Neural event detection

Information

  • Patent Grant
  • 10869616
  • Patent Number
    10,869,616
  • Date Filed
    Friday, June 1, 2018
    6 years ago
  • Date Issued
    Tuesday, December 22, 2020
    4 years ago
Abstract
A neural monitoring system for detecting an artificially-induced mechanical muscle response to a stimulus provided within an intracorporeal treatment area includes a mechanical sensor, a stimulator, and a processor. The processor is configured to provide a periodic stimulus via the stimulator, and monitor the output from the mechanical sensor in an expected response window that follows one stimulus, yet concludes before the application of the next, subsequent stimulus to determine if the stimulus induced a response of the muscle.
Description
TECHNICAL FIELD

The present disclosure relates generally to a surgical diagnostic system for detecting the presence of one or more nerves.


BACKGROUND

Traditional surgical practices emphasize the importance of recognizing or verifying the location of nerves to avoid injuring them. Advances in surgical techniques include development of techniques including ever smaller exposures, such as minimally invasive surgical procedures, and the insertion of ever more complex medical devices. With these advances in surgical techniques, there is a corresponding need for improvements in methods of detecting and/or avoiding nerves.


SUMMARY

A neural monitoring system is provided that is capable of detecting an artificially-induced mechanical response of a muscle to stimulus that is provided within an intracorporeal treatment area of a human subject. The intracorporeal treatment area generally includes a nerve that innervates the monitored muscle. The present system utilizes advanced filtering techniques to aid in discriminating an induced response from all other responses.


The neural monitoring system includes a non-invasive mechanical sensor, a stimulator, and a processor. The mechanical sensor is configured to be placed in mechanical communication with the muscle and is operative to generate a mechanomyography output signal that corresponds to a sensed mechanical movement of the muscle. The stimulator is configured to provide a periodic stimulus within the intracorporeal treatment area, where the periodic stimulus includes at least a first stimulus beginning at a first time (T1), and a second, consecutive stimulus beginning at a second time (T2).


The processor is in communication with both the mechanical sensor and the stimulator, and is operative to provide the periodic stimulus to the stimulator for the ultimate delivery to the intracorporeal treatment area, and to receive the mechanomyography output signal from the mechanical sensor. The processor may be configured to analyze a response window of the mechanomyography output signal to determine if the first stimulus induced a response of the muscle. If an induced response is detected, the processor may provide a corresponding indication to a user, such as in the form of an alert, sound, altered color on a coupled display, or the like. Conversely, if an induced response is not detected within the response window, the processor may provide a different indication to the user to indicate that the stimulus did not induce a muscular response. In one configuration, the response window corresponds to a period of time when an induced response to the first stimulus is likely to occur. This response window generally extends between a third time (T3) and a fourth time (T4) such that T1≤T3<T4<T2.


In some embodiments, the processor is configured to determine if the first stimulus induced a response of the muscle by examining one or more characteristics of the mechanomyography output signal within the response window using a supervised learning algorithm that is operative to classify the response window as being either representative of an induced response of the muscle, or not representative of an induced response of the muscle. In an embodiment, the supervised learning algorithm may include an image-based classifier operative to analyze one or more graphical aspects of a graph of the mechanomyography output signal.


In an embodiment, the mechanical sensor may be a tri-axis accelerometer operative to monitor acceleration in three mutually orthogonal axes. The processor may then be configured to determine if the first stimulus induced a response of the muscle using a magnitude of a resultant vector calculated from the monitored acceleration in each of the three axes. In some embodiments, the processor may be configured to only determine if the first stimulus induced a response of the muscle if a magnitude of a movement of the muscle in a direction normal to the skin surface is greater than a magnitude of a movement of the muscle in a direction that is tangential to the skin surface.


As an additional background removal filter, in an embodiment, the processor may be further configured to identify signal content from the mechanomyography output signal that exists at least partially outside of the response window; determine a frequency component of that signal content; and attenuate the frequency component from the mechanomyography output signal within the response window. This filtered response window may then be used to determine if the first stimulus induced a response of the muscle. In some embodiments, the signal content exists at least partially between T1 and T2. Likewise, in some embodiments, the signal content may exist across a plurality of stimuli.


In some embodiments, the processor may be configured to use techniques described herein to more accurately determine a change in muscle response latency or nerve conduction velocity. For example, the processor may be configured to identify a time corresponding to a detected induced muscle response within the response window; determine a first response latency between the first stimulus and the time corresponding to a detected induced muscle response; identify a time corresponding to a subsequently detected muscle response that is induced by a subsequent stimulus provided by the stimulator; determine a second response latency between the subsequent stimulus and the time of the subsequently detected muscle response; and provide an alert if the second response latency differs from the first response latency by more than a predetermined amount.


In some embodiments, the current magnitude of the applied stimulus may be controlled in a closed loop manner to identify the lowest current that induces a threshold response of the muscle. This may operate by examining a difference between the mechanomyography output signal magnitude and a threshold output signal magnitude, and attempting to minimize that difference using a model describing how the response corresponds to the muscle output.


A method of detecting an artificially-induced mechanical response of a muscle to a stimulus provided within an intracorporeal treatment area of a human subject includes: transmitting a periodic electrical stimulus to a stimulator within the intracorporeal treatment area, receiving a mechanomyography output signal from a non-invasive mechanical sensor in mechanical communication with the muscle, detecting motion from the received mechanomyography output signal, and providing an indication to a user that the motion is an artificially-induced muscle response only if the motion occurs within a response window that exists between a first stimulus and a second, consecutive stimulus.


The above features and advantages and other features and advantages of the present technology are readily apparent from the following detailed description when taken in connection with the accompanying drawings.


“A,” “an,” “the,” “at least one,” and “one or more” are used interchangeably to indicate that at least one of the item is present; a plurality of such items may be present unless the context clearly indicates otherwise. All numerical values of parameters (e.g., of quantities or conditions) in this specification, including the appended claims, are to be understood as being modified in all instances by the term “about” whether or not “about” actually appears before the numerical value. “About” indicates that the stated numerical value allows some slight imprecision (with some approach to exactness in the value; about or reasonably close to the value; nearly). If the imprecision provided by “about” is not otherwise understood in the art with this ordinary meaning, then “about” as used herein indicates at least variations that may arise from ordinary methods of measuring and using such parameters. In addition, disclosure of ranges includes disclosure of all values and further divided ranges within the entire range. Each value within a range and the endpoints of a range are hereby all disclosed as separate embodiment.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 is a schematic diagram of a neural monitoring system for detecting an artificially-induced mechanical muscle response.



FIG. 2 is a schematic front view of the placement of a plurality of mechanical sensors on the legs of a subject.



FIG. 3 is a schematic side view of an intracorporeal treatment area including a portion of the lumbar spine.



FIG. 4 is a schematic time-domain graph of a mechanomyography output signal in response to a periodic electrical stimulus.



FIG. 5 is a schematic time-domain graph of an induced mechanical response of a muscle within a response window that exists after the application of an inducing stimulus.



FIG. 6 is a schematic diagram of a signal processing algorithm, including a supervised learning algorithm, for classifying a sensed muscle motion as being either an induced response or not an induced response.



FIG. 7 is a schematic flow diagram of a method of removing background noise that occurs at least partially outside of the response window.



FIG. 8 is a schematic time-domain graph of a technique for comparing a latency between the application of a stimulus and the occurrence of an induced response occurring within a response window.



FIG. 9 is a schematic graph illustrating a stimulus current control algorithm that adjusts stimulus current on the basis of a relationship between a stimulus current, a sensor output signal magnitude, and a distance between the stimulator and a nerve.



FIG. 10 is a schematic flow diagram of a method of detecting an artificially-induced mechanical response of a muscle to a stimulus provided within an intracorporeal treatment area of a human subject.





DETAILED DESCRIPTION

The present disclosure provides a neural monitoring system with improved capabilities for detecting an artificially-induced response of a muscle to a stimulus. More specifically, the processing techniques described herein enable a more robust event detection capability, while reducing the occurrence of false positives.


Referring to the drawings, wherein like reference numerals are used to identify like or identical components in the various views, FIG. 1 schematically illustrates a neural monitoring system 10 that may be used to identify the presence of one or more nerves within an intracorporeal treatment area 12 of a subject 14. As will be described in greater detail below, the system 10 may monitor one or more muscles of the subject 14 for a mechanical motion, and may be capable of discriminating an artificially-induced mechanical response of a muscle (also referred to as an “artificially-induced mechanical muscle response”) from a subject-intended muscle contraction/relaxation and/or an environmentally caused movement. If an artificially-induced mechanical muscle response is detected during the procedure, the system 10 may provide an indication to a user.


As used herein, an artificially-induced mechanical muscle response refers to a contraction or relaxation of a muscle in response to a stimulus that is not received through natural sensory means (e.g., sight, sound, taste, smell, and touch). Instead, it is a contraction/relaxation of a muscle that is induced by the application of a stimulus directly to a nerve that innervates the muscle. Examples of stimuli that may cause an “artificially-induced” muscle response may include an electrical current applied directly to the nerve or to intracorporeal tissue or fluid immediately surrounding the nerve. In this example, if the applied electrical current is sufficiently strong and/or sufficiently close to the nerve, it may artificially cause the nerve to depolarize (resulting in a corresponding contraction of the muscle innervated by that nerve). Other examples of such “artificial stimuli” may involve mechanically-induced depolarization (e.g., physically stretching or compressing a nerve, such as with a tissue retractor), thermally-induced depolarization (e.g., through ultrasonic cautery), or chemically-induced depolarization (e.g., through the application of a chemical agent to the tissue surrounding the nerve).


During an artificially-induced mechanical muscle response, a muscle innervated by the artificially depolarized nerve may physically contract or relax (i.e., a mechanical response). Such a mechanical reaction may primarily occur along a longitudinal direction of the muscle (i.e., a direction aligned with the constituent fibers of the muscle), though may further result in a respective swelling/relaxing of the muscle in a lateral direction (which may be substantially normal to the skin for most skeletal muscles). This local movement of the muscle during an artificially-induced mechanical muscle response may be measured relative to the position of the muscle when in a non-stimulated state, and is distinguished from other global translations of the muscle


The neural monitoring system 10 may include a processor 20 that is in communication with at least one mechanical sensor 22. The mechanical sensor 22 may include, for example, a strain gauge, a force transducer, a position encoder, an accelerometer, a piezoelectric material, or any other transducer or combination of transducers that may convert a physical motion into a variable electrical signal.


Each mechanical sensor 22 may be specially configured to monitor a local mechanical movement of a muscle of the subject 14. For example, each sensor 22 may include a fastening means, such as an adhesive material/patch, that allows the sensor 22 to be adhered, bandaged, or otherwise affixed to the skin of the subject 14 (i.e. affixed on an external skin surface). Other examples of suitable fastening means may include bandages, sleeves, or other elastic fastening devices that may hold the sensor 22 in physical contact with the subject 14. Alternatively, the mechanical sensor 22 (and/or coupled device) may be configured to monitor a local mechanical movement of a muscle by virtue of its physical design. For example, the sensors/coupled devices may include catheters, balloons, bite guards, orifice plugs or endotracheal tubes that may be positioned within a lumen or natural opening of the subject to monitor a response of the lumen or orifice, or of a muscle that is directly adjacent to and/or connected with the lumen or orifice. In one configuration, the mechanical sensor may be a non-invasive device, whereby the term “non-invasive” is intended to mean that the sensor is not surgically placed within the body of the subject (i.e., via cutting of tissue to effectuate the placement). For the purposes of this disclosure, non-invasive sensors may include sensors that are placed within naturally occurring body lumens that are accessible without the need for an incision.


In one configuration, the sensor 22 may include a contact detection device, that may provide an indication if the sensor 22 is in physical contact with the skin of the subject 14. The contact detection device may, for example, include a pair of electrodes that are configured to contact the skin of the subject 14 when the sensor 22 is properly positioned. The sensor 22 and/or contact detection device may then monitor an impedance between the electrodes to determine whether the electrodes are in contact with the skin. Other examples of suitable contact detection devices may include capacitive touch sensors or buttons that protrude slightly beyond the surface of the sensor.


The system 10 may further include one or more elongate medical instruments 30 that are capable of selectively providing a stimulus within the intracorporeal treatment area 12 of the subject 14 (i.e., also referred to as a stimulator 30). For example, in one configuration, the elongate medical instrument 30 may include a probe 32 (e.g., a ball-tip probe, k-wire, or needle) that has an electrode 34 disposed on a distal end portion 36. The electrode 34 may be selectively electrified, at either the request of a user/physician, or at the command of the processor 20, to provide an electrical stimulus 38 to intracorporeal tissue of the subject. In other configurations, the elongate medical instrument 30 may include a dilator, retractor, clip, cautery probe, pedicle screw, or any other medical instrument that may be used in an invasive medical procedure. Regardless of the instrument, if the intended artificial stimulus is an electrical current, the instrument 30 may include a selectively electrifiable electrode 34 disposed at a portion of the instrument that is intended to contact tissue within the intracorporeal treatment area 12 during a procedure.


During a surgical procedure, the user/surgeon may selectively administer the stimulus to intracorporeal tissue within the treatment area 12 to identify the presence of one or more nerve bundles or fibers. For an electrical stimulus 38, the user/surgeon may administer the stimulus, for example, upon depressing a button or foot pedal that is in communication with the system 10, and more specifically in communication with the stimulator 30. The electrical stimulus 38 may, for example, be a periodic stimulus that includes a plurality of sequential discrete pulses (e.g., a step pulse) provided at a frequency of less than about 10 Hz, or from about 1 Hz to about 5 Hz, and preferably between about 2 Hz and about 4 Hz. Each pulse may have a pulse width within the range of about 50 μs to about 400 μs. In other examples, the discrete pulse may have a pulse width within the range of about 50 μs to about 200 μs, or within the range of about 75 μs to about 125 μs. Additionally, in some embodiments, the current amplitude of each pulse may be independently controllable.


If a nerve extends within a predetermined distance of the electrode 34, the electrical stimulus 38 may cause the nerve to depolarize, resulting in a mechanical twitch of a muscle that is innervated by the nerve (i.e., an artificially-induced mechanical muscle response). In general, the magnitude of the response/twitch may be directly correlated to the distance between the electrode and the nerve, the impedance between the electrical stimulus and the ground patch, and the magnitude of the stimulus current. In one configuration, a lookup table may be employed by the processor 20 to provide an approximate distance between the electrode and the nerve, given a known stimulus magnitude and a measured mechanical muscle response.


Prior to beginning a surgical procedure, the one or more mechanical sensors 22 may be placed in mechanical communication with one or more muscles of the subject 14. In the present context, a sensor 22 may be in mechanical communication with the muscle if it can physically detect a movement, velocity, acceleration, strain or other physical response of the muscle, either via direct contact with the muscle, or via a mechanical relationship through one or more intermediate materials and/or tissues (e.g., skin and/or subcutaneous tissue).



FIG. 2 illustrates an example of the placement of a plurality of mechanical sensors 22 for a surgical procedure that may occur proximate the L2, L3, and/or L4 vertebrae of the lumbar spine (shown schematically in FIG. 3). The nerves 50, 52 and 54 exiting the L2, L3 and L4 foramen 56, 58, 60 may therefore either lie within the treatment area 12 (i.e., the area surrounding the L2, L3, and/or L4 vertebrae), or may be immediately proximate to this area. Using common anatomical knowledge, the surgeon may understand that damage to these nerves 50, 52, 54 may affect the functioning of the vastus medialis muscles and the tibialis anterior muscles. As such, the surgeon may place mechanical sensors 22a-22d on or near the vastus medialis muscles and the tibialis anterior muscles to guard against inadvertent manipulation of the nerves during the procedure. For example, mechanical sensors 22a and 22b are placed on the vastus medialis muscles, which are innervated by the nerves 50, 52 exiting the L2 and L3 foramen 56, 58, and sensors 22c and 22d are placed on the tibialis anterior muscles, which are innervated by the nerves 54 exiting the L4 foramen 60.


In general, each mechanical sensor 22 may generate a mechanomyography (MMG) output signal (schematically shown at 62) that corresponds to a sensed mechanical movement/response of the adjacent muscle. The MMG output signal 62 may be either a digital or analog signal, and the sensor 22 may further include communication circuitry operative to transmit the mechanomyography output signal to the processor through a wired or wireless communication protocol (e.g., through one or more wired data transmission protocols operative to communicate data over a physical wire such as I2C, CAN, TCP/IP, or other wired protocols; or through the use of one or more wireless/radio frequency-based data transmission protocols, such as according to IEEE 802.11, Bluetooth, ZigBee, NFC, RFiD or the like). As a specific signal, the MMG output signal 62 is intended to be separate and distinct from any electrical potentials of the muscle or skin (often referred to as electromyography (EMG) signals). While electrical (EMG) and mechanical (MMG) muscle responses may be related, their relationship is complex, and not easily described (e.g., electrical potentials are very location specific, with a potentially variable electrical potential across the volume of the muscle of interest).


Referring again to FIG. 1, the processor 20 may be in communication with the stimulator 30 and the mechanical sensor 22, and may be configured to receive the MMG output signal 62 from the mechanical sensor 22. The processor 20 may be embodied as one or multiple digital computers, data processing devices, and/or digital signal processors (DSPs), which may have one or more microcontrollers or central processing units (CPUs), read only memory (ROM), random access memory (RAM), electrically-erasable programmable read only memory (EEPROM), a high-speed clock, analog-to-digital (A/D) circuitry, digital-to-analog (D/A) circuitry, input/output (I/O) circuitry, and/or signal conditioning and buffering electronics.


The processor 20 may be configured to automatically perform one or more signal processing algorithms 70 or methods to determine whether a sensed mechanical movement (i.e., via the MMG output signal 62) is representative of an artificially-induced mechanical muscle response or if it is merely a subject-intended muscle movement and/or an environmentally caused movement. These processing algorithms 70 may be embodied as software or firmware, and may either be stored locally on the processor 20, or may be readily assessable by the processor 20.



FIG. 4 generally illustrates a graph 80 of an MMG output signal 62 in response to a periodic electrical stimulus 38 provided proximate to a nerve. It should be noted that the graph 80 is provided for illustrative purposes to show a generalized muscular response to a periodic stimulus provided at about a 3 Hz stimulation frequency. As shown, the MMG output signal 62 has an amplitude 84 that varies as a function of time 86 and includes a plurality of generally discrete contraction events 88. Each contraction event 88 may include, for example, an initial response 90 (e.g., an M-wave), and a plurality of subsequent peaks/valleys 92 (e.g., an H-reflex).



FIG. 5 provides an enlarged view of the first event 88 of FIG. 4. In addition to the graph 80 of the MMG output signal 62, FIG. 5 additionally includes a graph 94 representing two consecutive stimuli 96, 98. As generally shown, the first stimulus 96 may be provided by the stimulator beginning at a first time, T1. The second, consecutive stimulus may be provided by the stimulator beginning at a second time, T2. The length of time 100 between T1 and T2 may also be regarded as the period 100 of the periodic stimulus 38. This period 100 may typically be between about 100 ms and 1000 ms, or more typically between about 250 ms and about 500 ms. Within the length of time 100 following the first stimulus 96, there may be a narrower window of time where a muscle event 88 is most likely to occur in response to the first stimulus 96 (i.e., the “response window 102”). The response window 102 generally begins at a time T3 that is on or shortly after T1 and that may represent the earliest time where a response of the muscle to the stimulus could be expected. Likewise, the response window 102 generally ends at a time T4 that is before the next stimulus 98 begins and that provides a large enough period of time from T3 to include at least the entire initial response 90, if one were to occur.


The offset 104 between T1 and T3, if one were to exist would be minimal, as the delay between stimulation and the initial muscle response 90 is only limited by the speed at which the nerve signal propagates, the length of the nerve, and the dynamics of the muscle to actually contract in response to the nerve signal. In most patients, motor nerves can conduct generally between about 40 m/s and about 80 m/s, which could result in about a 5-20 ms delay until the start of the muscular contraction. In some embodiments, the start time T3 of the response window 102 could be further refined by accounting for specific attributes of the patent, such as body mass index (BMI), diabetes, neuropathy, degenerative nerve conditions, or other such factors that are known to affect nerve conduction velocity and/or muscular response.


The relative location of T4 within the period 100 may generally be selected such that if a muscle event 88 were to occur in response to the first stimulus 96, a sufficient amount of information related to the event would fall within the response window 102 to properly categorize it as an induced/evoked muscle response. This later bound may generally depend on the amount of time 106 between T1 and the initial onset and/or peak of the muscle response, as well as on the expected duration of the event 88. From a clinical perspective, it is most important that T3 and T4 are selected to capture at least the initial M-wave response 90 within the response window 102. Similar to T3, the offset of T4 relative to T1 may be further refined by accounting for specific attributes of the patient, such as body mass index (BMI), diabetes, neuropathy, degenerative nerve conditions, muscle fatigue, or other such factors that are known to affect nerve conduction velocity and/or muscular response.


Properly sizing the response window 102 within the period 100 between the stimuli may enable the processor 20 to summarily reject some muscle events (or other detected movements) if those events occur outside of the expected response window 102. For example, if a periodic stimulus was applied to a subject at a frequency of 2 Hz (500 ms period), any given pulse may be expected to elicit a response within about the first 100 ms of the onset of the pulse (i.e., with slight variability based on the health of the patient). If a purported muscle event 88 was detected in the later 400 ms of the period 100, it may be safe to assume that the applied stimulus did not cause that motion.


Using these assumptions, in one embodiment, the processor 20 may be configured to only perform the signal processing algorithms 70 on sensed motion or muscle events that occur within the response window 102. Such a time-gating filter may reduce the total number of potential events that must be analyzed, which may conserve processing power, improve processing speed, and reduce the potential for false positives. As mentioned above, the response window should be sized such that T1≤T3<T4<T2, however, to best realize the processing improvements, it is preferable for (T4−T3)≤(T2−T1)/2.


In some embodiments, the signal processing algorithms 70 may involve one or more analog detection techniques such as described, for example, in U.S. Pat. No. 8,343,065, issued on Jan. 1, 2013 (the '065 Patent), which is incorporated by reference in its entirety, and/or one or more digital detection techniques, such as described in US 2015/0051506, filed on Aug. 13, 2013 (the '506 Application), which also is incorporated by reference in its entirety. In the analog techniques, the processor 20 may examine one or more aspects of the MMG output signal 62 in an analog/time domain to determine if the sensed response is an artificially-induced response of the muscle to the stimulus. These analog aspects may include, for example, the time derivative of acceleration, or the maximum amplitude of the M-wave/initial response 90.


In a digital context, such as described in the '503 Application, the processor 20 may compare the frequency components of the MMG output signal (i.e., in the frequency domain) with the frequency of the applied stimulation to determine whether the sensed muscle responses and/or “events” were induced by the applied stimulus. Such a technique may be made more robust by considering only events or muscle activity that occurs within the reference window 102 and/or by aggressively filtering/attenuating or ignoring the signal outside of the response window 102 prior to applying the signal processing algorithms 70.


In some embodiments, the signal processing algorithms 70 may include one or more supervised learning algorithms that are operative to classify any sensed motion into one of a plurality of classifications that include at least whether the signal 62 is, or is not representative of an artificially-induced mechanical response of the muscle. Both classifications may provide valuable information to an operating surgeon during a procedure. Affirmatively detecting a response informs the surgeon that a nerve is proximate to the stimulator/tool, and to proceed with caution. Conversely, determining that no induced response occurred, particularly if a stimulus is provided, informs the surgeon that the nerve is not present and they can proceed in their normal manner.


In a general sense, a supervised learning algorithm is an algorithm that attempts to classify a current sample using observations made about prior samples and their known classifications. More specifically, the algorithm attempts to construct and/or optimize a model that is capable of recognizing relationships or patterns between the training inputs and training outputs, and then the algorithm uses that model to predict an output classification given a new sample. Examples of supervised learning algorithms that may be employed include neural networks, support vector machines, logistic regressions, naive Bayes classifiers, decision trees, random forests, or other such techniques or ensembles of techniques.



FIG. 6 schematically illustrates an embodiment of a supervised learning algorithm 110 that may be used to classify a current sample 112 of an MMG output signal 62 into a binary classification (i.e., an artificially induced muscle response 114, or not an artificially induced response 116). As shown, the processor 20 may initially characterize the MMG output signal 62 and/or recognized muscle event (i.e., any sensed motion relative to a baseline) according to one or more analog characteristics 118, frequency characteristics 120, and/or time-series/image characteristics 122. Using a model 124 constructed/optimized on the basis of a plurality of pre-classified training samples 126, the supervised learning algorithm 110 may then make an informed classification that minimizes an established error function or maximizes the probability of an accurate prediction.


In an embodiment, the one or more analog characteristics 118 may include, for example, max/min acceleration amplitudes, max/min velocity amplitudes, time derivative of acceleration, signal rise time, or curve fitting coefficients. Likewise, the one or more frequency characteristics 120 may include, for example, FFT coefficients, peak frequencies, peak frequency magnitudes, harmonic frequencies, or frequency fall-off. Finally, the time-series/image characteristics 120 may include a snapshot of a graph 80 of the MMG output 62 over time (similar to what is shown in FIG. 5). In general, as discussed in the '065 Patent and in the '506 Application, artificially-induced muscle responses have certain analog and frequency characteristics that non-induced responses do not. As such, the supervised learning algorithm 110 may model these characteristics 118, 120 in the aggregate to predict the nature of the muscle event with a greater accuracy. Furthermore, in some situations, the visual attributes of an induced response may tell a more complete story than any one parameter or collection of parameters could. As such, in an embodiment, the supervised learning algorithm 110 may include an image based classifier that may attempt to classify a muscle response on the basis of a visual similarity with other previously identified induced responses.


In some embodiments, the supervised learning algorithm 110 may employ an ensemble approach to generating the output classification. In such an approach, the model 124 may include a plurality of different models/approaches that may be combined according to a weighting/costing formula to provide improved redundancy/voting. In another embodiment, the ensemble approach may use the output of one or more approaches/models as an input of another model. For example, the analog and/or frequency based detection techniques discussed in the '065 Patent and/or in the '506 Application may output a probability or likelihood that an event in question is representative of an induced response. These estimations may then be fed into, for example, a supervised learning algorithm as another input (i.e., where the supervised learning algorithm may understand situations when the pre-determined algorithms are to be trusted or not trusted). In another embodiment, each model, including any supervised learning algorithm may feed into a separate algorithm that may output a binary response or probability based upon the outcomes of the various models. This approach may use voting algorithms, probability combinations, and/or separate supervised learning algorithms to provide an output based on the prediction of each constituent model.


While each of the above-referenced signal processing algorithms 70 may alone, or in combination, provide reliable detection functionality, in some embodiments, the detection functionality may be made more robust by using one or more techniques to increase the signal to noise ratio of the MMG output signal 62. In a general sense, the signal-to-noise ratio represents how recognizable a muscle event is when occurring amidst other sensed movement, signal noise, or other occurrences within the operating room. Already, MMG technology provides a vastly improved signal-to-noise ratio from previously used EMG technology, however, further improvements are still available.


In one embodiment, the time gating approach that is reliant on the response window 102 may be used to identify and remove background noise with a higher degree of confidence than might be performed in a continuous monitoring approach. More specifically, activity that at least partially occurs outside of the response window 102 may be assumed to not have been caused by the applied stimulus, and thus may be classified as “background noise” when attempting to identify an induced muscle response. Furthermore, it may be assumed that signal content occurring across a plurality of stimuli is also not representative of an artificially induced muscle response since an induced response tends to settle out prior to the application of the next sequential stimulus. Therefore, in some embodiments, activity that occurs at least partially outside of the reference window 102 may be viewed as noise (to the induced-response detection algorithms 70) and used to tune a digital filter. This filter may then be applied to the signal prior to any of the signal processing algorithms 70 described above.



FIG. 7 schematically illustrates a method 130 of removing background noise that occurs at least partially outside of the response window 102. This method 130 begins at 132 by identifying signal content from the mechanomyography output signal 62 that exists at least partially outside of the response window 102. In some embodiments, the processor 20 may identify this signal content, for example, by converting the mechanomyography output signal 62 into the frequency domain (e.g. via a fast Fourier transform), and searching for signal content having a period (i.e., inverse of frequency) that is greater than the length of the response window 102 and/or having a frequency that is less than about the frequency of the applied stimulus. This signal content may represent motion that may extend across a plurality of stimuli/response windows and therefore is at least partially outside of any given response window 102. Alternatively, or additionally, the processor 20 may search for signal content with a faster frequency that appears in both a response window 102 and an adjacent period of time outside of the response 102. While it is preferable for each response window 102 to be filtered using content that at least partially exists in a directly adjacent period of time outside of that response window, in some embodiments, the signal content may be previously detected and recognized to occur on a recurring basis (e.g., a 10 Hz signal occurring on a 0.1 Hz period, or a half-wave rectified signal).


The processor 20 may then determine a frequency characteristic of this signal content, for example, using a fast Fourier transform (FFT) at 134. Frequency characteristics may include an identification of the dominant frequencies, harmonics, phase angles, etc.


Once this out-of-window content is identified, its frequency and phase may be used to tune a digital filter to attenuate this frequency content from the mechanomyography output signal 62 within at least the response window 102 (at 136). This cleaned up response window may then be passed to the one or more signal processing algorithms 70 (at 138), which may be used to determine the occurrence of an artificially-induced response of the muscle.


As may be appreciated, this background identification and removal technique may improve signal-to-noise ratio of the MMG output signal 62 by reducing the noise (i.e., the denominator). In some embodiments, the signal-to-noise ratio may also be improved using techniques that improve the quality of the signal during an event (i.e., the numerator). In one embodiment, the quality of the signal may be improved through the use of an MMG sensor 22 that is capable of sensing motion in three orthogonal axes (i.e. a “tri-axis mechanical sensor”).


In an embodiment, one or more of the mechanical sensors 22 described above may be a tri-axis mechanical sensor that is specially configured to monitor a local mechanical movement of a muscle of the subject 14 in three orthogonal axes. In a first configuration, the sensed motion from each of the three axes may be independently fed into the signal processing algorithms 70. In doing so, the algorithms 70 may have more information about the event upon which they can base their classification. This technique may be particularly useful with the supervised learning algorithms 110, which may identify patterns between the various channels that are indicative of an induced muscle response.


In some embodiments, the sensed motion in each of the three orthogonal axes may be combined to form a resultant vector that more accurately describes the magnitude and direction of the sensed response. More specifically, the resultant vector will always have a magnitude that is greater than or equal to the magnitude of any one axis; and, with the larger magnitude comes a greater signal. As an additional benefit, the use of a tri-axis mechanical sensor may reduce any signal variance/error that is attributable to improper sensor placement. For example, if a sensor is not generally centered on a muscle group, the sensed motion may include some component that is tangential to the skin surface (i.e., where the contracting of the muscle causes off-center portions of the skin to rotate inward or outward while the central region may move in a substantially normal direction).


As an additional filtering technique, in one configuration, the resultant vector and/or any constituent vectors may only be considered by the signal processing algorithms 70 only if the magnitude of the sensed motion normal to the skin surface is greater than the sensed motion in any one axis that is tangential to the skin surface (and/or greater than the resultant vector formed between the two tangential axes). Such a filtering technique is premised on the understanding that an induced muscle response is primarily represented by motion in a direction normal to the skin surface. If the sensed motion tangential to the skin surface is too large relative to the motion normal skin, then there is a high probability that the sensed motion is not an induced muscle response, and therefore may be disregarded. In an embodiment, the sensed motion may be disregarded unless the magnitude of the normal motion is more than twice the magnitude of the resultant tangential motion. In other embodiments, the sensed motion may be disregarded unless the magnitude of the normal motion is more than three times, or four times, or even five times the magnitude of the resultant tangential motion.


Following the filtering and performance of the one or more signal processing algorithms 70, if the processor 20 concludes that a sensed motion and/or muscle event is an artificially-induced muscle response, then the processor 20 may provide an indication to a user corresponding to the detected event. In one configuration, this indication may include one or more of an illuminated light/LED, a colored light/LED, a textual or symbolic alert on a display device associated with the processor 20, a vibration in the handle of the stimulator, and an audible alert such as a single frequency alert, a multiple frequency alert, and/or an audible natural language alert. Moreover, the indication/alert may include an estimation of the proximity between the electrode and the nerve, such as may be derived using a lookup table as described above, or as explained in U.S. Pat. No. 8,343,065 to Bartol, et al., entitled “NEURAL EVENT DETECTION,” which is hereby incorporated by reference in its entirety and for all of the disclosure set forth therein.


In addition to simply detecting an artificially induced muscle response, in an embodiment, the processor 20 may further be configured to examine the timing between a provided stimulus and a muscle response induced by this stimulus. If this timing changes by more than the threshold amount, the processor 20 may provide an alert to a user to indicate a change in the health of the nerve that innervates the responding muscle. As a general premise, nerve conduction velocity and/or muscle response latency should be faster with a healthy nerve than with an injured or impinged nerve.


Therefore, as generally illustrated in FIG. 8, in an embodiment, the processor 20 may be configured to identify a time 150 of a first muscle event 152 that occurs within a first response window 154. The first muscle event 152 is induced by a first stimulus 156 that begins at the first time 158. As generally shown, the muscle event includes an initial M-wave response 160 having a peak magnitude 162, followed by later responses 164 such as the H-reflex. The processor 20 may be configured to determine a first response latency 166 between the first time 156 and the time 150 of the muscle event 152. While it is not critical where the time of the stimulus is recorded, it important that the latency 166 is consistently recorded between measurements. As such, the most optimal times to log the time of the stimulus is on either the rising or falling edge, and the most optimal time to log the time of the event is at the maximum peak (i.e., as peak detection techniques are easily implemented).


Once a baseline latency is established, either by computing a single latency, or an average of many successively computed latencies, future latencies (e.g., subsequent latency 168) may be computed in a similar manner and compared to the baseline. More specifically, the processor 20 may be configured to identify a time 170 of a second muscle event 172 within a second response window 174 following a subsequent stimulus 176 provided by the stimulator. The processor 20 may determine the response latency 168 between the stimulus 176 the second muscle event 172, and may then provide an alert if the second response latency 168 differs from the baseline latency by more than a predetermined threshold amount that is set to indicate either a meaningful improvement in the health of the nerve, or a meaningful impairment of the nerve. Additionally, or alternatively, the system 10 may display a constant readout that compares the nerve conduction velocity and/or muscle response latency to either a baseline level measured from that patient, or to a standard or expected velocity/latency, from which changes throughout the procedure can be gauged.


In an embodiment, the processor 20 may be configured to provide the electrical stimulus 38, via the stimulator, with a varying current magnitude that is a function of a difference between the maximum amplitude of the sensed M-wave response, and a threshold amplitude (alternatively, the current magnitude is a function of the difference between a sensed peak MMG output signal magnitude and a threshold MMG output signal magnitude).


In some surgical techniques, it may be useful for a surgeon to understand what is the minimum current amplitude of a an electrical stimulus 38 provided by the stimulator 30 to elicit a mechanical response that is greater than or equal to a predetermined threshold response. FIG. 9 illustrates an example of a graph that represents the relationship between current magnitude 180, MMG output signal (peak) magnitude 162, the distance 184 between the stimulator 30 and the nerve, and the threshold 186 response sought. If the processor 20 applies a stimulus at a known first current 188, which elicits a first MMG output magnitude 190, then the known relationships may enable the processor to use various closed-loop control techniques (e.g., various combinations of proportional, derivative, and integral control methods) to minimize the difference 192 between the sensed magnitude 190 and the threshold 186. In this example, such a closed loop control scheme would eventually arrive at a reduction of the current to the second level 194.


This closed-loop threshold hunting technique is highly dependent on an accurate model and the ability to get a consistent output signal from the sensor, which both exist using MMG technology (though are not generally possible with noisier signals such as may exist with other sensing methodologies such as EMG technology).


While the control technique generally illustrated in FIG. 9 assumes a stationary stimulator (i.e., the distance 184 does not change between the first and second current levels 188, 194, in another embodiment, the motion of the stimulator 30 may be tracked in an effort to approximate changes in distance between the stimulator and the nerve. The motion of the stimulator 30 may be tracked, for example, by including an accelerometer, inertial measuring unit, and/or gyroscope on the stimulator 30 or stimulator handle. Likewise, the motion of the stimulator 30 may be known if the stimulator is robotically controlled, or is sensed through another non-contact positioning technique. While motion of the stimulator is important, ultimately the control technique must understand motion of the stimulator relative to the nerve. Therefore, in some embodiments, the system may employ nerve detection and mapping techniques such as described in U.S. Patent Application No. 2017/0020611, filed on Oct. 5, 2016, which is incorporated by reference in its entirety.



FIG. 10 schematically illustrates a method 200 of detecting an artificially-induced mechanical response of a muscle to a stimulus provided within an intracorporeal treatment area of a human subject. In general, the method 200 begins with the processor 20 transmitting a periodic electrical stimulus to a stimulator within the intracorporeal treatment area (at 202). Similar to that described above, the periodic stimulus includes at least a first stimulus beginning at a first time (T1), and a second, consecutive stimulus beginning at a second time (T2).


Concurrently with the transmission of the stimulus, the processor 20 may be receiving a mechanomyography output signal from one or more non-invasive mechanical sensors in mechanical communication with one or more muscles of the subject (at 204). The processor 20 may analyze the mechanomyography output signal (at 206) specifically within a response window that corresponds to a period of time when an induced response of the muscle to the first stimulus is likely to occur. The response window may extend between a third time (T3) and a fourth time (T4) such that T1≤T3<T4<T2.


In some embodiments, the step of analyzing the mechanomyography output signal within the response window may include performing one or more signal processing algorithms 70 on the sensed MMG output signal. In one embodiment, these signal processing algorithms 70 may be performed only if the motion occurs within the response window. In one embodiment, the signal processing algorithms 70 may include a supervised learning algorithm that examines one or more characteristics of the MMG output signal within the response window to determine if the sensed motion is an artificially-induced muscle response. The supervised learning algorithm may generally be operative to classify the motion into one of a plurality of classifications that include either that the sensed motion (and/or response window as a whole) is representative of an induced muscle response, or that the sensed motion (and/or response window) is not representative of an induced muscle response.


In some embodiments, the signal processing algorithms 70 may be performed on a “cleaned” signal that has background noise dynamically reduced or attenuated. Such a cleaning process my include identifying signal content from the mechanomyography output signal that exists at least partially outside of the response window; determining a frequency component of the signal content; and attenuating the frequency component from the mechanomyography output signal within the response window.


At step 208, the processor 20 may then provide an indication to a user that the sensed motion was an artificially-induced muscle response only if the motion occurs within the response window.


In addition to use as a stand alone, or hand-held nerve monitoring apparatus, the present nerve monitoring system 10 and described artificially-induced mechanical muscle response detection algorithms (as described within method 100) may be used by a robotic surgical system, such as described in U.S. Pat. No. 8,855,622, issued Oct. 7, 2014 entitled “ROBOTIC SURGICAL SYSTEM WITH MECHANOMYOGRAPHY FEEDBACK,” which is incorporated by reference in its entirety and for all of the disclosure set forth therein. In such a system, the above-described neural monitoring system 10 may be used to provide one or more control signals to a robotic surgical system if an artificially-induced mechanical muscle response is detected. In such an embodiment, the one or more elongate medical instruments 30 described above may be robotically controlled in up to 6 or more degrees of freedom/motion by a robotic controller. This instrument may be configured to perform a surgical procedure within an intracorporeal treatment area at the direction of the robotic controller, and may provide an electrical stimulus 38 in the manner described above. If an artificially-induced mechanical muscle response is detected, the neural monitoring system 10 may instruct the robotic controller (via the provided control signal) to limit the range of available motion of the elongate medical instrument 30 and/or to prevent an actuation of an end effector that may be disposed on the instrument 30 and controllable by the robotic controller.


While the best modes for carrying out the present technology have been described in detail, those familiar with the art to which this technology relates will recognize various alternative designs and embodiments that are within the scope of the appended claims. It is intended that all matter contained in the above description or shown in the accompanying drawings shall be interpreted as illustrative only and not as limiting.


Various advantages and features of the disclosure are further set forth in the following clauses:


Clause 1: A neural monitoring system for detecting an artificially-induced mechanical response of a muscle to a stimulus provided within an intracorporeal treatment area of a human subject, the intracorporeal treatment area including a nerve that innervates the muscle, the neural monitoring system comprising: a non-invasive mechanical sensor configured to be placed in mechanical communication with the muscle and to generate a mechanomyography output signal that corresponds to a sensed mechanical movement of the muscle; a stimulator configured to provide a periodic stimulus within the intracorporeal treatment area, the periodic stimulus including at least a first stimulus beginning at a first time (T1), and a second, consecutive stimulus beginning at a second time (T2); and a processor in communication with the mechanical sensor and the stimulator, the processor configured to: provide the periodic stimulus to the stimulator; receive the mechanomyography output signal from the mechanical sensor; analyze a response window of the mechanomyography output signal to determine if the first stimulus induced a response of the muscle; and provide an indication to a user if it is determined that the first stimulus induced a response of the muscle within the response window; wherein the response window corresponds to a period of time when an induced response to the first stimulus is likely to occur; and wherein the response window extends between a third time (T3) and a fourth time (T4) such that T1≤T3<T4<T2.


Clause 2: The neural monitoring system of clause 1, wherein the processor is further configured to determine if the first stimulus induced a response of the muscle by analyzing the mechanomyography output signal only within the response window.


Clause 3: The neural monitoring system of any of clauses 1-2, wherein the processor is configured to determine if the first stimulus induced a response of the muscle by examining one or more characteristics of the mechanomyography output signal within the response window using a supervised learning algorithm; and wherein the supervised learning algorithm is operative to classify the response window into one of a plurality of classifications comprising: the response window is representative of an artificially-induced mechanical response of the muscle; and the response window is not representative of an artificially-induced mechanical response of the muscle.


Clause 4: The neural monitoring system of clause 3, wherein the one or more characteristics of the mechanomyography output signal includes a graph of the amplitude of the mechanomyography output signal throughout the response window as a function of time; and wherein the supervised learning algorithm includes an image-based classifier operative to analyze one or more graphical aspects of the graph.


Clause 5: The neural monitoring system of any of clauses 1-4, wherein the mechanical sensor is a tri-axis accelerometer operative to monitor acceleration in three mutually orthogonal axes; and wherein the processor is configured to determine if the first stimulus induced a response of the muscle using a magnitude of a resultant vector calculated from the monitored acceleration in each of the three axes.


Clause 6: The neural monitoring system of clause 5, wherein the processor is configured to determine if the first stimulus induced a response of the muscle only if a magnitude of a movement of the muscle in a direction normal to the skin surface is greater than a magnitude of a movement of the muscle in a direction that is tangential to the skin surface.


Clause 7: The neural monitoring system of any of clauses 1-6, wherein (T4−T3)≤(T2−T1)/2.


Clause 8: The neural monitoring system of any of clauses 1-7, wherein the processor is further configured to: identify signal content from the mechanomyography output signal that exists at least partially outside of the response window; determine a frequency component of the signal content; attenuate the frequency component from the mechanomyography output signal within the response window; and wherein the processor is configured to determine if the first stimulus induced a response of the muscle using the attenuated mechanomyography output signal within the response window.


Clause 9: The neural monitoring system of clause 8, wherein the signal content from the mechanomyography output signal exists at least partially between T1 and T2.


Clause 10: The neural monitoring system of any of clauses 8-9, wherein the periodic stimulus includes a plurality of stimuli; and wherein the signal content exists across the plurality of stimuli.


Clause 11: The neural monitoring system of any of clauses 1-10, wherein the processor is further configured to identify a time corresponding to a detected induced muscle response within the response window; determine a first response latency between the first stimulus and the time corresponding to a detected induced muscle response; identify a time corresponding to a subsequently detected muscle response that is induced by a subsequent stimulus provided by the stimulator; determine a second response latency between the subsequent stimulus and the time of the subsequently detected muscle response; provide an alert if the second response latency differs from the first response latency by more than a predetermined amount.


Clause 12: The neural monitoring system of any of clauses 1-11, wherein the first stimulus has a first current magnitude, a subsequent stimulus has a second current magnitude, and a detected induced muscle response to the first stimulus has a mechanomyography output signal magnitude; and wherein the second current magnitude is: different from the first current magnitude; and is a function of a difference between the mechanomyography output signal magnitude and a threshold output signal magnitude.


Clause 13: The neural monitoring system of clause 12, wherein the second current magnitude is proportional to the difference between the mechanomyography output signal magnitude and a threshold output signal magnitude.


Clause 14: A method of detecting an artificially-induced mechanical response of a muscle to a stimulus provided within an intracorporeal treatment area of a human subject, the intracorporeal treatment area including a nerve that innervates the muscle, the method comprising: transmitting a periodic electrical stimulus to a stimulator within the intracorporeal treatment area, the periodic stimulus including at least a first stimulus beginning at a first time (T1), and a second, consecutive stimulus beginning at a second time (T2); receiving a mechanomyography output signal from a non-invasive mechanical sensor in mechanical communication with the muscle, wherein the mechanomyography output signal corresponds to a sensed mechanical movement of the muscle; analyzing the mechanomyography output signal within a response window of time to determine if the sensed motion is representative of an artificially-induced response of the muscle, wherein the response window corresponds to a period when an induced response of the muscle to the first stimulus is likely to occur, the response window extending between a third time (T3) and a fourth time (T4) such that T1≤T3<T4<T2; and providing an indication to a user that the sensed motion is an artificially-induced muscle response only if the motion occurs within the response window.


Clause 15: The method of clause 14, further comprising: analyzing the mechanomyography output signal only within the response window to determine if the sensed motion is an artificially-induced muscle response.


Clause 16: The method of any of clauses 14-15, further comprising: examining one or more characteristics of the mechanomyography output signal within the response window using a supervised learning algorithm to determine if the sensed mechanical movement of the muscle is an artificially-induced muscle response; and wherein the supervised learning algorithm is operative to classify the mechanomyography output signal within the response window into one of a plurality of classifications comprising: the response window is representative of an artificially-induced mechanical response of the muscle; and the response window is not representative of an artificially-induced mechanical response of the muscle.


Clause 17: The method of any of clauses 14-16, wherein (T4−T3)≤(T−2−T1)/2.


Clause 18: The method of any of clauses 14-17, further comprising: identifying signal content from the mechanomyography output signal that exists at least partially outside of the response window; determining a frequency component of the signal content; attenuating the frequency component from the mechanomyography output signal within the response window; and determining the occurrence of a muscle event using the attenuated mechanomyography output signal within the response window.


Clause 19: The method of any of clauses 14-18, further comprising: identifying a time of the muscle response within the response window; determining a first response latency between T1 and the time of the muscle response; identifying a time of a second muscle response within a second response window following a third stimulus provided by the stimulator beginning at a third time (T3); determining a second response latency between T3 and the time of the second muscle response; providing an alert if the second response latency differs from the first response latency by more than a predetermined amount.


Clause 20: The method of any of clauses 14-19, wherein the first stimulus has a first current magnitude, the second stimulus has a second current magnitude, and the muscle response has a mechanomyography output signal magnitude; and wherein transmitting the periodic electrical stimulus includes transmitting the second current magnitude such that it is: different from the first current magnitude; and is a function of a difference between the mechanomyography output signal magnitude and a threshold output signal magnitude.


Clause 21: A mechanomyography sensor configured to be placed in mechanical communication with a muscle of a human subject, the mechanomyography sensor comprising: a non-invasive mechanical sensor operative to sense a mechanical movement of the muscle and to generate a mechanomyography output signal that corresponds to the sensed mechanical movement; a communication means for transmitting the mechanomyography output signal to a processor that is operative to: provide a periodic stimulus to a stimulator, including at least a first stimulus beginning at a first time (T1), and a second, consecutive stimulus beginning at a second time (T2); receive the mechanomyography output signal from the mechanical sensor; analyze the mechanomyography output signal within a response window to determine if the first stimulus induced a response of the muscle; wherein the response window corresponds to a period of time when an induced response to the first stimulus is likely to occur; and wherein the response window extends between a third time (T3) and a fourth time (T4) such that T1≤T3<T4<T2; and provide an indication to a user if it is determined that the first stimulus induced a response of the muscle within the response window.


Clause 22: The mechanomyography sensor of clause 21, wherein the mechanical sensor is a tri-axis accelerometer operative to monitor acceleration in three mutually orthogonal axes; and wherein the processor is further operative to determine if the first stimulus induced a response of the muscle using a magnitude of a resultant vector calculated from the monitored acceleration in each of the three axes.


Clause 23: The mechanomyography sensor of clause 22, wherein the processor is further operative to determine if the first stimulus induced a response of the muscle only if a magnitude of a movement of the muscle in a direction normal to the skin surface is greater than a magnitude of a movement of the muscle in a direction that is tangential to the skin surface.

Claims
  • 1. A neural monitoring system for detecting an artificially-induced mechanical response of a muscle to a stimulus provided within an intracorporeal treatment area of a human subject, the intracorporeal treatment area including a nerve that innervates the muscle, the neural monitoring system comprising: a non-invasive mechanical sensor configured to be placed in mechanical communication with the muscle and to generate a mechanomyography output signal that corresponds to a sensed mechanical movement of the muscle;a stimulator configured to provide a periodic stimulus within the intracorporeal treatment area, the periodic stimulus including at least a first stimulus beginning at a first time (T1), and a second, consecutive stimulus beginning at a second time (T2); anda processor in communication with the mechanical sensor and the stimulator, the processor configured to: provide the periodic stimulus to the stimulator;receive the mechanomyography output signal from the mechanical sensor;analyze a response window of the mechanomyography output signal to determine if the first stimulus induced a response of the muscle; andprovide an indication to a user if it is determined that the first stimulus induced a response of the muscle within the response window;wherein the response window corresponds to a period of time when an induced response to the first stimulus is likely to occur; andwherein the response window extends between a third time (T3) and a fourth time (T4) such that T1≤T3<T4<T2.
  • 2. The neural monitoring system of claim 1, wherein the processor is further configured to determine if the first stimulus induced a response of the muscle by analyzing the mechanomyography output signal only within the response window.
  • 3. The neural monitoring system of claim 1, wherein the processor is configured to determine if the first stimulus induced a response of the muscle by examining one or more characteristics of the mechanomyography output signal within the response window using a supervised learning algorithm; and wherein the supervised learning algorithm is operative to classify the response window into one of a plurality of classifications, the plurality of classifications comprising: a first classification wherein the mechanomyography output signal within the response window is indicative of an artificially-induced mechanical response of the muscle; anda second classification wherein the mechanomyography output signal within the response window is not indicative of an artificially-induced mechanical response of the muscle.
  • 4. The neural monitoring system of claim 3, wherein the one or more characteristics of the mechanomyography output signal includes a graph of an amplitude of the mechanomyography output signal throughout the response window as a function of time; and wherein the supervised learning algorithm includes an image-based classifier operative to analyze one or more graphical aspects of the graph.
  • 5. The neural monitoring system of claim 1, wherein the mechanical sensor is a tri-axis accelerometer operative to monitor acceleration in three mutually orthogonal axes; and wherein the processor is configured to determine if the first stimulus induced a response of the muscle using a magnitude of a resultant vector calculated from the monitored acceleration in each of the three axes.
  • 6. The neural monitoring system of claim 5, wherein the processor is configured to determine if the first stimulus induced a response of the muscle only if a magnitude of a movement of the muscle in a direction normal to a skin surface is greater than a magnitude of a movement of the muscle in a direction that is tangential to the skin surface.
  • 7. The neural monitoring system of claim 1, wherein (T4−T3)≤(T2−T1)/2.
  • 8. The neural monitoring system of claim 1, wherein the processor is further configured to: identify signal content from the mechanomyography output signal that exists at least partially outside of the response window;determine a frequency component of the signal content;attenuate the frequency component from the mechanomyography output signal within the response window; andwherein the processor is configured to determine if the first stimulus induced a response of the muscle using the attenuated mechanomyography output signal within the response window.
  • 9. The neural monitoring system of claim 8, wherein the signal content from the mechanomyography output signal exists at least partially between T1 and T2.
  • 10. The neural monitoring system of claim 8, wherein the periodic stimulus includes a plurality of stimuli; and wherein the signal content exists across the plurality of stimuli.
  • 11. The neural monitoring system of claim 1, wherein the processor is further configured to identify a time corresponding to a detected induced muscle response within the response window;determine a first response latency between the first stimulus and the time corresponding to a detected induced muscle response;identify a time corresponding to a subsequently detected muscle response that is induced by a subsequent stimulus provided by the stimulator;determine a second response latency between the subsequent stimulus and the time of the subsequently detected muscle response; andprovide an alert if the second response latency differs from the first response latency by more than a predetermined amount.
  • 12. The neural monitoring system of claim 1, wherein the first stimulus has a first current magnitude, a subsequent stimulus has a second current magnitude, and a detected induced muscle response to the first stimulus has a mechanomyography output signal magnitude; and wherein the second current magnitude is: different from the first current magnitude; andis a function of a difference between the mechanomyography output signal magnitude and a threshold output signal magnitude.
  • 13. The neural monitoring system of claim 12, wherein the second current magnitude is proportional to the difference between the mechanomyography output signal magnitude and a threshold output signal magnitude.
  • 14. A method of detecting an artificially-induced mechanical response of a muscle to a stimulus provided within an intracorporeal treatment area of a human subject, the intracorporeal treatment area including a nerve that innervates the muscle, the method comprising: transmitting a periodic electrical stimulus to a stimulator within the intracorporeal treatment area, the periodic stimulus including at least a first stimulus beginning at a first time (T1), and a second, consecutive stimulus beginning at a second time (T2);receiving a mechanomyography output signal from a non-invasive mechanical sensor in mechanical communication with the muscle, wherein the mechanomyography output signal corresponds to a sensed mechanical movement of the muscle;analyzing the mechanomyography output signal within a response window of time to determine if the sensed motion is representative of an artificially-induced response of the muscle, wherein the response window corresponds to a period when an induced response of the muscle to the first stimulus is likely to occur, the response window extending between a third time (T3) and a fourth time (T4) such that T1≤T3<T4<T2; andproviding an indication to a user that the sensed motion is an artificially-induced muscle response only if the motion occurs within the response window.
  • 15. The method of claim 14, further comprising: analyzing the mechanomyography output signal only within the response window to determine if the sensed motion is an artificially-induced muscle response.
  • 16. The method of claim 14, further comprising: examining one or more characteristics of the mechanomyography output signal within the response window using a supervised learning algorithm to determine if the sensed mechanical movement of the muscle is an artificially-induced muscle response; and wherein the supervised learning algorithm is operative to classify the mechanomyography output signal within the response window into one of a plurality of classifications, the plurality of classifications comprising: a first classification wherein the mechanomyography output signal within the response window is indicative of an artificially-induced mechanical response of the muscle; anda second classification wherein the mechanomyography output signal within the response window is not indicative of an artificially-induced mechanical response of the muscle.
  • 17. The method of claim 14, wherein (T4−T3)≤(T2−T1)/2.
  • 18. The method of claim 14, further comprising: identifying signal content from the mechanomyography output signal that exists at least partially outside of the response window;determining a frequency component of the signal content;attenuating the frequency component from the mechanomyography output signal within the response window; anddetermining an occurrence of a muscle event using the attenuated mechanomyography output signal within the response window.
  • 19. The method of claim 14, further comprising: identifying a time of the muscle response within the response window;determining a first response latency between T1 and the time of the muscle response;identifying a time of a second muscle response within a second response window following a third stimulus provided by the stimulator beginning at a third time (T3);determining a second response latency between T3 and the time of the second muscle response; andproviding an alert if the second response latency differs from the first response latency by more than a predetermined amount.
  • 20. The method of claim 14, wherein the first stimulus has a first current magnitude, the second stimulus has a second current magnitude, and the muscle response has a mechanomyography output signal magnitude; and wherein transmitting the periodic electrical stimulus includes transmitting the second current magnitude such that the second current magnitude is: different from the first current magnitude; andis a function of a difference between the mechanomyography output signal magnitude and a threshold output signal magnitude.
US Referenced Citations (325)
Number Name Date Kind
3200814 Taylor et al. Aug 1965 A
3565080 Ide et al. Feb 1971 A
3797010 Adler et al. Mar 1974 A
4155353 Rea et al. May 1979 A
4493327 Bergelson et al. Jan 1985 A
4807642 Brown Feb 1989 A
4817628 Zealear et al. Apr 1989 A
4940453 Cadwell Jul 1990 A
4994015 Cadwell Feb 1991 A
5047005 Cadwell Sep 1991 A
5078674 Cadwell Jan 1992 A
5116304 Cadwell May 1992 A
5178145 Rea Jan 1993 A
5284153 Raymond et al. Feb 1994 A
5284154 Raymond et al. Feb 1994 A
5482038 Ruff Jan 1996 A
5566678 Cadwell Oct 1996 A
5593429 Ruff Jan 1997 A
5631667 Cadwell May 1997 A
5775331 Raymond et al. Jul 1998 A
5860939 Wofford et al. Jan 1999 A
5888370 Becker et al. Mar 1999 A
5993630 Becker et al. Nov 1999 A
5993632 Becker et al. Nov 1999 A
6030401 Marino Feb 2000 A
6093205 McLeod et al. Jul 2000 A
6181961 Prass Jan 2001 B1
6183518 Ross et al. Feb 2001 B1
6206921 Guagliano et al. Mar 2001 B1
6221082 Marino et al. Apr 2001 B1
6224603 Marino May 2001 B1
6251140 Marino et al. Jun 2001 B1
6264659 Ross et al. Jul 2001 B1
6266394 Marino Jul 2001 B1
6266558 Gozani et al. Jul 2001 B1
6280447 Marino et al. Aug 2001 B1
6287832 Becker et al. Sep 2001 B1
6290724 Marino Sep 2001 B1
6324432 Rigaux et al. Nov 2001 B1
6361508 Johnson et al. Mar 2002 B1
6368325 McKinley et al. Apr 2002 B1
6387070 Marino et al. May 2002 B1
6387130 Stone et al. May 2002 B1
6436143 Ross et al. Aug 2002 B1
6466817 Kaula et al. Oct 2002 B1
6478805 Marino et al. Nov 2002 B1
6485518 Cornwall et al. Nov 2002 B1
6491626 Stone et al. Dec 2002 B1
6500128 Marino Dec 2002 B2
6519319 Marino et al. Feb 2003 B1
6530930 Marino et al. Mar 2003 B1
6533797 Stone et al. Mar 2003 B1
6540747 Marino Apr 2003 B1
6564078 Marino et al. May 2003 B1
6638281 Gorek Oct 2003 B2
6641708 Becker et al. Nov 2003 B1
6654634 Prass Nov 2003 B1
6739112 Marino May 2004 B1
6760616 Hoey et al. Jul 2004 B2
6764452 Gillespie et al. Jul 2004 B1
6764489 Ferree Jul 2004 B2
6802844 Ferree Oct 2004 B2
6805668 Cadwell Oct 2004 B1
6807438 Brun Del Re et al. Oct 2004 B1
6843790 Ferree Jan 2005 B2
6852126 Ahlgren Feb 2005 B2
6870109 Villarreal Mar 2005 B1
6887248 McKinley et al. May 2005 B2
6923814 Hildebrand et al. Aug 2005 B1
6945973 Bray Sep 2005 B2
6964674 Matsuura et al. Nov 2005 B1
6972199 Lebouitz et al. Dec 2005 B2
6981990 Keller Jan 2006 B2
7001432 Keller et al. Feb 2006 B2
7025769 Ferree Apr 2006 B1
7050848 Hoey et al. May 2006 B2
7072521 Cadwell Jul 2006 B1
7079883 Marino et al. Jul 2006 B2
7160303 Keller Jan 2007 B2
7162850 Marino et al. Jan 2007 B2
7166113 Arambula et al. Jan 2007 B2
7175662 Link et al. Feb 2007 B2
7177677 Kaula et al. Feb 2007 B2
7207949 Miles et al. Apr 2007 B2
7214197 Prass May 2007 B2
7214225 Ellis et al. May 2007 B2
7216001 Hacker et al. May 2007 B2
7230688 Villarreal Jun 2007 B1
7236832 Hemmerling et al. Jun 2007 B2
7267691 Keller et al. Sep 2007 B2
7296500 Martinelli Nov 2007 B1
7320689 Keller Jan 2008 B2
7338531 Ellis et al. Mar 2008 B2
7341590 Ferree Mar 2008 B2
7367958 McBean et al. May 2008 B2
7374448 Jepsen et al. May 2008 B1
7379767 Rea May 2008 B2
7470236 Kelleher et al. Dec 2008 B1
7485146 Crook et al. Feb 2009 B1
7522953 Kaula et al. Apr 2009 B2
7527629 Link et al. May 2009 B2
7527649 Blain May 2009 B1
7553307 Bleich et al. Jun 2009 B2
7555343 Bleich Jun 2009 B2
7569067 Keller Aug 2009 B2
7578819 Bleich et al. Aug 2009 B2
7582058 Miles et al. Sep 2009 B1
7583991 Rea Sep 2009 B2
7611522 Gorek Nov 2009 B2
7618423 Valentine et al. Nov 2009 B1
7628813 Link Dec 2009 B2
7634315 Cholette Dec 2009 B2
7657308 Miles et al. Feb 2010 B2
7664544 Miles et al. Feb 2010 B2
7666195 Kelleher et al. Feb 2010 B2
7668588 Kovacs Feb 2010 B2
7691057 Miles et al. Apr 2010 B2
7693562 Marino et al. Apr 2010 B2
7708776 Blain et al. May 2010 B1
7713463 Reah et al. May 2010 B1
7722613 Sutterlin et al. May 2010 B2
7722673 Keller May 2010 B2
7738968 Bleich Jun 2010 B2
7738969 Bleich Jun 2010 B2
7740631 Bleich et al. Jun 2010 B2
7766816 Chin et al. Aug 2010 B2
7776049 Curran et al. Aug 2010 B1
7776094 McKinley et al. Aug 2010 B2
7785248 Annest et al. Aug 2010 B2
7785253 Arambula et al. Aug 2010 B1
7815682 Peterson et al. Oct 2010 B1
7819801 Miles et al. Oct 2010 B2
7828855 Ellis et al. Nov 2010 B2
7833251 Ahlgren et al. Nov 2010 B1
7857813 Schmitz et al. Dec 2010 B2
7862592 Peterson et al. Jan 2011 B2
7862614 Keller et al. Jan 2011 B2
7867277 Tohmeh Jan 2011 B1
7883527 Matsuura et al. Feb 2011 B2
7887538 Bleich et al. Feb 2011 B2
7887568 Ahlgren Feb 2011 B2
7887595 Pimenta Feb 2011 B1
7892173 Miles et al. Feb 2011 B2
7901430 Matsuura et al. Mar 2011 B2
7905840 Pimenta et al. Mar 2011 B2
7905886 Curran et al. Mar 2011 B1
7914350 Bozich et al. Mar 2011 B1
7918849 Bleich et al. Apr 2011 B2
7918891 Curran et al. Apr 2011 B1
7920922 Gharib et al. Apr 2011 B2
7927337 Keller Apr 2011 B2
7935051 Miles et al. May 2011 B2
7938830 Saadat et al. May 2011 B2
7942104 Butcher et al. May 2011 B2
7942826 Scholl et al. May 2011 B1
7946236 Butcher May 2011 B2
7959577 Schmitz et al. Jun 2011 B2
7962191 Marino et al. Jun 2011 B2
7963915 Bleich Jun 2011 B2
7963927 Kelleher et al. Jun 2011 B2
7981058 Akay Jul 2011 B2
7981144 Geist et al. Jul 2011 B2
7991463 Kelleher et al. Aug 2011 B2
8000782 Gharib et al. Aug 2011 B2
8005535 Gharib et al. Aug 2011 B2
8012212 Link et al. Sep 2011 B2
8016767 Miles et al. Sep 2011 B2
8027716 Gharib et al. Sep 2011 B2
8048080 Bleich et al. Nov 2011 B2
8050769 Gharib et al. Nov 2011 B2
8055349 Gharib et al. Nov 2011 B2
8062298 Schmitz et al. Nov 2011 B2
8062300 Schmitz et al. Nov 2011 B2
8062369 Link Nov 2011 B2
8062370 Keller et al. Nov 2011 B2
8063770 Costantino Nov 2011 B2
8068912 Kaula et al. Nov 2011 B2
8070812 Keller Dec 2011 B2
8074591 Butcher et al. Dec 2011 B2
8075499 Nathan et al. Dec 2011 B2
8075601 Young Dec 2011 B2
8083685 Fagin et al. Dec 2011 B2
8083796 Raiszadeh et al. Dec 2011 B1
8088163 Kleiner Jan 2012 B1
8088164 Keller Jan 2012 B2
8090436 Hoey et al. Jan 2012 B2
8092455 Neubardt et al. Jan 2012 B2
8092456 Bleich et al. Jan 2012 B2
8103339 Rea Jan 2012 B2
8114019 Miles et al. Feb 2012 B2
8114162 Bradley Feb 2012 B1
8123668 Annest et al. Feb 2012 B2
8133173 Miles et al. Mar 2012 B2
8137284 Miles et al. Mar 2012 B2
8147421 Farquhar et al. Apr 2012 B2
8147551 Link et al. Apr 2012 B2
8165653 Marino et al. Apr 2012 B2
8167915 Ferree et al. May 2012 B2
8172750 Miles et al. May 2012 B2
8206312 Farquhar Jun 2012 B2
8255044 Miles et al. Aug 2012 B2
8255045 Gharib et al. Aug 2012 B2
8303515 Miles et al. Nov 2012 B2
8337410 Kelleher et al. Dec 2012 B2
8343065 Bartol et al. Jan 2013 B2
8343079 Bartol et al. Jan 2013 B2
8394129 Morgenstern Lopez et al. Mar 2013 B2
8500653 Farquhar Aug 2013 B2
8500738 Wolf, II Aug 2013 B2
8517954 Bartol et al. Aug 2013 B2
8535224 Cusimano Reaston et al. Sep 2013 B2
8538539 Gharib et al. Sep 2013 B2
8556808 Miles et al. Oct 2013 B2
8562539 Marino Oct 2013 B2
8562660 Peyman Oct 2013 B2
8568317 Gharib et al. Oct 2013 B1
8591431 Calancie et al. Nov 2013 B2
8641638 Kelleher et al. Feb 2014 B2
8731654 Johnson et al. May 2014 B2
8784330 Scholl et al. Jul 2014 B1
8792977 Kakei et al. Jul 2014 B2
8855822 Bartol et al. Oct 2014 B2
8864654 Kleiner et al. Oct 2014 B2
8936626 Tohmeh et al. Jan 2015 B1
8945004 Miles et al. Feb 2015 B2
8958869 Kelleher et al. Feb 2015 B2
8983593 Bartol et al. Mar 2015 B2
8989855 Murphy et al. Mar 2015 B2
8989866 Gharib et al. Mar 2015 B2
9014776 Marino et al. Apr 2015 B2
9014797 Shiffman et al. Apr 2015 B2
9037250 Kaula et al. May 2015 B2
9066701 Finley et al. Jun 2015 B1
9084551 Brunnett et al. Jul 2015 B2
9131947 Ferree Sep 2015 B2
9192415 Arnold et al. Nov 2015 B1
9295396 Gharib et al. Mar 2016 B2
9295401 Cadwell Mar 2016 B2
9301711 Bartol et al. Apr 2016 B2
9392953 Gharib Jul 2016 B1
9446259 Phillips et al. Sep 2016 B2
20010031916 Bennett et al. Oct 2001 A1
20020038092 Stanaland et al. Mar 2002 A1
20020165590 Crowe et al. Nov 2002 A1
20030074037 Moore et al. Apr 2003 A1
20040077969 Onda et al. Apr 2004 A1
20040082877 Kouou et al. Apr 2004 A1
20040186535 Knowlton Sep 2004 A1
20040243018 Organ et al. Dec 2004 A1
20050075578 Gharib et al. Apr 2005 A1
20050085741 Hoskonen et al. Apr 2005 A1
20050102007 Ayal et al. May 2005 A1
20050240086 Akay Oct 2005 A1
20050245839 Stivoric et al. Nov 2005 A1
20050280531 Fadem et al. Dec 2005 A1
20050283204 Buhlmann et al. Dec 2005 A1
20060020177 Seo et al. Jan 2006 A1
20060052726 Weisz et al. Mar 2006 A1
20060135888 Mimnagh-Kelleher et al. Jun 2006 A1
20060270949 Mathie et al. Nov 2006 A1
20070038155 Kelly et al. Feb 2007 A1
20070049826 Willis Mar 2007 A1
20070232958 Donofrio et al. Oct 2007 A1
20070265675 Lund et al. Nov 2007 A1
20070276270 Tran Nov 2007 A1
20070296571 Kolen Dec 2007 A1
20080051643 Park et al. Feb 2008 A1
20080058656 Costello et al. Mar 2008 A1
20080167695 Tehrani et al. Jul 2008 A1
20080234767 Salmon et al. Sep 2008 A1
20080287761 Hayter et al. Nov 2008 A1
20080306363 Chaiken et al. Dec 2008 A1
20080306397 Bonmassar et al. Dec 2008 A1
20080312560 Jamsen et al. Dec 2008 A1
20080312709 Volpe et al. Dec 2008 A1
20090036747 Hayter et al. Feb 2009 A1
20090062696 Nathan et al. Mar 2009 A1
20090069709 Schmitz et al. Mar 2009 A1
20090069722 Flaction et al. Mar 2009 A1
20090076336 Mazar et al. Mar 2009 A1
20090171381 Schmitz et al. Jul 2009 A1
20090192416 Ernst et al. Jul 2009 A1
20090228068 Buhlmann et al. Sep 2009 A1
20090247910 Klapper Oct 2009 A1
20090306741 Hogle et al. Dec 2009 A1
20090318779 Tran Dec 2009 A1
20100137748 Sone et al. Jun 2010 A1
20100152619 Kalpaxis et al. Jun 2010 A1
20100152622 Teulings Jun 2010 A1
20100152623 Williams Jun 2010 A1
20100168559 Tegg et al. Jul 2010 A1
20100262042 Kim Oct 2010 A1
20100292617 Lei et al. Nov 2010 A1
20110004207 Wallace et al. Jan 2011 A1
20110230782 Bartol et al. Sep 2011 A1
20110237974 Bartol et al. Sep 2011 A1
20110270121 Johnson et al. Nov 2011 A1
20110301665 Mercanzini et al. Dec 2011 A1
20120053491 Nathan et al. Mar 2012 A1
20120191003 Garabedian et al. Jul 2012 A1
20130123659 Bartol et al. May 2013 A1
20130197321 Wilson Aug 2013 A1
20130204097 Rondoni et al. Aug 2013 A1
20130213659 Luyster et al. Aug 2013 A1
20130253533 Bartol et al. Sep 2013 A1
20140020178 Stashuk et al. Jan 2014 A1
20140066803 Choi Mar 2014 A1
20140088029 Sugimoto et al. Mar 2014 A1
20140121555 Scott et al. May 2014 A1
20140148725 Cadwell May 2014 A1
20140163411 Rea Jun 2014 A1
20140275926 Scott et al. Sep 2014 A1
20140276195 Papay et al. Sep 2014 A1
20140358026 Mashiach et al. Dec 2014 A1
20150032022 Stone et al. Jan 2015 A1
20150045783 Edidin Feb 2015 A1
20150051506 Wybo et al. Feb 2015 A1
20150051507 Wybo Feb 2015 A1
20150112325 Whitman Apr 2015 A1
20150230749 Gharib et al. Aug 2015 A1
20150342521 Narita et al. Dec 2015 A1
20150342621 Jackson Dec 2015 A1
20160051812 Montgomery, Jr. et al. Feb 2016 A1
20160121109 Edgerton et al. May 2016 A1
20170347941 Ejiri et al. Dec 2017 A1
Foreign Referenced Citations (5)
Number Date Country
1095670 May 2001 EP
1575010 Sep 2005 EP
2920087 Feb 2009 FR
0078209 Dec 2000 WO
2007024147 Mar 2007 WO
Non-Patent Literature Citations (13)
Entry
International Search Report issued in International Application No. PCT/IB2017/056372 dated Feb. 14, 2018.
Bartol, Stephen MD, and Laschuk, Maria MD, “Arthroscopic Microscopic Discectomy in Awake Patients: The Effectiveness of Local/Neurolept Anaesthetic”, Canadian Spine Society Meeting, Vernon, BC, Canada, Mar. 2002.
Bartol, Stephen MD, and Laschuk, Maria MD, “Use of Nerve Stimulator to Localize the Spinal Nerve Root During Arthroscopic Discectomy Procedures”, Canadian Spine Society Meeting, Vernon, BC, Canada, Mar. 2002.
Begg et al. “Computational Intelligence for Movement Sciences: Neural Networks and Other Emerging Techniques” 2006.
Bourke et al. “A Threshold-Based Fall-Detection Algorithm Using a Bi-Axial Gyroscope Sensor” Medical Engineering and Physics 30 (2008) 84-90.
Fee Jr., James W.; Miller, Freeman; Lennon, Nancy; “EMG Reaction in Muscles About the Knee to Passive Velocity, Acceleration, and Jerk Manipulations”; Alfred I. duPont Hospital for Children, Gait Laboratory, 1600 Rockland Road, Wilmington, DE 19899, United States Journal of Electromyography and Kinesiology 19 (2009) 467-475.
Koceja D.M. Bernacki, R.H. and Kamen, G., “Methodology for the Quantitative Assessment of Human Crossed-Spinal Reflex Pathways,” Medical & Biological Engineering & Computing, Nov. 1991, pp. 603-606, No. 6, US.
Tarata, M.; Spaepen, A.; Puers, R.; “The Accelerometer MMG Measurement Approach, in Monitoring the Muscular Fatigue”; Measurement Science Review; 2001; vol. 1, No. 1.
Murphy, Chris; Campbell, Niall; Caulfield, Brian; Ward, Tomas and Deegan, Catherine; “Micro Electro Mechanical Systems Based Sensor for Mechanomyography”, 19th international conference Biosignal 2008, Brno, Czech Republic.
Nijsen, Tamara M.E.; Aarts, Ronald M.; Arends, Johan B.A.M.; Cluitmans, Pierre J.M.; “Model for Arm Movements During Myoclonic Seizures”; Proceedings of the 29th Annual International Conference of the IEEE EMBS Cite Internationale, Lyon, France Aug. 23-26, 2007.
Ohta, Yoichi; Shima, Norihiro; Yabe, Kyonosuke; “Superimposed Mechanomyographic Response at Different Contraction Intensity in Medial Gastrocnemius and Soleus Muscles”; International Journal of Sport and Health Science, vol. 5, 63-70, 2007.
Anderson, Edward; Wybo, Christophe;, An analysis of agreement between MMG vs EMG systems for identification of nerve location during spinal procedures Spine Journal, Suppl. 10.9, 93S-94S Sep. 2010.
Bartol, Stephen; Wybo, Christopher; The use of Mechanomyography MMG to locate nerves during spine surgery procedures, Spine Journal, Suppl. 10.9, 128S, Sep. 2010.
Related Publications (1)
Number Date Country
20190365288 A1 Dec 2019 US