Total Disc Arthroplasty for Treating Lumbar Degenerative Disc Disease

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Abstract

Introduction

The appropriate surgical technique to treat lumbar degenerative diseases has been controversial, particularly that for chronic lumbago. Advances in the field of lumbar spine surgery have transformed the management of lumbar degenerative disk diseases. Among these techniques, total arthroplasty through an anterior or anterolateral approach has been widely used by spinal surgeons [1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22]. The anterior approach allows complete access to the lumbar discs without incising paravertebral muscles and removing posterior structures. Therefore, this approach does not compromise biomechanical stability or functionality of posterior lumbar facets.

We present our experience with total disc arthroplasty for treating lumbar degenerative diseases and evaluate outcomes following this technique.

Materials and Methods

A total of 104 patients underwent total disc arthroplasty (Prodisc, Synthes Inc., West Chester, PA, USA) at the Department of Neurosurgery of Colmar in France from April 2002 to October 2008. All patients were included in the study. We studied the files of these patients retrospectively, and the clinical history, examinations, and radiological findings were reviewed for each patient (Fig. 1). Surgery was performed in the following circumstances: lumbalgia caused by chronic and invalidating discopathy, and resistance to 6 months of medical treatment in an adult <60 years suffering symptomatic discopathy lumbar or lumbosacral discopathy without associated sciatica [1,2,3,8,9,11,12,13,14,16,19]. Patients were evaluated during the preoperative period. The patients were examined clinically at 6 and 12 weeks postoperatively and evaluated with a visual analogue scale (VAS) ranging from 0 (no pain) to 10 (worst pain imaginable) and with the Oswestry disability index (ODI), which ranges from 0-100. All patients underwent X-ray imaging of the lumbar spine on week 6 postoperatively. Among the patients, 21 had undergone previous lumbar spine surgery using a posterior approach.

Fig. 1

Preoperative magnetic resonance image of the lumbar spine. Sagittal view reveals both a bulging disc and endplate Modic changes at L5-S1.

Results

A total of 104 patients (67 females and 37 males; median age, 35.1 years; range, 20-58 years) were included (Fig. 2). Mean follow-up was 20 months (range, 3-38 months).

Fig. 2

Age distribution of patients.

Twenty-one patients had been operated on previously using a posterior approach for different reasons, including disk herniation, lumbar canal stenosis, and other causes. We did not intervene surgically if the level had been instrumented previously. Eighty-three patients (79.81%) suffered from pure lumbago without radiculopathy, and 21 patients (20.19%) had associated radiculopathy.

All patients benefited from a magnetic resonance imaging (MRI) scan of the lumbar spine conducted at the time of diagnosis. We were compelled to carry out a discography in 22 patients because there were doubts about the symptomatic degenerated disc level.

More than one symptomatic degenerated disk level was detected in 17 cases; 13 patients with two levels and four patients with three levels.

Clinical radiculopathy was discordant with symptomatic degenerated disk level in radiological findings of nine patients. The most frequent symptomatic degenerated disk level was L4-L5 (62 cases; 59.62%), followed by the L5-S1 level (52 cases; 50 %). Higher levels were less frequent with seven cases (6.73%) at the L3-L4 level and four cases (3.85%) at the L2-L3 level (Figs. 3, 4).

Fig. 3

Intraoperative photograph of disk space.

Fig. 4

Level distribution of patients as sick disc.

Eighty-seven patients (83.65%) underwent surgery for one level, 13 (12.50%) for two levels, and four patients (3.85%) underwent operations for three levels.

MRI showed the following results: 43 patients had Modic sign 0, 43 patients had Modic sign I, 15 patients had Modic sign II, and three patients had Modic sign III.

All patients had preoperative computed tomography angiography to assess the vascular system of the region as well as anteroposterior (AP) and lateral lumbar spine radiographs and dynamic X-rays.

The average length of stay in the hospital was 3.5 days (range, 2-15 days). Patients were encouraged to ambulate on day 1 and were authorized to restart their activities at the first consultation.

The postoperative complications are summarized in Table 1.

Table 1

Postoperative complications

All patients responded to the VAS and the ODI before, during the immediate preoperative period, and 6 and 12 weeks after surgery. Table 2 summarizes the results of this evaluation. All patients improved after 6 weeks except one who lost 1 point on the VAS at 6 weeks but returned to the preoperative level at 12 weeks, and three patients did not improve on the VAS. All patients improved on the ODI at 6 and 12 weeks. Patients were followed up for a mean of 20 months clinically and radiologically every 3 months

Table 2

Clinical and preoperative assessment data of patients

Discussion

Treatment for lumbalgia has been problematic for spine specialists, as the surgical treatment is controversial. According to Burke et al. [5], lumbar degenerative disc diseases lead to mechanical instability that stimulates nociceptive intradiscal fibers. This source of pain is removed by replacing the symptomatic degenerated disk with an artificial disc. In addition, mobility, disc height, and segmental stability are restored. The ProDisc was designed by Marnay in 1987 [3]. Thereafter, this technique spread rapidly, and several clinical trials were conducted in the USA. Numerous studies with positive results support this technique. Our results demonstrated satisfactory outcomes with significant improvement on the VAS and ODI. All patients were consulted 6 and 12 weeks postoperatively, and AP and lateral lumbar spine radiographs were obtained. Among the 104 patients, 51 (49.03%) returned to work within 6 weeks and 92 (88.46%) returned within 12 weeks. Forty-five patients had dynamic X-rays that confirmed persistence of the mobile section. Twenty-three patients participated in strenuous and regular sports activity before surgery. Among them, 19 (82.6%) started complete sports and physical activities after 12 weeks. Four patients were hospitalized in medical physical and rehabilitation centers. The minimum VAS pain score preoperatively was 5. Thirty-six (34.62%) patients had zero pain (VAS=0) 6 weeks postoperatively, and 68 (66.35%) had VAS scores ≤6. Among the patients with radiculopathy, 17 became asymptomatic (Table 3). The clinical radiculopathy was discordant with the symptomatic degenerated disk level in the radiological findings of nine patients. One study [9] suggested that patients with radiculopathy without herniation may be suboptimal candidates for the procedure.

Table 3

Preoperative and postoperative VAS and ODI

Studies have reported complication rates of 1%-40% for this procedure [1,2,3,8,9,11,12,13,14,15,16,17,18,19,22], whereas we had a relatively lower 9.61% of complications. This large difference can be explained by the use of various techniques and approaches and the level of experience of the surgeon. In our study, 91 patients (87.5%) were operated on using a transperitoneal approach and 13 cases (12.5%) by an anterior paramedian retroperitoneal approach. We have more experience with the transperitoneal approach than the retroperitoneal approach. We believe that the retroperitoneal approach does not provide the opportunity for symmetry, as there is no straight axis of vision, and the iliac artery and iliac vein (at left because this approach is usually performed by the left side) must be retracted medially. We operated on four patients (3.86%) due to complications (Tables 1, 4). These complications included wound dehiscence, retroperitoneal hematoma, abdominal wall hematoma, and a prosthesis dislocation.

Table 4

Distribution of patient as number of sick disc

One of the most important complications in the literature is major vessel injury with an incidence of 1.9%-2.9% [5,6]. We had one retroperitoneal hematoma (0.96%). The incidence of retrograde ejaculation is 0%-4.1% in the literature. We had two cases (1.92%).

Our results following artificial total disc replacement were promising, particularly in comparison with posterior fusion results. In the latter cases, patients suffered postoperative back pain for various reasons. A meta-analysis of artificial total disc replacement vs. fusion for lumbar degenerative disc diseases performed by Yajun et al. [20] showed that total disc arthroplasty provides for slightly better functioning and back pain status and significantly greater patient satisfaction. The follow-up was 2 years in that meta-analysis. Another study performed in South Korea [8] with a 5-year follow up showed 88% satisfied or somewhat satisfied patients. Our study produced similar results with 86.54% satisfied and somewhat satisfied patients at 6 weeks and 87.5% satisfied at 12 weeks. Our average follow-up was 20 months (range, 3-38 months), which was relatively short but we noticed that the most important improvement occurs in the first 6 weeks and the evolution becomes slower and more discrete as time passes. According to the meta-analysis by Yajun et al. [20], ODI and VAS scores are typically lower than our results (on average 2 and 10, respectively).

Conclusions

We demonstrated satisfactory clinical and radiographic results. Total disc arthroplasty is a valid, simple and effective treatment for lumbar degenerative disk disease.

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