Clinical StudyIncidence of contraindications to total disc arthroplasty: a retrospective review of 100 consecutive fusion patients with a specific analysis of facet arthrosis
Introduction
The role of total disc arthroplasty (TDA) in the treatment of spinal pathology is unclear [1], [2], [3], [4]. TDA has been touted as an alternative to fusion which would allow resolution of discogenic pain while still maintaining spine motion [1], [2], [3], [4], [5], [6], [7] and reducing the incidence of adjacent segment degeneration [3], [8], [9]. However, it is recognized that not all mechanical back pain is discogenic in origin [9] and that there are a number of decisive and relative contraindications to TDA (Table 1, Table 2) [3], [8], [9], [10], [11], [12], [13], [14], [15], [16], [17], [18], [19], [20]. At Spine Week in Porto, Portugal, June 2004, Huang and Cammisa's group from the Hospital for Special Surgery in New York presented their study evaluating the presence of 10 relatively decisive contraindications to TDA [10] (Table 1) evaluated in a single-surgeon consecutive series of 100 patients undergoing spinal surgery at their institution. The results have subsequently been published [10]. They found that 56/56 (100%) of the patients having a lumbar fusion had one or more of 10 recognized definite contraindications to TDA. Only 5 of the 44 patients having decompressive/nonfusion operations were without TDA contraindications on review of their medical records. En face, this seems to be an extremely high number of patients with contraindications to TDA.
These results highlight the profound difficulty of accurately defining the limits in the lumbar degenerative process that would be optimal for the use of the TDA. Kirkaldy-Willis et al. [21], [22] divided the stages of degeneration of a spinal motion segment into three phases (normal, unstable, stable). Macnab [23] defined X-ray signs of the transition between the normal and unstable phases (the Macnab “Traction Spur”). Farfan and Kirkaldy-Willis [24] suggested that in the degenerative process, the spinal motion segment be viewed as primarily a “three joint complex” (disc and two facet joints). These concepts worked well even in the era before more modern and sophisticated imaging studies and still form the basis for subsequent classifications that have been proposed to take into account pathologic changes seen by more modern techniques of histologic analysis and imaging modalities such as magnetic resonance imaging. Thompson et al. [25] described a five-stage classification based on a pathological analysis of disc degeneration. Thalgott et al. [26] proposed a classification which also began to look at the posterior elements.
The 10 contraindications to TDA used by Huang and Cammisa in their review appear to be the most consistent and decisive through various publications (facet arthrosis, central spinal stenosis, lateral recess spinal stenosis, spondylolysis, spondylolisthesis, herniated disc with radiculopathy, scoliosis, osteoporosis, pseudoarthrosis, deficient posterior elements) (Table 1). Although these 10 represent the most definite contraindication to TDA, more than 50 other contraindications have also been cited (Table 2).
In our view, facet arthrosis appeared to be the contraindication with a relatively imprecise diagnosis and wide clinical spectrum that was most likely to represent a patient selection dilemma for the spine surgeon.
The Hospital for Special Surgery study [10] brought attention to the issue that TDA may not represent a “better” or even an “alternative” surgical procedure to the majority of patients presently undergoing spinal fusion. Their paper broke new ground on this issue. However, as their study was a single-surgeon (F. Cammisa) series, performed in an orthopedic department at an academic medical center, their paper generates another tier of questions to be answered:
- 1)
Do the results reflect the referral pattern of one particular orthopedic spine surgeon, or do they apply over multiple surgeon practices?
- 2)
Are the findings consistent across different subspecialties (orthopedic surgery, neurosurgery)?
- 3)
Are the findings consistent across different practice settings (academic vs. private medical center)?
- 4)
Was the incidence of the 10 contraindications specified weighted more towards the “hard” contraindications (such as herniated disc or spinal stenosis with radiculopathy) or more frequently a relatively “soft” contraindication (such as facet arthrosis)?
- 5)
If facet arthrosis is viewed as a relative rather than absolute contraindication to TDA, what is the clinical spectrum of this pathology in patients having surgical fusion?
- 6)
Can patients with facet arthrosis be subdivided into clinically relevant subgroups in a manner that would assist with surgical treatment decision?
This study was undertaken to compare the contraindications found in a cohort of patients undergoing fusion at our private medical center with the group at the Hospital for Special Surgery. Patients from both the Orthopedic and Neurosurgery Departments, from several different practice groups were reviewed. A further in-depth chart review was performed to analyze the diagnosis of facet arthrosis and determine the incidence of clinically significant facet disease which likely represented a definite contraindication to TDA.
Section snippets
Methods
This was a retrospective review of the medical records of 100 consecutive patients undergoing a primary 1–3 level lumbar spinal fusion at Presbyterian St. Luke's Medical Center, Denver between January 2003 and May 2004. Patients from all five spinal surgeons on staff were included (two neurosurgeons and three orthopedic spine surgeons from three separate practices). The patients' medical records were reviewed independently by Presbyterian St. Luke's Medical Center's director of spinal research,
Results
All 100 patients had at least one contraindication to TDA. Only one patient had facet arthritis as their only contraindication. The average number of contraindications per patient was 3.69 (Fig. 1). At the low end of the range, three patients had a single contraindication. The maximum number of contraindications was seven in one patient.
The relative incidence of the 10 specific contraindications was quite varied (Fig. 2), but appeared to self-stratify into three segments. Only one diagnosis
Discussion
The ideal indication for lumbar TDA seems clear (isolated discogenic low back pain only). However, the relative frequency of this decisive clinical circumstance in the population in general and even in the cohort of patients undergoing lumbar spinal fusion appears extremely indefinite. There has been great enthusiasm in some quarters that TDA would obviate spinal fusion in a large percentage of the patients presently undergoing a fusion procedure. Cammissa's study [10] directly contradicts this
Conclusions
Significant contraindications to TDA appear to exist in some patient populations presently having lumbar spinal fusion surgery. Both the present study and the original similar review at the Hospital for Special Surgery [10] found that 100% of the patients having fusion surgery at our two institutions have one or more recognized contraindications to TDA.
Careful analysis of pain generators will be necessary to define appropriate candidates for TDA.
The role of clinically significant facet disease
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2015, Journal of BiomechanicsCitation Excerpt :Several clinical studies have demonstrated satisfactory clinical results for monosegmental TDR, but these results were demonstrated only in carefully selected patients (Freeman and Davenport, 2006; Guyer et al., 2009; Siepe et al., 2014). Various contraindications have been identified for TDR (Chin, 2007; Huang et al., 2004; McAfee, 2004; Wong et al., 2007), and the success of TDR in the clinic has fallen short of its initial high expectations. In particular, the spino-pelvic alignment (‘sagittal balance’) is a key factor for surgical success (Mehta et al., 2012; Pellet et al., 2011; Roussouly et al., 2005).
FDA device/drug status: approved for this indication (spinal instrumentation).
The authors acknowledges a financial relationship (all authors—grant research support from Stryker, Zimmer, Archus, Cervitech; AK, GG, SJat.—consultants and speakers for Stryker) that may indirectly relate to the subject of this research.