Inflammatory Seropositive Arthritis: RA, SLE, Sjogrens, Scleroderma Flashcards
Rheumatoid arthritis
-pathophysiology
-risk factors
-presentation
-investigations
-monitoring response
-management
Synovial inflammation => joint damage
Genetic (HLA DR4) + environmental (smoking)
Female 30-40
Symmetrical - PIP, MCP, MTP
Morning stiffness (30mins+)
Swelling
Fatigue
Constitutional - fever, weight loss
Insiduous onset, gradual development
Extra-articular manifestations
-rheumatoid nodules
RF - more sensitive but associated with other conditions
Anti CCP - more specific
Xray changes - LESS
-loss of joint space
-erosions (late)
-soft tissue swelling
-soft bones (early osteopenia/osteoporosis)
Monitor CRP, DAS28
Initial DMARD therapy - methotrexate
-must monitor FBC (myelosuppression), LFT (cirrhosis)
Inadequate response to 2 DMARDs => TNF inh
-infliximab, adalimumab
-must do CXR before hand to assess risk of TB reactivation
Flares - IA/IM CS
Extraarticular presentation of RA
Resp - IDL, effusion, nodules, methotrexate pneumonitis
Eyes - dry eyes, episcleritis, scleritis, keratitis
Inflammation => osteoporosis, CVD
Medication - IC
Impact of condition - depression
SLE
-pathophysiology
-risk factors
-presentation
-investigations
-monitoring response
-management
T3 hypersensitivity - HLA B8, DR2-3
-immune complex formation => deposits in tissues
Genetic
Environmental
-UV light
-drug induced - procainamide, hydralazine, isonaizid
Systemic - fever, weight loss
Joint - non erosive arthritis, Raynaud’s, nailfold capillaries
Skin - photosensitivity, malar/discoid rash, non scarring alopecia, livedo reticularis
Mouth - ulcers
Renal - lupus nephritis
Resp - pleuritis
CV - pericarditis
Neuropsych - headache, seizure, psychosis
FBC
High ESR with normal CRP
ANA - most important test
Anti dsDNA - specific
U&E - deranged in lupus nephritis (proteinuria, haematuria)
4/11 signs => diagnosis
Initial - HCQ + NSAID
Mild flare - add PO/IM GC
Moderate - add IV
Severe - cyclophosphamide, rituximab considered
Regular urinalysis for lupus nephritis
Lupus nephritis
-presentation, investigations
-management
Proteinuria
Reduced GFR
HTN
Edema
Management
-HTN + CS + azathiopurine
Sjogrens syndrome
-pathophysiology
-relationship with other AI conditions
-presentation
-investigations
-management
AI affecting exocrine glands => mucosal dryness
-primary or secondary to RA, other connective tissue disorders
Female
Dry eyes, mouth, vagina
Muscle, joint pain, Raynauds
Clinical diagnosis
Schirmer’s test - assess tear production with filter paper
AntiRo, La, ANA, RF - not specific
Artificial saliva, tears
Pilocarpine
Systemic sclerosis
-pathophysiology
-risk factors
-types
-management
Chronic AI connective tissue - fibrosis of skin, internal organs, vasculature, immune dysregulation
Female, 60-70s
Limited
-Raynauds + FACE and DISTAL LIMB scleroderma
CREST - calcinosis, Raynaud’s, esophageal dysmotility, sclerodactyly, telangectasia
Diffuse
-Raynauds + TRUNK and PROXIMAL LIMB scleroderma + RESP INVOLVEMENT
Cause of death often due to
-interstitial lung disease
-pulmonary arterial HTN
-renal disease - treat with captopril
ANA in all
Limited - anti centromere
Diffuse - anti scl70
Early - low dose steroid
Late - symptomatic
Drug induced lupus
-presentation
-causative drugs
-how to differentiate from SLE
-management
Arthralgia
Myalgia
Skin + lung involvement
-malar rash
-pleurisy
PROCAINAMIDE
ISONIAZID
HYDRALAZINE
ANA +ve
dsDNA -ve
ANTI HISTONE +ve
anti-Ro, Smith +ve
Stop causative meds