rheum 2 Flashcards

1
Q

summarise psoriatic arthritis

A

a seronegative inflammatory condition- associated with psoriasis

mild assocation with HLA b27
genetic and environmental factors play a role in development of disease.

rare (0.1%) in gen pop but high 6-41% in psoriasis patients. higher prevalence in northern europe.

prevents with oligoarthritis- 2-4 joints affected asymetrically.

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2
Q

signs and symptoms of psoriatic arthritis + some risk factors

A

plaques on extensor surfaces
nail dystrophy
asymetrical oligo/poly arthritis
DIPJ joints affected.
dactylitis
anterior uveitis, ulcerative colitis.
enthesopathy

can affect the spine in a simalar manner to AS

RF:
ginetics, stress- chronic or acute.
alcohol + smoking.

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3
Q

investigations and classification of psoriatic arthritis

A

no specific lab tests- CRP and ESR might be raised- but 50/50.

X-rays- errosive changes, gross joint destruction, narrowing, pencil in cup deformitiy. —— look for bone destruction and formation within the same joint.

spinal changes- but unilateral, skipping levels, as opposed to AS changes.

Classification criteria- CASPAR
Skin psoriasis: present =2, prev present = 1. none=0
nail lesions =1
dactylitis=1
RF: if -ve =1
Juxta articular bone formation=1

if 3 points- quite likely.

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4
Q

management of psoriatic arthritis

A

PTOT, stop smoking + drinking.

NSAIDS
DMARD (meth, or sulfasalazine- though sulf not effective for skin disease)

biologics- better for axial disease- TNF inhibitors are best.

less use of oral steroids as can cause psoriasis to flare.

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5
Q

definition, epidaemiology, aetiology + risk factors for Systemic lupus erythmatosis

A

an autoimmune chronic inflam connective tissue disorder- can involve skin, joints, mucous membranes, kidneys, blood vesels. autoantibodies are made to antigens - forming immune complexes - which accumulate.
type 3 hypersensitivity reaction

Epi: women of child bearing age 9:1 men.
afro-carribean/ asian

Aetiology: waste disposal- defected cells undergo apoptosis- defect + not cleared- release nuclear antigens- generation of antibodies.

RF:
genetic C4null, or variant in FC receptors
C3 deficiency.

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6
Q

signs and symptoms of SLE

A

malar/ erythematous rash
photosensitive rash
non-scarring alopecia
ulcers oral/nasally.
synovitis- more than 30 mins pain in the morning
pleurisy, effusions, rub, pericardial pain
seziures, psychosis, lethargy
thrombocytopaenia

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7
Q

pathophysiology of SLE

A

loss of B cell tolerance.
Antigen-antibody complexes then accumulate-

on renal basement mambrane
synovium
skin
small blood vessels
cell surfaces

compliment gets activated- lowering their levels in the blood stream.- releasing cytokines they promote inflammation.
Il-6 released- hepatocytes release more fibrinogen.

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8
Q

investigations of SLE

A

ANA- antinuclear antibody- most sensitive test
infirect immunofluorescence Crithidia test- checks for double straned DNA antibodies- specific but not sensitive.

Check compliment- C3 + C4 will be low. - use this to monitor disease activity.
ESR,CRP, U&E, LFT- CRP is usually low.

6/6 specific antibodies to check for
(DS-DNA, SMITH< RIBONUCLEOPROTEINS, RO, LA)

RO+LA cross placenta and can cause heart block in foetus.

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9
Q

Rx of SLE + prognosis

A

high factor sunblock, hydroxycholoroquine, topical steroids for skin

Maintenance: NSAIDS, hydroxycholoroquine,

Mild flare: low dose steds + hydroxy
mod flare- mycophenolate
severe flares- urgen high dose steds, myco, rituximab

reduce proteinurea with ACEi

prognosis-
80% survival at 15 years.

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10
Q

complications of SLE- anti-phospholipid syndrome

A

specific antibodies to

cardioliptin- a component in the inner mitochondrial membrane- which activated protein C.

by binding cardioliptin + inhibiting factor c from working factor 5 cannot be degreaded and is always active.

B2 glycoprotein antibodies- leading to activation of thrombin

lupus coagulant- bind to prothrombin- helping it be cleaved to thrombin.

to diagnose - must have antiphospholipid antibodies on 2 tests 12/52 apart

Causes: CLOT
Coagulation defecit
livedo reticularis
obstetric- recurrent misscarrage
thrombocytopaenia

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11
Q

management of antiphospholipid sydrome

A

thrombophrophylaxis- low dose aspirin 75mg

if not pregnant with thrombosis- LMWH + warfarin

pregnant with thrombosis- LMWH + aspirin

if post thrombotic event- lifelong warfarin 2-3 INR
if recurrent 3-4 INR

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