Literature DB >> 10641695

Charcot arthropathy in spina bifida.

D G Nagarkatti1, J V Banta, J D Thomson.   

Abstract

This multicenter study was undertaken to identify the prevalence of Charcot arthropathy in the spina bifida population; to evaluate the relationship of neurosegmental level, ambulatory level, and distribution of joint involvement; and to assess treatment results and make treatment recommendations. Sixteen patients were identified with Charcot arthropathy based on clinical and radiographic criteria ranging in age from 9 to 42 years. There were 15 ankles, seven knees, and four hips identified with Charcot arthropathy. Six patients underwent surgery and modification of orthoses, eight had a modification of orthoses only, one had no modification, and one was lost to follow-up. Mean follow-up was 4 years and 9 months (with four good, 17 fair, and five poor results). The best results were seen in 13 compliant patients with a brace modification, whereas poor results were seen in three patients with poor brace compliance. Based on our study, we have noted the prevalence of Charcot arthropathy in spina bifida to be one in 100 cases.

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Year:  2000        PMID: 10641695

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


  2 in total

1.  Charcot's arthropathy secondary to herpetic encephalitis sequelae: an unusual presentation.

Authors:  Samuel Katsuyuki Shinjo; Jozélio Freire de Carvalho
Journal:  Rheumatol Int       Date:  2009-06-18       Impact factor: 2.631

Review 2.  Myelomeningocele: neglected aspects.

Authors:  Christopher R J Woodhouse
Journal:  Pediatr Nephrol       Date:  2008-01-17       Impact factor: 3.714

  2 in total

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