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DOI 10.2147/tcrm.s106014

Медицинская библиотека · Therapeutics and clinical risk management · 2016

Vojta method in the treatment of developmental hip dysplasia - a case report.

Kiebzak Wojciech, Żurawski Arkadiusz, Dwornik Michał

Клинический случайСтатьяПеревод в очереди

Аннотация

BACKGROUND

Developmental dysplasia of the hip joint is one of the most common congenital defects and often results in functional and structural disorders. Such cases particularly demand optimizing therapeutic effects and maximally reducing the duration of therapy.

PURPOSE: The aim of this case report is to present the therapeutic process in a child with developmental hip dysplasia.

CASE REPORT: This is a case report of a female child with a birth weight of 2,800 g and an Apgar score of 9 points born to a gravida 3 para 3 mother at 37 weeks. The child was delivered by cesarean section, and the pregnancy was complicated by oligohydramnios. Subluxation of the left hip joint was diagnosed by an orthopedist in the third month of life. The treatment followed was the Vojta method (the first phase of reflex turning and reflex crawling).

RESULTS

During the 6 weeks of the Vojta treatment, the left half of the femoral head was centralized, and the process of formation of the hip joint acetabulum was influenced effectively enough to change the acetabulum's Graff type from the baseline D to IIb after 41 days of treatment.

CONCLUSION

The diagnostic work-up of congenital hip joint dysplasia should involve a physiotherapist who will investigate the child's neuromuscular coordination, in addition to a neonatologist and a pediatrician. The therapy for a disorder of hip joint development of neuromotor origin should involve the application of global patterns according to Vojta. Children with congenital dysplasia of the hip joint should commence rehabilitation as early as possible.

Для цитирования: Kiebzak Wojciech, Żurawski Arkadiusz, Dwornik Michał. Vojta method in the treatment of developmental hip dysplasia - a case report.. Therapeutics and clinical risk management. 2016. DOI: 10.2147/tcrm.s106014.
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