Patho EXAM review Flashcards

1
Q

what is delirium

A

acute decline in the cognitive process of the brain (attention and cognition)

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2
Q

what age group does delirium generally affect?

A

65+

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3
Q

How does delirium influence cognitive function throughout the day?

A

cognitive function fluctuates through the day

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4
Q

What rate and why is delirium underreported?

A

2/3 cases are unreported because it is under-recognized due to variable signs and symptoms

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5
Q

what is the 1 year mortality rate?

A

35-40%

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6
Q

why is it important to address delirium?

A

delirium initiates a cascade of pathophysiological changes that can lead to loss of independence, increased morbidity and death.

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7
Q

what is the diagnostic criteria for delirium?

A
  • disturbance in attention and awareness
  • develops over a short period of time
  • change from baseline attention and awareness and - fluctuates in severity during the day
  • additional disturbance in cognition
  • disturbances are not well explained by other/pre-existing neurocognitive disorders
  • evidence from history/labs/physical exams show that the disturbance is a direct physiological consequence of another medical condition/intervention
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8
Q

what are the clinical features of delirium?

A
  • acute onset
  • fluctuating course
  • inattention
  • disorganized thinking
  • altered LOC
  • cognitive deficits
  • perceptual disturbances (illusions)
  • psychomotor disturbances
  • altered sleep-wake cycles
  • emotional disturbances
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9
Q

how does delirium differ form dementia, how are they the same

A

Similarities:

  • both have impaired recent and remote memory
  • orientation is impaired in delirium and may be impaired in dementia

Differences

  • onset delirium is quick dementia is chronic
  • course: delirium is short and worse at night and on awakening. Dementia is long, symptoms progress and stable over time
  • progression: delirium is abrupt. Dementia is slow but even
  • duration: delirium takes hours to less than one month. Dementia takes months to years
  • awareness: delirium is reduced. Dementia is clear
  • Attention: delirium is impaired and fluctuates. Dementia is generally normal
  • thinking: delirium had disorganized, disoriented, incoherent and fragmented. Dementia there are impoverished thoughts, words are hard to find and poor judgment
  • perception: delirium perception is disoriented, delusions & hallucinations, difficulty distinguishing between reality and misperceptions. Dementia, misperceptions are often absent
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10
Q

how does delirium differ from depression, how are they similar?

A

Similarities:
-diurnal effects (worse in the mornings)

Differences in

  • onset
  • course
  • Progression
  • duration
  • awareness
  • alertness
  • attention
  • orientation
  • memory
  • thinking
  • perception
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11
Q

what are the types of delirium?

A

hyperactive, hypoactive and mixed

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12
Q

what are the characteristics if hyperactive delirium?

A
  • restlessness, constant movement and agitation
  • insomnia, hyper-vigilance, irritabilty, rpaid speech, distractibility
  • may be mistaken for shizophrenia, bipolar or agitated dementia
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13
Q

what are the characteristics of Hypoactive delirium?

A
  • most common in 65+
  • slow or lacking movement, paucity (little to no) speech with or without prompting, unresponsiveness, decreased alertness
  • may be mistaken for depression and is associated with higher mortality
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14
Q

what are the characteristics of mixed delirium

A
  • more disruptive

- alternates between hypoactive and hyperactive

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15
Q

what causes delirium?

A

predisposing factors and precipitating factors

- 3 or more increase the risk of delirium by 60%

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16
Q

what is the pathophysiology of delirium?

A

The pathophysiology of delirium is poorly understood. The fluctuating course is the hallmark of delirium. there are multiped interacting risk factors. Most likely more than one neurobiological mechanism

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17
Q

what does the neuroinflammatory hypothesis of delirium entail?

A
  • systemic inflammation is a predominant feature of many surgical and medical conditions associated with delirium
  • delirium has clinical features of sepsis, UTIs, pneumonia, MIs, fractures etc
  • delirious patients have higher blood plasma levels of inflammatory cytokines than pts. without delirium
  • this creates an increased permeability of the BBB
  • change occurs in all places that combat acute infections (ie. cytokine production, neuronal cell proliferation and HPA axis activations
  • this explains how peripheral changes can affect brain function
  • also explains why older individuals are more susceptible
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18
Q

what does the neurotransmitter hypothesis of delirium entail?

A
  • acetylcholine is decreased and responsible for memory & cognition
  • anticholinergic drugs cause delirium in healthy adults in the elderly population
  • dopamine has an inhibitory effect on cholinergic activity. This means that dopamine agonists induce delirium and antagonists can treat delirium
  • there are precipitating factors that can decrease acetylcholine synthesis in the brain
  • high levels of serum anticholinergic activity are associated with increased risks of delirium
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19
Q

how can delirium be prevented

A
  • modify risk factors
    Interventions include:
  • orientation and therapeutic activity protocols, non-pharmacological sleep and sleep enhancement protocols, early mobilization protocol, vision protocol, hearing protocol, dehydration protocol
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20
Q

how is delirium managed

A
  • monitor changes in mental status
  • perform CAM
  • identify and treat the underlying cause
  • provide supportive care and prevent complications
21
Q

what drugs are used to treat delirium

A
  • antipsychotics are durg of choice
  • low dose haloperidol
  • atypical antipsychotics (not great tho)
  • non-pharm interventions should be attempted first
22
Q

how are delirium and dementia, related?

A

-dementia is a predisposing risk factor for delirium (interrelated)
- both are associated with decreased cerebral blood flow, cholinergic deficiency and inflammaiton
- delirium worsens
dementia
-2/3 delirium patients have dementia

23
Q

what tool is used to screen for delirium?

A
  • Confusion Assessment Method
24
Q

what are the benefits and draw-backs of the CAM

A

Benefits

  • questions are answered using yes or no
  • uses components form the clinical features of delirium
  • scoring is based on presence of acute onset AND fluctuating course and inattention and disorganized thinking or altered LOC

Draw-backs
- lacks ability to rate the severity

25
Q

what are predisposing factors for delirium?

A

baseline characteristics

  • demographics
  • cognitive status
  • functional status
  • sensory impairment
  • decreased oral intake
  • drugs
  • coexisting medical conditions
26
Q

what are precipitating factors for delirium?

A
  • drugs
  • primary neurologic diseases
  • incurrent illness (shock, hypoxia, fever)
  • surgery
  • environmental (ICU, restraints)
  • prolonged sleep deprivation
27
Q

what is the most significant risk factor for persistent delirium?

A

physical restraints

28
Q

what is the primary goal of adaptive immunity?

A

maintain homeostasis by protecting the body from pathogens, foreign molecules and harmful toxins

29
Q

what are the first line barriers?

A
first-line INTRINSIC barriers 
physical barriers (skin and mucous membranes), mechanical (cough, sneeze), chemical (decreased pH of the stomach), microbiological (commensal flora, resource competition)
30
Q

what are the second line barriers?

A

second line INNATE barriers (broad-spectrum): phagocytes, NK cells, inflammation, antimicrobial proteins (interferons, compliment), fever

31
Q

what are the third line barriers?

A

third line ADAPTIVE immunity: cellular response (targeted killing of infected abnormal cells), humoral response (production of soluble immunoglobulins or antibodies that confer protection from specific pathogens by many functions)

32
Q

what are the hallmarks of adaptive immunity response?

A
  • specificity (self vs. non-self)

- Memory: the ability to recall past exposures

33
Q

what are the differences between innate and adaptive immunity

A

INNATE

  • broad specificity (recognize broadly conserved PAMPs which are recognized by TLRs on phagocytes)
  • limited repertoire (PRRs are encoded by germ line DNA limiting PAMPs)
  • immediate response
  • lacks memory

ADAPTIVE

  • narrow specificity
  • vast repertoire
  • slow repsonse
  • memory
34
Q

where does the adaptive response originate from?

A

secondary lymphoid tissues which include…

  • spleen
  • MALT
  • lymph nodes
35
Q

what is the function of each of the secondary lymphoid tissues?

A

Spleen: filters blood of pathogens
MALT (mucosal-associated lymphoid tissue): filters pathogens of mucosal surfaces before spreading
Lymph nodes: immune surveillance

36
Q

lymph nodes are places systematically through the body so that what can occur

A

slows the blood flow so that T and B cells have enough time to respond to pathogens

37
Q

what do lymph nodes contain?

A

they contain macrophages and dendritic cells that migrated from infected areas leading to the area where innate and adaptive systems interact

38
Q

where do proliferating B cells differentiate?

A

germinal cnetre

39
Q

how does lymph enter and leave the nodes?

A

afferent and efferent vessels

40
Q

where to T cells originate?

A

red bone marrow

41
Q

where do B cells maure?

A

red bone marrow

42
Q

where to b cells originate from?

A

red bone marrow

43
Q

where do T cells mature?

A

thymus

44
Q

what do B cells target

A

extracellular pathogens

45
Q

what do T cells target?

A

intracellular pathogens and cancers

46
Q

what kind of response do b cells have?

A

cell-mediates response that secretes cytokines

47
Q

what kind of response do T cells have?

A

antibody/ humoral response

48
Q

T/F: B and T cells can damage host tissues?

A

true

49
Q

what are PAMPs?

A

pathogen-associated molecular patterns