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. Author manuscript; available in PMC: 2024 Feb 15.
Published in final edited form as: J Pain. 2022 Oct 2;24(2):204–225. doi: 10.1016/j.jpain.2022.08.010

Table 1.

(Adapted from Vollert et al., 2017). Predicted Benefits of Different Analgesic Classes in 3 DFNS-defined Subgroups

Cluster Characteristics, Hypotheses About Underlying Pathophysiology, and Expected Treatment Efficacy
Sensory Loss Thermal Hyperalgesia Mechanical Hyperalgesia
Sensory profile
Sensory Loss Touch, thermal, pain None Mostly thermal
Hyperalgesia None Mostly cold & heat Mostly pressure & pain
DMA Little Little Much
PHS Much Little Little
Pathophysiology
Sensory Loss Small & large fibers Mostly small fibers
Hyperalgesia Peripheral sensitization Central sensitization
Ongoing Pain Ectopic activity Spontaneous activity Ectopic activity
Predicted Findings
IENFD Loss None Mild loss
CCM Loss None Mild loss
Peripheral MRI Damage None Mild damage
LEP Reduction Normal or gain Mild reduction
RIII Reduction Normal or gain Gain
μENG Denervation Sensitization Little denervation
Predicted Efficacy
NSAIDS (+)
Botox +
Topical capsaicin +
NMDA antagonist +
SNRI ++ + +
Gabapentinoid + + ++
Sodium channel blocker + ++ ++
Opioid ++ + +

CCM, confocal corneal microscopy; DMA, dynamic mechanical allodynia; IENFD, intraepidermal nerve fiber density; LEP, laser-evoked potentials; μENG, microneurography; PHS, paradoxical heat sensation; RIII, nociceptive flexion reflex; SNRI, serotonin-norepinephrine reuptake inhibitor.