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Abstract—The coordination and combination of motion and sensation are critical to realize a natural and precise control of prosthetic hands. Transcutaneous electrical stimulation (TES) is one of possible methods to develop an intuitive perception feedback for limb amputees. However, the perception afferent sites would be a critical issue that is still unexplored in depth. This paper reports a preliminary study on using somatosensory evoked potentials (SEP) to determine the proper afferent sites of perceptions on residual arms of transradial amputees. In this study, two transradial amputees with phantom finger perception (PFP) were recruited and SEP for the stimulation of median nerves and ulnar nerves were recorded and analyzed. PFP distribution maps on subjects’ stumps were obtained by mechanical stimulations performed manually. Electrical stimulation was then applied to some selected sites on the stumps of their residual arms with surface electrodes to evoke SEP. In the experiments, SEP were successfully recorded, which means that the proposed method might be a suitable approach for localizing the afferent sites of perceptions, and could provide technique support for possible intuitive neural feedback for limb amputees in future work. I. INTRODUCTION Now available prostheses is helpful for amputees in doing their activities, but a major drawback with current hand prostheses is that they do not provide the users with proper sensory feedback [1]. For human beings, the interaction between sensory and motor functions is essential [2]. Transfering the sensor-detected sensation signals into users’ nerve systems is very critical to realize intuitive feedback of perception for arm amputees [3]. Many methods have been proposed to provide sensation feedback for amputees, including indirect stimulation methods (visual, vibrotactile or auditory feedback) and direct neural stimulation methods (electrical stimulation of somatosensory cortex or peripheral nerves) [3]. Electrical stimulations of both somatosensory cortex and peripheral This work was supported in part by the National Key Basic Research Program of China (#2013CB329505), the National Natural Science Foundation of China (#61203209, #91420301, #61135004), the Guangdong Province Natural Science Fund for Distinguished Young Scholars (#2014A030306029), the Shenzhen Peacock Plan Grant (#JCYJ20130402113127532) and the Guangdong Innovation Research Team Fund for Low-cost Healthcare Technologies. H. Wang, P. Fang, L. Tian, Y. Zheng, H. Zhou and G. Li are with the Key Lab of Human-Machine Intelligence-Synergy Systems, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, 518055 China. H. Wang is also with the Shenzhen College of Advanced Technology, University of Chinese Academy of Sciences, Shenzhen, 518055 China. X. Zhang is with National Research Center for Rehabilitation Technical Aids, Beijing, China. (Corresponding author: Guanglin Li; Tel: +86-755-86392219; Fax: +86-755-86392299; E-mail: gl.li@siat.ac.cn). nerves are possible approaches to regenerate intuitive and accurate perception feedback for limb amputees [4-6]. But the direct neural stimulation methods require delicate surgery to implant the electrodes. In addition, more research work and clinical verification should be performed before actual applications. Electrical stimulation of sensory afferents using transcutaneous electrical nerve stimulation (TES) has been confirmed to generate somatic sensations in an amputee's phantom limb directly and invasively [7]. TES can induce various types of sensation, including touch, vibration, warmth, wetness and so on [8, 9]. Tactile perception was found to be induced more easily on the median and ulnar aspects than the dorsal and radial aspects of the forearm with TES [8]. Phantom limb sensation (PLS) is a remarkable and important sensory phenomena [10]. More than 80% of amputees report phantom limb sensation, which refers to non-painful sensations that are felt at a missing limb or a portion of the missing limb [11]. Transradial amputees often experience sensation on specific phantom fingers (phantom finger perception, PFP) with cutaneous stimulation of specific stump areas [12]. Some amputees experienced a “hand-map phenomenon” corresponding to somatic sensations in specific phantom finger elicited by touch of specific localized parts of the amputation stump skin [13]. Although the neuronal basis of referred phantom limb sensations is unclear, several existing studies have demonstrated that deafferented cortex remains responsive when provided with artificial phantom input and could provide a neuronal substrate for spontaneous phantom limb sensations [14]. By stimulating the forearm stump skin, PLS may be an important method for sensation input for amputee [15, 16]. The users of prosthesis can understand the source location of sensation with stimulating the phantom finger area. PFP evoked by TES may be a promising technique to establish sensory feedback from the prosthetic fingers to the amputees [11]. One of the critical problems for sensory feedback based on TES technology is how to determine the proper stimulation sites. Stimulation sites are usually chosen along the arm nerves. The location of the sensations is evaluated subjectively when the stimulations are applied on the forearm skin. And an objective evaluation of sensation site is needed. Somatosensory evoked potentials (SEP) is a useful and noninvasive approach for assessing somatosensory system. By combining SEP recordings at different levels of the somatosensory pathways, it is possible to assess the transmission of the afferent volley from the periphery up to the cortex. In that way, we can monitor the afferent nerve pathway of perception, from the residual limbs to the Towards determining the afferent sites of perception feedback on residual arms of amputees with transcutaneous electrical stimulation Hui Wang, Peng Fang, Member, IEEE, Lan Tian, Yue Zheng, Hui Zhou, Guanglin Li, Senior Member, IEEE , and Xiufeng Zhang. 978-1-4244-9270-1/15/$31.00 ©2015 IEEE 3367 somatosensory cortical hand area. SEP may be an objective tool to evaluate sensory feedback. As far as we know, there are no systematic studies of regional distribution of phantom fingers and how to determine reliable and proper stimulation site of TES for amputee sensory feedback. The goal of this work is to explore the method to evaluate the stimulation site for TES using the phenomenon of phantom finger perception by SEP in amputees for sensory feedback of prosthetic hand. Our preliminary results of this study indicated that SEP would be a promising technique to determine the stimulation sites for establishing sensory feedback from fingers of the prosthetic hand to amputee with TES and PFP. II. MATERIALS AND METHODS A. Principle The median nerve innervation territory includes thumb, index finger and middle finger. Ulnar nerve dominates the little finger and part of ring finger (Fig. 1). We can reasonably assume that stump median nerve can be identified from stump ulnar nerve by identifying the phantom thumb perception and phantom little finger perception. PFP can be aroused by touching a specific part of the skin in the stump area of amputees. TES can evoke a similar PFP in amputees with electrodes placed at the same skin area and we hypothesized that the stimulation sites that aroused the PFP were along the stump nerves. So in that way, we can evaluate the sensory feedbackfunction with SEP. In this study, we firstly identified the PFP points in stump skin of amputees, so as to prove that PFP area is located along the forearm stump nerves. In order to evaluate the stimulation site, we then measured the SEP when electrocutaneous nerve stimulation was employed with electrodes site along the PFP area Figure 1.Schematic diagram for brachial plexus nerves innervations and the phenomenon of phantom finger perceptions B. Subjects and Data Acquisition Two male transradial amputees (designated as A1 and A2) with ages of 31 and 27, and amputated in 2007 and 2010, respectively, were recruited in the study. The two subjects reported spontaneous phantom limb sensations but no phantom limb pain. A1 was was with left forearm amputation , and A2 was with right foream amputaion.Results from subject A1 were typically presented. The protocol of this study was approved by the Institutional Review Board of Shenzhen Institutes of Advanced Technology. The subjects gave the written informed consent and provided permission for publication of photographs with a scientific and educational purpose. We used an 8-channel EMG/EP system (NTS-2000-A38, Shanghai NCC Electronic co) with one current stimulator and eight EMG recording channels. The stimulation parameters were: square wave pulses, current intensity 2 mA, pulse width 0.2 ms, inter-pulse delay 0.2 ms, and frequency 4.7 Hz. C. Procedures We first identified the PFP area in the remaining arm of amputee, so as to prove that PFP area is along the forearm stump nerves. The experiment protocol was as follows: Subject was asked to be seated on a chair, with his eyes always closed. The subject’s residual forearm was properly surrounded with a clinical sterile cloth with coordinate scales. Pressures were applied directly on the subject’s residual forearm with a hard plastic stick (such as a pen), and the corresponding perceptions of different fingers or imperceptions were subjectively reported by the subject. SEP to median nerve stimulation and ulnar nerve stimulation were recorded for intact limb and amputated limb. For intra individual side-to-side comparisons (amputated vs. intact side), a mixed sensory-motor arm nerve (median or ulnar nerve) was stimulated electrically 100 times proximal to the amputation site. N9 was recorded at the Erb's point (reference electrode: contralateral Erb's point), N13 was measured over the fifth cervical spine (reference electrode: FPz), and the N20 was recorded over the somatosensory cortex (reference electrode: FPz). The experiment protocol for intact limb SEP followed the standard procedure [17]. Surface electrodes were used to record SEP. Stimulation electrode and reference electrode were positioned carefully so as to evoke sensation projected exclusively to the median nerve's territory or ulnar nerve’s territory (above the motor threshold for the healthy hand, causing a thumb or a little finger to shake with amplitude about 1 cm). The detailed experiment protocol for stump limb SEP was as follows [11]: 1) Marked the PFP regions in the subject stump limb; 2) Attached the SEP recording electrodes to the assigned position; 3) Attached the stimulation electrode to labeled skin area, and the reference electrode was positioned carefully so as to evoke sensation projected exclusively to the median nerve's territory in the amputated phantom hand through phantom thumb perception; 4) Turned on the stimulator, increased current intensity from 0 until pricking sensation was reached, and recorded this current level as upper limit of stimulation; 5) Chose the stimulator parameter 3368 to arouse phantom thumb perception and the subject reported that phantom thumb was shaking and without painful sensation; 6) Used the selected stimulation site and parameter for SEP recording; 7) Chose stimulation site among the phantom little finger points, so as to stimulate the ulnar nerve territory, and did steps 5-6 again. III. RESULTS A. Phantom finger perception As Fig. 2 shows, the central part indicated the “hand –map” for different phantom finger perception. The areas of single finger-PFP representing the thumb (1), index (2), middle (3), ring (4) and little finger (5) were marked. Some peculiar points with mixed finger-PFP were also labeled. For example, (1+2) indicates mixed PFP of thumb and index fingers, and (3+4+5) for mixed PFP for middle, ring and little fingers. Those areas not eliciting any perception of touch were identified with (0). These labeled single finger-PFP points are exactly the positions of stimulating electrode. In this way, the accurate hand-map for PFP can be drawn and digitized. The results showed that most points were for phantom thumb perception or phantom little finger perception.Few points were for other phantom fingers perception. It was in accordance with our hypotheses that stump median nerve can be distinguished from stump ulnar nerve by identifying the phantom thumb perception and phantom little finger perception. Figure 2.Experiment set up with identifying ‘hand-map’ for phantom finger perception. The right part of the figure is about the identification of PFP points on the stump skin and marking points of PFP with a plastic rod. The central part is a continuous ‘hand-map’ on the stump skin B. Somatosensory evoked potentials SEP to median nerve and SEP to ulnar nerve were recorded. N9, N13 and N20 were detected for SEP to median nerve at the corresponding recording site. Only N20 was detected on C3/C4 for stimulation on the ulnar nerve. The two amputees showed significant SEP responses upon electrical stimulation of the truncated nerve on the residual limb (phantom thumb points or phantom little finger points) as well as of the nerve at the intact side. These preliminary results showed the amplitude and latency of corresponding SEP. Representative SEP component can be obtained when choosing phantom thumb points or phantom little finger points as simulation sites (Fig. 3). Results from subject A2 were similar, the hand-map for PFP and reasonable SEP component were obtained. Figure 3.Median SEP and ulnar SEP (amputated side vs. intact side). a) Shows the amplitudes of N9, N13, N20 for median SEP, and N20 for ulnar SEP. b) Shows the latency. 3369 IV. DISCUSSION To our best knowledge, this is the first study for evaluating stimulation site with SEP for limb amputee sensory feedback based on TES and PFP. According to our results,a continuous “hand-map” for phantom finger perception was determined through mechanical stimulation of a manual touch applied to skin surface of the stump in forearm amputees (Fig. 2). The continuous map of the hand on the stump skin for PFP was digitized and the coordinates for PFP points were obtained. We generally believed that there was a correlation relationship between the PFP distribution and brachial plexus nerves innervations. These preliminary results demonstrated that the distribution of PFP points was along the stump nerves. Phantom limb phenomena are very complex, and individual differences for PFP are great. The above way may be a useful approach for understanding PFP distribution [10]. The coordination and combination of motion and sensation is very critical to achieve a natural and precise grasp for prosthetic hands. However, prosthetic hands still neither provide an intuitive sensation neural feedback for prosthesis users, nor accurately adjust the grasp motion and strengthaccording to the sensation information. It is possible to relay the sensation information from the prosthetic hand to the brain of amputees with finger-to-finger specificity via TES evoked PFP [11]. It is hard to choose a very efficient and robust stimulation site for amputated limb. PFP points are along stump nerves innervations, which make them suitable stimulation site candidates for TES. The mechanisms for phantom limb sensations is unknown [16]. It is interesting to note that most points of PFP are about the phantom thumb or little finger; the points of phantom ring finger are usually congregate with other phantom fingers. The phenomenon for PFP distribution can be explained by brachial plexus nerves innervations. The accurate hand-map for PFP can be used for further study. SEP recordings after electrocutaneous nerve stimulation were employed to monitor afferent sensory pathway. We firstly use SEP for stimulation site selection. Stump median nerve can be distinguished from stump ulnar nerve by identifying the phantom thumb perception and phantom little finger perception. The N20 amplitudes and lantency in response to median nerver stimulation were similar with N20 to ulnar nerver stimulation. Although statistical anlaysis is needed, SEP may be a reliable and objective character to evaluate the PFP points.In future work, more subjects would be recruited to investigate the rules of perception input and verify the reliability of the proposed method. V. CONCLUSION The results obtained in this study demonstrated that stump median nerve or stump ulnar nerve can be distinguished by identifying the phantom thumb perception and phantom little finger perception. SEP may be a promising tool for evaluating stimulation site for PFP induced by TES in amputees to build an indirectly and invasively sensory feedback system. ACKNOWLEDGMENT The authors would like to thank the two amputees who participated in this study. We would also thank the technical support provided by the members of Research Center for Neural Engineering, at Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences. REFERENCES [1] C. Antfolk, C. Balkenius, B. Rosen, G. Lundborg, and F. Sebelius, "SmartHand tactile display: a new concept for providing sensory feedback in hand prostheses," Scand J Plast Reconstr Surg Hand Surg, vol. 44, pp. 50-3, Feb 2010. [2] D. M. Rager, D. Alvares, I. Birznieks, S. J. Redmond, J. W. Morley, N. H. Lovell, et al., "Generating tactile afferent stimulation patterns for slip and touch feedback in neural prosthetics," Conf Proc IEEE Eng Med Biol Soc, vol. 2013, pp. 5922-5, Jul 2013. [3] C. Antfolk, M. D'Alonzo, B. Rosen, G. Lundborg, F. Sebelius, and C. Cipriani, "Sensory feedback in upper limb prosthetics," Expert Rev Med Devices, vol. 10, pp. 45-54, Jan 2013. [4] J. E. O'Doherty, M. A. Lebedev, P. J. Ifft, K. Z. Zhuang, S. Shokur, H. Bleuler, et al., "Active tactile exploration using a brain-machine-brain interface," Nature, vol. 479, pp. 228-31, Nov 10 2011. [5] M. Ortiz-Catalan, B. Håkansson, and R. Brånemark, "An osseointegrated human-machine gateway for long-term sensory feedback and motor control of artificial limbs," Science Translational Medicine, vol. 6, p. 257re6, October 8, 2014. [6] D. W. Tan, M. A. Schiefer, M. W. Keith, J. R. Anderson, J. Tyler, and D. J. Tyler, "A neural interface provides long-term stable natural touch perception," Science Translational Medicine, vol. 6, p. 257ra138, October 8, 2014. [7] M. R. Mulvey, H. J. Fawkner, H. E. Radford, and M. I. Johnson, "Perceptual embodiment of prosthetic limbs by transcutaneous electrical nerve stimulation," Neuromodulation, vol. 15, pp. 42-6; discussion 47, Jan-Feb 2012. [8] B. Geng, K. Yoshida, L. Petrini, and W. Jensen, "Evaluation of sensation evoked by electrocutaneous stimulation on forearm in nondisabled subjects," J Rehabil Res Dev, vol. 49, pp. 297-308, 2012. [9] B. Geng and W. Jensen, "Human ability in identification of location and pulse number for electrocutaneous stimulation applied on the forearm," J Neuroeng Rehabil, vol. 11, p. 97, 2014. [10] A. Woodhouse, "Phantom limb sensation," Clin Exp Pharmacol Physiol, vol. 32, pp. 132-4, Jan-Feb 2005. [11] G. H. Chai, S. Li, X. H. Sui, Z. Mei, L. W. He, C. L. Zhong, et al., "Phantom finger perception evoked with transcutaneous electrical stimulation for sensory feedback of prosthetic hand," in Neural Engineering (NER), 2013 6th International IEEE/EMBS Conference on, 2013, pp. 271-274. [12] A. Björkman, A. Weibull, J. Olsrud, H. Henrik Ehrsson, B. Rosén, and I. M. Björkman-Burtscher, "Phantom digit somatotopy: a functional magnetic resonance imaging study in forearm amputees," European Journal of Neuroscience, vol. 36, pp. 2098-2106, 2012. [13] H. H. Ehrsson, B. Rosén, A. Stockselius, C. Ragnö, P. Köhler, and G. Lundborg, Upper limb amputees can be induced to experience a rubber hand as their own vol. 131, 2008. [14] B. M. Mackert, T. Sappok, S. Grusser, H. Flor, and G. Curio, "The eloquence of silent cortex: analysis of afferent input to deafferented cortex in arm amputees," Neuroreport, vol. 14, pp. 409-12, Mar 3 2003. [15] RAMACHANDRAN, #160, V. S., HIRSTEIN, #160, and W., The perception of phantom limbs : The D.O. Hebb lecture vol. 121. Oxford, ROYAUME-UNI: Oxford University Press, 1998. [16] M. J. Giummarra, S. J. Gibson, N. Georgiou-Karistianis, and J. L. Bradshaw, "Central mechanisms in phantom limb perception: The past, present and future," Brain Research Reviews, vol. 54, pp. 219-232, 4// 2007. [17] M. Tinazzi, G. Zanette, A. Polo, D. Volpato, P. Manganotti, C. Bonato, et al., "Transient deafferentation in humans induces rapid modulation of primary sensory cortex not associated with subcortical changes: a somatosensory evoked potential study," Neuroscience Letters, vol. 223, pp. 21-24, 2/14/ 1997. 3370
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