E2-Immune System-Horners Syndrome Flashcards

1
Q

what is an innate cell

A

non specific from birth
monocytes, neutrophils, basophils, mast cells, natural killer cells

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2
Q

what are adaptive cells

A

acquire following exposure
remember foreign invaders
B and T cells/lymphocytes

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3
Q

what are macrophages and dendritic cells

A

innate and adaptive cells

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4
Q

where do stem cells occur and what do they generate

A

bone marrow
immune cells

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5
Q

what are neutrophils

A

predominantly leukocyte or WBC
1st cells to arrive
phagocytosis

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6
Q

what are monocytes and macrophages

A

long lived
monocytes mature into macrophages
filter pus/bacteria from neutrophils and kill larger pathogens

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7
Q

what are eosinophils

A

next cells to participate
handle larger invading pathogens

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8
Q

what do eosinophils release

A

histamine- vasodilator to improve circulation

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9
Q

what are B lymphocytes

A

produce antibodies in reaction to antigens or foreign bodies

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10
Q

what are T lymphocytes

A

stimulate B lymphocytes that are directly kill infected host cells

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11
Q

what are presenting antigens

A

they present antigens to T lymphocytes to ingest/digest pathogens

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12
Q

what are natural killer cells

A

large lymphocytes
directly kill cells infected by pathogens
activate macrophages

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13
Q

what is our first line of defense

A

innate cells
resolve most threats
external/internal defenses

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14
Q

what are our external defenses

A

physical, chemical, and mechanical barriers that limit host penetration
skin, mucus, coughing, sneezing, stomach acid, etc

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15
Q

what are our internal defenses

A

soluble factors- modify cell behavior and enhance inflammatory response
innate cells and components from birth

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16
Q

what is our 2nd line of defense

A

inflammatory response
vascular response and plasma protein systems

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17
Q

what is the vascular response

A

activated at time of injury or exposure
series of vascular and cellular activities
possibly start a fever
natural killer cells

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18
Q

what is the plasma protein systems

A

clotting to control bleeding
kinin

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19
Q

what is kinin

A

produces vasodilation and vascular permeability
makes debris/pathogen vulnerable to phagocytosis

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20
Q

what is the 3rd line of defense

A

adaptive immunity

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21
Q

what is adaptive immunity

A

acquired and reactive
characterized by specificity and memory of a pathogen- B/T cells
days to weeks to respond
develops throughout life
responds with exposure

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22
Q

what is active immunity

A

concept of most vaccinations using a harmless virus to produce a secondary immune response with antibodies and memories

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23
Q

what is passive immunity

A

passing of antibodies through birth/breast feeding but is only temporary due to lack of memory cells

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24
Q

what is cell mediated immunity

A

not involving antibodies but instead cells like WBCs and B and T cells that can kill antigens

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25
Q

what are the phases of the immune response

A

recognition phase
amplification phase
effector phase
termination phase
memory

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26
Q

what factors negatively affect immunity

A

aging
hormonal imbalances
environment pollution
trauma or illnesses
inadequate sleep
lack of exercise
stress
dysfunctional gut

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27
Q

how does exercise affect immunology

A

enhanced or suppressed
moderate intensity is beneficial
overtraining without adequate recovery can impair immunity

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28
Q

what is a primary immunodeficiency disease

A

genetic defect involving T cells, B cells, or lymphoid tissues

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29
Q

what is secondary immunodeficiency

A

results from an underlying disease or factor that depresses or blocks the immune response
most common

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30
Q

what is acquired immunodeficiency syndrome (AIDS)

A

massive destruction of the immune system by HIV

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31
Q

what is AIDS patho

A

HIV depletes T lymphocytes along with other immunity cells
very high mutation rate

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32
Q

what are the S&S of AIDS

A

constitutional S&S
distal peripheral neuropathy, balance/gait deficits, myalgia and arthralgia, bone degradation
integumentary breakdown
lipodystrophic syndrome

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33
Q

what conditions can increase morbidity and mortality in AIDS

A

cardiopulmonary

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34
Q

what is lipodystrophic syndrome

A

central fat accumulation in neck and trunk but a decrease in extremities

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35
Q

what are the PT implications for AIDS

A

unrestricted with usual benefits for initial asymptomatic HIV
more limited with symptomatic and advanced HIV= less beneficial

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36
Q

What is chronic fatigue syndrome

A

Immune dysfunction syndrome characterized by unexplained fatigue >4 months limiting ADLs

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37
Q

What are the risk factors for chronic fatigue syndrome

A

Minority females with lower socioeconomic status
Immune deficits
Traumatic events
Poorly managed stress
Abnormal neuroendocrine function

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38
Q

What are the S&S of chronic fatigue syndrome

A

Varied
Overwhelming fatigue
Muscle pain and weakness
Forgetfulness
Hypotension that worsens through the day

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39
Q

What are the PT implications of chronic fatigue syndrome

A

Lifestyle management for stress, sleep, diet, actively levels
Gentle graded exercise

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40
Q

What is hypersensitivity disorder

A

Inaccurate response of the immune system
No response the first time, but occurs 2nd exposure

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41
Q

What is type 1 hypersensitivity disorder

A

Immediate type
Seasonal or food allergy
Anaphylactic or severe

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42
Q

What is type 2 hypersensitivity

A

Tissue or organ specific
Autoimmune condition- tissue and it’s cell function are diminished
Antibody binds to antigen on tissue or cell surface

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43
Q

What is type 3 hypersensitivity

A

Immune complex mediated
Antibody binding to antigen and then released in circulation
Systemic lupus erythematosus attacks immune tissue throughout the body
Tissue but not organ specific

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44
Q

What is type 4 hypersensitivity

A

Cell mediated immunity
Only hypersensitivity not involving antibodies
T lymphocytes are present and kill target cells it does not recognize
Graft rejection, RA, MS, diabetes, contact allergen

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45
Q

What is autoimmune diseases and RF

A

Can’t distinguish body from non self
Genetic
Hormonal
Environment
Infections

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46
Q

What are the S&S of autoimmune diseases

A

GI S&S
Gradual onset
Inflammation
Swollen lymph nodes
Affects more than 1 area of body
Emotional changes

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47
Q

What are PT implications of autoimmune diseases

A

Infection control
Exercise prescription
Nutritional guidance
Sleep health
Corticosteroids medications

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48
Q

What are the side effects for corticosteroid medications in PT setting

A

Bone loss
More susceptible to fx, osteoporosis, avascular necrosis
Offset ideally with WB and resistance exercises
Avoid jt mobilization
Decrease healing
Increase susceptibility to infection

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49
Q

what are the RF and S&S for lupus

A

primarily young women and minorities
all systems maybe involved

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50
Q

what are the PT implications for lupus

A

protection with bracing/assistive devices
energy conservation
monitor symptoms
gentle and regular exercise

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51
Q

what is spondyloarthropathies or spondyloarthritides

A

group of diverse autoinflammatory conditions that affect the spine more than extremity jts

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52
Q

what are the common features of spondyloarthropathies or spondyloarthritides

A

gradual onset
> 30 minutes of P! after prolonged positions
chronic inflammation of axial skeleton
extraarticular involvement- eyes, skin, GI tract, renal and cardiac

53
Q

what are the RF for sjogren syndrome

A

postmenopausal women

54
Q

what is the patho of sjogren syndrome

A

exocrine glands, mainly salivary and lacrimal glands destruction

55
Q

what are the S&S of sjogren syndrome and the hallmark

A

spondyloarthritide S&S
peripheral neuropathy due to vasculitis
fatigue
sleep disturbance
DRY EYES AND MOUTH

56
Q

what is fibromylagia

A

chronic widespread myalgia

57
Q

what are the RF of fibromyalgia

A

women
20-55 yrs
minimal fitness levels

58
Q

what can trigger fibromylagia

A

prolonged anxiety and stress
trauma
rapid steroid withdrawal
thyroid disorders
infections

59
Q

what is the patho of fibromyalgia

A

misprocessing of pain with sensitization and nociplastic pain
micro spasms of muscles - impaired circulation and fatigue
hypothalmic pituitary adrenal gland dysfunction - response to stress

60
Q

how does the ANS respond to fibromyalgia

A

hyperactive flight or fight
hypoactive parasympathetic
increase of immune cells

61
Q

how does pain affect immune system

A

more cells = more release of pain neurotransmitters = same nociplastic pain response

62
Q

what are the results for test and measures with fibromyalgia

A

all imaging and blood tests are negative
Dx by exclusion

63
Q

how would we treat fibromyalgia

A

pt education and exercise prescription

64
Q

what is the MET for fibromyalgia

A

low to moderate global aerobic and resistance exercise
2-3x/wk
60-90 min
> or = to 13 weeks

65
Q

what are PT implications for fibromyalgia

A

nutritional guidance
stress management
minimal benefits

66
Q

what is multiple sclerosis

A

chronic and progressive neurodegenerative disorder of the CNS

67
Q

what is MS RF

A

white females between 20-50 years
autoimmune response
genetic link

68
Q

what is MS patho

A

demyelination
block neural transmission

69
Q

What are the S&S of MS

A

specific to CNS involvement
exacerbations and remissions
FATIGUE
optic neuritis

70
Q

what is the 1st S&S to be manifested with MS

A

optic neuritis

71
Q

what gives a sudden transient shock pain to the face

A

trigeminal neuralgia

72
Q

what are the neuromusculoskeletal S&S

A

abnormal speech or swallowing
incoordination and muscle tone
bowel and bladder
sexual dysfunction

73
Q

what are the S&S found in the scan for MS

A

resisted testing with multiple jt weakness
neuro tests - UMN findings

74
Q

what special tests can be done to confirm MS

A

balance
central vertigo
lhermitte sign

75
Q

what is our course of Rx for MS

A

urgent referral

76
Q

what is the etiology of CVA

A

ischemic and hemorrhagic

77
Q

what is the leading cause of long term disability

78
Q

what are the nonmodifiable RF for CVA

A

age
african americans
women

79
Q

what are the modifiable RF for CVA

A

CV disease and HTN
diabetes
lifestyle

80
Q

what is CVA

A

disrupted blood flow to the brain

81
Q

what are the S&S of CVA

A

all SUDDEN onset
multisegmental hemi face
visual disturbance
speech and swallowing impaired
severe headache
unexplained dizziness or falls

82
Q

what is found in scan for CVA

A

resisted testing with multiple jt weakness
neuro tests - UMN findings, hyperreflexive/clonus

83
Q

what is our course of Rx for CVA

84
Q

what can cause posterior circulation compromise

A

CVA
patho jt instability
atherosclerosis - ICA
sudden arterial dissection
tumors
VBI
presyncope

85
Q

what artery supplies the trigeminal n

86
Q

what are the 5 D’s And 3 N’s

A

dysphagia
dysarthria
diplopia
dizziness
drop attacks
Ataxia - incoordination
headache
nausea
nystagmus
numbness

87
Q

what is our course of Rx for posterior circulation compromise

88
Q

what is presyncope dizziness

A

near fainting and lightheadedness without the spinning

89
Q

what can cause presyncope dizziness

A

stress or medications (cardiovascular)

90
Q

what are the S&S of dizziness presyncope

A

generalized weakness
giddiness
pallor
5 D and 3 N

91
Q

what is our course of Rx for dizziness presyncope

92
Q

what is vertigo

A

the illusion of spinning or rotary motion

93
Q

what is peripheral vertigo

A

BPPV
crystals become from free floating in semicircular canals

94
Q

what is primary central vertigo

A

CVA or tumor

95
Q

what is secondary vertigo

A

trauma creating brain injury
infection
demyelination
migraine

96
Q

what is central vertigo patho

A

due to ischemia to cerebellum, brainstem, vestibular

97
Q

what are the S&S of peripheral vertigo

A

severe nausea
greater spinning primarily with horizontal nystagmus
worse with head movements
hearing loss
refer to vestibular PT

98
Q

what are S&S of central vertigo

A

UMN signs including 5 D and 3 N
severe perception with linear perception
vertical nystagmus
occurs at rest
severe imbalance
emergency

99
Q

what is BPPV

A

most common type of peripheral vertigo

100
Q

why is central vertigo an emergency referral

A

due to ischemia to cerebellum, brainstem, and vestibular neclei

101
Q

what is dysequilibrium

A

unsteadiness without illusion of spinning

102
Q

what are the 3 primary systems affected during dysequilibrium

A

proprioception
vestibular
visual

103
Q

what can cause dysequilibrium

A

brain degeneration
aging
neuromusculoskeletal diseases

104
Q

what do we do for dysequilibrium

A

assess/treat any MSK condition to improve somatosensory function and balance triad
potential urgent referral for vestibular or vision

105
Q

what is non specific dizziness

A

may be due to psychophysiological or cervical origins

106
Q

how can psychophysiological cause dizziness

A

vasoconstriction with SNS response

107
Q

what are the S&S for psychophysiological dizziness

A

motion sickness
giddiness
feeling removed from the body
sensation of floating
subjective postural balance with normal balance tests

108
Q

what is the Rx for psychophysiological dizziness

A

urgent referral to psych

109
Q

what can cause cervicogenic dizziness

A

C2-3 dysfunction
abnormal afferent signals from neck to trigeminal nucleus

110
Q

what is the S&S for cervicogenic dizziness

A

dizziness with neck motion
head and face parasympathetic symptoms
no illusion of spinning or nystagmus

111
Q

what is cervical myelopathy

A

slow gradual and often progressive compression on cord

112
Q

what can cause cervical myelopathy

A

lax and buckling lig flavum
ARJC
ARDC
vertebral body collapse

113
Q

what are S&S of cervical myelopathy

A

multiple directions of weak and painful resisted testing
wide based gait
incoordination
Cooks CPR +

114
Q

how do we treat cervical myelopathy

A

emergency referral with immobilization

115
Q

what is meningitis

A

infection leading to inflammation of the brain and spinal cord meningeal membrane

116
Q

what can meningitis cause that can affect the cord

A

scar tissue that restricts CSF that can lead to hydrocephalus or decreased blood flow leading to a stroke

117
Q

what are the typical S&S for meningitis

A

constitutional S&S (fever and N&V)
neck pain and stiffness
photophobia
HA

118
Q

what are the S&S for intracranial pressure

A

altered mental status
cranial n deficits
seizures
motion of bending over, lying down, lifting heavy weight

119
Q

what are the S&S of viral meningitis

A

infection and GI

120
Q

what are the S&S of bacterial meningitis

A

infection and respiratory

121
Q

what test to rule out meningitis

A

jolt accentuation of HA test
HA worsened by neck RT (2-3 turns in a sec)

122
Q

what test to rule in meningiits

A

Kernig- low back and posterior thigh pain combined with hip flexion and knee ext
Brudzinski- neck flexion produces hip and knee flexion

123
Q

how do we treat meningitis

A

emergency referral

124
Q

where can the brain tumor come from

A

lung- most common
breast and skin

125
Q

what can the brain tumor do

A

compression of cerebral tissue
at times erosion of bone with growth
edema and intracranial pressure

126
Q

what are the S&S for brain tumor

A

cancer S&S
HA increased with activity (looking down, coughing, straining, exercise)
ataxia
diplopia
painful eye motion
tinnitus
seizures
speech impairment

127
Q

what causes horners syndrome

A

pancoast tumor in apical of lung that compresses the sympathetic ganglion at cervicothoracic junction

128
Q

what does the the compression of the sympathetic ganglion in horners syndrome cause

A

interruption of sympathetic n supply to the eye

129
Q

what are the S&S of horners syndrome

A

unilateral
ptosis
lack of face sweating
sunken eyeball
miosis
possibly pain at top of shoulder