Evoked potentials to nociceptive stimuli delivered by CO2 or Nd:YAP lasers
Abstract Objective This study compares the amplitude, latency, morphology, scalp topography and intracranial generators of laser-evoked potentials (LEPs) to CO2 and Nd:YAP laser stimuli. Methods LEPs were assessed in 11 healthy subjects (6 men, mean age 39 ± 10 years) using a 32-channel acquisition...
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Published in: | Clinical neurophysiology Vol. 119; no. 11; pp. 2615 - 2622 |
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Main Authors: | , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Oxford
Elsevier
01-11-2008
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Subjects: | |
Online Access: | Get full text |
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Summary: | Abstract Objective This study compares the amplitude, latency, morphology, scalp topography and intracranial generators of laser-evoked potentials (LEPs) to CO2 and Nd:YAP laser stimuli. Methods LEPs were assessed in 11 healthy subjects (6 men, mean age 39 ± 10 years) using a 32-channel acquisition system. Laser stimuli were delivered on the dorsum of both hands (intensity slightly above pain threshold), and permitted to obtain lateralised (N1) and vertex components (N2-P2) with similar scalp distribution for both types of lasers. Results The N1-YAP had similar latencies but significantly higher amplitudes relative to N1-CO2 . The N2-P2 complex showed earlier latencies, higher amplitudes (N2) and more synchronised responses when using Nd:YAP stimulation. The distribution of intracranial generators assessed with source localization analyses (sLORETA) was similar for Nd:YAP and CO2 lasers. The insular, opercular, and primary sensorimotor cortices were active during the N1 time-window, whereas the anterior midcingulate, supplementary motor areas and mid-anterior insulae were active concomitant to the N2-P2 complex. Conclusions Earlier latencies and larger amplitudes recorded when using Nd:YAP pulses suggest a more synchronized nociceptive afferent volley with this type of laser. Significance This, together with its handy utilization due to optic fibre transmission, may favour the use of Nd:YAP lasers in clinical settings. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1388-2457 1872-8952 |
DOI: | 10.1016/j.clinph.2008.06.021 |