Evidence map›Paper›PMID 37982637›Full record

ArticleNeurosurgery2024

Reconnecting the Hand and Arm to the Brain: Efficacy of Neural Interfaces for Sensorimotor Restoration After Tetraplegia.

Eric Z Herring, Emily L Graczyk, William D Memberg, Robert Adams, Gaudalupe Fernandez Baca-Vaca, Brianna C Hutchison, John T Krall, Benjamin J Alexander, Emily C Conlan, Kenya E Alfaro and 9 more

Open access · greenAbstract readCase Reports
In one paragraph

Article in Neurosurgery, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
5.5field-weighted citation impact, top 3% of its field
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

24 citing papers in PubMed, 31 citations in OpenAlex.

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  17. Clinical Applications and Future Translation of Somatosensory Neuroprostheses.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 4 institutions in 1 country.

Eric Z HerringSchool of Medicine, Case Western Reserve University, Cleveland , Ohio , USA.
Emily L GraczykSchool of Medicine, Case Western Reserve University, Cleveland , Ohio , USA.
William D MembergSchool of Medicine, Case Western Reserve University, Cleveland , Ohio , USA.
Robert AdamsSchool of Medicine, Case Western Reserve University, Cleveland , Ohio , USA.
Gaudalupe Fernandez Baca-VacaSchool of Medicine, Case Western Reserve University, Cleveland , Ohio , USA.
Brianna C HutchisonDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland , Ohio , USA.
John T KrallDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland , Ohio , USA.
Benjamin J AlexanderDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland , Ohio , USA.
Emily C ConlanDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland , Ohio , USA.
Kenya E AlfaroDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland , Ohio , USA.
Preethisiri BhatDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland , Ohio , USA.
Aaron B Ketting-OlivierDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland , Ohio , USA.
Chase A HaddixDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland , Ohio , USA.
Dawn M TaylorDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland , Ohio , USA.
Dustin J TylerSchool of Medicine, Case Western Reserve University, Cleveland , Ohio , USA.
Jennifer A SweetSchool of Medicine, Case Western Reserve University, Cleveland , Ohio , USA.
Robert F KirschSchool of Medicine, Case Western Reserve University, Cleveland , Ohio , USA.
A Bolu AjiboyeSchool of Medicine, Case Western Reserve University, Cleveland , Ohio , USA.
Jonathan P MillerSchool of Medicine, Case Western Reserve University, Cleveland , Ohio , USA.ORCID 0000-0001-5441-1751
Case Western Reserve University · USLouis Stokes Cleveland VA Medical Center · USThe Neurological Institute · USCleveland Clinic · US

Funding

Integrated Neural Engineering and Rehabilitation Training ProgramT32EB004314 · NIBIB · CASE WESTERN RESERVE UNIVERSITY · PI Jeffrey R Capadona, Robert F. Kirsch · 2004 to 2026
$6.1M
Improving intracortical control of reaching after paralysisR01NS119160 · NINDS · CLEVELAND CLINIC LERNER COM-CWRU · PI AJIBOYE, ABIDEMI BOLU, TAYLOR, DAWN MARIE · 2020 to 2024
$2.8M
NIBIB NIH HHS T32 EB004314NINDS NIH HHS R01 NS119160
6 · The paper itself

Abstract

BACKGROUND AND

objectivesParalysis after spinal cord injury involves damage to pathways that connect neurons in the brain to peripheral nerves in the limbs. Re-establishing this communication using neural interfaces has the potential to bridge the gap and restore upper extremity function to people with high tetraplegia. We report a novel approach for restoring upper extremity function using selective peripheral nerve stimulation controlled by intracortical microelectrode recordings from sensorimotor networks, along with restoration of tactile sensation of the hand using intracortical microstimulation.

methodsA 27-year-old right-handed man with AIS-B (motor-complete, sensory-incomplete) C3-C4 tetraplegia was enrolled into the clinical trial. Six 64-channel intracortical microelectrode arrays were implanted into left hemisphere regions involved in upper extremity function, including primary motor and sensory cortices, inferior frontal gyrus, and anterior intraparietal area. Nine 16-channel extraneural peripheral nerve electrodes were implanted to allow targeted stimulation of right median, ulnar (2), radial, axillary, musculocutaneous, suprascapular, lateral pectoral, and long thoracic nerves, to produce selective muscle contractions on demand. Proof-of-concept studies were performed to demonstrate feasibility of using a brain-machine interface to read from and write to the brain for restoring motor and sensory functions of the participant's own arm and hand.

resultsMultiunit neural activity that correlated with intended motor action was successfully recorded from intracortical arrays. Microstimulation of electrodes in somatosensory cortex produced repeatable sensory percepts of individual fingers for restoration of touch sensation. Selective electrical activation of peripheral nerves produced antigravity muscle contractions, resulting in functional movements that the participant was able to command under brain control to perform virtual and actual arm and hand movements. The system was well tolerated with no operative complications.

conclusionThe combination of implanted cortical electrodes and nerve cuff electrodes has the potential to create bidirectional restoration of motor and sensory functions of the arm and hand after neurological injury.

Indexed as

ArmBrain-Computer InterfacesAdultBrainClinical Trials as TopicElectrodes, ImplantedHandHumansMaleQuadriplegiaUpper Extremity

Identifiers

PMID37982637
PMCPMC12245341
OpenAlexW4388826070

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.