Overview
Posterior lumbar interbody fusion (PLIF) after lumbar disk removal was first reported by Jaslow in 1946, and Cloward presented his first 100 cases at the Harvey Cushing Society meeting in 1947. More recently, Steffe, Brantigan, and Ray have reported on the use of posterior segmental instrumentation or cage implants for PLIF, a surgical technique that allows fusion across two adjacent vertebrae by inserting grafts, titanium-threaded cages, bone dowels, or carbon-fiber spacers filled with bone graft into the disk space. All PLIF techniques require removal of the disk material from within the disk space; bone grafts and spacing devices are then used to create a bony “bridge” that will fuse the two adjacent vertebral bodies.
PLIF is a valuable way of achieving a spinal fusion. If spinal instability is present (i.e., spondylolisthesis or slippage of the vertebrae), PLIF should be performed with spinal stabilizing instruments, such as pedicle screws or hooks and rods to immobilize the loose vertebrae. The many advantages in instrumented PLIFs, or 360-degree fusions, include a decrease in pain and an increase in functional activities. Compared with anterior-posterior (AP) fusions, instrumented PLIFs also have equal patient satisfaction, much lower costs, and faster return to work and other activities. Furthermore, a recent biomechanical study by Bennett and associates found that PLIFs double the spinal stiffness produced by transpedicular fixation following laminectomy and facetectomy. Other theoretical advantages of PLIF are technical and include the fact that a much larger area of bone surface exists for the fusion, with the fusion at the center of motion and at the site of maximum compression loading. The disk space is maintained in a distracted position without the collapse that is often seen in transverse-process fusion using transpedicular fixation. In addition, the blood supply is better at the decorticated end plate than at the transverse process.
Perhaps the greatest concern with a standard PLIF is the amount of neural retraction needed. An inappropriate amount could potentially lead to nerve root injury, cauda equina injury, dural laceration, and epidural fibrosis. Consequently, the unilateral posterior transforaminal lumbar interbody fusion (TLIF) was developed to address some of these problems. The concept of a unilateral approach to the anterior column was refined and popularized by Harms. The purpose of this approach was to obtain the same goals as a PLIF without the potential risks and complications.
The TLIF technique allows clearance of the entire intervertebral disk compartment by opening the neural foramen on one side. After appropriate clearance, it is possible to achieve further enlargement of the cleared intervertebral compartment by posterior transpedicular distraction. This enables definitive anterior column support and certain fusion by transforaminally introduced bone material and support structures. After the introduction of these anterior fusional elements, segment stability is restored by converting the distraction force into compression force. The TLIF approach helps to avoid damage to important anatomic structures, such as the nerve roots, dura, ligamentum flavum, and interspinous ligament.
Preservation of the ligamentous structures is of great importance to restoring biomechanical stability of the segment and its adjacent counterparts. The advantages of unilateral TLIF over the standard PLIF include the ability to provide bilateral anterior column support through a single posterolateral approach of the disk space. The transforaminal approach preserves the anterior and most of the posterior longitudinal ligamentous (PLL) complex, which provides a tension band for compression of the graft and prevents retropulsion of the graft. It avoids excessive soft-tissue dissection, which may help prevent scarring, instability of adjacent segments, and injury to the exiting nerve root. Epidural bleeding is less of a problem than with the standard bilateral PLIF because of the unilateral transforaminal approach, and with experience, proper cage placement within the disk space is consistently achieved.
Indications and Contraindications
Indications
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Broad-based herniations
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Totally degenerated disks with marked instability (spondylolisthesis, some cases of scoliosis)
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Recurrent disk herniation
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Pseudarthrosis of transverse process fusion (as an alternative to anterior lumbar fusion) in the absence of epidural scarring
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Back pain as a result of symptomatic spondylosis and/or symptomatic degenerative disk disease
Contraindications
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Conjoined nerve root precluding access to the disk space
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Osteoporotic patients
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Active infection
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Previous anterior lumbar interbody fusion
Operative Technique
Equipment
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Radiograph-compatible operating table
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Jackson table, Wilson frame, or chest rolls
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Fluoroscopy
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Headlight system
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Pneumatic compression stockings or antiembolic stockings for both legs
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Lumbar laminectomy set
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Steinmann pins
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Bone graft source
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Lumbar pedicle screw system
Posterior Lumbar Interbody Fusion Procedure
Laminectomy
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Patient is placed in prone position with chest rolls, on a Wilson frame, or using the Jackson table.
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A midline longitudinal skin incision is made.
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Subperiosteal dissection extends laterally beyond the border of the articular facet joints.
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Laminectomy and complete decompression of nerve roots are performed in the desired level. Total or subtotal laminectomy is easier than the partial laminectomy to handle the thecal sac and nerve roots ( Fig. 45-1 ).
Figure 45-1
L4 subtotal laminectomy.
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Medial facetectomy is recommended for preservation of posterior column function.
Traditional Diskectomy
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After gently retracting the nerve roots and thecal sac, the epidural space is identified, and epidural vessels are coagulated ( Fig. 45-2 ).
Figure 45-2
Careful retraction of the nerve roots and thecal sac.
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Carefully retracting the nerve root at risk, a No. 15 scalpel is used to incise the annulus widely. A large rectangle of annulus and available disk is removed ( Fig. 45-3 ).
Figure 45-3
Removal of the annulus with a No. 15 scalpel.
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Traditional bilateral diskectomy requires removal of as much disk as possible to ensure that none bunches up to the midline, compressing the dural sac, when bone grafts or cages are placed laterally ( Fig. 45-4 ).
Figure 45-4
Traditional diskectomy before end plate removal.
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An up-biting pituitary forceps is used to remove disk beneath the thecal sac without manipulating it.
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Ring curettes are often used to further empty the disk space.
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Backward-angled curettes are carefully placed between the dural sac and the annulus to push down any bulging disk or osteophyte near the midline.
End Plate Preparation
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A vertebral spreader is used to widen the disk space.
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The size of the reamer-distractor varies from 8 to 12 mm practically. Once the reamer-distractor is attempted within the disk space, it is turned 90 degrees to distract the space ( Fig. 45-5 ). The next larger sized reamer-distractor is then tried, and this is repeated using progressively larger reamer-distractors until the ideal disk height is achieved. The final dilator is left within the disk space in the distracted position.
Figure 45-5
Reamer-distractors of progressively increasing size are inserted to widen the disk space, until optimal distraction is achieved.
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A Penfield dissector or ruler is placed into the disk space, and images are obtained.
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The osteotome should not be placed more than 50% to 60% through the AP diameter of the vertebral body.
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Osteotomes are placed parallel to the end plates at both the superior and inferior aspects of the disk space and then are placed medial and lateral.
Bone Graft Preparation
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Separate the skin incision on the posterior superior iliac crest.
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Remove the long tricortical iliac bone.
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Shape the bone as three pieces of bone graft material, with the height measuring the distracted disk space near the vertebral spreader ( Fig. 45-6 ).
Figure 45-6
Iliac bone harvesting. A, Graft harvest. B, Location of graft harvesting from the iliac crest.
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Donor site bleeding control is achieved with bone wax and closure.
Bone Graft Placement
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The nerve root and dural sac should be very carefully protected with handheld retractors that are regularly released.
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The prepared tricortical grafts or cage filled with autograft are then tapped into the widened disk space.
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A bleeding cancellous bone surface should then be available on the cephalad and caudal edges of the space and possibly laterally as well.
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We generally prefer to place the more medial bone grafts first, to minimize total mobilization of the dural sac ( Fig. 45-7 ).
