| Literature DB >> 27928445 |
T Nedelcu1, I Georgescu2, J Leroux3, J Lechevallier3, A Barbilian4, I Tuhar5.
Abstract
The article represents a retrospective clinical and radiological study. Objective. To assess the safety and the stability in time of the Unit Rod instrumentation in the treatment of severe neuromuscular scoliosis in children and adolescents. Summary. The treatment of patients with neuromuscular scoliosis always represents a challenge. The patients are debilitated and usual interventions are very long with great loss of blood. Serious complications can compromise the result of the surgery. The technique we used (the Unit Rod) is worldwide recognized, is simple, and gives excellent stability with a low rate of complications. Methods. We conducted a clinical and radiological retrospective study with a follow-up of at least 4 years in 58 patients with serious neuromuscular conditions, most of them being non-walkers. They were surgically treated by using mostly the Unit Rod technique, in the department of Paediatric Orthopaedics of the Rouen University Hospital, France, between 2000 and 2008. The back fusion was generally from T2 to pelvis. We used the Galveston technique for the patients who needed a pelvic fixation. Results. The mean Cobb angle correction was of 67% immediately after surgery; the correction of the curve decreased in time only in 4% of the cases. Pelvic obliquity was also very well corrected: 73% immediately and 70% at the last radiological follow-up. The mean operative time was of 175 minutes compared to 269 minutes for screws and hooks instrumentation. The most common complication for our technique was the radiolucent halo that appeared around the pelvic inserts. There was no significant degradation in time of the correction obtained. Conclusions. The use of this technique is safe, gives excellent results, achieving significant improvements in the postoperative functional status of the patients. The intra- and postoperative complications were minor. The advantage of using this method is the low cost of the material and technical simplicity, the corrective results being the same as the ones obtained with other techniques.Entities:
Keywords: Unit Rod; cerebral palsy; neuro-muscular scoliosis; sublaminar wires; vertebral arthrodesis
Mesh:
Year: 2016 PMID: 27928445 PMCID: PMC5141401
Source DB: PubMed Journal: J Med Life ISSN: 1844-122X
Incidence of scoliosis depending on aetiology
| Pathology | Incidence |
|---|---|
| Cerebral Palsy | |
| GMFCS I and II (ambulatory) | 25% |
| GMFCS III and IV (non-ambulatory) | 80-90% |
| Neuropathies (Charcot-Marie-Tooth) | 30% |
| Lumbar syringomyelia | 60% |
| Thoracic syringomyelia | 100% |
| Spinal muscular atrophy | 70% |
| Friedreich’s ataxia | 80% |
| Duchenne muscular dystrophy | 90% |
| Spinal cord injuries | 100% |
Patients’ aetiology and demographics
| Name | Sex | Birthdate | Disease | Walker/ Non-walker W/ NW | Year of the intervention | Age at the operation (years, months) | Follow-up (Years) |
|---|---|---|---|---|---|---|---|
| A.N. | M | 10/06/1985 | Friedreich ’s Ataxia | W | 2002 | 17+2 | 6 |
| A.E. | M | 25/12/1985 | Cerebral Palsy | NW | 2000 | 14+10 | 8 |
| A.E. | F | 29/07/1996 | RETT's Syndrome | NW | 2007 | 11+6 | 8 |
| A.G. | M | 09/09.1987 | Traumatic spinal cord injury | NW | 2000 | 13+2 | 11 |
| A.M. | M | 13/07/1992 | Metabolic disease: Juvenile Ceroid lipofuscinosis | NW | 2006 | 14+1 | 4 |
| A.M/ | F | 19/01/1994 | Spinal muscular atrophy type II | NW | 2006 | 12+6 | 5 |
| B.T. | M | 20/08/1992 | Cerebral Palsy | NW | 2006 | 15+10 | 4 |
| B.S. | F | 01/09/1992 | Arthrogryposis | W | 2005 | 13+0 | 7 |
| B.M. | M | 14/02/1990 | Cerebral Palsy | NW | 2006 | 15+9 | 5 |
| B.J. | M | 28/08/1989 | Duchenne muscular dystrophy | NW | 2004 | 15+0 | 10 |
| B.V. | M | 15/11/1994 | Duchenne muscular dystrophy | NW | 2008 | 13+4 | 5 |
| B.O. | M | 27/11/1980 | Cerebral Palsy | W | 2006 | 26+1 | 6 |
| B.I. | F | 03/11/1984 | Congenital myopathy (merozyne deficit) | NW | 2005 | 10+5 | 9 |
| B.M. | F | 17/07/1989 | Cerebral Palsy | NW | 2004 | 15+6 | 4 |
| B.B. | M | 23/05/1992 | Duchenne muscular dystrophy | NW | 2004 | 11+11 | 5 |
| C.J. | F | 14/01/1984 | Unknown genetic syndrome | NW | 2004 | 20+0 | 4 |
| D.T. | M | 02/01/1987 | Cerebral Palsy | NW | 2003 | 16+8 | 4 |
| D.E. | F | 30/04/1991 | Unknown genetic syndrome | W | 2003 | 12+1 | 5 |
| D.P. | M | 19/10/1987 | Cerebral Palsy | NW | 2004 | 16+8 | 4 |
| D.V. | M | 13/10/1987 | Alcoholic fetopathy | W | 2001 | 13+10 | 9 |
| D.Q. | M | 06/10/1993 | Duchenne muscular dystrophy | NW | 2005 | 11+7 | 8 |
| D.H. | M | 16/06/1992 | Unknown genetic syndrome | NW | 2008 | 15+8 | 6 |
| D.E. | F | 22/04/1985 | Arthrogryposis | NW | 2000 | 15+2 | 11 |
| D.C. | F | 03/02/1987 | Cerebral Palsy | NW | 2002 | 14+0 | 5 |
| F.A. | M | 13/05/1993 | Cerebral Palsy | NW | 2006 | 13+4 | 8 |
| F.G. | M | 16/10/1991 | Duchenne muscular dystrophy | NW | 2006 | 15+0 | 8 |
| F.R. | M | 02/08/1988 | Duchenne muscular dystrophy | NW | 2002 | 13+4 | 6 |
| G.N. | M | 22/10/1990 | Duchenne muscular dystrophy | NW | 2002 | 11+7 | 4 |
| G.P. | F | 20/08/1987 | Cerebral Palsy | NW | 2006 | 18+10 | 4 |
| H.A. | M | 05/08/1984 | Cerebral Palsy | NW | 2004 | 20+1 | 4 |
| H.B. | M | 20/04/1990 | Duchenne muscular dystrophy | NW | 2003 | 12+10 | 5 |
| H.J. | M | 26/12/1988 | Cerebral Palsy | NW | 2004 | 15+6 | 6 |
| H.K. | F | 30/07/1985 | Cerebral Palsy | NW | 2006 | 20+10 | 7 |
| I.A. | F | 09/07/1993 | Congenital Nemalin myopathy | NW | 2005 | 12+6 | 9 |
| K.H. | M | 10/12/1985 | Cerebral Palsy | NW | 2000 | 15+0 | 7 |
| L.C. | F | 16/05/1986 | Cerebral Palsy | NW | 2001 | 15+3 | 5 |
| L.L. | M | 04/06/1997 | Duchenne muscular dystrophy | NW | 2008 | 11+2 | 6 |
| L.A. | M | 11/07/1986 | Cerebral Palsy | W | 2000 | 14+0 | 4 |
| L.K. | M | 17/06/1988 | Arthrogryposis | NW | 2004 | 16+5 | 4 |
| L.F. | M | 02/09/1984 | Cerebral Palsy | NW | 2001 | 16+2 | 4 |
| L.J. | M | 13/07/1993 | Duchenne muscular dystrophy | NW | 2006 | 12+10 | 7 |
| L.K. | F | 19/12/1985 | Cerebral Palsy | NW | 2001 | 15+11 | 13 |
| M.N. | M | 26/10/1980 | Cerebral Palsy | NW | 2002 | 21+1 | 8 |
| M.A. | M | 20/07/1992 | Duchenne muscular dystrophy | NW | 2003 | 11+3 | 9 |
| M.D. | M | 01/07/1989 | Syringomyelia type I | W | 2006 | 17+2 | 7 |
| M.N. | M | 19/11/1981 | Sensitive motor neuropathy (Charcot Marie Tooth) | W | 2001 | 20+1 | 10 |
| M.A. | F | 26/05/1984 | Cerebral palsy | NW | 2002 | 17+10 | 12 |
| M.F. | M | 15/06/1988 | Duchenne muscular dystrophy | NW | 2002 | 13+9 | 10 |
| N.M. | F | 28/11/1984 | Unknown genetic syndrome | NW | 2003 | 18+10 | 5 |
| O.D. | M | 29/02/1984 | Cerebral Palsy | NW | 2001 | 17+9 | 6 |
| P.D. | F | 19/05/1992 | Medullary tumor | NW | 2004 | 12+0 | 10 |
| Q.F. | M | 04/10/1992 | Cerebral Palsy | NW | 2008 | 15+1 | 6 |
| R.V. | M | 07/08/1989 | Duchenne muscular dystrophy | NW | 2002 | 15+9 | 7 |
| R.E. | F | 24/06/1991 | RETT's Syndrome | NW | 2003 | 11+7 | 8 |
| R.L. | F | 24/06/1991 | RETT's Syndrome | NW | 2004 | 12+10 | 7 |
| V.B. | M | 04/11/1989 | Sensitive motor neuropathy (Charcot Marie Tooth) | W | 2006 | 16+9 | 4 |
| V.D. | F | 09/07/1984 | RETT's Syndrome | NW | 2002 | 17+10 | 6 |
| W.T. | M | 10/10/1989 | Encephalitis | NW | 2004 | 15+1 | 10 |
Dynamic evaluation of radiological parameters
| Radiological parameters | Pre-operatively | Post operatively | |
|---|---|---|---|
| Immediate | > 4 years | ||
| Cobb angle (°) | 63 (20-122) | 20.8 (0-65) | 22.9 (0-70) |
| Pelvic obliquity (°) | 25.2 (0-53) | 4.3 (0-20) | 4.9 (0-21) |
Mean surgery time
| Unit Rod | Segmental CD* | ||
|---|---|---|---|
| Mean surgery time (minutes) | 175 (115-240) | AVP 269 (200-320) | AVA+AVP 340 (300-420) |
| *CD – Cotrel – Dubousset |