Rheum/osteo arthritis Flashcards

(42 cards)

1
Q

Rheumatoid Arthritis

Pathophysiology:

A

chronic inflammatory disease with uncontrolled proliferation of synovial tissue and a wide array of multisystem comorbidities. The body confuses synovial tissue for a foreign body and attacks synovial surfaces

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2
Q

Rheumatoid Arthritis

general

Swelling in PIP and MCP joints R > L ; note the decrease in skin creases over PIP
A

Most commonly diagnosed inflammatory arthritis

Females > males ( 3:1) between 30-50 years of age
Can be triggered by stress, infection, environmental, smoking; genetic

Higher likelihood to also have IBS, FM, SLE, Sjogren’s, thyroiditis

Present with pain worse in am improves as the day goes on, “stiffness,” deformity, muscle weakness, fatigue, malaise

Can have extraarticular manifestations

DIP joints are usually uninvolved
Most common joints: PIP, wrist, metacarpals

Most common cause of death is cardiovascular
More joints involved worse prognosis
On average life expectancy is 12 years less than the general population

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3
Q

RA

Physical Exam Findings

A

Low-grade fever
Slightly elevated pulse
Rheumatoid nodules on extensor surfaces of the forearm
Bilateral Joint swelling ( fingers, wrists, elbows, shoulders, hips, knees, ankles, toes, and neck) without erythema; decreased range of motion and possible heat
Distal interphalangeal joints are rarely involved
Epitrochlear, axillary, and cervical lymphadenopathy

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4
Q
A
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5
Q

RA

Extra-articular manifestations of RA (18% to 41%)

A

Cardiovascular: pericarditis and myocarditis

Pulmonary: Pleural effusions and pulmonary rheumatoid nodules most common manifestations, pleurisy, pneumonitis, and fibrosis

Vasculitis: skin ulcerations, infections, or neuropathy

Ocular: retinitis, scleritis, uveitis, and peripheral ulcerative keratitis (corneal melt), Sjogren’s disease

Osteopenia and osteoporosis
Anemia of chronic disease

Spine instability: caution in patient post-fall/trauma, increases fall risk
Rheumatoid nodules: (20%) elbows and finger joints

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6
Q

Rheumatoid Arthritis

Workup and Tx

A

Xray hand and feet (r/o osteo; will show soft tissue swelling and demineralization of joint) “periarticular osteopenia”
aspiration of joint fluid ( r/o gout/septic arthritis)
labs ( ESR and CRP elevated, RF + 80%, ACPA/anti-CCP + 95%)
CBC, CMP

  • if going to treat with biological need negative Hepatitis C/B and TB testing

Treatment: rheumatology collaboration, physical therapy/occupational therapy, Rx therapy

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7
Q

RA

A
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8
Q

RA

differential diagnoses

A

+ skin changes: SLE, systemic sclerosis, psoriatic arthritis

+ shoulder/hip pain in elderly: polymyalgia rheumatica

Recurrent self-limiting symptoms: crystal arthropathy

+ multiple trigger points: FM ( can co-exist with RA)

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9
Q

RA

Tx

A

Nonbiologic DMARD
Methotrexate- 1st line
Alternative therapies leflunomide ( GI SE), Sulfasalazine or hydroxychloroquine- if low disease activity, seronegative
Add folic acid daily

Biologic DMARD
TNF inhibitors-1st line

Pain control
NSAIDS and/or corticosteroids
1,200–1,500 mg of calcium and 800–1,000 IU of vitamin D daily to prevent glucocorticoid-induced osteoporosis

Therapeutic Lifestyle Changes
Complimentary Therapies
Exercise
Physical Therapy

*remission in 10-50% of patients. Remission more likely in males, non-smokers, < 40 years, late on set disease ( > 65), seronegative

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10
Q
A
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11
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12
Q

Rheumatoid Arthritis Summary

A

Female, 30-50 years age ( fam hx/smoker) with at least one joint swelling unexplained other etiology
Symmetrical pain w morning stiffness > 6 weeks, spares DIP

Diagnosis
RF+, anti-CCP+, elevated CRP, ESR
Treatment ( baseline GFR/LFTs)
DMARD (methotrexate preferred)
Biologics (r/o hepatitis/TB)

Tumor necrosis factor usually add on/second line

Goal of therapy
Pain management and maintain joint space
Long term
Monitor for cardiovascular disease and lymphoma; extraarticular manifestations

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13
Q

Which of the following is an extra-articular manifestation of rheumatoid arthritis?

A. vasculitis
B. xanthelasma
C. coronary artery aneurysms
D. malar rash

A

A. vasculitis

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14
Q

Juvenile Rheumatoid Arthritis ( juvenile idiopathic arthritis)

general

A

Chronic synovitis and extra-articular manifestations age < 16 at onset lasting > 6 weeks

Female/male ratio 2:1; female age of onset 1-3 yoa; males age of onset 8-12 yoa

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15
Q

Juvenile Rheumatoid Arthritis

work up

A

Labs: 10-15% + RF, + ACPA antibody; usually have elevated CRP, ESR;

if have + ANA increased risk uveitis

Imaging: soft tissue swelling, periarticular osteoporosis, joint destruction uncommon

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16
Q

Juvinile RA- subtypes

Systemic ( 15% cases)

A

Fever spikes, myalgias, polyarthralgia, salmon-pink maculopapular rash in pm w fever
Minimal articular findings

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17
Q

Juvinile RA- subtypes

Pauciarticular (50% cases)

A

Involves 4 or fewer joints; if + ANA increased risk for asymptomatic uveitis may lead to blindness

18
Q

Juvinile RA- subtypes

Polyarticular (35% of cases)

A

Systemic involvement of 5 or more joints; assoc low grade fever, fatigue, rheumatoid nodules

19
Q

Which of the following diseases usually has a symmetric presentation?

Which of the following diseases usually has a symmetric presentation?
A) osteoarthritis
B) gout
C) septic arthritis
D) rheumatoid arthritis

A

D) rheumatoid arthritis

20
Q

What is most common complication associated with juvenile rheumatoid arthritis and a positive ANA?

A. glomerulonephritis
B. Myocarditis
C. Sjogren syndrome
D. Uveitis
E. Vasculitis

21
Q

Which of the following describes the pathophysiology associated with rheumatoid arthritis?
A) degenerative wear and tear of joint
B) T cell-mediated pannus formation that attacks synovial tissues
C) joint damage from repetitive microtrauma
D) joint damage from bacteria

A

B) T cell-mediated pannus formation that attacks synovial tissues

22
Q

45-year-old female presents with recurrent flare up of rheumatoid arthritis. She is currently taking ibuprofen. What medication is indicated to slow progression and prevent further joint destruction?

A. diclofenac (NASID)
B. prednisone (glucocorticoid)
C. infliximab (TNF-inhibitor)
D. methotrexate (DMARD)

A

A- no benefit to another nsaid
b. Prednisone used for acute flare symptom relief- no improvement on disease
c. 2nd line after conventional DMARD consider biologic ( for TNF need to monitor labs and make sure no active infection – Hepatitis B, TB, HIV)
d. DMARD

23
Q

Which antibody is most specific to Rheumatoid arthritis?
A. Anti-cyclic citrullinated peptide (anti-CCP)
B. ANA
C. Rheumatoid Factor
D. ESR

A

A-
B- not specic
c. Can be seronegative

24
Q

A patient presents with acute diarrhea after starting a medication to treat gout. What medication is most likely the cause of his symptoms?
A. ibuprofen
B. prednisone
C. allopurinol
D. colchicine

A

D. colchicine

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Characteristics of Synovial Joints
**Articular cartilage** Made of hyaline Covers the ends of bones Provides shock absorption, stability, and lubrication **Synovial membrane** Loose, vascularized connective tissue **Secretes synovial fluid** into the joint cavity for lubrication **Joint/articular capsule** A fibrous connective tissue that surrounds the bony ends forming the joint
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# Osteoarthritis (OA) general
Irreversible, progressive multifactorial disease affecting the entire joint **Most common form of arthritis** (> 70% of all cases of arthritis) Traditionally known as “wear and tear arthritis” Incidence: Affects ~41 million people in the United States (www.arthritis.org) Prevalence increases with age 80–90% of individuals < 65 years have radiographic osteoarthritis (OA) Symptoms are generally not noticed until after the age of 50
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# OA Primary and Secondary OA
Primary Osteoarthritis Idiopathic form Secondary Osteoarthritis Caused by another disease or condition **Obesity** Repeated trauma or surgery to the joint Infection Congenital abnormalities (scoliosis) **Metabolic disorders:** Gout Hemochromatosis- MCPs Bone disorders: Paget’s disease
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# OA RF
**Age - ↑ with age Obesity** Sex: Women > Men Physical activity and repetitive use Joint injury Muscle weakness or dysfunction Genetics and family history
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# OA Commonly Affected Joints
Hands **PIP and DIP joints CMC joint** Feet **1st MTP joint** Shoulder Hips…younger age! Knees Spine Neck Low back
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# OA Patho
**Degradation of the articular cartilage** and **remodeling of bone** due to an active response of **chondrocytes** in the cartilage and the **inflammatory cells** in the surrounding tissues Release of degradative enzymes from **chondrocytes causes breakdown of collagen and proteoglycans**→ destruction of the articular cartilage Exposure of underlying subchondral bone → **sclerosis** and reactive **remodeling changes** (**formation of osteocytes and subchondral bone cysts**) Progressive **loss of joint space** over time
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# OA Joint pain
Gradual onset of achy pain **Asymmetric** More severe with: Activity and Weight bearing Relieved with rest Later in the disease:  Pain is more constant Affects sleep and level of activity **Radicular pain** results from: (pain that shoots down) Spondylolisthesis Nerve impingement ## Footnote Spondylolisthesis: displacement of a vertebra forward in relation to the vertebra below
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# OA Joint stiffness
Most noticeable upon awakening or after being inactive Duration **< 30 minutes** Improves with movement **Swelling of the joint** **Limited range of motion** (ROM) Sensation of **joint instability, locking, buckling Crepitus**- Crackling, crunching, grinding or grating noise
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# OA PE
Joint line tenderness Limited range of motion (ROM) Crepitus with passive ROM Evidence of osteophytes **DIP joints: Heberden’s nodes PIP joints: Bouchard’s nodes First CMC joint: thumb squaring** Knee varus or valgus deformities
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# OA Dx
Clinical diagnosis that is confirmed with imaging Radiography Classic findings: Joint space narrowing (asymmetric) Subchondral sclerosis Osteophytes Subchondral cysts (late) Findings do not correlate well with symptoms No specific blood test for the diagnosis of osteoarthritis
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1 - Joint space narrowing 2 - Osteophytes 3 - Joint destruction 4 - Involvement of the carpometacarpal (CMC) joint which is very common
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# OA Supportive Labs
Used to exclude other causes of arthritis Everything should be normal Arthrocentesis with synovial fluid analysis Non-inflammatory with a **WBC count < 2,000 cells/μL** Crystal analysis to rule out gout and pseudogout Laboratory testing  Negative rheumatoid factor (RF) and anti-cyclic citrullinated peptide (anti-CCP) Normal erythrocyte sedimentation rate (ESR) or C-reactive protein (CRP) Negative antinuclear antibody (ANA)
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# OA TLC Tx
Goals of management include alleviating pain and minimizing the loss of physical function General conservative measures Lifestyle modifications:  Minimize weight bearing activities Good posture Sleeping on a firm mattress Wearing supportive shoes **Weight loss** **Physical therapy** to increase: Strength Flexibility Range of motion Endurance Assistive devices:  Cane, brace, splints, and taping Hot and cold therapy
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# OA Pharm tx
Acetaminophen (Tylenol) Oral and topical nonsteroidal anti-inflammatory drugs (NSAIDs) Muscle relaxants Cyclobenzaprine, methocarbamol Relieve pain from strained muscles Use with caution in elderly patients Duloxetine (Cymbalta) – second-line agent Can be used in patients with contraindications to NSAIDs Alternative for those who do not respond to first-line therapies Corticosteroids Should not be used chronically Can be used orally or as an intra-articular injection Hyaluronic acid Intra-articular injection Supplements Glucosamine & chondroitin Evidence is limited Opioids – BE CAREFUL! Can be considered for short-term use For patients who fail or are not candidates for other treatments Consider referral to a chronic pain management clinic ## Footnote Tramadol (Ultram) is the only opioid medication listed as a medication option through the Arthritis Foundation
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# OA Surgical Management
Reserved for patients with advanced disease who have failed other treatments Total joint arthroplasty (replacement) is the most common procedure
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