2009
DOI: 10.1109/tnsre.2009.2032603
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Stimulation Stability and Selectivity of Chronically Implanted Multicontact Nerve Cuff Electrodes in the Human Upper Extremity

Abstract: Nine spiral nerve cuff electrodes were implanted in two human subjects for up to three years with no adverse functional effects. The objective of this study was to look at the long term nerve and muscle response to stimulation through nerve cuff electrodes. The nerve conduction velocity remained within the clinically accepted range for the entire testing period. The stimulation thresholds stabilized after approximately 20 weeks. The variability in the activation over time was not different from muscle-based el… Show more

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Cited by 121 publications
(88 citation statements)
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“…In the mid-forearm, 8-contact FINEs were implanted around the median and ulnar nerves and a 4-contact CWRU spiral electrode was implanted around the radial nerve. Cuff leads were routed subcutaneously to percutaneous leads [22,24,25] in the upper arm ( figure 1(A)). The intraluminal size of the FINEs was 10 mm × 1.5 mm.…”
Section: Surgical Implantationmentioning
confidence: 99%
“…In the mid-forearm, 8-contact FINEs were implanted around the median and ulnar nerves and a 4-contact CWRU spiral electrode was implanted around the radial nerve. Cuff leads were routed subcutaneously to percutaneous leads [22,24,25] in the upper arm ( figure 1(A)). The intraluminal size of the FINEs was 10 mm × 1.5 mm.…”
Section: Surgical Implantationmentioning
confidence: 99%
“…Extraneural electrodes surround a peripheral nerve, but do not insert elements within the nerve, causing the least disturbance to the neural tissue. Circular, self-sizing electrodes, such as the spiral [86] and helical electrode [87], have been stable in clinical applications for decades [88][89][90]. A circular configuration has the minimum surface area to interact with the neural tissue.…”
Section: Physical Interactionmentioning
confidence: 99%
“…Forschung im Hinblick auf komplexere Implantate und die Verwendung von Nervenelektroden [7] wird weiterhin betrieben, die Zulassung eines neuen Systems als Medizinprodukt ist jedoch gegenwärtig nicht absehbar. Ein Grund für das Scheitern des Unternehmens war, dass die Zahl der Patienten, für die das System infrage kamen, -entgegen anfänglichen Schätzungen -doch zu gering war.…”
Section: Greifenunclassified