Seropositive Arthropathies Flashcards

1
Q

list all the seropositive arthropathies

A
rheumatoid arthritis 
SLE
systemic sclerosis 
sjogrens 
vasculitis
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2
Q

what do seropositive arthropathies have in common

A

all diagnosed through blood tests as have certain auto-antibodies present in disease

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3
Q

what is the most common seropositive arthropathy

A

rheumatoid arthritis

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4
Q

what is the aetiology for RA

A

females > males
peak incidence between 35-50 years
certain HLA subtypes and environmental factors such as smoking increase risk

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5
Q

describe the pathogenesis of RA

A

immune response against synovium, immune cells attack which destroys articular cartilage
lining of the joint thickens producing excess fluid and wears away bone underneath

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6
Q

which joints are affected in RA

A

small joints, PIPs, MCP, MTP, wrists but not DIPs

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7
Q

describe the presentation of RA

A

morning stiffness >30 mins
pain improves on movement
joints symmetrically affected
visible synovitis - hands appear boggy and soft

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8
Q

RA increases risk of spinal cord compression true/false

A

true - atlanto-axial subluxation is later complication

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9
Q

describe a swan neck deformity

A

hyperextension at PIP, flexion at DIP

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10
Q

describe a boutonniere deformity

A

flexion at PIP, hyperextension at DIP

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11
Q

list some of the extra-articular manifestations of RA

A

rheumatoid nodules - found on extensor surfaces
increased cardiovascular morbidity
interstitial lung disease
ocular involvement

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12
Q

list the ocular symptoms of RA

A

uveitis, scleritis

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13
Q

which auto-antibodies are present in RA

A

rheumatoid factor

anti-CCP

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14
Q

describe the x-ray findings of early and late RA

A

early - normal x-ray possibly with swelling

late - erosions of bone and subluxations

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15
Q

what factors must be present to diagnose RA

A

involvement of several joints, positive serology, acute phase reactants positive eg CRP and duration longer than 6 weeks

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16
Q

what is the first line treatment for RA

A

DMARDs - specifically methotrexate unless contraindicated

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17
Q

what is the window of time DMARDs must be commenced from start of disease

A

3 months

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18
Q

what must initially be added to methotrexate and why

A

corticosteroid as lag time - acts as short term pain relief

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19
Q

list some other examples of DMARDs and their side effects

A

leflunomide, sulfalazine and hydroxychloroquine

methotrexate and leflunomide are teratogenic, all increase risk of infection and bone marrow suppression

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20
Q

if RA doesnt respond to DMARDs what is the next line of treatment and give examples

A

biologics
TNFalpha inhibitors - infliximab and adalinumab
B cell depletion - rituximab

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21
Q

what calculator is used to assess severity of RA

22
Q

DAS28 score of what indicates remission of RA

23
Q

DAS28 score of what indicates severe disease requiring biologics

24
Q

describe the pathogenesis of SLE

A

defect in apoptosis causing increased cell death - allows inadequate clearance of antigens and deposition of immune complexes - type 3 hypersensitivity

25
who is lupus most likely to present in
women of child bearing age, more common in black women
26
describe the skin and mucocutaneous presentation of lupus
skin - butterfly malar rash with sparing of nasolabial fold, discoid dermatitis too muco-cutaneous - oral ulceration and Raynauds phenomenon
27
describe the other organ involvement of lupus
``` renal - lupus nephritis resp - interstitial lung disease and pleurisy neuro - seizures and psychosis cardiac - pericarditis and ischaemia MSK - myalgia and inflammatory arthritis ```
28
there is one specific diagnostic test for lupus true/false
false
29
list some of the investigation findings of lupus
FBC showing thrombocytopenia and leucopenia | Anti-dsDNA positive, ANA positive, Anti-sm (low sensitivity)
30
what happens to C3/4 levels in active lupus disease
lowered
31
which test is used in lupus to assess for renal involvement
urinalysis
32
what is the treatment for lupus
depends on manifestations, skin disease and arthralgia give hydroxychloroquine and NSAIDs, arthritis or organ involvement requires immunosuppression if unresponsive may require IV immunoglobulin
33
what is Sjogrens syndrome
autoimmune condition characterised by lymphatic infiltrates in exocrine glands - causes dryness, arthralgia and fatigue
34
list the clinical features of Sjogrens
reduced salivary and lacrimal gland production vaginal dryness polyarthritis peripheral neuropathy and interstitial lung disease
35
which connective tissue disease has an increased risk of lymphoma
Sjogrens
36
which test is used to assess ocular dryness in Sjogrens
Schrimers test
37
other than Schrimers test, list investigations for Sjogrens
lip gland biopsy for dryness | positive anti-Ro and anti-La antibodies
38
what is the management of systemic sclerosis
symptom management as no cure lubricating eye drops, saliva replavements, hydroxychloroquine for joint pain, immunosuppressant if extreme organ involvement
39
what is systemic sclerosis
connective tissue disease causing vasculopathy and autoimmunity due to excessive collagen deposition
40
describe the difference between limited and diffuse systemic sclerosis
limited - confined to hands, feet and forearms | diffuse - spread all across limbs and trunk
41
what is usually the first manifestation of systemic sclerosis
Raynauds phenomenon - blanching, acrocyanosis and reactive hyperaemia
42
what is the treatment for raynauds
calcium channel blockers, ARBs and nitrates
43
what is the pneumonic for limited systemic sclerosis
CREST - calcinosis, raynauds, oesophageal dysmotility, sclerodactyly and telangiectasia
44
list some symptoms of systemic sclerosis
dysphagia telangiectasia skin tightening - beaking of the nose calcinosis - deposition of calcium in the digits
45
state the antibodies present in systemic sclerosis
limited - anti-centromere | diffuse - anti-scl-70
46
how is systemic sclerosis managed
no curative treatment, manage underlying organ damage | immunosuppressant for lung disease, PPI for GI symptoms
47
how does anti-phospholipid syndrome present
migraines increased risk of stroke, MI esp in younger patients recurrent loss of pregnancy typically in second and third trimester recurrent pulmonary emboli
48
what type of rash presents with anti-phospholipid syndrome
livedo reticularis - mottled vascular rash with lace like purple discolouration
49
what investigations are carried out for anti-phospholipid syndrome
bloods - thrombocytopenia | lupus anticoagulant and anti-beta 2 glycoprotein positive
50
what is the management of anti-phospholipid syndrome
if one episode of thrombosis - lifelong anticoagulation eg warfarin, if pregnant give LMWH instead