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  • Oral presentation
  • Open Access

The use of the SpineCor Dynamic Corrective Brace in Greece: a preliminary report

  • 1,
  • 2,
  • 2,
  • 3 and
  • 4
Scoliosis20094 (Suppl 1) :O35

  • Published:


  • Public Health
  • Observational Study
  • Successful Treatment
  • Research Society
  • Preliminary Report


The purpose of this observational study was to quantify the efficacy of the SpineCor Dynamic Corrective Brace for patients who were still actively being treated in Greece. It also, evaluated the effectiveness of the Brace for adolescent idiopathic scoliosis in accordance with the new standardized criteria proposed by the Scoliosis Research Society (SRS) [1].


From 2003–2007, 109 patients were treated. 82 patients met the inclusion criteria proposed by the SpineCorporation [2]. 26 patients met the criteria for inclusion proposed by the SRS [1]. There were no patients with an outcome. Assessment of the brace effectiveness included (1) percentage of patients who had an initial Cobb angle reduction of 5° or greater; (2) percentage of patients who had an initial Cobb angle increase or decrease of less than 5° (3) percentage of patients who had an initial Cobb increase of 5° or greater and (4) the number of cases progressing to require surgery or undergone surgery.


Successful treatment (correction >5°, or stabilization +/- 5°) was achieved in 79 of the 82 patients and 25 of the 26 patients studied from the time of fitting of the Brace to the point which last Cobb angle was measured. This meant 96% correction/stabilization. Two out of 82 patients (2,4%) had curve progression and 1 patient (1,2%) underwent surgery. 1 patient out of 26 (3,8%) had a curve progression and has been recommended surgery.


The SpineCor Brace is an effective for the treatment of adolescent idiopathic scoliosis.

Authors’ Affiliations

Osteopath, Private Practice and Biomagnetic Ltd, Greece
Private Company, Greece
Asclepios Centre, Private Practice, Greece
Central Clinic of Athens, Private Clinic, Greece


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© Tsakiri et al; licensee BioMed Central Ltd. 2009

This article is published under license to BioMed Central Ltd.