Transcript Gout/R
Autoimmune Disorders
That Affect the
Musculoskeletal System
Rheumatoid Arthritis
Rheumatoid Arthritis (RA)
Chronic,
systemic autoimmune disease
Inflammation of connective tissue in
diarthrodial (synovial) joints
Periods of remission and exacerbation
Frequently accompanied by extra-articular
manifestations
Incidence
Occurs
globally, affecting all ethnic groups
Occurs at any time of life
Incidence increases with age
Peaks between 30s and 50s
Nearly
2.1 million Americans affected
Women have incidences three times
higher than men
Etiology
Cause
of RA is unknown
No infectious agent found
Two etiologies
Autoimmune etiology
• Most widely accepted
Genetic factor etiology
Pathophysiology
Chronic
inflammation of the joints leads to:
Scar tissue (pannus) & joint cartilage
destruction
Joint laxity, subluxation (dislocation), &
contracture
Pathophysiology
Fig. 65-3
As the synovitis expands inside and outside of the joint,
it can damage the bone and cartilage of the joint and the
surrounding tissues, such as ligaments, tendons, nerves,
and blood vessels.
With articular cartilage destruction, vascular granulation
tissue grows across the surface of the cartilage (pannas)
with loss of cartilage beneath the expanding pannas
Etiology and Pathophysiology of
Rheumatoid Arthritis
Inflammatory
pannus causes destruction
of bone.
This
leads to joint deformities.
Pathophysiology
If
unarrested, RA progresses in 4 stages
Stage 1: Early
• No destructive changes on x-ray, possible x-ray
evidence of osteoporosis
Stage 2: Moderate
• X-ray evidence of osteoporosis, with or without
slight bone or cartilage destruction
• No joint deformities, adjacent muscle atrophy,
possibly presence of extra-articular soft tissue
lesions
Etiology and Pathophysiology
RA
progresses in four stages (cont'd)
Stage 3: Severe
• X-ray evidence of cartilage and bone destruction in
addition to osteoporosis; joint deformity; extensive
muscle atrophy; possible presence of extraarticular soft tissue lesions
Stage 4: Terminal
• Fibrous or bony ankylosis, stage III criteria
Clinical Manifestations
Onset
Onset
is typically insidious
Nonspecific manifestations may precede
onset of arthritic complaints
Some
report a history of precipitating
events
Clinical Manifestations
Joints
Specific articular
involvement
Symptoms occur
symmetrically
Frequently affect small
joints of hands and
feet
Larger peripheral joints
may also be involved
Typical Deformities of
Rheumatoid Arthritis
Fig. 65-4
Clinical Manifestations
Joints
Patient
experiences joint stiffness after
periods of __________
Morning stiffness may last from 60
minutes to several hours or more
MCP and PIP joints typically swollen
Fingers may become spindle shaped from
synovial hypertrophy and thickening of
joint capsule
Clinical Manifestations
Joints
Joints
become tender, painful, and warm
Joint pain
Increases with ______
Varies in intensity
May not be proportional to degree of
inflammation
Tenosynovitis
frequently affects extensor and
flexor tendons near wrists
RA progresses
Extraarticular Manifestations of
Rheumatoid Arthritis
Fig. 65-5
Clinical Manifestations
Extraarticular Manifestations
Three
most common
Rheumatoid
nodules develop in up to 25%
of all patients with RA
Those
affected usually have high RF titers
Clinical Manifestations
Extraarticular Manifestations
Sjögren’s
syndrome
Seen in 10% to 15% of patients with RA
Can occur as a disease by itself or in
conjunction with other arthritic disorders
• RA and systemic lupus erythematosus (SLE)
Complaints of burning, gritty, itchy eyes
Decreased tearing, photosensitivity
Clinical Manifestations
Extraarticular Manifestations
Felty’s
syndrome
Most commonly in patients with severe,
nodule-forming RA
Characterized by
•
•
•
•
•
Inflammatory eye disorder
Splenomegaly
Lymphadenopathy
Pulmonary disease
Blood dyscrasias
Complications
Joint
destruction begins as early as first
year of disease without treatment
Flexion contractures and hand deformities
Cause diminished grasp strength
Affect patient’s ability to perform
self-care tasks
Cataract
development and loss of vision
can result from scleral nodules
Complications
Rheumatoid
nodules
On the skin can ulcerate, similar to
pressure ulcers
On vocal cords leads to progressive
hoarseness
In vertebral bodies can cause bone
destruction
Complications
Cardiopulmonary
effects may occur later
in RA
Pleurisy, pleural effusion, pericarditis,
pericardial effusion, cardiomyopathy
Carpal
tunnel syndrome can result from
swelling of synovial membrane
Diagnostic Studies
RA is defined as having at least 4 of the
following seven criteria. Following must
be present for at least 6 wks:
Morning stiffness that lasts ≥1 hour
Swelling in three or more joints
Swelling in hand joints
Symmetrical joint swelling
Erosions or decalcification seen on hand
x-rays
6. Rheumatoid nodules
7. Presence of serum RF
1.
2.
3.
4.
5.
Diagnostic Studies
Accurate
diagnosis is essential to initiation
of appropriate treatment and prevention of
unnecessary disability
Diagnosis is often made
Based on history and physical findings
Some laboratory tests are useful for
confirmation and to monitor disease
progression
Diagnostic Studies
Positive
RF
Titers rise during active disease
Antinuclear antibody (ANA) titers
Indicators
of active inflammation
ESR
C-reactive protein (CRP)
Diagnostic Testing
Blood
Studies
Rheumatoid factor (RF)
Erythrocyte sedimentation rate (ESR)
C-reactive protein (CRP)
Antinuclear antibodies (ANA) titers are seen in some
Synovial
fluid analysis
Straw-colored fluid with fibrin flecks
WBC is elevated to >25,000/μl
X-rays
Will not diagnosis – only show bone changes
Collaborative Care
Care
begins with a comprehensive
program of education and drug therapy
Education of drug therapy
Patient and family educated about disease
process and home management strategies
NSAIDs are prescribed to provide comfort
Collaborative Care
Physical
therapy helps maintain joint
motion and muscle strength
Occupational therapy develops extremity
function and encourages joint protection
Drug Therapy
Drugs
remain cornerstone of treatment
DMARDs can lessen permanent effects of
RA
Choice of drug is based on
Treatment and Nursing Care for
Rheumatoid Arthritis
See
Table 65-3 for meds used for arthritis
p. 1698-1700.
Salicylates
NSAIDs
Antibiotics
Topical analgesics
Corticosteroids
DMARDs
Gold compounds
Antimalarials
Immunosupressants
Biologic/Targeted therapy
Drug Therapy
DMARD
Many
of the drugs used to treat RA are
expensive
Methotrexate (Rheumatrex) is drug of
choice
Rapid antiinflammatory effect decreases
clinical symptoms in days to weeks
Inexpensive
Lower toxicity compared to other drugs
Drug Therapy
Effective
DMARDs for mild to moderate
disease
Sulfasalazine (Azulfidine)
Antimalarial drug hydroxychloroquine
Leflunomide
(Arava) is a newer synthetic
DMARD that blocks immune cell
overproduction
Drug Therapy
Biologic/targeted
drug therapies can also
slow disease progression in RA
Can be used in patients with moderate to
severe disease who have not responded
to DMARDs or in combination therapy with
an established DMARD
Drug Therapy
Corticosteroid
therapy can aid in symptom
control
Intraarticular injections may relieve pain and
inflammation associated with flare-ups
• Long-term use should not be a mainstay
Risk osteoporosis, avascular necrosis
Low-dose prednisone for a limited time to
decrease disease activity until DMARD effect is
seen
Drug Therapy
Various
NSAIDs and salicylates to treat
arthritis pain and inflammation
Aspirin is often used in high dosages of 4
to 6 g/day (10 to 18 tablets)
NSAIDs have antiinflammatory, analgesic,
and antipyretic properties
Drug Therapy
NSAIDs
Do not alter natural history of RA
Full effectiveness may take 2 to 3 weeks
• Some relief may be noted within days
May be used when patient cannot tolerate
high doses of aspirin
Relieve Pain
NSAIDs
DMARDs
Non-Pharmacological
Heat or Cold applications
Rest
Relaxation techniques
Nursing Implementation
Acute Intervention
Usually
treated on an outpatient basis
Hospitalization may be necessary for
patients with extraarticular complications
or advancing disease
Reconstructive surgery for disabling
deformities
Nursing
intervention begins with a careful
physical assessment
Nursing Management
Assessment
Nurse
must also
Evaluate psychosocial needs and
environmental concerns
After problem identification, coordinate a
carefully planned program for rehabilitation
and education for interdisciplinary health care
team
Nursing Management
Problems
Chronic
pain
Impaired physical mobility
Activity intolerance
Self-care deficit
Ineffective therapeutic regimen
management
Disturbed body image
Nursing Management
Planning
Overall
goals
Satisfactory pain relief
Minimal loss of functional ability of affected
joints
Perform self-care
Participate in planning and carrying out
therapeutic regimen
Maintain a positive self-image
Nursing Management
Interventions
Discuss
with patient
Many
patients take several different drugs
so the nurse must make the drug regimen
as understandable as possible
Careful
attention to timing is critical to
Nursing Management
Interventions
Nonpharmacologic
relief of pain
Therapeutic heat and cold
Rest
Relaxation techniques
Joint protection
Biofeedback
Transcutaneous electrical stimulation
Hypnosis
Nursing Management
Interventions
Lightweight
splints may be prescribed to
rest an inflamed joint and prevent
deformity
Should be removed regularly to perform skin
care and ROM exercises
Should be reapplied as prescribed
Occupational therapist may help identify
additional self-help devices to assist in
activities of daily living
Nursing Management
Interventions
Morning
care and procedures should be
planned around morning stiffness
To
relieve joint stiffness and increase
comfort
Ambulatory and Home Care
Rest
Alternate
scheduled rest periods with
activity throughout day
Helps relieve pain and fatigue
Amount of rest varies
Total
bed rest
Rarely necessary
Should be avoided to prevent stiffness and
immobility
Ambulatory and Home Care
Rest
Good
body alignment while resting can be
maintained through use of a firm mattress
or bed board
Encourage positions of extension
Avoid flexion positions
Splints
and casts can help maintain proper
alignment and promote rest
Ambulatory and Home Care
Heat and Cold Therapy
Help
relieve pain, stiffness, and muscle
spasm
Ice
Superficial
Moist
heat
heat sources
Ambulatory and Home Care
Exercise
Inadequate
joint movement can result in
progressive joint immobility and muscle
weakness
Overaggressive exercise can result in
increased pain, inflammation, and joint
damage
Gentle ROM exercises are usually done
daily to keep joints functional
Ambulatory and Home Care
Psychologic Support
Patient’s
value system and perception of
disease must be considered
Patient is constantly challenged by
problems of
Limited function and fatigue
Loss of self-esteem
Altered body image
Fear of disability or deformity
Gout
Gout
Deposits
of sodium urate crystals in
articular, periarticular, and subcutaneous
tissues
May
be primary or
secondary
Primary – hereditary error of purine
metabolism
Secondary – drugs that inhibit uric acid
excretion or another acquired disorder
Incidence and Risk Factors
Primary
Affects
Risk
gout accounts for 90% of cases
primarily middle aged men
factors: obesity, HTN, thiazide
diuretics, excess alcohol use
Pathophysiology
Uric
acid is end product of purine
metabolism and is excreted by the kidneys
Causes
Diet
of hyperuricemia
high in purines will not cause gout,
but may trigger an attack in a susceptible
person
Clinical Manifestations
Gouty
arthritis in one or more joints (but
less than four)
Great toe joint most common first
manifestation; other joints may be the foot,
ankle, knee, or wrist
Joints are tender & cyanotic
May be precipitated by trauma, surgery,
alcohol ingestion, or infection
Clinical Manifestations
Onset
usually nocturnal, with sudden
swelling and excruciating pain
May have low grade fever
Usually subsides within 2-10 days
Joints are normal, with no symptoms
between attacks
Complications
Joint
deformity
Osteoarthritis
Tophi
may produce draining sinuses that
may become infected
Renal
stones, pyelonephritis, obstructive
renal disease
Diagnosis
History
& physical examination
Family
history of gout
Diagnostic
studies
Diagnostic Studies
Serum uric acid levels
May be caused by other factors
WBC elevated during acute attack
ESR
24 hour urine uric acid levels
Synovial fluid aspiration contains uric acid
crystals
Seldom necessary
X-rays appear normal in early stages; tophi
appear as eroded areas of bone
Collaborative Care
Acute
attack
Colchicine produces dramatic antiiflammatory
effects with relief within 24-48 hours
NSAIDs for additional pain relief
Corticosteroids (po or intraarticular)
Adrenocorticotropic hormone (ACTH)
Joint aspiration to decompress
Collaborative Care
Prevention
of acute attacks
Colchicine combined with:
• allopurinol (Zyloprim, Alloprim) – blocks production
of uric acid
• probenecid (Benemid), sulfinpyrazone (Anturane)
– inhibit tubular reabsorption of uric acid
• febuxostat (Uloric) – inhibits xanthine oxidase,
recently shown to reduce serum uric acid levels
Collaborative Care
Uricosuric
Agents
Probenecid (Benemid)
Precautions
Sulfinprazone (anturan) block resorption uric acid
High fluid intake, alkaline urine
Not effective if creatinine clearance is elevated
Cozaar
Angiotension II receptor angonist
• Monitoring
Force Fluids while on these medications!!
Collaborative Care
Dietary
measures
Weight reduction
Avoidance of alcohol
Avoidance of foods high in purines
• High: Sardines, anchovies, herring, mussels, liver,
kidney, goose, venison, meat soups, sweetbreads,
beer & wine
• Moderate: Chicken, salmon, crab, veal, mutton,
bacon, pork, beef, ham
Treatment and Nursing Care
Bedrest and position for comfort
Joint immobilization and protect joint from pressure
Local application of heat or cold
Assess for complications
Formation of kidney stones
Hypertriglyceridemia
Hypertension
Collaborative Care
Prevention
of renal stones
Increase fluid intake to maintain adequate
urine output
Allopurinol
ACE inhibitor losartin (Cozaar) – promotes
urate diuresis
Nursing Care
Acute
gouty arthritis – pain control
Gentle, supportive care of affected joints
Immobilize and rest affected joints – bed rest
or NWB
Cradle or footboard to prevent pressure from
bedcovers
Monitor ROM and degree of pain
Nursing Care
Patient/Family
teaching
Gout is a chronic disease
Drug teaching
Need to monitor serum uric acid levels
Precipitating factors
Systemic Lupus
Erythematosus (SLE)
Chronic multisystem disease involving
vascular and connective tissue
Incidence
SLE
affects 2 to 8 persons per 100,000 in
United States
Most cases occur in women of
childbearing years
African, Asian, Hispanic, and Native
Americans three times more likely to
develop than Whites
Etiology
Etiology
is unknown
Most probable causes
Genetic influence
Hormones
Environmental factors
Certain medications
SLE
Pathophysiology
Chronic
multisystem inflammatory disease
Associated with abnormalities of immune
system
Results from interactions among genetic,
hormonal, environmental, and
immunologic factors
Because the antibodies and
accompanying cells of inflammation can
affect tissues anywhere in the body, lupus
can affect a variety of areas
Systemic Lupus Erythematosus
A
variable disease
Chronic
Unpredictable
Characterized by exacerbations & remissions
Clinical Manifestations
Ranges
from a relatively mild disorder to
rapidly progressing, affecting many body
systems
Most commonly affects the skin/muscles,
lining of lungs, heart, nervous tissue, and
kidneys
Systematic Lupus
Erythematosus
Affects the
Skin
Joints
Serous membranes
Renal system
Hematologic
system
Neurologic system
Clinical Manifestations
Dermatologic
Cutaneous vascular lesions
Butterfly rash
Oral/nasopharyngeal ulcers
Alopecia
Clinical Manifestations
Musculoskeletal
Polyarthralgia with morning stiffness
Arthritis
• Swan neck fingers
• Ulnar deviation
• Subluxation with hyperlaxity of joints
Clinical Manifestations
Cardiopulmonary
Tachypnea
Pleurisy
Dysrhythmias
Accelerated CAD
Pericarditis
Clinical Manifestations
Renal
Lupus nephritis
• Ranging from mild proteinuria to
glomerulonephritis
• Primary goal in treatment is slowing the
progression
Clinical Manifestations
Nervous
system
Generalized/focal seizures
Peripheral neuropathy
Cognitive dysfunction
• Disorientation
• Memory deficits
• Psychiatric symptoms
Clinical Manifestations
Hematologic
Formation of antibodies against blood cells
Anemia
Leukopenia
Thrombocytopenia
Coagulopathy
Anti-phospholipid antibody syndrome
Clinical Manifestations
Infection
Susceptibility to infections
Fever should be considered serious
Infections such as pneumonia are a common
cause of _____
Diagnostic Studies
No specific test
SLE is diagnosed primarily on criteria relating to
patient history, physical examination, and
laboratory findings
Diagnosis
Autoantibody
Anti-DNA- specific
Anti- Smith antibody (Anti-Sm)
Anti nuclear antibody (ANA)
Inflammatory
Testing:
Activity:
ESR
C-reactive protein
These are not diagnostic for SLE, but
help in the diagnosis
Diagnostic Tests
CBC
UA
X-rays
Chest
ECG
x-ray
Collaborative Care
Prognosis
is improved with
Earlier diagnosis
Earlier and better treatment regimens
Careful monitoring for organ
involvement
Collaborative Care
Drug
therapy
NSAIDs
Antimalarial drugs
Steroid-sparing drugs
Corticosteroids
Immunosuppressive drugs
Treatment and Nursing Care
What is the single most important medication
used in the treatment of SLE?
Other Medications:
Anitmalarial
Immunosuppressive agents
Nursing Management
Nursing Assessment
Assess
patient’s physical, psychologic,
and sociocultural problems with long-term
management of SLE
Assess pain and fatigue daily
Obtain subjective and objective data
Educate and counsel on expected issues
Nursing Management
Nursing Diagnoses
Fatigue
Acute
pain
Impaired skin integrity
Ineffective therapeutic regimen
management
Body image disturbance
Nursing Management
Nursing Implementation
Health
promotion
Prevention of SLE is not possible
Promote early diagnosis and treatment
Relieve pain and discomfort and fatigue
Application of heat and cold
Encourage to alternate rest and activity
Support devices – braces, splints, firm
mattress
Analgesics and anti-inflammatory medications
Nursing Care
Maintain Skin Integrity
Apply topical antiinflammatory
Avoid direct sunlight
Increase Mobility
ROM
Assistive devices
Nursing Management
Nursing Implementation
Acute
intervention
During exacerbation, patient will become
abruptly, dramatically ill
Record severity of symptoms and response to
therapy
Observe for
•
•
•
•
•
Fever pattern
Joint inflammation
Limitation of motion
Location and degree of discomfort
Fatigability
Nursing Management
Nursing Implementation
Acute
intervention (cont’d)
Monitor ______ & _ _ _
Collect 24-hour urine sample
Assess neurological status
Explain nature of disease
Provide support
Nursing Management
Nursing Implementation
Ambulatory
and home care
Reiterate that adherence to treatment does
not necessarily halt progression
Minimize exposure to precipitating factors –
Teach energy conservation and relaxation
exercises
For joint problems, all the teaching for RA
related to joint protection, ROM, and
positioning to prevent contractures
Treatment and Nursing Care
Facilitate self care
Improve body image
Provide adaptive equipment for eating, bathing,
toileting, dressing
Allow patient extra time to complete care
Encourage patient to verbalize feelings, perceptions,
and fears
Monitor for complications
Assess for serious adverse effects of medications
used in treatment
Avoid ____________ ____ ____ _______
Nursing Management
Nursing Implementation
Lupus
and pregnancy
Infertility
SLE is associated with complications of
pregnancy
Pregnancy & post partum
Women with serious SLE
Nursing Management
Nursing Implementation
Psychosocial
issues
Counsel patient and family that SLE has good
prognosis
Physical effects can lead to isolation, selfesteem, and body image disturbances
Assist patient in developing goals
Nursing Management
Evaluation
Expected
outcomes
Completion of priority activities
Verbalization of having more energy
Expression of satisfaction with pain relief measures
Performance of activities of daily living without pain
Limitation of direct exposure to sun
No open skin lesions
Expression of satisfaction with activity level
Pacing of activities to match level of tolerance
Expression of confidence in ability to manage SLE
over time and in home environment