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Orthopaedic Proceedings
Vol. 87-B, Issue SUPP_III | Pages 242 - 243
1 Sep 2005
Fairbank J Frost H MacDonald J Yu L Rivero-Arias O Campbell H Gray A
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Study Design: Prospective randomized study.

Objectives: To compare the strategy of spinal fusion with that of rehabilitation for patients with chronic low back pain.

Methods: A multicentre trial of 349 candidates for spinal fusion (where both patient and surgeon were uncertain of the outcome) were randomised to either an operation that the surgeon considered was most appropriate for that patient or to an intensive rehabilitation programme. Rehabilitation was based on a 3 week (15 day) model of exercise therapy, spine stabilisation techniques and education using cognitive behavioural principles. Follow-up was at least 2 years from randomisation. The trial was 90% powered to show a 4 point difference between groups at α= 0.05. A full economic analysis is available.

Outcomes Measures: Oswestry Disability Index (ODI); the Shuttle Walking Test (SWT); SF-36 and EuroQol EQ-5D.

Results: 176 patients were randomized to surgery and 173 to rehabilitation. Demographic features including sex, age, diagnosis (spondylolisthesis, post-laminectomy syndrome, others) duration of back pain, smoking history, litigation, employment status, planned numbers of fused levels and baseline ODI were similar for both groups.

Results: For the surgery group the mean ODI improved from 46.6 (SD 14.5) to 34.9 (SD 21) at two years. For the rehabilitation group mean ODI improved from 44.8 (SD 14.8) to 36.2 (SD 20.6) at two years. For the surgery group the mean SWT improved from 254 (SD 209) to 350 (SD 244.8) at two years. For the rehabilitation group mean SWT improved from 247 (SD 185) to 310 (SD 203) at two years. For the surgery group the mean SF-36 Physical component score improved from 22.2 (SD 18) to 43.6 (SD 32.1) at two years. For the rehabilitation group the mean SF-36 Physical component score improved from 24.0 (SD 20.6) to 40.5 (SD 31.1) at two years.

Conclusions: This is a comparison of treatment strategies: There was no clinical or statistical difference in outcome between the strategy of spinal fusion and that of rehabilitation. Patients randomised to surgery (spinal stabilisation) and patients randomised to rehabilitation have indicated a treatment effect, but this may be due to natural history. The surgery results parallel those reported in other trials. At two years the treatment costs of the surgery arm were approximately twice those of the rehabilitation arm. The costs of rehabilitation depend on how many patients opt for surgery (22% in this trial). “Failed” non-operative treatment is commonly listed as an indication for surgery. “Failed” non-operative treatment should include intensive rehabilitation appropriately supported by the treating surgeon.


Orthopaedic Proceedings
Vol. 87-B, Issue SUPP_III | Pages 291 - 291
1 Sep 2005
Fairbank J Frost H Wilson-MacDonald J Yu L Barker K Collins R
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Introduction and Aims: A multicentre trial of 349 patients of candidates for spinal fusion (where both patient and surgeon were uncertain of the outcome) were randomised to either an operation or to an intensive rehabilitation program. Rehabilitation was based on a three-week (15-day) model of exercise therapy and education using cognitive behavioural principles.

Method: The main outcome measures were the Oswestry Disability Index (ODI); Shuttle Walking Test; SF-36 and EuroQol EQ-5D recorded at baseline and six, 12 and 24 months after randomisation. The trial was 90%-powered to show a four-point ODI difference between groups at a= 0.05. Full economic analysis is available.

Results: Patients in both treatment arms made statistically significant improvements on all outcome measures between baseline and two-year follow-up. There was a small difference between the treatment arms favouring surgery on one of the main outcome measures, the Oswestry Disability Index; there were no statistically significant differences between the two treatment strategies for the rest. The difference in the change of score for the ODI was a decrease of 3.2 (C.I -7.3 – 0.9) in favour of surgery (p< 0.1), an improvement of 30 metres on the shuttle walking test in favour of the surgery group (p< 0.2), a difference of 0.01 on the Euroqol (p< 0.9) and an increase of 2.7 points on the SF-36 (p< 0.4).

The surgery results parallel those reported in other trials. At two years, the treatment costs of the surgery arm were approximately twice those of the rehabilitation arm. The costs of the rehabilitation strategy depend on how many patients opt to have surgery after rehabilitation (22% in this trial). This is a comparison of treatment strategies: there was no clinical or statistical difference in outcome between the strategy of spinal fusion and rehabilitation.

Conclusion: Patients randomised to both surgery (spinal stabilisation) and rehabilitation have indicated a treatment effect, but this may be due to natural history. ‘Failed’ non-operative treatment is commonly listed as an indication for surgery, this should only be considered once an intensive rehabilitation program backed by the treating surgeon has been tried.