Meningitis Flashcards

1
Q

… refers to inflammation of the meninges, which are the outer membranes covering the brain and spinal cord.

A

Meningitis refers to inflammation of the meninges, which are the outer membranes covering the brain and spinal cord.

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2
Q

Epidemiology of bacterial meningitis

A

The annual incidence of bacterial meningitis in developed countries is estimated at 2-5 per 100,000 population.

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3
Q

Meningitis has been reported to be … times more common in developing countries due to less well developed preventative programmes (e.g. vaccination).

A

Meningitis has been reported to be ten times more common in developing countries due to less well developed preventative programmes (e.g. vaccination).

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4
Q

The meninges are composed of … individual layers.

A

The meninges are composed of three individual layers.

The meninges form the outer membranes covering of the brain and spinal cord. These are divided into three structures.

Dura mater: tough outer membrane. Lies directly beneath the skull. Composed of two layers: outer periosteal layer and inner meningeal layer.
Arachnoid mater: avascular layer of connective tissue that sits beneath the dura mater. Beneath the arachnoid mater is the subarachnoid space that contains cerebrospinal fluid.
Pia mater: thin inner membrane. Tightly adherent to the brain and spinal cord.

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5
Q

The meninges are composed of three individual layers - list these

A

The meninges form the outer membranes covering of the brain and spinal cord. These are divided into three structures.

Dura mater: tough outer membrane. Lies directly beneath the skull. Composed of two layers: outer periosteal layer and inner meningeal layer.
Arachnoid mater: avascular layer of connective tissue that sits beneath the dura mater. Beneath the arachnoid mater is the subarachnoid space that contains cerebrospinal fluid.
Pia mater: thin inner membrane. Tightly adherent to the brain and spinal cord.

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6
Q

…: thin inner membrane. Tightly adherent to the brain and spinal cord.

A

Pia mater: thin inner membrane. Tightly adherent to the brain and spinal cord.

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7
Q

Arachnoid mater: … layer of connective tissue that sits beneath the dura mater. Beneath the arachnoid mater is the … space that contains cerebrospinal fluid.

A

Arachnoid mater: avascular layer of connective tissue that sits beneath the dura mater. Beneath the arachnoid mater is the subarachnoid space that contains cerebrospinal fluid.

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8
Q

Dura mater: … outer membrane. Lies directly beneath the skull. Composed of two layers: outer … layer and inner meningeal layer.

A

Dura mater: tough outer membrane. Lies directly beneath the skull. Composed of two layers: outer periosteal layer and inner meningeal layer.

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9
Q

Meningitis may be caused by a series of infectious and non-infectious aetiologies.

List some non-infectious casues

A

Non-infectious causes include malignancy, systemic inflammatory conditions (e.g. systemic lupus erythematous, Behçet’s disease), head injury, medications (e.g. NSAIDs, co-trimoxazole) or surgery.

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10
Q

Bacterial meningitis usually occurs acutely (< 1 day) and can lead to profound sepsis and subsequent complications.

Commonly implicated organisms include:
(5)

A

Commonly implicated organisms include:

Neisseria meningitidis
Streptococcus pneumoniae
Haemophilus influenzae
Listeria monocytogenes
Escherichia coli
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11
Q

Bacterial meningitis usually occurs acutely (< 1 day) and can lead to profound sepsis and subsequent complications.

The table summarises the likely organisms based on age.

A
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12
Q

Several viruses are implicated in meningitis - list them

A
Enteroviruses (most common): examples include echovirus and Coxsackieviruses
Herpes simplex virus (HSV)
Human immunodeficiency virus (HIV)
West Nile virus (WNV)
Varicella-zoster virus (VZV)
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13
Q

Several viruses are implicated in meningitis

What are the most common?

A

Enteroviruses (most common): examples include echovirus and Coxsackieviruses

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14
Q

Cryptococcus neoformans is a particularly devastating meningitis that is usually seen in patients with poorly controlled HIV. It is a …-like … that is a major cause of HIV-associated mortality worldwide.

A

Cryptococcus neoformans is a particularly devastating meningitis that is usually seen in patients with poorly controlled HIV. It is a yeast-like fungus that is a major cause of HIV-associated mortality worldwide.

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15
Q

Fungal - meningitis

Fungal infections usually occur in the setting of HIV or signifiant immunosuppression.

A
Cryptococcus neoformans
Coccidioides immitis
Candida species
Histoplasma capsulatum
Blastomyces dermatitidis
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16
Q

TB - meningitis

A

Mycobacterium tuberculosis (TB) should always be considered in patients who are immunosuppressed. In addition, have a low threshold for suspecting TB meningitis in patients with aseptic meningitis (initial bacterial cultures negative), chronic meningitis (> 7 days duration), or from high prevalence area.

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17
Q

…. meningitidis can cause a rapidly progressive, and devastating meningitis with profound bacteraemia.

A

N. meningitidis can cause a rapidly progressive, and devastating meningitis with profound bacteraemia.

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18
Q

N. meningitidis is a gram … diplococci. It is found as a commensal organism in the upper respiratory tract of 5-11% of the adult population. Around 25% of adolescents are asymptomatic carriers.

A

N. meningitidis is a gram negative diplococci. It is found as a commensal organism in the upper respiratory tract of 5-11% of the adult population. Around 25% of adolescents are asymptomatic carriers.

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19
Q

N. meningitidis is a gram negative …. It is found as a commensal organism in the upper respiratory tract of 5-11% of the adult population. Around 25% of adolescents are asymptomatic carriers.

A

N. meningitidis is a gram negative diplococci. It is found as a commensal organism in the upper respiratory tract of 5-11% of the adult population. Around 25% of adolescents are asymptomatic carriers.

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20
Q

N. meningitidis is a gram negative diplococci.

The organism typically causes meningitis in patients of all ages, except the very young (< … months). The incubation period for infection is usually ..-… days and the spectrum of disease is wide. Some patients may develop a mild self-limiting illness, whereas others may present with fulminant meningococcal disease characterised by septic shock and multi-organ failure.

A

The organism typically causes meningitis in patients of all ages, except the very young (< 3 months). The incubation period for infection is usually 2-7 days and the spectrum of disease is wide. Some patients may develop a mild self-limiting illness, whereas others may present with fulminant meningococcal disease characterised by septic shock and multi-organ failure.

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21
Q

N. meningitidis is a gram negative diplococci.

The majority of cases are caused by 6 serogroups, which are categorised according to its polysaccharide capsule. These include A, B, C, W, X and Y. More than 95% of cases of meningitis are caused by serogroups …

A

The majority of cases are caused by 6 serogroups, which are categorised according to its polysaccharide capsule. These include A, B, C, W, X and Y. More than 95% of cases of meningitis are caused by serogroups B, C and Y.

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22
Q

The UK currently offers …s vaccinations to children and young adults as part of the UK vaccination programme. This includes the MenB and MenACWY vaccines.

A

The UK currently offers N. meningitidis vaccinations to children and young adults as part of the UK vaccination programme. This includes the MenB and MenACWY vaccines.

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23
Q

… pneumoniae is commonly implicated in cases of meningitis, pneumonia, and ear infections.

A

Streptococcus pneumoniae is commonly implicated in cases of meningitis, pneumonia, and ear infections.

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24
Q

S. pneumoniae is a gram positive ….

A

S. pneumoniae is a gram positive diplococci.

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25
Q

S. … is a gram positive diplococci.

A

S. pneumoniae is a gram positive diplococci.

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26
Q

S. pneumoniae is a gram positive diplococci. It is a very common cause of … and usually transmitted by close contacts through droplet or direct contact with secretions from the respiratory tract. It colonises 5-10% of asymptomatic adults and up to 40% of children.

A

S. pneumoniae is a gram positive diplococci. It is a very common cause of pneumonia and usually transmitted by close contacts through droplet or direct contact with secretions from the respiratory tract. It colonises 5-10% of asymptomatic adults and up to 40% of children.

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27
Q

The UK currently offers S. pneumoniae vaccination to children as part of the UK vaccination programme. It also offers the vaccine to patients with significant co-morbidities (e.g. diabetes mellitus) and all adults > … years old.

A

The UK currently offers S. pneumoniae vaccination to children as part of the UK vaccination programme. It also offers the vaccine to patients with significant co-morbidities (e.g. diabetes mellitus) and all adults > 65 years old.

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28
Q

Routes of infection

Bacteria cause meningeal inflammation by two major routes:

A

Invasion of bloodstream: subsequent haematogenous spread to meninges (commonly seen with N. meningitidis and S. pneumoniae)
Direct contiguous spread: usually as a result of ear, nose or throat infections (e.g. sinusitis, otitis media). Alternatively trauma.

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29
Q

Once bacteria penetrate the blood-brain barrier (BBB), they spread quickly within the meninges and can eventually damage underlying brain tissue.

Mild vs severe cases?

A

Once bacteria penetrate the blood-brain barrier (BBB), they spread quickly within the meninges and can eventually damage underlying brain tissue.

Mild cases: infection usually confined to the subarachnoid space.
Severe cases: brain parenchyma underlying pia mater can be affected leading to widespread destruction.

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30
Q

Once bacteria penetrate the blood-brain barrier (BBB), they spread quickly within the meninges and can eventually damage underlying brain tissue.

As the immune system is activated, there is infiltration of immune cells and release of inflammatory cytokines. The combination of inflammatory cell infiltration, cytokine-mediated damage and replicating bacteria can perpetuate the infectious process. This leads to a number of complications:

A
Damage to cranial nerves
Obstructive hydrocephalus (disruption of CSF flow, leading to fluid accumulation)
Local ischaemia (local inflammatory reactions causes vessel inflammation and thrombophlebitis)
Cerebral oedema: secondary to interstitial oedema (due to altered CSF and venous flow), cytotoxic oedema (due to inflammation reaction) and vasogenic oedema (due to increased BBB permeability)
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31
Q

If left untreated, progressive cerebral oedema leads to diffuse neuronal injury. This is usually combined with systemic complications due to bacteraemia, which include … … and …

A

If left untreated, progressive cerebral oedema leads to diffuse neuronal injury. This is usually combined with systemic complications due to bacteraemia, which include septic shock and multi-organ failure.

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32
Q

Meningitis is characterised by meningism, which describes a triad of …, … … and ….

A

Meningitis is characterised by meningism, which describes a triad of headache, neck stiffness and photophobia.

33
Q

… meningitis is more likely to present with a sudden onset illness (up to 50% within 24 hours of symptom onset) and systemic upset (e.g. signs of sepsis). … meningitis has a slightly longer prodrome and usually less severe symptoms. Meningism is characteristic of both, which describes a triad of headche, neck stiffness and photophobia.

A

Bacterial meningitis is more likely to present with a sudden onset illness (up to 50% within 24 hours of symptom onset) and systemic upset (e.g. signs of sepsis). Viral meningitis has a slightly longer prodrome and usually less severe symptoms. Meningism is characteristic of both, which describes a triad of headche, neck stiffness and photophobia.

34
Q

Over 95% of cases of meningitis present with at least two of the following symptoms: …, fever, neck stiffness, and altered … ….

A

Over 95% of cases of meningitis present with at least two of the following symptoms: headache, fever, neck stiffness, and altered mental status.

35
Q

Symptoms of meningitis (9)

A
Neck stiffness
Photophobia: dislike for bright lights
Headache (>80%)
Fever (>70%)
Nausea & vomiting
Fatigue
Confusion
Irritable or unsettled behaviours: particularly in children
Altered mental status (>70%)
36
Q

Signs of meningitis (8)

A
Tachycardia
Hypotension
Marked neck stiffness
Photophobia
Non-blanching rash: concerning sign of meningococcal septicaemia from ‘leaky’ blood vessels. May be seen with other organisms. 
Seizures
Focal neurological deficits
Reduced consciousness and coma
37
Q

Classic signs in meningitis ?

A

Kernig’s sign: inability to fully extend at the knee when the hip is flexed at 90º due to pain
Brudzinski’s sign: spontaneous flexion of the knees and hips on active flexion of the neck due to pain

38
Q

… sign: inability to fully extend at the knee when the hip is flexed at 90º due to pain

A

Kernig’s sign: inability to fully extend at the knee when the hip is flexed at 90º due to pain

39
Q

… sign: spontaneous flexion of the knees and hips on active flexion of the neck due to pain

A

Brudzinski’s sign: spontaneous flexion of the knees and hips on active flexion of the neck due to pain

40
Q

Both Kernig’s and … are classical signs of meningeal irritation. However, absence of these signs does not exclude meningitis.

A

Both Kernig’s and Brudzinski’s are classical signs of meningeal irritation. However, absence of these signs does not exclude meningitis.

41
Q

The diagnosis of meningitis can be challenging. Why?

A

Due to the potentially life-threatening nature of meningitis (esp. bacterial meningitis), a diagnosis is initially made on clinical suspicion and treatment instigated whilst further investigations are organised.

Definitive diagnosis of an infectious meningitis (e.g. bacterial meningitis) is by isolation of a pathogen from a CSF sample following a lumbar puncture (LP). However, it may be difficult to isolate an organism, especially with administration of antibiotics prior to LP. Given this, a confident diagnosis of bacterial meningitis may be made in patients with a bacterial pathogen isolated from blood cultures with a CSF sample suggesive of infection (e.g. raised WCC), even if cultures are negative

42
Q

Clinical assessment in meningitis

Prompt clinical assessment should focus on: (4)

A

ABCDE assessment: if critically unwell
Focused history: important to determine any preceeding illnesses that increase risk of meingitis (e.g. sinusitis, otitis media, contact with an affected patient)
Allergy status
Formal examination: assess for meningeal irritation, look for non-blanching rash and signs of sepsis (e.g. hypotension, tachycardia).

43
Q

A … rash refers to identification of petechiae (<2mm red lesions) or purpura (>2mm), which are both a sign of abnormal vessel integrity. In meningitis, it is indicative of … and is most commonly seen in meningococcal infection. Importantly, the disease may already be quite advanced before the rash develops.

A

A non-blanching rash refers to identification of petechiae (<2mm red lesions) or purpura (>2mm), which are both a sign of abnormal vessel integrity. In meningitis, it is indicative of septicaemia and is most commonly seen in meningococcal infection. Importantly, the disease may already be quite advanced before the rash develops.

44
Q

A non-blanching rash refers to identification of … (<2mm red lesions) or … (>2mm), which are both a sign of abnormal vessel integrity. In meningitis, it is indicative of septicaemia and is most commonly seen in meningococcal infection. Importantly, the disease may already be quite advanced before the rash develops.

A

A non-blanching rash refers to identification of petechiae (<2mm red lesions) or purpura (>2mm), which are both a sign of abnormal vessel integrity. In meningitis, it is indicative of septicaemia and is most commonly seen in meningococcal infection. Importantly, the disease may already be quite advanced before the rash develops.

45
Q

NOTE: in the early stages of meningitis and septicaemia, the rash may be …. Important to regularly reassess.

A

NOTE: in the early stages of meningitis and septicaemia, the rash may be blanching. Important to regularly reassess.

46
Q

Patients with a suspected meningitis and a non-blanching rash should be given prompt parenteral (intravenous or intramuscular) antibiotics and referred urgently to hospital. Unless there is a clear penicillin allergy, the choice is …..

A

Patients with a suspected meningitis and a non-blanching rash should be given prompt parenteral (intravenous or intramuscular) antibiotics and referred urgently to hospital. Unless there is a clear penicillin allergy, the choice is benzylpenicillin. Paramedics can administer benzylpenicillin for suspected meningococcal meningitis.

47
Q

Paramedics can administer … for suspected meningococcal meningitis.

A

aramedics can administer benzylpenicillin for suspected meningococcal meningitis.

48
Q

Benzylpenicillin dosing for suspected meningococcal meningitis prior to transfer to hospital:

A

Children 1-11 months: 300 mg
Children 1-9 years: 600 mg
Child 10-17 years: 1200 mg
Adults: 1200 mg

49
Q

Patients with suspected meningitis undergo a series on investigations including blood tests, …, neuroimaging (if indicated) and …

A

Patients with suspected meningitis undergo a series on investigations including blood tests, cultures, neuroimaging (if indicated) and LP.

50
Q

If there is concern about a non-blanching rash, sepsis, or rapidly-progressive disease, patients should be given urgent intravenous antibiotics (e.g. … 2 g STAT or chloramphenicol if severe penicillin allergy) whilst awaiting further tests.

A

If there is concern about a non-blanching rash, sepsis, or rapidly-progressive disease, patients should be given urgent intravenous antibiotics (e.g. ceftriaxone 2 g STAT or chloramphenicol if severe penicillin allergy) whilst awaiting further tests.

51
Q

Bedside tests for suspected meningitis

A

Throat swab

Respiratory viral screen (nasopharyngeal swab)

52
Q

Blood tests in suspected meningitis

A
Full blood count
Urea & electrolytes
Liver function tests
Bone profile
Coagulation
C-reactive protein
Blood cultures
Venous blood gas
Meningococcal PCR
53
Q

A CT head is often completed as part of the work-up for meningitis. This is predominantly to look for any contraindications to lumbar puncture instead of being used as a diagnostic tool.

Not all patients require a CT head. In general, the main indications include:(6)

A

Immunocompromised patient
History of CNS disease (e.g. tumour, stroke, abscess)
New-onset seizures (within a week of illness)
Swollen optic discs: assess with direct ophthalmoscope or slit-lamp
Abnormal conscious level
Focal neurological deficit (e.g. limb weakness, cranial nerve palsy)

54
Q

Not all patients require a CT head. In general, the main indications include:

Immunocompromised patient
History of CNS disease (e.g. tumour, stroke, abscess)
New-onset seizures (within a week of illness)
Swollen optic discs: assess with direct ophthalmoscope or slit-lamp
Abnormal conscious level
Focal neurological deficit (e.g. limb weakness, cranial nerve palsy)

Why do we do this?

A

The reason to perform a CT head in these situations is because of the small, but increased, risk of brain herniation with lumbar puncture with raised intracranial pressure (ICP). On CT, features of raised ICP include effacement of the ventricles, basal cisterns and/or other CSF areas, brain herniation or loss of grey-white matter differentiation. Effacement refers to obliteration of a cavity or space by mass effect (e.g. raised ICP or tumour).

In addition, neuroimaging is useful at looking for an alternative diagnosis or complication of meningitis (e.g. abscess). These would be suggested by the clinical situations described above.

55
Q

Why do we perform a CT head in some individuals with suspected meningitis?

A

The reason to perform a CT head in these situations is because of the small, but increased, risk of brain herniation with lumbar puncture with raised intracranial pressure (ICP). On CT, features of raised ICP include effacement of the ventricles, basal cisterns and/or other CSF areas, brain herniation or loss of grey-white matter differentiation. Effacement refers to obliteration of a cavity or space by mass effect (e.g. raised ICP or tumour).

In addition, neuroimaging is useful at looking for an alternative diagnosis or complication of meningitis (e.g. abscess). These would be suggested by the clinical situations described above.

56
Q

Lumbar puncture with analysis of the … is the key investigation in the work-up of meningitis.

A

Lumbar puncture with analysis of the CSF is the key investigation in the work-up of meningitis.

57
Q

Every patient with suspected meningitis should undergo …

A

Every patient with suspected meningitis should undergo LP and CSF evaluation. Ideally, an LP should be performed before the administration of antibiotics to improve the diagnostic yield of CSF culture. However, in ‘real-life’ clinical practice this is often difficult and therefore antibiotics have usually already been administered.

58
Q

An LP involves the insertion of a spinal needle into the … space and taking a sample of CSF. It is important to determine the opening pressure with the patient lying on their side in a lateral position. This is a surrogate marker of ICP.

A

An LP involves the insertion of a spinal needle into the subarachnoid space and taking a sample of CSF. It is important to determine the opening pressure with the patient lying on their side in a lateral position. This is a surrogate marker of ICP.

59
Q

CSF samples should be sent to biochemistry and microbiology for the following tests: (meningitis) - 7

A

Cell count and differential
Protein
Glucose (paired with serum glucose)
Microscopy, cultures & sensitivity (MC&S)
Viral PCR
Save sample (can subsequently be used to run other tests)
Others (if indicated): cryptococcal antigen (paired with serum), TB PCR

60
Q

Interpretation - CSF sample in suspected meningitis

A

Isolation of a pathogen on MC&S (e.g. bacteria) or PCR (e.g. virus) will confirm the diagnosis. However, this may take time to come back, especially if the initial gram stain for a bacterial pathogen is negative. Therefore, the general appearance, opening pressure, cell count, protein and glucose concentration are used in combination to determine the suspected diagnosis.

61
Q

Isolation of a pathogen on MC&S (e.g. bacteria) or PCR (e.g. virus) will confirm the diagnosis. However, this may take time to come back, especially if the initial gram stain for a bacterial pathogen is negative. Therefore, the general appearance, opening pressure, cell count, protein and glucose concentration are used in combination to determine the suspected diagnosis. (CSF)

A
62
Q

In bacterial meningitis, the prompt administration of … is the principle treatment.

A

In bacterial meningitis, the prompt administration of antibiotics is the principle treatment.

63
Q

The first-line antibiotic for bacterial meningitis is …, which is a 3rd generation cephalosporin.

This should be given as 2 grams twice daily. It should be used with caution in patients with penicillin allergy due to cross-reactivity. If there is a severe penicillin allergy (e.g. anaphylaxis) it should be avoided. Further choice antibiotic choices depends on the suspected, or isolated, bacterial pathogen (e.g. amoxicllin if concern about L. monocytogenes.

A

The first-line antibiotic for bacterial meningitis is ceftriaxone, which is a 3rd generation cephalosporin. This should be given as 2 grams twice daily. It should be used with caution in patients with penicillin allergy due to cross-reactivity. If there is a severe penicillin allergy (e.g. anaphylaxis) it should be avoided. Further choice antibiotic choices depends on the suspected, or isolated, bacterial pathogen (e.g. amoxicllin if concern about L. monocytogenes.

64
Q

The second line antibiotic in bacterial meningitis after ceftriaxone is … (~25 mg/kg, max dose 1 gram QDS). This should be given to those with a severe penicillin allergy. In these situation it is usually recommended to discuss with microbiology.

A

The second line antibiotic is chloramphenicol (~25 mg/kg, max dose 1 gram QDS). This should be given to those with a severe penicillin allergy. In these situation it is usually recommended to discuss with microbiology.

65
Q

… can be considered as a treatment adjunct in patients highly suspected of having bacterial meningitis, especially pneumococcal meningitis. It may reduce development of neurological complications. It should be given in close association with the initial antibiotic dose for maximal effect. It can be continued in confirmed S. Pneumoniae meningitis.

A

Dexamethasone can be considered as a treatment adjunct in patients highly suspected of having bacterial meningitis, especially pneumococcal meningitis. It may reduce development of neurological complications. It should be given in close association with the initial antibiotic dose for maximal effect. It can be continued in confirmed S. Pneumoniae meningitis.

66
Q

Management of viral meningitis

A

Supportive treatment with rest, hydration, analgesia and antipyretic can be considered. If there is concern about encephalitis or HSV infection then aciclovir can be considered.

67
Q

Acute meningitis is a … disease.

A

Meningitis is a notifiable disease and many pathogens that cause meningitis (e.g. N. meningitidis, invasive S. pneumoniae) are notifiable organisms. This means PHE, usually via notification of the ‘proper officer’ at a local council or local health protection unit, need to be informed once the disease is confirmed or organism isolated.

68
Q

Contact tracing and … should be considered in close contacts following a case of acute meningitis.

A

Contact tracing and chemoprophylaxis should be considered in close contacts following a case of acute meningitis.

69
Q

Contact-tracing in meningitis

A

This involves identifying individuals who have come into close contact with the patient affected by meningitis. This is usually close household contacts. Contact-tracing is orchestrated by the local health protection team.

70
Q

Examples of close contacts:

A

Prolonged contact within 7 days of illness onset (e.g. household member, sharing halls of residence, partner)
Transient close contact but exposed to large respiratory secretions (usually around time of hospital admission)

71
Q

Chemoprophylaxis

A

This is the administration of antibiotic prophylaxis in at-risk close contacts to prevent the risk of developing acute meningitis in case they have asymptomatic carriage of the pathogen

This should be completed following confirmed cases of meningococcal meningitis regardless of vaccination status. Antibiotic choices in adults:

Ciprofloxacin: 500 mg single dose
Rifampicin: 600 mg twice daily for two days

72
Q

The UK vaccination programme is important for prevention of bacterial meningitis. The programme includes vaccines against H. …, N…. S. pneumoniae.

A

The UK vaccination programme is important for prevention of bacterial meningitis. The programme includes vaccines against H. influenza, N. meningitidis, S. pneumoniae.

73
Q

… vaccine: protects against H. influenzae type B. Given as part of childhood vaccination programme, in patients with complement deficiency and hyposplenism

A

Hib vaccine: protects against H. influenzae type B. Given as part of childhood vaccination programme, in patients with complement deficiency and hyposplenism

74
Q

… and MenACWY vaccines: protects against different serogroups of N. meningitidis. Given as part of childhood vaccination programme, in patients with complement deficiency and hyposplenism

A

MenB and MenACWY vaccines: protects against different serogroups of N. meningitidis. Given as part of childhood vaccination programme, in patients with complement deficiency and hyposplenism

75
Q

Pneumococcal conjugate vaccine: protects against 13 serogroups of S. …. Given as part of childhood vaccination programme, to all adults > 65 years old and those with major co-morbidities (including complement deficiency and hyposplenism).

A

Pneumococcal conjugate vaccine: protects against 13 serogroups of S. pneumoniae. Given as part of childhood vaccination programme, to all adults > 65 years old and those with major co-morbidities (including complement deficiency and hyposplenism).

76
Q

Vaccination against encapsulated bacteria is important in patients with hyposplenism. Why?

A

Vaccination against encapsulated bacteria is important in patients with hyposplenism. This is because encapsulated bacteria are poorly opsonised (i.e. attachment of complement) and reliant on removal by resident splenic phagocytes. Without a spleen, patients are at risk of overwhelming infections.

77
Q

Immediate complications of bacterial meningitis

A

Severe sepsis and multi-organ failure
Seizures (20-30% of adults)
Cerebral oedema
Death

78
Q

Chronic complications of meningitis

A
Hearing loss and deafness
Seizure disorder
Focal paralysis
Cranial nerve defects
Hydrocephalus
Cognitive impairment
Gait disturbance
Peripheral gangrene
Blindness
79
Q

Waterhouse–Friderichsen syndrome - what is this?

A

This describes a classical syndrome causing primary adrenal insufficiency (Addison’s disease) due to bilateral adrenal gland haemorrhage. It usually occurs in association with severe bacterial infection such as meningococcal septicaemia.