Impact of Bobath Based Rehabilitation Program and Conventional Physiotherapy: Children with Hydrocephalus

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Abstract

Introduction. Hydrocephalus is an abnormal enlargement of the brain ventricles caused by increased amounts of cerebrospinal fluid. The aim of the study was to determine the efficacy of Bobath Based Rehabilitation Program and conventional physiotherapy for improving motor function in children with hydrocephalus and reducing levels of anxiety in parents of children with hydrocephalus.

Materials and methods. The study design was quasi experimental in nature. Twenty patients with hydrocephalus, aged below 10 years, both males and females were included as per the eligibility criteria. All parents provided their written informed consent for participations in the study. These subjects were randomly divided into two equal groups using computer generated table: group A (n = 10) and group B (n = 10). All patients were assessed for motor function using GMFM-88 scale, whereas their parents were evaluated for anxiety levels using STAI tool. Group A received Bobath Based Rehabilitation Program whereas group B received conventional physiotherapy. Both groups received interventions for a total of 8 weeks, with 1 60-minute session per week and their parents were taught an individualized program of home exercises and encouraged to practice daily. Then the subjects were re-assessed after completing 8 weeks of interventions. Statistical analysis was performed using paired t-test and unpaired t-test.

Results. Our study revealed statistically significant difference in the GMFM-88, STAI-S and STAI-T scores in group A (p = 0.032, 0.0001, 0.0001) and group B (p = 0.0001, 0.001, 0.003), respectively.

Discussion. These two interventions have their benefits in improving gross motor function in children with hydrocephalus. These interventions can indeed be customized to address specific needs of children with hydrocephalus, such as muscle weakness, impaired coordination, and balance issues. This personalized approach optimizes the intervention effectiveness directly targeting the areas of difficulty experienced by each child. Moreover, these therapeutic approaches engage mechanisms of neuroplasticity through repetitive and task-specific exercises. Training general physiotherapists to deliver both therapies efficiently could maximize access to rehabilitation services in areas with inadequate healthcare infrastructure.

Conclusion. Bobath Based Rehabilitation Program and conventional physiotherapy are effective interventions for improving motor function in children with hydrocephalus and in reducing levels of anxiety in their parents.

About the authors

Tanpreet Kaur Bakshi

Baba Farid University of Health Sciences

Author for correspondence.
Email: tanpreetbakshi1010@gmail.com
ORCID iD: 0009-0002-1244-1252

student, University College of Physiotherapy

India, 151203, Faridkot, Punjab

Jaspreet Singh Vij

Baba Farid University of Health Sciences

Email: tanpreetbakshi1010@gmail.com
ORCID iD: 0009-0006-8445-4449

PhD (Med), Associate Professor, University College of Physiotherapy

India, 151203, Faridkot, Punjab

Ashish Chhabra

Guru Gobind Singh Medical College and Hospital

Email: tanpreetbakshi1010@gmail.com
ORCID iD: 0000-0002-0406-3389

MS (General Surgery), MCh (Peds Surgery), Associate Professor, (Peds Surgery)

India, Faridkot, Punjab

References

  1. Bondurant CP, Jimenez DF. Epidemiology of cerebrospinal fluid shunting. Pediatr Neurosurg. 1995;23(5):254–259. doi: 10.1159/000120968
  2. Hochstetler A, Raskin J, Blazer-Yost BL. Hydrocephalus: historical analysis and considerations for treatment. Eur J Med Res. 2022;27(1):168. doi: 10.1186/s40001-022-00798-6
  3. Munawaroh N, Nurhasanah L, Isma R. Case report of speech and ambulation ability after five years therapy in a six-year-old boy with habilitation sixth lumbar spina bifida with meningocele post resection and hydrocephalus post VP shunt. Indonesian Journal of Physical Medicine & Rehabilitation. 2022;11(01):13–23. doi: 10.36803/ijpmr.v11i01.324
  4. Singh R, Prasad RS, Singh RC. et al. Evaluation of pediatric hydrocephalus: clinical, surgical, and outcome perspective in a Tertiary Center. Asian J Neurosurg. 2021; 16(4):706–713. doi: 10.4103/ajns.AJNS_132_21
  5. Chi JH, Fullerton HJ, Gupta N. Time trends and demographics of deaths from congenital hydrocephalus in children in the United States: National Center for Health Statistics data, 1979 to 1998. J Neurosurg. 2005;103(2 Suppl):113–118. doi: 10.3171/ped.2005.103.2.0113
  6. Wiswell TE, Tuttle DJ, Northam RS, Simonds GR. Major congenital neurologic malformations: a 17-year survey. Am J Dis Child. 1990;144(1):61–67. doi: 10.1001/archpedi.1990.02150250071035
  7. Isaacs AM, Riva-Cambrin J, Yavin D, et al. Age-specific global epidemiology of hydrocephalus: systematic review, metanalysis and globalб birth surveillance. PloS One. 2018;13(10):e0204926. doi: 10.1371/journal.pone.0204926
  8. Dewan MC, Rattani A, Mekary R, et al. Global hydrocephalus epidemiology and incidence: systematic review and meta-analysis. J Neurosurg. 2018;130(4):1065–1079. doi: 10.3171/2017.10.JNS17439
  9. Jaiswal A, Jaiswal J. Incidence of hydrocephalus in pediatric age in a tertiary care centre of Chhattisgarh. Journal of Evolution of Medical and Dental Sciences. 2015;4(83):14564–14572. doi: 10.14260/jemds/2015/2070
  10. Khalatbari H, Parisi MT. Management of hydrocephalus in children: anatomic imaging appearances of CSF shunts and their complications. AJR Am J Roentgenol. 2021;216(1):187–199. doi: 10.2214/AJR.20.22888
  11. Kirkpatrick M, Engleman H., Minns RA. Symptoms and signs of progressive hydrocephalus. Arch Dis Child. 1989;64(1):124–128. doi: 10.1136/adc.64.1.124
  12. Wald NJ. Folic acid and the prevention of neural-tube defects. New England Journal of Medicine. 2004;350:101–103. doi: 10.1056/NEJMp038186
  13. Yu M, Peterson MR., Cherukri V, et al. Infection diagnosis in hydrocephalus CT images: a domain enriched attention learning approach. J Neural Eng. 2023;20(3):10.1088/1741-2552/acd9ee. doi: 10.1088/1741-2552/acd9ee
  14. Bawa M, Dash V, Mahalik S, Rao KL. Outcome analysis of patients of congenital hydrocephalus with ventriculoperitoneal shunt at a tertiary care hospital in North India. Pediatr Neurosurg. 2019;54(4):233–236. doi: 10.1159/000501018
  15. Walters S. Benefits of a group exercise program on a student with congenital hydrocephalus and multiple co-diagnoses (2013). PTHMS Undergraduate Publications. 2. URL: https://digitalcommons.sacredheart.edu/pthms_honors/2
  16. Kahle KT, Kulkarni AV, Limbrick DD, Warf BC. Hydrocephalus in children. Lancet. 2016;387(10020):788–799. doi: 10.1016/S0140-6736(15)60694-8
  17. Barnes K, Zimmerman K, Herbey I, et al. Understanding and identifying the needs of parent caregivers of children with hydrocephalus: a qualitative study. J Neurosurg Pediatr. 2023;31(5):433–443. doi: 10.3171/2022.12.PEDS22425
  18. Duzgun MV, Erdem Y. Factors affecting the anxiety level and quality of life of parents of children with hydrocephalus. International Journal of Caring Sciences. 2020;13(2):1382–1391.
  19. Russell DJ, Palisano RJ, Walter S, et al. Evaluating motor function in children with Down syndrome: validity of the GMFM. Dev Med Child Neurol. 1998;40(10):693–701. doi: 10.1111/j.1469-8749.1998.tb12330.x
  20. Adair B, Said CM, Rodda J, Morris ME. Psychometric properties of functional mobility tools in hereditary spastic paraplegia and other childhood neurological conditions. Dev Med Child Neurol. 2012;54(7):596–605. doi: 10.1111/j.1469-8749.2012.04284.x
  21. Wang HY, Yang YH, Jong YJ. Correlations between change scores of measures for muscle strength and motor function in individuals with spinal muscular atrophy types 2 and 3. Am J Phys Med Rehabil. 2013;92(4):335–342. doi: 10.1097/phm.0b013e318269d66b
  22. Russell DJ, Avery LM, Rosenbaum PL, et al. Improved scaling of the gross motor function measure for children with cerebral palsy: evidence of reliability and validity. Phys Ther. 2000;80(9):873–885.
  23. Lee KH, Park JW, Lee HJ, et al. Efficacy of intensive neurodevelopmental treatment for children with developmental delay, with or without cerebral palsy. Ann Rehabil Med. 2017;41(1):90–96. doi: 10.5535/arm.2017.41.1.90
  24. Veličković TD, Perat MV. Basic principles of the neurodevelopment treatment. Medicina. 2005; 41:112–120.
  25. Bertenthal B, Von Hofsten C. Eye, head and trunk control: the foundation for manual development. Neurosci Biobehav Rev. 1998;22(4):515–520. doi: 10.1016/s0149-7634(97)00038-9
  26. Assaiante C, Mallau S, Viel S, et al. Development of postural control in healthy children: a functional approach. Neural Plast. 2005;12(2-3):109–118. doi: 10.1155/NP.2005.109
  27. Sah AK, Balaji GK, Agrahara S. Effects of task-oriented activities based on neurodevelopmental therapy principles on trunk control, balance, and gross motor function in children with spastic diplegic cerebral palsy: a single-blinded randomized clinical trial. J Pediatr Neurosci. 2019;14(3):120–126. doi: 10.4103/jpn.JPN_35_19
  28. Mwiinga FB, Malekani N, Mwape M. Caregivers’ experiences in caring for children with hydrocephalus at the University Teaching Hospitals, Lusaka Zambia. Medical Journal of Zambia. 2024;50(4):347–354. doi: 10.55320/mjz.50.4.436
  29. El-Zraigat I, Al-Dhafairi F. Coping strategies with the psychological stress among parents of children with intellectual disabilities and slow learners in light of selected variables in the State of Kuwait. British Journal of Education, Society & Behavioural Science. 2017;19(3):1–13. doi: 10.9734/BJESBS/2017/31637
  30. King G, Law M, Hanna S, et al. Predictors of the leisure and recreation participation of children with physical disabilities: a structural equation modeling analysis. Children’s Health Care. 2006;35(3):209–234. doi: 10.1207/s15326888chc3503_2
  31. Plant KM, Sanders MR. Predictors of care-giver stress in families of preschool-aged children with developmental disabilities. J Intellect Disabil Res. 2007;51(Pt 2):109–124. doi: 10.1111/j.1365-2788.2006.00829.x
  32. Raina P, O’Donnell M, Rosenbaum P, et al. The health and well-being of caregivers of children with cerebral palsy. Pediatrics. 2005;115(6):e626–636. doi: 10.1542/peds.2004-1689
  33. Bright T, Wallace S, Kuper H. A systematic review of access to rehabilitation for people with disabilities in low- and middle-income countries. Int J Environ Res Public Health. 2018;15(10):2165. doi: 10.3390/ijerph15102165

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