The GALS Screen Flashcards

1
Q

what is the purpose of the locomotion examination?

A

identify abnormal joints

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2
Q

what does GALS stand for?

A

Gait
Arms
Legs
Spine

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3
Q

what is observed in gait?

A

observe the patient walk, turn and walk back

o Smoothness and symmetry of legs.
o Normal stride length.
o Ability to turn quickly.

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4
Q

what are the key questions asked in the GALS examination?

A

o Have you any pain in your muscles, joints or back?

o Can you dress yourself completely without any difficulty?

o Can you walk up and down the stairs without any difficulty?

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5
Q

what are the signs inflammation?

A
o	Rubor (Red)
o	Calor (Hot)
o	Tumor (Swelling)
o	Dolor (Pain)
o	Funcio laesa (Loss of function)
or SWELT:
Swelling
Warmth
Erythema
Loss of function 
Tenderness
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6
Q

what can be examined in the arms?

A
pronation and supination 
grip
MCP squeeze
tip of fingers to thumb 
shoulder movement
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7
Q

what is the significance of the MCP and MTP squeeze?

A

indicative of synovitis when there is discomfort

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8
Q

what is examined in the legs?

A
  • flexion of hip and knees
  • examine knee for fluid (patellar tap sign where patella bounces)
  • MTP squeeze
  • sole of feet inspected for rashes/callosities
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9
Q

what is the difference between arthritis and arthralgia?

A

Arthritis – refers to a definite inflammation of a joint(s).

Arthralgia – refers to a pain within a joint(s) WITHOUT demonstrable inflammation by physical examination

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10
Q

what is dislocation and subluxation?

A

Dislocation – articulating surfaces are displaced and no longer in contact.

Subluxation – partial dislocation.

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11
Q

what is the difference between varus deformity and valgus deformity?

A

Varus deformity – lower limb deformity whereby distal part is directed towards the midline
– e.g. varus knee with medial compartment osteoarthritis.

Valgus deformity - lower limb deformity whereby distal part is directed distally from the midline
– e.g. hallux valgus.

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12
Q

what are some indicators of inflammation occurring?

A
  • gout (example of arthritis)
  • joint swelling
  • enthesopathy (enthesis)
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13
Q

what is the enthesis?

A

where the ligament/tendon connective inserts into the bone

e.g. in the spine or knee

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14
Q

what does deposition of monosodium urate (MSU) crystals in the tissue lead to?

A

o Gouty arthritis (commonly affects the 1st MTP joint) aka podagra.

o Tophi
– aggregated deposits of MSU in tissue

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15
Q

what is the cause of deposition of monosodium urate (MSU) crystals in the tissue?

A

hyperuricaemia

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16
Q

what are the different sites of inflammation?

A
  • Articular soft tissue (Inflammatory joint disease)
  • Peri-articular soft tissue (Inflammatory joint disease)
  • Non-articular synovial (Inflammation of structure)
  • Bony areas (Osteoarthritis)
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17
Q

what are some example of enthesopathies?

A

Achilles tendonitis

plantar fasciitis

18
Q

what are some signs of irreversible joint damage?

A

o Joint deformity.

o Crepitus
– sound upon articulating joint i.e. in osteoarthritis.

o Loss of joint range or abnormal movement.

19
Q

what are the signs of mechanical defects due to inflammation, degenerative arthritis or trauma?

A

o Painful restriction of motion in absence of features of inflammation
– e.g. knee “locking”.

o Instability
– e.g. side-to-side movement of tibia on femur.

20
Q

what are the terms to indicate the number of joints involved the arthritis?

A

o Polyarthritis= >4.
o Oligoarthritis= 2-4.
o Monoarthritis= 1.

21
Q

what is observed when describing the pattern of arthritis?

A
  • Note symmetrical involvement.
  • Note size of involved joints.
  • Note any axial involvement.
22
Q

how is the pattern of arthritis described in RA?

A

Bilateral
symmetrical
large and small joints

23
Q

how is the pattern of arthritis described in ReaA?

A

Lower limb
asymmetrical
Oligoarthritis
axial involvement.

24
Q

what joint is commonly affected in gout?

A

1st MTP joint involvement.

25
Q

name an additional diagnostic feature of RA

A

subcutaneous nodules

26
Q

name an additional diagnostic feature of gout

A

tophi (monosodium urate deposition due to hyperuricaemia)

27
Q

name an additional diagnostic feature of SLE

A

malar rash sparing nasolabilal folds

28
Q

where is synovial fluid produced?

A

synovial lining cells(1-3 cells deep).
o Type A – macrophage-like cells.

o Type B – fibroblast-like cells – secrete hyaluronic acid and increased viscosity of synovial fluid.

29
Q

what is synovial effusion?

A

abnormal increase in synovial fluid volume

can be:
•	Normal.
•	Non-inflammatory (Osteoarthritis)	
•	Inflammatory (Gout)		
•	Infectious (Bacterial infections)
30
Q

what happens to the composition of synovial in OA? how does this change the volume of synovial fluid?

A

increases hyaluronic acid production

more oncotic pressure increased synovial volume.

31
Q

how does synovial fluid normally look? how does it change in inflammation?

A

normally clear or pale yellow

becomes more turbid in disease

32
Q

how is synovial fluid sampled?

A

arthrocentesis

look for pathogens (ABs assay) and crystals (polarising light microscopy)

33
Q

what are the contraindications and complications of arthrocentesis?

A

o Contraindications
– bleeding disorders (genetics or drugs like warfarin), overlying skin infection.

o Complications
– introducing infection, Haemarthrosis, damage to structures.

34
Q

what diseases can be determined with synovial fluid examination?

A
  • septic arthritis (postive gram stain and culture)

- olecranon bursitis (crystals present)

35
Q

name some connective tissue disorders

A

o SLE.
o Inflammatory muscle diseases – polymyositis, dermatomyositis.
o Systemic sclerosis.
o Sjogren’s syndrome.
o Overlap syndrome – a mixture of the above.

36
Q

what is the Raynaud’s phenomenon?

A

is often associated with arthritis and arthralgia in connective tissue disorders (not exclusively)

  • Intermittent vasospasm of digits on exposure to the cold.
  • Colour changes (blue to red)
    – vasospasm blanches digit, cyanosis as static venous blood deoxygenates, reactive hyperaemia.
37
Q

what is Sjogren’s Syndrome?

A

Autoimmune exocrinopathy

– lymphocytic infiltration of exocrine glands e.g parotid, hence the parotid gland enlargement

38
Q

what does Sjogren’s Syndrome result in? what are signs in relation to connective tissue disorders in general?

A
o	Dry eyes 
– xerophthalmia.
o	Dry mouth 
– xerostomia.
o	Parotid gland enlargement 

importantly non-erosive arthritis and Raynaud’s phenomenon.
“Secondary Sjogren’s syndrome” if occurs with another connective tissue disorder like SLE

39
Q

what is inflammatory muscle disease?

A

Proximal myopathy (AI-mediated inflammation) with either dermatomyositis (rash) or polymyositis (no rash).

40
Q

what is systemic sclerosis?

A

thickened skin with raynauds syndrome (skin changes are diffuse or limited)

41
Q

what is Overlap Syndrome?

A

has features of more than one connective tissue disorder e.g. SLE plus inflammatory muscle disease