10 - 65 - PSORIATIC ARTHRITIS Flashcards

1
Q

PsA characteristically involve which joints?

A

distal interphalangeal joints

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2
Q

Classification Criteria for PsA (CASPAR)

A
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3
Q

Clinical predictors of PsA

A
  • nail psoriasis,
  • severe psoriasis,
  • scalp, intergluteal, or perianal psoriasis,
  • presence of uveitis
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4
Q

psoriasis in what areas are more likely to be associated with PsA?

A

Scalp and intergluteal psoriasis

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5
Q

In PsA, what is the nail disease prevalence?

A

80%

  • Both the nail plate and nail matrix are affected, with nail pitting being the most common
  • Association of onycholysis with axial PsA has recently been described.
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6
Q

most common Psoriatic Arthritis Phenotype

A

Oligoarthritis

  • These phenotypes tend to overlap with cumulative disease duration. For example, the oligoarticular presentation tends to become symmetric over time as more joints become involved
  • Joint inflammation in PsA is more vascular and less tender than in rheumatoid arthritis, and joint tenderness and swelling each predict subsequent joint damage
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7
Q

full-thickness inflammation of a digit (finger or toe)

A

Dactylitis

  • sign of disease severity associated with radiographic damage
  • Inflammation affects the joints, entheses, and subcutaneous tissues of the digits.
  • Dactylitis assessed with high-resolution MRI is characterized by multiple lesions spanning multiple musculoskeletal structures: diffuse extracapsular soft tissue edema (92%), diffuse or focal increased bone marrow edema (83%), enthesitis at the collateral ligament (75%) and extensor tendon (50%) insertions, flexor tenosynovitis (75%), synovitis (68%), signal intensity changes in the tendon pulleys (fingers), and fibrous sheaths (toes).
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7
Q

inflammation at entheseal sites and has an important role in PsA pathophysiology, with studies supporting a link between biomechanical damage as the initiating event of autoimmunity in PsA.

A

Enthesitis

  • Clinically, enthesitis is diagnosed as tenderness to pressure at entheseal insertion sites.
  • The most common sites of involvement are the Achilles tendons, plantar fascia, and lateral epicondyles at the elbows
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8
Q

has the strongest evidence for being a genetic risk factor for PsA in people with psoriasis

A

HLA-B27

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8
Q

Risk factors for axial PsA

A

presence of onycholysis, inflammatory back pain symptoms, PsA duration/young age at onset, positive HLA-B27, and inflammatory bowel disease

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8
Q

inflammatory arthritis affecting the axial skeleton leading to spondylitis and/or sacroiliitis.

A

Spondyloarthritis

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9
Q

population at greatest risk for developing PsA

A

people with psoriasis

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10
Q

risk factors associated with developing PsA have been identified in people with psoriasis:

A
  • psoriasis type/location such as scalp and intergluteal, psoriasis severity, psoriatic nail disease, positive HLA-B27, and uveitis
  • In addition to these clinical factors, the following environmental and individual factors increase the risk of PsA: physical trauma, smoking, overweight, and obese physique
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11
Q

Psoriatic arthritis diagnostic algorithm

A
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12
Q

window of opportunity to initiate therapy to maximize chances of minimal disease damage in Psoriatic Arthritis

A

6 months

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13
Q

first-line agents for PsA

A

The disease-modifying antirheumatic drugs (DMARDs) methotrexate, sulfasalazine, and leflunomide

13
Q

preferred DMARD in peripheral spondyloarthritis considering risk and benefits in individual patients

A

Sulfasalazine

13
Q

first-line biologic agents for PsA

A

TNF inhibitors (adalimumab, certolizumab, golimumab, etanercept, infliximab)

13
Q

first-line treatment for enthesitis and axial PsA

A

TNF inhibitors (adalimumab, certolizumab, golimumab, etanercept, infliximab)

15
Q

Reactive arthritis is typically an oligoarthritis that develops how many weeks following an enteric or urethral infection?

A

1 to 4 weeks

16
Q

classic triad of reactive arthritis

A

urethral, ocular and articular inflammation

*rarely present

17
Q

Inciting infections in reactive arthritis

A

Chlamydia trachomatis, Yersinia, Shigella, Salmonella, Campylobacter, Clostridium difficile, and Escherichia coli.

18
Q

Cutaneous manifestations of reactive arthritis

A

keratoderma blenorrhagicum, circinate balanitis, aphthous ulcers, and nail changes.

19
Q

This HLA haplotype appears to be a risk factor of reactive arthritis and is associated with a more chronic prognosis.

20
Q

cutaneuos manifestation of reactive arthritis characterized as inflammatory skin lesion that develops on the shaft or glans of the penis and more rarely on the scrotum

A

Circinate balanitis

21
Q
  • cutaenous manifestation of reactive arthritis that resembles a pustular psoriasis and is generally found on the **palms and soles. **
  • Initially it is an erythematous vesicular lesion that develops into pustular keratotic lesions before coalescing into psoriatic-like plaques.
A

Keratoderma blenorrhagicum

22
Q

criteria for diagnosing ReA

A

■ The arthritis should predominantly involve the lower limb, involve one or only a few joints, and not equally involve both sides of the body (asymmetric).

■ There should be evidence or a history of preceding infection. Although it is ideal to have a culture that is positive for an infectious agent that is recognized to be associated with this condition, if the patient has documented diarrhea or urethritis in the prior 4 weeks, laboratory confirmation is not required.

■ The patient should not have evidence that the joint itself is infected (ie, septic arthritis). Also, other causes of monoarthritis (such as gout) or oligoarthritis (such as rheumatoid arthritis) should be ruled out.