Pain Oriented Sensory Testing
The ANZCA have published guidelines on pain oriented sensory testing (POST) which can be found here
Neurophysiology
- See also: Nociception
Peripheral transmission follows transduction. Figure 1 shows a response being recorded from a sciatic nerve after an applied stimulus. The recording electrode experiences large changes in electrical potential. There are three major waves corresponding to three groups of nerves - A wave, B wave, and a smaller later C wave. Velocities can be calculated, and we find that the diameter of the nerve fibres are proportional to their conduction velocities.
The Aα and Aγ nerves are largely made up of motor neurons. The Aβ waves are produced by large diameter sensory nerve fibres that information related to proprioception, touch, and pressure. All fibres capable of transmitting nociception are Aδ fibres or C fibres.
There is no such thing as a "pain fibre" or specific nociceptive fibre. There are a variety of nerve fibres that are capable of transmitting nociception, but that may not be their only function. In various situations there may be more than one fibre involved in transmitting nociceptive information.
- Characteristics of sensory nerve fibres
Nerve fibre | Myelinated axons | Diameter (µm) | Conduction velocity (m/s) | Sensory information | Usefulness of electroneuromyography | Usefulness of QST |
---|---|---|---|---|---|---|
Aα | Yes | 13-20 | 80-120 | Proprioception, muscle spindle primary endings (Ia), golgi tendon organs (Ib) (and alpha motor neurons) | Yes (H reflex) | No |
Aβ | Yes | 6-12 | 33-75 | Discriminative mechanoreception (touch, vibration), proprioception, pain modulation (block nociceptive information, allodynia in sensitisation) | Yes (sensory nerve conduction) | Yes |
Aγ | Yes | 4-8 | 15-40 | Touch, pressure (and gamma motor neurons) | No | |
Aδ | Thin | 1-5 | 3-30 | "rapid" pain, crude touch, pressure, temperature. AMH type I for rapid mechanical pain (high heat threshold >53C), AMH type II for rapid heat pain (lower heat threshold 43-47C). | No | Yes |
C | No | 0.3-1.5 | 0.5-2.0 | "slow" pain, touch, pressure temperature (and postganglionic autonomic). Polymodal. | No | Yes |
Examination
Below is a table comparing clinical vs QST methods that I have modified from several sources.
Fibres | Sensation | Finding Descriptor | Clinical Relevance | Testing Equipment and Instructions | ||
---|---|---|---|---|---|---|
Clinical | QST | Laboratory | ||||
Aβ | Touch | Dynamic mechanical allodynia | Common to most NP. Central sensitisation. | cotton wool or camel hairbrush - 2cm stroke over 1 second and repeat | Von Frey filaments | NCS, SEPs |
Aβ | Vibration | Vibration detection threshold | Infrequent but strongly suggestive of NP | Tuning fork (128 Hz) | Vibrameter† | NCS, SEPs |
Aδ | Pinprick, sharp pain | Punctate mechanical allodynia and hyperalgesia | Common to most NP. Central sensitisation. | Punctate mechanical allodynia - use a toothpick apply 2 stimuli per second (2 Hz) and repeat.
Punctate mechanical hyperalgesia - optionally tested with a neurotips needle. |
Weighted needles | LEPs, IENF |
Aδ | Touch | Static or Pressure-evoked mechanical allodynia | Common to most NP, also observed in inflammatory pain. Central sensitisation. | Finger tip - apply pressure until blanching of nail bed for 1 second and repeat. | Von Frey filaments | |
Aδ | Cold | Cold allodynia | Infrequent but strongly suggestive of NP. Central sensitisation. | Stainless steel 128 Hz tuning fork prongs applied to the skin for 1 second and repeat | Thermode‡ | None |
Aδ | Touch, Pain | Temporal summation indicating hyperpathia | Central sensitisation, test for "wind-up" | Toothpick applied 2 stimuli per second (2Hz) for 30 seconds. Assess change in pre- and post- pain scores, and aftersensation. | ||
C | Warmth | Warm allodynia | Infrequent but strongly suggestive of NP. Peripheral sensitisation. | Thermoroller or warmed C size battery at 45° applied for 1 second and repeat | Thermode‡ | LEPs, IENF |
† or other device providing graded vibratory stimuli
‡ or other device providing graded thermal stimuli |
The function of the various sensory peripheral nerves are reproduced below.See Also
- Neuropathic Pain
- Central Sensitisation
- Allodynia, Hyperalgesia, and Hyperpathia
- Nerve Conduction Studies and Electromyography
References
- ↑ Cruccu & Truini. Tools for assessing neuropathic pain. PLoS medicine 2009. 6:e1000045. PMID: 19360134. DOI. Full Text.
- ↑ Zhu et al.. Concurrent validity of a low-cost and time-efficient clinical sensory test battery to evaluate somatosensory dysfunction. European journal of pain (London, England) 2019. 23:1826-1838. PMID: 31325385. DOI. Full Text.
- ↑ Backonja et al.. Value of quantitative sensory testing in neurological and pain disorders: NeuPSIG consensus. Pain 2013. 154:1807-1819. PMID: 23742795. DOI.
- ↑ Faculty of Pain Medicine. Pain Oriented Sensory Testing Guidelines. 2018.