Meningitis by Prof Khin


Published on

Published in: Health & Medicine
  • Be the first to comment

No Downloads
Total views
On SlideShare
From Embeds
Number of Embeds
Embeds 0
No embeds

No notes for slide
  • Neurocutaneous lesions:Café-au-lait spot,vitiliginous lesions of tuberous sclerosis using an UV light, ademonasebaceum, shagreen patch, nevus flammeus, retinal phakomaNeck stiffness not very well exhibited in <1yr old
  • meningitisPoints supporting – fever, seizure, irritablePoints against – fever is just 1 day duration, no drowsiness, no poor-feeding, no bulging of fontenelle, no vomiting. Cerebral malariaPoints supporting – fever, seizurePoints against – no exposure to malaria endemic area, fever duration only 1 day, no vomiting, no hepatoslenomegaly.
  • LP must if any sign of intracranial infection, prior antibiotic therapy, persistent lethargy & not fully interactive 6hr after seizureStrongly recommended in <1y.o., 1st complex febrile convulsion, no pediatrician, parent have problem bringing the child again
  • Especially if they are staying far from hospital.
  • Meningitis by Prof Khin

    1. 1. Pyogenic Meningitis ACUTE BACTERIAL MENINGITIS Asso. Prof. Dr.Khin Htwe
    2. 2. Pathophysiology of convulsions• Seizures are paroxysmal manifestations of the electrical properties of the cerebral cortex• A seizure results when a sudden imbalance occurs between the excitatory and inhibitory forces within the network of cortical neurons in favour of a sudden- onset net excitation
    3. 3. • Impairment of the γ-aminobutyric acid (GABA)–ergic inhibitory system• Excitatory glutamatergic synapses (excitatory amino acid neurotransmitters glutamate, aspartate)• Seizures may arise from areas of neuronal death, and these regions of the brain may promote development of novel hyperexcitable synapses that can cause seizures eg temporal lobe lesions can cause seizures
    4. 4. Brain injury –• One suggests that inhibitory neurons are selectively damaged and remaining principal excitatory neurons become hyperexcitable• The other hypothesis suggests that aberrant excitatory circuits are formed as part of reorganization after injury
    5. 5. Seizures more common in chhildren• Underdeveloped brain is more susceptible to specific seizures than is the brain of an older child or adult (age specific – infantile spasm)• Immature brain is more excitable than the mature brain, reflecting the greater influence of excitatory glutamate-containing circuits• Actions of GABA, the major inhibitory neurotransmitter, are often paradoxically excitatory in the immature brain
    6. 6. Differential diagnoses of acute onset of fever and fits• Febrile convulsion• Acute bacterial meningitis• Cerebral malaria• Encephalitis
    7. 7. Meningitis• Inflammation of leptomeninges• Viral infection – commonest, self- resolving in most cases• Bacterial meningitis – may have severe consequences
    8. 8. Clinical featuresNewborn - 2 months- Signs and symptoms are not typical as in older children. • Poor sucking Poor tone • Staring eyes Poor cry • Irritability Drowsiness • Convulsion• There may be history of • Prematurity LBW • Complicated labour PROM • Maternal sepsis.
    9. 9. Clinical featuresInfants and older children• Preceding history of • Ear discharge • Head injury • Sinusitis may be present
    10. 10. Signs and Symptoms• Less common - Dramatic onset - Meningococcal infection may progress rapidly leading to shock, purpura, DIC and reduced level of conciousness and died within 24 hours• Commonly – several days of fever with URT or GI symptoms followed by non- specific CNS symptoms
    11. 11. • Infants and young children – fever, poor feeding, vomiting, irritability, lethargy, drowsiness, seizures or reduced consciousness• Older children – fever, Vomiting, headache, photophobia, neck stiffness, drowsiness, convulsion, coma
    12. 12. Signs and Symptoms• Bulging and tense fontanelle.• Signs of meningeal irritation • Neck stiffness • Kernig’s sign • Brudzinski’s Sign.
    13. 13. Increased ICP suggested by• Head ache, vomiting, bulging fontanelle or diastasis (widening ) of sutures• Ocular or abducens nerve paralysis• Hypertension with bradycardia• Apnea or hyperventilation• Decorticate or decerebrate posture• Stupor or coma.• Pappilloedema is uncommon (chronic process).
    14. 14. Meningococcal meningitisMeningococcemia• Petaechiae, and/or purpura, or maculopapular rashes• Signs of shock may be present.
    15. 15. Organisms causing bacterial meningitisNeonatal to 3 months - Group B streptococcus E.coli and other coliforms Listeria monocytogenes1 month – 6 year - Nisseria meningitidis Streptococcus pneumoniae Haemophilus influenzae>6 years - Nisseria meningitidis Streptococcus pneumoniae
    16. 16. Acute bacterial meningitis (Causal organisms) (M Protocol)• 0-1 month - GBS E. coli• 1-3 m – GBS, E.coli, Strep.pneumoniae H.influenzae type b• >3 mo - N. meningitidis S. pneumoniae H. influenzae type b
    17. 17. Investigations for Diagnosis- CSF examination including Gram stain & culture• CSF Examination • Raised CSF pressure • Appearance - Turbid or opalescent • Raised protein • Increased cell count, may be numerous, mainly neutrophils • Reduced sugar
    18. 18. Infection Pressure Leucocyte Leucoc Protein Glucose mm Hg s ytes g/l Mmol/l Total/cum (Differ) mNormal 50-80 <5 lympho 0.2-0.4 2.8 - 4.4 cytesBacterial 100-300 100- PMN 1.0 – 5.0 0.5 – 1.5meningiti >50,000sTB increased 10 - 500 Lymphoc 1 - 5 0-2meningiti ytess
    19. 19. CSF Gram Stain• Results within hours• Gram (+) cocci, Gram (-) cocci, Gram (-) coccobacilli or bacilliCSF Culture & Sensitivity• 3 to 7 days to get the results• Organisms identifiedCSF Antigen – Latex agglutination testCSF PCR - organism
    20. 20. Blood• Culture may identify organisms dose• FBC – Neutrophil leucocytosis• Latex agglutination test of blood for antigen• PCR – organism• Glucose
    21. 21. Investigations for complications• BUSE SIADH - urea level normal : serum Na level low, high urine Na• Coagulation screen (DIC)• CT/MRI brain scan and EEG - for hydrocephalus, subdural effusion, brain abscess, cerebral infarct• Ultrasound for infants - confirm with CT/MRI brain scan
    22. 22. Contraindications to LP• Cardiorespiratory instability• Focal neurologic signs• Signs of increased ICP Glasgow coma scale <8 Abnormal dolls’ eye reflex, Unequal pupils Papilloedema, High BP low HR• Coagulopathy, thrombocytopenia• Local infection at the site of LP• Immediately after recent seizure
    23. 23. Fever and S&S of bacterial meningitis LP contraindicated No(carry out Yes (withhold LP) LP) • do blood,urine • Start antibiotic dexamethasone Abnormal CSF Normal CSF,wait for CSF culture and Latex agglutination Continue antibiotic positive negative improvement No improvement Re-evaluate, consider discontinu antibioticComplete course of treatment Change antibiotic No response- consider TB,fungus or encephalitis
    24. 24. Treatment• Antibiotics• Dexamethasone• Supportive treatment • Fluid balance, Fluid restriction • Monitor vital signs and signs of raised ICP, Input and output • Fit chart • Daily neurological assessment • Measure OFC daily• Follow up• Prevention
    25. 25. Dexamethasone• Use of steroids – Antiinflammatory to prevent cytokine release- Best given before or with first antibiotic dose- Dose: dexamethasone 0.15mg/kg 6hly for 4 days or 0.4mg/kg 12hly for 2 days
    26. 26. Fluid • Maintanence • Fluid restriction (2/3 of maintenance) • Fluid replacement if shock is present in cases of meningococcal meningitis.
    27. 27. Cerebral monitoring (Neuro-observation Chart)Cerebral oedema • IV 20 % mannitol 7 to 10 ml/kg/20 mins, can be repeated 8 hourlySeizure – anticonvulsantsApnoea – mechanical ventilationCare of unconscious patient – Nursing, bladder, bowel, skin.
    28. 28. Complications• Immediate • Seizures • Cerebral or cerebellar herniation • Increase Intracranial pressure • Cranial nerve palsies • Subdural effusion • SIADH • Hydrocephalus • Waterhouse Friderichsen syndrome
    29. 29. Complications• Remote • Neurological deficit • eg. hemiplegia, aphasia, ocular palsies • Deafness • Blindness • Learning difficulty • Brain abscess • Hydrocephalus • Epilepsy
    30. 30. Follow upFollow Up (long term FU is important)• Developmental assessment• Measurement head circumference• Ask about any occurrence of fits or any beh. abnormalities (for epilepsy and behavioural problems)• Assess vision, hearing and speech• Neurological assessment
    31. 31. Prevention1. Antibiotic prophylaxis• Meningococcal infection (all contacts) • Rifampicin 10 mg/kg OD for 2 days• H. influenzae infection (only if <5yr child at home) • Rifampicin 20 mg/kg OD for 4 days • Alternative – Ciprofloxacin (for adult contacts)
    32. 32. Prevention• 2. Vaccination • HiB vaccine • Meningococcal vaccine • Pneumococcal vaccine• 3. Adequate treatment of pyogenic infection elsewhere in the body
    33. 33. Lumbar Puncture
    34. 34. Lumbar Puncture• Informed consent from the parents are needed. • Parents should be told on why the test is needed • How the procedure are going to be carried out • The complications that can occur & its risk
    35. 35. To seek verbal consent for LP• Introduce yourself• Check knowledge about condition of the child and need for LP• Clearly explain about LP - why is it necessary and what is involved (a technique to sample the fluid surrounding the brain and spinal cord, put a needle on the back and take few mls of fluid)
    36. 36. Why LP is necessary• Meningitis is potentially serious• The most serious forms of meningitis can be effectively treated with antibiotics• Delay in making the diagnosis and starting treatment worsens the outlook• LP is the only way of excluding meningitis• While it is possible to give an antibiotic without performing a LP, there is less chance of making an accurate diagnosis
    37. 37. • Explain about analgesia, antiseptic• Explain what to expect afterwards – the fluid sample will be sent to the laboratory for analysis to see any evidence of infection• Explain risks – infection, leak, headache, technically unsuccessful• Explain benefits – confirm diagnosis and management, selection of treatment, length of treatment, follow-up arrangements• Invite patient any further questions, check understanding• Ask permission, using and open-ended, non- diirective question
    38. 38. References• Illustrated Paediatrics 4th edition• Nelson Textbook of Paediatrics 19th edition• Paediatric Protocols for Malaysia Hospitals 2nd edition 2010
    39. 39. • A 12 year-old boy was in his normal state of health until 5 days ago, when he developed a fever of 105.8 F (41C). Over the next 2 days, he developed stiff neck and began vomiting. He was brought to the emergency department (ED) when he developed altered mental status. In the ED, his heart rate is 135 bpm, blood pressure 120/70 mm Hg, respiratory rate 25 breaths/min, and temperature 104F (40C). He is combative, unaware of his surroundings,• and does not follow instructions. Kernig and Brudzinski signs are present.• ➤ What is the most likely diagnosis?• ➤ How would you confirm the diagnosis?• ➤ What treatment is indicated?• ➤ What are possible complications?
    40. 40. Investigation findings• FBC – WBC – 16,000/cmm N 80%, L 15%• LP CSF – turbid cell – 1000/cmm, N 80% Protein – 1 G/L Sugar – 1.3 mmol/l
    41. 41. CASE STUDY
    42. 42. A one year 6 months old malay boy, came to A&E accompanied by his mother, with chief complaint of fits and fever.Questions• State the immediate management• State the differential dx• Mention information you would like to know.• Physical signs you would look for
    43. 43. Case study• Fever – started in the morning, 39.5°C, not relieved by paracetamol• Fits – started around 1.20pm, around 4 hrs after the onset of fever. Generalized tonic- clonic, uprolling of eyes, drooling of saliva and urinary incontinence. It lasted for 5 minutes.• Postictal – crying, No drowsiness, no weakness of limbs and the baby did not sleep.
    44. 44. • Not drowsy, not irritable, no weaknesses, still feeding well during fever. No fast breathing, no cyanosis, no ear discharge, no rashes.• No hx of head injury, no recent travelling to other country• He had similar episode 2 mths ago. The fever was 38°C and fits 5 hrs after onset of fever. Similar generalized tonic-clonic with uprolling of eyes, drooling of saliva and incontinence. No post-ictal drowsiness or weakness and the fits lasted for 10 minutes. The baby was admitted in hospital for 1 day. No medication given.
    45. 45. Case study• Antenatal history – GDM with insulin injection. C-sec, birthweight 4.03kg. After birth, baby was having respiratory distress and was given O2 via headbox, not intubated• Developmental – normal• Family hx – youngest of 4, no similar presentations in family or afebrile convulsion in family
    46. 46. • Physical examination?
    47. 47. Physical examination• Anthropometry - normal• Neurologic examination – power and sensory intact. No signs of cranial nerves palsy• Anterior fontanelle not bulging• Neck stiffness absent• Eyeground (fundoscope): no abnormalities detected• Liver and spleen not palpable
    48. 48. • Provisional diagnosis? • Recurrent Simple Febrile seizure• Differential Diagnosis • Cerebral malaria • Meningitis • Encephalitis
    49. 49. • Investigation?
    50. 50. Investigation• FBC – for presence of Infections• RBS• BUSE with creatinine, Ca, Mg• Infection screen • Blood culture • Urine culture • Lumbar puncture (indication?)
    51. 51. Investigation• Unnecessary in this case • EEG • Neuroimaging (MRI, CT) • Toxicology screening if suspicious of drug exposure
    52. 52. Management