2. Introduction
T.B. spine with neurological
involvement
20% incidence
M/c in dorsal spine
As spinal canal is narrowest in
dorsal spine
3. Pathology
Pressure on neural tissues within
canal by the products from diseased
vertebrae
Inflammatory edema
Extradural abscess and granulation
tissue
Sequestra of extruded disc
5. Types of Pott’s paraplegia
Early onset : paraplegia during active stage of
disease.
Usually within 2 yrs of onset of disease.
Late onset: paraplegia occuring several years after
disease has become quiescent.
Usually occurs at least 2 years after the onset of
the disease.
6. Causes of paraplegia in T.B. spine
Early onset :
Inflammatory causes
Abscess-m/c
Granulation tissue
Circumscribed tuberculous
focus
Posterior spinal disease
Infective thrombosis of spinal
blood supply
8. Late onset
Recurrence of disease
Prominent anterior wall of spinal canal
in case of severe kyphosis ( internal
gibbus)
Fibrous septae following healing
More than one cause may be responsible
for particular patient
9. Clinical features
Onset : gradual, some cases may be
sudden
Spastic to start
Clonus is most prominent early
sign
Clinical features of associated
tuberculosis spine: weight loss,
night sweat, night cries, evening
rise of temperature
10. Stages of paraplegia
Muscle weakness, spasticity and
incoordination: due to pressure on
corticospinal tract, anteriorly placed.
Paraplegia in extension: tone of muscle
increased
11. Paraplegia in flexion: absence of paraspinal tract
functions in addition to corticospinal tract.
Complete flaccid paraplegia: all transmission
across cord stops
12. Grades of Pott’s paraplegia
Grade 1: patient unaware of neural deficit
Doctor elicits babinski positive, ankle or patellar
clonus.
Grade 2: spasticity while walking
Patient is able to walk with or without support
13. Grade 3 : patient not able to walk because of severe
weakness.
Paraplegia in extension.
partial loss of sensation.
Grade 4: unable to walk.
Paraplegia in flexion
Near complete loss of sensation with sphincter
disturbances
14. Investigations
+/- History of spinal tuberculosis
Clinical features: paraplegia
Blood investigation: raised ESR, lymphocytosis
X ray
CT scan: vertebral destruction
MRI : investigation of choice
16. Conservative
ATT: mainstay of treatment
Intensive phase: 2 months HRZE
Continuation phase: 8 to 16 months HRE
MDR TB: 5 drugs in intensive phase.
( pyrazinamide+ 4 second line drugs)
17. Absolute rest
Cervical spine : sling traction
Dorsolumbar spine: bed rest
Repeated neurological examination of
limb is carried out to detect any
deterioration or improvement
Bracing 6-12 months.
18. Operative treatment
Indications
Paraplegia occuring during
conservative treatment
Paraplegia deteriorates or remains
stationary despite conservative
treatment
Severe paraplegia with rapid onset
19. Complete loss of motor power for
one month despite adequate
treatment
Motor or sensory loss for more
than 6 months
paraplegia with uncontrolled
spasticity
20. Relative indication of surgery
Recurrant paraplegia
Paraplegia in old age
Painful paraplegia: spasm or
root compression
22. Anterolateral decompression
Removal of rib, transverse
process, pedicle and part of
body of vertebra is done
laminae and facet joint are
not removed.
23. Other surgeries
Radical debridement and
arthrodesis
Dead and diseased vertebrae
excised and replaced with rib
graft
Laminectomy : spinal cord
syndrome
25. Prognosis of pott’s paraplegia
Good prognosis
Children respond better than
adults
Acute onset has better prognosis
Poor prognosis
Long duration paraplegia
More severe grade( eg. With
sphincter involvement)
Sudden progress