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. 2018 Oct 26;3(6):e668.
doi: 10.1097/PR9.0000000000000668. eCollection 2018 Nov.

Dynamic of the somatosensory system in postherpetic neuralgia

Affiliations

Dynamic of the somatosensory system in postherpetic neuralgia

Janne Gierthmühlen et al. Pain Rep. .

Abstract

Introduction: In postherpetic neuralgia (PHN) different types of patients can be distinguished regarding their predominant peripheral nociceptor function.

Objective: The aim was to examine somatosensory profiles in the course of disease with special regard to the different subtypes existing in PHN.

Methods: Twenty patients with PHN (7 men and 13 women, age 67 ± 9.6 years) were examined at baseline (disease duration 18.1 ± 26 months) and follow-up (31.6 ± 23.8 months later) with quantitative sensory testing (protocol of the German Research Network on Neuropathic Pain).

Results: Fourteen (70%) PHN patients presented with impaired (iPHN) and 6 (30%) with preserved (pPHN) C-fiber function. Groups did not differ regarding age, disease duration, or pain intensity at baseline. Both groups did not differ regarding change in pain intensity (-0.5 ± 2.3 vs -1.7 ± 2.6 numerical rating scale, P = n.s.) at follow-up. Impaired PHN improved in thermal and mechanical detection thresholds as well as allodynia independent from change in pain intensity. By contrast, pPHN showed an increase in mechanical pain sensitivity (1.4 ± 2.5 vs -0.4 ± 2.2, P < 0.05) and a trend towards a stronger loss of detection (66% vs 33%, P = n.s.) on follow-up.

Conclusion: Results demonstrate that patients with preserved C-fiber function are more predisposed to develop signs of central sensitization as demonstrated by an increased mechanical pain sensitivity. Impaired C-fiber function is able to improve even in chronic cases, but a functional loss is unlikely to play a role here. The knowledge of development of somatosensory profiles in the course of the disease offers possibilities to optimize a mechanism-based treatment.

Keywords: Chronic pain; Mechanism-based treatment; Postherpetic neuralgia; QST; Somatosensory profiles.

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Conflict of interest statement

Sponsorships or competing interests that may be relevant to content are disclosed at the end of this article.

Figures

Figure 1.
Figure 1.
Somatosensory profile and the presence of dynamic mechanical allodynia and paradoxical heat sensations (A) as well as frequencies of abnormal values (B) on baseline (white circles and white columns) and follow-up (black circles and black columns) examination in PHN patients with impaired C-fiber function. CDT, cold detection threshold; CPT, cold pain threshold; DMA, dynamic mechanical allodynia; HPT, heat pain threshold; MDT, mechanical detection threshold, MPS, mechanical pain sensitivity; MPT, mechanical pain threshold; NRS, numerical rating scale; PHN, postherpetic neuralgia; PHS, paradoxical heat sensitivity; PPT, pressure pain threshold; QST, quantitative sensory testing; TSL, thermal sensory limen; VDT, vibration detection threshold; WDT, warm detection threshold; WUR, wind-up ratio. *P < 0.05 and **P < 0.01 for comparison of baseline vs follow-up measurement.
Figure 2.
Figure 2.
Somatosensory profile and the presence of dynamic mechanical allodynia and paradoxical heat sensations (A) as well as frequencies of abnormal values (B) on baseline (white circles and white columns) and follow-up (black circles and black columns) examination in PHN patients with preserved C-fiber function. CDT, cold detection threshold; CPT, cold pain threshold; DMA, dynamic mechanical allodynia; HPT, heat pain threshold; MDT, mechanical detection threshold; MPS, mechanical pain sensitivity; MPT, mechanical pain threshold; NRS, numerical rating scale; PHN, postherpetic neuralgia; PHS, paradoxical heat sensitivity; PPT, pressure pain threshold; QST, quantitative sensory testing; TSL, thermal sensory limen; VDT, vibration detection threshold; WDT, warm detection threshold; WUR, wind-up ratio. *P < 0.05 for comparison of baseline vs follow-up measurement.

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