2. Definition:
Meningitis is defined as inflammation
(swelling) of the membranes surrounding
the brain and spinal cord, including dura,
arachnoid and pia matter.
Meningoencephalitis represents
inflammation of both the meninges and
the cortex of the brain.
3.
4. AETIOLOGY
Bacterial meningitis- caused by bacteria and can e deadly
Viral meningitis- caused by viruses and often less severe
Fungal meningitis- caused by fungi and its mostly rare, people get it by
inhaling fungal spores
Parasitic meningitis- much less common
Amebic meningitis- primary amebic meningoencephalitis is rare but
devastating infection caused by Naegleria fowleri
Non infectious meningitis- sometime cancers, SLE, certain drugs, head injury
and brain surgery can also cause this.
5. PYOGENIC MENINGITIS
INCIDENCE it can occur at all ages but more common in infancy
CAUSATIVE AGENTS RESPONSIBLE AT DIFF AGES
6. CLINICAL FINDINGS
High grade fever ( 100 F or 38. 2 C)
Infant does not look well, feeds poorly and develop hypothermia, vomiting,
irritability
Bulging ant fontanelle, head retraction, high pitched cry
Seizures
Neck stiffness, Kernig's positive (flexion of leg 90 deg at hip with pain on
extension of leg thereafter) positive Brudzinski ( involuntary flexion of legs
when neck is placed in flexion)
Cranial nerves palsy and papilledema
Hemiplegia, ataxia
Generalized pruritic rash, purple mottling of skin, peripheral cyanosis
Otitis media or mastoiditis
9. DIAGNOSIS
CSF culture
Blood culture its mostly positive in case of H. influenza, and 80 percent in
case of S. pneumonia
Blood count total and differential count
Chest Xray to rule out pneumonia and tb
CT scan
Rapid diagnostic tests ELISA, CSF lactase ldh, enzyme radioisotope assay,
latex particle agglutination test lpa
Gram staining pneumococci- gram positive diplococci
Influenzas- gram neg coccobacilli
E.coli- gram neg bacilli
Meningococci- gram neg intracellular diplococci
10. MANAGEMENT
SUPPORTIVE MEASURES
The first 3- 4 days of treatment of bacterial meningitis are critical and
requires intensive care
Vitals should be monitored every 15-30 mins until pt. is stable
Frequent neurological assessment like papillary reflexes, LOC, cranial nerves
signs
Measure head circumference
Strict intake output record
Pt daily body weight and serum electrolytes
Control temperature with sponging and antipyretics
Feeding should be continued
Fluid restriction to 60-70% because of fear of SIADH
For seizures IV diazepam is given as 0.1-.2 mg/kg/dose
13. MANAGEMENT
Steroids:
DEXAMTHASONE in a dose of 0.6 mg/kg/day in 2-4 divided doses for –
days
TREATMENT OF COMPLICATIONS:
Cerebral edema and raised icp: elevate the head, steroid therapy an
mannitol
Subdural effusions: aspiration of effusion
SIADH: fluid restriction and diuretics
Shock ( warehouse Friedrichsen syndrome): normal saline or plasma,
steroids, dopamine infusions
15. PREVENTION
VACCINATION:
1. Pneumococcal polysaccharide- it’s a 23 valent vaccine, effective
in children older than 17 months. Dose is 0.5 ml IM single dose.
2. Meningococcal vaccine- it’s a quadrivalent vaccine (A, C, Y,
W135), Recommended in children with defects of the terminal component of
complement cascade.
3. H. Influenza vaccine- given to all infants above 2 months of age.
ANTIBIOTIC PROPHYLAXIS:
1. Meningococcal- Rifampicin, dose is 10mg/kg (max 600mg)
given every 12 hourly.
2. H. Influenza- Rifampicin, dose is 20mg/kg ( max 600mg) given
once daily for 4 days.
16. TUBERCULOUS MENINGITIS
It’s a inflammation of leptomeninges (pia, arachnoid) by Mycobacterium
tuberculosis
The max risk of TBM is within 6months of primary infection.
CLINICAL FINDINGS:
STAGE 1 (PRODROMAL) it lasts for 1-2 weeks, non specific symptoms, child
becomes listless, irritable, loses interest in playing, fever, wt. loss, headache.
No foal neurologic signs
STAGE 2 Its onset is abrupt, signs of meningeal irritation appears, positive
Kernig's and Brudzinski sign, neck stiffness present, headache is cardinal
symptom, fever. CN 3, 6, 7 palsy common, in infants ant fontanelle bulges
and sutures become separated ( crackpot sign )
STAGE 3 Child becomes comatose, hemi and paraplegia, opisthotonos
develops. Taches-cerebral is seen by stroking the skin with blunt obj
18. MANAGEMENT
GENERAL MEASURES:
Corticosteroid therapy, Prednisolone is given in a dose of 1-2 mg/kg/d for
6-8 weeks
Record vitals
Phenobarbitone, to control convulsions, dose is 5 mg/kg/day
Antipyretic
Pyridoxamine- 10mg daily,
Give tube feeding
Prevent bed sores
Care of comatose, bowl and bladder
19. MANAGEMENT
SPECIFIC TREATMENT:
Isoniazid- dose is 10-15mg kg/day
Rifampicin – dose is 10-20mg/kg/day
Pyrazinamide- dose is 30mg/ k/day
Streptomycin- dose is 20-40mg/kg/day
Ethambutol- dose is 15-25m/k/day
20. COMPLICATIONS
Mental retardation
CN palsy 3. 6. 7
Blindness due to optic atrophy
Deafness
hydrocephalus,
Epilepsy
Hemi para or monoplegia
Endocrine disturbances like DI
Tuberculoma