Outcome of Surgery for Sciatica - a Comparison of Data From Three National Quality Registries

December 2, 2017 updated by: Paul Gerdhem, Karolinska Institutet

Purpose: The incidence of surgery for lumbar disc hernia varies. According to the national spine registries in Sweden, Norway and Denmark, there is a 30-60% difference in surgical incidence between these countries. The cause for this difference is not known. It may reflect a difference in incidence of lumbar disc hernia, but with a similar socio-economic and ethnical background in these countries, it is more likely that the differences are due to varying surgical indications. Comparing indications for surgery, patient reported outcome and factors predictive for outcome after surgery for lumbar disc hernia in these countries could provide information about optimal indications for surgery.

Hypotheses: (i) there are no differences in patient-reported outcome after surgery between these countries, (ii) there are no differences in indications for surgery between these countries and (iii), factors that predict outcome are similar in these countries.

Method of research: By using data from three Nordic national spine registers, we will compare baseline data, indications for surgery and patient reported outcome one year after surgery for lumbar disc herniation. Register based studies have advantages such as large sample sizes, reflecting real life, but they also have limitations such as lower follow-up rates than clinical trials. A non-response analysis will be performed to take this into account.

Study Overview

Status

Completed

Detailed Description

This is an observational register based study, with prospective data registration and a retrospective study design. Included are individuals treated surgically for a lumbar disc herniation between the ages of 18 through 65 years, without a history of previous lumbar spine surgery. Surgery has been performed in Denmark, Norway or Sweden during 2011, 2012 or 2013. Data will be presented according to the STROBE criteria.

The registers

All registries have the aim of studying outcome after spine surgery. All departments and patients participate voluntarily. At the time of admission, the patient reports data consisting of information on social factors, comorbidity and previous surgery. After surgery, the surgeon records diagnosis and type of surgery performed.

The Swespine Register has included individuals treated with surgery for lumbar disc herniation 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 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 36 of 40 centers performing lumbar spine surgery in Norway report to NORspine. Coverage is approximately 90%. The completeness is approximately 65%.

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. In total 17 of 19 centers performing lumbar spine surgery in Denmark report to DaneSpine. Coverage is approximately 90%. The completeness is approximately 60%.

Quality assurance

As for all studies, there is a risk that 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. Preliminary data indicates that predictors of outcome after lumbar disc herniation surgery are comparable with data in a study with a very high follow-up rate and with the Swespine register.

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 discectomy only.

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, numeric rating scale leg pain, numeric rating scale back pain, 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 (ANCOVA), Chi-square or logistic regression tests will be used and the crude (unadjusted) data will be presented.

The baseline variables will be used as covariates in the ANCOVA and the adjusted data presented. Additionally, the results from the ANCOVA will be compared with results from propensity score matching or ANCOVA with the propensity score as a covariate.

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.

Study Type

Observational

Enrollment (Actual)

7500

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

This is an observational register based study, with prospective data registration and with a retrospective study design. Individuals treated surgically for lumbar disc herniation in Denmark, Norway and Sweden during 2011, 2012 and 2013 are included.

Description

Inclusion Criteria:

  • Patients treated with surgery for lumbar disc herniation in Denmark, Sweden or Norway and registered in a national quality register.

Exclusion Criteria:

  • Patients not treated with discectomy for the lumbar disc herniation.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Disc hernia patients treated in Sweden
Individuals undergoing lumbar disc hernia surgery and included in the Swespine register
Other Names:
  • Surgery for sciatica due to lumbar disc herniation
Disc hernia patients treated in Norway
Individuals undergoing lumbar disc hernia surgery and included in the NORspine register
Other Names:
  • Surgery for sciatica due to lumbar disc herniation
Disc hernia patients treated in Denmark
Individuals undergoing lumbar disc hernia surgery and included in the Danespine register
Other Names:
  • Surgery for sciatica due to lumbar disc herniation

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Oswestry disability index
Time Frame: preoperative and 1 year postoperative

Index at baseline, index change from preoperative to 1 year follow-up and actual index at 1 year follow-up.

Oswestry disability index version 2.1 (from 0; no disability to 100; maximum disability)

preoperative and 1 year postoperative

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Numerical rating scale for leg pain
Time Frame: preoperative and 1 year postoperative

Index at baseline, index change from preoperative to 1 year follow-up and actual index at 1 year follow-up.

Numerical rating scale for leg pain (from 0; no pain to 10; maximum pain). The numerical rating scale is used in Norway. The visual analogue scale (0-100) used in Sweden and Denmark will be converted to the numerical rating scale.

preoperative and 1 year postoperative
Numerical rating scale for back pain
Time Frame: preoperative and 1 year postoperative

Index at baseline, index change from preoperative to 1 year follow-up and actual index at 1 year follow-up.

Numerical rating scale for back pain (from 0; no pain to 10; maximum pain). The numerical rating scale is used in Norway. The visual analogue scale (0-100) used in Sweden and Denmark will be converted to the numerical rating scale.

preoperative and 1 year postoperative
EQ-5D
Time Frame: preoperative and 1 year postoperative

EQ-5D is a 5-item questionnaire measuring mobility, self-care, usual activities, pain/discomfort and anxiety/depression. The answers are translated to an index representing the societal perspective of health. Index at baseline, change from preoperative to 1 year follow-up and actual index at 1 year follow-up will be presented.

The EQ-5D-index is constructed using the British tariff (UK-TTO; from -0.59; worst possible health to 1; perfect health).

preoperative and 1 year postoperative
Return to work rate
Time Frame: Preoperative work rate. Work rate at the 1 year follow-up.
The participants are asked to what extent they work preoperatively and at the 1 year follow-up.
Preoperative work rate. Work rate at the 1 year follow-up.
Additional surgery in the same segment of the lumbar spine
Time Frame: During the 1 year follow-up
During the 1 year follow-up

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Paul Gerdhem, MD, PhD, Karolinska University Hospital and Karolinska Institutet, K54, Huddinge, SE-141 86 Stockholm, Sweden

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

January 1, 2011

Primary Completion (Actual)

December 1, 2013

Study Completion (Actual)

June 1, 2015

Study Registration Dates

First Submitted

August 18, 2016

First Submitted That Met QC Criteria

August 30, 2016

First Posted (Estimate)

September 5, 2016

Study Record Updates

Last Update Posted (Actual)

December 5, 2017

Last Update Submitted That Met QC Criteria

December 2, 2017

Last Verified

August 1, 2016

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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