- Also know as congenital talipes equinovarus
- Commonest congenital and ankle deformity in UK
- Should be differentiated from
- Talipes calcaneovalgus
- Postural talipes equinovarus
- Affects about 3 per 1000 live births
- Male to female ratio is 3 to 1
- 40% cases are bilateral
- Low incidence in far east asians and Polynesians
- High incidence in black South Africans
- Genetic factors seem to important in its aetiology
- Most cases are idiopathic
- Occasionally associated with neuromuscular disorders
- Aetiological factors include
- Developmental arrest or delay
- Intrauterine moulding
- Retracting fibrosis
- Neuromuscular factors
Clinical features
- Many cases are diagnosis with prenatal ultrasound
- Ultrasound can not assess the severity of the condition
- The anatomical features of talipes equinovarus include:
- Equinus deviation in the sagital plane
- Varus deviation in the frontal plane
- Adduction of the forefoot in the horizontal plane
- Deviation of the whole foot with respect to the talus
- The severity of the deformity can be graded
- Grade 1 - foot can be held in neutral position
- Grade 2 - fixed equinus or varus deformity of less then 20 degrees
- Grade 3 - fixed equinus or varus deformity of more than 20 degrees
- Surgery is required in:
- 10% patients with Grade 1 deformity
- 50% patients with Grade 2 deformity
- 90% patients with Grade 3 deformity

Management
- Treatment should be begun within the first week of life
- Initial management should involve conservative therapy involving
- Manipulation and serial casting
- Continuous physical therapy
- With both methods the deformities are addressed in the following
order
- Forefoot adduction and cavus deformity
- Whole foot varus deformity
- Equinus deformity
- False correction of deformity can occur
- Leads to 'rocker-bottom foot'
Surgery
- By 3 months of age it is usually clear whether conservative
management will be effective
- Timing of surgery is controversial
- Most surgeons recommend surgery between 9 and 12 months of age
- Plaster can then be removed at the time the child begins to walk
- Aim of surgery is release all the tight structures and lengthen
muscles
- Structures that may need to be divided include:
- Plantar fascia
- Tendon sheaths of tibialis posterior, flexor hallucis longus,
flexor digitorum longus
- Posterior part of deltoid ligament
- Posterior part of ankle joint and subtalar joint capsules
- Fibulocalcaneal and fibulotalar ligaments
- Peroneal tendon sheaths
- Talonavicular joint capsule
- Tendons that may require lengthening include:
- Achilles tendon
- Tendon of flexor digitorum longus
- Tendon of flexor hallucis longus
- Tendon tibialis posterior
- Percutaneous wires may be need to maintain correction
- Foot is kept in plaster for about 6 weeks
- Following plaster removal a splint is required until the child is
walking normally
- Late problems following surgery include
- Dynamic forefoot adduction and varus
- Recurrent deformity
- Overcorrection
- Most children undergoing surgery achieve a plantigrade foot
- Most can wear normal shoes
Bibliography
Macnicol M F. The management of clubfoot: issues for
debate. J Bone Joint Surg Br 2003; 85: 167-170.
Noonan K J. Richards B S. Nonsurgical management of
idiopathic clubfoot. J Am Acad Orth Surg 2003; 11:
392-402.
Scher D M. The Ponseti method for the treatment of congenital
club foot. Curr Opin Pediatr 2006; 18: 22-25. |