Key Words
Lumbar interbody fusion, Lumbar spine surgery, Spine fusion assessment
Introduction
The ultimate goal of lumbar interbody fusion procedures is to relieve debilitating pain or prevent neurologic compromise. Fusion is achieved via the promotion of solid ossification across a lumbar disk space, known as solid arthrodesis ( Fig. 24.1 ). Interbody fusion (in other words, fusion across the disk space) can be performed by various surgical approaches. The aim is to restore and maintain disk space height, conserve normal lordotic sagittal contours, and increase the stability of the segments of concern. In their normal taut and stretched position, the disk annulus fibrosus and supporting ligaments of the spine are better able to provide a biomechanically sound and firm construct to limit abnormal motion and thus permit solid fusion to develop over time. This restoration and maintenance of disk space height (otherwise known as “ligamentotaxis”) is of particular importance for the establishment of stability, which is essential for fusion development.
Although spinal interbody fusion techniques, devices, and materials continue to evolve, a few basic concepts endure. Fusion success requires mechanical stability and a favorable environment, including adequate osseous substrate/graft material.
Overview
Interbody Fusion Approaches and Techniques
Interbody fusion can be performed via several surgical approaches including anterior lumbar interbody fusion (ALIF), posterior lumbar interbody fusion (PLIF), and transforaminal lumbar interbody fusion (TLIF) ( Fig. 24.2 ). The ideal setting for fusion to develop across the disk space is a clean bone surface across apposing endplates. Therefore regardless of the surgical approach, a total diskectomy is performed at the level of concern through a surgical window in the annulus fibrosus. An osseous substrate is then implanted into the disk space in between the decorticated bleeding surfaces of the adjacent endplates, which serves as a favorable environment for fusion by means of bone formation and healing. The insertion of bone graft material may be conducted with or without interbody spacers (to achieve ligamentotaxis). The implanted osseous substrates placed in the disk space are generally in the form of interbody spacers that are either solid or openwork structures usually filled with bone graft material. The spacer is meant to maintain alignment, provide spinal column support, and promote fusion. Fusion may be attempted at a single or multiple spinal segments.
In addition, supplemental segmental hardware instrumentation (posterior rods and pedicle screws, plates, and intervertebral implants) may accompany the interbody fusion ( Fig. 24.3 ). Instrumentation itself is not meant to fuse but to stabilize, so that osseous fusion may develop. The aim of the hardware is to immediately stabilize the spine, maintain alignment, limit postoperative segmental motion, and replace excised anatomic components. The hardware limits motion by acting as a rigid internal fixation device and thus provides the stability that favors osseous fusion. An understanding of this point is essential, since it is acknowledged that instrumentation without osseous fusion will be generally unsuccessful. In other words, hardware itself is insufficient for fusion.
Anterior Lumbar Interbody Fusion
If an interbody fusion is large enough, it can on its own provide sufficient motion limitation and biomechanical stability to promote fusion. ALIF provides optimal disk space access allowing for complete anterior and central disk removal, which in turn allows for an optimally sized device to be placed. Therefore ALIF is the only approach that does not require supplemental posterior hardware to ensure stability and motion limitation throughout the fusion process. ALIF utilizes single large cages typically supplemented by an anterior plate ( Fig. 24.4 ). The ALIF approach avoids damage to the motion limiting posterolateral vertebral elements, avoids damaging the posterior musculature, and decreases the risk of epidural fibrosis. If delayed arthrodesis is evident after stand-alone ALIF, a second posterior instrumentation procedure can be performed to further promote solid arthrodesis. Importantly, the approach requires skilled surgical expertise to avoid abdominal and vascular complications.
Posterior Lumbar Interbody Fusion
This approach typically requires laminectomies and often facetectomies. The posterior approach allows direct access to the spinal canal allowing for complete decompression of the thecal sac and nerve roots. Retraction of the thecal sac and nerve roots is necessary to access the disk. The size of the devices that can be placed is therefore limited, which in turn reduces the stability of the construct ( Fig. 24.5A ). Supplemental posterior instrumentation is therefore frequently performed and the approach facilitates optimal placement of posterior hardware.
Transforaminal Lumbar Interbody Fusion
A more lateral approach than the posterior approach permits foraminal decompression with safer access to the disk by reducing the need for retraction. This approach allows for wider access to the anterior half of the disk space as compared to PLIF (see Fig. 24.5B ). Although this approach allows for placement of larger intradiskal grafts than PLIF, the size limitations do not permit stand-alone fusion without supplemental posterior instrumentation. Ipsilateral removal of the pars interarticularis and facet joint is usually performed.
From the above discussion, one can see that the improved disk space access of anterior and lateral approaches better allow for restoration of height in cases where loss of disc space is the primary problem. A posterior approach, on the other hand, allows for decompression of focal posterior disk herniations or significant spinal stenosis in need of decompression.
Lumbar Interbody Fusion Devices
There are numerous interbody fusion devices of differing size and morphology. While the nuances of each device are beyond the scope of this discussion, it is important to note that they fall under three general categories: metal devices, composite devices, and biologic devices. Therefore not only do their morphologies differ, but so do their attenuation and visibility on computed tomography (CT) imaging. These include bone graft substitutes such as recombinant human bone morphogenetic protein (rhBMP-2). rhBMP-2 acts as signaling molecule to initiate bone formation and is radiolucent at the time of placement.