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| Name | Class |
|---|---|
| St. Olavs Hospital | OTHER |
| Haukeland University Hospital | OTHER |
| Helse Stavanger HF | OTHER_GOV |
| University Hospital of North Norway |
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During the past 25-30 years, surgery with total disc replacement (TDR) has become an option for a selection of patients with chronic low back pain (LBP) traditionally treated conservatively or operated on with spinal fusion. Randomized trials comparing TDR with fusion have found the clinical outcome of TDR at least equivalent to that of fusion, and the only study comparing TDR to non-surgical treatment (The Norwegian TDR study) concludes that TDR is significantly more effective than multidisciplinary rehabilitation (REHAB) after 2 years. However, the long-term effects of TDR in terms of clinical results, costs, reoperation- and revision rate, degenerative changes and prognostic factors have not been investigated in high quality prospective trials. This is very much required since TDR surgery is offered a great number of patients world wide, and is associated with high complexity and risk of serious complications and difficult revision. Hence, the overall aim of the present study is to evaluate the long term (eight years follow-up) effect of The Norwegian TDR study where TDR surgery were compared to modern multidisciplinary rehabilitation in patients with chronic low back pain and localized degenerative disc changes.
Two-year results of the Norwegian TDR study were published in BMJ in May 2011 (Hellum et al). The current protocol is 8-year follow-up of patients included in the Norwegian TDR study.
Hypothesis of the 8-year follow-up:
Main hypothesis (H0): There are no differences in change between TDR and REHAB for pain and disability measured by Oswestry Disability Index (main outcome), back pain, quality of life, psychological variables, work status, patients satisfaction, drug use, urinary incontinence, and back surgeries after 8 years.
Secondary Hypothesis:
Statistical analysis:
The investigators will use the same analysis as for 2-years results: two-way ANOVA, mixed model, regression analysis. p<0.05 will be considered statistically significant
Additional analysis (not conducted at 2 years):
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Surgery | Experimental | Replacement of the degenerative intervertebral lumbar disc with an artificial lumbar disc device (degeneration had to be restricted to the two lower levels (L4/L5 and/or L5/S1)) |
|
| Multidiciplinary rehabilitation | Active Comparator |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Lumbar total disc replacement | Procedure | The surgical intervention consisted of replacement of the degenerative intervertebral lumbar disc with a artificial lumbar disc device in one or two of the lover lumbal levels (L4/L5 or/and L5/S1). The ProDisc consists of three pieces, two metal endplates and a polyethylene core that is fixed to the inferior endplate when the device is implanted, and is implanted through a retroperitoneal (or transperitoneal) access. |
| Measure | Description | Time Frame |
|---|---|---|
| Oswestry Disability Index Oswestry Disability Index | Version 2.0 | Baseline, 6 weeks, 3 months, 6 months, 1, 2 and 8 years after inclusion to trial |
| Measure | Description | Time Frame |
|---|---|---|
| Low back pain | Measured by a VAS scale (0-100 mm) | Baseline, 6 weeks, 3 months, 6 months, 1, 2 and 8 years after inclusion to trial |
| EQ-5D | general health status |
| Measure | Description | Time Frame |
|---|---|---|
| Time to surgery | For patients randomized to TDR surgery: time to fixation For patients randomized to REHAB: time to TDR surgery or fixation | From baseline to 8 years after inclusion to the study |
Inclusion Criteria:
Exclusion Criteria:
Patients were examined by an orthopaedic surgeon and a specialist in physical medicine and rehabilitation together, which had to agree on inclusion.
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| Name | Affiliation | Role |
|---|---|---|
| Kjersti Storheim, PhD | Oslo University Hospital Ullevål | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Oslo University Hospital Ullevål | Oslo | Oslo | 0407 | Norway |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 21596740 | Background | Hellum C, Johnsen LG, Storheim K, Nygaard OP, Brox JI, Rossvoll I, Ro M, Sandvik L, Grundnes O; Norwegian Spine Study Group. Surgery with disc prosthesis versus rehabilitation in patients with low back pain and degenerative disc: two year follow-up of randomised study. BMJ. 2011 May 19;342:d2786. doi: 10.1136/bmj.d2786. | |
| 22246644 |
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| Type | Date | Date Unknown |
|---|---|---|
| Release | Nov 23, 2017 | |
| Unrelease | Jul 11, 2018 | |
| Release | Oct 12, 2018 | |
| Reset | Feb 20, 2019 |
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| Release Date | Unrelease Date | Unrelease Date Unknown | Reset Date | MCP Release Number |
|---|---|---|---|---|
| Nov 23, 2017 | Jul 11, 2018 | |||
| Oct 12, 2018 |
| OTHER |
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|
| Multidisciplinary rehabilitation | Behavioral | The intervention is based on a treatment model described by Brox et al (Spine 2003;28:1913-1921) and is also described in details by Hellum et al (BMJ, May 2011). It consisted of a cognitive approach and supervised physical exercise and was delivered by a team of physiotherapists and specialists in physical medicine and rehabilitation. The rehabilitation programme lasted for about 60 hours over three to five weeks. |
|
| Baseline, 6 weeks, 3 months, 6 months, 1, 2 and 8 years after inclusion to trial |
| HSCL-25 | Hopkins Symptom Check List 25 for emotional distress | Baseline, 3 months, 6 months, 1, 2 and 8 years after inclusion to trial |
| Work status | Baseline, 6 weeks, 3 months, 6 months, 1, 2 and 8 years after inclusion to trial |
| Satisfaction with treatment outcome | 7 point Likert scale | Baseline, 6 weeks, 3 months, 6 months, 1, 2 and 8 years after inclusion to trial |
| Satisfaction with care | 5 point Likert scale | Baseline, 6 weeks, 3 months, 6 months, 1 and 8 years after inclusion to trial |
| Drug consumption | Daily, weekly, type | Baseline, 6 weeks, 3 months, 6 months, 1, 2 and 8 years after inclusion to trial |
| Urinary incontinence | Stress incontinence, urge incontinence | Baseline, 3 months, 6 months, 1, 2 and 8 years after inclusion to trial |
| Back surgeries and multidisciplinary rehabilitation | All surgeries and multidisciplinary rehabilitation due to low back pain will be registered | Baseline, 6 weeks, 3 months, 6 months, 1, 2 and 8 years after inclusion to trial |
| Disc degeneration | Disc degeneration at adjacent level | Baseline, 2 and 8 years after inclusion to trial |
| Facet joint degeneration | Facet joint degeneration at index level | Baseline, 2 and 8 years after inclusion to trial |
| Cost-effectiveness | The EQ-5D questionnaire will be used to estimate patient utilities | Baseline, 6 weeks, 3 months, 6 months, 1, 2 and 8 years after inclusion to trial |
| Hellum C, Johnsen LG, Gjertsen O, Berg L, Neckelmann G, Grundnes O, Rossvoll I, Skouen JS, Brox JI, Storheim K; Norwegian Spine Study Group. Predictors of outcome after surgery with disc prosthesis and rehabilitation in patients with chronic low back pain and degenerative disc: 2-year follow-up. Eur Spine J. 2012 Apr;21(4):681-90. doi: 10.1007/s00586-011-2145-3. Epub 2012 Jan 13. |
| 22706091 | Background | Hellum C, Berg L, Gjertsen O, Johnsen LG, Neckelmann G, Storheim K, Keller A, Grundnes O, Espeland A; Norwegian Spine Study Group. Adjacent level degeneration and facet arthropathy after disc prosthesis surgery or rehabilitation in patients with chronic low back pain and degenerative disc: second report of a randomized study. Spine (Phila Pa 1976). 2012 Dec 1;37(25):2063-73. doi: 10.1097/BRS.0b013e318263cc46. |
| 24150435 | Background | Johnsen LG, Hellum C, Storheim K, Nygaard OP, Brox JI, Rossvoll I, Ro M, Andresen H, Lydersen S, Grundnes O, Pedersen M, Leivseth G, Olafsson G, Borgstrom F, Fritzell P; Norwegian Spine Study Group. Cost-effectiveness of total disc replacement versus multidisciplinary rehabilitation in patients with chronic low back pain: a Norwegian multicenter RCT. Spine (Phila Pa 1976). 2014 Jan 1;39(1):23-32. doi: 10.1097/BRS.0000000000000065. |
| 23982421 | Background | Berg L, Hellum C, Gjertsen O, Neckelmann G, Johnsen LG, Storheim K, Brox JI, Eide GE, Espeland A; Norwegian Spine Study Group. Do more MRI findings imply worse disability or more intense low back pain? A cross-sectional study of candidates for lumbar disc prosthesis. Skeletal Radiol. 2013 Nov;42(11):1593-602. doi: 10.1007/s00256-013-1700-x. Epub 2013 Aug 28. |
| 23622053 | Background | Johnsen LG, Hellum C, Nygaard OP, Storheim K, Brox JI, Rossvoll I, Leivseth G, Grotle M. Comparison of the SF6D, the EQ5D, and the oswestry disability index in patients with chronic low back pain and degenerative disc disease. BMC Musculoskelet Disord. 2013 Apr 26;14:148. doi: 10.1186/1471-2474-14-148. |
| 23307678 | Background | Johnsen LG, Brinckmann P, Hellum C, Rossvoll I, Leivseth G. Segmental mobility, disc height and patient-reported outcomes after surgery for degenerative disc disease: a prospective randomised trial comparing disc replacement and multidisciplinary rehabilitation. Bone Joint J. 2013 Jan;95-B(1):81-9. doi: 10.1302/0301-620X.95B1.29829. |
| 22430564 | Background | Berg L, Gjertsen O, Hellum C, Neckelmann G, Johnsen LG, Eide GE, Espeland A. Reliability of change in lumbar MRI findings over time in patients with and without disc prosthesis--comparing two different image evaluation methods. Skeletal Radiol. 2012 Dec;41(12):1547-57. doi: 10.1007/s00256-012-1394-5. Epub 2012 Mar 20. |
| 34049574 | Derived | Garratt AM, Furunes H, Hellum C, Solberg T, Brox JI, Storheim K, Johnsen LG. Evaluation of the EQ-5D-3L and 5L versions in low back pain patients. Health Qual Life Outcomes. 2021 May 28;19(1):155. doi: 10.1186/s12955-021-01792-y. |
| Feb 20, 2019 |