Rheum Flashcards

Meds SE, RA, seronegative spondylo - ank spond, reactive, psoriatic,, SLE, psoriasis, systemic sclerosis, sjogrens, PMR, polymyosits/dermatomyositis, GCA, fibromyalgia

1
Q

Cautions/ side effects of NSAID use

A

Gastric ulceration; other GI upset nausea, diarrhoea

Haemorrhage

Renal injury/ failure

Increase risk of MI, stroke (prothrombic effects)

Exacerbate HF ( blood pressure elevation, reduced renal perfusion, fluid retention)

Miscarriage and congenital malformation, fetal renal dysfunction

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2
Q

Side effects of corticosteroids

A
  • increased susceptibility to infection in those >20mg per day > 2/weeks - eg. candidiasis, pneumocystis jiroveci pneumonia
  • oesophageal and peptic ulceration
  • osteoporosis, fractures
  • Cushingoid features: easy bruising, purple striae of skin, cheek telangiectasia, thin skin, acne and hirsuitism, buffalo hump
  • growth suppression, adrenal suppression
  • depression; mania
  • cataract, glaucoma, papilloedema
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3
Q

Side effects of methotrexate and sulfasalazine (dmard)

A

Both
- GI intolerance - nausea
- myelosuppression - rbc, wcc, platelet
- hepatotoxicity

Methotrexate
- pneumonitis at start
- oral ulcers

sulfasalazine
- allergic rashes, mood changes, hallucinations

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4
Q

Hydroxychloroquine (dmard) SE

A
  • photosensitivity
  • retinal toxicity (>5years >5mg/kg/d)
  • hyperpigmentation
  • cardiotoxicity rare but QTC prolongation
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5
Q

Leflunomide, mycophenolate and azathioprine (dmard) SE

A
  • diarrhoea, myelosuppression, hepatotoxicity

Leflunomide : + hypertension

azathioprine: - diarrhoea

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6
Q

TnFa inhibitor SE eg. Humira, adalimumab, infliximab, remicade

A
  • injection reaction (pain swelling around site)
  • worsening heart failure
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7
Q

SE/ cautions of rituximab - monoclonal ab against B cells CD20 (used for nh lymphoma/leukaemia, severe RA)

A

infections from immunosuppression including TB, septicaemia, Hep B reactivation

caution in hx of cvd/cardiotoxic chemo as causes exacerbation of angina, arrthymia, HF.

progressive multifocal leucoencephalopathy (monitor for cognitive/neurological. psychiatric signs)

transient hypotension - withhold antihypertensives 12 hrs before infusion.

Infusion related reactions 30-120 min after starting infusion -fever, chills, rigors, nausea, vomiting uritcaria, dyspnoea

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8
Q

SE of tocilizumab (actemra)
IL 6 blocer

A

Infection
GI perforation : UGIB
myelosuppression + hepatotoxicity : fatigue, jaundice
- metabolic derangement : hypertension, weight gain

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9
Q

Presentation of Rheumatoid arthritis - articular, non articular5, rare-7

A

Articular
- pain, swelling, morning stiffness

Non-articular
- sjogren
- RA nodules
- anaemia
faitgue
- lung fibrosis

Rare:
o Skin – Raynaud’s, ulcers
o Eyes – dry eyes, epi/scleritis, cataracts (from steroids), NOT iritis
o Lungs – dyspnea (pleural effusion), pleuritic chest pain
o Heart – chest pain owing to pericarditis, valve disease
o Hoarseness, sore throat, neck pain from C1-C2 subluxation (atlantoaxial joint disease)
o Neuro – peripheral neuropathy,
mononeuritis multiplex, cord compression, entrapment neuropathy
Systemic features
o anorexia, weight loss, polymyalgia

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10
Q

Exam for RA

A

General - cushingoids feature

Look
Dorsum -wrist swelling and radial deviation, dorsum wasting and nodules,
MCP swelling, ulnar deviation and subluxation
- Phalanges - swan neck deformity, boutonniere’s deformity, Z-thumb deformity
- Nails - Vasculitic changes
- Volar - Palmar erythema, carpel tunnel scar,
fixed flexion

Feel
- Temperature
- Joints for crepitus, swelling and tenderness
- Nodules for character, mobility, tenderness

Move
- All joints, active ROM\
Function
- Grip strength, key strength, opposition strength, do up a button, hold a pen and
write name

Neurology
Face

  • eyes for scleritis, cataracts and pallor
  • enlarged parotids in Sjogren’s
  • mouth for dryness and oral ulcer
  • TMJ for crepitus

Neck
- cervical spine tenderness and reduced ROM
- Cervical lymphadenopathy

Chest
- Lungs for pulmonary fibrosis or effusion
- Heart for pericardial rub or regurg murmur

Abdomen
- Hepato/splenomegaly
- Inguinal lymph nodes

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11
Q

Investigations for RA - bloods , imaging , soft

A

BLoods
FBC, Hb, ESR , CRP , normocytic anaemia
Rheumatoid Factor + ACPA Anti CCP abs

Imaging
Xray - normal - soft tissue swelling, juxta-articular osteopenia, reduced bone space, bony erosions, subluxation
USS and MRI - synovitis

DAS-28 questionaire use to look at disease activity over time - Tender swollen joint, ESR, and global health (confirmed RA)

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12
Q

Management of RA - non pharm, symptom relief , pharm, monitoring, surgery

A

Non pharm
- education, regular exercise, alcohol cessation
PT and OT for aids/splints
- Manage for CV risk as RA accelerates atherosclerosis
- DAS 28
- Contraception, even after stopping depending on the drug
- flu vaccine but not live vaccines

Symptom relief
- Steroids - good in acute flares but would avoid giving until seen by rheum - IM or oral not long term
NSAIDS - not for long term use as DMARDS

Pharm
1st line : MTX
If not controlled add another until triple therapy
2nd sulfasalazine, hydoxychloroquine, leflunomide, prednisone

Monitor
- FBC for myelosuppression, LFTS for hepatotoxicity ,
- hydroxy - opthal review 5 years if under 60, no liver disease, no retinal disease) or annual if high risk
Creatinine for azathioprine, ciclosporin
Blood pressure

Biologics if active infection, severe heart failure, haem malignancy
- Anti-TNFa - adalimumab and entanercept
- Rituxamab + mtx if have failed
-tocilizumab

Surgery
- replace joints, carpal tunnel release

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13
Q

What are the shared features of seronegative spondyloarthropathies (ank spond, psoriatic, enteropathic, reactive) (SEA SHED)

A

-Seronegativity (rheumatoid factor –ve)

  • Enthesitis (inflammation of the site of insertion of tendon or ligament into bone) e.g. plantar fasciitis, Achilles tendonitis, costochondritis
  • Asymmetrical large joint oligoarthritis (< 5 joints) or monoarthritis
  • Spine and SI joints (axial skeleton)
  • HLA B27 association
  • Extra-articular features (iritis, rashes, oral ulcers, aortic valve incompetence, IBD)
  • Dactylitis (inflammation of the entire digit due to soft tissue oedema, tenosynovial and joint inflammation)
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14
Q

What 4 categories are used to diagnose RA

A
  1. Joint involvement - # of joints with small joints favoured
  2. Serology - high positive RF +/- ACPA
  3. acute phase reactants - abnormal CRP and/or ESR
  4. Duration of sx - >6 weeks big points
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15
Q

What is the typical presentation and examination of ankylosing spondylitis
-“chronic inflam disease of spine and sacroiliac joints, 1:3 FM

A

Hx
- lower back pain worse at night + morning stiffness, relieved by exercise
- pain radiates from SI joints to hips/buttocks
- progressive loss of spinal movements
- peripheral arthritis esp in lower limbs oligoarthritis
- symptoms of enthesitis and iritis

Exam
- Looking for deformity - kyphosis & neck hyperextension
- Enthesitis - achilles , plantar, tibial tuberosity, ischial tuberosity, iliac crests
- sacroilitis - pain over SI joint through FABER test

extra joint findings
- - eyes for iritis (red, poorly reactive pupils, photophobia, pain, blurred vision)
-heart for AR
- lungs for apical pulmonary fibrosis

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16
Q

What are the general investigations for ankylosing spondylitis

A

Bloods – normocytic anaemia, raised ESR, CRP,
HLA-B27

Imaging
– MRI most sensitive.
Look for irregular
erosions and sclerosis around SI joints,
bone marrow oedema, vertebral syndesmophytes
which can fuse with bone above to cause ankylosis, calcification of ligaments leads to bamboo spine.

X-ray will show sacroiliitis but may appear late.

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17
Q

What is the dx and management of ankylosing spondylitis

A

Diagnosis =Clinical with support from imaging

Management
- Exercise (www.nass.co.uk) and NSAIDS
- TNF a blockers (adalimumab)
- Local steroid injections for short term relief
- Surgery including hip replacement and
rarely spinal osteotomy

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18
Q

How does psoriatic arthritis present in hx and exam

A
  1. Skin changes precede arthropathy in 75%

Hx
- symmetrical polyarthropathy OR asymetrical oligoarthropathy
- Can affect DIPS and axial skeleton
- psoriatic arthritis mutilans rare
- skin and nail changes

exam
- look at skin - extensor surfaces, scalp, umbilicus
- nail for onycholysis
- fingers for dactylitis
- examine affected joints for pain, swelling and stiffness

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19
Q

Co morbidities associated with psoriatic arthritis

A

Ocular involvement: uveitis (7%) and conjunctivitis (20%).
Cardiovascular disease
Inflammatory bowel disease
Metabolic syndrome
Hypertension
Diabetes
Atherosclerosis
Depression and anxiety.

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20
Q

What are the ix and treatment of psoriatic arthritis - dx - exam + xray

A

Ix
- Xray - assymetric SI joint involvement, erosions of bone next to joint space
-pencil in cup deformity
- ankylosis - fusion of bones together across joint space

management
- NSAIDS
- mTX / sulfasalazine
- anti-TnFa

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21
Q

What is the definition and presentation of reactive arthritis
- can be part of Reiter’s syndrome = triad of urethritis,
arthritis and conjunctivitis

A

Reactive arthritis = sterile arthritis affecting lower limb 1-4 weeks after urethritis
(eg. chlamydia) or dysenter (campylobacter, salmonella, shigella)

Hx
- chronic or replapsing arthopathy
- hx of infection (may be subclinical)
- iritis , ulcers, enthesitis

22
Q

Ix and treatment of reactive arthritis

A

ESR and CRP
stool culture, infectious serology,
sexual health review
Chylamidia and gonorrhoea urine PCR + syphilis blood test

Imaging - Xray or USS = enthesitis with periosteal reaction (he formation of new bone in response to injury or other stimuli of the periosteum surrounding the bone)

Treatment
- rest and splint affected joints
- NSAIDS , local steroid injection
MTX or sulfasalazine if persistent

23
Q

what is enteropathic arthritis

A

joint pain associated with IBD or GI bypass

24
Q

What are 11 diagnostic features of Systemic lupus Erythematosis - DRAMA SIPHON (need 4 for dx)

A

D: discoid rash
R: renal - lupus (glomerulo-nephritis) cause persistent proteinuria and casts (red, cell, granular, mixed)

A: Arthritis - non erosive >2 peripheral joints

M: malar rash sparing the nasolabial folds
A: ANA positive

S: serositis:
- pleuritis (pleuritic CP + SOB) and pericarditis (rub, CP, ECG)

Immunological
- antiDsDNA
and or
-anti SM +/- Ro, La, U1RNP

Photosensitivity
Haematological - haemolytic anaemia or lymphopenia/leukopenia/thrombocytopenia

Oral Ulcers - painless (or nasopharyngeal
N: neuro - seizures, psychosis in absence of other triggers

25
Q

What is the aetiology of SLE and what are commonly associated diseases

A

B cell secretion of autoantibodies to variety of antigens creating immune complexes that deposit in a range of sites

associated with sjogrens, autoimmune thyroid disease,
antiphospholipid syndrome (- anticardiolipid and lupus anticoagulant antibodies cause clots. Coagulation defect, livedo reticularis, recurrent miscarriages, thrombocytopenia)

26
Q

What are the symptoms you would ask about for SLE + extra history question
Most present with rash

A

General – malaise, weight loss, fever

  • MSK – arthralgia/arthritis,
    myalgia/myositis
  • Derm – rash, alopecia, oral and nasal ulcers
  • Neuro – delirium, dementia, convulsions, loss
    of vision, stroke, headache, MS symptoms,
    anxiety, depression
  • Renal – haematuria, oedema, high BP
  • Resp – dyspnea and pleuritic chest pain
  • Cardio – pericarditis, myocarditis, murmers,
    angina (premature coronary artery disease)
  • Haem – lymphadenopathy, anaemia, thrombophlebitis
  • GI – nausea, vomiting, pseudo obstruction
  • Antiphospholipid – recurrent miscarriage,
    DVT/PE
  • Sjogrens symptoms – dry eyes, mouth,
    enlarged parotid

Drug History
- procainamide, hydrasalazine, minocycline can induce

27
Q

What are the investigations for SLE

A

Bloods
- anaemia : chronic disease or may be haemolytic (high retics and bili, low haptoglobins, coombs + and high LDH if immune

  • high ESR, normal CRP
  • platelets, white cells low
  • prolonged APTT not corrected by addition of normal plasma

Immunological
- ANA (sens/not spec)
- AntidsDNA and Anti-SM
-low C3 and C4

Other
renal biopsy - glomerulonephritis

28
Q

Management and maintenance of SLE, lupus nephritis, cutaneous symptoms and antiphospholipid syndrome

A

Acute flare
- prednisone
- IV cyclophosphamide (life threatening flare)

Maintenance
- NSAIDS + hydroxychloroquine for joint and skin
- steroids for lungs, CNS, heart and haem involvement
- tapering of steroids with other DMARDS - MTX, mycophenolate or azathioprine
- warfarin for hypercoagulability if previous DVT/PE
- Belimumab or Rituxamab for severe

Treatment of lupus nephritis
- steroids + cyclophosphamide, mycophenolate and rituxamab for glomerulonephritis (needs renal r/v)
- Control BP with ACEi or CCB

Cutaneous symptoms
- topical steroids
- sunscreen/ avoiding sun

Treatment of APS - aspirin or warfarin

29
Q

What are the risk factors and associations of psoriasis

A

RISK FACTORS/TRIGGERS
- Recent strep infection
- Stress
- Skin trauma
- Drugs (lithium, NSAIDS, B blockers)
- Alcohol, smoking
- Obesity
- Family history (HLA associations)

ASsociated with
- Inflammatory arthritis (30% of psoriasis
patients develop psoriatic arthritis)
- Inflammatory bowel disease
- Uveitis
- Coeliac Disease
- Metabolic Syndrome

30
Q

Ix and management of psoriasis
DDX
- Eczema
- Tinea
- Mycosis fungoides
- Seborrheic dermatitis

A

Non-Pharmacological
- Education – control not cure is the aim
- Encourage a support group
- Remove triggers

Pharmacological
- Mild
o Daivobet Cream (Vit D analogue calcipotriol + betamethasone)
o Emollients
o Tar preparations
o Salicylic Acid

  • Moderate/Severe
    o Warrants treatment with systemic
    agent and/or phototherapy
    o Methotrexate, ciclosporin, acitretin
    o Narrowband UVB, broadband UVB,
    photochemotherapy (PUVA)
    o Consider biologic drugs e.g.
    etanercept if no improvement with
    non-biologics + PUVA
  • Psoriatic Arthropathy
    o Etanercept, infliximab or
    methotrexate
31
Q

what is difference from systemic sclerosis / crest /crest syndrome

A

scleroderma: autoimmune skin fibrosis from over production of collagen

Systemic sclerosis = scleroderma + vascular disease
- can be limited cutaneous (to face and extremities)
or diffuse cutaneous (also affect whole organs

CREST - calcinosis, raynauds phenomena, oesophageal dysmotility, sclerodactyly

32
Q

What are the risk factors for systemic sclerosis or crest and presentation/ exam findings

A

Risk factors
- fam hx, silica dust exposure

Hand Exam
Skin
- bilateral skin thickening extending to MCP joints,
- symmetrical thickening of fingers, puffy, sclerodactyly
- prayer signs
-pigmentation

finger tip ulcers, pitting scars
telangectasia
abn nailfold capillaries
- carpal tunnel secondary to flexion contracture
- calcinosis on extensor surface
- raynauds

Other
- GORD
- interstitial lung disease - pul htn

33
Q

Ix for systemic sclerosis and ongoing monitoring

A

Bloods
- FBC
o Anaemia
o Reactive thrombocytosis
o Hemolysis

  • Renal function (Cr)
  • ANA/ENA
    o ANA+ (nucleolar pattern)
    o RF+ (30%)
    o Anti-centromere Ab (75%) - LcSSc
    o Anti-topoisomerase (scl70) + (40%)

– DcSSc
o Anti-RNA poly+ (20%) – dcSSc
o Anti-Ro +/-
o ESR N/raised

Echo
- PA pressure and RH enlarged

Lung FTs
- Initial evaluation. Low lung diffusion capacity suggests PAH, decr FVC precede ILD

Monitoring
- FBC, Renal function, ECHO, PFTs

34
Q

Management of systemic sclerosis features -
Lifestyle
Antifibrotic therapy
- digital ischaemia/ raynauds analgesia, raynauds,
dysphagia, calcinosis, inflam arthritis , acute renal crisis

A

Lifestyle
- Smoking cessation, reg exercise/PT
- splints decr ROM and CTS

Immunosuppression
- MTX/ hydroxychloroquine (arthritis/myositis)
- Mycophenolate (lung involvement)
- cyclophosphamide

Digital ischaemia
- iloprost or sildenafil

Analgesia
- paracetamol, nsaids

Raynaud
- analgesia
- nifedipine, amlodipine
fluoxetine
topical nitrate
sildenafil

Dysphagia
- supportive, dilitation, PPI if GORD

Calcinosis
- NSAIDS, excision

Inflam arthritis
- hydroxychloroquine, mtx,
- prednisone <5mg daily otherwise renal crisis in pt with diffuse scleroderma rnp 3.

Acute renal crisis ( new onset hypertension, raised Cr, intravascular haemolysis).

35
Q

Sjogrens presentation
- dry eyes, mouth from lymphocyte infiltrate into lacrimal and salivary glands. Can occur alone (1) or w other AI diseases (2).

A
  • Fatigue, sleep disturbance
  • Keratoconjunctivitis sicca >3m
  • Xerostoma, (altered swallow/taste)
  • Vasculitis (skin rash)
  • Dental carries, incr oral infections
  • arthralgia, myalgia
  • Interstitial kidney disease (RTA)
  • corneal ulceration, no saliva pool
  • trigeminal neuralgia
  • peripheral neuropathy (sensory)
  • VTE Hx (incr risk)
36
Q

Management of Sjogrens

A

Dry Eyes – optometry review

  • Meds
    o artificial tears
    o ciclosporin ophthalmic drops BD
    o Cholinergic pilocarpine 5mg TDS
     CI: resp disease, HTN
  • spectacle eye shield, humidifiers
  • Punctal plugging

Dry Mouth – dental review
- gels, lozenges, gum, mouthwash
- Pilocarpine
- Lip balm

MSK Sx
- Paracetamol, NSAIDs
- Prednisone 15mg daily for 2/52
- Hydroxychloroquine, methotrexate

Vasculitis
- prednisone 1mg/kg OD or
- IV Ig 0/4mg/kg/day IV 5days
RTA
- Kt repletion, alkali

37
Q

Ix for sjogrens and diagnosis

A

Schirmer’s test - <5mm wet in 5mins

Bloods
- RF+ close to 100%
- ANA+ (70%)
- anti-RO (SSA), anti-La (SSB)

Urine
- deranged P, K, Ca,

Salometery - decrd
/Salivary gland Bx
Lisamine green test, fluorescein

Criteria for diagnosis
- Clinical diagnosis – no clear criteria
- Objective findings of ocular or oral dryness
or of glandular parenchymal damage
- Serologic or histopathologic evidence of
autoimmunity

38
Q

Presentation - Polymyositis / dermatomyositis

  • Rare. Insidious onset of progressive symmetrical
    proximal muscle weakness, autoimmune striated
    muscle inflam, myalgia/arthralgia +/- skin
    involvement.
A

Proximal muscle weakness
- Gottren’s papules (pathognomic);
Violaceous fat-topped plaques on dorsal
knuckles/wrists/knees/elbows/malleoli

  • Heliotrope rash: dusky-red rash periorbital, symmetrical
  • Macular violaceous rash:
    o Gottren’s sign
    o Shawl sign: neck, shoulders
    o V sign: neck, chest
    o Holsters sign: lateral thigh
    o Linear extensor erythemas
    o Facial rash, perioral sparing
    o Scalp rash
  • Finger tips: periungal erythema, nailfold
    capil dilatation, cuticle overgrowth
  • mechanic’s hands – hyperkeratosis
  • sub cute proximal symmetrical weakness
  • photosensitive, pruritis
  • poikiloderma vascular atrophicans
  • fatigue, malaise, minor weight loss
  • Sob (2 to weakness)
39
Q

Ix for polymyositis/dermatomyositis

A

INVESTIGATIONS
Bloods
- raised serum CK (more with polymyositis), LDH, aldolase

  • ANA+, anti-Jo+, anti-Mi2 (ILD, acute)

EMG
- abnormal spontaneous activity, abnormal
voluntary movements

Muscle Bx
- perivascular or interfascicular inflam, endo
hyperplasia

Imaging
- MRI: muscle oedema, fibrosis, calcification
- CXR: interstitial changes
- echo/ECG: arrhythmias, conduction defects

40
Q

Management of polymyositis, dermatomyositis

A

May need to screen for malignancy
Severe/acute flare
- IV prednisone 1g OD
- IV Ig

Derm manifestations

  • Conservative
    o moisturiser
    o sunscreen
    o exercise – PT
    o healthy diet
  • Meds
    o topical Urea
    o topical doxepin
    o topical tacrolimus
    o oral prednisone
    o DMARDs
41
Q

What are the complications of polymyositis/ dermatomyositis

A

COMPLICATIONS
Steroid toxicity
Respiratory infection, ILD
Cardiac disease
dysphagia

MONITORING
- Specialist r/v of muscle strength and markers of
severity
- regular assessment for development for
pulmonary and cardiac involvement

42
Q

Gout presentation, investigations, diagnostic criteria

A

Presentation
- rapid onset severe pain (w/I 1hr)
- morning stiffness
- monoarticular or oligo
- 50% 1st MTP (podagra)
- red, hot, swollen, tender
- tophi: elbows, knees, Achilles

Ix
Arthrocentesis
- raised WBC
- negative bifringent needle crystals

Bloods
- raised WBC, +/- raised serum Urate

Xray
- periarticular erosions, Normal joint space,
ST swelling

Dx
Monosodium urate crystals in joint
fluid/tophus
- Plus >6 of;
o >1 attack acute arthritis
o developed w/I day
o monoarthritis, redness observed
o 1st MTP painful/swollen
o tophus
o hyperuricaemia
o unilateral 1st MTP or tarsal joint
o abnormal swelling on x-ray
o subcortical cyst w/o erosion

43
Q

Management of Gout - prophylaxis and acute attack

A

Acute Attack
- Naproxen 500mg PO BD 10-14d
or Celecoxib 100-200mg PO BD or prednisone 1mg/kg stat (renal)
or colchicine 1.2 PO, then 0.6mg (
GI bleed)
- Steroid injection of affected joint can be
very effective.

Prophylaxis
- Allopurinol starting dose 1.5mg x eGFR,
max 100mg

o SE: decr WBC, rash, fever
o Don’t stop during flare
o May trigger attack initially, cover w NSAID or colchicine
- Probenecid
- Febuxostat

Lifestyle
- Lose weight, if overweight/ avoid fasting/alcohol excess/ /low dose aspirin.

44
Q

Presentation and investigations of Polymyalgia rheumatica

  • Inflam syndrome of pain and morning stiffness in
    neck/shoulder/pelvic girdles, >50yrs, +/- GCA.
A

Presentation
- Subacute onset (<2/52)
- Bilateral ache, tenderness, morning stiffness
(>1hr)
- Shoulder girdle (~80%); Pelvic (~60%)
- Tenosynovitis, CTS
- Low-grade fever, fatigue, anorexia, depress
- Response to steroids
- Think about rheumatoid arthritis if there is
significant peripheral joint involvement. Approx.
10% of RA presents initially like PMR.

Investigation
Bloods
- CRP, ESR >40 (emerging IL-6)
- FBC, Serum electrophoresis (r/o myelo)
- TSH, CK normal

45
Q

Management and monitoring of polyyalgia rheumatica

A

MANAGEMENT
Meds
- Prednisone 15mg PO OD (taper to 10mg
over 4-6wks, then 1by 1mg/month)
- Cholecalciferol 1.25mg monthly
Alendronate 70mg PO weekly – if BMD low
- Omeprazole 20mg PO OD
- Methotrexate – ask advice

Advice
- Warn pt. of GCA Sx – seek advice

MONITORING
- monthly for 3m; exam, Hx, ? ESR. If methotrexate do bloods.

46
Q

Giant cell arteritis
- presentation and investigations

Granulomatous vasculitis of large & medium
arteries (branches of ECA). Serious consequence is
irreversibly vision loss of optic nerve d/t ischemia.

A

PRESENTATION
- New Headache
- Scalp tenderness
- Jaw claudication
- visual loss- painless, uni-/bilateral,
amaurosis fugax (disc pallor, oedema)
- temporal artery thickening/nodule/tender
- upper extremity claudication
- Other CN abnormalities

INVESTIGATIONS
Bloods
- ESR >50, CRP raised
- FBC:
o normocytic, normochromic anemia
o raised plts
o mild WBC raise, ALP rise

Biopsy
- Temporal artery, w/I 7 days starting steroid (beware skip lesions)

Imaging
- Thickening of temporal artery

47
Q

Dx, management and monitoring of GCA

A

CRITERIA
3/5; age >50, new HA, ESR >50, temporal artery
abnormality, abnormal Bx

MANAGEMENT
- If suspected – do ESR and start
o Prednisone 1mg/kg PO OD 4weeks
 Taper over 6-12m
 w Sx /ESR improvement

o IV Prednisolone if visual/neuro Sx  1g 3 days

  • If confirmed – aspirin 75mg OD
  • Consider bone protection (vit D, BP)

MONITORING
- for steroid SE: BP, DM, bones
- FBC
- incr. risk abdo aneurysms (? USS, echo, CXR)

48
Q

Fibromyalgia -how is it diagnosis, risk factors, associations,

A

Fibromyalgia is a condition characterized by
chronic widespread pain and fatigue.

Commonly associated with depression, anxiety, and
PTSD

Part of same diffuse group of diseases as chronic
fatigue syndrome, however more orientated around
the pain. Many doctors consider them to be the
same disease.

Essentially a functional diagnosis. Investigations are
ALL normal.
Scoring systems for how many painful joints are present are used for diagnosis.
Must be chronic and widespread.
Important to rule out other pathological causes of
pain.

RISK FACTORS
FMHx, rheumatological conditions, 20-60y, F

49
Q

Presentation and investigations for fibromyalgia

A

PRESENTATION
- Chronic, diffuse pain
diffuse tenderness o/e
- fatigue unrelieved by rest
- sleep & mood disturbance (d, A)
- cognitive dysfunction
- HA – axial, extend to neck, shoulders
- numbness, tingly – variable nature
- stiffness, swelling feeling
- fluid retention (not observed)
- incr sensitivity to sensory stimuli

Investigations
Clinical
- Chronic, widespread pain in muscles &
joints
- Fatigue, wakening unrefreshed, cognitive sx
- >11/18 tender points - lower neck in front. edge of upper breast, below side bone of elbow. inside of knee, hip bone, upper outer buttock. upper inner shoulder, neck and shoulder, base of skull
Bloods
- ESR, TFT, FBC, RF, anti-CCP, vit D NORMAL
- ANA – sometimes positive

50
Q

Management of fibromyalgia

A

MANAGEMENT
Education
- Thorough explanation about nature of
‘disorder’ – relapsing-remitting (discuss
with chronic pain service)
- No simple cure
- Reassurance no serious pathology, mindful of patient’s perspective of sx

Medication
- Nortriptyline 10mg nocte
- gabapentin 300mg OD then titrate up
- Pregabalin 75 PO BD
- High dose Venlafaxine

Psychology
- CBT
Lifestyle
- Exercise
- Good sleep hygiene