Somatosensory function (pain) Flashcards

1
Q

examples of pain types

A
nociceptive
muscle
superficial somatic
visceral
referred 
neuropathic.
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2
Q

types of muscular pain

A
	Metabolic		
	Overuse		
	Tension		
	Compression		
	Ischaemia		
	Tearing		
	Viral infection
	Fibromyalgia
	Angina
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3
Q

what are the typical features of pain?

A
Aching
Burning (lactic acidosis)
Cramping
Tightness
Crushing
Tenderness
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4
Q

why is visceral pain vague, diffused and poorly localised?

A

low density of sensory innervation

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5
Q

visceral pain

A

may be referred
often midline
associated with autonomic symptoms
may show visceral hyperalgesia, viscerovisceral cross-talk

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6
Q

types of somatic pain

A
	Often nociceptic	
	Related to skin	
	Pressure		
	Too hot/cold		
	Inflammation		
	Injury		
	Infection		
	Burns
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7
Q

features of somatic pain

A
Well-localised
Sharp
Stinging
Aching
Burning
Throbbing
Tightness
Sensitive
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8
Q

where does referred pain often occur?

A

at sites of the body wall where innervation enters the spinal cord at the same level as the organ
pain is sharper and better localised than visceral pain

e.g in angina

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9
Q

what are Wind Dynamic neurones

A

o Receive input from A, A and C fibres.
o The most populous cell whose soma is located in the dorsal horn.
o Respond to a full range of stimuli (touch, heat and chemical) but fire more frequently to noxious stimuli.
o They fire APs in a graded fashion.
o Exhibit “wind-up”.

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10
Q

what is the Wind-Up phenomenon

A

exponentially progressive increase in firing of WDR neurons with repeated stimulation

increase in pain intensity over time when a given stimulus is delivered repeatedly above a critical rate

o Short-lasting synaptic plasticity.
o Repetitive stimulation of WDRs which induce increased evoked response and post discharge with each stimulus.
o May precipitate long-term potentiation (LTP) – i.e. long lasting increase in efficacy of synaptic transmission.
o Wind-up and LTP related to neuropathic sensitisation.

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11
Q

what are the two types of sensitisation?

A

peripheral and central

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12
Q

peripheral sensitisation

A

injury in late nerve

small area of sensitisation

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13
Q

central sensitisation

A

injury in the early nerve in spinal cord

possible large area of sensitisation if in tracts

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14
Q

what is neuropathic pain

A

pain source in the somatosensory nervous system

pain in area of neuronal dysfunction
sharp, burning, electric shcck and squeezing pain
has poor response to usual analgesic drugs
can last after an area has completely healed

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15
Q

allodynia

A

pain due to stimulus that does not usually cause pain

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16
Q

hyperalgesia

A

increased pain from a stimulus that normally causes pain

17
Q

hypoalgesia

A

decreased pain from a stylus that normally causes pain

18
Q

what is sensitisation?

A

increased responsiveness of nociceptive neurones to their normal input

19
Q

hyperpathia

A

painful syndrome caused by abnormally painful reaction to a stimuli
especially a repetitive stimulus and an increased threshold

20
Q

paraesthesia

A

abnormal sensation (spontaneous or evoked)

pins and needles

21
Q

dysaesthesia

A

unpleasant abnormal sensation (spontaneous or evoked)

22
Q

examples of neuropathic pain

A

complex regional pain (CRPS) syndrome

phantom limb pain
sciatica

23
Q

Complex Regional Pain Syndrome

A

o Sensory, vasomotor, pseudomotor/oedema, motor/trophic symptoms must be present.
 Characterised by neurogenic inflammation.
 Displays overexpression of nociceptive nerve endings.

24
Q

phantom limb pain

A

common among amputees
stump neuroma association
may be due to remapping of brain

treatment:
o Antidepressants – Amitriptyline, Nortriptyline, Duloxetine.
o Anticonvulsants – Gabapentin, Pregabalin.
o Opioid trial – Tramadol, Buprenorphine, Methadone, Morphine.
o Hybrid – Tapentadol.
o Topical – 5% Lidocaine, Capsaicin 0.075% cream and capsaicin 8% patches.