Arthritic Diseases Flashcards

1
Q

Osteoarthritis (OA)

A
  • progressive deterioration of articular cartilage and its underlying bone and overgrowth of periarticular bone
  • as we get older, our joints get overused
  • obesity has been linked to OA due to excessive loading (joints are not meant to have excessive weight on them - not moving, maintaining their ability, looseness, and decreased strength)
  • incidence rises sharply after the age 50 and peaks in the 70-79 year old age group
  • 1 in 10 adults aged 60 years and older have significant clinical problems attributable to OA

Result of tissue damage to a joint and the immune reaction that occurs as a result of that damage
- swelling of cartilage
- reduction in the thickness of the joint surface (having less padding)
- loss of elasticity of the cartilage (cannot absorb much force as it used to)

  • most common type of arthritis
  • primarily affects cartilage, the tissue that cushions the ends of bones within the joints
  • affects hands and weight-bearing joints
  • can cause joint pain and stiffness
  • usually develops slowly over many years
  • common areas = lower back, neck, hip, knees, and hands (getting lately more on the shoulder and thumbs)
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2
Q

Risk factors of OA

A

Modifiable:
- decrease in muscle strength and joint proprioception
- obesity = increase strength and aerobic exercise
- history of joint trauma
Non-Modifiable
- age
- gender
- hereditary
- race
- ethnicity
Age in and of itself does not cause OA = it does in relation to past experiences, activities, and comorbidities

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3
Q

Clinical signs and symptoms of OA

A
  • pain worsens with activity and relieve by “rest”
  • joint stiffness and achness
  • swollen and “tight” joints
  • joint enlargement and crepitus
  • decreased ROM, muscle weakness, and posture abnormalities

*for people with arthritis on their back, it’s hard for them to stand all the way up, so they hunch their backs

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4
Q

Primary OA

A
  • without a known cause (just part of your genes)
  • usually affects hips, knees, hands, and wrist
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5
Q

Secondary OA

A
  • results from a previous joint injury
  • metabolic, anatomic, traumatic, or inflammatory incident
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6
Q

Prevalence of OA

A
  • 5th most common cause of disability in adults
  • arthritis cause pain while doing activity (people rest because it hurts too much and then it leads to obesity, HP, DM)
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7
Q

Signs and symptoms of OA

A
  • primarily impacts the knees, hips, hands, and spine
  • pain first appears to a particular joint
  • visible and palpable swelling with tender points
  • significant joint stiffness following a prolonged period of inactivity = resolves around 15-20 minutes following the movement
  • post-activity flare-ups of swelling and pain that reoccur with prolonged activity, extensive use, and weather changes (barometric pressure putting pressure on the joints)
  • joint locking (when straighten out the joint but cannot bend it back, sort of gets locked) or instability
  • crepitus during ROM = crunching feeling or sound coming from the articular surface
  • guard motion and avoid use of the painful joint = leads to the development of muscle weakness, feeling of fatigue, and reluctance to maintain typical habits and routines and to engage in desired or needed occupations
  • 12.4% of individuals with OA are reported to have depression (not because of arthritis but because they cannot engage in the occupations)
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8
Q

Diagnosis of OA

A
  • first step to diagnose regardless of its cause is to rule out other conditions like fracture, tumor, metabolic bone disease, bursitis, tendinitis, rheumatoid disease, internal derangement, soft tissue injury, and viral infection
  • physical examination is best suited to diagnosing OA
  • assessment of pain during movement and limitations in ROM
  • bony nodules due to overgrowth of damaged bone
  • x-rays
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9
Q

Course and prognosis of OA

A
  • fat around the knuckles and skinny on the finger parts
    Lifestyle changes can prevent further damage:
  • greater the body mass index, the more rapid the progression of disease of the weight-bearing joints
  • highly repetitive tasks
  • not considered a life-threatening disease
  • disruption, imbalance, and ultimately inflammation of supportive structures leads to joint instability, limited movement, pain with use and sometimes at rest, weakness, disfigurement, and dysfunction
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10
Q

Medical management of OA

A
  • slows the progression of the disease, reduce pain, and improve functional abilities that are limited by pain, ROM deficits, and weakness
    Medications:
  • acetaminophen (Tylenol which affects your GI tract) = eventually may fail to reduce comfort
  • NSAID (Motrin) = can cause GI bleeding and peptic ulcer and can accelerate joint destruction
  • topical creams
  • supplements
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11
Q

Surgical procedures of OA

A
  • arthrodesis = fusion of joints such as vertebrae, DIP, PIP joints, and wrists
  • joint replacement for shoulders, hips, and knees and thumb CMC joints
  • significantly reduce pain and prevent the progressive nature of the disease but may impact function = loss of ROM
  • joint replacement, fully remove the damaged bone, and ultimate provide significant pain relief, deformity correction, and functional improvements, although they may not restore every facet of previous function
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12
Q

Osteoarthritis vs Rheumatoid arthritis

A

Osteoarthritis:
- degenerative joint disease caused by the breakdown of cartilage between the joint bones
- the overuse of the cartilage
- local (joint)
- joint deformity
- acute joint injury
- occupational factors
- joint laxity
- muscle weakness
- sports participation
Rheumatoid arthritis:
- chronic, inflammatory type of arthritis
- also classified as systemic autoimmune disease
- systemic (all throughout the body)
- gender
- genetic factors
- obesity
- nutritional factors
- bone density
- age
- inflammation of the fluids around the joints (the inflammation and pressure causes the bone to erode)

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13
Q

Rheumatoid arthritis (RA)

A
  • a chronic, systemic, inflammatory, autoimmune disorder created through a complex interplay of contextual factors, genes, and abnormal immune response
  • significant joint inflammation leading to changes in the synovial membrane
  • systemic condition = can also involve internal organs such as lungs, the skin, eyes, and the cardiovascular system
  • RA leads to complications that impair function
  • reduce the person’s ability to engage in meaningful daily activities and reduce quality of life
  • ultimately and especially if left untreated, RA leads to increased morbidity and mortality
  • bursitis
  • tendinitis
  • erosion of bone and cartilage
  • synovitis
  • polymorphonuclear leukocytes
  • inflammation in subchondral bone
  • affects the hips, knees, wrist, hand, big toe, shoulders, and neck
  • causes redness, warmth, and swelling of joints
  • usually affects the same joint on both sides of the body
  • often causes a general feeling of sickness, fatigue, weight loss, and fever
  • may develop suddenly within weeks or months
  • most often begins between ages 25-50
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14
Q

Etiology of RA

A
  • a combination of genetic and environmental factors
  • autoimmune
  • if left untreated, the autoimmune reactions cause joint damage, ligament laxity, and muscle imbalance
  • affects women 3 times more than men because there is a hormonal component to it
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15
Q

Risk factors of RA

A
  • age = likelihood increases with age (the onset of RA is highest among adults in their 60s)
  • sex = 2-3 times higher on women than men
  • genetics/inherited traits = people born with specific genes are more likely to develop RA (the risk of RA may be highest when people with these genes are exposed to environmental factors like smoking or when a person is obese)
  • smoking = increases a person’s risk of developing RA and can make the disease worse
  • obesity
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16
Q

Signs and symptoms of RA

A
  • initial signs = fatigue and generalized weakness
  • morning stiffness (lasts for an hour when you wake up)
  • some exacerbations and remissions, some more consistent course
  • can be symmetrical or asymmetrical
  • once it gets super bad, it breaks down ligaments and bones which leads to physical bone changes
  • loss of ROM
  • pain
  • limiting ROM may lead to contractures
  • MCP and PIP joints are most severely impacted by RA = Swan-neck deformities and Boutonniere deformities
  • ulnar drifts
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17
Q

How RA affects the body

A
  • systemic!!!
  • fever (constantly trying to fight off the inflammation)
  • red, dry eyes
  • breathing problems
  • anemia
  • fatigue
  • skin lumps (nodules)
  • stiff, swollen joints
  • dry mouth
  • depression
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18
Q

Stages of RA

A

Stage 1 - Early-stage = Initial inflammation in the joint capsule and swelling of synovial tissue. The swelling causes the symptoms of joint pain, swelling, and stiffness.
Stage 2 - Moderate stage = Inflammation of the synovial tissue that becomes severe enough to create cartilage damage. Symptoms consist of loss of mobility and decreased joint ROM becomes more frequent
Stage 3 - Severe stage = Inflammation in the synovial is now destroying not only the cartilage of the joint but the bone as well. Potential symptoms includes increased pain and swelling and a further decrease in mobility and even muscle strength. Physical deformities of the joint may start to develop as well
Stage 4 - End stage = Inflammatory processes ceases and joints stoic functioning altogether. Pain, swelling, stiffness, and loss of mobility are still the primary symptoms in this stage (everything is broken down)

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19
Q

Diagnosis of RA

A
  • blood test
  • synovial fluid testing
  • imaging (x-ray)
  • individuals will often self-manage 2-4 years prior to seeking medical intervention
  • family medical history
  • physical exam
  • ESR test
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20
Q

Objective qualifications of RA

A
  • morning stiffness = in and around the joints lasting at least 1 hour before the maximal improvement
  • arthritis of 3 or more joint areas = at least 3 joint areas at the same time have had soft tissue swelling or fluid observed by a physician (14 possible areas are right or left PIP, MCP, wrist, elbow, knee, ankle, and MTP joints)
  • arthritis of hand joints = at least one area swollen in a wrist, MCP, or PIP joint
  • symmetric arthritis = simultaneous involvement of the same joint areas on both sides of the body (bilateral involvement of PIPs, MCPs, or MTPs is acceptable without absolute symmetry)
  • rheumatoid nodules = subcutaneous nodules over bony prominences or extensor surfaces or in juxta-articular regions, observed by a physician
  • serum rheumatoid factor = demonstration of abnormal amounts of serum RF by any method for which the result has been positive in 5% of normal subjects
  • radio graphic changes = Regino graphic changes typical of RA on posters anterior hand and wrist radiographs, which must include erosions or unequivocal bony decalcification localized in involved joints
21
Q

Medical management of RA

A
  • there are no medications that cure RA, but it does slow it down
    Focus of management:
  • relief of pain
  • reduction of edema (helps to not break down the joints as much)
  • preservation of normal joint function, musculature, and soft tissue support structures
  • minimization of the unintended consequence of medication
  • promotion of normal growth and development
  • maintenance of ADL independence
  • if early diagnosis can occur and proper interventions can be initiated within the first 2 years, disease progress may be halted and in some cases, reversed
22
Q

Medications for RA

A

Nonsteroidal anti-inflammatory drugs (NSAIDs):
- ibuprofen (Advil, Motrin, others) and Naproxen sodium (Aleve)
- side effects can include upset stomach and much less often, kidney and liver problems
Disease-modifying antirheumatic drugs (DMARDs):
- used when NSAIDs alone fail to relieve symptoms of joint pain and swelling
- used if there is a high risk of damage in the future
- Methotrexate (Trexall, Xatmep, others)
- side effects may include nausea, low blood counts, liver problems, and a mild increased risk of infection
Biological agents = a newer class of drugs also known as biological, response modifiers:
- Etanercept (Enbrel, Erelzi, Eticovo), adalimunab (Humira), golmunab (Kineret), and tocilzumab (Actemra)
- can increase risk of infection
Steroids and corticosteroids:
- prednisone may be used to control symptoms until another medication takes affect
- used to treat inflammation when it is not in the joints, such as inflammation of the sac around the heart
- can interfere with normal growth and increase susceptibility to infection, so they generally should be used for the shortest possible duration

23
Q

Surgical intervention for RA

A
  • joint replacement
  • pain relief, deformity correction, and functional improvements
  • may not restore every facet of previous function of the joint itself
  • RA is systemic so you will still have fatigue and inflammation

*can have both OA and RA

24
Q

Gout

A
  • more so acute, not chronic
  • a crystalline form of inflammation arthritis that is marked by significant pain that first presents in the metatarsophalangeal joint of the big toe (also called podagra)
  • related to how the body metabolizes food
  • build up in the body and are not excreted, crystals can accumulate and lead to inflammation
  • monosodium urate (MSU) crystals in affected joints resulting from excessive Uris acid in the body
  • gout will often flare up and then go into remission
  • it is not cured but can be managed
  • common areas = big toe and wrist
  • episodic and chronic components
  • causes severe pain
  • joint deformities
  • end-organ damage
  • with early treatment and diagnosis long-term effects can be eliminated
  • medication needed to help lower hyperuricemia (hyperuricemia causes organ breakdown)
25
Q

Hyperuricemia

A
  • a risk factor for gout
  • high serum uric acid
  • uric acid = waste product that is created when your body breaks down chemicals called purines in food and drinks
  • most uric acid dissolves in your blood, passes through your kidneys and leaves your body in your pee (urine)
  • occurs if too much uric acid stays in your body
  • associated with an imbalance of production and excretion through the urine, or gut bacterial breakdown
  • related to a metabolic syndrome, obesity, and diet
  • often associated with a “rich man”s diet” = high in purines (red meat, organ meat, fish and shellfish, and high fructose corn syrup)
26
Q

Signs and symptoms of gout

A
  • can attack suddenly and often flares at night while the individual is sleeping
  • severe pain, to the point of the inability to tolerate even the slightest pressure or breeze to the affected area (gout attack)
  • joint can feel like it is on fire and may be red or purple as well as swollen
  • pain may last 5-10 days and then disappear
  • ankles, midfoot joints, knees, wrists, fingers, and elbows
  • gout left untreated leads to persistent swelling, stiffness, and pain
  • eventually leads to joint damage
  • high uric acid can also contribute to kidney disease, diabetes, hypertension, and cardiovascular disease
27
Q

Medical management of gout

A
  • NSAIDs with steroids and colchicine = medication that reduces buildup of uric acid crystals
  • can be managed with diet
28
Q

Systemic lupus erythematosus (SLE)

A
  • NOT a type of arthritis
  • a chronic disease with no cure that causes pain and inflammation in any part of the body (inflames your whole body)
  • an autoimmune disease in which the body attacks otherwise health tissue (will attack anything)
29
Q

Incidence and prevalence of lupus

A
  • can affect, skin, heart, kidneys, blood, muscles, and joints
  • autoimmune disease
  • commonly diagnosed between age 15-44
  • 90% of patients are women
  • black people have higher risk
  • treated by a rheumatologist
  • most people test positive to an ANA blood test
  • hydroxychloroquine is most common medication
30
Q

Etiology of lupus

A
  • contributing factors believed to be a combination of hormones, genetics, and environment
  • looking at the role of estrogen
  • appears to run in families
  • these factors go into your T cells which goes to the organs, causing damage
31
Q

Signs and symptoms of lupus

A
  • severe and prolonged fatigue
  • stiffness and pain in hands, wrists, elbows, and knees
  • fever
  • butterfly rash
  • sunlight sensitivity (gets sunburned a lot quicker)
  • Raynaud phenomenon (white due to lack of blood flow; blue due to lack of oxygen; red when blood flow returns)
  • mouth sores
  • hair loss
  • chest pain or cough
  • swollen glands
  • swelling in legs and around eyes
  • headaches
  • symptoms can come and go
  • inflammation of the kidney (lupus nephritis) = can lead to the need for dialysis or a kidney transplant
  • inflammation of the nervous system = can lead to memory problems, confusion, headaches, and strokes
  • inflammation of the blood vessels in the brain = can lead to seizures, fever, and behavioral changes
  • hardening of the arteries or coronary artery disease = can lead to heart attack
  • inflammation of the skin = can cause rashes, sores, and ulcers
  • about half of those diagnosed will acquire the malar or butterfly rash on their nose and cheeks
32
Q

Diagnosis of lupus

A
  • lack of single confirmatory test
  • diagnosis can take months or years
  • diagnosis typically requires review of symptoms, medical history, family history, and available lab tests
  • lab test for antinuclear antibodies (ANAs)
33
Q

Stages of lupus

A

Quiescent SLE:
- the patient leads a normal life
- may only have a rash and/or fatigue
- treatment would include a nonsteroidal anti-inflammatory drugs and topical applications
Stable SLE:
- involves occasional flares where the individual presents with rash and/or chest pain and occasionally reaches out for medical advice
- treatment includes intravenous or oral corticosteroids
Serious SLE:
- presents with kidney, hematological, and/or brain involvement
- treatment includes continuous corticosteroids and immunosuppressive drugs

34
Q

Impact on ADLS with occupational performance (arthritis)

A
  • pain, fatigue, reduced strength and movement, and reduced motor function needed for skilled movements
  • some conditions require surgery that temporarily limit the ability to engage in occupations (reduced strength and movement leads to sedentary life)
  • limited movements cause difficulty in reading, extending extremities, grasping (trouble dressing, washing hair, transferring)
  • fine motor limitations due to hand deformities
  • caregivers help with ADLs
35
Q

Impact on IADLs with occupational performance (arthritis)

A
  • the physical body has become painful, fatigued, weak, and stiff
  • with joint erosion leading to deformity, the multiple steps, multiple sub tasks, and extended time are needed to be able to complete IADLs
  • IADLs can be impacted before ADLs
  • trouble cleaning, doing laundry, vacuuming, and cooking
36
Q

Impact on health management with occupational performance (arthritis)

A
  • highly important for individuals to take care of their health
  • learning about proper nutrition (takes lots of brain power to watch what you eat)
  • how to create a medication routine and be compliant with dosing
  • maintaining mobility and strength through exercise and activity
  • being a self-advocate and having health literacy
  • vigilant with medication, medical appointments, daily exercise, and symptom monitoring
37
Q

Impact on rest and sleep with occupational performance (arthritis)

A
  • recognition of what is creating sleep difficulties is helpful in determining the best course of action for improving sleep
  • possible that the individual with arthritis is not active enough during the day, so they are not tired at a reasonable bedtime
  • an inconsistent schedule can create difficulties obtaining quality restful sleep
38
Q

Impact on work with occupational performance (arthritis)

A
  • almost all jobs are impacted in some way
  • heavy physical jobs that require extensive walking, lifting, and maneuvering involvement
  • fatigue and malaise also make it difficult to maintain the ability to work in heavy, physical jobs
  • moderate and light work types of employment may also be impacted and require modifications to technique or equipment if extended times in one position are expected, or that it included repetitive nature to the work or that it requires fine motor skills
39
Q

Impact on social participation with occupational performance (arthritis)

A
  • emotional toll and isolation that can ensure when one is in pain, has impaired mobility, fatigued, and is simply not well
  • person is living with a chronic and in some cases (such as SLE) a potentially dangerous disease
  • long-term effects of pain and lack of control over one’s life can negatively impact relationships and lead to social isolation
  • physical changes to the body can also cause individuals to give up many activities that they used to do with other people such as attending theater events, school events, and events outside of work with colleagues
  • your body has been fighting inflammation all day and then cannot go to social events in the evening because they are tired
40
Q

Juvenile arthritis

A
  • an umbrella term for several types of arthritis that occur in children under the age of 16
  • prevalence = affects approximately 1 in 1,000 children
  • types = juvenile idiopathic arthritis and juvenile lupus
41
Q

7 facts about juvenile arthritis

A
  • an umbrella term for different types of childhood arthritis
  • affects children under the age of 16
  • affects more girls than boys
  • symptoms include joint pain, stiffness, fever, fatigue
  • cause is unknown but genetics may play a role
  • physical and occupational therapy is beneficial
42
Q

Symptoms of juvenile arthritis

A
  • joint swelling, pain, and stiffness
  • fatigue, fever, and loss of appetite
  • difficulty with mobility or performing daily activities
43
Q

Juvenile idiopathic arthritis (JIA)

A
  • used to be known as juvenile rheumatoid arthritis
  • most common
  • characterized by inflammation in one or more joints for at least 6 weeks
    Subtypes:
  • oligoarticular JIA = affects 4 or fewer joints
  • polyarticular JIA = affects 5 or more joints
  • systemic JIA = involve joint swelling along with systemic symptoms like fever, rash, and organ involvement
  • onset = typically occurs before the age of 16, with peak incidence between ages 1-3 and 8
44
Q

Symptoms of JIA

A
  • muscle weakness
  • fatigue
  • difficulty climbing stairs or lifting objects
  • distinctive skin rashes, especially on the knuckles and eyelids
45
Q

Juvenile lupus

A
  • an autoimmune condition where the immune system attacks the body’s tissues, affecting multiple systems
  • onset = commonly diagnosed in children ages 11-15, with higher prevalence in girls
46
Q

Symptoms of juvenile lupus

A
  • joint pain
  • butterfly rash
  • kidney inflammation
  • sensitivity to light
47
Q

Common symptoms of juvenile arthritis across all types

A

Joint-related symptoms
- persistent joint pain, swelling, and stiffness, especially in the morning or after inactivity
- warmth and redness around affected joints
- reduced range of motion and joint function
Systemic symptoms:
- fever, fatigue, and weight loss
- rash or changes in the skin
- general malaise and irritability

  • growth and developmental concerns
  • occupation of play helps with developmental skills, so if the kids cannot engage, they will struggle
48
Q

Managing juvenile arthritis

A
  • lots of therapy (PT and OT)
    Medical treatments:
  • NSAIDs
  • corticosteroids
  • DMARDs
  • biologic agents
  • have to be careful with meds for kids because they are taking it longer than if you were to take it at age 50
    Lifestyle modifications:
  • balanced diet
  • regular exercise
  • adequate rest
49
Q

Impact on daily life and occupational performance (juvenile arthritis)

A
  • physical impact = difficulty in walking, running, or participating in sports
  • psychosocial impact = increased risk of anxiety, depression, and social isolation
  • school and activities = challenges in maintaining school attendance and participation in extracurricular activities
  • visual - illustration showing areas of difficulty in daily life for children with JA