Week 6: Rheumatology (2) (conditions and investigations) Flashcards

1
Q

hypermobility spectrum disorder

A
  • Pain syndrome in people with joints that move beyond normal limits (often referred to as being “double-jointed”).
  • There is no precise definition as joint mobility is a graduated phenomenon. It may affect any number of joints.
  • Pathophysiology- It is due to laxity of ligaments, capsules and tendons.
    • It is thought that the origin of pain is from microtrauma
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2
Q

RF for hypermobility spectrum disorder

A
  • 10% of pop- very few symptomatic
  • Familial
  • More common in women and Asian people
  • Presents in childhood or young adulthood
  • Recurrent subluxations or dislocations
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3
Q

presentation of hypermobility spectrum disorder

A

Pain around the joints, worse after activity, but pain may generalize and fatigue is prominent too.
Other features:

  • soft tissue rheumatism e.g. epicondylitis
  • abnormal skin: papyraceous scars, hyperextensible, thin, striae
  • marfanoid habitus
  • arachnodactyly
  • drooping eyelids, myopia
  • hernias and uterine/rectal prolapses
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4
Q

HSD Treatment

A

aims to improve pain and reduce disability

  • Non-drug therapy (mainstay)
    • strengthening exercises to reduce joint subluxation
    • work on posture and balance
    • splinting and evening surgical intervention
    • advice on pacing and goal setting
    • specialist pain management
  • Pharmacological therapy
    • No good evidence base on which to advise
    • Paracetamol mainstay
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5
Q

osteoarthritis

A

This is the commonest type of arthritis: a degenerative joint disorder in which there is progressive loss of articular cartilage accompanied by new bone formation and capsular fibrosis.

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6
Q

OA pathophysiology

A

3 possible scenarios

  • Failure of normal cartilage subject to abnormal or incongruous loading for long periods
  • Damaged or defective cartilage failing under normal conditions of loading
  • Break up of cartilage due to defective stiffened subchondral bone passing more load to it
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7
Q

key features of OA

A
  • loss of elasticity with a reduced tensile strength
  • cellularity and proteoglycan content are reduced
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8
Q

risk factors for OA

A
  • age
  • women
  • obesity
  • trauma
  • hereditary
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9
Q

presentation of OA

A
  • hip knee and spine most commonly affected
  • pain is provoked by movement and weight-bearing
  • at first intermittent, but later constant
  • at the knee inactivity gelling a feeling that the joint will give way are common
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10
Q

investigation for OA

A

x-ray

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11
Q

OA x-ray findings

A

· Joint space narrowing

· Subarticular sclerosis

· Bone cysts

· Osteophytes

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12
Q

treatment of OA- non pharmacological

A
  • Strengthening and range of movement exercises
  • Weight loss to reduce joint loading
  • Laterally wedged insoles/ walking stick
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13
Q

treatment of OA- pharmacological

A
  • Paracetamol regularly
  • NSAIDs short-term
  • Topical NSAIDs
  • Intraarticular corticosteroids (evidence of benefit from glucosamine or chondroitin sulphate supplements not convincing
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14
Q

treatment of OA - surgery

A
  • Surgery
    • If pharmacological and physical modalities of treatment don’t work
    • Younger patients have higher chance of revision surgery int eh future
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15
Q

osteoporosis

A

A skeletal condition characterized by low bone mass, deterioration of bone tissue, and disruption of bone architecture that leads to compromised bone strength and an increased risk of fracture

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16
Q

risk factors for osteoporosis: non-mdoifiable

A

Non-modifiable

  • Advanced age (>65 years)
  • Female gender
  • Caucasian or south Asians
  • Family history of osteoporosis-genetic
  • History of low trauma fracture (fall from standing height or less, at walking speed or less.
17
Q

risk factors for osteoporosis - modifiable

A
  • Low body weight (58 kg or body mass index [BMI] <21)
  • Premature menopause (age<45)
  • Calcium/vitamin D deficiency
  • Inadequate physical activity
  • Cigarette smoking
  • Excessive alcohol intake (>3 drinks/day)
  • Iatrogenic: e.g. corticosteroids, aromatase inhibitors
18
Q

secondary causes of osteoporosis

A

coeliac, eating disorders, hyperparathyroidism and hyperthyroidism, MM

19
Q

investigations for osteoporosis

A
  • Dual energy x-ray absorptiometry (DEXA) of the lumbar spine and hip is considered the gold standard for the diagnosis of osteoporosis.
  • T-score is the number of SDs from the mean bone density of persons of same gender at age of peak density (25 years)
  • T-score minus 2.5 or less = osteoporosis
  • Normal BMD = T-score ≥ −1
  • Osteopenia = T-score between −1 and −2.5
20
Q

important considerations for osteoporosis

A
  • The Z-score is a comparison of the patient’s BMD with an age- & gender-matched population.
  • A Z-score
  • Plain radiographs lack sensitivity to diagnose osteoporosis, but rib fractures or vertebral compression fractures without trauma history should prompt evaluation for osteoporosis.
21
Q

dexa score: osteopenia vs osteoporosis

A
  • For osteopenia (BMD between -1 and 2.5)
    • Risk modification: weight-bearing exercise, VitD3 supplementation (800-20000 IU/day), limiting alcohol and smoking cessation. Dietary advice regarding calcium intake
  • For osteoporosis (BMD -2.5)
    • VitD +- calcium supplementation
    • Oral bisphosphonates or IV if oral not tolerated
    • 2nd line: `Denosumab or teriparatide
22
Q

advice for taking bisphosphonates for osteoporosis

A

Always take on an empty stomach with a full glass of water. Stand or sit upright for 30 mins after taking them. Wait between 30 mins and 2 hours before eating or drinking

23
Q

prevention of osteoporosis

A

Regular weight-bearing exercise prevents osteoporosis

24
Q

Fibromyalgia

A

A common disorder of central pain processing characterised by chronic widespread pain in all 4 quadrants of the body (both sides and above and below the waist).

  • Allodynia, a heightened and painful response to innocuous stimuli, is often present.
25
Q

fibromyalgia pathogenesis

A
  • It can be induced by deliberate sleep deprivation.
  • Sleep disturbance is probably the trigger in most patients -EEG studies show reduced REM sleep and delta wave sleep.
  • This causes hyper-activation in response to noxious stimulation, and neural activation in brain regions associated with pain perception in response to non-painful stimuli.
26
Q

risk factor of fibromyalgia

A
  • affects 5% of population
  • female : male = 9 : 1
  • peak age of onset 40-50
  • onset may have an obvious trigger – emotional or physical e.g. painful arthritis
27
Q

presentation of fibromyaglia

A

Fibromyalgia symptoms are not restricted to pain

  • joint/muscle stiffness
  • profound fatigue
  • unrefreshed sleep
  • numbness
  • headaches
  • irritable bowel/bladder syndrome
  • depression and anxiety
  • poor concentration and memory “fibrofog”

On examination, there should be no physical abnormalities to the MSK or neurological systems. Patients may have “tender points” on palpation of their muscles. These are present if the patient experiences excess discomfort when palpating with just sufficient pressure to blanch your finger nails. There is no specific diagnostic test.

28
Q

management of fibromyalgia

A
  • treatment modalities should be specifically tailored to pain intensity, function and associated features such as depression, fatigue and sleep disturbance
  • improve sleep and physical activity levels
  • low dose amitriptyline and pregabalin
  • opiates not recommended
  • CBT
29
Q

describe and diagnose this condition

A

aysmmetrical oligoarthritis

→ psoriatic arthritis

→ usually have had psoriasis before onset of arthritis

→ nail involvement → pitting in the nails

→ drug treatment for both arthritis and psoriasis: methotrexate

30
Q

describe and diagnose

A

reactive arthritis

  • sterile inflammaotry arthriits preceiptated by a distant infection
  • usually oligoarhtirits of lowe limb
  • young patients
  • chamydia trachomatis, chlamydia pneumonia, shigella, slamonells
  • can occur up to a month post infection
  • prompt antimicrobial treatment of infection may improve outcomes
  • most resolve <6 months
31
Q

differential diagnosis of widespread pain

A

fibromyalgia

  • diagnosis of exclusion
  • middle aged women
  • fatigue and unrefreshing sleep
  • treatment withe exercise, CBT, SSRIs and tricyclics
32
Q

describe and diagnose

A

acute monoarticular joint disease

→ septic arthritis

→ RFL extremes of age, prosthetic joint, diabetic, immunosuppression, IVDU

→ staph aureus

→ investigate (mc&s of joint aspirate and blood cultures- best before antibiotics), CRP FBC

33
Q

to diagnose gout you need at least 2 of

A

typical history

tophi

raised serum urate

crystals in joint during attach

34
Q

differential diagnosis of chronic monoarticular joint diseaser

A

inflammatory arthritis e.g. psoriatic

osteoarthritis

foreign body

35
Q

key finding of MRI spine in patient with ankylosing spondylitis

A

bamboo spine and sclerosis of SIJ joint (erosion)- fusion

36
Q

risk factors for osteoporosis

A

FRACTURES
family Hx

RA

alcohol

cigarettes

thin

UC

reduced mobility

endocrinopathies

steroid use

37
Q

what is the most likely diagnosis

A

systemic lupus erythematosus

afrocaribbean > south asian > caucasians