2019
DOI: 10.1088/1741-2552/ab4a24
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Selectivity of afferent microstimulation at the DRG using epineural and penetrating electrode arrays

Abstract: Objective. We have shown previously that microstimulation of the lumbar dorsal root ganglia (L5-L7 DRG) using penetrating microelectrodes, selectively recruits distal branches of the sciatic and femoral nerves in an acute preparation. However, a variety of challenges limit the clinical translatability of DRG microstimulation via penetrating electrodes. For clinical translation of a DRG somatosensory neural interface, electrodes placed on the epineural surface of the DRG may be a viable path forward. The goal o… Show more

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Cited by 18 publications
(24 citation statements)
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References 59 publications
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“…Our data suggest that clinical DRGS directly activates myelinated neurons, regardless of electrode position, stimulation configuration, and stimulus pulse parameters (i.e., frequency, pulse width). This corroborates our previous study's findings that clinical DRGS is likely driving the activity of large‐diameter myelinated Aβ‐LTMRs, without directly activating small‐diameter nonmyelinated C‐nociceptors (19) and is supported by recent experimental findings that DRGS applied with nonpenetrating electrode arrays activates neurons with conduction velocities in the Aδ‐ to Aβ‐axon range (70). Furthermore, our data also suggest that clinical DRGS activates Aα‐neurons, and may activate Aδ‐neurons, though in a considerably smaller proportion than Aα‐ and Aβ‐neurons.…”
Section: Discussionsupporting
confidence: 91%
“…Our data suggest that clinical DRGS directly activates myelinated neurons, regardless of electrode position, stimulation configuration, and stimulus pulse parameters (i.e., frequency, pulse width). This corroborates our previous study's findings that clinical DRGS is likely driving the activity of large‐diameter myelinated Aβ‐LTMRs, without directly activating small‐diameter nonmyelinated C‐nociceptors (19) and is supported by recent experimental findings that DRGS applied with nonpenetrating electrode arrays activates neurons with conduction velocities in the Aδ‐ to Aβ‐axon range (70). Furthermore, our data also suggest that clinical DRGS activates Aα‐neurons, and may activate Aδ‐neurons, though in a considerably smaller proportion than Aα‐ and Aβ‐neurons.…”
Section: Discussionsupporting
confidence: 91%
“…Therefore, we used stimulus-triggered averaging to detect responses evoked by stimulation. The presence of a compound action potential on each nerve was determined by comparing responses following stimulation to baseline recordings in which no stimulation occurred, using a previously-published method 67,68 . To determine the response detection threshold, we calculated the 99% confidence interval on the root mean squared baseline amplitude.…”
Section: Compound Action Potential Detectionmentioning
confidence: 99%
“…A binary search procedure was used to determine the minimum stimulus current necessary to recruit each nerve according to methods published previously 67,68 . First, we delivered 50 stimulation pulses through each electrode on the array in a random order using high amplitude pulses at 20 Hz to determine which electrodes could evoke responses in the peripheral nerves.…”
Section: Determining Recruitment Thresholdsmentioning
confidence: 99%
“…We filtered the ENG using a second-order high-pass filter with a cutoff frequency of 300 Hz, and we stimulation-triggered averaged the responses to 600 stimulus pulses. We determined the presence of an ECAP at a particular stimulation amplitude by comparing the root-mean-square (RMS) amplitude of the ENG to a threshold value, as shown in prior work (Ayers et al, 2016;Nanivadekar et al, 2019). We used a bootstrapping method to verify consistency of the evoked responses.…”
Section: Eng Analysismentioning
confidence: 99%