Trauma and Orthopedics Flashcards

1
Q

How can fractures be classified?

A

Oblique – fracture lies oblique to the long axis of bone
Commuted fracture – >2 fragments
Segmental fracture – more than one fracture alone a bone
Transverse fracture – perpendicular to long axis of bone
Spiral fracture – severe oblique fracture with rotation along long axis

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2
Q

How are open fractures classified?

A

Gustilo and Anderson Classification system
Grade 1 – low energy wound < 1cm
Grade 2 – greater than 1cm wound with moderate soft tissue damage
Grade 3 – high energy wound > 1cm with extensive soft tissue damage

Grade 3 subdivided into:
A. Adequate soft tissue coverage
B. Inadequate soft tissue coverage
C. Associated arterial injury – use mangled extremity scoring system (MESS) can be used to help predict need for amputation

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3
Q

How should open fractures be investigated?

A

Routine bloods
Clotting
Group and Save and Crossmatch
Plain film X-ray

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4
Q

How are open fractures managed?

A
  • ABCDE
  • IV broad spectrum antibiotics for open injuries as soon as possible consider tetanus prophylaxis
  • Continuous assessment of neurovascular status particularly following reduction and immobilization
  • Immobilise the fracture including proximal and distal joints then realignment and splinting of the fracture
  • Dress with saline soaked gauze
  • Immediate surgery if vascular impairment or compartment syndrome
  • Thoroughly debride in theatre within 6 hours of injury with external fixation devices as internal fixation should be avoided or used with extreme caution
  • Open reduction and internal fixation if required
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5
Q

What is the first principle in managing closed fractures?

A

Reduction – restoring the anatomical alignment of a fracture and is important because it:
• Tamponades the bleeding
• Reduces traction on surrounding tissues and so swelling
• Reduces traction on surrounding neurovascular

Closed reduction requires analgesia either via regional block or conscious sedation

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6
Q

What is the second principle in managing closed fractures?

A

Hold – immobilising a fracture, consider if traction is required on the bony fragments whilst they heal to keep them in the correct anatomical place. Most commonly this is done via splints and plaster casts.

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7
Q

What are three important aspects of plaster casts?

A

Should not be circumferential for the first 2 weeks to prevent compartment syndrome
Should cover joint above and below if there is a possibility of axial instability e.g. combined tibia/fibula fractures, metaphyseal fractures or combined radio-ulna fractures

Consider the need of the patient for thromboprophylaxis if they are immobilised

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8
Q

What is the final important principle in closed fractures management?

A

Rehabilitate – intensive period of physiotherapy required following fracture management

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9
Q

What is ORIF and what are the indications for it?

A
Open reduction and Internal Fixation 
The majority of fractures involving articulations will be managed with ORIF 
Other indications include: 
•	Failed conservative management 
•	2 fractures in one limb 
•	Bilateral identical fractures 
•	Intraarticular fractures 
•	Open fractures and displaced unstable fractures 

Methods for internal fixation

  1. Plates
  2. Screws
  3. Intramedullary nails
  4. Kirschner wires (k-wires)
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10
Q

When is external fixation utilised?

A

Useful in the case of burns, loss of skin and/or bone or in open fractures as external fixation causes less soft tissue disruption. Can be definitive or temporary. It usually involves pins/wires being places away from the zone of injury giving varying degrees of stability.

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11
Q

What are the 8 physiological steps in fracture healing?

A
Haematoma 
Vascular granulation tissue 
Subperiosteal osteoblast stimulation 
Bone matrix 
Endochondral ossification 
Deformable woven bone (callus) 
Lamellar bone
Fracture union
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12
Q

What complications can occur as a result of fractures?

A
  • Fat embolism – altered mental state, pyrexia, SOB, hypoxia, tachycardia and rash – consider ITU as management is mainly supportive
  • Neurovascular injury
  • Infection
  • Delayed union – not healed within expected time frame usually as a result of poor blood supply, bone finished growing, infection, systemic disease or distraction of bone ends by muscle (ORFI prevents this)
  • Non-union – no evidence of progression towards healing clinically of radiologically after 6 months – manage by optimising healing factors and think avascular necrosis
  • Malunion – fracture heals in non-anatomical positions causing loss of function and risk of secondary osteoarthritis and contractures
  • DVT
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13
Q

What is septic arthritis?

A

Definition – Infection within the joint capsule of a joint. 50% of the time it is the knee which is affected. Joint will de destroyed within 24 hours and mortality rate is up to 11%. Common in 0-6 years old and children rarer in adults unless immunocompromised

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14
Q

What organisms commonly cause septic arthritis?

A

Staph Aureus
Streptococci
Neisseria gonococcus
Gram-negative bacilli

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15
Q

What are the main risk factors for septic arthritis?

A

Pre-existing joint disease such as Rheumatoid arthritis
Diabetes or Immunosuppression
Chronic Renal failure
Recent joint surgery
Prosthetic joints (also particularly difficult to treat)
IV drug use
80 years and over

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16
Q

What are the clinical features of septic arthritis?

A

Hot swollen joint with effusion
Systemic fever
Non-weight bearing
Very painful on both active and passive movement
Usually preceding history of trauma or infection
Joint held in position of maximal comfort

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17
Q

How should septic arthritis be investigated?

A

Urgent joint aspiration with USS to assess effusion and guide aspiration
Do not aspirate if prosthesis is present
X-ray may show joint space widening or subluxation
Crystallography on aspirate
Blood cultures and culturing of aspirate
Routine bloods

CT or MRI rarely required unless need specific detail e.g. mediastinal or pelvic extension from sternoclavicular or sacroiliac respectively

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18
Q

What are the Kocher criteria?

A
Non-weight bearing 
CRP > 4
Fever > 38.5
WCC > 12000 
1 = 3%, 2 = 40% 3 = 93% and 4 = 99%
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19
Q

How is septic arthritis managed?

A

IV antibiotics for at least 4-6 weeks (IV for only 2 weeks)
Fluid resuscitation
Open or arthroscopic drainage of the joint with irrigation

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20
Q

What complications can follow septic arthritis?

A

Sepsis
Loss of joint
Osteoarthritis
Osteomyelitis

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21
Q

What are the features of a normal, non-inflammatory arthritis, inflammatory arthritis and septic joint aspirate?

A

Normal – clear <200 WC and <25% neutrophils
Non-inflammatory arthritis – clear/straw coloured, <2000 WC and < 25% neutrophils
Inflammatory arthritis – clear or cloudy yellow, >2000 WC and < 50% neutrophils
Septic arthritis – turbid, > 50’000 WC and >75% neutrophils

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22
Q

What is haematogenous osteomyelitis?

A

Haematogenous osteomyelitis
This occurs from bacteraemia and is usually monomicrobial. It is the most common form in children and usually affects the vertebrae in adults.

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23
Q

What are the risk factors for haematogenous osteomyelitis?

A

Risk factors
• Sickle cell anaemia
• Intravenous drug user and alcohol excess
• Immunosuppression due to either medication or HIV
• Infective endocarditis

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24
Q

What is non-haematogenous osteomyelitis?

A

Non-haematogenous osteomyelitis
This occurs from the contiguous spread of infection from adjacent soft tissues to the bone or from direct injury/trauma to bone. It is often polymicrobial and is the most common form in adults.

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25
Q

What are the risk factors for non-haematogenous osteomyelitis?

A

Risk factors
• Diabetic foot ulcers/pressure sores
• Diabetes mellitus
• Peripheral arterial disease

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26
Q

What are the clinical features of osteomyelitis?

A
Raised inflammatory markers 
Constant pain with gradual onset and worse at night
Low grade pyrexia 
Tender to touch
Warm and erythematous 
Slight effusion 
Systemic infection 
Inability to weight bear
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27
Q

What organisms causes osteomyelitis?

A

Staph Aureus is the most common
Pseudomonas, E. coli and streptococci
Salmonella species predominate sickle cell patient

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28
Q

How should osteomyelitis be investigated?

A

Routine bloods
Blood cultures
X-rays – show nothing in first 10-14 days but later show haziness and loss of density
MRI is the most sensitive modality
Bone biopsy and culture is gold standard but rarely required

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29
Q

How is osteomyelitis managed?

A

Drain any abscess
When organism and sensitivities not known – 6 weeks of IV vancomycin and cefotaxime
Flucloxacillin for 6 weeks and clindamycin if penicillin allergic may also be appropriate
Ciprofloxacin in pseudomonas infections

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30
Q

What is chronic osteomyelitis and why does it occur?

A

Chronic Osteomyelitis
If osteomyelitis is poorly treated this will result in progression to chronic characterised by pain, fever, infected dead bone (sequestrum), sinus suppuration (pathognomonic) and long remissions. Suspect in vascular insufficiency with non-healing tissue ulceration overlying bony prominences.

Sequestrum acts as a reservoir for infection as it is avascular and so is not penetrated by antibiotics.

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31
Q

How does chronic osteomyelitis appear on X-ray?

A

X-rays will show thick irregular bone and if bone can be felt on probing an ulcer this is sufficient to diagnose chronic osteomyelitis.

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32
Q

How is chronic osteomyelitis managed?

A

Management – excision of dead bone, skeletal stabilisation, dead space management and antibiotics as for acute or modified for sensitivities.

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33
Q

What is compartment syndrome?

A

Definition – build up of pressure in a muscle compartment that results in compression of blood vessels and muscles causing ischaemia and death of the muscle. Fractures at highest risk of this are supracondylar fracture and tibial shaft fractures.

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34
Q

What causes compartment syndrome?

A

Reperfusion of ischaemic limb
Plaster cast
Physical trauma especially fractures
Crush injuries

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35
Q

What are the clinical features of compartment syndrome?

A

Severe pain especially on movement
Excessive requirement of breakthrough analgesia should raise suspicion
Pulseless (although the presence of a pulse does not rule out compartment syndrome)
Paralysis
Paraesthesia
Pallor

Death of muscle will occur within 4-6 hours

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36
Q

How should compartment syndrome be investigated?

A

Clinical diagnosis
Can measure intercompartmental pressure – anything in excess of 20mmHg are abnormal and > 40mmHg is diagnostic
Routine bloods including creatinine kinase
Note no pathology will be seen on X-ray

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37
Q

How is compartment syndrome managed?

A

Removal of cause if present and placement of limb at heart level
Emergency fasciotomy with wound closure around 7 days afterwards
Management of rhabdomyolysis with aggressive IV fluids
If muscle groups are frankly necrotic at fasciotomy they should be debrided and amputation may be required

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38
Q

What is osteoarthritis?

A

Definition – progressive loss of articular cartilage and remodelling of underlying bone, originally thought to be simple wear and tear now its thought it may be due to slight deformities within joints causing inflammation over time.

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39
Q

What are the general risk factors for osteoarthritis?

A

Obesity
Advancing age
Female
Manual labour jobs

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40
Q

What are the clinical features of osteoarthritis?

A

Painful and stiff joints – most commonly, fingers, hips and knees
Reduced movements
Typically insidious onset, chronic and gradually worsening
Relieved by rest and worsened through activity
Pain gets worse through day but stiffness improves
Localised swelling
Crepitus

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41
Q

How does osteoarthritis appear on X-ray?

A

Loss of joint space
Subchondral Sclerosis (bright white)
Osteophytes
Subchondral cysts

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42
Q

How should osteoarthritis be investigated?

A

X-ray

Routine blood tests to rule out other disorders

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43
Q

How is osteoarthritis managed?

A

Education on protection and physiotherapy strengthening exercises
Loss of weight
First line analgesics such as Paracetamol and NSAIDs (topical NSAIDs or knee and hand only)
Second line analgesics such as opioids, capsaicin cream and intraarticular steroid injections
Replacement of joint in surgery

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44
Q

What is osteoarthritis of the hand sometimes referred to as?

A

Osteoarthritis (OA) of the hands is sometimes referred to as nodal arthritis. The presence of hand OA increases the risk of future hip and knee OA (higher for hip OA than for knee OA)

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45
Q

What are the risk factors for osteoarthritis of the hand?

A
Family history
Female (M:F 1:3)
Increasing age (rare to present before 55 years of age)
Previous trauma of a joint 
Obesity
Hypermobility 
Occupation e.g. cotton workers and farmers are more susceptible to hand OA
Osteoporosis reduces the risk of OA
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46
Q

What are the clinical features of osteoarthritis of the hand?

A
  • Radiologic signs are more common than symptoms
  • Usually bilateral with one joint affected at a time over several years.
  • The carpometacarpal joints (CMCs), distal interphalangeal joints (DIPJs) are affected more than the proximal interphalangeal joints (PIPJs)
  • Episodic joint ache provoked by movement and relieved by resting the joint
  • Stiffness worse after long periods of inactivity such as in the morning, stiffness lasts only a few minutes compared to the morning joint stiffness seen in rheumatoid arthritis
  • Painless nodes – Heberden’s nodes at the DIPJs, Bouchard’s Nodes at the PIPJs, these nodes are the result of osteophyte formation
  • Squaring of the thumbs, deformity of the carpometacarpal joint of the thumb resulting in fixed adduction of the thumb
  • Functionally patients do not usually have any problems unless there is severe involvement of the DIPJs, there may be reduced grip strength which can result in disuse atrophy
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47
Q

How is osteoarthritis of the hands investigated?

A

X-ray signs as for standard OA – osteophyte and joint space narrowing

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48
Q

What are the risk factors for osteoarthritis of the hip?

A
Increasing age
Female gender (twice as common)
Obesity
Developmental dysplasia of the hip
AVN of the hip
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49
Q

What are the clinical features of osteoarthritis of the hip?

What scoring system can be used to assess severity?

A

Chronic history of groin ache following exercise and relieved by rest
Red flag features suggesting an alternative cause include rest pain, night pain and morning stiffness > 2 hours

Oxford Hip Score is used to assess severity

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50
Q

What investigations should be done in someone with suspected osteoarthritis of the hip?

A

NICE recommends that if the features are typical then a clinical diagnosis can be made
otherwise, plain x-rays are the first-line investigation

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51
Q

How is osteoarthritis of the hip managed?

A

Oral analgesia
Intra-articular injections: provide short-term benefit
Total hip replacement remains the definitive treatment

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52
Q

What are the complications of total hip replacement?

A

Venous thromboembolism
Intraoperative fracture
Nerve injury

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53
Q

What reasons are there for a revision of a total hip replacement?

A

Aseptic loosening (most common reason)
Pain
Dislocation
Infection

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54
Q

What are the 3 main techniques for hip arthroplasty?

A
  • Cemented hip replacement – metal femoral component is cemented into the femoral shaft accompanied by a cemented acetabular polyethylene cup
  • Uncemented replacement, more popular in younger patients but expensive
  • Hip resurfacing – metal cap placed over the femoral head and is often used in younger patients as it preserved the femoral neck in case its needed for conventional surgery later on in life
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55
Q

What advice should be given to patients following hip arthroplasty to prevent dislocation?

A
  • Avoid flexing hip > 90 degrees
  • Avoid low chairs
  • Do not cross your legs
  • Sleep on your back for first 6 weeks
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56
Q

What causes osteoarthritis of the knee?

A

Primary osteoarthritis appears idiopathic although research is suggesting small underling defects may be the cause.

Secondary Causes 
Post traumatic 
Postoperative 
Post-infection 
Malposition 
Mechanical instability 
Osteochondritis dissecans
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57
Q

What are the risk factors for osteoarthritis of the knee?

A
Obesity 
Female 
Genetics 
Age 
Occupation
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58
Q

What are the clinical features of osteoarthritis of the knee?

A

Pain on initiating movement
Stiffness following inactivity but resolves in 30minutes
Posterior patellar and medical compartment most affected leading to varus deformity
Limited range of movement
Crepitus during active and passive movement

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59
Q

How is osteoarthritis of the knee managed?

A

NSAIDs topical or oral
Physiotherapy focusing on quadriceps strengthening exercises
Weight loss
Steroid injections
Total knee replacement – lasts about 15 years
If young then osteotomies are preferred and can delay TKR for 10 years

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60
Q

What are the two most common types of rotator cuff injuries?

A

A syndrome comprising two aetiologies
• Subacromial impingement – impingement syndrome or painful arc syndrome
• Rotator cuff tears – tear in supraspinatus tendon, subscapularis, or infraspinatus

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61
Q

What actually causes subacromial impingement

A

Definition – supraspinatus becomes inflamed due to impingement below acromion and coraco-acromial ligament.

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62
Q

What cause subacromial impingement?

A

Osteoarthritis of the acromio-clavicular joint and resulting osteophytes
Thickening or calcification of the coracoacromial ligament
Rotator cuff injuries destabilising the joint
Bursitis of the subacromial bursa

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63
Q

What are the clinical features of subacromial impingement?

A

Painful mid arc (60-120 degrees)

Positive Neer’s impingement test or Hawkins-kennedy test

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64
Q

What are the clinical features of a rotator cuff tear?

A

Positive test for rotator cuff tears (Jobe’s test, Bell-press test, infraspinatus, and teres minor tests and drop arm sign)
If there is a rotator cuff tear, then there may be pain in the first 60 degree of abduction and an inability to abduct above 90 degrees
Particularly pain at night disturbing sleep

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65
Q

How are rotator cuff tears investigated?

A

If suspecting tear, then X-ray to exclude fracture
USS scan of the arm – can determine tear or no tear
MRI – size characteristic and location of tear

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66
Q

Subacromial impingement is a clinical diagnosis but how can it be confirmed?

A

MRI used to confirm impingement

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67
Q

How is subacromial impingement managed?

A

Conservative management of impingement with analgesia, physio, and steroid injection
If after 6 months of conservative management there is no response then surgical management can be considered such as arthroscopic acromioplasty, bursectomy or repair of muscle tears

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68
Q

How are rotator cuff tears managed?

A

For tears conservative management preferred if presenting within 2 weeks of injury and especially in patients not limited by pain and those with co-morbidities and unsuitable for surgery. Surgery indicated if presenting >2 weeks since the injury or remaining symptomatic despite conservative management.

Incomplete tendon tear – surgery only if symptoms persist
Complete tendon tear – open or arthroscopic repair

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69
Q

What is frozen shoulder syndrome?

A

Frozen Shoulder Syndrome (adhesive capsulitis)
Idiopathic severe pain and then persisting stiffness. Fairly common especially in middle aged females, associated with diabetes mellitus thyroid disease, and cervical spondylosis.

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70
Q

What is primary vs secondary adhesive capsulitis?

A

Primary – idiopathic

Secondary – rotator cuff tendinopathy, impingements, biceps tendinopathy, previous surgery, trauma or joint arthropathy

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71
Q

What are the clinical features of adhesive capsulitis?

A

External rotation affected more than internal rotation or abduction, loss of arm swing
Both active and passive movements are affected
Split into 3 phases that last over 6-24 months
1. Deep and constant painful freezing phase (up to 12 months)
2. Adhesive phase (6-12 months)
3. Recovery or thawing phase (12-36 months)
Stiffness and pain is worse at night and often disturbs sleep
Bilateral in 20% of cases

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72
Q

How is adhesive capsulitis investigated?

A

Typically, a clinical diagnosis

Imaging may be required in atypical or persistent symptoms and MRI scan is the modality of choice in this case

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73
Q

How is adhesive capsulitis managed?

A

No single intervention has been shown to improve outcomes
NSAIDs, physiotherapy, oral corticosteroids, and intra-articular corticosteroids
Surgical release with manipulation under anaesthetic or arthroscopic arthrolysis

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74
Q

How common is shoulder dislocation and when does it occur?

A

This is the most common joint in the body to dislocate accounting for 50% of all major dislocations. Typically young males in contact sport where arm was forced into abduction, extension, and external rotation. In the elderly may simply be a FOOSH.

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75
Q

What can dislocate in a shoulder dislocation?

A

Types of Shoulder dislocation
• Glenohumeral dislocation – 95% are anterior
• Acromioclavicular dislocation – next most common and clavicle loses all attachment to the scapula
• Sternoclavicular – uncommon

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76
Q

What are the two main types of Glenohumeral shoulder dislocation?

A

Anterior – occurs due to external rotation and abduction, 40% of cases will become recurrent. Associated with greater tuberosity fracture, Bankert lesion (avulsion of glenoid labrum from the glenoid) and Hill-sachs lesion (impaction fracture of humeral head).

Posterior – often misdiagnosed, Rim’s, Light bulb sign and Trough sign. Present with limited external rotation, usually occurs following epileptic seizures or electric shock

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77
Q

What are the clinical features of shoulder dislocation?

A
Pain
Reduced mobility 
Asymmetry on examination 
Loss of contours – flattened deltoid 
Anterior bulge from head of humerus
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78
Q

How should shoulder dislocation be investigated?

A

Trauma X-ray of shoulders – AP, Y scapular and axial views (Lightbulb sign seen in posterior dislocation)
Must check neurovascular status before and after reduction as well as an x-ray to confirm no fracture has occurred
If soft tissue damage suspected such as rotator cuff tears then MRI shoulder may be indicated

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79
Q

How are anterior shoulder dislocations managed?

A

If dislocation recent then reducing may be done without analgesia
Some patients may require sedation/analgesia to make sure rotator cuffs are relaxed - usually Entonox, parenteral opioid or intra-articular local anaesthetic)
Support the arm in a broad arm sling and refer to fracture clinic and physiotherapy
In recurrent dislocation surgical repair will be required

Simple reduction – apply longitudinal traction to the arm in abduction and replace head of the humerus with gentle pressure

Kocher’s method – flex elbow to 90 degrees, abduct the shoulder, externally rotate the shoulder and then abduct the upper arm back across the body before internally rotating the shoulder

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80
Q

What is a proximal humerus fracture and when do they occur?

A

Common fracture that usually occurs through the surgical neck (very rare for it to happen through the anatomical neck) usually after FOOSH in the elderly causing a stable osteoporotic fracture. Can sometimes occur in the young in high energy trauma and often associated with tissue or neurovascular injuries.

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81
Q

What types of proximal humeral fracture carries the greatest risk of AVN?

A

Avascular necrosis risk if there is an anatomical neck fracture with displacement of >1cm

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82
Q

What proximal humeral fracture is most common in children?

A

In children the most common pathology is a greenstick fracture through the surgical neck.

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83
Q

What are the clinical features of proximal humeral fractures?

A

Pain
Restricted arm movement
Significant swelling
Check neurovascular status, especially axillary distribution

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84
Q

How are proximal humeral fracture investigated and classified?

A

Trauma shoulder X-ray – AP, Y scapular and axial views

Neer Classification – classification based on relationship between greater tuberosity, less tuberosity, articular segments (anatomical neck) and humeral shaft (surgical neck)

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85
Q

How are proximal humeral fractures managed?

A

Majority managed conservatively with immobilisation and early mobilisation. Use polysling that allows the arm to hand aiding the reduction of fragments

If significantly displaced, open or neurovascular compromise then will require ORIF with use or intramedullary nailing. ORIF usually preference is head splitting fracture and intramedullary nail if fracture involved surgical neck or combined humeral fracture

Hemiarthroplasty in complex injuries where ORIF and intramedullary nails are inappropriate.

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86
Q

What causes fractures of the shaft of the humerus

A

Typically direct blow to the arm rather than a FOOSH, be aware of radial nerve injury (seen in 10%) so document neurovascular status before and after intervention. Typically occur from FOOSH or falling laterally onto an adducted arm.

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87
Q

What is a Holstein-Lewis fracture?

A

Holstein-Lewis fracture – distal third of humerus resulting in entrapment of the radial nerve – loss of sensation in radial distribution and wrist drop deformity. Surgical management required.

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88
Q

How are humeral shaft fractures managed?

A

Typically does not need surgery, simple splinting with a humeral brace and gravity traction by means of collar and cuff gives satisfactory reduction. Must immobilise for 8-12 weeks. Full union expected with 8-12 weeks.

In minority of cases ORIF with a plate is required and may involve faster healing times
Intramedullary nailing indicated in pathological fracture, polytrauma or severe osteoporosis

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89
Q

When do clavicular fracture occur?

A

Most commonly occurs following direct blow to the clavicle and is common in cycling accidents. The most common location in the middle third where the medial fragment is pulled superiorly by sternocleidomastoid and the lateral fragment is displaced inferiorly from weight of the arm.

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90
Q

What is the Allman classification of clavicular fractures?

A
  1. Type 1 – middle third of the clavicle (75% of all clavicular fractures), generally stable but significant deformity may be present
  2. Type 2 – lateral third and make up 20% of clavicular fractures. When displaced these are often unstable
  3. Type 3 – remaining 5% in the medial third of the clavicle usually involving multi system polytrauma. Must check neurovascular compromise due to proximity of mediastinum. Think pneumothorax and haemothorax
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91
Q

How are clavicular fractures managed?

A

Broad arm sling with follow up X-ray at 6 weeks to ensure union, encourage early mobilisation of shoulder to prevent adhesive capsulitis. Sling maintained until there is pain free movement. If fragments failed to unite then ORIF
ORIF if severely displaced, open fracture or bilateral

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92
Q

What is epicondylitis?

A

Inflammation of the epicondyles of the elbow termed tennis elbow if the lateral epicondyle and golfer’s elbow if the medial epicondyle.

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93
Q

Describe the features of lateral epicondylitis?

A

Lateral Epicondylitis (Tennis elbow)

Pain and tenderness localised to the lateral epicondyle
Pain worse on resisted wrist extension with the elbow extended or supination of the forearm with the elbow extended
Patients in acute pain for 6-12 weeks
Episodes typically last between 6-24 months
Cozen’s and Mill’s tests

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94
Q

Describe the features of medial epicondylitis?

A

Medial Epicondylitis (Golfer’s elbow)

Pain and tenderness localised to the medial epicondyle
1/5 less common than tennis elbow
Pain aggravated by wrist flexion and pronation
Symptoms may be accompanied by numbness/tingling in the 4th and 5th finger due to ulnar nerve involvement

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95
Q

How is epicondylitis managed?

A

Most cases will spontaneously resolve via restriction of activity within 1 year and analgesia
Physiotherapy in motivated patients may speed this up as well as corticosteroid injections

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96
Q

What is bicep tendinopathy and who does it occur in?

A

Painful swollen and weak tendon that can pose a risk of rupture. This can occur proximally or distally (most common) and is most common in young active individuals or in older people with a degenerative tendinopathy.

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97
Q

How does bicep tendinopathy present?

A

Presentation – pain, worse on stressing the tendon, weakness and stiffness. Tender to examine and muscular atrophy due to disuse atrophy. Specific tests – speed test (proximal tendon) and Yorgason’s test (distal tendon)

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98
Q

How should bicep tendinopathy be investigated?

A

Investigations – blood tests and play x-ray to exclude other causes. US and MRI may be used but are rarely warranted.

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99
Q

How is bicep tendinopathy managed?

A

Management – conservative with analgesia, ICE and physiotherapy. US guided steroid injections if persistent and very rarely surgical intervention with arthroscopic tenodesis or tenotomy.

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100
Q

What is a bicep rupture?

A

Two tendons, long from glenoid and the short from the coracoid process that insert distally together onto the radial tuberosity. Tendon rupture occurs when one of these separate form their attachment site or is torn across its full width. Typically, this involves the long tendon (90%) but can rarely occur at the distal tendon.

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101
Q

What are the risk factors for bicep rupture?

A
Male (3:1 ratio) 
Elderly – over age of 60
Distal rupture usually in 40s and almost always men 
Heavy overhead activities 
Shoulder overuse or underlying shoulder injuries 
Smoking 
Corticosteroid 
Bicep tendinopathy
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102
Q

What are the mechanisms of bicep ruptures?

A

Long tendon – typically occurs when biceps are lengthened and contracted, and a load is applying e.g. descent phase of a pull-up
Distal tendon – flexed elbow is suddenly and forcefully extended whilst bicep is contracted

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103
Q

What are the clinical features of bicep ruptures?

A

Sudden pop or tear in the shoulder or elbow followed by pain, bruising and swelling
If long tendon rupture then Popeye deformity, also less reliable reverse Popeye in distal tendon rupture
Weakness in shoulder and elbow especially with supination
Hood test – flex elbow to 90 degrees fully supinated and attempt to hook index finger underneath lateral edge of bicep tendon (can’t be done if ruptured)

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104
Q

How are bicep ruptures investigated?

A

General examination of elbow and shoulder and assess neurovascular function
Bicep squeeze test – if intact then squeeze should cause forearm supination
USS by skilled clinician usually done to confirm diagnosis
Urgent MRI if suspected distal tendon rupture

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105
Q

How are bicep rupture managed?

A

Long tendon rupture – conservative management with analgesia and physiotherapy
Distal tendon rupture – surgical intervention

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106
Q

What are distal humeral fractures and who do they most often occur in?

A

Supracondylar Fracture

Most common fracture in childhood (but very rare in adults) and usually due to FOOSH with hyperextension.

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107
Q

What is the presentation of a supracondylar fracture?

A

Clinical features – pain, swelling and inability to move elbow
Neurovascular problems are common due to the proximity of surrounding structures

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108
Q

How should suspected supracondylar fracture be investigated for?

A

Investigations – X-ray in AP and lateral views. Look for posterior fat pad sign and displacement of the anterior humeral line which should intersect the middle of the capitellum in children > 5 years

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109
Q

How are supracondylar fractures classified?

A

Gartland Classification (lateral x-ray)

  1. Anterior humeral line passes through the middle of the capitellum (undisplaced)
  2. Anterior humeral line passes anterior to the capitellum (displaced with intact posterior cortex)
  3. Unstable with posterior displacement, if medial then threatens the radial nerve, if lateral displacement then threatens the median nerve
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110
Q

How are supracondylar fractures managed?

A

Keep elbow in extension to minimise brachia artery damage
Type 1 – above elbow back slab and sling – conservative management
Type 2 – closed reduction under GA (and fixation with k wires)
Type 3 – closed reduction under GA and fixation with k wires

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111
Q

What causes fracture of the head of the radius?

A

Most common elbow fracture in adults usually through indirect trauma with axial load being placed on the forearm causing radial head to be pushed against the capitulum of the humerus, usually this is during extension and pronation.

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112
Q

What are the clinical features of a fracture of the head of a radius?

A

History of FOOSH with swollen and tender elbow over the radial head
Flexion/extension may be possible, but supination and pronation hurt
Effusion on x-ray or sail sign

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113
Q

How are radial head fractures classified?

A

Mason Type 1 – non-displaced or minimally displaced
Mason Type 2 – partial articular fracture with displacement > 2mm or angulation
Mason Type 3 – Comminuted fracture and displacement (complete articular fracture)

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114
Q

How are radial head fractures managed?

A

Check for position and neurovascular compromise before and after intervention
Undisplaced – collar and cuff e.g. Mason Type 1 and some Type 2
Displaced or fragments prevent supination/pronation then ORIF or excision of radial head such as in Mason Type 3 and some Type 2.

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115
Q

How do elbow dislocations occur?

A

Almost always posterior due to fall on not quite fully outstretched hand with partially flexed elbows causing posterior ulna displacement on the humerus. Often have ulnar nerve deficit.

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116
Q

How are elbow dislocations managed?

A

Manage with closed reduction +/- GA which is confirmed by hearing a clunk. Must have post reduction image and check neurovascular status before and after. Keep immobilised in a backslab for 10 days. Check neurovascular status and X-ray before and after.
Dislocations complicated by fractures, open injury or neurovascular compromise requires ORIF of the coronoid, radial head or olecranon with appropriate soft tissue repair.

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117
Q

What is the terrible triad?

A

Terrible triad – elbow dislocation with lateral collateral ligament injury, radial head fracture and coronoid fracture. This will cause a very unstable elbow. This usually occurs with falls onto extended arm with rotation resulting in posterolateral dislocation.

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118
Q

How do olecranon fractures occur?

A

All olecranon fracture are intraarticular and occur after direct blow or avulsion when triceps contacts during a fall on semiflexed, supinated arm.

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119
Q

How do olecranon fractures present?

A

Presentation is with tenderness and inability to extend the elbow against gravity

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120
Q

How are olecranon fractures managed?

A

Conservative management if displacement < 2mm – immobilisation in 60–90-degree elbow flexion and early introduction of movement from week 1-2. Increasingly conservative management is used in elderly patients despite a larger displacement.

Surgical management if displacement is > 2mm with ORIF and tension band or a plate. Often requires a high rate of removal of metal work due to how superficial everything is over the olecranon.

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121
Q

What is olecranon bursitis?

A

Inflammation of the olecranon bursa – sometimes referred to as student’s elbow due to it occurring from resting elbows on a desk for long periods of time. Can also have an infective cause.

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122
Q

How does olecranon bursitis present and how is it managed?

A

Presents with pain and swelling over the olecranon but with range of movement preserved and can be definitively diagnosed with aspiration of the fluid.

If infective manage with IV antibiotics and washout, noninfective treated with rest and analgesia.

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123
Q

What causes fracture of the distal radius and/or Ulna?

A

Usually caused by a fall on the outstretched hand or FOOSH and is very common in elderly osteoporotic women. Be aware of compartment syndrome and injuries to ulnar, radial, and medial nerve as well as the radial and ulnar arteries.

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124
Q

Describe a colles’ fracture

A

Colles’ Fracture
Distal transverse radial fracture (usually 1 inch proximal to the radio-carpal joint) with posterior displacement of the fragments and ulnar deviation. Described as a dinner fork type deformity.

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125
Q

Describe a Smith’s or reverse colles’ fracture

A

Smith’s or reverse Colles’ fracture
Falling onto flexed wrists (falling backwards and arms flexed behind you) or direct blow to the forearm resulting in volar angulation (anterior displacement) of the distal radial fragment described as a Garden spade deformity.

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126
Q

Describe a Barton’s fracture

A

Barton’s Fracture
Intra-articular fracture of the distal radius (Colles’/Smith’s) with associated radiocarpal dislocation, usually due to fall onto extended and pronated wrist.

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127
Q

Describe a Bennett’s fracture?

A

Bennett’s Fracture
Intraarticular fracture of the first carpometacarpal joint due to impact on flexed metacarpal such as in fist fight. On X-ray triangular fragment at ulnar base of metacarpal is seen.

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128
Q

Describe Monteggia’s and a Galeazzi’s fracture

A

Monteggia’s Fracture
Dislocation of the proximal radioulnar joint in association with an ulnar fracture. Fall on outstretched hand with forced pronation. Need prompt diagnosis to avoid disability.

Galeazzi Fracture
Radial shaft fracture with associated dislocation of the distal radioulnar joint due to direct blow to the forearm.

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129
Q

How should suspected wrist fracture be investigated?

A

X-ray looking for: intra articular extension and ulnar styloid fractures which indicate a more unstable fracture.

130
Q

How are wrist fractures managed?

A

Analgesics will always be needed
Closed reduction in ED in cases where there is neurovascular compromise or where manipulation is likely to be a definitive treatment.
Plaster immobilisation for 6 weeks with below elbow backslab casts and Physiotherapy
Significantly displaced or unstable fractures ORIF +/- K wires

Ulnar styloid fractures often do not require fixation
Smith’s fracture are more unstable and treated with a volar buttress plate in their plaster

131
Q

What are the common complications following wrist fractures?

A

Involvement of the scaphoid bone
AVN
Malunion or Non-union
Median nerve compression

132
Q

What is a scaphoid fracture and why is it important?

A

Must always examine for scaphoid fracture in anyone presenting with wrist pain acutely for medico legal reasons as the blood supply comes dorsally from the radial artery and so there is high risk of avascular necrosis.

133
Q

What tends to cause scaphoid fractures?

A

Fall onto outstretched hand
Contact sports – football and rugby (see a peak in autumn with start of school season)
Road traffic accidents – holding steering wheel

134
Q

What are the clinical features of a scaphoid fracture?

A

Pain along the radial aspect of the wrist at the base of the thumb
Loss of grip strength/pinch
Maximal tenderness over the anatomical snuff box (sensitive but not specific)
Wrist joint effusion – unless hyper acute (<4h) or delayed (>4days) presentation
Pain elicited by telescoping of the thumb (longitudinal compression)
Tenderness of the scaphoid tubercle
Pain on ulnar deviation of the wrist

135
Q

How should scaphoid fractures be investigated?

A

X-ray in AP and lateral views (can also request scaphoid views – PA, lateral oblique and ziter) – be wary as x-ray may be normal in early phases so repeat in 7-10 days’ time after wrist immobilisation
CT scan is superior to X-ray
MRI is definitive to confirm or exclude diagnosis and should be considered first line

136
Q

How are scaphoid fractures managed?

A

Immobilisation with a thumb spica splint or below the elbow back slab. Undisplaced fractures – cast for 6-8 weeks, union achieved in 95%, if professional sportsman then early surgical intervention. If fracture is displaced, then surgical fixation usually with percutaneous variable-pitched screw.

137
Q

What is Trigger finger?

A
Trigger Finger (Tendon nodules)
Associated with abnormal flexion of the digits that is thought to occur due to disparity between the size of the tendon and the pulleys.
138
Q

What are the risk factors for trigger finger?

A
Female 
Rheumatoid arthritis 
Diabetes 
Prolonged gripping 
Increasing age
139
Q

What are the clinical features of trigger finger?

A

More common in thumb, middle or ring finger
Stiffness, locking and snapping when extending a flexed digit
Nodule may be felt at the base of the finger
May become painful, especially over the volar aspect of the MCP joint

140
Q

How is trigger finger managed?

A

If mild then conservative management with advice and small splint
Steroid injection works in most cases
Finger splint applied after the injection and rest
Surgery reserved for patients who do not respond to injections

141
Q

What is De Quervain’s tenosynovitis?

A

Definition – inflammation of the sheath containing extensor pollicis brevis and abductor policis longus tendons.

142
Q

What are the risk factors for De Quervain’s tenosynovitis?

A

Aged 20-50
Female
Pregnant
Activities involving repetitive wrist movement

143
Q

What are the clinical features of De Quervain’s tenosynovitis?

A

Pain near the base of the thumb
Tenderness and swelling over the radial styloid process
Pain when grasping or pinching are particularly painful and difficult e.g. lifting a teapot
Positive Finkelstein’s test

144
Q

How can you examine/ investigated for De Quervain’s tenosynovitis?

A

No investigation required as clinical diagnosis

Finkelstein’s test – patient makes a fist with their thumb inside the fist then ulnar deviates, positive test if pain felt over the radial styloid region.

145
Q

How is De Quervain’s tenosynovitis managed?

A

Conservative – lifestyle advice to reduce repetitive movements and a thumb splint (spica)
ICE and NSAIDs
Steroid injections to reduce inflammation and relieve pain in first 6 months
Surgical decompression by splitting the tendon sheaths

146
Q

What is Dupuytren’s contracture?

A

Contraction of the longitudinal palmer fascia due to fibroblastic hyperplasia and altered collage matrix.

147
Q

What are the risk factors for Dupuytren’s contracture?

A
6:1 Male to Female 
Smoking 
Alcoholic Liver disease 
Diabetes 
Occupational exposures (vibration tools or heavy manual work)
148
Q

What are the clinical features of Dupuytren’s contracture?

A

Typically starts as painless nodules
Can lead to severely limited digital movement
Most commonly affects the ring and little finger
Heuston’s test

149
Q

How is Dupuytren’s contracture investigated?

A

Diagnosis is clinical
Good practice to check LFTs and glucose
USS might be used for accuracy when applying intralesional injections

150
Q

How is Dupuytren’s contracture managed?

A

Conservative – hand physiotherapy, injectable collagens clostridium histolyticum
Surgical – excision of disease fascia, fasciectomy

151
Q

What are ganglionic cysts?

A

Noncancerous soft tissue lumps that can occur along any tendon or joint and are usually filled with synovial fluid. They are soft and transilluminate on examination.

152
Q

How are ganglionic cysts managed?

A

Management if symptom free then conservative and simply monitor.
If interfering with daily functioning, then can aspirate +/- steroid injection or excise the cyst.

153
Q

What is carpal tunnel syndrome?

A

Definition – compression of the median nerve due to raised pressure underneath the flexor retinaculum the wrist

154
Q

What are the risk factors for carpal tunnel syndrome

A
Female
Increasing age
Pregnancy and the pill
Obesity 
Previous Joint injury 
Diabetes
Rheumatoid arthritis 
Hypothyroidism 
Gout and pseudogout 
Cardiac failure acromegaly
Premenstrual state
155
Q

What are the causes of carpal tunnel syndrome?

A
Idiopathic 
Pregnancy 
Oedema 
Lunate fracture 
Rheumatoid arthritis
156
Q

What are the clinical features of carpal tunnel syndrome?

A

Pain/Pins and needles in the thumb, index and middle finger (palmer aspect usually spared as a result of the early cutaneous branch of the median nerve)
Symptoms may ascend proximally
Worst during the night
Patient may shake their hand to obtain relief

Weakness of thumb abduction (abductor pollicis brevis)
Wasting of thenar eminence

157
Q

How is carpal tunnel syndrome investigated?

A

Percuss over median nerve to bring back symptoms – Tinel’s test
Hold wrist in full flexion for a few minutes should re-create pain – Phalen’s test

Nerve conduction studies – prolongation of action potential
US and MRI if required to identify lesions

158
Q

How is carpal tunnel syndrome managed?

A

Conservatively with wrist splint at night
Corticosteroid injection and NSAIDS to reduce swelling
Carpel tunnel surgery if really severe symptoms – surgical decompression (flexor retinaculum division)

159
Q

What is cubital tunnel syndrome?

A

Compression of the ulnar nerve as it passes through the cubital fossa

160
Q

What are the clinical features of cubital tunnel syndrome?

A

Tingling and numbness in the 4th and 5th finger
Tingling starts off intermittent and then becomes constant
Weakness and muscle wasting
Pain worse on leaning on the affected elbow
History of osteoarthritis or prior trauma

161
Q

How is cubital tunnel syndrome investigated?

A

Clinical diagnosis
Nerve conduction studies

Froment’s sign – hold piece of paper between patient’s thumb and index finger – then attempt to pull it away, if ulnar palsy then adductor policis muscle doesn’t work and patient tried to compensate by flexing thumb at interphalangeal joint

162
Q

How is cubital tunnel syndrome managed?

A

Avoid aggravating activity
Physiotherapy
Steroid injections
Surgery in resistant cases

163
Q

What is radial tunnel syndrome?

A

Most are due to compression of the posterior interosseous branch of the radial nerve and though to occur due to overuse.

Clinical Features
Very similar to lateral epicondylitis making it difficult to diagnose
Pain tends to be around 4-5cm distal to the lateral epicondyle
Symptoms exacerbated by extending the elbow and pronating the forearm

164
Q

What modalities do the dorsal column and spinothalamic tract carry?

A

Dorsal Column – vibration, and proprioception

Spinothalamic – pain, sensation, and temperature

165
Q

What is discitis?

A

Infection in the intervertebral disc space which can lead to serious complications such as sepsis or epidural abscess.

166
Q

What causes discitis?

A

Usually due to haematogenous seeding of the vertebrae implying the patient has bacteraemia and seeding could have occurred elsewhere

Bacterial – staphylococcus aureus is most common
Viral
TB
Aseptic

167
Q

What are the clinical features of discitis?

A

Back pain
Pyrexia, rigors, and sepsis
Neurological features- changing lower limb neurology
Features of epidural abscess

168
Q

How should suspected discitis be investigated?

A

MRI is most sensitive
CT guided biopsy may be required to guide microbial treatment
Assess for endocarditis with transthoracic echo or TOE

169
Q

How is discitis managed?

A

6-8 weeks of IV antibiotics – really important to tailor to positive cultures

170
Q

What causes non-specific back pain?

A

One of the most common presentations to general practice with the majority being non-specific muscle problems. When diagnosing focus on the fact you have rule out sinister causes of back pain.

171
Q

Describe the red flag signs to be aware of in red flag lower back pain?

A

Red Flags associated with Lower back pain
• Age < 20 or > 50 – malignancy
• Violent trauma or minor trauma in osteoporosis – fracture
• History of previous malignancy – metastatic disease
• Night pain
• Systemically unwell – weight loss of fever
• Faecal/urinary incontinence/saddle anaesthesia – cauda equina syndrome
• Immunosuppression, ICDU and unexplained fever – infection
• Chronic steroid use – fracture or infection

172
Q

How should non specific lower back pain be investigated?

A

NO need for lumbar spine X-ray
MRI – only if the result is likely to change management or where there is suspicion of malignancy, infection, fracture, cauda equina or ankylosing spondylitis or if symptoms persist for > 4 weeks.

173
Q

How should non specific lower back pain be managed?

A

Should be self-managed
Stay physically active and exercise
NSAIDs are first line (plus PPI if >45yrs) – ibuprofen, naproxen and paracetamol. Consider morphine early if pain not controlled
Treat sciatica with the usual neuropathic guidance
Warmth and swimming

Consider exercise programmes along side manual therapy
Radiofrequency denervation
Epidural injections of local anaesthetic and steroid for acute and severe sciatica

174
Q

What yellow flags impair recovery from lower back pain?

A

Yellow flags that impair recovery
• Belief that pain and subsequent activity is harmful
• Pain behaviour – extended rest, avoidance, or normal activities
• Over reliance on passive treatments such as ice packs and analgesia
• Psychiatric disorders – anxiety, depression, and personality disorders
• Unsupportive home environment or over protective family
• Inappropriate expectations and failing to actively engage with treatment

175
Q

What are the referral criteria for lower back pain?

A

Any red flags = immediate referral to secondary care
Progressive/severe neurological deficit = seen be specialist within 1 week
Disabling pain > 2 weeks = early referral to physio and consider corticosteroid injections
Disabling pain > 6 weeks = to be seen by specialist within 2 weeks

176
Q

What are the clinical features of a prolapsed disc?

A

Clear dermatomal leg pain and neurological deficits
Pain often worse when sitting and may come on insidiously or suddenly
L4/L5 and L5/S1 are the most common locations for a disc prolapse
Disc may seize a few days after a back strain following severe coughing, sneezing, or twisting

177
Q

What symptoms would a patient get from radiculopathy in L3, L4, L5 and S1?

A

Features based on level of prolapse
• L3 root compression – sensory loss over anterior thigh, weak quadriceps, reduced knee reflex and positive femoral stretch test
• L4 root compression – sensory loss anterior aspect of knee, weak quadriceps, reduced knee reflex, positive femoral stretch test
• L5 root compression – sensory loss dorsum of foot, weakness in foot and big tow dorsiflexion, reflexes intact and positive sciatic nerve stretch test
• S1 root compression – sensory loss posterolateral aspect of leg and lateral aspect of foot, weakness in plantar flexion of foot, reduced ankle reflex and positive sciatic nerve stretch test

178
Q

How should suspected prolapsed disc be investigated?

A

Straight leg raising (Lasegue Test) – stretches the sciatic nerve attempting to reproduce root pain, if this pain occurs within 30-70 degrees then this is said to be a positive sign
MRI indicated if radiculopathy persistent for > 6 weeks, red flags present, evidence of spinal cord compression or imaging will significantly alter management.

179
Q

How is a prolapsed disc managed?

A

Initially brief rest with early mobilisation and pain relief works in 90% of patients
Analgesia
Physiotherapy
Exercises
If symptoms persist after 4-6 weeks, then referral for consideration of MRI

Surgery – discectomy, indications:
Cauda equina
Progressive muscular weakness
Continuing pain

180
Q

What are the risk factors for osteoporotic fractures?

A
  • Previous history of a fragility fracture
  • Frequent or prolonged use of glucocorticoids
  • History of falls
  • Family history of hip fracture
  • Alternative causes of secondary osteoporosis e.g. Cushing’s disease, hyperthyroidism, chronic renal disease
  • Low BMI (< 18.5)
  • Tobacco smoking
  • High alcohol intake: > 14 units/week for women, > 21 units/week for men
181
Q

What are the clinical features of a osteoporotic vertebral fracture?

A

Asymptomatic usually discovered incidentally
Acute back pain
Breathing difficulties: due to compression the lungs, heart and intestine
Gastrointestinal problems due to compression of abdominal organs
A minority will have a history of fall or trauma
Loss of height
Kyphosis (curvature of the spine)
Localised tenderness on palpation of spinous processes at the fracture site

182
Q

How should vertebral fracture be investigated?

A

X-ray of the spine: This should be the first investigation ordered and may show wedging of the vertebra due to compression of the bone. An X-ray of the spine may also show old fractures (which can have a sclerotic appearance)
CT spine
MRI spine: Useful for differentiating osteoporotic fractures from those caused by another pathology e.g. a tumour

183
Q

What are Jefferson’s fractures?

A

A Jefferson fracture is the eponymous name given to a burst fracture of the atlas. It is caused by axial loading of the cervical spine resulting in the occipital condyles being driven into the lateral masses of C1. They are often associated with head injuries and other concurrent cervical spinal injuries. These fractures are usually unstable and account for approximately a third of all C1 fractures.

184
Q

What is a Hangman’s fracture?

A

A Hangman’s fracture, also termed as traumatic spondylolisthesis of the axis, describes a fracture through the pars interarticularis of C2 bilaterally usually with subluxation of the C2 vertebra on C3. These are caused by cervical hyperextension and distraction (historically the forces that were delivered by a noose). These fractures can be unstable; in such cases, surgical fixation will be required.

185
Q

What is an odontoid or peg fracture?

A

Odontoid peg fractures are common cervical fractures, most common in older patients. Patients can present following low-impact injuries, neck pain being common. The condition can be fatal, especially with significant displacement of the odontoid; those who survive can have no neurology.

186
Q

What is scoliosis?

A

Consists of curvature of the spine in the coronal plane, usually accompanied by a degree of rotation of the spine. The majority of cases are idiopathic with no serious underlying pathology and usually involves muscle spasm. This most commonly affects girls and is called adolescent idiopathic scoliosis.

187
Q

What are the clinical features of scoliosis?

A

Clinical features – later in life may have issues with pain, cosmesis and impaired lung function. As curvature continues with growth the earlier the onset the worse the prognosis.

188
Q

How should patients with scoliosis be managed?

A

Patients should be referred to specialist clinics for observation and regular measurement of Cobb’s angle (lateral curvature). Only 1/6 of patients will require treatment and only a ¼ of those require surgery.

189
Q

How is scoliosis managed?

A

Braces may be trialled if curvature is progressing to slow the progression (it will not treat)
Severe, or progressive structural disease is managed surgically with bilateral rod stabilisation of the spine

190
Q

What is cervical spondylosis?

A

Very common condition occurring as a result of osteoarthritis

Clinical Features
Neck pain +/- referred pain that can mimic headaches
Radiculopathy
Myelopathy

191
Q

How does cervical spondylosis present?

A

Clinical spectrum of presentation and severity ranging from asymptomatic to quadriparesis and sensory loss due to compression of the cord.

Neck stiffness 
Crepitus 
Stabbing or dull arm pain 
Forearm/wrist pain 
Limited painful neck movement 
Neck flexion inducing tingling down the spine (Lhermitte’s sign)
192
Q

How does cervical spondylosis affecting C5 present?

A

C5 (C4/5 disc)

Weak deltoid and supraspinatus
Reduced supinator jerks and numb elbow

Neck/shoulder radiating to elbow

193
Q

How does cervical spondylosis affecting C6 present?

A

C6 (C5/6 disc)

Weak biceps and brachioradialis
Reduced biceps jerk, numb thumb and index finger

Pain in shoulder radiating down arm to below elbow

194
Q

How does cervical spondylosis affecting C7 present?

A

C7 (C6/7 disc)

Weak triceps and fingers extension
Reduced triceps jerks and numb middle finger

Pain in upper arm and dorsal forearm

195
Q

How does cervical spondylosis affecting C8 present?

A

C8 (C7/T1 disc

Weak finger flexors and small muscles of hand. Numb 5ht and ring finger

Pain in upper arm and dorsal forearm

196
Q

What is the difference between radiculopathy and myelopathy?

A

Radiculopathy – root compression – pain/electrical sensations in arms or fingers at the levels of the compression. Numbness, dull reflexes, UMN weakness and wasting of muscles (long term)

Myelopathy – cord compression – progressive symptoms e.g. weakness, clumsy hands and gait disturbance, UMN leg signs, LMN arms signs, incontinency, hesitancy and urgency.

197
Q

How is cervical spondylosis managed?

A

MRI urgently and specialist referral if you suspect cord compression
Analgesia via WHO ladder
Encourage gentle activity but avoid driving if neck movement is restricted
Cervical collars can give respite
If no improvement in 6 weeks, then repeat MRI and referral
Surgery if indicated – interlaminar cervical epidural injections, transforaminal injection or surgical decompression

198
Q

What is spondylolisthesis?

A

This occurs when one lumbar vertebra is displaced relative to its immediate inferior vertebral body and may occur as a result of stress fracture, osteoarthritis, or spondylolysis, a congenital or acquired (usually age related) deficiency of the pars interarticularis of the neural arch of a particular vertebral body, usually affecting L4/ L5.

199
Q

How does spondylolisthesis present?

A

Patients usually present with back pain in adolescence, patients may also have sciatica and a waddling gait due to tight hamstrings. Traumatic cases may show the classic ‘Scotty Dog’ appearance on plain films.

200
Q

How is spondylolisthesis investigated?

A

X-ray and MRI to assess for nerve compression

201
Q

How is spondylolisthesis managed?

A

Management depends upon the extent of deformity and associated neurological symptoms; minor cases may be actively monitored. Individuals with radicular symptoms or signs will usually require spinal decompression and fusion/stabilisation.

202
Q

What is lumbar spinal stenosis?

A

Lumbar spinal stenosis is a condition in which the central canal is narrowed by, usually as a result of facet joint osteoarthritis and osteophytes but can also occur due to tumours, trauma, and osteoporosis

203
Q

How does lumbar spinal stenosis present?

A

Patients may present with a combination of back pain, neuropathic pain and symptoms mimicking claudication. One of the main features that may help to differentiate it from true claudication in the history is the positional element to the pain. Sitting is better than standing and patients may find it easier to walk uphill rather than downhill in contrast to disc prolapse symptoms. The neurogenic claudication type history makes lumbar spinal stenosis a likely underlying diagnosis, the absence of such symptoms makes it far less likely.

204
Q

How is lumbar spinal stenosis investigated?

A

Diagnosis is via MRI

205
Q

How is lumbar spinal stenosis managed?

A

Management at first is with NSAIDs, epidural injections and corsets but if these fail to help then decompressive Laminectomy.

206
Q

What causes rib fractures?

A

Blunt trauma to the chest wall
Polytrauma with chest injuries being present in 25% of major trauma
Spontaneous rib fractures can occur rarely following coughing or sneezing: usually there is a past medical history of osteoporosis, steroid use or chronic obstructive pulmonary disease
pathological rib fractures can also occur due to cancer metastases: the most common cancers which predispose to these are prostate in men and breast in women

207
Q

What are the clinical features of a rib fracture?

A

Severe, sharp chest pain that is worse with deep breaths or coughing
Significant chest wall tenderness over the site of the fractures and visible bruising
Crackles or reduced breath sounds
Poor oxygenation in cases of flail chest or contusion and pain limiting breathing
Pneumothorax

208
Q

How is a rib fracture investigated?

A

CT will show the fractures in 3D as well as the associated soft tissue injuries.
Chest x-rays provide suboptimal views and are rarely used

209
Q

How is a rib fracture managed?

A

Majority are managed conservatively with analgesia to ensure breathing not impaired
Surgical fixation can be considered to manage pain if this is still an issue and the fractures have failed to heal following 12 weeks of conservative management
Flail chest segments must be urgently discussed with cardiothoracic surgery

210
Q

What is avascular necrosis of the hip?

A

Death of bone tissue secondary to loss of blood supply, most commonly this affects epiphysis of long bones such as the femur.

211
Q

What can cause avascular necrosis of the hip?

A

Long-term steroid use
Chemotherapy
Alcohol excess
Trauma

212
Q

What are the clinical features of avascualr necrosis of the hip?

A

Initially asymptomatic

Pain in the affected joint

213
Q

How should avascular necrosis of the hip be investigated?

A

Plain X-ray – may be normal initially, or osteopenia and microfracture may be seen
Collapse of the articular surface may result in crescent sign
MRI investigation of choice

214
Q

How is avascular necrosis of the hip managed?

A

Joint replacement

215
Q

What are the risk factors for NOF?

A

Increasing age
Female
Osteoporosis/osteopenia

216
Q

What are the clinical features of a NOF?

A

Inability to weight bear (unless non-displaced or incomplete)
Leg will be externally rotated and shortened (Measure from ASIS to medial malleolus) if intracapsular
Pain

217
Q

How are NF fractures classified?

A

Intracapsular (subcapital, transcervical and basicervical) from edge of the femoral head to the insertion of the capsule of the hip joint
Extracapsular – intertrochanteric/pertrochanteric or subtrochanteric (lesser trochanter is the dividing line). Also reverse oblique or transtrochanteric which is at right angles to an intertrochanteric fracture

218
Q

How are Intracapsular NOFs classified?

A

Garden System for Intracapsular fractures
This is based purely on the AP X-ray
1. Type 1 – incomplete, undisplaced fracture with inferior cortex intact
2. Type 2 – complete undisplaced fracture through the neck
3. Type 3 – complete partially displaced fracture, usually rotated and angulated but still has bony contact
4. Type 4 – fully displaced fracture

Be wary of blood supply disruption in types 3 and 4 (i.e. when displaced)

219
Q

How are intracapsular NOFs managed?

A

Intracapsular Hip Fracture
Undisplaced/minimal displacement – internal fixation in situ or hemiarthroplasty if unfit

Displaced – if fit then total hip replacement if older and reduced mobility, then hemiarthroplasty

Intracapsular hip fracture have a high risk of AVN

220
Q

How are extracapsular NOFs managed?

A

Dynamic hip screw

If reverse oblique transverse or sub trochanteric then intramedullary hip screw

221
Q

What are the complications from NOF?

A
Non-union 
Avascular necrosis 
Malunion 
Fixed deformities
Septic arthritis 
Reduced mobility
222
Q

What cause distal femur fractures?

A

Usually occur in young patients from high energy trauma or in older patents from low energy, pathological or osteoporotic fractures.

223
Q

How are distal femur fractures classified?

A

Type A = extra-articular
Type B = Partial articular
Type C = complete articular

224
Q

How are distal femur fractures managed?

A

If significant misalignment then closed reduction and realignment with immobilisation using skin traction initially.
Surgical management with ORIF or retrograde nailing is usually indicated for most fractures following this

225
Q

What causes femoral shaft fractures

How are femoral shaft fractures classified?

A

Classification – Winquist and Hansen Classification
Type 0 – no comminution
Type I – insignificant comminution
Type II – greater than 50% cortical contact
Type III – less than 50% cortical contact
Type IV – segmental fracture with no contact between fragments

226
Q

How are femoral shaft fractures managed?

A

Fascia iliaca block for analgesia
Immediate reduction and immobilisation to near anatomic alignment to ensure appropriate haematoma. Traction splinting such as Kendrick traction splint are used in isolated fractures.
Most femoral shaft fractures require surgery – within 24-48 hours usually with intramedullary nails
Long leg casts can be indicated in undisplaced femoral shaft fractures

227
Q

What causes dislocation of the hip?

A

Extremely painful condition and due to the high impact and trauma required usually associated with other potentially life-threatening injuries. Prompt diagnosis and management are important to reduce morbidity.

228
Q

How are hip dislocations classified?

A
  • Posterior dislocation – most common accounting for 90% of hip dislocations, the affected leg is adducted, shortened, and internally rotated
  • Anterior dislocation – affected leg is abducted and externally rotated without any leg shortening
  • Central dislocation
229
Q

How are hip dislocations managed?

A

ABCDE
Analgesia
Reduction under general anaesthesia within 4 hours to reduce risk of avascular necrosis
Long-term management – physiotherapy to strengthen the surrounding muscles
Will take 2-3 months for the hip to heal after traumatic dislocation. Reducing the hip in less than 12 hours gives better prognosis

230
Q

What are the complications of hip dislocations?

A

Sciatic or femoral nerve injury
Avascular necrosis
Osteoarthritis
Recurrent dislocation due to damage of supporting ligaments

231
Q

What is an iliopsoas abscess?

A

An iliopsoas abscess describes a collection of pus in iliopsoas compartment (iliopsoas and iliacus).

232
Q

What causes iliopsoas abscess?

A

Primary
Haematogenous spread of bacteria – Staphylococcus aureus: most common

Secondary
Crohn's (commonest cause in this category)
Diverticulitis, colorectal cancer
UTI, GU cancers
Vertebral osteomyelitis
Femoral catheter, lithotripsy
Endocarditis
Intravenous drug use
233
Q

What are the clinical features of an iliopsoas abscess?

A

Fever
Back/flank pain
Limp
Weight loss

Specific tests to diagnose iliopsoas inflammation:
Patient in the supine position with the knee flexed and the hip mildly externally rotated
• Place hand proximal to the patient’s ipsilateral knee and ask patient to lift thigh against your hand. This will cause pain due to contraction of the psoas muscle.
• Lie the patient on the normal side and hyperextend the affected hip. This should elicit pain as the psoas muscle is stretched.

234
Q

How should a suspected iliopsoas abscess be investigated?

A

CT abdomen is the investigation of choice

235
Q

How are iliopsoas abscess managed?

A

Note the mortality rate can be up to 19-20% in secondary iliopsoas abscesses compared with 2.4% in primary abscesses.

Antibiotics
Percutaneous drainage is the initial approach and successful in around 90% of cases
Surgery is indicated if:
1. Failure of percutaneous drainage
2. Presence of another intra-abdominal pathology which requires surgery

236
Q

What is the difference between a total hip replacement and a hemiarthroplasty?

A

Total hip replacement – both the articular surfaces of the femur and acetabulum are replaced either by conventionally be replacing femoral head and neck or simply resurfacing the femoral head.
Hemiarthroplasty – on the articular surface of the femoral head is replaced, usually indicated in NOF fractures with no arthritis but high risk of avascular necrosis of the femoral head.

237
Q

What are the common complications following hip surgery?

A
VTE – 4% 
Dislocation – 3% 
Deep infection – 2% 
Fracture – 1% 
Nerve palsy – 1% 
Limb length discrepancy – 1% 
Death – 0.4-0.7%
238
Q

What causes failure of a hip or knee arthroplasty?

A
  • Dislocation (mostly in hip)
  • Prosthetic loosening (mostly knee) presenting with chronic pain or fracture
  • Periprosthetic fractures (mostly hip) typically after minor trauma
  • Infection either early or late but either way is disastrous
239
Q

How does an infection post arthroplasty present?

A

Can present acutely with fever and systemic symptoms or more subtly with pain and loss of function.

240
Q

What are the risk factors for post arthroplasty infection?

A
Wound complications 
Obesity 
Increasing age 
Diabetes mellitus 
Steroid use
Rheumatoid arthritis 

Cause – most commonly coagulase negative staphylococci

241
Q

How should a suspected infection following arthroplasty be investigated?

A

Routine bloods
Joint aspiration – showing high WCC
Blood cultures
Plain X-ray

242
Q

How is an infection post arthroplasty managed?

A

Early debridement and antibiotics may be sufficient
If later on then radical debridement with removal of all prosthetics and involved bone
Antibiotics may be required for months
Revision is usually in 2 stages with wash out and insertion of antibiotic loaded cement spacer (which is functionally debilitating to patient) if successful then reimplantation after 2 months if still desired.

243
Q

What usually results in anterior cruciate ligament injuries

A

Anterior – usually torn in twisting injury with foot fixed to the ground during sport, much more common in women.

244
Q

What are the clinical features of anterior cruciate injuries?

A

Patient may have felt a pop or crack
Pain and rapid effusion usually within an hour
Difficult to examine in first 2 weeks

245
Q

How are anterior cruciate injuries investigated?

A

X-ray to exclude bony injury (Segond fracture (bony avulsion of lateral proximal tibia is pathognomonic of ACL injuries)
Increased laxity on anterior draw test (done at 90 degrees) and positive Lachman test (done at 30 degrees and is more reliable)
MRI

246
Q

How are anterior cruciate ligament injuries managed?

A

Very poor healing
RICE immediately then 3-week rest and intense physiotherapy
Arthroscopic graft reconstruction in young or particularly unstable joint

247
Q

Discuss posterior cruciate injuries

A

Posterior – hyperextension injuries due to high energy trauma such as direct blows to the flexed knee e.g., dashboard injury

Clinical Features
Increased posterior laxity on posterior draw test

Management
Rest with analgesics
Surgery is usually required

248
Q

What causes medial collateral ligament injuries?

A

Damage commonly occurs from skiing and valgus stress (lateral force)

249
Q

What are the clinical features and classification of medial collateral ligament injuries?

A

Clinical Features
Abnormal passive abduction of the lower leg
Laxity when testing collateral ligaments and painful
Effusion
Tender

Grade 1 – mild with minimal tearing and no loss of integrity
Grade 2 – moderate with incomplete tear and increased laxity
Grade 3 – severe with complete tear and gross laxity

250
Q

How are medial collateral injuries investigated?

A

X-ray

MRI is gold standard

251
Q

How are medial collateral ligaments managed?

A

Grade 1 – RICE, return to normal in 6 weeks
Grade 2 – RICE, analgesia, knee brace and physiotherapy, return to normal in 10 weeks
Grade 3 – RICE, analgesia, knee brace, crutches and consider surgery is distal avulsion. Return to normal in 12 weeks

252
Q

Discuss lateral collateral ligament injuries

A

Lateral Collateral – isolated injuries are uncommon but usually more severe

Clinical Features
Laxity when testing collateral ligaments and painful
Effusion
Tender

Investigations
X-ray
MRI is gold standard

Management
Treated with rest and support can take between sever weeks to months to heal
Surgery if very severe

253
Q

What causes meniscal tears?

A

Causes – twisting injury usually during sport for medial meniscus and adduction and internal rotation cause lateral meniscus tears

254
Q

What are the clinical features of meniscal injuries?

A

Delayed swelling but still within a few hours
Sharp localised medial or lateral pain exacerbated by hyperextending/twisting of knee and this may cause it to lock or give
Tender over affected joint line
Recurrent episodes of pain and effusions common often following minor trauma
Still good range of movement

Positive McMurrays test
Positive Thessaly’s test – weight bear at 20 degrees of knee flexion, support patient, positive is pain on twisting knee

255
Q

How are meniscal injuries investigated?

A

X-ray to exclude bony injuries
MRI
Arthroscopy

256
Q

How are meniscal injuries managed?

A

Non-serious require rest elevation, compression, and ice

Serious injuries may require surgery to repair the meniscus

257
Q

What is the unhappy triad?

A

Unhappy triad injury occurs from a lateral blow to the knee and involves anterior cruciate, medial collateral and one of the meniscus (usually the medial but more recent evidence suggests lateral is actually more common). This almost always required surgery.

258
Q

What is a Baker’s cyst?

A

Baker’s cysts also known as a popliteal cyst are not true cysts but a distention of the gastrocnemius-semimembranosus bursa.

Primary – no underlying pathology, typically seen in children
Secondary – underlying condition such as osteoarthritis, typically seen in adults

259
Q

How do baker’s cysts present?

A

Swelling in the popliteal fossa behind the knee
Rupture may occur resulting in similar symptoms to a deep vein thrombosis such as pain, redness and calf swelling however the majority of ruptures are asymptomatic

260
Q

How are baker’s cysts managed?

A

Must rule out DVT
In children the cysts typically resolve and do not require treatment
In adults the underlying cause should be treated where appropriate

261
Q

Describe the two most common types of patellar bursitis and their causes

A

Prepatellar Bursitis – prolonged periods of upright kneeling (Housemaid’s knee)
Infrapatellar Bursitis – prolonged kneeling (Clergyman’s knee)

Causes
Infection
Crystal arthropathies
Rheumatoid arthritis

262
Q

How does patellar bursitis present?

A

Localised swelling and tenderness over patella

Normal range of movement

263
Q

How should baker’s cyst be investigated?

A

Aspiration of effusion to check for infection or crystal arthropathies if indicated

264
Q

How are baker’s cysts managed?

A

Rest and NSAIDS

Corticosteroid injections

265
Q

What is iliotibial band syndrome?

A

Iliotibial band syndrome is a common cause of lateral knee pain in runners, occurring in around 1 in 10 people who run regularly. Tenderness 2-3cm above the lateral joint line

266
Q

How is iliotibial band syndrome managed?

A

Activity modification and iliotibial band stretches
If not improving, then physiotherapy referral
Local steroid injections

267
Q

What causes dislocation of the patella?

A

Traumatic primary event through direct trauma or severe contraction of quadriceps with knee stretched in valgus and external rotation. Typically the patella goes laterally and the knee will be in a flexed position.

20% recurrence rate

268
Q

How should patellar dislocation be investigated?

A

Skyline x-ray view of patella required but should be clinically obvious

269
Q

How are patellar discloations managed?

A

Reduction with medial pressure in an extended leg. Post reduction X-ray required to check for fracture, and check function of extensors of knee. Must immobilise the joint for next few weeks in cast or splint and refer to physiotherapy for quadricep strengthening.

270
Q

How are patellar fractures classified?

A

2 Fracture types:
• Direct blow to patella causing undisplaced fragments, extensor mechanism intact
• Quadriceps forceful contraction can cause a transverse patella fracture and sometimes an avulsion fracture

271
Q

What is the most important thing to assess in patella fracture?

A

Important to assess extensor function of the patella following fracture. If not too painful ask patient to attempt straight leg raising – can be made easier to lying on side to remove gravity resistance.

272
Q

How are patellar fractures managed?

A

Undisplaced fracture especially vertical fracture with intact extensor mechanism can be managed non-operatively in a hinged knee brace for 6 weeks with patients allowed to weight bear.

Displaced fractures and those with loss of extensor mechanisms require surgical management with ORIF plus either tension band wire, inter-fragmentary screws or cerclage wires. Patients are then put in a hinged knee brace for 6 weeks and allowed to weigh bear

273
Q

How do tibial plateau fractures present?

A

Occur in the elderly or following significant trauma in the young. Knee forced into varus or valgus position but the bone fractures before ligament rupture. Varus injury causes medial plateau fracture whilst valgus injury causes lateral plateau fracture.

274
Q

How are tibial plateau fractures classified?

A
  1. Lateral split fracture
  2. Lateral split with depressed fracture
  3. Lateral pure depression fracture (rare)
  4. Medial plateau fracture
  5. Bicondylar fracture (rare)
  6. Metaphyseal – diaphyseal disassociation
275
Q

What are the clinical features of tibial plateau fractures?

A
Sudden onset pain 
Unable to weight bear 
Swelling of the joint 
Tenderness
Ligament instability 
Full neurovascular assessment before and after intervention
276
Q

How are tibial plateau fractures investigated?

A

Plain X-ray anterior and lateral

CT required in almost all cases unless undisplaced

277
Q

How are tibial plateau fracture managed?

A

Uncomplicated fractures can be managed without surgery – hinged knee brace with non or partial weight bearing for 8-12 weeks
Complicated fractures require ORIF and post operatively a hinged knee brace with limited or no weight bearing for 8-12 weeks

278
Q

What causes tibial shaft fractures?

A

High risk of open fracture and compartment syndrome due to the limited soft tissue compartments surrounding the tibial shaft.

279
Q

What are the clinical features of tibial shaft fractures?

A

History of trauma
Severe pain inability to weight bear
Usually a clear deformity and significant swelling
Often associated fibular fracture as well

280
Q

How are tibial shaft fractures investigated?

A

X-ray – AP and lateral

CT usually indicated as well

281
Q

How are tibial shaft fractures managed?

A

Realignment should take place as soon as possible under conscious sedation
Above knee backslab in slight flexion at knee and neutral dorsiflexion at ankle
Almost all are managed surgically with intramedullary nailing and post op patient are usually able to fully weight bear
ORIF with locking plate required if extending into either joints

282
Q

What is osteochondritis dissecans?

A

Osteochondritis dissecans (OCD) is a pathological process affecting the subchondral bone (most often in the knee joint) with secondary effects on the joint cartilage, including pain, oedema, free bodies and mechanical dysfunctions. OCD may progress to degenerative changes if untreated.

It affects children and adolescents with open growth plates (juvenile OCD) and young adults with closed growth plates (adult OCD). Most common age of presentation is between 12 and 19 years (age of presentation is decreasing likely due to the decreasing age of children participating in active sports)

283
Q

What are the risk factors for osteochondritis dissecans?

A

Trauma
Male
Genetic

284
Q

What are the clinical features of osteochondritis dissecans?

A

Knee pain and swelling, typically after exercise
Knee catching, locking and/or giving way - more constant and severe symptoms are associated with the presence of loose bodies
Feeling a painful ‘clunk’ when flexing or extending the knee - indicating the involvement of the lateral femoral condyle

Signs
Joint effusion
Full range of movement in the joint without signs of ligamentous instability
External tibial rotation when walking – if medial femoral involvement
Tenderness on palpation of the articular cartilage of the medial femoral condyle, when the knee is flexed

Wilson’s sign for detecting medial condyle lesion - with the knee at 90° flexion and tibia internally rotated, the gradual extension of the joint leads to pain at about 30°, external rotation of the tibia at this point relieves the pain.

285
Q

How is osteochondritis dissecans investigated?

A

Early diagnosis is important. Clinical signs may be subtle in the early stages hence there should be a low threshold for imaging and/or orthopaedic opinion.

X-ray (anteroposterior, lateral and tunnel views) – subchondral crescent sign or loose bodies
MRI – to evaluate cartilage, visualise loose bodies, stage and assess the stability of the lesion
CT – used in preoperative planning and in cases where MRI is not available/contraindicated
Scintigraphy – used to guide treatment as it may show increased uptake in the fragments – a sign of osteoblastic activity

286
Q

What are the clinical features of achilles tendinopathy?

A

Gradual onset of posterior heel pain that is worse following exercise
Morning pain and stiffness

287
Q

How is achilles tendinopathy managed?

A

Simple analgesia
Reduction of precipitating activities
Calf muscle eccentric exercises – self direction or under physio guidance

288
Q

What are the risk factors for achilles tendon rupture?

A

Quinolone e.g. ciprofloxacin

Hypercholesterolaemia – predisposes to tendon xanthomata

289
Q

What are the clinical features of achilles tendon rupture?

A

Audible pop in the ankle
Sudden onset significant pain in calf or ankle
Likened to being kicked in the back of the foot
Inability to walk or continue the sport

290
Q

How are suspected achilles tendon ruptures investigated?

A

Investigation and Examination – Simmond’s triad
• Patient lies prone with feet over the edge of the bed – look for abnormal angle of declination (rupture may lead to greater dorsiflexion compared to uninjured foot
• Feel for gap in the tendon
• Gently squeeze calf muscles – if ruptured the foot will stay in the neutral position
USS of the tendon

291
Q

How are achilles tendon ruptures managed?

A

If presenting within 2 weeks:
Analgesia and immobilisation for 2 weeks with moon boot (able to weight bear) or splinted plaster in full equinus with no weight bearing. Then half equinus for 4 weeks and following this another 4 weeks in the neutral position
Conservative management often preferred for smokers, diabetics and those > 50yrs

If presenting after 2 weeks or re-rupture requires surgical end-to-end tendon repair

292
Q

Which bones are involved in an ankle fracture?

A

Definition – a fracture of the any of the malleoli (lateral, medial or posterior) with or without disruption of the syndesmosis.

293
Q

What generally causes ankle fractures?

A

Low energy – twisting, inversion/eversion injuries usually due to a fall from standing height
High energy – direct blow to tibia or fibula

294
Q

What are the clinical features of an ankle fracture?

A

Tenderness
Pain
Obvious deformity

295
Q

How are ankle fractures investigated?

A

Check neurovascular status
Ottawa Ankle rules - plain X-ray with 2 views required if pain in the malleolar zone and one of the following findings:
• Bony tenderness at the lateral malleolar zone (from the top of the lateral malleolus to include the lower 6cm of posterior border of the fibular)
• Bony tenderness at the medial malleolar zone (from the top of the medial malleolus to the lower 6cm of the posterior border of the tibia
• Inability to walk four weight bearing steps immediately after the injury and in A&E

296
Q

How are ankle fractures involving the lateral malleolus classified?

A

Type A – fibula fracture below syndesmosis
Type B – fracture that starts at the level of the tibial plafond and may extend proximally to involve the syndesmosis
Type C – above the level of the syndesmosis which may itself be damaged

Subtype – Maisonneuve fracture – spiral fibular fracture of the proximal 1/3 leading to disruption of the syndesmosis with widening of the ankle joint – surgery required

Pott’s Fracture – bimalleolar ankle fracture from forced foot eversion

297
Q

How are ankle fractures managed?

A

Give lots of analgesics and check neurovascular status before and after intervention

All ankle fractures should be reduced and realigned under conscious sedation to remove pressure on the overlying skin and subsequent necrosis

Stable or minimally displaced (Weber A and B) can be treated non operatively in a below knee backslab. Elderly patients even with unstable injuries usually fare better with attempts at conservative management as their weaker bones do not hold metalwork well.

ORIF is often required and indicated in:
Displaced bimalleolar or trimalleolar fractures, Weber C, Weber B with talar shift and open fractures.

298
Q

What is an ankle sprain?

A

Sprain = stretching or a partial or complete tear of a ligament. In the ankle we divide this into high ankle sprains involving the syndesmosis and low ankle sprains involving the lateral collateral ligaments.

299
Q

What are the clinical features of low ankle sprains?

A

Most common ankle sprain (90%) with injury to the ATFL the most common cause
Mechanism is usually as a result of inversion
Pain swelling and tenderness over affected ligaments and sometimes bruising
Usually are still able to weight bear unless severe

300
Q

How are low ankle sprains classified?

A
Grade I (mild) – stretch or micro tear, minimal bruising and swelling and normal weight bearing without pain 
Grade II (moderate) – partial tear with moderate welling and bruising and minimal pain on weight bearing 
Grade III (severe) – complete tear, severe bruising and swelling and severe pain on weight bearing
301
Q

How are ankle sprains investigated?

A

X-ray should be done according to Ottawa ankle rules as 15% of sprains are associated with a fracture. MRI if persistent pain and useful for evaluating peroneal tendons.

302
Q

How are low ankle sprains managed?

A

RICE protocol – Rest, ICE, Compression, and Elevation
Removable orthosis, case and/or crutches may be required for short-term symptom relief
If symptoms fail to settle or there is significant join instability, then MRI and surgical intervention can be considered
In significant sprains with ligament rupture and inability to weight bear then below knee immobilisation is required for 10 days

303
Q

What are the clinical features of high ankle sprains?

A

Injuries to the syndesmosis are rare and severe
Mechanism of injury is usually external rotation of the foot causing talus to push the fibula laterally
Weight bearing often very painful in comparison to low ankle injury
Pain when tibia and fibula are squeezed together at the lever of the mid-calf (Hopkin’s squeeze test)

304
Q

How are high ankle sprains investigated?

A

X-ray may show widening of the tibiofibular joint (diastasis) or ankle mortise
MRI if high suspicion of syndesmotic injury

305
Q

How are high ankle sprains managed?

A

If no diastasis then non-weight bearing orthosis or cast until pain subsides
If diastasis or failed non-operative management then operative fixation is usually required

306
Q

What is Morton’s neuroma?

A

Morton’s neuroma is a benign neuroma affecting the intermetatarsal plantar nerve, most commonly in the third inter-metatarsophalangeal space. The female to male ratio is around 4:1.

307
Q

What are the clinical features of a Morton’s neuroma?

A

Forefoot pain, most commonly in the third inter-metatarsophalangeal space
Worse on walking
Shooting or burning pain
Patients may feel they have a pebble in their shoe
Loss of sensation distally in the toes

Mulder’s click: one hand tries to hold the neuroma between the finger and thumb. The other hand squeezes the metatarsals together. A click may be heard as the neuroma moves between the metatarsal heads

308
Q

How are Morton neuromas investigated?

A

Diagnosis is usually clinical

USS may be helpful in confirming the diagnosis.

309
Q

How are Morton neuromas managed?

A

Avoid high heels
Metatarsal pad
CKS recommends referral if symptoms persist for > 3 months despite footwear modifications and the use of metatarsal pads
Orthotists may give the patient a metatarsal dome orthotic
Other secondary care options include corticosteroid injection and neurectomy of the involved interdigital nerve and neuroma

310
Q

What is planter fasciitis?

A

Definition – Not actually inflammation but due to weakness in the plantar fascia of the foot and can occur unilaterally or bilaterally. It is the most common cause of heel pain and is most common between 40-60yrs

311
Q

What causes plantar fasciitis?

A

Micro tears in the plantar fascia due to chronic breakdown of the structure and not just inflammation. Any anatomical abnormalities that affect the gait cycle may increase the risk of this.

312
Q

What are the risk factors for plantar fasciitis?

A
Anatomical factors
Weak plantar flexors
Prolonged standing or excessive running
Leg length discrepancy
Obesity
Unsupportive footwear
Inactivity
313
Q

What are the clinical features of plantar fasciitis?

A

Sharp pain across plantar aspect of the foot felt most severely in the heel
Worst with first few steps of the day or after periods of inactivity

314
Q

How is plantar fasciitis investigated?

A

On examination look for evidence of over pronation, high arches and leg length disparity.
Clinical diagnosis
Plain x-ray to exclude bone injury
MRI occasionally useful if uncertainty

315
Q

How is plantar fasciitis managed?

A

Rest the foot where possible
Adjust footwear to have good arch support and cushioned heels
Regular analgesics, typically NSAIDs
Physiotherapy is very useful
Corticosteroid injection
Plantar fasciotomy (results in some instability)

316
Q

What are hallux valgus?

A
Hallux Valgus (Bunions)
Definition – deformity at the first metatarsophalangeal joint causing deviation medially. It is the most common foot problem in the adult population – 35% in those aged >65 and is more common in women.
317
Q

What causes hallux valgus?

A

1st metatarsal of the foot is inherently unstable and relies heavily on the stabilising structures of muscles and tendons to keep in in place. As a result, it is at greater risk of becoming disturbed. If it does escape these stabilisers, then the extrinsic tendon slowly deform the foot.

Anatomic variants, genetic predisposition, and environmental factors all further contribute

318
Q

What are the risk factors for hallux valgus?

A
Female
Connective tissue disorders
Hypermobility syndromes 
Type of footwear (ideal is wide low-heeled shoes) 
Family history
319
Q

What are the clinical features of a hallux valgus?

A

Medial deviation of the first metatarsal and lateral deviation of the hallux with associated joint subluxation.
Painful medial prominence
For some the deformity is painless other than in shoe fitting
Aggravated by walking, weight bearing and wearing narrow shoes
Typically bilateral

320
Q

How are hallux valgus investigated and managed?

A

Investigations
Plain X-ray

Management
Sufficient analgesia
Advice on adjusting footwear – wide and low heeled
Physiotherapy providing stretching exercises and gait re-education
Surgical intervention may be considered for those whose quality of life is affected