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For Phase 2

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For Phase 2 Katie Knappett Phase 3B The Peer Teaching Society is not liable for false or misleading information – PowerPoint PPT presentation

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Title: For Phase 2


1

Rheumatology
  • For Phase 2
  • Katie Knappett
  • Phase 3B

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or misleading information
2
Aims
  • Go over basic sciences from Phase 1
  • Aetiology / Risk Factors
  • Pathophysiology
  • Epidemiology
  • Clinical Presentation
  • Diagnostic Tests
  • Treatment

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or misleading information
3
Conditions
  • Osteoarthritis
  • Rheumatoid Arthritis
  • SLE
  • Seronegative Spondyloarthropathies
  • Crystal Arthropathies

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or misleading information
4
Rheumatology
  • Rheumatic diseases
  • Joints
  • Connective Tissues
  • Immunology

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or misleading information
5
Joint Pain
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6
Synovial Joints
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7
Osteoarthritis
  • Most common type of arthritis
  • Age-related degenerative
  • Synovial joints affected
  • Epidemiology
  • Prevalence increased with age. Uncommon lt45
  • Familial

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8
Risk Factors for OA
  • Age
  • Sex (FgtM)
  • Genetic predisposition (polyarticular)
  • Obesity
  • Local factors
  • Abnormal biomechanics
  • Occupation (farming, footballer)

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or misleading information
9
Pathogenesis of OA
  • There is a difference between structural OA and
    symptomatic OA

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10
Clinical 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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or misleading information
11
The Peer Teaching Society is not liable for false
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12
Investigations
  • 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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13
OA X-Ray shows LOSS Loss of joint
space Osteophyte formation Subchondral
cysts Subarticular sclerosis
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14
Management of OA
Non-Pharmacological
Surgical
  • Low impact activity
  • Weight loss
  • Physiotherapy
  • Joint Replacement

Pharmacological
  • Analgesia
  • Regular Paracetamol (1g QDS)
  • NSAIDs PRN (PPI if regular)

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15
Rheumatoid Arthritis
  • Inflammatory
  • Autoimmune disease
  • Chronic symmetrical, deforming, polyarthritis of
    synovial joints
  • Systemic involvement
  • Typically female patients aged 30-50

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16
Risk Factors for RA
  • Female sex
  • Genetic predisposition
  • Smoking

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17
Pathophysiology 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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18
Clinical 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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19
Deformities in RA
Boutonniere Swan neck deformities
Ulnar Deviation
Z Thumb
Joint Subluxation (wrist/MCPJ)
Muscle Wasting
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20
The Peer Teaching Society is not liable for false
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21
Rheumatoid Nodules
  • Subcutaneous nodules
  • Firm, intradermal
  • Occur over pressure points (elbows, finger
    joints, Achilles tendon)

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22
Ring of macrophages and fibroblasts
Necrotic centre
Cuff of connective tissue containing lymphocytes
and plasma cells
23
Extra-Articular Features of RA
  • RA is a SYSTEMIC disease

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24
Investigations
  • 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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25
Management 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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26
Disease-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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27
RA vs OA
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28
RA 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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29
Systemic 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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30
SLE Epidemiology
  • Afro-Caribbean / Asian ethnicity
  • Female Male ratio is 91
  • Peak age onset 20-40

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31
SLE 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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32
SLE 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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33
SLE Pathology
  • Skin/Kidneys
  • Deposition of complement and IgG antibodies
  • ? neutrophils and lymphocytes
  • Vasculitis
  • Joints
  • Immune complexes deposited in synovium

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34
SLE 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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35
SLE 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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36
SLE 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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37
Management 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
  • Renal transplant

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38
Prognosis 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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or misleading information
39
Seronegative 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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40
Seronegative Spondyloarthropathies
  • 3 main conditions
  • Ankylosing Spondylitis
  • Psoriatic Arthritis
  • Reactive Arthritis

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41
Ankylosing 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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42
Clinical 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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43
Classification 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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44
AS 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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45
Management 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
  • Spinal osteotomy

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or misleading information
46
Psoriatic 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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47
Psoriatic Arthritis Treatment
  • Responds to
  • NSAIDs
  • Methotrexate
  • Cyclosporin
  • Anti-TNFa Therapies

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48
Reactive 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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49
Reactive 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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50
Reactive Arthritis
  • Reiters Syndrome
  • Cant See, Cant Pee, Cant climb a tree.
  • Reactive Arthritis
  • Urethritis
  • Conjuncivitis

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51
Crystal Arthritis
  • Gout/Pseudogout
  • 2 main types of crystal involved
  • Soduim Urate
  • Calcium pyrophosphate

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52
Gout
  • Inflammatory arthritis
  • Hyperuricaemia
  • Intra-articular sodium urate crystals
  • VERY painful

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53
Hyperuricaemia
  • 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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54
Precipitants 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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55
Clinical 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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56
Investigations 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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57
Management 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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58
Recurrent 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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or misleading information
59
Pseudogout
  • AKA Calcuim Pyrophosphate Dihydrate (CPPD)
    arthropathy
  • Similar to gout but affects different joints
    mainly wrist/knee
  • More common in Women

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60
Pseudogout Risk Factors
  • Dehydration
  • Intercurrent illness
  • Hyperparathyroidism
  • Myxoedema
  • Low Phosphate or magnesium
  • Osteoarthritis
  • Haemochromotosis
  • Acromegaly

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61
Pseudogout
  • Diagnosis
  • Synovial fluid microscopy
  • Positively birefringent rhomboidal crystals
  • Purulent aspirate
  • Bloods
  • Raised ESR, CRP and WCC

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62
Pseudogout Treatment
  • Aspiration reduces pain
  • NSAID/Colchicine as with gout
  • Intra-articular steroid injection

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63
Other Rheumatology not covered
  • Septic Arthritis
  • Systemic Scerosis
  • Polymyalgia Rheumatica
  • Vasculitis
  • Polymyositis / Dermatomyositis

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or misleading information
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