Rheumatology Flashcards

(37 cards)

1
Q

Urate targets in gout treatment

A

Low disease burden <0.36 mmol/L High disease burden <0.3 mmol/L

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2
Q

What is this?

A

Double conture sign

Seen in gout due to a layer of crystals on the surface of the cartilage

Sens 44% Spec 99%

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3
Q

What type of crystal is seen in gout?

A

Monosodium urate

Strongly negatively birefringent needle shapped crystals:

‘Yellow when parrallel to the polariser’

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4
Q

What is the HLA association with allopurinol hypersensitivity?

A

HLA -B*58:01

Test Han Chinese, Thai, Korean

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5
Q

What are the key inflammatory components of gout attack?

A

Inflammasone assembly

IL1 production

Phagocytosis by macrophages

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6
Q

What non-traditional urate lowering drugs can lower serum urate?

A

Losartan

Fenofibrate

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7
Q

What are the XR changes seen in osteoarthritis?

A

L - Loss of joint space

O - Osteophytes

S - Subchondral cysts

S - Subchondral sclerosis

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8
Q

What is the HLA association with rheumatoid arthritis?

A

Increased risk with HLA-DRB1

Felty syndrome is associated with HLA DR4

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9
Q

What pattern is rheumatoid associated interstitial lung disease?

A

Usually UIP, worse prognosis than NSIP

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10
Q

What is Felty Syndrome?

A

Triad of persistant rheumatoid arthritis, splenomegaly and neutropenia

Can have other extra-articular manifestations

Associated with HLA-DR4

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11
Q

What are the key cytokines seen in RA?

A

TNF-a

IL-6

IL-1

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12
Q

What is the classification of lupus nephritis?

A
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13
Q

What are the principles of the 2019 EULAR-ACR SLE classification criteria?

A

Must have ANA > 1:80 at any point in time

Must have at least 1 clinical criteria and total score >10

The clinical criteria contain - fever, cutaneous, arthritis, neurological, serositis, haematological and renal manifestations

Immunological criteria - anti-phospholipid, complement, dsDNA, anti-SM

If there is a renal biopsy demonstrating lupus nephritis this is diagnostic

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14
Q

What are the changes in complement seen in SLE?

A

Low C3 C4 in active disease

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15
Q

How is disease acitvity in lupus monitored?

A

Clinically

ESR>CRP

dsDNA

Complement levels

Proteinuria

Disease activity scoring systems

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16
Q

What is the management of lupus nephritis?

A
  1. General measures with ACEI, BP management, CVD management, hydroxychloroquine
  2. Immunosuppress class III, IV and possibly V
    - Induction with steroids + mycophenolate or cyclophosphamide
    - Maintance with low dose steroids + mycophenolate or azathioprine
17
Q

What are anti-Ro and anti-La antibodies associated with?

A

Sjogrens

Sjogren manifestations in SLE

Congentital heart block, neonatal lupus

18
Q

What antibodies are associated with neurolupus?

A

Anti-ribosomal P

19
Q

What are the risk factors for poor pregnancy outomes in SLE?

A

Disease activity in preceeding 6 months

Stopping hydroxychloroquine

Serological activity

Lupus nephritis

Anti-phosopholipid syndrome

Organ damage

Anti Ro and Anti La (SSA and SSB)

20
Q

What are the antibodies seen in scleroderma and whar are they associated with?

A

Centromere - limited, Pul HTN

Topoisomerase 1 (Scl-70) - ILD

RNA polymerase III - diffuse, renal involvement

21
Q

What antibody is associated with mixed connective tissue disease?

A

ANA speckled

ENA - U1RNP

22
Q

What is the classic clinical feature of mixed connective tissue disease?

23
Q

What types of rash are seen in dermatomyositis?

A

Gotrans patches - over knuckles of hands

Shawl sign - back of neck/shoulders

Heliotrope rash - eye lids

24
Q

What is the muscle involvement pattern with inclusion body myositis?

A

Distal upper limb

Proximal lower limb

Can be asymmetric

25
What is the HLA association with immune mediated necrotizing myopathy? What is the antibody?
HLA DRB1\*11:01 ANti0HMGCR antibodies highly specific
26
What is anti-synthetase syndrome?
ILD Raynauds Mechanics hands Arthritis Myositis Most commonly Jo-1 positive
27
What is Lofgren syndrome?
A particular sarcoidosis syndrome - hilar lymphadenopathy - Joint pain - often ankle - Erythema nodosum
28
What are the key inflammatory drivers of ankylosing spondylitis?
IL-23 driving Th17 picture which produces IL-17 and TNFa
29
What are the cardiac manifestations of ankylosing spondylitis?
Ischaemic heart disease Conduction defects Aortic regurgitation
30
What types of lung disease is seen in ankylosing spondylitis?
Restrictive lung defect from reduced chest wall expansion Interstitial fibrosis - in the upper lobes
31
What is the treatment for ankylosing spondylitis?
1st - NSAID (continous) and physio, education, smoking cessation \*\*Extra-axial disease - local steroid injections, MTX, sulfasalazine 2nd - anti-TNFa or secukinumab (anti-IL17)
32
In ankylosing spondylitis what agents should not be used in co-existing IBD?
Etanercept (anti-TNF) - not effective in IBD Secukinumab (anti-IL17) - not effective, may be harmful
33
What forms of arthritis affect the DIP joints?
Osteoarthritis Psoriatic arthritis Gouty arthrtitis
34
What are the radiographic features of psoriatic arthritis?
Pencil in cup deformity Marginal erosions with adjacent proliferation Small joint ankylosis Asymmetric sacroiliitis
35
What antibody is associated with inclusion body myositis?
Anti-5NT1A Highly specific but not sesnitive Associated with more severe disease
36
Which dermatomyositis anibody is associated with highest malignancy risk?
TIF gamma antibody NXP2 Anti-P155
37
What are the common ANA patterns? What are they associated with?
Homogenous - dsDNA, histone, chromatin Rim or peripheral staining - dsDNA, sclerosis Speckled - most eg SS-A, SS-B Nucleolar - sclerosis, polymyositis Centromere - sclerosis, primary biliary cirrhosis