Evidence map›Paper›PMID 39020366›Full record

ArticleBioelectronic medicine2024

The role of spinal cord neuroanatomy and the variances of epidurally evoked spinal responses.

Danny V Lam, Justin Chin, Meagan K Brucker-Hahn, Megan Settell, Ben Romanauski, Nishant Verma, Aniruddha Upadhye, Ashlesha Deshmukh, Aaron Skubal, Yuichiro Nishiyama and 12 more

Erratum issuedAbstract read
In one paragraph

Article in Bioelectronic medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors.

Danny V LamNeural Lab, Abbott Neuromodulation, Plano, TX, USA.
Justin ChinDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, USA.
Meagan K Brucker-HahnDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA.
Megan SettellWisconsin Institute for Translational Neuroengineering (WITNe), Madison, WI, USA.
Ben RomanauskiDepartment of Neurosurgery, Mayo Clinic, Rochester, MN, USA.
Nishant VermaNeural Lab, Abbott Neuromodulation, Plano, TX, USA.
Aniruddha UpadhyeDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, USA.
Ashlesha DeshmukhDepartment of Biomedical Engineering, University of Wisconsin Madison, Madison, USA.
Aaron SkubalDepartment of Biomedical Engineering, University of Wisconsin Madison, Madison, USA.
Yuichiro NishiyamaDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.
Jian HaoDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.
J Luis LujanDepartment of Neurosurgery, Mayo Clinic, Rochester, MN, USA.
Simeng ZhangNeural Lab, Abbott Neuromodulation, Plano, TX, USA.
Bruce KnudsenDepartment of Biomedical Engineering, University of Wisconsin Madison, Madison, USA.
Stephan BlanzDepartment of Biomedical Engineering, University of Wisconsin Madison, Madison, USA.
Scott F LempkaDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA.
Kip A LudwigDepartment of Biomedical Engineering, University of Wisconsin Madison, Madison, USA.
Andrew J ShoffstallDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, USA.
Hyun-Joo ParkNeural Lab, Abbott Neuromodulation, Plano, TX, USA.
Erika Ross EllisonNeural Lab, Abbott Neuromodulation, Plano, TX, USA.
Mingming ZhangNeural Lab, Abbott Neuromodulation, Plano, TX, USA. zmmhoney@gmail.com.
Igor LavrovDepartment of Neurology, Mayo Clinic, Rochester, MN, USA. igor.lavrov@gmail.com.ORCID http://orcid.org/0000-0002-3885-4509

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSpinal cord stimulation (SCS) has demonstrated multiple benefits in treating chronic pain and other clinical disorders related to sensorimotor dysfunctions. However, the underlying mechanisms are still not fully understood, including how electrode placement in relation to the spinal cord neuroanatomy influences epidural spinal recordings (ESRs). To characterize this relationship, this study utilized stimulation applied at various anatomical sections of the spinal column, including at levels of the intervertebral disc and regions correlating to the dorsal root entry zone.

methodTwo electrode arrays were surgically implanted into the dorsal epidural space of the swine. The stimulation leads were positioned such that the caudal-most electrode contact was at the level of a thoracic intervertebral segment. Intraoperative cone beam computed tomography (CBCT) images were utilized to precisely determine the location of the epidural leads relative to the spinal column. High-resolution microCT imaging and 3D-model reconstructions of the explanted spinal cord illustrated precise positioning and dimensions of the epidural leads in relation to the surrounding neuroanatomy, including the spinal rootlets of the dorsal and ventral columns of the spinal cord. In a separate swine cohort, implanted epidural leads were used for SCS and recording evoked ESRs.

resultsReconstructed 3D-models of the swine spinal cord with epidural lead implants demonstrated considerable distinctions in the dimensions of a single electrode contact on a standard industry epidural stimulation lead compared to dorsal rootlets at the dorsal root entry zone (DREZ). At the intervertebral segment, it was observed that a single electrode contact may cover 20-25% of the DREZ if positioned laterally. Electrode contacts were estimated to be ~0.75 mm from the margins of the DREZ when placed at the midline. Furthermore, ventral rootlets were observed to travel in proximity and parallel to dorsal rootlets at this level prior to separation into their respective sides of the spinal cord. Cathodic stimulation at the level of the intervertebral disc, compared to an 'off-disc' stimulation (7 mm rostral), demonstrated considerable variations in the features of recorded ESRs, such as amplitude and shape, and evoked unintended motor activation at lower stimulation thresholds. This substantial change may be due to the influence of nearby ventral roots. To further illustrate the influence of rootlet activation vs. dorsal column activation, the stimulation lead was displaced laterally at ~2.88 mm from the midline, resulting in variances in both evoked compound action potential (ECAP) components and electromyography (EMG) components in ESRs at lower stimulation thresholds.

conclusionThe results of this study suggest that the ECAP and EMG components of recorded ESRs can vary depending on small differences in the location of the stimulating electrodes within the spinal anatomy, such as at the level of the intervertebral segment. Furthermore, the effects of sub-centimeter lateral displacement of the stimulation lead from the midline, leading to significant changes in electrophysiological metrics. The results of this pilot study reveal the importance of the small displacement of the electrodes that can cause significant changes to evoked responses SCS. These results may provide further valuable insights into the underlying mechanisms and assist in optimizing future SCS-related applications.

Indexed as

Epidural Spinal RecordingsEvoked Compound Action PotentialNeuroanatomyNeuromodulationSpinal cord stimulationSpinally Evoked Motor Potentials

Identifiers

PMID39020366
PMCPMC11253499

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.