Outcome of Surgery for Lumbar Spinal Stenosis - a Comparison of Data From Three National Quality Registries

Spinal Stenosis Clinical Trial

Official title: Outcome of Surgery for Lumbar Spinal Stenosis - a Comparison of Data From Three National Quality Registries

Status Completed

Clinical Trial Summary

There is no international consensus on evaluation and surgical treatment of Lumbar Spinal Stenosis (LSS). The indication for operative treatment is relative, and the variation in surgical rates and procedures is significant, both within and between countries. Understanding practice-based variety is critical since these differences may reflect a disparity in quality of the health care in different institutions, regions, or countries. Norway, Sweden, and Denmark do all have National spine registers for research and quality assessment. Comparing indications for surgery, selected procedure, patient reported outcomes, and factors predicting outcome after surgery for LSS between these countries could provide information about optimal indications and strategy for surgery. Register-based studies have advantages such as large sample sizes and high external validity, but also limitations such as lower follow-up rates, and inferior data quality compared to clinical trials.

Hypotheses: Between these three countries, there are no differences in (i) indications for surgery, (ii) patient-reported outcome after surgery or (iii) risk factors associated to outcome are similar.

Clinical Trial Description

This is an observational register based study, i.e. prospective data registration and a retrospective study design. Eligible patients are those 50 years or older treated surgically for LSS in Denmark, Norway or Sweden during 2011, 2012, or 2013 with no history of previous lumbar spine surgery. Register-based studies have advantages such as large sample sizes and greater external validity, but also limitations such as lower follow-up rates, inferior data quality compared to clinical trials. Data will be presented according to the STROBE criteria.

The registers:

All registries have the aim of studying outcome after spine surgery. All departments participate voluntarily. Patients participate voluntarily after signing an informed consent. At the time of admission, the patient reports data on demographics, social factors, comorbidity and previous surgery. After surgery, the surgeon records diagnosis and type of surgery performed.

The Norwegian Spine register, NORspine, is based on experiences from the Swespine register and previous validation studies from a local clinical registry, and was founded in 2007. In total 38 of 40 centers performing lumbar spine surgery in Norway report to NORspine. Coverage is approximately 95%. The completeness is approximately 65%.

The Swespine Register has included individuals treated with surgery for lumbar spinal stenosis since 1993. During the last decade, the number of departments participating in the registry has varied between 35 and 41 of the 42 to 45 departments providing spinal surgery services in Sweden. Coverage is approximately 90%. The completeness (number of patients reported to Swespine at the time of surgery) is approximately 80%.

The Danish spine register, DaneSpine, is based on Swespine and was acquired by the Danish Spine Society from the Swedish Society of Spinal Surgeons in 2009 and has successively been implemented. Coverage and completeness for DaneSpine has not been determined.

Quality assurance:

Loss to follow-up may bias the results. Solberg et al. (2011) studied 633 patients, who were operated on for degenerative disorders of the lumbar spine in Norway, and found that a loss to follow-up of 22% would not bias conclusions about overall treatment effects. There were no indications of worse outcomes in the non-responders group. In a similar one-center study of the DaneSpine. Højmark et al. (2016) found that a loss to follow-up of 12% at did not seem to bias the conclusions that can be drawn from DaneSpine at that center.

Data handling Anonymized individual level data from all three registers will be pooled in one database. The cohort will be divided by country for comparisons.

Missing data and out of range data: In case of missing data case exclusion analysis by analysis, will be used. Out of range data will be deleted.

Analysis The data will be cleaned by excluding patients with missing or incorrect date of surgery, missing date for follow-up, previous lumbar spine surgery and surgery other than decompression for lumbar spinal stenosis with or without concomitant arthrodesis.

After data cleaning, we aim to perform blinded statistical analyses, in which the independent statistician performing the analyses is unaware of group belonging (i.e. country). The code will not be broken until the analyses and interpretations have been performed.

Comparisons of indications for surgery Analysis of baseline data will include age at surgery, sex, anthropometrics, number of smokers, Oswestry Disability Index, EQ-5D, number on sick leave, employment status, and duration of leg and back pain and presented as mean (SD), mean (95% confidence interval), or number (%).

Variables will be analyzed by analysis of variance, Chi-square or logistic regression tests. Data will be presented as crude (unadjusted) data to elucidate any differences between the countries.

Comparisons of outcome Comparisons of the change of the outcome variables from baseline to 1 year, as well as comparisons of the actual value at 1 year will be performed. Analysis of covariance, Chi-square or logistic regression tests and the crude (unadjusted) data will be presented.

In addition, baseline variables will be used as covariates in the analysis of covariance and the adjusted data presented. Propensity scores will also be considered as covariates.

Comparison of surgical method used Based on the decompression with or without concomitant arthrodesis. Non-response analysis A non-response analysis will be performed comparing all available baseline variables between those that responded to the 1 year follow-up with those that did not respond.

Sample size A study of similar character has never been performed before. Due to the nature of the study, the sample size is not formulated in the guise of power, risk level, or clinical difference. The number of patients participating in the study is estimated to 7500. The sample is so large that differences in the Oswestry Disability Index of as low as 2 points may be detected (power 90%, significance level 5%), but in the interpretation the minimal important difference of 10-15 points in the Oswestry Disability Index often referred to has to be taken into account. ;

Related Conditions & MeSH terms

• Constriction, Pathologic
• Intermittent Claudication
• Spinal Stenosis

• NCT number: NCT02897947
• Study type: Observational [Patient Registry]
• Source: St. Olavs Hospital
• Status: Completed
• Start date: January 2011
• Completion date: June 2015