Title: Meningitis.
1Meningitis.
2definition
- Inflammatory disease of leptomeninges, the tissue
surrounding the brain and spinal cord. - The meninges consist of three parts the pia,
arachnoid and dura maters. - It involves the arachnoid mater and the
cerebrospinal fluid in the subarachnoid space as
well as in the cerebral ventricles.
3Types
- Acute either pyogenic or viral.
- Chronic due to tuberculosis or fungal.
4Pyogenic meningitis.
5ETIOLOGICAL AGENT
"Normal" Adults (6-21 yrs) Neisseria
meningitidis Streptococcus pneumoniae
Children (3 months - 6 years) Haemophilus
influenzae Neisseria meningitidis
Streptococcus pneumoniae Staphylococcus
aureus Mycobacterium tuberculosis Infants
(½ - 3 months) Streptococcus, Group B
Listeria monocytogenes Escherichia coli
6Neonates Escherichia coli
Streptococcus, Group B Staphylococcus aureus
Listeria monocytogenes Streptococcus,
Group A Diabetics, alcoholics, elderly,
debilitated, diseased (untreated) Listeria
monocytogenes Streptococcus pneumoniae
Treponema pallidum
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8Clinical feature.
- Fever and headache in majority.
- Headache severe and generalized.
- Most have fever but small percentage have
hypothermia. - CNS symptoms photophobia, and cloudy sensorium.
Changes in mentation and level of consciousness,
seizures, and focal neurological signs tend to
appear later in the course of the disease.
9Nuchal rigidity.
- The patients might not complain of neck stiffness
but easy to find it by passive or active flexion
of the neck will usually result in inability to
touch the chin to the chest. - Brudzinski sign refers to spontaneous flexion of
the hips during attempted passive flexion of the
neck. - The kernig signs refers to the inability to allow
full extension of the knee when the hip is flexed
90 degree.
10Other finding.
- Skin manifestation in form of petechiae and
palpable purpura.( N. meningitides ). - If sequelae of infection in other part of the
body, there may the feature of that infection. (
sinusitis and otitis).
11Laboratory features.
- Increased WBC.
- Low platelets if there is intravascular
coagulation. - Electrolytes abnormalities mainly low sodium. (
SIADH ). - Blood culture at least one half have positive
before antibiotics.
12CSF.
- Can be diagnostic should be done in all only if
there is contraindication. - Can distinguish viral from bacterial.
- Gram stain should be done if suspected bacterial.
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14Complication.
- Cerebrovascular involvement.
- Cerebral odema.
- Hydrocephalus.
- Septic shock.
- Disseminated intravascular coagulation.
- Acute respiratory distress syndrome.
15Treatment.
- Empiric ceftriaxone has a potent activity for
causative organism except Listeria . - Ampicilin should be added if Listeria infection
possible. - Dexamethazone reduced the complication.
16H- influenza.
- Ceftriaxone 2 gm twice a day.
- Cefotaxime 2gm 6 hourly.
- Rifampicin 6oo mg daily for 4 days to clear the
colonization. - Should be treated 5 7 days.
17Neisseria meningitis.
- Penicillin, but there resistant cases.
- Third generation cephalosporin.
- Treatment for 5 days at least.
- Rifampicin if penicillin used in treatment.
- Rifampicin or ciprobay for contact.
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19PREVENTION
Neisseria meningitidis - each dose of the
multivalent vaccine provides A, C, Y and W-135
capsular polysaccharides. Effective in children
over 3 months of age.
Streptococcus pneumoniae - each dose of the
multivalent vaccine provides 23 types of capsular
polysaccharide covering the majority of
strains causing meningitis. Recommended for
children over 2 years of age.
months of age.
Haemophilus influenzae each dose of the
monovalent vaccine provides the capsular
polysaccride from serotype b. organisms.
Recommended for children over 18 months of age.
20Viral meningitis
21ETIOLOGICAL AGENTS
Mumps virus Polio virus
Coxsackie B virus Echovirus
Arboviruses Human Herpesvirus 1 (Herpes
simplex 1 virus) Lymphocytic
choriomeningitis viruses-Arenavirus
Encephalomyocarditis viruses Louping
ill virus Pseudolymphocytic meningitis
virus Hepatitis viruses
Adenovirus Rhinovirus
Coxsackie A virus
22CHRONIC MENINGITIS
NAMES OF DISEASE Fungal meningitis
Cryptoc
occosis Torulosi
s
Tubercular meningitis
Amoebic meningitis
Syphilitic meningitis
23ETIOLOGICAL AGENTS
Cryptococcus neoformans (Serotypes A,B,C,D)
Treponema pallidum
) All slow Mycobacterium
tuberculosis )
growers in Naegleria fowleri
) the CNS
Human immunodeficiency virus
) Coccidioides
immitis
)
24Fungal meningitis-predisposing factors.
- 1. Glucosteroid therapy
- 2. Malignancy (particularly of the
lymphoreticular system) - 3. Collagen - vascular disease.
- 4. Sarcoidosis - a disorder involving
many organs where there is formation of
epithelioid cell tubercles. - 5. Diabetes mellitus
- 6. Pregnancy
- 7. Alcoholism
- 8. Genetic impairment of host defense
mechanisms - 50. T-cell diseases (Di George
Syndrome, Nezelof's syndrome) - 9. AIDS
25Clinical feature fungal.
- 1. Headache - frontal, temporal or
retro-orbital. Most common feature and it becomes
progressively more frequent and severe. - 2. Mental aberrations (from simple
irritability to psychosis) - 3. Motor abnormalities (altered reflexes to
paralyses) - 4. Cranial nerve dysfunctions (aphasia,
visual disturbances, hearing loss) - 5. Cerebellar signs (dyssynergia, dysmetria,
dysrhythmia, intentional tremor, slurring of
speech) - 6. Evidence of increased intracranial
pressure - 7. Fever in about 1/3 of patients
26CSF in fungal
- 1. Increased CSF pressure
- 2. Protein is elevated
- 3. Leukocytosis (40-400/mm3 - mostly
mononuclear cells) - 4. Glucose is decreased (45 of blood
glucose) - 5. C. neoformans present in India ink
preparations - 6. Serological tests for cryptococcal
antigen
27TREATMENT
- 1. Amphotericin B injected I.V. and into
the subarachnoid space. NOTE This is poorly
absorbed into CSF. Treat for 6 weeks. Toxic. - 2. Flucytosine (5-fluorocytosine)-penetrat
es into all body fluids, including CSF. Less
toxic but higher doses required. - 3. Miconazole-an imidazole derivative
- 4. Amphotericin B methyl ester
28Tuberculous meningitis.
- Clinical feature.
- Diagnosis.
- Treatment.
29Clinical feature TB.
- Atypical presentations Rapid progressive as
pyogenic or slow dementia. - Stage 1 lucid with no focal neurological signs.
- Stage 11 are confused or focal signs such as
hemiparesis or cranial nerve palsies. - Stage 111 advanced illness with delirium ,
stupor, coma and dense hemiplegia.
30Diagnosis.
- High degree of suspicion.
- CSF high protein, low sugar and a mononuclear
pleocytosis. - Early in the illness the cellular reaction is
atypical with low cell or polymorphonuclear
leukocyte. - AFB smear in 37.
- Polymerase chain reaction 70.
- CT Scan of the brain with contrast or MRI.
31Treatment.
- INH, Rifampicin and pyrazinamid for 2 months then
discontinue PYZ. - In endemic areas where resistance to INH is high
the streptomycin or ethambutol added. - The duration for 12 months but if PYZ not
tolerated the duration extended to 18 months and
in case multiple drugs resistance for 18-24
months. - Steroid improve morbidity and mortality,
prednisone 60 mg to be tapered over 4 weeks. - Surgery in case of hydrocephalus or increase
intracranial pressure.( deterioration in
conscious level and stupor).