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Tuberculous Meningitis
SANJAY GEORGE
Epidemiology
 India has one fifth of the world’s TB burden.
 2 million new cases in 2009.
 Around 10% develop CNS disease.
Etiology
 Mycobacterium tuberculosis.
 Risk Factors:
 Delay in diagnosis and treatment
 HIV, Immunocompromised state.
Pathophysiology
 50% cases : History present, Hematogenous spread
 Seed meninges or brain – Sub-pial/Sub-ependymal foci of
metastatic caseous lesion – Rich Foci.
 Proximity to S.A Space determines type of CNS involvemeny.
 Rupture into S.A space – Meningitis
 Deep in parenchyma cause Tuberculoma or Abscesses.
Contd.
 Paresis of C.N nerves common as involvement more at base of
brain.
 Disease evolves over 1-2 weeks.
 Thick gelatinous exudate infiltrates the cortical, meningeal blood
vessels, producing inflammation, obstruction, or infarction.
 Ultimate evolution to coma, with hydrocephalus and intracranial
hypertension.
Clinical Features
 Headache
 Vomiting
 Low Grade Fever
 Malaise, Anorexia, Irritability
 Severe Headache
 Confusion
 Lethargy
 Altered Sensorium
 Neck Rigidity
Initially
Late
Signs
 Meningism (maybe absent)
 Occulomotor palsies
 Papilloedema
 Depression of conscious level
 Focal hemisphere signs.
Differential Diagnosis
 Other Infectious causes of meningitis
 Acute hemorrhagic leukoencephalopathy
 Behçet disease
 Chemical meningitis
 Chronic benign lymphocytic meningitis
 Neoplastic: metastatic, lymphoma
 Systemic lupus erythematosus
 Vascular: Multiple emboli, subacute bacterial endocarditis, sinus
thrombosis
 Vasculitis
 Vogt-Koyanagi-Harada syndrome
Investigations
 Lumbar Puncture:
 High leucocyte count (upto 1000/μL) with lymphocytic predominance.
 Elevated Protein (100-800 mg/dL).
 Mildly Decreased Glucose Concentration (20 – 40 mg/dL)
 AFB – 1/3rd cases
 CSF culture (Gold Standard) – diagnostic in 80% cases.
 PCR
 Imaging Studies – MRI, CT
Management
 Initiate if high index of suspicion.
 Initial Therapy:
 Isoniazid – 300mg/d
 Rifampicin – 10mg/kg/d
 Pyrazinamide – 30mg/kg/d
 Ethambutol – 15-25 mg/kg/d
 Pyridoxine – 50mg/d
 Good Response : Discontinue Pyrazinamide after 2 months continue
H & R for 6 – 12 months
 Inadequate Resolution : Continue for 9 – 12 months
 Dexamethasone in HIV –ve Patients. 12 -16mg/day for 3
weeks, tapered over next 3 weeks
Contd.
 Obstructive hydrocephalus and neurological deterioration :
ventricular drain or ventriculoperitoneal or ventriculoatrial shunt.
 Prevention:
 BCG Vaccine
Tuberculous meningitis

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Tuberculous meningitis

  • 2. Epidemiology  India has one fifth of the world’s TB burden.  2 million new cases in 2009.  Around 10% develop CNS disease.
  • 3. Etiology  Mycobacterium tuberculosis.  Risk Factors:  Delay in diagnosis and treatment  HIV, Immunocompromised state.
  • 4. Pathophysiology  50% cases : History present, Hematogenous spread  Seed meninges or brain – Sub-pial/Sub-ependymal foci of metastatic caseous lesion – Rich Foci.  Proximity to S.A Space determines type of CNS involvemeny.  Rupture into S.A space – Meningitis  Deep in parenchyma cause Tuberculoma or Abscesses.
  • 5. Contd.  Paresis of C.N nerves common as involvement more at base of brain.  Disease evolves over 1-2 weeks.  Thick gelatinous exudate infiltrates the cortical, meningeal blood vessels, producing inflammation, obstruction, or infarction.  Ultimate evolution to coma, with hydrocephalus and intracranial hypertension.
  • 6.
  • 7.
  • 8. Clinical Features  Headache  Vomiting  Low Grade Fever  Malaise, Anorexia, Irritability  Severe Headache  Confusion  Lethargy  Altered Sensorium  Neck Rigidity Initially Late
  • 9. Signs  Meningism (maybe absent)  Occulomotor palsies  Papilloedema  Depression of conscious level  Focal hemisphere signs.
  • 10. Differential Diagnosis  Other Infectious causes of meningitis  Acute hemorrhagic leukoencephalopathy  Behçet disease  Chemical meningitis  Chronic benign lymphocytic meningitis  Neoplastic: metastatic, lymphoma  Systemic lupus erythematosus  Vascular: Multiple emboli, subacute bacterial endocarditis, sinus thrombosis  Vasculitis  Vogt-Koyanagi-Harada syndrome
  • 11. Investigations  Lumbar Puncture:  High leucocyte count (upto 1000/μL) with lymphocytic predominance.  Elevated Protein (100-800 mg/dL).  Mildly Decreased Glucose Concentration (20 – 40 mg/dL)  AFB – 1/3rd cases  CSF culture (Gold Standard) – diagnostic in 80% cases.  PCR  Imaging Studies – MRI, CT
  • 12. Management  Initiate if high index of suspicion.  Initial Therapy:  Isoniazid – 300mg/d  Rifampicin – 10mg/kg/d  Pyrazinamide – 30mg/kg/d  Ethambutol – 15-25 mg/kg/d  Pyridoxine – 50mg/d  Good Response : Discontinue Pyrazinamide after 2 months continue H & R for 6 – 12 months  Inadequate Resolution : Continue for 9 – 12 months  Dexamethasone in HIV –ve Patients. 12 -16mg/day for 3 weeks, tapered over next 3 weeks
  • 13. Contd.  Obstructive hydrocephalus and neurological deterioration : ventricular drain or ventriculoperitoneal or ventriculoatrial shunt.  Prevention:  BCG Vaccine