invasive meningoccal disease Flashcards

(48 cards)

1
Q

what is meningitis

A

inflammation of the meninges (membranes) which cover the brain and spinal cord

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2
Q

what are the 3 layers of meninges

A

dura mater
arachnoid mater
pia mater

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3
Q

usual causes of meningitis

A

infection with
- bacteria
- viruses
- less common ones: fungi, protoza &other parasites

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4
Q

non infectious causes of meningitis

A
  • medications eg antibiotics, NSAIDS
  • cancers eg melanoma, lung cancer
  • autoimmune diseases eg SLE, Behcets syndrome
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5
Q

differential diagnoses for acute bacterial meningitis

A

• Viral meningitis
• Fungal meningitis
• TB meningitis
• Drug-induced meningitis Loading…
• Sepsis from other causes
• Encephalitis – inflammation of the brain
• Brain abscess – collection of pus in the brain
• Subarachnoid haemorrhage
• Brain tumour
• HIV infection

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6
Q

what is invasive meningococcal disease

A

infection with NEISSERIA MENINGITIDIS

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7
Q

describe neisseria meningitidis

A

gram negative dipolococci
carried by 10-24% of population
humans are the only known reservoir

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8
Q

describe transmittion of neisseria meningitidis

A

by respiratory droplets/nano-pharyngeal secretions

usually requires either frequent or prolonged close contact

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9
Q

incubation period of neisseria meningitidis

A

2- 10 days

usually 3-4 days

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10
Q

2 main manifestations of neisseria meningitidis

A

meningitis - a localised infection of the meninges with ‘local’ symptoms

septicaemia - a systemic infection with widespread signs, and generalised organ damage

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11
Q

how many sero groups of neisseria mengitidis

A

12 sero groups based on the capsular polysaccharide

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12
Q

when is meningitis more prominently

A

winter

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13
Q

which is worse - bacterial or viral meningitis

A

viral

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14
Q

risk factors for invasive meningococcal disease

A

Extremes of age
• Immunocompromised (e.g. HIV) or immunosuppressed (e.g. chemotherapy)
• Asplenia/hyposplenia
• Cancer – people with leukaemia and lymphoma
• Sickle cell disease
• Organ dysfunction – e.g. liver or kidney disease
• Cranial anatomical defects
• Cochlear implants
• Contiguous infection - e.g. otitis media, sinusitis, mastoiditis, pneumonia
• Smokers
• Living in overcrowded households, college dormitories or military barracks
• People who have had contact with a case
• Travellers abroad to high risk area - increased risk of encountering the pathogen

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15
Q

classic symptoms of meningococcal meningitis

A

fever
stiff neck
headache
confusion
increased sensitivity to light
nausea and vomiting

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16
Q

babies symptoms of meningococcal meningitis

A

slow or inactive
irritable
vomiting
feeding poorly
bulging anterior fontanelle - soft spot of the skull

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17
Q

meningococcal septicaemia symptoms

A
  • fever and chills
  • fatigue
  • vomiting
  • cold hands & feet
  • severe aches or pains in the muscles, joints, chest or abdomen
  • rapid breathing
  • diarrhoea
  • nom blanching rash (petechiae)
  • in later stage - a dark purple rash (purpura)
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18
Q

what happens if you press a glass against a petechiae rash

A

the rash does not fade if you press the side of a clear glass firmly against the skin

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19
Q

what can sepsis cause

A

Disseminated intravascular coagulation - the activation of coagulation pathways that results in formation of intravascular thrombi and depletion of platelets and coagulation facors

these clots cause arterial occlusionsleading to gangrene of extremities & auto amputations

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20
Q

natural history of disease

A

acute onset

fulminating infection - occurs quickly, escalates uickly

prolonged and persistent coccaemia (bloodstream infection)

surovioprs may have long term complications -eg deafness, amputations, seizures

21
Q

what specimens do you take on hospital admission before initiating antibodies

A

blood sample for culture & PCR
CSK for microscopy, culture and PCR

for other localised infections - aspirate from sterile site for microscopy, culture and PCR

throat swab for culture

additional samples for enhanced national surveillance

22
Q

why do you notify public health about the disease

A

To find out how the patient caught it

23
Q

when do you notify

A

on suspicion
don’t wait for confirmation

24
Q

what action can public health take

A

contract tracing

chemoprophylaxis

vaccination

alerting and informing close contacts and the public

25
define confirmed case for public health purposes
clinical diagnoses with lab confirmation (immediate pH action)
26
define probable case for public health purposes
clinical case with no lab confirmation, but meningococcal disease is most likely (immediate PH action)
27
define possible case for public health purposes
no lab confirmation and other diagnoses is equally likely (no immediate PH action)
28
define close contacts
- people living in the same household as the case - anyone who slept overnight in the same household in previous 7 days - other household members if case stayed overnight elsewhere in previous 7 days - intimate kissing contacts in lass 7 days
29
what type of antibiotics is given
chemoprophylaxis
30
why are antibiotics given for meningitis s
to eradicate throat carriage
31
main type of antibiotic given
ciprofloxacin single dose doesn’t interact well with oral contraceptives readily available
32
alternative antibiotic given
rifampicin
33
what happens if there is delayed report of a case
offer prophylaxis to household contacts up to 4 weeks after case became ill
34
what do you give for meningococcal conjunctivitis
prophylaxis
35
further public health actions
Contact school/nursery/university etc Standard letter to warn and inform Customised letter if unusual circumstances e.g. death Offer leaflets Offer information/support/helpline Media handling
36
do we get cluster cases in this country
no its rare less than 5% most cases are individual
37
what age range is most popular
teenagers / youths outbreaks occur in schools/colleges
38
what does action depend on
attack rate isolation of the same organism establishing a link between cases public anxiety
39
describe clusters in schools
Two probable or confirmed cases of the same type within 4 weeks Need to define the risk group Class, Year group, or Whole school
40
describe clusters in the community
Look for links Define an at risk population Calculate age-specific attack rates Loading... No specific threshold, but look for a substantial increase
41
describe global epidemiology
Occurs sporadically, and in small clusters worldwide Seasonal variation: October-May in Northern Hemisphere Groups B&C most common in Europe and Americas Group A most common in Africa and Asia
42
causes of epidemic meningitis s
• Dry season (Dec – Jun) dust laden winds • Upper Respiratory Tract Infection (URTI) due to cold nights • Decrease in “local immunity” in pharynx • Overcrowded housing • Large population displacements due to pilgrimages and traditional markets • Herd immunity leads to cyclical epidemics
43
3 goals of WHO to defeat meningitis by 2030
Elimination of bacterial meningitis epidemics Reduction of cases of vaccine-preventable bacterial meningitis by 50% and deaths by 70% Reduction of disability and improvement of quality of life after meningitis due to any cause
44
4 types of vaccines for meningococcal
MenC conjugate vaccine Hib/MenC conjugate vaccine MenACWY quadrivalent conjugate vaccine multi component protein vaccine (MenB)
45
immunisation schedule for meningococcal routine vaccination
8 weeks 16 weeks one year 14 years
46
describe polysaccharide vaccines
- Polysaccharide vaccines give only short term (3-5 years) protection • Polysaccharide vaccines will not evoke an immune response in children under 2 years
47
describe conjugate vaccines
Polysaccharide-conjugate vaccines are immunogenic across all ages. In infants and young children, conjugation increases the immunogenicity of the vaccines compared to polysaccharide only vaccines • also prevents acquisition of carriage so interrupt transmission of meningococci to others and induces population protection • Serogroup specific and do not provide any cross-protection against other meningococcal serogroups
48
describe meningitis B vaccine
Biologically difficult to produce. Antigenically similar to brain protein. • In UK, multiple strains of serogroup B, so not easy to produce a “one size fits all” vaccine. • Group B vaccine developed, given routinely for infants, but issues with uncertain effectiveness and high costs • Not used in outbreaks 38