Title: For Phase 2
1 Rheumatology
- For Phase 2
- Katie Knappett
- Phase 3B
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2Aims
- Go over basic sciences from Phase 1
- Aetiology / Risk Factors
- Pathophysiology
- Epidemiology
- Clinical Presentation
- Diagnostic Tests
- Treatment
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3Conditions
- Osteoarthritis
- Rheumatoid Arthritis
- SLE
- Seronegative Spondyloarthropathies
- Crystal Arthropathies
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4Rheumatology
- Rheumatic diseases
- Joints
- Connective Tissues
- Immunology
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5Joint Pain
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6Synovial Joints
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7Osteoarthritis
- Most common type of arthritis
- Age-related degenerative
- Synovial joints affected
- Epidemiology
- Prevalence increased with age. Uncommon lt45
- Familial
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8Risk Factors for OA
- Age
- Sex (FgtM)
- Genetic predisposition (polyarticular)
- Obesity
- Local factors
- Abnormal biomechanics
- Occupation (farming, footballer)
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9Pathogenesis of OA
- There is a difference between structural OA and
symptomatic OA
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10Clinical Features of OA
- Symptoms
- Joint pain
- Stiffness
- Gelling
- Instability
- Loss of function
- Worse in evening
- Signs
- Tenderness
- Swelling
- Limited ROM
- Crepitus
- Joint instability
- Bony swelling (Heberdens Nodes, DIPJ)
- Muscle wasting
- Altered gait
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11The Peer Teaching Society is not liable for false
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12Investigations
- Bloods ESR normal, hsCRP may be raised. RF and
ANA negative. - X-Rays abnormal only when advanced
- MRI subchondral bone changes, early cartilage
injury - Arthroscopy
- Aspiration of synovial fluid viscous fluid with
few leucocytes
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13OA X-Ray shows LOSS Loss of joint
space Osteophyte formation Subchondral
cysts Subarticular sclerosis
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14Management of OA
Non-Pharmacological
Surgical
- Low impact activity
- Weight loss
- Physiotherapy
Pharmacological
- Analgesia
- Regular Paracetamol (1g QDS)
- NSAIDs PRN (PPI if regular)
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15Rheumatoid Arthritis
- Inflammatory
- Autoimmune disease
- Chronic symmetrical, deforming, polyarthritis of
synovial joints - Systemic involvement
- Typically female patients aged 30-50
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16Risk Factors for RA
- Female sex
- Genetic predisposition
- Smoking
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17Pathophysiology of RA
- Widespread persistent synovitis
- Synovial hypertrophy
- Synovial proliferation
- Inflammatory infiltration
- Pannus of inflamed synovium
- Damages underlying articular cartilage by
blocking nutrition / direct cytokine effect - Cartilage becomes thinned bone is exposed
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18Clinical Features of RA
- Slowly progressive, symmetrical, peripheral
polyarthritis evolving over weeks months.
- Symptoms
- Pain Stiffness typically in the morning
- Tiredness
- Systemically unwell
- Disturbed sleep
- Signs
- Inflammation
- Redness
- Heat
- Swelling
- Pain
- Limited ROM
- Muscle wasting
- Deformities
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19Deformities in RA
Boutonniere Swan neck deformities
Ulnar Deviation
Z Thumb
Joint Subluxation (wrist/MCPJ)
Muscle Wasting
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20The Peer Teaching Society is not liable for false
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21Rheumatoid Nodules
- Subcutaneous nodules
- Firm, intradermal
- Occur over pressure points (elbows, finger
joints, Achilles tendon)
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22Ring of macrophages and fibroblasts
Necrotic centre
Cuff of connective tissue containing lymphocytes
and plasma cells
23Extra-Articular Features of RA
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24Investigations
- Bloods
- Raised ESR
- Normocytic anaemia
- RF may be negative at the start, becoming
positive in 80 - ANA ve in 30
- Anti-CCP
- X-rays
- Decreased joint space
- Bony erosions
- Subluxation
- Carpal destruction
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25Management of RA
Non-Pharmacological
Pharmacological
- Regular exercise
- Physiotherapy
- Occupational therapy
- Orthotics (e.g. wrist splint)
- NSAIDs
- Ibuprofen
- Consider COX II selective if needing max doses
(e.g. Celecoxib) - PPI cover
- Steroids
- Intra-articular
- Systemic
- DMARDS
Surgical
- Joint replacement
- Pain relief, improve function
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26Disease-Modifying Drugs (DMARDs)
- Problem Inflammation
- Solution Stop the inflammation!
Sulfasalazine Methotrexate Ciclosporin Gold Azath
ioprine Penicillamine Hydroxychloroquine
- Biologics
- Anti-cytokine treatments
- Infliximab (anti -TNF-a antibody)
- Etanercept (TNF-a receptor blocker)
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27RA vs OA
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28RA vs OA
Rheumatoid Arthritis Osteoarthritis
Pain Eases with use Increases with use
Stiffness Significant (gt60 mins) Early morning After rest Not prolonged (lt30 mins) Morning/Evening
Swelling Synovial /- bony Bony / None
Inflammation Hot, red joints No inflammation
Demographics Young, FH Older, occupation
Joint distribution Small joints Hands feet 1st CMCJ, DIPJ Knees
NSAIDs Good response Less convincing response
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29Systemic Lupus Erythmatosus
- Inflammatory multisystem
- disorder
- Autoantibody (ANA)
- Deposition of immune
- complexes
- Most common Sx rash arthralgia
- Most serious Sx renal cerebral involvement
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30SLE Epidemiology
- Afro-Caribbean / Asian ethnicity
- Female Male ratio is 91
- Peak age onset 20-40
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31SLE Aetiology
- ? Cause
- Predisposing Factors
- Genetics (HLA A1, B8, DR3 Complement
deficiencies, Family history) - Sex Hormone Status (Premenopausal women, XXY, HRT
can cause flare up) - Drugs (hydralazine, isoniazid, penicillmine can
cause mild SLE) - EBV ?trigger for SLE
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32SLE Pathophysiology
- Cells die by apoptosis self-antigens presented
to immune system for phagocytosis - Antibodies to these self-antigens are produced
- Immune system fails to inactivate B and T cells
responding to these self-antigens - Autoantibody production
- Complement activation
- Neutrophil influx
- Inflammation
- Abnormal cytokine production
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33SLE Pathology
- Skin/Kidneys
- Deposition of complement and IgG antibodies
- ? neutrophils and lymphocytes
- Vasculitis
- Joints
- Immune complexes deposited in synovium
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34SLE Clinical Features
- Great variety! - Most patients fatigue,
arthralgia, skin involvement - Major organ
involvement is less common, but more serious
SKIN gt85 of cases Butterfly erythema Photosensi
tivity Malar/Discoid rash Livedo
reticularis Raynauds Alopecia
HEART/CVS 25 of cases Pericarditis Pericardial
effusions Myocarditis Cardiomyopathy ?IHD/Stroke A
ntiphospholipid syndrome
JOINTS/MUSCLES gt90 have joint involvement Like
RA symmetrical small joints Painful but
clinically normal Deformity is RARE
LUNGS gt50 of cases Recurrent pleurisy Pleural
effusions Pneumonitis Pulmonary
fibrosis Intrapulmonary haemorrhage (vasculitis)
KIDNEYS 30 of cases Lupus Nephritis Glomeruloneph
ritis
NERVOUS SYSTEM 60 of cases Depression Severe
psychiatric disturbance Epilepsy Migraines
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35SLE Clinical Features
O R D E R H I S A N A
Oral ulcers Rash (malar) Discoid rash Eye
involvement Renal disorders / recurrent
abortion Haematological Immunological Serositis Ar
thritis Neurological involvement Alopecia
- Diagnostic Criteria
- Malar (butterfly) rash
- Discoid rash
- Photosensitivity
- Oral ulcers
- Arthritis
- Serositis (pleutiris / pericarditis)
- Renal disorders (persistent proteinuria)
- CNS disorders (seizures / psychosis)
- Haematological disorders (haemolytic anaemia,
leukopenia, lymphopenia, thrombocytopenia) - Immunological disorders (Antiphospholipid
antibody, anti-DNA antibody, anti-SM antibody) - Antinuclear antibody positive in 95
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36SLE Investigations
Routine Bloods Low WCC (neutophils and
lymphocyres) Low platelets Normocytic
anaemia/ Haemolytic anaemia Raised ESR Normal
CRP Raised Urea and Creatinine in renal
involvement
Autoantibodies ANA Anti-dsDNA Anti-Ro Anti-La
Anti-SM Antiphospholipid antibodies (in
APS) Complement ? C3 and C4
Histology Skin/Renal biopsy deposition of IgG
and complement complexes Imaging CT Head
infartcs/ Haemorrhage/ cerebral atrophy
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37Management of SLE
- Avoidance of sunlight / sunblock
- Reduce CV Risk factors
- Rheum referral
Non-Pharmacological
Pharmacological
- NSAIDs for arthralgia, serositis
- Hydroxychloroquine for joint/skin problems if
NSAIDs insufficient. - High dose prednisolone for severe episodes.
Other immunosuppresives/steroid sparing agents
(cyclophosphamide, azathioprine, methotrexate)
can be used. - Longterm anticoagulant in APS
Surgical
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38Prognosis of SLE
- Episodic relapsing/remitting course
- 10 year survival 90
- Deaths ltage 50 usually due to cerebral/renal
involvement, or infection - gt50, deaths due to stroke / CAD
- Increased lymphoma risk
- Fertility usually normal though increased
miscarriages
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39Seronegative Spondyloarthropathies
- Familial HLA-B27
- Different distribution of joint involvement
- Spine/Sacroiliac joints
- Asymmetrical large joint oligo- or
monoarthropathies - Enthesitis (inflammation of site of attachment of
tendon/ligament to bone) - Extra-articular features
- No RF production (Seronegative)
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40Seronegative Spondyloarthropathies
- 3 main conditions
- Ankylosing Spondylitis
- Psoriatic Arthritis
- Reactive Arthritis
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41Ankylosing Spondylitis
- Inflammatory spinal disorder
- Affects young adults
- Men present earlier
- MF age 16 is 61
- MF age 30 is 21
- 95 are HLA-B27 ve
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42Clinical Features of AS
- Early Features / Presentation
- Typically young male
- Low back pain / stiffness
- Buttock pain
- Worse in the morning relieved by exercise
- Episodic but persistent for 3/12
- Associations
- Chest pain
- Hip involvement
- Knee involvement
- Enthesitides plantar faciitis
- Crohns/UC/Amyloid
- Psoriaform rashes
- Iritis / sterile uveitis
- Late Features
- Kyphosis
- Neck hyperextension (question mark posture)
- Spino-cranial ankylosis
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43Classification Criteria
- High sensitivity and specificity
- 3 out of the following in adults under 50
indicates AS - Morning stiffness gt30 mins
- Improvement with exercise but not rest
- Awakening due to back pain in the 2nd half of the
night only - Alternating buttock pain
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44AS Investigations
- Clinical diagnosis
- Radiological findings
- Early Normal, or erosions/sclerosis affecting
both sides of lower sacroiliac joints - Late Squaring of vertebra,
- bamboo spine
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45Management of AS
Non-Pharmacological
- Exercise, not rest
- Intense exercise regimens
Pharmacological
- NSAIDs for pain / stiffness
- Sulfasalazine / Methotrexate help peripheral
arthritis / enthesitis - Infliximab
- Long term bisphosphontes to help prevent
osteoporotic spinal fractures
Surgical
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46Psoriatic Arthritis
- Arthritis / Enthesitis in patients with psoriasis
or FH or psoriasis - Skin disease may develop after the arthrtitis
- Asymmetrical arthritis involving DIPJ and spine
- Dactylitis (due to synovitis/tenosynovitis)
- Arthritis mutilans
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47Psoriatic Arthritis Treatment
- Responds to
- NSAIDs
- Methotrexate
- Cyclosporin
- Anti-TNFa Therapies
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48Reactive Arthritis
- Large joint mono- or oligoarthritis occurring
following an infection - Men gt Women
- Typical triggers
- NSU e.g. Chlamydia trachomats
- Gut infections salmonella, shigella, yersinia
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49Reactive Arthritis
- May be chronic or relapsing
- Management
- Rest
- Splint joints
- NSAIDs / Steroids
- Consider sulfasalazine / Methotrexate
- Treating original infection has little benefit
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50Reactive Arthritis
- Reiters Syndrome
- Cant See, Cant Pee, Cant climb a tree.
- Reactive Arthritis
- Urethritis
- Conjuncivitis
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51Crystal Arthritis
- Gout/Pseudogout
- 2 main types of crystal involved
- Soduim Urate
- Calcium pyrophosphate
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52Gout
- Inflammatory arthritis
- Hyperuricaemia
- Intra-articular sodium urate crystals
- VERY painful
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53Hyperuricaemia
- Uric acid is the end product of purine metabolism
- Blood levels depend on purine synthesis, dietary
purines and elimination of urate by the
kidney/intestine - Risk factors for hyperuricaemia (. Gout!)
- Renal function
- Body weight
- Blood pressure
- Alcohol intake
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54Precipitants of Gout Attack
- Aggressive induction/cessation of hypouricaemic
therapy (Allopurinol) - Alcohol / shellfish binges
- Sepsis / MI / Acute severe illness
- Truma / Surgery / Dehydration (diuretics)
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55Clinical Features of Gout
- Middle aged older men
- Sudden onset (ususally during the night)
- Agonising pain
- Red, shiny joint (polished apple)
- Tender
- Chronic gout urate deposits
- (tophi) found in peripheries
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56Investigations of Gout
- Clinical picture is diagnostic, as is the
response to treatment - Joint Aspiration Microscopy of Synovial fluid
Sodium Urate seen which is negatively
birefringent needles under polarised light - X-Ray soft tissue swelling, periarticular
erosions, normal joint space - Bloods raised serum uric acid (gt600µmol/L)
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57Management of Acute Gout
- Strong NSAID e.g. naproxen
- Or
- Colchicine
- Or
- Steroids
- Prevent future attacks by avoiding high purine
foods, alcohol XS, weight loss
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58Recurrent Gout
- Reduction of serum urate with long-term
Allopurinol (Inhibitor of Xanthine oxidase which
converts Xanthine to Urate) - Start alongside NSAID/Colchicine as initiation
can precipitate acute attack - Check serum urate levels and adjust dose
accordingly
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59Pseudogout
- AKA Calcuim Pyrophosphate Dihydrate (CPPD)
arthropathy - Similar to gout but affects different joints
mainly wrist/knee - More common in Women
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60Pseudogout Risk Factors
- Dehydration
- Intercurrent illness
- Hyperparathyroidism
- Myxoedema
- Low Phosphate or magnesium
- Osteoarthritis
- Haemochromotosis
- Acromegaly
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61Pseudogout
- Diagnosis
- Synovial fluid microscopy
- Positively birefringent rhomboidal crystals
- Purulent aspirate
- Bloods
- Raised ESR, CRP and WCC
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62Pseudogout Treatment
- Aspiration reduces pain
- NSAID/Colchicine as with gout
- Intra-articular steroid injection
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63Other Rheumatology not covered
- Septic Arthritis
- Systemic Scerosis
- Polymyalgia Rheumatica
- Vasculitis
- Polymyositis / Dermatomyositis
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