SLE Flashcards

1
Q

What is SLE?

A

It is a multisystem autoimmune disease that primarily affects women of child-bearing age

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2
Q

Who gets SLE the most?

A

-It is 10x more common in women and between 20-40 years

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3
Q

what is the aetiology of SLE?

A

-genetic predispositions:
HLA DR2 and HLA DR3
-hormonal factors: increased oestrogen
-environmental factors: UV light, EBV, medications: hydralazine

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4
Q

What is the clinical presentation of SLE?

A

Skin: 70% of cases

  • malar rash(sparing of the nasolabial folds)
  • photosensitivity
  • discoid rash
  • oral ulcers
  • alopecia

Joints:

  • arthritis and arthralgia(90% of the cases)
  • non-erosive polyarthritis
  • fever and fatigue
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5
Q

What other organ systems are affected by SLE?

A
  1. musculoskeletal-lymphadenopathy
  2. serositis-pleuritis and pericarditis presenting as chest pain
  3. kidneys: nephritis
  4. Heart: Libman sacks endocarditis
  5. Lungs- interstitial lung disease
  6. vascular: Raynauds phenomenon
  7. Neurological: psychosis, seizures
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6
Q

What are the different types of lupus erythematosis?

A
  1. Discoid lupus erythematosus
  2. Drug induced lupus erythematosus
  3. Subacute cutaneous lupus erythematosus
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7
Q

How do we diagnose SLE?

A
  1. First we suspect it if more than 2 organ systems are indicated according to the American College Of Rheumatology
  2. Screening with Anti-nuclear Antibody titre
  3. If the antibody antinuclear test is increased then we do a confirmatory test:
    - Anti-dsDNA antibody testing which is positive in 70% o patients
    - Anti Smith antibody testing which is highly specific
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8
Q

What are the 11 diagnostic criteria for SLE?

A

SOAP BRAIN MD

  1. Serositis
  2. orla ulcers
  3. arthritis
  4. Photosensitivity
  5. Blood disorders: thrombocytopenia, autoimumune hemolytic anaemia with reticulocytes, leucopenia
  6. Renal involvement: persistent proteinuria >0,5g per day or cellular casts
  7. Anti-nuclear antibodies
  8. Immunological phenomena: Anti-dsDNA antibodies, anti-Smith antibodies, anti-phospholipid antibodies
  9. Neurological disorders: psychosis and seizures
  10. Malar rash
  11. Discoid Rash
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9
Q

What is the treatment of SLE?

A
  1. Basic therapy: hydrochloroquine
  2. Induction therapy:
    - mild symptoms with no organ involvement- low dose and oral glucocorticoids
    - severe symptoms with no organ involvement- medium dose oral glucocorticoids
    - organ involvement: IV glucorticoids
  3. Immunosupressives- cyclophosphamide
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10
Q

What are the common complications of SLE?

A
  1. Lupus nephritis-50%
  2. accelerated atherosclerosis leading to myocardial infarction
  3. Pulmonary hypertension
  4. Antiphospholipid syndrome
  5. Pancytopenia
  6. Osteopenia/osteoporosis
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11
Q

what is lupus nephitis?

A

It is a crucial prognostic factor for SLE

  • it can present as either nephrotic or nephritic syndrome
  • the pathophysiology is when there are immune complex deposition in the mesangial or subendothelial cells(Anti-smith, anti-dsDNA) this then causes inflammation and damage which allows the protein or blood to flow into the system causing proteinuria or haematuria
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12
Q

How do we diagnose lupus nephritis?

A
  1. Do urine tests: proteinuria, haematuria, red cell casts,

2. kidney biopsy

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13
Q

What is the treatment of lupus nephritis?

A
  1. Prednisone

2. cyclophosphamide (immunosuppresives)

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14
Q

What is the most common cause of death in SLE?

A
  1. Myocardial infarction

2. end stage renal disease

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