Literature DB >> 16557146

Effects of intramuscular psoas lengthening on pelvic and hip motion in patients with spastic diparetic cerebral palsy.

Mauro C Morais Filho1, Wagner de Godoy, Carlos A Santos.   

Abstract

The effects of intramuscular psoas lengthening on gait in cerebral palsy patients have been the subject of debates, and the indications for such procedure are still controversial. The purpose of this study was to evaluate the effects of intramuscular psoas lengthening on sagittal plane pelvic and hip motion in patients with spastic diparetic cerebral palsy and identify the factors linked to the best possible outcome. A retrospective study was performed in 26 independent ambulatory patients. All of them had undergone an intramuscular psoas lengthening over the pelvic brim. The mean age at the time of surgery was 11.10 years, and most cases went through additional simultaneous procedures. A complete gait analysis was performed before and, on average, at 17.69 months (range, 6-39 months) after surgery. The Thomas test values, maximum hip extension in stance, and pelvic tilt were analyzed before and after surgical intervention, and the results were statistically compared. The most significant postoperative effect was the reduction of pelvic range of motion (P < 0.01). Reduction of anterior pelvic tilt was observed only in those patients with no previous need of an external aid (P < 0.01), and the studied group did not show a significant improvement of hip extension at terminal stance. According to the results, intramuscular psoas lengthening was useful in reducing pelvic range of motion at the sagittal plane, but this study also suggests that pelvic and hip disruptions of the same plane (sagittal) seem to have a multifactorial etiology. The use of external assistive devices in patients with balance problems may lead to increased anterior pelvic tilt as well as reduction of hip extension at terminal stance.

Entities:  

Mesh:

Year:  2006        PMID: 16557146     DOI: 10.1097/01.bpo.0000194700.06398.a2

Source DB:  PubMed          Journal:  J Pediatr Orthop        ISSN: 0271-6798            Impact factor:   2.324


  6 in total

1.  No detectable major changes in gait analysis after soft tissue release in DDH.

Authors:  Hakan Omeroğlu; Güneş Yavuzer; Ali Biçimoğlu; Haluk Ağuş; Yücel Tümer
Journal:  Clin Orthop Relat Res       Date:  2008-03-12       Impact factor: 4.176

2.  Treatment of fixed knee flexion deformity and crouch gait using distal femur extension osteotomy in cerebral palsy.

Authors:  Mauro C de Morais Filho; Daniella Lins Neves; Fábio Peluzo Abreu; Yara Juliano; Leandro Guimarães
Journal:  J Child Orthop       Date:  2008-01-03       Impact factor: 1.548

3.  Treatment of Hip Flexion Contractures with Psoas Recession Through the Middle Window of the Ilioinguinal Approach.

Authors:  Daniel J Gittings; Jonathan R Dattilo; George Fryhofer; Derek J Donegan; Keith Baldwin
Journal:  JBJS Essent Surg Tech       Date:  2017-08-23

4.  Validity of gait parameters for hip flexor contracture in patients with cerebral palsy.

Authors:  Sun Jong Choi; Chin Youb Chung; Kyoung Min Lee; Dae Gyu Kwon; Sang Hyeong Lee; Moon Soek Park
Journal:  J Neuroeng Rehabil       Date:  2011-01-23       Impact factor: 4.262

5.  Outcome of medial hamstring lengthening in children with spastic paresis: A biomechanical and morphological observational study.

Authors:  Helga Haberfehlner; Richard T Jaspers; Erich Rutz; Jaap Harlaar; Johannes A van der Sluijs; Melinda M Witbreuk; Kim van Hutten; Jacqueline Romkes; Marie Freslier; Reinald Brunner; Jules G Becher; Huub Maas; Annemieke I Buizer
Journal:  PLoS One       Date:  2018-02-06       Impact factor: 3.240

6.  DOES RECTUS FEMORIS TRANSFER INCREASE KNEE FLEXION DURING STANCE PHASE IN CEREBRAL PALSY?

Authors:  Mauro César de Morais; Francesco Camara Blumetti; Cátia Miyuki Kawamura; José Augusto Fernandes Lopes; Daniella Lins Neves; Michelle de Oliveira Cardoso
Journal:  Acta Ortop Bras       Date:  2016 Jan-Feb       Impact factor: 0.513

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.