screws traversing the facets. With this technique he achieved a fusion rate of 91% without prolonged postoper­ative external fixation. Boucher (4) adopted this idea and improved the technique. He achie v ed a 100% fusion rate in single level fusions by penetrating the ipsilateral pedicle with the tip of the screw, thus improving the bony pur­chase. This method of screw insertion implied that the tip of the screw had to be placed near the foramen and the nerve root and carried the risk of nerve injury. In addition, there was a risk of decreased stability of this construct if the screw broke through the cortex of the posterior aspect of the facet. These complications of screw f ixation in the lumbar spine made them unpopular despite the simplicity of the technique. It was Magerl 1984 (5) who modified and improved the technique of screw f ixation and popularized revival of this type of immobilization. By inserting the screws from the contralateral side through the lamina, through the facet and ending in the base of the transverse process, most of the disadvantages of the former tech­niques were eliminated without losing their advantages.
Bony purchase was increased by the passage of the screw through the lamina, and the procedure was less risky because: (a) the insertion of the screw was clearly posterior to the neural elements; (b) the technique could be per­formed under direct visualization; and (c) the direction of screw insertion was parallel to the exiting nerve root, thereby minimizing the risk of injury to the nerve.
BIOMECHANICAL CONSIDERATIONS
A simplified but practical biomechanical concept of the lumbar spine with a three-column model was con­ceived by Louis (6). The anterior column is represented by the disc, the vertebral body, and the two posterior columns by the facets. In the course of evolution, anatomy adapted to the physiologic requirements of the spine; therefore, it seems reasonable to assume that the facets developed in response to mechanical necessity.
The importance of the facets has been demonstrated by several in vitro experiments in which partial or total resec- tion of the facets led to dysfunction of the functional spinal motion unit (7,8). Together with the intervertebral disc, the facets share and support the axial load of the spine. Although the disc appears to be the primary load-bearing structure (8), the facets function as an indispensable part of the three-column concept to transmit part of the axial load, which varies according the position of the individual (9,10). Structural and morphologic changes that occur with destruction of cartilage and osteophyte formation under­score the important mechanical properties of the facets. Because the load passes partially through the facets, the lever arm acting on an internal fixation device through the facets remains small. A low-prof ile fixation device is suf­ficient to block segmental motion efficiently enough to enhance solid bony fusion (11,12).
Despite the fact that translaminar screw fixation repre­sents the lowest prof ile implant for the lumbar spine, the stability in flexion achieved with this technique in vitro is similar to that provided b y pedicle scre w fixation (13,14).
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