ORTHO 218 Hip Fracture Flashcards

1
Q

What is a fracture?

A

A loss of continuity of the substance of a bone due to physical force

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2
Q

What is a dislocation?

A

Complete loss of contact between articulating surfaces of a joint

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3
Q

What types of fractures can you get in Long bones?

A

Transverse, spiral, oblique, comminuted, segmental

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4
Q

What fractures do you get in cancellous bones?

A

Impacted/crush or compression

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5
Q

What type of fractures due you get peri-articularly?

A

Avulsion fractures

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6
Q

What are the two types of hip fracture (broadly speaking)

A

Intracapsular and Extra capsular

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7
Q

Describe an intracapsular hip fracture?

A

Proximal to the intertrochanteric line

Usually presents with external rotation, adduction and shortening

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8
Q

What is avascular necrosis and what type of hip fracture is it more likely in?

A

Disruption of blood supply to the femoral head more likely in an intracapsular fracture

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9
Q

What is the blood supply to the femoral head?

A

Medial and lateral femoral circumflex arteries

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10
Q

What is an extracapsular fracture?

A

Distal to the intertrochanteric line

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11
Q

What are the three R’s for treating a fracture?

A

Reduction - open/close and how accurate?
Retention - stabilise surgically or not
Rehab - Get them weight bearing asap

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12
Q

What type of fracture needs to be reduced very accurately - therefore surgically?

A

Fracture through a joint

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13
Q

What are the options for treating an extracapsular fracture?

A

Dynamic hip screw - providing optimal stability whilst still allowing micromovement
Cannulated screw can be added if additional stability is required

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14
Q

What are the main treatments for an intracapsular fracture?

A

Hemiarthroplasty or THR

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15
Q

What are some of the complications of fractures?

A

Fat embolism, nerve, vessel or visceral damage, union problems, joint stiffness or myositis ossificans

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16
Q

What is the 1st stage of fracture healing?

A

Formation of the fracture haematoma containing required cells for required regeneration - fibrin clot, polymorphs, platelets and monocytes. Later - fibroblasts, osteoprojenitor cells and vascular in growth

17
Q

What is the 2nd stage of fracture healing?

A

Soft callous
Bony fragments become united by fibrous/cartilagenous tissue, usually when swelling and pain subside
Still possible to angulate however

18
Q

What is the 3rd stage of fracture healing?

A

Hard callous - as the cartilage/fibrous tissue becomes mineralised and converted into endochondral and membranous bone by osteoblasts
= increased stiffness and external callous formation

19
Q

What is the 4th Stage of fracture healing?

A

Remodelling - where woven bone becomes lamellar bone and excess callous is removed and the medullary canal reconstituted

20
Q

What is osteoporosis?

A

Disease characteristics by low bone mass and micro architectural deterioration of bone tissue and an increased fracture risk

21
Q

How do you diagnose osteoporosis?

A

DEXA scan

Tscore >2.5 Standard deviations from the gender matched young adult mean

22
Q

How do you diagnose osteopenia?

A

T score between 1-2.5 Standard deviations

23
Q

What is the Z score?

A

Bone density and number of standard deviations away from the gender and age matched mean - used more in children

24
Q

What are some risk factors for the osteoarthritis?

A
Hypogonadism in men
Smoking
Alcohol
Low BMI
Inactivity
Caucasian
Medication: aromatase inhibitors and GnRH agonists
25
Q

What are the treatments for osteoporosis?

A

Lifestyle : exercise and falls prevention
AdCalD3
Drugs:
to increase bone formation and decrease bone resorption

26
Q

What drug treatment increases bone formation?

A

Teriparatide - recombinant human PTH given in pulses (paradoxically increases BMD!)

27
Q

What drug treatments decrease bone resorption?

A

Bisphosphanates - alendronic acid inhibits osteoclasts

RANK ligand inhibitor - denosuman prevents osteoclast differentiation, activation and survival

28
Q

What is osteomalacia(OM) and ricketts?

A

Inadequate mineralization of the osteoid due to vitamin D deficiency

29
Q

What are some causes of OM and ricketts?

A

Lack of sunlight and diet deficiency/malabsorption
Medication : rifampicin and phenytoin
Liver or renal disease
Low phosphate

30
Q

How do children with ricketts look?

A

Protruding forehead/large head
Kyphosis and pigeon chest
Protruding abdomen
Curved tibia and fibula

31
Q

What are the clinical features of OM?

A

Bone pain
Proximal muscle weakness
Back pain
Stress fractures

32
Q

What is pagets disease?

A

Disorder of bone metabolism

33
Q

What is the pathophysiology behind pagets disease?

A

There is initial overactivity - excessive resorption followed by increased osteoblast activity and bone formation however new bone is woven bone (disordered not lamellar)

34
Q

Where does pagets disease common affect?

A

Spine, pelvis, skull and femur

35
Q

What can some symptoms be of pagets disease?

A
Often asymptomatic
Bone pain - worse on weight bearing
Pathological
High cardiac output
Compression effects - CN palsies, sciatica and cauda equina
36
Q

How do you diagnose pagets disease?

A

Xray, increased ALP and isotope scan

37
Q

How do you treat pagets disease?

A

Bisphosphonates - stimulate production of lamellar bone