Multicenter Retrospective Evaluation of the Surgical Management of Spinal Growth Dystrophy (DRC)

Spinal growth dystrophy (CRD), also called Scheuermann's disease, corresponding to impaired vertebral structure occurring in children and adolescents with involvement of the growth cartilage causing impaired growth and kyphosis.

There are forms thoracolumbar and thoracic conventional forms of DRC with variable clinical expressions; the most important being kyphosis with spinal stiffness associated with painful elements.

The radiographic definition according Sorenson is uniformisation 5 ° affecting at least three adjacent vertebrae.

Scheuermann's disease and three problems. First, the thoracic kyphosis generates back pain which may be thoracic or lumbar indirectly attributed to compensatory lordosis. Moreover disruption sagittal balance frequently causes a significant aesthetic discomfort. Finally, scalability because the curvature may increase the likelihood of degenerative lesions disc degeneration or lumbar spinal stenosis for example.

When the disease is diagnosed early, treatment is most often associated with orthopedic physiotherapy. However, for patients with active deformation, despite an orthopedic brace treatment with chronic pain, neurological deficit or for aesthetic reasons, surgical decision can be taken.

The goal of surgical treatment of DRC is a correction of the thoracic kyphosis. It goes through a spinal fusion must be released from his column stiffness in a bad position, changing the equilibrium profile and ensure that it remains in a good position.

This surgery usually requires a prior operative time (thoracic surgery to remove the intervertebral discs) and a posterior surgical time (blockage of the vertebrae together with a bone graft and osteosynthesis). Currently different surgical strategies are practiced there is no real consensus between the teams.

Study Overview

• Status: Completed
• Conditions: Hip Replacement; Acetabular Fractures
• Intervention / Treatment: Other: No intervention. Observational and descriptive study

Detailed Description

objectives:

1. Evaluation of the rate and type of complications in different age categories and surgical strategies.
2. Evaluation of clinical results based on surgical strategies.
3. Evaluation of sagittal balance and correction obtained based surgical strategies

Methodology and duration of the research

This is a multicenter retrospective cohort on the assessment of surgical practices cited objectives. Also, this research is in Chapter X of the Data Protection Act and allows the collection of personal data for the purpose of evaluation of care and prevention practices with authorization request to the CNIL; the opinion of CCTIRS therefore not required in this case.

This study concerns the data of patients operated with the techniques mentioned in addition with a decline of more than 20 years.

Patients are aware of the potential use of their data in their files for medical research through oral information provided by the doctor at the signing by the patient's consent related to the surgery and most recently contained in the Home booklet setting for patients.

Nature of the data collected

The data is anonymous and not identifiable (for each subject a number of inclusion is given). The name of the surgeon is also anonymized.

The data collected concern the characteristics of the patient, as well as its history, the operating data including technical, suites and possible post-operative complications and patient monitoring.

Data collection will be done on the basis KEOPS https://www.keops-spine.fr

• Study Type: Observational
• Enrollment (Actual): 16

Contacts and Locations

Study Locations

• France
  • Ile-de-France
    • Paris, Ile-de-France, France, 75014
      • Groupe hospitalier Paris saint Joseph

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 10 years and older (Child, Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

• Sampling Method: Non-Probability Sample

Study Population

Patients operated on for an arthrodesis Dystrophy Spinal Growth (DRC)

Description

Inclusion Criteria:

• patients operated on for an arthrodesis Dystrophy Spinal Growth (DRC)
• Age> 10 years
• monitoring of minimum one year

Exclusion Criteria:

• deformation in the frontal plane
• kyphosis malformation
• osteoporotic or degenerative kyphosis
• post laminectomy kyphosis
• constitutional bone disease
• connective Tissue Disease
• myopathy

Study Plan

How is the study designed?

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Surgery complication type	Statement from the database keops	Day 30

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Assessment od the clinical results based on surgical strategies	Evaluation of clinical results based on surgical strategies. Statement from the database keops : Worse,; Acceptable,; Good	Day 30
Assessment of sagittal balance and correction Score obtained	Evaluation of sagittal balance score obtained based surgical strategies. Statement from the database keops: Worse,; Acceptable,; Good	Day 30
Assessment of correction Score obtained	Evaluation of sagittal correction score obtained based surgical strategies. Statement from the database keops: Worse,; Acceptable,; Good	Day 30

Collaborators and Investigators

• Sponsor: Groupe Hospitalier Paris Saint Joseph

Study record dates

Study Major Dates

• Study Start (Actual): December 1, 2014
• Primary Completion (Actual): January 30, 2015
• Study Completion (Actual): April 15, 2016

Study Registration Dates

• First Submitted: August 31, 2016
• First Submitted That Met QC Criteria: September 13, 2016
• First Posted (Estimate): September 19, 2016

Study Record Updates

• Last Update Posted (Actual): September 6, 2017
• Last Update Submitted That Met QC Criteria: September 4, 2017
• Last Verified: September 1, 2017

More Information

Terms related to this study

• Other Study ID Numbers: DRC

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: UNDECIDED