MSK - Arthritides Flashcards

1
Q

What is osteoarthritis and primary cause? / RFs?

A

Asymetrical degenerative synovial disease where cartilage destruction exceeds repair = pain and instability

‘wear and tear’ cause

Obesity, age, female, occupation, hereditary predisposition?postemnopausal?

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2
Q

Secondary cause?

A

Altered joint architecture and stability = further damage.

Pre-existing condition s.e.g. Rh or septic arthritis,
developmental dyspasia o hip
Wilsons, acromegaly, haemochromotosis
Trauma

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3
Q

Presentation of osteoarthritis?

A

Morning stiffness <30mins, joint pain with gradual nset, worse with activity and better with rest
High-use and weight bearing joints HIP, KNEE, DIP, PIP, 1st CMV, wrist

Late = night pain, instability, deformity and loss of function

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4
Q

Osteoarthritis O/E?

A

SQUARING BASE OF THUMB, heberdens and bouchards nodes, effusion and erytherma

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5
Q

Ix for osteoarthritis?

A
XRAY = LOSS
Loss of joint pasce
Osteophytes
Subarticular sclerosis
Subchondral cysts

Joint aspirationn = straw coloured aspirate with high viscosity

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6
Q

what is the management of osteoarthritis?

A
Lifestyle + physio
Occ.therapy
Intra-articular steroids
Joint replacement 
Stepwise analgesia:
1) Oralparacetomol +- topical NSAID/capsaicin
2) Oral NSAID + PPI
3) Opiates
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7
Q

WHat is rheumatoid arthritis (RA) and Rfs?

A

Autoimmune condition causing chronic > 6weeks inflammation of the synovial lining, tendon sheaths and bursa, Characterised by symetrical polyarthritis >4 + extraarcticular manifestations

HLADR4 (common)
HLADR1
Smoking
Dhx
Women more than men in middle age
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8
Q

Articular presentation of RA?

A

small joints = wrist, ankle. MCP, PIP, MTP (knees, elbows, hips, shoulders)

DIP SPARING

rapid onset or chronic

Systemic = weight loss, fatigue, malaise

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9
Q

Signs of articular RA?

A

Swan Neck = hyperextended PIP and flexed DIP
Boutonnieres = DIP extendsion and PIP flexion

Radial deviation of wrist
Ulnar deviation at CP
Z deformity on thumb

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10
Q

Extra-articular presentation of RA?

A
RHEUMATOID NODULES
episcleritis/scleritis
Secondary Sjorens/sicca
Lymphadenopathy
Pulmonary fibrosis/pleuritis/bronchiolitis obliterans
Pericarditis
Carpel tunnel syndrome
Tenosynovitis/bursitis

Amyloidosis, Feltys syndrome and ACD

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11
Q

What is Feltys syndrome?

A

RA, neutropenia and splenomgealy

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12
Q

Ix for RA?

A

Serology for RF Abs, CCP Abs,
Bloods = elevated CRP, ESR, anaemia and low albumin

Xray = joint space narrowing, joint destruction, deformity, boney reosions at joint margimns , periarticular osteopaenia
Soft tissue swelling

ELAR score 6+ = RA

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13
Q

Mx for RA?

A

SHort course steroids
NSAIDS/COX2 (PPIs)
Surgery
DMARDS

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14
Q

Progression of DMARDS for RA?

A

hydroxychloroquine if mild

1) Methotrextae, leflunomide, sulfasalazine
2) 2 in combo
3) methotrexate + biologic e.g. anti-TNF (infliximab/adalimumab)
4) Methotrextae + rituximab

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15
Q

Risk of rituximab and anti-TNF?

A

immunosuppression -> serious infections or TB/hep B reactivation

Rituximab can cause night sweats and thrombocytopaenia

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16
Q

what are the seronegative spondyloathropathies?

A

No Rh factor
HLA-B27 association and Men>women

PEAR
Psoriatic athritis
Enterohepatic arthritis
Ankylosing sponylitis
Reactive athritis
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17
Q

What is ankylosing athritis and RFs?

A

Inflammatory athropathy of axial skeleton and peripheral joints, tendos/ligamens and extraarticular sites

+ve FHx
HLA-B27
ERAP-1 or IL-23R genes

Early in males, usually early 20s

18
Q

What is reactive athritis?

A

Sterile, seronegative joint inflammatio n that develops in response to extra-articular infection

RFS: HLAD-B27 (70-80%)
?sexual behaviour and STIs

20-30 years M>F

19
Q

What is Reiters syndrome?

A

Triad of reactive arthritis, urethritis and conjunctivitis

20
Q

Articular presentation of AS?

A

> 3months inflammatory back pain, sacrolilac joints and axial spine>peripheral joints

Early = pain and stiffness
late = spinal fusion, kyphosis, loss of lumbar lordosis and eneck extesnion
21
Q

articular Presentation of Reactive athritis?

A

1-4 weeks post infection
GI = salmonella, shigella, yesinina, campylobacter
GU = chamydia trachomatic, gonorrhoea

Asymetrical, oligoarthritis and lower extremitis >upper

22
Q

Extraarticular presentation of AS?

A

Anterior uveitis >40%
Apical lung fibrosis and aortic regurgitation

Psoriasis
IBD symptoms

23
Q

Reactive Arthritis extra-articular presentation?

A

Reitiers = urethritis + conunctivitis

Keratoderman blenorrhagicum

Circinate balantis

oral ulcers
Cystitis/prostatis

24
Q

How to test for AS?

A

Schobers Test = lumbar mobility
Tragus to wall (increased in AS)

Stress tests e.g. Gaenslens = sacrolilac joint pain

25
Xray features or psoriatic arthitis and Eneterohepatic arthritis?
``` P = pencil-in-cup appearance E = marginal syndesmophytes ```
26
Ix for reactive arthritis?
Joint aspiration gram stain, culture and sensitivies to rule out septic joint and cyrstal athropathices
27
Types of amyloidosis?
Primary = deposit of immunoglobulin light chains. Associated with MM, lymphoma, waldenstrons macroglobulinaemia Secondary = Serum amyloid A Association with RA, IBC< chronic infections e.g. TB
28
Ix for amyloidosis?
Apple green birenfringence under polarised light - congo red stain
29
Presentation of amyloidosis?
``` Periorbital purpura Carpal tunnel syndrome Hepatomegaly Nephrotic syndrome Peripheral neuropathy ``` Primary as well = macroglossia and restrictive cardiomyopathy
30
What is septic arthritis and features?
Acute monoarthritis - very painful, erythermatous, swollen, restricted ROm and fever Caused by current infection S.Aureus >30, Neisseria gonorrhoea<30
31
What is Gout and what causes it?
Acute monoarthritis, 1st MTP is podagra Precipitated by trauma or infection. Crystal is monosodium urate adn caused bu hyperuricaemia from increased intake, increased production and decreased excretion
32
Specific causes of hyperuricaemia?
High pruine diet and alcohol, malignancy e.g. tumour lysis syndrome
33
What is pseudogout?
Acute monoarthritis of large joints e.g. knee. Can be polyarticular if chronic Precipitated by illness of trauma. Calcium pyrophsophate crystals
34
Causes of psuedogout?
Idiopathic, hyperPTH, hyperPO4, hypoMg, metabolic e.g. haemochromotosis, wilsons and acromegaly
35
RFs and Ix for septic athritis?
IV drug use, DM< immunosuppression, Joint damage: RA, prosthetic joint or gout Aspirate = tubid yellow low viscosirt fluid. Raised WCC 90% neutrophils MC&S organsim Bloods for elevated WCC and CRP
36
Gout RFs and Ix?
Alcohol, high purine diet, obesity, male and diabetes Aspirate -> yellow, turbid, low viscosity with raised WCC (neutrophils). Needle shaped vely birefringent crystals Bloods = elevated WCC, CRP and uric acid XR = rat bite erosions
37
Pseudogout RFs and Ix?
Elderly and female Aspirate -> turbid yellow low viscosity fluid. WCC (neutrophils). Rhomboid shaped, +vly birefringent crystals Bloods = elevated WCC and CRP Xray = chondrocalconosis
38
Mx for septic, gout and pseudogout?
SA = IV Abx for 2 weeks and 4 weeks oral and stop biologic therapies Got acute : NSAIDS +- PPI, colchicine, corticosteroids Gout prophylaxis: allopurinaol (dont give in acute) . febuxostat, probenecid Pseudogout: intra-articular coritcosteroids +-paracetomol Polyarticular = NSAIDS +-colchicine +-paracetomil
39
What is osteomyelitis?
Infection of bone from haematogenous spread, contiguous spread and direct inoaculation Haematogenous = IVDU, immunosuppression, DM and Sickle cell Contiguus = cellulitis and localised infection Direct - penetrating injury, ulcers and surgery Leads to inflammation, necrosis and new bone formation. Mostly Staph A, Potts diease if TB
40
presentation of ostemyelitis?
Nonspecific pain in affected area, fever, malaise, rigors, preceding skin lesion, sore throat trauma or operation O/E = localised erytherma, swellign and warmth, reduced ROM, and discharge from wound or affected area
41
Ix for osteomyelitis?
Raised WCC and CRP/ESR No chnages onxray 1st 2 weeks then darkening and periosteal thickening Bone culture = +ve culture
42
Causative organisms in osteomyelitis>
Here is a breakdown of most common causative organisms of Osteomyelitis by age group (Source BMJ Best practice): Infants: S aureus, Group B streptococci, Aerobic gram-negative bacilli (e.g., Escherichia coli), Candida albicans. Children 3 months – 5 years: S aureus, Kingella kingae (increased incidence in children <4 years), Group A streptococcus, Streptococcus pneumoniae, Haemophilus influenzae (if not vaccinated), Pseudomonas (from foot puncture wounds). Children > 5 years: Staph aureus, Group A streptococcus Adults: Staph aureus, Coagulase negative staphylococci, aerobic gram negatives, anaerobic gram positive Peptostreptococcus spp. Elderly: Gram negative bacilli