Mimic Inflammatory Conditions Flashcards

1
Q

What is fibromyalgia?

A

Centralised pain disorder characterised by severe pain and other somatic symptoms
Widespread pain in multiple regions of body for more than 3 months

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2
Q

What is the features of fibromyalgia?

A

Intrusive fatigue - physical, cognitive, and emotional
Increased sensitivity to sound, light, and fluctuations in temp.
Symptoms can fluctuate in severity and type over time

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3
Q

What are important conditions to think of when diagnosing fibromyalgia?

A

Malignancy, rheumatic conditions, polymyalgia rheumatica, endocrine disorders, drug induced conditions, sleep disorders, neurological disorders, functional neurological disorders and depression

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4
Q

What can help with general examination for fibromyalgia?

A

GALS screen
PIP tuck, thumb to little finer, wrist and fore/mid/hindfoot
Enthesitic points
Joint hypermobility

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5
Q

What is involved in joint examination for fibromyalgia?

A

Joint swelling
Bony/ firm
Soft tissue/ boggy/ spongy - synovitis (like a grape)
Dactylitis - think SpA
Pressure on palpation

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6
Q

What is the predisposition for fibromyalgia?

A

Common beliefs/ situations, usually coping strategies, coping skills not good, significant psychosocial stress, and physical illness now resolved (trigger)
Infections (viral), trauma, and prolonged stressful situations

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7
Q

What are the maintaining factors for fibromyalgia?

A

Fear of symptoms and consequences leads to activity avoidance, reduced external external stimulation, sleep problems leading to pain and fatigue

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8
Q

What are symptoms of fibromyalgia?

A

Widespread pain, intrusive fatigue, longevity of symptoms, feeling overwhelmed, poor concentration, poor refreshment from rest and ineffective treatments so far

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9
Q

What type of pain if fibromyalgia?

A

Nociplastic - caused by disturbance in peripheral and/ or central nervous system pain processing
Cant be alleviated from surgery

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10
Q

How is fibromyalgia diagnosed?

A

Symptoms present for more than 3 months
Use ACR criteria
Use symptom severity index
Use widespread pain index

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11
Q

What is the management for fibromyalgia syndrome (FMS)?

A

Pain related anxiety/ depression - CBT and SSRIs
Severe sleep disturbance - low dose amitriptyline and night time pregabalin
Severe pain - amitriptyline, gabapentin, pregabalin, duloxetine and tramadol
Physio

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12
Q

What can be a cause of MSK pain in children and adults?

A

Hypermobility

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13
Q

What are some features of hypermotility?

A

More females than males
Not every hypermobile person gets pain
Strongly genetically determined
Definitely a link with chronic pain

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14
Q

What is the difference between localised and widespread hypermotility (HM)?

A

Localised may be advantageous
Widespread may be disadvantageous

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15
Q

What is the spectrum of HM?

A

Wide - Ehler’s Danlos syndrome (EDS) - Marfan’s syndrome - Osteogenesis imperfecta
Hypermobility and pain - Hypermotility spectrum disorder (HSD) or hypermobile EDS (hEDS)
Pathophysiology - true connective tissue disorders

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16
Q

What are the symptoms of hypermobile spectrum disorder (HSD) and hypermobile Ehler’s Danlos syndrome?

A

Arthralgia - joint pain
Myalgia - muscle pain
Joint effusions
Soft tissue problems - bursitis, epicondylitis and tendinopathies

17
Q

What are other symptoms linked to HSD/hEDS?

A

Cardiovascular autonomic disturbance - postural orthostatic hypotension tachycardia (POTS), orthostatic hypotension and vasovagal syncope
History of clumsiness
GI disturbances - pain/ constipation/ diarrhoea/ bloating

18
Q

What are the clinical signs of HSD/ hEDS?

A

Hypermotility may be localised
Paradoxical tightness
Soft skin
Papery scars
Striae - unusual places
Easy bruising
Peizogenic papules

19
Q

What are peisogenic papules?

A

Herniation of fat through dermis

20
Q

What is the Beighton diagnostic criteria?

A

1 point for each -
5th finger hyperextended more than 90 degrees
Thumb opposable to forearm
Elbows or Knees hyperextended more than 10 degrees
Hands flat to floor or feet
More than 4/9 is widespread hypermotility

21
Q

What are the problems with Beighton Diagnostic criteria?

A

Does not diagnose HM
Not good for children as 1/3 of children have HM
Only covers limited regions/ joints
Other symptoms need to be considered

22
Q

What are features of HSD/hEDS?

A

Soft tissue vulnerability
Acute and chronic pain
Altered proprioception
Autonomic disturbance
Anxiety and phobia

23
Q

What is the management for HSD/hEDS?

A

Appropriate physical therapy advice - stretching
Correct posture - core stability
Correct foot deformity
OT input