Bone And Joint Disorders Flashcards

1
Q

what is avascular necrosis

A

Failure of the blood supply to the end of a bone, resulting in ischaemic necrosis of bone and marrow

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2
Q

where is most commonly affected by avascular necrosis

A

head of the femur

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3
Q

who usually presents with avascular necrosis

A

males 35-50

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4
Q

clinical presentation of femoral head AVN

A

commonly bilateral
insidious onset of groin pain exacerbated by stairs or impact

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5
Q

hanging rope sign

A

femoral head AVN

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6
Q

how is osteoarthritis often described

A

wear and tear

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7
Q

x-ray changes seen in osteoarthritis

A

Loss of joint space
Osteophytes
Subarticular sclerosis
Subchondral cysts

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8
Q

clinical presentation of osteoarthritis

A

joint pain and stiffness, worse on activity

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9
Q

clinical signs of osteoarthritis in the hands

A

heberdens nodes
bouchards nodes
squaring at the base of the thumb
weak grip, reduced ROM

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10
Q

clinical marker of generalised OA

A

heberdens nodes

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11
Q

clinical signs in osteoarthritis

A

joint line tenderness
crepitus
joint effusion

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12
Q

management of osteoarthritis

A

physio, weight loss, NSAIDs, activity modification

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13
Q

surgical management of osteoarthritis

A

joint replacements
arthroscopic surgery to remove loose bodies

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14
Q

who is more likely to have joint hypermobility syndrome

A

females

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15
Q

name some genetic syndromes associated with joint hypermobility syndrome

A

marfans, ehlers danlos

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16
Q

when does joint hypermobility syndrome usually present

A

childhood or 3rd decade

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17
Q

clinical presentation of joint hypermobility syndrome

A

pain
thin stretchy skin

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18
Q

what is used to classify joint hypermobility syndrome

A

modified beighton score

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19
Q

what is septic arthritis

A

inflammation of joint space caused by infection

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20
Q

most common cause of septic arthritis in adults

A

staph aureus

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21
Q

most common cause of septic arthritis in the elderly

A

e.coli

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22
Q

what predisposes to salmonella arthritis

A

sickle cell

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23
Q

clinical presentation of septic arthtitis

A

acute monoarthropathy, knee most commonly affected

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24
Q

clinical signs of septic arthritis

A

reduced ROM and swelling
systemic fever

25
Q

name some risk factors for a prosthetic joint infection

A

corticosteroids
prior infection/surgery
prolonged duration of surgery

26
Q

most common organisms in prosthetic joint infection

A

staph aureus, staph epi

27
Q

management of early prosthetic joint infection

A

debridement, antibiotics, implant retention

28
Q

what is osteomyelitis

A

infection of the bone/bone marrow

29
Q

who usually presents with osteomyelitis

A

children

30
Q

risk factors of osteomyelitis

A

immunocompromised, chronic disease

31
Q

most common cause of osteomyelitis

A

staph aureus

32
Q

clinical presentation of osteomyelitis

A

fever, pain/tenderness, erythema, swelling

33
Q

best diagnostic tool for osteomyelitis

A

MRI

34
Q

what is osteoporosis

A

a significant reduction in bone density

35
Q

what is a less severe version of osteoporosis

A

osteopenia

36
Q

when does physiological loss of bone density start

A

30 yrs

37
Q

who is more likely to have osteoporosis

A

females

38
Q

what is type 1 osteoporosis

A

exacerbated loss of bone in the post‐menopausal period

39
Q

what is type 2 osteoporosis

A

osteoporosis of old age with a greater decline in bone mineral density than expected

40
Q

name a drug that can exacerbate osteoporosis

A

corticosteroids

41
Q

what can be used to measure bone mineral density

A

DEXA scan

42
Q

lifestyle advice for osteoporosis

A

increase calcium intake
high intensity strength training
avoid smoking and excess alcohol

43
Q

pharmacological management of osteoporosis

A

calcium + vit d supplements
oral bisphosphonates
zoledronic acid

44
Q

what is osteomalacia

A

a condition where defective bone mineralisation causes “soft” bones

45
Q

what is the most common cause of osteomalacia

A

vitamin D deficiency

46
Q

symptoms of osteomalacia

A

bone pain
pathological fractures
symptoms of hypocalcaemia

47
Q

symptoms of hypocalcaemia

A

paraesthesia, muscle cramps, irritability, fatigue

48
Q

bloods in osteomalacia

A

↓ calcium and serum phosphate, ↑ serum ALP

49
Q

x-ray of osteomalacia

A

pseudofractures

50
Q

management of osteomalacia

A

vit D + calcium and phosphate supplementation

51
Q

what is pagets disease

A

excessive bone turnover due to increased osteoclast and osteoblast activity

52
Q

where does paget’s particularly affect

A

axial skeleton

53
Q

presentation of pagets

A

can be asymptomatic
Bone pain
Bone deformity
Fractures
Hearing loss

54
Q

what are the 3 main stages of pagets

A

osteolytic
mixed
osteosclerotic

55
Q

bloods in pagets

A

↑ alkaline phosphatase with otherwise normal LFTs

56
Q

x-ray appearance of pagets

A

cotton wool appearance
bone enlargement and deformity

57
Q

management of pagets

A

bisphosphonates

58
Q

complications of pagets

A

osteosarcoma, fibrosarcoma