Viral CNS Infections Flashcards

1
Q

Two primary ways that viruses get into the CNS?

A

Blood and Neurons

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2
Q

What is meningitis?

A

Inflammation of the lining of the brain

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3
Q

What is Encephalitis?

A

Inflammation of the brain tissue

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4
Q

What is Meningoencephalitis?

A

Widespread infection of the meninges and brain

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5
Q

What is encephalopathy? Common cause?

A

Damage to brain tissues: Prions

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6
Q

What is aseptic meningitis?

A

Meninges are inflamed and pyogenic bacterial source is not to blame; Infectious bug cannot be determined.

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7
Q

What are typical causes of aseptic meningitis? What is the most common type of viral infection?

A

Virus, fungi, TB; Enterovirus (90%)

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8
Q

Describe lumbar puncture findings of aseptic meningitis

A

Increased WBCs but no CSF

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9
Q

What Tx is used for aseptic meningitis?

A

Not many options but few options for herpes, fungal, and mycobacterial infections

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10
Q

What is Brudzinski’s sign?

A

Lift patient’s head upward when in the supine position and knees will bend up indicating meningitis

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11
Q

Describe the general progression of encephalitis

A

Virus (generally) -> influx of immune cells in brain -> Cerebral edema destroys neurons -> Hemorrhage

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12
Q

What are some urgent Syx of encephalitis?

A

Unresponsive/Coma, Seizures/Weakness/Paralysis, Memory Loss/Flat Affect/Withdrawal/Poor Judgement

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13
Q

How do you diagnose encephalitis?

A

Spinal tap indicates inflammation in CSF, blood (possibly), PCR for viruses; EEG/MRI/CT

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14
Q

What is the treatment for encephalitis? If herpes?

A

Supportive care/Syx relief, sedate (phenytoin), anti-inflamm/reduce edema (dexamethasone); Acyclovir

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15
Q

What are typical complications of meningitis? Encephalitis?

A

Generally benign, resolve in 2 wks; Permanent neurologic ipairments to memory, speech, vision, hearing, muscle control, or sensation

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16
Q

What are risk factors for viral CNS infection?

A
  • Age (older)
  • Immune status (Immunoincompetent)
  • Genetics (Innate resistance of viruses)
  • Exercise (may increase dissemination of virus)
17
Q

What is Acute Disseminated Encephalomyelitis (ADEM)?

A

Postinfectious encephalitis following viral infection by 1-2 wks; possibly autoimmune etiology

18
Q

What are the Alphaherpesviruses?

A

HSV-1/2, VZV;

19
Q

When can herpetic meningitis occur?

A

In both primary and recurrent infections

20
Q

What is the most common herpes virus that causes meningitis? What are other less frequent offenders?

A

HSV-1/2; VZV, CMV, EBV;

21
Q

Tx for herpesvirus meningitis?

A

Acyclovir, valaciclovir, famciclovir

22
Q

Describe the dessemination of Rabies Virus. Why is this relatively easy to treat?

A

Inoculated within an injured site -> Replicated w/i muscle -> Travel up nerve (slowly) -> Brain; It is so slow!

23
Q

How is rabies spread? What does the virus have a tropism for?

A

Through salivary glands! or organ transplants!

24
Q

What is the transmission of picornaviruses? Who does it affect? What are two to major Picornaviruses and which one are we currently worried about? What do we have a vaccine for?

A

Fecal-oral; Young children (mild disease), Old children, adult (asymp - paralytic); Polio and entero; Only to Polio

25
Q

What is the general rount of dissemination of picornavirus?

A

Mouth -> Oral/GI Mucosa -> Blood -> Brain

26
Q

What is the general circulating pattern of Arboviruses? What are the dead end hosts?

A

Betwixt birds and mosquitos; Horses and humans

27
Q

Name 4 Togaviruses

A

Venezuelan equine encephalitis, Eastern Equine Encephalitis, Western Equine Encephalitis, Chikungunya virus

28
Q

What are the subtypes of arbovirus we should know about?

A

Togavirus (WEE, VEE, EEE, Chikungunya) and Flavivirus (Japanese Encephalitis, St. Louis Encephalitis)

29
Q

When during the year are arboviruses most common?

A

Summer months

30
Q

How are arboviruses spread?

A

Mosquito

31
Q

Describe the basic pathogenesis of prion disease

A

Proteins (Prions) misfold -> aggregate -> fibril formation -> Disease (May come from exogenous causes as well)

32
Q

What is the major etiology of CJD? 2nd most? 3rd?=

A

Sporadic; Genetic; Iatrogenic

33
Q

Describe the pathology found in CJD? Time frame? Prognosis?

A

Brain atrophy, spongiform pathology; Dementia, loss of brain fn., 6-9 months until dead;

34
Q

Describe the Dx process for CJD

A

MRI (only suggestive), 14-3-3 protein in CSF, post-mortem analysis (autopsy general way to make Dx)

35
Q

Describe precautions for prion diseases. What are the highest risk body parts?

A

Currently all surgical/medical equipment is thrown out/incincerated; Brain, spinal cord, eye tissue

36
Q

What is a distinguishing feature of encephalitis?

A

Intracerebral hemorrhage

37
Q

What type of viral encephalitis would a patient likely get in the summer?

A

Enterovirus

38
Q

What is the route other than viremia where a virus may disseminate to the brain?

A

Retrograde transport from peripheral nerve endings or nasal mucosa!