FRCS Revision

This site is private

Enter the password to open the revision library.

Personal revision library · not clinical advice
FRCSRevision
Home / Foot and Ankle / Hindfoot and knee malalignment
Foot and Ankle

Hindfoot and knee malalignment

Hindfoot calcaneus alignment and limb deformity patterns including genu valgum and recurvatum

29 questions 2 source pages 1 images

Images appear with the first question taken from each source page — tap a question to open it.

29 questions
Q1Describe the deformity in this spina bifida patient.📷▸
HF calcaneus (not varus)
HF calcaneus (not varus)
  • Hindfoot calcaneus (not varus)
  • Midfoot cavus with 1st ray plantarflexion
  • Claw toes
  • Scar at heel from previous TA lengthening
  • Calf muscle wasting
Q2How does a calcaneus foot present and how is it managed?▸
  • History of instability and pain, previous TA lengthening
  • Neuromuscular causes: spina bifida and polio
  • Gait: slapping (lack of gastrocnemius eccentric contraction); heel ulcer
  • XR: pistol grip deformity
  • Mx: non-operative; tibialis anterior to TA transfer; dome calcaneal osteotomy with posterior tuberosity proximalisation
Q3What is spina bifida?▸
  • Neural tube defect
  • Failure of neural tube closure at 3 weeks
Q4What are the risk factors for spina bifida?▸
  • Folate deficiency
  • Maternal diabetes
  • Valproic acid
Q5What prenatal screening is done for spina bifida?▸
  • Maternal AFP level (high = bad)
  • Amniotic fluid AFP
  • Structural scan
Q6What is the postnatal treatment of spina bifida and what must you beware of?▸
  • Neurosurgery: untethering of cord, drainage of syrinx, screen for Arnold-Chiari syndrome
  • Beware malignant hyperthermia
  • Beware latex allergy
  • Beware neurogenic bladder
Q7Classify spina bifida.▸
  • Occulta: vertebral arch failure
  • Meningocele: meninges protrusion, no neural element
  • Myelomeningocele: meninges and neural elements protrusion
  • Rachischisis: neural elements protrusion with no coverings
Q8What are the features of a pre-L3 spina bifida lesion?▸
  • Hip FABER contracture
  • Knee flexion contracture (FFC)
  • Feet equinovarus + claw toe
  • Non-ambulatory
Q9What are the features of an L4 (L5 defect) spina bifida lesion?▸
  • Hip: full quadriceps, Trendelenburg gait
  • Knee: recurvatum (unopposed knee extension)
  • Feet: calcaneus
  • Limited community ambulator
Q10What are the features of an L5 (S1 defect) spina bifida lesion?▸
  • High normal
  • Knee normal
  • Feet: calcaneus
  • Community ambulator
Q11What are the features of S1 or below spina bifida lesions?▸
  • Only claw toe
  • Near normal
Q12Why must VP shunt function be checked before spine surgery in spina bifida?▸
  • Check VP shunt function before spine surgery
  • Otherwise it may result in death
Q13Describe the limb deformity in this polio patient.▸
  • Right lower limb: hip extension, knee extension +/- recurvatum
  • Ankle plantarflexed, tibial external rotation, genu valgum
  • Contralateral hip and knee flexion compensating for LLD
  • Pelvic obliquity; no claw toes
Q14What do you assess in a polio patient with deformity?▸
  • Check shoewear
  • Gait: Trendelenburg, short limb, recurvatum, hand-knee gait
  • Sitting: inspect for neuropathic ulcers and callosity
  • Contractures: Silverskiold (Achilles), knee FFC (recurvatum), hip FABER (Ober)
  • Power of antigravity muscles: ankle plantarflexion, knee extension, hip extension
Q15What is the current disability history in this polio patient?▸
  • Pain from ulcers, callosity, stress fracture
  • Instability
Q16How does quadriceps weakness cause knee flexion contracture and how is it managed?▸
  • Knee collapse and unopposed hamstrings perpetuate flexed knee posture
  • Ankle PF + hip flexion bring CG forward to lock knee; FFC becomes contracture over time
  • Hand-knee gait; first line hinged KAFO
  • Flexible: biceps femoris to quadriceps transfer (needs normal hip extension/ankle PF, no recurvatum)
  • Rigid: <15 degrees serial casting, 15-30 degrees hamstring/ITB/posterior capsule release, 30-70 degrees distal femoral extension osteotomy, >70 degrees staged release then osteotomy
Q17How is knee recurvatum managed in polio?▸
  • <15 degrees: observe
  • Solid AFO
  • Triple tenodesis (gracilis, hamstrings, ITB)
  • Posterior capsular advancement; gracilis/semitendinosus or biceps femoris/tibialis tenodesis
Q18How does exaggeration of the passive stance phase cause knee recurvatum in polio?▸
  • By exaggeration of passive stance phase: knee recurvatum assists in locking of the knee (ITB becomes extensor, CG falls in front of knee)
  • Posterior knee capsules and hamstrings act as restraints, counterbalanced by hip extension and ankle PF
  • Over time the knee loses its posterior constraint causing instability; pain occurs over the anterior knee from excessive hyperextension (perpetuated by fixed equinus)
Q19What are the aims of management in polio deformity?▸
  • Maximise gait efficiency
  • Prevent deformity with growth
  • Prevent upper limb contractures and scoliosis
Q20How does gluteal weakness present in polio and how is it managed?▸
  • Gluteus medius/minimus weakness -> Trendelenburg gait
  • Gluteus maximus weakness -> back lurch
  • Abductors: external oblique transfer
  • Glut max (iliopsoas to GT transfer)
Q21What is the FABER contracture in polio and what problems does it cause?▸
  • Frog posture: hamstring, hip flexors, TFL spasm -> ITB contracture
  • Secondary pelvic obliquity
  • Leads to scoliosis and increase contralateral hip dislocation
Q22How is FABER contracture managed in polio?▸
  • Mild: fasciotomy
  • Moderate: Ober release
  • Ober release: ASIS - sartorius + TFL; AIIS - rectus femoris; GT - anterior fibres of glut med/min; LT - iliopsoas
  • Severe: Campbell procedure
  • Campbell: outer table glut med/min + TFL; inner table iliacus; AIIS rectus femoris; ASIS distalisation of sartorius
Q23What is poliomyelitis?▸
  • Non progressive motor paralysis secondary to polio virus infection at anterior horn cells
  • Enterovirus, faecal-oral route
Q24What is the pattern of poliomyelitis infection?▸
  • 80% asymptomatic
  • 10% flu-like
  • 10% neurological symptoms, of which 2% paralysis
Q25What are the phases of poliomyelitis?▸
  • Acute: flu-like symptoms, flaccid paralysis
  • Recovery: no more muscle ache, some recovery of power
  • Residual: >2 years, deformity
Q26What is post-polio syndrome?▸
  • New onset weakness after a prolonged period of recovery
  • Occurs in 50% of patients
Q27What are the diagnostic criteria for post-polio syndrome?▸
  • History of paralytic poliomyelitis by clinical/NCT
  • Complete recovery >15 years with neurological and functional stability
  • New onset weakness
  • New onset muscle/joint pain, deformity, cold intolerance
  • Exclude other causes
Q28What is the pathophysiology of post-polio syndrome?▸
  • Immunological/viral reactivation
  • Aging/degeneration of neurons
Q29What are the 5 potential problems after the residual paralysis stage?▸
  • Isolated muscle weakness - splintage, passive mobilisation
  • Deformity
  • Shortening (LLD)
  • Flail joint - may need arthrodesis or splintage
  • Vascular dysfunction