Pathologies Flashcards

1
Q

HIV Etiology and definition

A

Definition: Destruction of T4 lymphocytes that progresses in various disease states: acute infection > asymptomatic HIV > early symptomatic HIV> advanced HIV (AIDS)

Etiology: virus causes cell death / inactivation of important immune cells that fight infection: macrophages, B cells, dendritic cells, and microglia. Body becomes immuno copmpromised due to lack of T4 cells

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2
Q

HIV Prevalnce/ Incidence, Risk Fxs, Gender and Age preference

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Prevalnce/ Incidence: 1.1 million with 14% not knowing dx. In: recent deline in past 2 years, about 40k new cases in 2018

Risk Fxs: IV drud use, intercourse, unprotected male-male contact

Gender and Age Preference: 77% reported in males, but is not gender specific. 1/2 of glabal cases are women.

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3
Q

Hypersensitivity Etiology and definition

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Definition: exaggerated or inappropriate immune response to allergen or antigen. Damage comes form immune response itself rather than from the substances that provoke it.

Etiology: complement cascade is activated under diff conditions: genetic (high affinity for IgE) or environmental fxs (allergen expose, diet)
1 IgE, instead of IgG is produced in response to antigen and causes response
2. own body’s tissue is attacked and clumped together 2/2 the activation of the cascade system.
3. antigen-antibody complexes are deposited into tissues and around small blood vessels ls and activate the complement cascade, causing inflammation and local tissue injury.
4. delayed response/ sensitization to an allergen

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4
Q

Hypersensitivity Risk Fxs, Gender and Age Preference

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Risk Fxs: exposure to allergens, 2- multiple blood transfusions,
Gender and Age Preference: 58% women. allergic rhinitis was highest in those ages 18-34 and 35-49, decreasing after age 50

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5
Q

Hypersensitivity Medical MGMT

A

H1 blockers, Mast cell stabilizers, Anti-inflammatory corticosteroids, Immunotherapy, Oral allergy pill, remove allergen, epinephrine.

Emergency attack: clear an airway block, and secure an airway is the highest priority in that situation.

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6
Q

Hypersensitivity Tests and measures

A

-Tests and measures
prick test, Allergen specific serum IgE tests to see if IgE binds, thorough hx of attacks and related info. Gathering hx and details is more reliable.

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7
Q

Hypersensitivity Physical Therapy Tests and Measures and Implications for Eval and Tx

A

-Physical TherapyTests and Measures and Implications for eval: NONE

-Best practice for Physical Therapy Treatment
make sure area is clean and allergen, powder and latex free

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8
Q

Scleroderma Definition and etiology

A

Definition: generalized connective tissue disorder characterized by immune dysregulation (autoantibody production), micro-angiopathy (vasculitis and obstruction of small vessels), andfibrosis of skin and internal organs. May occur in the heart, lungs, GI and kidneys. 3 sub groups:
Limited: less risk of systemic involvement. Pulmonary HTN adn espagus pathoolgy can occur. Skin tightness is limited to the hands and face.

Diffuse: Most debilitating - more frequent renal and pulmonary involvement. Classified on all body + skin

Systemic: Fibrosis of the skin, joints, blood vessels, and internal organs from deposition of excessive amounts of collagen. Can last months- lifetime

Etiology: Possibly triggered by auotimmunte response, otherwise unknown

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9
Q

Scleroderma Clinical Presentation

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  • Clinical Presentation: Signs/symptoms: not all peeps pass through all stages but Raynaurds is common btwn all exposures.
  • *Stage 1:** edematous stage: bilateral, non-pitting edema is present in the fingers, hands, and, less commonly, feet. progresses to other body areas. PItting edema is replaced with thick, hard skin that has less sensation and vasoconstriction.

Stage 2: sclerotic stage tight, waxy, smooth skin. hyper-or hypo-pigmented. Facial skin may also be affected and take on a tight, mask-like appearance with thin lips and a pinched nose

** 3rd stage atrophic stage** tightening and calcification of subcutaneous skin over joints (elbow, knee fingers) which may lead to flexion contractures. Decr GI motility, decr fxn of esophagus andanorectal regions, frequent reflux, heartburn, dysphagia, and bloating, pulmonary heart and kidney issues.

Atrophy can occur 2/2 limited use/ mobility

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10
Q

Scleroderma Medical MGMT

A

-Medical MGMT: due to systemic involment treatment can consider Pulmonary arterial hypertension and digital ulcers, GI tract, heart, and joints. For tx, stage and involvement must be determined, the earlier tx the better.

Organ involvement: immunosuppressant, paniculonin, and anti-inflammatories)
Renal failure: ACE inhibitors
NSAIDS for pn mmgmt 2/2 active and passive stretching

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11
Q

Scleroderma Tests and measures

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-Tests and measures Distinctive serum autoantibodies are found in more than 90% of cases. No single laboratory test for scleroderma. Skin biopsy, urinalysis, blood studies, presence of rheumatoid factor, and presence of antinuclear antibodies are used to determine the extent

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12
Q

Scleroderma Physical Therapy Tests and Measures and Implications for Eval and TX:

A
  • Physical Therapy Tests and Measures and Implications for eval: Vitals (for CP involment), check capillary refill, joint pain, skin integrity, edema girth, facial tightness, 2 point discrimination for neuropathy, vitals, depression, MMT for atrophy, tinnels for carpal tunnel.
  • Best practice for Physical Therapy Treatment: menthol and other soothing no itch creams, aquatic therapy, ROM and Ex, precaution of skin which can be V sensitive to pressure, ulcer mgmt- protect and dress it form trauma and pressure, flexibility for joints NSAIDS to help control pain which can be a limiting fx. Exercise should be done for pulmonary/cardiac involvement bu should consider tolerance and premorbid state. Address phsyco-social fxs as needed. Splints, but monitor skin changes.
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13
Q

Scleroderma Risk Fxs and Gender and Age Preference

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Risk Fxs: Fetomaternal cell trafficking, emotional shock, chemical exposure
Gender and Age Preference: Fetomaternal cell trafficking, mortality rate higher in men. Affects 35-50 years of age

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14
Q

Sjogrens Definition and etiology

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Definition: T-lymphocyte infiltrate or B cell hyperactivity cause autoimmune disease which causes destruction of exocrine glands like the salivary and lacrimal glands.

Etiology: perhaps genetic component - disrupted neurogenic regulation of salivary glands on a genetic level does not allow stemcells to make acinar cells

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15
Q

Sjogrens Risk Fxs, gender and age

A

Risk Fxs: having RA, as well as other autoimmune diseases or familial connection

Gender and Age Preference: Second most common rheumatic disease, 9 times more likely to affect women > men. more common in postmenopausal women, however, can affect men and women of all ages

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16
Q

Sjogrens Medical MGMT

A

-Medical MGMT:

local+ systemic stimulators for tear production for eyes, oral hygiene, prevention/treatment of oral infections d utilization of saliva stimulants and mouth lubricants for dry mouth.

Avoidance activities that cause dryness, use moisturize for skin.

NSAIDS, prednisone, or hydroxychloroquine + proper nutrition and exercise can help with joint/muscle stiffness and fatigue.

NSAIDS with proper nutrition for joint pain and gabapetin fro nueropathy

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17
Q

Sjogrens Tests and measures

A
  • Tests and measures: (SSLP )
  • Slit lamp test-detects damage to the eyes
  • Schirmer Test-measures the dryness of the eyes
  • Lip biopsy-detects inflammation of the salivary glands
  • Blood test-checks for antibodies present in primary SS
18
Q

Sjogrens Clinical Presentation

A

Clinical Presentation: Signs/symptoms: Problems with the integumentary, respiratory, renal, hepatic, neurologic, and vascular systems can lead to DRYNESS throat/ eyes esophagitis, gastritis, cavities in the teeth due to lack of saliva, vaginal and kidney dryness, fatigue, joint and muscle pain/stiffness, swelling, rashes, and peripheral neuropathy. keratoconjunctivitis and xerostomia = Dry eyes and mouth.

19
Q

Sjogrens PT implications for Eval ,TX, tools and outcomes

A
  • Physical Therapy Tests and Measures and Implications for eval: monofilmanet tests, Vo2 max for aerobic capacity (AC), 6 min walk test, 1 RM
  • Best practice for Physical Therapy Treatment: Similar to RA. Fatigue is a huge fx, therefore create a baseline fo where activity tolerance is with tests to progress and track aporp. Moderate-high intensity exercise will increase AC. Use RPE to make sure pt. isnt sore after 1 hour of session and include strength and ROM EX to address stiffness, depression, body mechanics and CV fitness. 1 RM and 60-70 of Vo2 via astrand methood for 1-8 week and 70-80% for 9-12 weeks of training.
20
Q

Ankylosing Spondylitis definition and etiology

A

Definition: chronic inflammatory joint disorder in axial skeleton. Can lead to fibrosis, calcification, and ossification of the involved structures: VB and assciated joitn inclding the costovertebral

Etiology: hereditary

21
Q

Ankylosing Spondylitis gender, age add Risk fxs

A

Risk Fxs: first-degree relative with the HLA-B27 antigen.

Gender and Age Preference: Men> women 15 and 30 years but Women may be under dx

22
Q

Ankylosing Spondylitis Medical MGMT, and tests/ measures

A
  • Medical MGMT: NSAIDS, COX-2 inhibitors, anti-rheumatic drugs (DMARDs), Tumor Necrosis Factor Alpha (TNF-α)antagonist for prgression prevention and peripheral symps.
  • Tests and measures: MRI, Schober test for patient’s ability to flex their low back(<15cm), and measurement of chest wall expansion(<2.5cm)
23
Q

Ankylosing Spondylitis Clinical Presentation

A

-Clinical Presentation: Signs/symptoms: Low back, hip, or buttock pain and stiffness lasting at least 3 months, Dull pain that is hard to locate, occasionally sharp. Morning stiffness > 1 hour, better with activity worse with immobility and pn can go into thigh but never below knee.

24
Q

Ankylosing Spondylitis PT implications for Eval ,TX, tools and outcomes

A

-Physical Therapy Tests and Measures and Implications for eval+ TX : Spine P/AROM (Schober test), CHest wall expansion, 6MW. Monitor for S/S of infection 2/2 supressed immune system if on TNF meds.. Avoiding flexion exercises, high impact exercises, contact sports, and other high risk activities due to increased risk of fractures. Gentle mobility exercises, passive physiological joint mobilizations, spine mus stretch and soft tissue, Aquatics program > land for benefits and pilates.

25
Q

Psoriatic Arthritis defiinition and etioligy

A

Definition: synovium in an individual’s joints becomes inflamed secondary to a diagnosis of dermatological inflammation of the skin(psoriasis). Slow progressing that can caise permenant damage if not treated. not associated with a rheumatoid factor and therefore cannot be diagnosed though blood testing.
Etiology: genetics

26
Q

Psoriatic Arthritis gender, age and risk Fxs

A

Risk Fxs: Family HX
Gender and Age Preference: anyone, common in Affects adult males and females equally. In children (9-12), there is a slight preference for females over males.

27
Q

Psoriatic Arthritis clinical presentation

A

Clinical Presentation:
Raised, red, scaly patches on skin -Morning fatigue and stiffness
-Tenderness/pain over and around tendons- digit joint Swelling/ rednesss
- Decreased joint ROM
-Uveitis (inflammation of the eye, particularly the middle layer)
-Pitting or splitting of nails

Common locations & their related symptoms:
Spondylitis(inflammation of the spinal column): C/L-spine pelvic stiffness, Enthesitis (inflammation at attachment sites of ligaments/tendons): fibrosis or ossification of affected tissues, Achilles’ tendon and plantar fascia inflammation-Dactylitis (inflammation of digits –distinguishing indicator of PsA): asymmetrical swelling of a few fingers or toes

28
Q

Psoriatic Arthritis Diagnostic tests

A

Diagnostic Tests:

no blood tests, exam: Absence of osteopenia, DIPs affected, Unilateral SI joint affected seen w. radiographs

29
Q

Psoriatic Arthritis medical mgmt

A

Med MGMT: TNF, NSAIDS, topicals, DMARDS, phototherapy.

30
Q

Psoriatic Arthritis PT implications for Eval ,TX, tools and outcomes

A

Tests and outcomes for PT:
RM,MMT, ARC Joint Count, Health Assessment Questionnaire for psoriasis (HAQ-SK)

PT Tx : strength and resistance aprop. monitored. Aquatic therapy may allow for jump start to ex progression/initiation

31
Q

Juvenile Idopathic Arthritis Definition and etiology

A

Definition: rheumatic disease in childhood, in which the immune cells attack joints and organs, causing inflammation, destruction, fatigue and other local/systemic effects.

Etiology: Maybe environmental factors and infection in those with a genetic predisposition.

32
Q

Juvenile Idopathic Arthritis Gender, age, Risk Fxs

A

Risk Fxs: Genetics, bacterial or viral infection maybe? not known
Gender and Age Preference: Girls > boys

33
Q

Juvenile Idopathic Arthritis Clinical presentation

A

Clinical Presentation:
Pauciarticular JIA(PaJIA)- MOst common. knees, elbows, wrists and ankles.
Polyarticular JIA(PoJIA)- 2nd most common. 5 joints in a symmetric pattern for UE and hand. ptenntial to turn severe
Systemic-onset JIA (SoJIA)- 1/2 make full recovery. 2 most common
Pain often dull and aching, presents in the morning and early during the day. Possible fever, swollen joints, antaglic gait

34
Q

Juvenile Idopathic Arthritis Med MGMT

A

Med MGMT: Early aggressive combination medications,DMARDS, Steroid injections into joint, immunosuppressants. Cervical fusion for Polyarticular

35
Q

Juvenile Idopathic Arthritis Tests

A

Diagnostic tests: blood tests for antigen

36
Q

Juvenile Idopathic Arthritis PT implications for Eval ,TX, tools and outcomes

A

PT Tx: an exercise program of at least 6 weeks improves aerobic fitness, screen for C1-2 instability before contact sports, Soft tissue, mobs, children can have time rating pan so make sure not to exacerbate during symp flare ups, use stretches aquatics (1xweek for 20 weeks) and low intensity interventions. Educate- sleep quialy, school acmodations, avoid deep flexion

37
Q

HIV clinical Presentation

A

Common s/s: eneral fatigue, muscle wasting, and peripheral neuropathy.
Due to time in btwn stages, each stages has unique presentation
Acute- pathogen no detectable, flu like symptoms, large lymphnoded
Asymptomatic- can last 1- 20 years with fatigue and large nodes. CD4 >500 = (+) test
symtomatic: weight loss, diarrhea, night sweats, fever, neurologic symptoms and fatigue CD4 200-500
AIDS- neuro deficts, dementia, extreme fatigue

38
Q

HIV Tests

A

Test: antibody test to determine if any HIV antibodies are present, P24 and NAT test (most $/least common)

39
Q

HIV Med MGMT

A

Med MGMT- HAART can be used to slow progression and replication of HIV when < 500

40
Q

HIV PT implications: tools, outcomes, best practices and eval

A

Test/ Measures: General muscle fatigue, strength and sensation loss, lack of respiratory endurance and R
OM, increased pain levels, and chronic pain, cardiovascular endurance. Strength: MMT 1RM. VO2max w. RPE, moderate intensity Ex for enhanced immune system benefits, QoL measures and other fxn tests: 5x sts , 6 min walk test