Percutaneous Lumbar Restabilization via a Posterolateral Approach

Published on 10/03/2015 by admin

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Last modified 10/03/2015

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Chapter 32 Percutaneous Lumbar Restabilization via a Posterolateral Approach

Minimally invasive percutaneous lumbar restabilization via a posterolateral approach is a valid and less aggressive procedure than conventional open surgery for the treatment of lumbar segmental insufficiency (LSI) or micro-instability. The potential for performing a percutaneous lumbar restabilization has been made possible by the development of a new expandable titanium device available in several sizes (B-Twin System [Disc-O-Tech Medical Technologies Ltd., Herzliya, Israel] or intervertebral holder [IVH]), which should serve as the first device of its nature in a series of new-generation implants conceived for the less invasive treatment of a number of spine conditions [15].

The advantages of this surgical option include the following:

The primary indication for percutaneous lumbar restabilization with the expandable interbody device is the treatment of lumbar segmental instability at the lower lumbar level (Fig. 32-1). This clinical feature is characterized by typical signs and symptoms associated with clear radiologic criteria (Table 32.1).

Table 32.1 Clinical and Radiologic Features of Lumbar Segmental Insufficiency (LSI)

Clinical Features
Clinical anamnesis
Clinical characteristics
Pathognomonic Radiologic Signs
Conventional radiography
Functional x-ray study Dynamic sagittal instability (flexion-extension > 6 mm)
Magnetic resonance imaging: the stage or degree of LSI and with regard to the Modic changes described below Local kyphosis and/or posterior articular subluxation on both T1-weighted and T2-weighted sequences
Modic changes Type I: Disruption and fissuring at the level of the end plates with low signal on T1-weighted images and increased signal on T2-weighted images
Type II: Fatty conversion with increased signal on T1-weighted images and isointense or increased signal on T2-weighted images
Type III: Marked sclerosis (osteochondrosis) with low or no signal on both T1- and T2-weighted images

To confirm the diagnosis of LSI, the patient must exhibit at least three of the radiologic signs or criteria listed in this table in addition to the standard clinical signs and corresponding anamnesis.

This surgical option may also be contemplated in the treatment of patients with failed back surgery syndrome if no decompression of the nerve roots or foramen is required and if there is no recurrent disc herniation. There is strong evidence that the device offers distraction by “jacking up” the segment, leading to a restabilization of the instable segment. The device also serves as an internal “strengthener” for the fusion process. There is an immediate reduction of the hypermobility contributing to the clinical indication of micro-instability, which is favorable for the fusion process over the months following surgery.

In cases of LSI, the disc of the mobile segment is often the cause of the degeneration of the segment (comprising the two adjacent vertebrae and the disc in between). Thus pain relief can be achieved by immediate restabilization with the device, and the pain relief can be maintained long term owing to the longer, definite bony fusion produced (spondylodesis).

Indications and Contraindications

See Table 32.1 for the indications for percutaneous lumbar restabilization via a posterolateral approach. Box 32.1 lists the contraindications. Degree of disc removal remains a matter of debate because the surgeon is limited as to the degree of motion (in-and-out movements and technical limitation to go laterally in the working channel). Eroders cannot be used for the percutaneous application of the device. They are used strictly in the microsurgical reduced open application. The curette and possibly a shaver must be used in the percutaneous technique.