Neuropediatrics 2011; 42(1): 18-23
DOI: 10.1055/s-0031-1275344
Original Article

© Georg Thieme Verlag KG Stuttgart · New York

Hip Lateralisation in Children with Bilateral Spastic Cerebral Palsy Treated with Botulinum Toxin Type A: A 2-Year Follow-Up

N. H. Jung1 , F. Heinen2 , B. Westhoff3 , L. Doederlein4 , A. Reissig5 , S. Berweck6 , M. Linder-Lucht1 , S. Schandelmaier1 , V. Mall1  on on behalf of the German Abo study group (For author list see Appendix) 
  • 1Division of Neuropediatrics and Muscular Disorders, Department of Pediatrics and Adolescent Medicine, University Hospital Freiburg, Freiburg, Germany
  • 2Department of Pediatric Neurology and Developmental Neurology, Dr. von Hauner's Children's Hospital, University of Munich, Munich, Germany
  • 3Department of Orthopedics, Heinrich-Heine-University, Düsseldorf, Germany
  • 4Orthopaedic Treatment Center Aschau, Aschau im Chiemgau, Germany
  • 5IPSEN Pharma GmbH, Ettlingen, Germany
  • 6Specialist Centre for Pediatric Neurology and Epilepsy for Children and Adolescents, Treatment Center Vogtareuth, Vogtareuth, Germany
Further Information

Publication History

received 5.08.2010

accepted 10.03.2011

Publication Date:
15 April 2011 (online)

Abstract

We investigated the effect of BoNT/A injection on hip lateralisation in children with bilateral spastic cerebral palsy and bilateral adductor spasticity. Pelvic radiographs using Reimers’ migration index (MI) were evaluated from 27 children (n=9 females, n=18 males; mean age 5.2±1.96 years; range: 2–10 years; initial MI <50%) with bilateral spastic cerebral palsy over a time period of 2 years. All received injections of BoNT/A (Dysport®) every 12 weeks with a dose of 30 Units per kilogram body weight into adductor and medial hamstring muscles on both sides. The MI was calculated before treatment and after 1 and 2 years. The mean MI increased from 25.5% (range: 0–48) to 26.7% (+1.2%, range: 0–79) on the right side and from 28.0% (range: 0–40) to 30.6% (+2.6%, range: 3–84) on the left side over 2 years, respectively. Hips of one patient dislocated bilaterally. The mean MI remained stable over 2 years. Although a specific BoNT/A effect cannot be proven because of the open design of this study, we provide strong evidence that the MI can be kept stable for a time period of 2 years under non-surgical management including therapy with BoNT/A even in CP patients with a high risk for hip dislocation.

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Appendix

German Abo study group: Bad Kreuznach (Dr. G. Romberg), Beelitz (Prof. Dr. J. Wissel), Braunschweig (Dr. U. Frank), Datteln (Dr. B. Dietz), Duisburg (Dr. J. Buckard), Göttingen (Dr. K. Brockmann), Halle (Dr. C. Fritzsch), Hannover (Dr. W. Voss), Heidelberg (Dr. N. Breitbach-Faller), Hochried Murnau (Dr. E. Waldeck), Innsbruck (Dr. Müller), Karlsruhe (Dr. M. Schaechtele), Konstanz (Dr. W. Kratzer), Kreischa (Dr. W. Deppe), Landstuhl (Dr. B. Stein-Bayet), Maulbronn (Dr. G. Nass), Neunkirchen (Dr. E. Feldmann), Oldenburg (Dr. M. Wagner), Rostock (Dr. B. C. Westphal), Schwerin (Dr. D. R. Boettcher), Würzburg (Dr. M. Haeussler).

Correspondence

Prof. Dr. Volker Mall

Division of Neuropediatrics and

Muscular Disorders

Department of Pediatrics and

Adolescent Medicine

University Hospital Freiburg

Mathildenstraße 1

79106 Freiburg

Germany

Phone: +49/761/270 4301

Fax: +49/761/270 4450

Email: volker.mall@uniklinik-freiburg.de

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