Week 12- Screening for Immunologic Disease Flashcards

1
Q

PART 1

A

PART 1

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2
Q

Immunology:

  • Response to defend against attacks by “_______ _______”.
  • Immunity is provided by _______ cells.
  • Immune disorders are classified as what (4) things?
A
  • “foreign invaders”
  • lymphoid cells
  • Autoimmune*, immunodeficiency, hypersensitivity, and immunoproliferative disorders
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3
Q

What are some questions to ask during the patient interview if immune disorder is suspected?

A
  • How long have you had this problem? (chronic and repetitive)
  • Has the problem gone away then recurred? (cyclical pattern)
  • Have additional symptoms developed or have other areas become symptomatic over time?
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4
Q

_________ may be the only risk factor for immunologic disease.

A

Family Hx

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5
Q

Immunologic Disease S/Sx. (7)

A
  • Soft tissue/joint pain***
  • Stiffness***
  • Swelling***
  • Generalized weakness***
  • Constitutional symptoms***
  • Raynaud’s phenomenon***
  • Sleep disturbances***
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6
Q

Soft Tissue/Joint Pain:

  • Specific joints affected.
  • What joints are affected with RA?
  • What joints are affected with Psoriatic Arthritis?
A
  • RA = wrist and proximal small joints of hands and feet

- Psoriatic Arthritis = distal joints of hands and feet

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7
Q

Stiffness:

  • Marked by prolonged stiffness >_____.
  • What is the gel phenomenon?
A
  • > 1 hour

- Gel phenomenon = Symptoms relieved with activity but recurs after sitting and then attempting to continue activity.

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8
Q

What would we do if we note a cluster of S/Sx associated with immunologic disease?

A
  • Immunologic ROS

- Rheumatologic ROS

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9
Q

PART 2: IMMUNE SYSTEM PATHOLOGIES

A

PART 2: IMMUNE SYSTEM PATHOLOGIES

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10
Q

Immune System Pathologies. (11)

A
  • Fibromyalgia
  • Rheumatoid Arthritis (RA)
  • Polymyalgia Rheumatica
  • Scleroderma
  • Systemic Lupus Erythematosus (SLE)
  • Ankylosing spondylitis (AS)
  • Reiter’s syndrome or reactive arthritis (ReA)
  • Psoriatic arthritis (PsA)
  • Multiple Sclerosis (MS)
  • Guillain-Barre Syndrome (GBS)
  • Myasthenia Gravis (MG)
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11
Q

Autoimmune Disorders Overview:

  • When do autoimmune disorders occur?
  • Body manufactures _________ directed against the body’s own cellular components or specific organs.
  • What does this result in?
  • Is the exact cause known?
A
  • Occurs when the immune system fails to distinguish self from non-self and misdirects immune response against body’s own tissues.
  • autoantibodies
  • Results in abnormal tissue reaction and tissue damage.
  • Exact cause not well understood.
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12
Q

Fibromyalgia:

  • What is fibromyalgia?
  • Is it more common in men or women?
  • Recent evidence suggests that chronic pain is _______ _______.
  • The new set of diagnostic criteria to diagnose fibromyalgia focuses on measuring ____________ rather than relying on tender point examination alone.
  • ___/___ tender points to diagnose as fibromyalgia.
A
  • Noninflammatory condition appearing with generalized MSK pain with associated tenderness to palpation in a large number of specific areas.
  • Women > Men
  • CENTRALLY MEDIATED
  • symptom severity
  • 11/18***
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13
Q

Fibromyalgia S/Sx. (5)

A
  • Aches and pains
  • Stiffness
  • Swelling in soft tissue
  • Tender points
  • Muscle spasms or nodules

-Fatigue, morning stiffness, and sleep disturbances may be present but not necessary for diagnosis.

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14
Q

Rheumatoid Arthritis (RA):

  • _______, _______, _______ disorder.
  • Is it more common in men or women?
  • Most common between ages ___-___.
  • What is the cause?
  • Affects various organs but predominantly ________ tissues of _______ joints.
A
  • Chronic, systemic, inflammatory disorder.
  • Women > Men (2-3x)
  • 20-40
  • Unknown cause (support for genetic predisposition)
  • synovial tissues of synovial joints
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15
Q

RA S/Sx. (7)

A
  • Swelling in 1 or more joints
  • Early morning stiffness (>1hr)
  • Recurring pain/tenderness in any joint (MTP, MCP)
  • Inability to move joint normally
  • Obvious redness and warmth in joint
  • Unexplained weight loss, fever, or weakness combined w/ joint pain
  • Symptoms lasting >2 weeks
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16
Q

What is a mnemonic to remember RA S/Sx?

A

SERIOUS

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17
Q

RA Referral/Diagnosis:

  • Why is early referral/diagnosis important in RA?
  • What are some early inflammatory symptoms of RA? (3)
A

-Studies show 70-90% of people with RA have SIGNIFICANT JOINT EROSION 2 YEARS AFTER ONSET.

  1. ) Significant discomfort with compression of metacarpal and metatarsal joints.
  2. ) Presence of 3 or more swollen joints.
  3. ) More than 1hr of morning stiffness.
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18
Q

RA Hands/Feet:

  • ________ pain often first complaint.
  • ________-____ deformities.
  • ______ ________ of MCP joint and ulnar deviation.
  • _____ ______ and __________ deformities may also be present.
A
  • Forefoot pain
  • Hammer-toe
  • Volar subluxation
  • Swan Neck and Boutonniere Deformities
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19
Q

RA Cervical Spine:

  • _________ may be reported in early onset of disease.
  • ___-___ laxity secondary to inflammation of ligaments. (Occurs more often _____ in disease)
  • Could result in _________ _________ with resultant spinal cord compression.
A
  • Neck stiffness
  • C1-C2 laxity (late in disease)
  • atlantoaxial subluxation
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20
Q

RA Shoulder:
-Chronic synovitis may result in limitations of shoulder ROM, dislocation, or spontaneous tears of the ___________ or ________________.

RA Elbow:
-Destruction or articulation may result in ________ contracture, loss of ________/_______, subluxation or _______ nerve neuropathy.

RA Wrist:
-Frequently affected and may result in _________ muscle atrophy, _______ or __________ (due to volar synovitis).

A
  • rotator cuff or adhesive capsulitis
  • flexion contracture, loss of supination/pronation, subluxation, or ulnar nerve neuropathy
  • interosseous muscle atrophy, ankylosis or carpal tunnel syndrome
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21
Q

What are some extraarticular manifestations of RA? (6)

A
  • Rheumatoid nodules
  • Arteritis (inflammation of artery walls)
  • Neuropathy
  • Scleritis (inflammation of sclera)
  • Pericarditis
  • Splenomegaly
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22
Q

Diagnosis is made if the patient has __/__ of what criteria?

A

-4/7

  1. ) Morning stiffness
  2. ) Arthritis of 3 or more joints
  3. ) Arthritis of hands
  4. ) Symmetric arthritis
  5. ) Rheumatoid nodules
  6. ) Serum rheumatoid factor
  7. ) Radiographic changes
23
Q

Polymyalgia Rheumatica:

  • _______, rheumatic inflammatory disorder with unknown cause.
  • Occurs almost exclusively in people >___.
  • Is it more common in men or women?
  • What patient population is it predominantly in?
  • Characterized by severe ______ and _________ primarily in the _______ as opposed to the joints.
A
  • Systemic
  • > 50
  • Women > Men (2x)
  • Caucasian population
  • severe aching and stiffness primarily in muscles
24
Q

Polymyalgia Rheumatica S/Sx. (8)

A
  • Muscle pain or aching (proximal muscle groups)***
  • Stiffness upon arising in the morning or after rest***
  • Weakness, fatigue, malaise
  • Low-grade fever, sweats
  • HA
  • Weight loss
  • Depression
  • Vision changes
25
Polymyalgia Rheumatica: - Condition is _____-________. - Typically lasts __-__ years. - What is used to suppress inflammation, treat symptoms and provide remission but does not cure? - Important for PTs to be aware of the possibility of _______-_______ osteopenia and _______. - Most pts with this condition do not have lasting effects with medical intervention.
- self-limiting - 2-3 years - oral corticosteroids - steroid-induced osteopenia and DM
26
Scleroderma: - Chronic _________ disease. - Characterized by _________ and _______ of many body parts including skin, blood vessels, synovium, skeletal muscle, and certain internal organs. - What are the (2) main categories of scleroderma? - Who is it more common in?
- multisystem - inflammation and fibrosis - limited cutaneous scleroderma, diffuse cutaneous scleroderma - young/middle-aged women
27
Limited Scleroderma: - Characterized by long hx of _________ phenomenon. - Skin thickening is limited to _____. - Esophageal ________ is common.
- Raynaud's phenomenon - limited to hand - esophageal dysmotility
28
Diffuse Scleroderma: - More _______ onset. - Many constitutional symptoms, arthritis, carpal tunnel and marked swelling of hands and legs. - Wide-spread skin thickening occurs and progresses from ________ to _______. - _____________ problems are common (GI effects and pulmonary fibrosis common, severe life-threatening involvement of heart/kidneys occurs)
- acute onset - from fingers to trunk - internal organ
29
Limited Cutaneous Scleroderma S/Sx. (5)
- Calcinosis - Raynaud's Phenomenon - Esophageal dysmotility, dysphagia, heartburn - Sclerodactyly (thickening of skin of digits of hands and feets) - Telangiectasia (dilated/broken blood vessels near surface of skin) CREST***
30
Diffuse Cutaneous Sclerosis S/Sx. (6)
- Raynaud's Phenomenon - Trunk and extremity skin changes - Ulceration of fingers - Polyarthralgia - Flexion contractures of large and small joints - Visceral involvement
31
Systemic Lupus Erythematosus (SLE): - In family of _________ _______ disease. - Chronic, systemic, inflammatory condition affecting skin, joints, kidneys, heart and blood-forming organs, nervous system and mucous membranes. - What is the most common characteristic of SLE? - What are the (2) primary forms of SLE?
- autoimmune rheumatic diseases - butterfly rash across cheeks/nose - discoid lupus, systemic lupus
32
SLE Risk Factors: - Appears to be result of ___________ disturbance caused by interplay of genetic, hormonal, chemical, and environmental factors. - ___________ factors that may trigger include infections, antibiotics/other medications, exposure to UV (sun) light and extreme physical/emotional stress. - There is a known genetic predisposition but no known gene associated with SLE. - Most common in ___-___ years of age. (can occur at any age) - Are men or women affected more?
- immunoregulatory disturbance - environmental factors - 15-40 years - Women > Men (10-15x)
33
SLE S/Sx. (12)
-Arthralgia*** -Arthritis*** -Constitutional symptoms (low-grade fever & fatigue) -Skin rash (malar) -Pulmonary involvement -Anemia -Kidney involvement -Sun or light sensitivity -Hair loss -Raynaud's phenomenon -Nervous system involvement Mouth, nose, or vaginal ulcers
34
Spondyloarthropathy: - Group of __________, _________, _________ rheumatic diseases. - What does it target? - Is it more common in men or women? - What are the (3) main types?
- noninfectious, inflammatory, erosive rheumatic diseases - Targets SI, bony insertion of annulus fibrosis of IV discs and facet joint - Men > Women - ankylosing spondylitis, Reiter's syndrome, Psoriatic arthritis
35
What are the (3) main types of spondyloarthropathy?
- Ankylosing Spondylitis - Reiter's Syndrome - Psoriatic Arthritis
36
Ankylosing Spondylitis: - _______, _________ inflammatory disorder of undetermined cause. - Inflammation of fibrous tissue affected insertions of _______/______/_______ into bone resulting in what? - What areas are primarily affected? (3)
- chronic, progressive, inflammatory - ligaments/tendons/capsules, results in fusion over time - SI, spine, and large peripheral joints
37
Ankylosing Spondylosis Early Stage S/Sx. (5)
- Intermittent LBP*** - Sacroiliitis*** - Spasm of paravertebral muscles*** - Loss of normal lumbar lordosis*** - Painful limitation of cervical joint motion***
38
Ankylosing Spondylosis Advanced Stage S/Sx. (4)
- Constant LBP*** - Loss of normal lumbar lordosis*** - Ankylosis of SI joints and spine*** - Muscle wasting in shoulder and pelvic girdle***
39
What are some complications of ankylosing spondylitis? (6)
- Prone to fracture from even minor trauma - Most common fracture site is lower cervical spine - Myelopathy - Spondylodiscitis (erosive & destructive lesions of vertebral bodies) - Cauda-equina syndrome - Spinal stenosis
40
Reiter's Syndrome: - Characterized by what triad? - Type of ________ arthritis. - Occurs mainly in young adult _____ ages ___-___.
- Triad of arthritis, conjunctivitis, and nonspecific urethritis - reactive arthritis - young adult men ages 20-40
41
Reiter's Syndrome S/Sx. (11)
- Plantar fasciitis*** - Polyarthritis - SI joint changes - Low back and buttock pain - Small joint involvement - Low-grade fever - Urethritis - Conjunctivitis and iritis, bilaterally - Skin involvement (resembling psoriasis) - May be preceded by bowel infection - Anorexia and weight loss
42
What are the (3) ways we can differentiate Reiter's Syndrome from Ankylosing Spondylitis?
1. ) Presence of urethritis and conjunctivitis. 2. ) Prominent involvement of distal joints. 3. ) Presence of asymmetric radiologic changes in SIJ and spine.
43
Psoriatic Arthritis (PsA): - ________, _________, erosive, inflammatory arthritis. - Associated with skin disease _________. - Does it affect men or women more? - Can occur at any age but usually ___-___. - Arthritis is usually preceded by _____ condition. - Causes and risk factors are unknown.
- Chronic, recurrent, erosive, inflammatory - skin disease psoriasis - Affects both genders equally - 20-30 - skin condition
44
Psoriatic Arthritis S/Sx. (6)
- Fever - Fatigue - Polyarthritis - Psoriasis - Sore fingers - Unique clinical features of PsA (DIP joint involvement, nail changes, dactylitis, spondylitis, iritis)
45
Multiple Sclerosis (MS): - Most common _________ ___________ disease of the CNS. - Affects areas of brain and spinal cord. - Symptoms appear between ___-___ years. - Does it affect men or women more? - __________ increases risk 10x. - 5x more prevalent in ______ climates of NA and EU. - Characterized by _________ _______ lesions that form scars (plaques) scattered in CNS white matter.
- inflammatory demyelinating disease of the CNS - 20-40 - Women > Men (2x) - Family Hx - colder climates - inflammatory demyelinating lesions
46
MS S/Sx. (16)
Symptoms (highest to lowest occurrence) - Unilateral visual impairment - Paresthesias - Ataxia - Vertigo - Fatigue - Muscle weakness - Bowel/bladder dysfunctions - Speech impairment Signs (highest to lowest occurrence) - Optic neuritis - Nystagmus - Spasticity or hyperreflexia - Babinski’s sign - Absent abdominal reflexes - Dysmetria or intention tremor - Labile or changed mood - Lhermitte’s sign (shock-like sensation in flexion)
47
Guillain-Barre Syndrome (GBS): - AKA _____ _________ _________ - _____, _______ autoimmune disorder. - Demyelination of _______. - Characterized by abrupt onset of _______. - Not related to race, sex, or age. - Exact cause unknown but frequently occurs after an _______.
- Acute Idiopathic Polyneuritis - acute, acquired - PNS - paralysis - illness
48
GBS S/Sx. (5)
- Muscular weakness (bilateral, progressing from legs and arms to chest and neck) - Diminished DTR - Paresthesias (w/o loss of sensation) - Fever, malaise - Nausea
49
Myasthenia Gravis (MG): - Develops when antibodies produced by immune system block receptors in muscles that receive signals of _______. - What does this result in? - What are the two peaks of onset?
- ACh (acetylcholine) - Impaired muscle function - 20-30 years, after 50 years
50
MG S/Sx. (9)
Muscle fatigue and proximal muscle weakness aggravated by exertion*** - Respiratory failure - Ptosis - Diplopia - Dysarthria - Alteration in voice quality - Dysphagia - Nasal regurgitation - Choking, difficulty in chewing
51
Clues to Immune System Dysfunction: - Insidious onset of episodic back pain in patient younger than 40 with family history of spondyloarthropathy. (_________) - Joint pain preceded or accompanied by burning and urinary frequency (urethritis) and/or accompanied by eye irritation. (_________) - Joint pain preceded or accompanied by a skin rash or lesions. (___________) - Development of neurological symptoms 1-3 weeks after infection. (___________)
- ankylosing spondylitis - Reiter's syndrome - Psoriatic Arthritis - GBS
52
Guidelines for immediate medical attention? (3)
- Dusky blue discoloration or erythema with exquisite tenderness in a joint - Evidence of spinal cord compression - Presence of incontinence in pt with AS
53
Guidelines for MD referral? (3)
- New onset of joint pain within 6 weeks of surgery accompanied by constitutional symptoms. - Symmetric swelling and pain in peripheral joints. - Development of progressive neurologic symptoms within 1-3 weeks of previous infection or recent vaccination.