Pain Flashcards

1
Q

Define pain

A

An unpleasant sensory and emotional experience associated with actual or potential tissue damage

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2
Q

Why do we feel pain?

A

Early warning system
Alerts to danger
Waning of actual or potential harm
Elicits change in behaviour
To try and avoid danger/ harm

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3
Q

What are the three different types of pain?

A

Somatic superficial, somatic deep, visceral

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4
Q

Somatic superficial=

A

On the skin, sharp (fast) pain, localised (brief)

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5
Q

Somatic deep=

A

In deep layers of skin, muscles and joints, is a burning/ itching/ aching (slow) pain, is diffuse (Long lasting)

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6
Q

Visceral=

A

In organs, is a dull ache/ burning/ gnawing (slow) pain, can cause nausea and sweating

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7
Q

Acute vs chronic pain

A

Acute= monetary or severe, weeks/ months, resolvable
Chronic= persistant, remains despite the healing process and lasts 3+ months

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8
Q

What is the congenital absence of pain disorder?

A

Someones central perception of pain mechanisms are disrupted so no pain is felt. This means there is an issue with the SCN9A voltage gated sodium channel.

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9
Q

Nociception=

A

neural process of encoding noxious stimuli

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10
Q

Pain perception=

A

the body’s interpretation of these signals

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11
Q

Nociceptor=

A

are sensory receptors that respond to pain. There are many types e.g., mechanoreceptors, bradykinin, prostaglandins, histamine, substance P. They are located on free nerve endings and respond to inflammatory mediators.

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12
Q

What are the role of free nerve endings?

A
  • Free nerve endings play an important role in nociception by detecting noxious stimuli. This initiates perception of pain.
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13
Q

Describe the differences between Aɗ (A-delta) and C-fibres.

A
  • Aɗ (A-delta) = sharp, pricking, fast pain. They are myelinated.
  • C-fibres= hot and burning sensation, slow deep pain. They are un-myelinated.
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14
Q

Describe the process of central sensitisation.

A
  • Involves two types of presynaptic cells which are both glutamate receptors: AMPA and NMDA. If there is a transient stimulus of the nociceptor then AMPA receptors are activated, releasing sodium ions into the cell. On a stronger stimulus of the nociceptor, NMDA receptors are activated on the 2nd order neuron allowing release of calcium ions into the cell, increasing the sensitivity of the neuron.
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15
Q

Describe the process of peripheral sensitisation.

A
  • It is a substance P mediated feedback loop where 1st order neurons are sensitised. There is an increase in nociceptive neurons so the pain will just get worse and worse.
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16
Q

Referred pain=

A
  • When you have an injury in one area of the body, but the pain is felt elsewhere. For example: issues with the gallbladder can cause pain on the skin of the shoulder. This is because of the interconnecting sensory nerves of the body.
17
Q

What is the neuromatrix theory of pain.

A
  • Suggests pain comes from a pattern of nerve impulses in the body. These impulses come from a neural network in the brain called ‘body’s-self neuromatrix’.
18
Q

Hyperalgesia=

A
  • Increased sense of painful sensation, primary/ secondary.
19
Q

Allodynia=

A
  • Pain from a stimulus that does not usually provoke pain.
20
Q

Explain the biomedical approach to pain.

A
  • Pain is felt in response to a painful situation. Meaning pain is felt as a sensation and has a singular cause.
21
Q

What are the pain paradoxes.

A
  • Battle wounds= Individuals with the same degree of injury will experience differences in reports to their painful situation. E.g., a study showed significant differences in soldiers requesting pain relief.
  • Phantom limb pain= 5-10% of amputees will experience pain in their absent limb.
  • Placebos.
22
Q

What is the biopsychological approach to understanding pain.

A
  • Acknowledges that pain is not just a psychical phenomenon but also a social, psychological and biological response.
  • Biological e.g., pain intensity, medication use and trauma/ injury
  • Psychological e.g., depression, pain perception and fear avoidance
  • Social e.g., work, disability, cultural and economic factors.
23
Q
A