SUMMARY
Background
People with chronic tetraplegia due to high cervical spinal cord injury (SCI) can regain limb movements through coordinated electrical stimulation of peripheral muscles and nerves, known as Functional Electrical Stimulation (FES). Users typically command FES systems through other preserved, but limited and unrelated, volitional movements (e.g. facial muscle activity, head movements). We demonstrate an individual with traumatic high cervical SCI performing coordinated reaching and grasping movements using his own paralyzed arm and hand, reanimated through FES, and commanded using his own cortical signals through an intracortical brain-computer-interface (iBCI).
Methods
The study participant (53 years old, C4, ASIA A) received two intracortical microelectrode arrays in the hand area of motor cortex, and 36 percutaneous electrodes for electrically stimulating hand, elbow, and shoulder muscles. The participant used a motorized mobile arm support for gravitational assistance and to provide humeral ab/adduction under cortical control. We assessed the participant’s ability to cortically command his paralyzed arm to perform simple single-joint arm/hand movements and functionally meaningful multi-joint movements. We compared iBCI control of his paralyzed arm to that of a virtual 3D arm. This study is registered with ClinicalTrials.gov, NCT00912041.
Findings
The participant successfully cortically commanded single-joint and coordinated multi-joint arm movements for point-to-point target acquisitions (80% – 100% accuracy) using first a virtual arm, and second his own arm animated by FES. Using his paralyzed arm, the participant volitionally performed self-paced reaches to drink a mug of coffee (successfully completing 11 of 12 attempts within a single session) and feed himself.
Interpretation
This is the first demonstration of a combined FES+iBCI neuroprosthesis for both reaching and grasping for people with SCI resulting in chronic tetraplegia, and represents a major advance, with a clear translational path, for clinically viable neuroprostheses for restoring reaching and grasping post-paralysis.
INTRODUCTION
High cervical spinal cord injury (SCI) resulting in tetraplegia prevents affected persons from performing reaching and grasping movements required for many activities-of-daily-living. Functional electrical stimulation (FES), in the absence of descending motor commands, applies spatiotemporal patterns of stimulation to peripheral nerves and muscles to reanimate paralyzed limbs for restoring lost functions. FES can be delivered through skin surface, intramuscular, or nerve cuff electrodes1–3, and has successfully restored grasping to persons with mid- to low-level cervical SCI, who retain both volitional shoulder and elbow movements for commanding stimulation4–6.
Restoring multi-joint reaching and grasping is more difficult in persons with high cervical SCI because the few available command options (sip-and-puff, eye tracking, retained head/neck movements) are unintuitive, scale poorly for commanding coordinated multi-joint movements, and interfere with intact head and face function. Intracortical brain-computer-interfaces (iBCIs) that directly map cortical activity to desired movement eschew the need for retained volitional movement, thereby potentially addressing these shortcomings. Intact non-human-primates (NHPs)7–9 and humans with paralysis10–13 have successfully used iBCIs to command cursor movements and reaching and grasping using robotic limbs. Temporarily paralyzed NHPs have used iBCIs to command implanted FES-actuated wrist and grasping movements14,15. A more recent study used an iBCI coupled with surface electrical stimulation to provide assistive hand grasping to an individual with C5/C6 SCI16 who retained volitional shoulder and elbow function. However, the 25-year-old Freehand implanted FES system4–6 already successfully restored hand grasping to persons who retained volitional arm function, without requiring an iBCI. We for the first time show an individual with chronic tetraplegia using an implanted FES system to make both reaching and grasping movements, intuitively and effectively commanded by an iBCI, with a translational path for future clinical viability.
METHODS
Cortical and FES Implications
The participant (ID# T8) enrolled into the BrainGate2 pilot clinical trial (ClinicalTrials.gov NCT00912041) and gave informed consent for study procedures as approved by the Institutional Review Boards of University Hospitals Cleveland Medical Center (Cleveland, OH) and Massachusetts General Hospital (Boston, MA). At the time of implant, he was a 53-year-old man who experienced traumatic high cervical SCI (C4, ASIA A) eight years before enrollment. On his dominant right side (contralateral to the intracortical implant), he retained limited and nonfunctional voluntary shoulder girdle motion, but no voluntary glenohumeral, elbow, or hand function, and no sensation below the shoulder. An implanted baclofen pump controlled spasticity of his dominant arm.
Two 96-channel microelectrode arrays (Blackrock Microsystems, Salt Lake City, Utah)17 were implanted into the hand area on the precentral gyrus18 of his motor cortex (Supplementary Figure 1). After four months of using the iBCI to command movements of a 3D virtual arm, the participant received, during two procedures (125 and 280 days-post-implant), 36 percutaneous muscle stimulating electrodes (Synapse Biomedical, Oberlin, OH)19 in his right upper and lower arm, including four percutaneous anodic current return electrodes, to restore finger and thumb (for a lateral hand grasp20), wrist, elbow, and shoulder movements (Supplemental Table 3 lists implanted muscles). Starting 142 days-post-implant, all implanted muscles were exercised using cyclical electrical stimulation patterns to improve strength, range-of-motion, and fatigue resistance. Exercise occurred 18 out of 45 weeks, averaging 8 hours/week spread over 2–3 days. Over the course of the study, the participant had four minor (and no serious) device-related adverse events, all of which were quickly treated, resolved, and appropriately reported to the governing IRBs.
FES+iBCI System Architecture and Neural Decoding
Figure 1A illustrates the FES+iBCI system. The iBCI consists of the implanted recording microelectrode arrays, with a neural decoder that translated recorded cortical activity into command signals for controlling muscle stimulation to produce coordinated reaching and grasping movements. The FES system consists of an external stimulator that delivered charge-balanced, biphasic, constant-current stimulation through percutaneous electrodes to produce muscle contractions and subsequent limb movement. The stimulation had a fixed current amplitude (20 mA) and frequency (12.5 Hz) and a variable pulse duration of 0–200 μs. The current pulse duration (“pulse-width”) applied at a given electrode determined the strength of the muscle contraction. The participant used a Mobile Arm Support (MAS) (Focal MEDITECH, Tilburg, Netherlands) for support against gravity and motorized humeral ab/adduction (also under cortical command), since neither his residual shoulder motion nor deltoid stimulation provided adequate humeral ab/adduction. Instrumented goniometers (Biometrics Ltd.-US, Ladysmith, VA) on his elbow, wrist, and hand measured joint motions.
Neural decoders were calibrated daily at the beginning of each experimental session to translate cortical activity patterns into movement commands for a virtual reality arm or the FES-actuated arm. Daily re-calibration helped to account for day-to-day variability in the recorded activity21. The decoders used two neural features from each electrode of the intracortical arrays: 1) unsorted threshold crossing “firing” rates, determined by counting all action potentials in a 20ms time window that crossed a preset noise threshold, and 2) average spectral high frequency power (250–3000 Hz) in a 20ms time window. The decoders used a linear transformation function, similar to the Kalman filter used in recent iBCI applications22, to map the neural features to three movement commands. For the virtual arm, decoded commands determined the instantaneous movement velocities for the virtual arm joints (shoulder, elbow, wrist, grasp). For the FES arm, decoded commands determined the change in the percent activation of stimulation patterns associated with elbow, wrist or hand movements (or determined the actuation of the MAS). The stimulation patterns made it easy for the participant to coordinate the activity of multiple electrodes in a graded fashion with only a few command signals20 (see Supplemental Methods). Figure 1B illustrates example stimulation patterns designed such that increases/decreases in the percent activation of the pattern smoothly coordinated multiple electrodes to cause joint extension/flexion. The decoded command signal for controlling the MAS caused no movement if it was below a certain threshold, and otherwise caused ab/adduction at a constant rate.
Session Overview
Figure 2A illustrates the timeline of surgeries and sessions. As part of the BrainGate2 pilot clinical trial, the study participant performed various virtual reality (VR) arm control sessions not directly related to the present study. For this study, he performed two types of sessions: (1) sessions where he controlled both the VR arm and the FES system in order to compare performance between the two, and (2) sessions where he controlled the FES system to complete meaningful functional tasks. Data reported in this study are from 26 VR vs. FES comparison sessions and functional task sessions collected after the second FES implant surgery.
Comparing Cortical Control of a Virtual Reality Arm vs FES-Actuated Arm
During the VR vs. FES comparison sessions, the participant cortically commanded single and multi-joint movements of both a 3D virtual arm and his FES arm to perform point-to-point target acquisitions. Since the virtual arm had no inertial or musculoskeletal dynamics, it was useful for demonstrating the quality of the decoded iBCI commands independently of any control difficulties added by the FES-actuated arm and the stimulation patterns.
Experimental sessions consisted of three conditions (Figure 2C). During the attempted movement condition (AM), the participant observed the virtual arm23 make goal-directed, point-to-point movements while he was instructed to attempt those same movements. Neural activity evoked during these attempted movements was used for decoder initialization. During the virtual reality condition (VR), the participant used this initial decoder to cortically command the real-time velocities of the elbow, wrist, hand, and/or shoulder joints to perform single and multi-joint movements of the opaque virtual arm to a target configuration represented by a translucent arm (Figure 2B). Decoder parameters were updated after each VR block by re-calibrating the decoder with all available data, and then held fixed for the FES condition. During the FES condition, the participant performed single and multi-joint movements of his own FES-actuated arm while receiving visual feedback of the arm movements and the target location via the VR system. The virtual arm’s joint angles were set equal to the joint angles recorded by the instrumented goniometers and the participant looked at the computer monitor during this phase instead of his own FES-actuated arm. This experimental set up (Supplemental Videos 1–2) enabled precise visualization of the target arm configurations during point-to-point FES arm movements and facilitated comparison between VR and FES movements (since visual feedback of the target location and the arm location was identical). The decoder output for the untested joints was set to zero. Supplementary Table 1 summarizes all sessions and joints tested during each day.
Functional Task Demonstrations
To demonstrate the potential of the system to restore meaningful function, the participant completed both a coffee drinking and a self-feeding task. For these sessions, we calibrated the decoder while he observed and controlled FES-actuated movements instead of virtual reality movements. First, we initialized the decoder using neural data recorded while his arm was automatically driven by the FES system (i.e. computer-controlled) to make elbow, hand, and shoulder (MAS) movements. He was instructed to simultaneously attempt to make the observed arm motions. We then refined the decoder by using neural data recorded while he performed user-controlled single-joint FES-actuated movements, cued by audio commands instead of the VR game. After refinement, the neural decoder was held constant for the functional tasks. We found that this calibration scheme worked better than calibrating with VR data, potentially because the difference in visual feedback between VR and physical reality caused the neural activity to change.
RESULTS
Quality of Recorded Neural Activity
Neural activity was strongly related to the participant’s intended movement commands during attempted movement (AM), VR, and FES movement conditions. Figure 2D illustrates example neural activity that was strongly tuned to wrist flexion over wrist extension during each condition (substantially more threshold crossings were observed during attempted wrist flexion over wrist extension). Similar consistency of neural tuning between task conditions (AM vs VR vs FES) on some channels was also observed for elbow flexion/extension, humeral ab/adduction, and hand opening/closing (Supplementary Figure 3). Of the 192 electrodes, we identified a neural feature (threshold crossing or spectral high frequency power) that coded for hand opening/closing on 15±2 (mean±SD) electrodes, for elbow flexion/extension on 25±2 electrodes, for wrist flexion/extension on 25±4 electrodes, and for humeral ab/adduction on 27±20 electrodes (Supplemental Figure 8). Supplementary Figure 9 reports the number of isolatable single neurons recorded over time.
Quality of Virtual and FES Arm Movements
Across the VR vs. FES comparison sessions, the participant consistently achieved 80–100% success rates during single-joint movements of the elbow, wrist, hand, and MAS (humeral ab/adduction) to specified target positions (Figure 3, Supplementary Video 1). To successfully acquire a target, he had to maintain the specified joint angle within a certain tolerance around the target for 500ms without exceeding a maximum movement time of 8–12 seconds. The starting position of each movement was equal to the ending position of the previous movement.
For some joint movements (elbow flexion/extension, MAS ab/adduction), the participant acquired targets with his FES-actuated arm as quickly and as successfully as the virtual arm (Figure 3A). For other joint movements (wrist flexion/extension, hand opening/closing), he achieved high success rates but targets were acquired more slowly and speeds varied non-uniformly as a function of joint angle (Figure 3A). Results for two and three-joint movements are shown in Supplementary Figures 4–5 and Supplementary Video 2. On average, he achieved fewer target acquisitions during control of his own arm as compared to control of the virtual arm (Figure 3B). However, FES movements were still far more successful (more target acquisitions) than chance movements for both single and multi-joint movements, and far more successful than what he could achieve with residual voluntary shoulder movements alone (Figure 3B, Supplementary Figure 6, Supplementary Table 4).
Failed reaching attempts were categorized as due to: (1) muscle fatigue making it impossible to reach the target even at full stimulation, (2) control interface (FES and MAS) challenges making it difficult to accurately stop within the target region, or (3) failure to decode the correct command signal to move the joint towards the target. Supplementary Figure 7 illustrates each failure mode. For single-joint movements, ~80% of failed trials were due to control interface challenges, predominantly due to the inability to maintain a desired hand grasp posture (Supplementary Table 2). These trials occurred primarily when the decoded commands for the hand were mapped to highly nonlinear portions of the stimulation pattern. Some portions of the pattern contained “dead space” that did not move the hand very much, while other portions caused large, quick movements, resulting in target overshoots. We alleviated this problem in later blocks by using an automatic procedure that warped the stimulation pattern so that command signals were mapped linearly to equilibrium positions (Supplementary Figure 8). ~15% of failed trials were due to muscle fatigue, while ~5% (only two trials) were due to failure to decode an appropriate command signal.
For multi-joint movements, the dominant failure mode was also control interface challenges (contributed to 67% of failed trials), and was due primarily to MAS movements causing undesired motion of other joints. Interestingly, failure to decode an appropriate command signal for at least one of the joints was more common for multi-joint movements (contributed to 38% of failed trials). Decoding failure may have been more common in multi-joint trials because of the cognitive burden of controlling multiple joints with real dynamics and SCI-musculoskeletal limitations. Muscle fatigue was a reason for failure in ~12% of multi-joint (mostly elbow and wrist) trials.
Performance of Functional Reach-to-Grasp Tasks
The participant was able to successfully acquire a cup of coffee and take a drink (Figure 4A, Supplementary Video 4) and feed himself using the FES+iBCI system (Supplementary Video 5). The coffee drinking task required him to 1) extend his elbow, 2) open his hand, 3) grasp the cup securely, 4) flex his elbow to transport it close to his mouth, 5) take a drink using the straw, 6) extend his elbow to return the cup, and 7) release his grasp. He required between 20–40 seconds to complete the drinking task and was successful in 11 of 12 attempts made during the illustrated session (Figure 4B). During self-feeding, he consistently and repeatedly scooped forkfuls of mashed potatoes, and navigated his hand to his mouth to take several bites. When asked to describe how he commanded the FES arm movements, he replied, “It’s probably a good thing that I’m making it move without having to really concentrate hard at it. … I just think ‘out’ and … it just goes”.
The participant was completely unable to perform meaningful movements with the FES system turned off (Figure 4C); his minor residual shoulder girdle motion only caused a small, uncontrolled elbow jerk and could not move his hand at all, despite his attempts to command the required arm movements. This indicates that no substantial motor recovery occurred due to the FES and/or iBCI (demonstrated more extensively in Supplementary Figure 6). Supplementary video 3 offers an additional qualitative comparison of the movements the participant could make with and without the FES+iBCI system, and also shows that he could move each joint individually with the FES+iBCI system while suppressing the motion of undesired joints. Finally, note that the participant required continuous visual feedback of his arm movements, as lack of proprioception prevented knowledge of arm position and hence an inability to perform meaningful movements without visual feedback.
DISCUSSION
FES+iBCI restoration of arm and hand functions, combined with a mobile arm support (MAS) (standard for persons with C4 SCI implanted with FES arm systems) under iBCI command, represents a neurotechnology-based circumvention of SCI, giving persons with chronic tetraplegia intuitive control over reaching and grasping movements using their paralyzed limbs. The study significantly extends previous iBCI research with individuals with paralysis controlling cursors or robotic limbs10–13. The movements afforded to the study participant (reaching out, grasping/scooping, reaching back to the face) allowed him to repeatedly take a drink of coffee and feed himself with his own arm and hand, solely of his own volition. These actions are representative of movements needed to perform a wide range of reaching tasks, suggesting that more functional activities are achievable with the current system.
FES movements were moderately slower and less accurate than the same movements of the VR arm under brain control (Figure 3, Supplementary Figure 4,5). This discrepancy may have been due to the difference in time spent practicing VR vs FES (65 vs. 15 hours), but may have also been caused by the more difficult control task presented by an FES-activated arm: dynamics due to arm mass, muscle contractile properties, interactions between joints, and MAS motor dynamics. We previously demonstrated that these control difficulties are addressable with a feedback control system24,25 that converts higher level movement commands decoded from the iBCI (e.g. desired joint velocities) into the lower level muscle stimulations needed to smoothly achieve that movement. The feedback controller incorporates joint angle sensors that continuously sense any movement “error” or deviation from the desired movement, and recruits the appropriate muscles to reduce that error while taking into account the dynamics of the musculoskeletal limb (similar to how robotic arms are controlled). It should be noted that even without an implemented feedback controller, the participant was able to modulate his neural activity and use visual feedback alone to perform meaningful FES arm movements, even on day one.
The percutaneous, readily removable, FES electrodes provide proof-of-concept for fully-implanted FES systems. While this choice limited the number of joints that could be restored and their ranges-of-motion, future fully implantable FES systems can take advantage of enhanced electrode design and surgical placement (e.g., more precisely located intramuscular electrodes implanted via open surgery, or peripheral nerve cuff electrodes for more distributed motor unit recruitment3) and associated techniques (e.g., model-based optimization of muscle stimulation patterns, muscle tendon transfers to replace the functions of denervated muscles6, and more extensive exercise programs) to restore motion more fully. The use of implanted FES is critical for clinical adoption of this technology. While some earlier studies have focused on the use of surface FES to restore only hand grasp to persons with lower-level SCI, either commanded by electroencephalography (EEG)26,27 or iBCIs16, surface FES systems do not have a history of wide spread and long term clinical adoption. In contrast, fully implanted systems for FES grasp restoration, specifically the Freehand1,4, have a history of successful clinical adoption, likely due to the seamlessness of day-to-day setup and use, and their durability (<1% of electrodes fail over 3 years1).
While iBCI-commanded systems (including robotic arms) have not yet restored movements with the same speed and precision of able-bodied movements, the current level of gross movement they can restore is still enough to achieve clinically relevant functions (such as self-feeding). Enhanced speed, precision, and multifunctional control may be achievable through electrode technologies that record more neurons from distributed cortical networks, improved decoding algorithms, implantable FES technologies, and restored somatosensation. Somatosensation restored through intracortical stimulation28 may also eventually allow users to make reach and grasp movements that are safer in the absence of constant visual feedback, due to sensory feedback of object properties (e.g. temperature) in the reachable workspace. Despite current limitations, iBCIs currently offer the best option for seamless clinical integration and greater functional performance, particularly over their non-invasive counterparts (e.g. continuous control of a high-dimensional robotic limb has been successfully demonstrated with iBCI systems12 but never with EEG). Research advances in intracortical electrode biocompatibility29 and fully-implanted brain recording interfaces30 continue to increase the clinical viability of iBCI-commanded systems.
The present FES+iBCI system offers persons with chronic tetraplegia from SCI the possibility of regaining lost arm and hand function to perform activities-of-daily-living. Continued clinical translation of this technology will be aided by iBCI and FES technological advances resulting in smoother and more dexterous arm and hand movements. Future systems inspired by this work may provide full-time and more accurate control of the arm and hand, enabling restoration of a wider range of functional activities and resulting in increased independence and quality-of-life.
Supplementary Material
PANEL: RESEARCH IN CONTEXT.
Evidence before this study
We initially performed a PubMed search using the search terms (“FES” OR “electrical stimulation”) AND (“BMI” OR “BCI” OR “brain-machine-interface” OR “brain-computer-interface”), with no language or date restrictions. We also considered our own extensive database of relevant studies. Our search resulted in a large number of studies in humans using predominantly non-invasive BCIs to command non-focal surface stimulation to restore state-based, all-or-nothing hand opening/closing. Other studies of note used non-invasive BCIs combined with an implanted Freehand FES neuroprosthesis to again restore state-based all-or-nothing hand opening/closing. A newer study used an intracortical microelectrode array with a surface FES system to restore hand grasping alone to a person with mid-level cervical SCI. Two non-human-primate (NHP) studies were of note that showed restoration of continuous (graded) control of implanted FES activation of wrist and hand function. Three recent studies in paralyzed humans have demonstrated BCI control of robotic arms. Yet we found no studies similar to our present study, either in humans with SCI or NHP paralysis models, that restored both continuous reaching and grasping function via electrical stimulation and that also had a clear path to clinical translation.
Added value of this study
Our study is the first to restore both reaching and grasping via FES to a person with chronic SCI resulting in complete loss of arm and hand function. By using both an intracortical BCI and percutaneous FES electrodes for muscle activation, as well as a Mobile Arm Support (MAS) for gravitational assistance, we have demonstrated a proof-of-concept combined technology that allows users to perform functional tasks requiring coordinated reaching-and-grasping. Although other non-invasive BCI and FES hand-only systems have been proposed, none have been shown to be readily adoptable for day-today use, and certainly not for restoring both reaching and grasping. The present work has a clear path to clinical translation due to already existing fully implantable FES technology, as well as continued efforts to develop fully implanted and wireless BCI systems.
Implications of all the available evidence
Our results show the potential of combining implanted FES and iBCI (with an MAS) for restoring self-initiated reaching and grasping movements to persons with SCI resulting in chronic paralysis. The work was a critical step for demonstrating feasibility. Future developments of fully implanted systems, as well as developments in advanced decoders and stimulators may lead to enhanced neuroprosthetic functional performance and greater independence for persons with paralysis.
Acknowledgments
Role of Funding Source
The funding source had no role in the experimental design, analysis, or manuscript preparation or submission. The funding source provided funds to complete the study, including investigator salaries, equipment costs, and research and clinical costs.
Funding: National Institutes of Health, Department of Veterans Affairs
We thank the study participant for his pioneering efforts participating in the present study. We thank the Louis Stokes Cleveland VA Medical Center Cares Tower Residence Center, for space and logistical support. We additionally thank Jaimie M. Henderson, MD and Krishna V. Shenoy, PhD for their feedback and support of the research efforts.
Support for this work was provided by the National Institutes of Health under grants NIH 1R01HD077220, NIH N01HD53403, NIH R01DC009899, and VA B6453R. The reported contents do not necessarily represent the views of the funding or parent institutions, or of the US Government. The funding sources had no role in the writing of this manuscript. The corresponding author confirms that he had full access to all the data in the study and had final responsibility for the decision to submit for publication, and received no payment for the writing of this manuscript.
Footnotes
Author Contributions
Overall conceptual design: ABA, PHP, JPD, LRH, RFK. Conception and design of scientific experiments: ABA, FRW, DRY, WDM, BAM, JDS, LRH, RFK. Software implementation of the FES+iBCI system and experiments: FRW, DRY. Performed the experiments: FRW, DRY, WDM, BAM. Analyzed the data: FRW, DRY. Interpreted the data: ABA, FRW, DRY, WDM, BAM, RFK. Surgical design and implementation: JPM, JAS, HAH, MWK. Post-surgical care: BLW. Contributed to the writing of the manuscript: ABA, FRW, DRY, WDM, BAM, BLW, JAS, HAH, MWK, PHP, JDS, JPD, JPM, LRH, RFK. IDE Sponsor-Investigator of the pilot clinical trial: LRH.
All authors had complete access to the data. All authors authorized submission of the manuscript, but the final submission decision was made by ABA (primary and corresponding author).
Declarations and Conflicts of Interest
No author has any declarations or conflicts of interest to report.
Publisher's Disclaimer: This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final citable form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.
References
- 1.Peckham PH, Keith MW, Kilgore KL, et al. Efficacy of an implanted neuroprosthesis for restoring hand grasp in tetraplegia: a multicenter study. Arch Phys Med Rehabil. 2001;82:1380–8. doi: 10.1053/apmr.2001.25910. [DOI] [PubMed] [Google Scholar]
- 2.Kilgore KL, Hoyen HA, Bryden AM, Hart RL, Keith MW, Peckham PH. An implanted upper-extremity neuroprosthesis using myoelectric control. J Hand Surg Am. 2008;33:539–50. doi: 10.1016/j.jhsa.2008.01.007. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Memberg WD, Polasek KH, Hart RL, et al. Implanted Neuroprosthesis for Restoring Arm and Hand Function in People With High Level Tetraplegia. Arch Phys Med Rehabil. 2014;95:1201–11. doi: 10.1016/j.apmr.2014.01.028. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Taylor P, Esnouf J, Hobby J. The functional impact of the Freehand System on tetraplegic hand function. Clinical Results. Spinal Cord. 2002;40:560–6. doi: 10.1038/sj.sc.3101373. [DOI] [PubMed] [Google Scholar]
- 5.Fromm B, Rupp R, Gerner HJ. The Freehand System: an implantable neuroprosthesis for functional electrostimulation of the upper extremity. Handchirurgie, Mikrochirurgie, Plast Chir Organ der Deutschsprachigen Arbeitsgemeinschaft für Handchirurgie Organ der Deutschsprachigen Arbeitsgemeinschaft für Mikrochirurgie der Peripher Nerven und Gefässe Organ der Vereinigung der Deut. 2001;33:149–52. doi: 10.1055/s-2001-15129. [DOI] [PubMed] [Google Scholar]
- 6.Keith MW, Kilgore KL, Peckham PH, Wuolle KS, Creasey G, Lemay M. Tendon transfers and functional electrical stimulation for restoration of hand function in spinal cord injury. J Hand Surg Am. 1996;21:89–99. doi: 10.1016/s0363-5023(96)80160-2. [DOI] [PubMed] [Google Scholar]
- 7.Taylor DM, Tillery SIH, Schwartz AB. Direct cortical control of 3D neuroprosthetic devices. Science (80-) 2002;296:1829–32. doi: 10.1126/science.1070291. [DOI] [PubMed] [Google Scholar]
- 8.Serruya MD, Hatsopoulos NG, Paninski L, Fellows MR, Donoghue JP. Instant neural control of a movement signal. Nature. 2002;416:141–2. doi: 10.1038/416141a. [DOI] [PubMed] [Google Scholar]
- 9.Velliste M, Perel S, Spalding MC, Whitford AS, Schwartz AB. Cortical control of a prosthetic arm for self-feeding. Nature. 2008;453:1098–101. doi: 10.1038/nature06996. [DOI] [PubMed] [Google Scholar]
- 10.Hochberg LR, Serruya MD, Friehs GM, et al. Neuronal ensemble control of prosthetic devices by a human with tetraplegia. Nature. 2006;442:164–71. doi: 10.1038/nature04970. [DOI] [PubMed] [Google Scholar]
- 11.Hochberg LR, Bacher D, Jarosiewicz B, et al. Reach and grasp by people with tetraplegia using a neurally controlled robotic arm. Nature. 2012;485:372–5. doi: 10.1038/nature11076. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Collinger JL, Wodlinger B, Downey JE, et al. High-performance neuroprosthetic control by an individual with tetraplegia. Lancet. 2013;381:557–64. doi: 10.1016/S0140-6736(12)61816-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Aflalo TN, Kellis S, Klaes C, et al. Decoding motor imagery from the posterior parietal cortex of a tetraplegic human. Sci Mag. 2015;348:906–10. doi: 10.1126/science.aaa5417. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Moritz CT, Perlmutter SI, Fetz EE. Direct control of paralysed muscles by cortical neurons. Nature. 2008;456:639–42. doi: 10.1038/nature07418. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Ethier C, Oby ER, Bauman MJ, Miller LE. Restoration of grasp following paralysis through brain-controlled stimulation of muscles. Nature. 2012;485:368–71. doi: 10.1038/nature10987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Bouton CE, Shaikhouni A, Nicholas V, et al. Restoring cortical control of functional movement in a human with quadriplegia. Nature. 2016;533:247–50. doi: 10.1038/nature17435. [DOI] [PubMed] [Google Scholar]
- 17.Maynard EM, Nordhausen CT, Normann RA. The Utah Intracortical Electrode Array: a recording structure for potential brain-computer interfaces. 1997;102:228–39. doi: 10.1016/s0013-4694(96)95176-0. [DOI] [PubMed] [Google Scholar]
- 18.Yousry TA, Schmid UD, Alkadhi H, et al. Localization of the motor hand area to a knob on the precentral gyrus. A new landmark. Brain. 1997;120:141–57. doi: 10.1093/brain/120.1.141. [DOI] [PubMed] [Google Scholar]
- 19.Memberg WD, Peckham PH, Thrope GB, Keith MW, Kicher TP. An analysis of the reliability of percutaneous intramuscular electrodes in upper extremity FNS applications. IEEE Trans Rehabil Eng. 1993;1:126–32. [Google Scholar]
- 20.Kilgore KL, Peckham PH, Thrope GB, Keith MW, Gallaher-Stone KA. Synthesis of Hand Grasp Using Functional Neuromuscular Stimulation. IEEE Trans Biomed Eng. 1989;36:761–70. doi: 10.1109/10.32109. [DOI] [PubMed] [Google Scholar]
- 21.Dickey AS, Suminski A, Amit Y, Hatsopoulos NG. Single-unit stability using chronically implanted multielectrode arrays. J Neurophysiol. 2009;102:1331–9. doi: 10.1152/jn.90920.2008. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Koyama S, Chase SM, Whitford AS, Velliste M, Schwartz AB, Kass RE. Comparison of brain-computer interface decoding algorithms in open-loop and closed-loop control. J Comput Neurosci. 2010;29:73–87. doi: 10.1007/s10827-009-0196-9. [DOI] [PubMed] [Google Scholar]
- 23.Ajiboye AB, Simeral JD, Donoghue JP, Hochberg LR, Kirsch RF. Prediction of imagined single-joint movements in a person with high-level tetraplegia. IEEE Trans Biomed Eng. 2012;59:2755–65. doi: 10.1109/TBME.2012.2209882. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Blana D, Kirsch RF, Chadwick EK. Combined feedforward and feedback control of a redundant, nonlinear, dynamic musculoskeletal system. Med Biol Eng Comput. 2009;47:533–42. doi: 10.1007/s11517-009-0479-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Chadwick EK, Blana D, Simeral JD, et al. Continuous neuronal ensemble control of simulated arm reaching by a human with tetraplegia. J Neural Eng. 2011;8:34003. doi: 10.1088/1741-2560/8/3/034003. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Lauer RT, Peckham PH, Kilgore KL. EEG-based control of a hand grasp neuroprosthesis. Neuroreport. 1999;10:1767–71. doi: 10.1097/00001756-199906030-00026. [DOI] [PubMed] [Google Scholar]
- 27.Pfurtscheller G, Mu GR, Ju H. ‘Thought’ – control of functional electrical stimulation to restore hand grasp in a patient with tetraplegia. 2003;351:33–6. doi: 10.1016/s0304-3940(03)00947-9. [DOI] [PubMed] [Google Scholar]
- 28.Flesher SN, Collinger JL, Foldes ST, et al. Intracortical microstimulation of human somatosensory cortex. Sci Transl Medicne. 2016:1–11. doi: 10.1126/scitranslmed.aaf8083. [DOI] [PubMed] [Google Scholar]
- 29.Jorfi M, Skousen JL, Weder C, Capadona JR. Progress towards biocompatible intracortical microelectrodes for neural interfacing applications. J Neural Eng. 2015;12:11001. doi: 10.1088/1741-2560/12/1/011001. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Capogrosso M, Milekovic T, Borton D, et al. A brain-spinal interface alleviating gait deficits after spinal cord injury in primates. Nature. 2016:284–8. doi: 10.1038/nature20118. In Press. [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.