Functional independence of one- to four-year-old children with myelomeningocele

Authors

  • Fabiane Ramos Ferreira Universidade Ibirapuera. SP. Brasil
  • Fernanda Pinheiro Bexiga Universidade Santa Cecília
  • Vivian Vargas de Moraes Martins Universidade Santa Cecília
  • Francis Meire Favero Universidade Ibirapuera
  • Cristina Dallemole Sartor Universidade Ibirapuera
  • Mariana Cunha Artilheiro Universidade Ibirapuera
  • Mariana Callil Voos Universidade Ibirapuera

DOI:

https://doi.org/10.1590/1809-2950/17006325022018

Keywords:

Myelomeningocele, Neural Tube Defects, Spinal Dysraphism, Disability Evaluation, Physical Therapy Modalities, Rehabilitation.

Abstract

Myelomeningocele is caused by neural tube closure defects and represents the second cause of locomotion disability in children. Functional independence depends on level of spine injury and assessment is important to determine proper therapeutic approaches. We aimed to describe functional Independence and level of injury in 15 children, aged one to four years and with complete spinal cord injury caused by myelomeningocele. This is an observational transversal study developed in the Ibirapuera University and Santa Cecília University. The Pediatric Evaluation of Disability Inventory (PEDI) was used to ask parents about the functional independence of children in daily life activities. The International Standards for Neurological Classification of Spinal Cord Injury of the American Spinal Injury Association was used to determine the motor and sensory levels. Nine girls and six boys were assessed (27.0 ±11.8 months of age). Three children showed thoracic level, nine showed high lumbar level, two were classified as low lumbar, and one as sacral level. PEDI scores varied from 15 to 60% on the self-care area, from 10 to 15% on mobility, and from 19 to 58% on social function. High variability was observed on the functional independence of children with myelomeningocele, detected by self-care and social function areas of PEDI. Mobility was the most affected domain.

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References

Zambelli H, Carelli E, Honorato D, et al. Assessment of

neurosurgical outcome in children prenatally diagnosed

with myelomeningocele and development of a protocol for

fetal surgery to prevent hydrocephalus. Childs Nerv Syst.

;23:421-5. doi: 10.1007/s00381-006-0261-x

Rocco FM, Saito ET, Fernandes AC. Acompanhamento

da locomoção de pacientes com mielomeningocele da

Associação de Assistência à Criança Deficiente (AACD) em

São Paulo, Brasil. Acta Fisiatr. 2007;14(3):126-9.

Tsai PY, Yang TF, Chan RC, Huang PH, Wong TT. Functional

investigation in children with spina bifida, measured by the

Pediatric Evaluation of Disability Inventory (PEDI). Childs

Nerv Syst. 2002;18:48-53. doi: 10.1007/s00381-001-0531-6

Norrlin S, Strinnholm M, Carlsson M, Dahl M. Factors of

significance for mobility in children with myelomeningocele.

Acta Paediatr. 2003;92:204-10. doi: 10.1111/j.1651-2227.2003.

tb00527.x

Danielsson AJ, Bartonek A, Levey E, McHale K, Sponseller

P, Saraste H. Associations between orthopaedic findings,

ambulation and health-related quality of life in children

with myelomeningocele. J Child Orthop. 2008;2:45-54. doi:

1007/s11832-007-0069-6

Warf BC. Hydrocephalus associated with neural tube defects:

characteristics, management, and outcome in sub-Saharan

Africa. Childs Nerv Syst. 2011;27:1589-94. doi: 10.1007/

s00381-011-1484-z

Schoenmakers MA, Uiterwaal CS, Gulmans VA, Gooskens

RH, Helders PJ. Determinants of functional independence

and quality of life in children with spina bifida. Clin Rehabil.

;19:677-85. doi: 10.1191/0269215505cr865oa

Roebroeck ME, Hempenius L, van Baalen B, Hendriksen JG,

van den Berg-Emons HJ, Stam HJ. Cognitive functioning

of adolescents and young adults with meningomyelocele

and level of everyday physical activity. Disabil Rehabil.

;28:1237-42. doi: abs/10.1080/09638280600551716

Hetherington R, Dennis M, Barnes M, Drake J, Gentili F.

Functional outcome in young adults with spina bifida and

hydrocephalus. Childs Nerv Syst. 2006;22:117-24. doi: 10.1007/

s00381-005-1231-4

Verhoef M, Barf HA, Post MW, van Asbeck FW, Gooskens

RH, Prevo AJ. Functional independence among young adults

with spina bifida, in relation to hydrocephalus and level of

lesion. Dev Med Child Neurol. 2006;48:114-9. doi: 10.1017/

S0012162206000259

Bartonek A, Saraste H, Danielsson A. Health-related quality

of life and ambulation in children with myelomeningocele

in a Swedish population. Acta Paediatr. 2012;101:953-6. doi:

1111/j.1651-2227.2012.02742.x

Sirzai H, Doqu B, Demir S, Yilmaz F, Kuran B. Assessment

on self-care, mobility and social function in children with

spina bifida in Turkey. Neural Regen Res 2014;15:1234-40. doi:

4103/1673-5374.135332

Mancini CM, Silva PC, Gonçalves SC, Martins MS. Comparação

do desempenho funcional de crianças portadoras de

síndrome de Down e crianças com desenvolvimento

normal aos 2 e 5 anos de idade. Arq Neuropsiquiatr. 2003;

(2-B):409-15. doi: 10.1590/S0004-282X2003000300016

Lundberg C. Validade e confiabilidade do questionário

de qualidade de vida de pessoas com espinha bífida

[dissertação]. São Paulo: Faculdade de Medicina da

Universidade de São Paulo; 2011.

Betz RR, Chafetz RS, Vogel LC, Samdani AF, Mulcahey MJ.

Description of sensory preservation in children and adolescents

with incomplete spinal cord injury. J Spinal Cord Med.

;34(3):297-300. doi: 10.1179/2045772311Y.0000000009

Brandão DA, Fujiwasa SD, Cardoso RJ. Características

de crianças com mielomeningocele: implicações para a

fisioterapia. Fisioter Mov. 2009;22:69-75.

Collange AL, Franco CR, Esteves NR, Collange ZN. Desempenho

funcional de crianças com mielomeningocele. Fisioter Pesqui.

;15:58-63. doi: 10.1590/S1809-29502008000100010

Medeiros MRD, Teixeira LL, Saraiva OL, Costa CSD, Nascimento

CGL. Plano terapêutico multidisciplinar para crianças com

mielomeningocele em um Hospital Universitário no Interior

do Rio Grande do Norte. Rev Bras de Ciênc Saúde. 2011;15-

:219-22. doi: 10.4034/RBCS.2011.15.02.13

Ramos FS, Macedo LK, Scarlato A, Herrera G. Fatores que

influenciam o prognóstico deambulatório nos diferentes

níveis de lesão da mielomeningocele. Rev Neurociênc.

(13):80-6.

Bartonek A. Motor development toward ambulation in

preschool children with myelomeningocele--a prospective

study. Ped Phys Ther. 2010;22:52-60. doi: 10.1097/

PEP.0b013e3181cc132b

Seitzber A, Lind M, Biering-Sorensen F. Ambulation in adults

with myelomeningocele. Is it possible to predict the level of

ambulation in early life? Child Nerv Syst. 2008;(24):231-7. doi:

1007/s00381-007-0450-2

Aizawa CY, Morales MP, Lundberg C, Soares de Moura MCD,

Pinto FCG, Voos MC, et al. Conventional physical therapy and

physical therapy based on reflex stimulation showed similar

results in children with myelomeningocele. Arq NeuroPsiquiatr. 2017;5(3):160-6. doi: 10.1590/0004-282x20170009

Luz CL, Soares de Moura MCD, Becker KK, Teixeira RAA,

Voos MC, Hasue RH. The relationship between motor

function, cognition, independence and quality of life

in myelomeningocele patients. Arq Neuro-Psiquiatr.

;75(8):509-14. doi: 10.1590/0004282x2017008

Published

2018-07-07

Issue

Section

Original Research

How to Cite

Functional independence of one- to four-year-old children with myelomeningocele. (2018). Fisioterapia E Pesquisa, 25(2), 196-201. https://doi.org/10.1590/1809-2950/17006325022018