Todd R. Farrell, M.S.1, Richard F. Weir, Ph.D.1-2 1Northwestern Univeristy Evanston, Illinois 2Jesse Brown VA Medical Center, Department of Veterans Affairs Chicago, Illinois
The use of surface electromyograms (EMG) to control a multiple degree-of-freedom prosthesis
has been investigated for several decades. A variety of approaches have been employed with
groups using different numbers of input channels (1-2), feature extraction methods (2-5) and
pattern recognition algorithms (2,6-7). While much work has been done, all of these efforts have
used surface EMG as the control signal.
It has been hypothesized that, due to the potential to provide a larger number of independent
control sites and the ability to record selectively from muscles of the forearm (in particular the
deep muscles), intramuscular EMG should be advantageous for multifunctional prosthesis
control (8).
Admittedly, the technology has not existed for chronic intramuscular recordings to be clinically
feasible for prosthetic use. The Implantable Myoelectric Sensor (IMES) that is being developed
at the Northwestern University Prosthetic Research Laboratory is an implantable sensor that will
allow for intramuscular EMGs to be chronically recorded directly from muscles in the forearm
(Fig.1) (9).
Figure 1 – A) A rendering of the proposed
Implantable Myoelectric Sensor (IMES).
B) An illustration of several IMES
implanted into individual muscles of the
forearm. The IMES will both receive power
and transmit the recorded EMG signals
without any wires passing through the skin.
Used with permission of NUPRL.
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We hypothesize and hope to demonstrate that by utilizing intramuscular EMG recordings it
will be possible to substantially increase the ability of a multifunctional prosthesis controller to
recognize the intended movement of the user, or ‘classification accuracy.’
Both surface and intramuscular EMG data were collected from the forearm of each subject.
Ten pairs of fine wire bipolar EMGs were recorded from 10 muscles in the forearm of four
subjects. These pairs of wires were separated by approximately 13 mm, to mimic those signals
that would be recorded by the IMES sensor. The muscles that were targeted were the extensor
carpi radialis, extensor carpi ulnaris, extensor digitorum communis, extensor pollicis longus,
flexor carpi radialis, flexor carpi ulnaris, flexor digitorum superficialis, flexor pollicis longus,
pronator teres, and supinator. In addition, six surface electrodes were placed in an equally
spaced array around the circumference of the forearm (Fig. 2).
Figure 2 - A photograph of the location of
the surface electrodes and fine wire
insertion sites. The writing on the forearm
indicates preliminary markings to assist in
locating the fine-wire sites. Used with the
permission of NUPRL.
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EMG was collected as the subjects produced a series of contractions for each of the movements
being investigated: hand close, hand open, pronation, supination, wrist extension and wrist flexion. For each trial the subject would produce four five-second contractions of the same
movement, each time starting from and returning to rest. Four of these trials were collected for
each movement with two trials used as training data for the pattern recognition system and the
other two used to test the efficacy of the system.
The signal amplitude was calculated for each channel. Additionally, because it has been
demonstrated that it is possible to significantly increase classification accuracies by presenting
EMG signal features in addition to signal amplitude (3-6+8) to the pattern recognition system. In
this study we chose to use auto-regressive (AR) parameters as our additional signal feature.
Four sets of input data were created for analysis:
Six surface channels: amplitude only
Six surface channels: amplitude + AR
Ten intramuscular channels: amplitude only
Ten intramuscular channels: amplitude + AR
Six intramuscular channels: amplitude only
Six intramuscular channels: amplitude + AR
Note: The subsets of six of the ten intramuscular channels used in input sets #5 and #6 were
selected using a process called multinomial logistic regression.
The classification accuracy was determined by comparing the intended movement of the user
to the output of a controller that uses a pattern recognition algorithm called a linear discriminant
analyzer (LDA).
The classification accuracies that resulted from the six input sets described above are shown in
Figure 3. When utilizing only EMG amplitude the surface data produced the worst classification
accuracy of any data set (78.9%). Adding the AR coefficients to the input data set increased the
classification accuracy substantially (89.7%).
Figure 3 – Classification accuracies of the
surface and intramuscular EMG. The
surface recordings are shown in black, the
full set of 10 intramuscular recordings are
shown in light gray and a subset of six of the
ten intramuscular channels are shown in
dark gray. The left column of each pair
shows classification accuracies when only
EMG amplitude is used and the right
column shows classification accuracies from
using autoregressive coefficients in addition
to EMG amplitude. Used with the
permission of NUPRL.
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When compared to the surface with AR data set the intramuscular data had slightly lower
classification accuracies when using only signal amplitude with 6 (87.9%) or 10 (86.8%)
channels. It was also demonstrated that the use of the AR parameters again reduced the error
substantially when applied to the intramuscular input sets 6 (92.8%) or 10 (93.7) channels.
The increased accuracy that is seen by implanting the electrodes is encouraging. However,
these results are based on a comparison of non-targeted surface channels to targeted
intramuscular channels and to achieve a truly fair comparison of surface vs. intramuscular EMG
we feel we need to target both recordings. In the near future we will be able to compare targeted
surface recordings with the targeted intramuscular data.
It was also interesting to note the considerable improvement that is achieved by adding the
auto-regressive parameters to each input set. The classifier error was reduced by more than half in two instances with the error being decreased by 51.7% for the surface inputs and 52.8% for
the 10 channel intramuscular inputs.
Finally, it was also interesting to observe that the smaller subsets of six intramuscular channels
performed as well as the full set of ten channels. This indicates that it may only be necessary to
record from a subset of forearm muscles to maximize classification accuracy for this six-class
problem. The muscles that were contained in these six-channel subsets were not consistent for
each subject however when a fixed subset of six channels was used for all subjects it performed
comparably (91.0 %) to the sets that were customized for each subject (92.8%).
Intramuscular and surface EMG data has been collected and preliminary analysis performed on
four normal subjects. The analysis shows that adding additional signal features to the input set
increases the ability of the classifier to accurately predict the subjects intended movement when
the surface or intramuscular EMG data is used. At this point only non-site-specific surface EMG
recordings have been obtained and this prevents any firm conclusions from being drawn
regarding the abilities of classifiers that use intramuscular versus surface EMG inputs. Future
experiments will target the surface EMG sites and allow for a comparison of the classification
accuracies of the two approaches.
The authors would like to acknowledge A. Bolu Ajiboye and Dr. Todd Kuiken for their
assistance with this work. This work was partially funded by the National Institute on Disability
and Rehabilitation Research (NIDRR) of the Department of Education under grant number
H133E030030. The opinions contained in this paper are those of the grantee and do not
necessarily reflect those of the Department of Education. This work was also supported in part
the by the National Institutes of Health (NIBIB/NICHD) under Grant 1 R01 EB01672 and by the
Department of Veterans Affairs, Rehabilitation Research and Development Service and is
administered through the Jesse Brown Veterans Affairs Medical Center, Chicago, IL.
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