System, method, and computer algorithm for measuring, displaying, and accurately detecting changes in electrophysiological evoked potentials

Information

  • Patent Grant
  • 12048567
  • Patent Number
    12,048,567
  • Date Filed
    Monday, December 13, 2021
    3 years ago
  • Date Issued
    Tuesday, July 30, 2024
    4 months ago
Abstract
An automated evoked potential analysis apparatus for improved monitoring, detecting and identifying changes to a patient's physiological system is described. The apparatus includes an input device for obtaining electrical potential data from the patient's physiological system after application of stimulation to a patient's nerve and a computing system for receiving and analyzing the electrical potential data. The computing system includes a processing circuit configured to: generate a plurality of evoked potential waveforms (EPs) based on the electrical potential data, measure changes or trends in the generated EPs utilizing a sliding window of analysis, display incremental changes in waveforms between full subsets of EPs, and determine an alert vote for each subset, representative of changes to the physiological system generating the EPs.
Description
BACKGROUND

The present invention relates generally to computer programs and methods for detecting changes in evoked potential (EP) waveforms, and more particularly to systems, methods, and computer-readable medium, which use a mathematical algorithm to assess and display EP waveforms, and calculate alerts to waveform changes.


Standard Attended Intraoperative Monitoring


Somatosensory evoked potentials are summated electrical potentials usually recorded from the head or neck area and a peripheral nerve after repeatedly stimulating a peripheral nerve. Monitoring patients using somatosensory evoked potentials during surgery has been shown to allow early identification of impending injury, particularly nerve injury.


Such monitoring generally requires highly trained technologists under physician supervision with sophisticated, multichannel amplifier and display equipment. Unfortunately, such personnel and equipment are limited in their availability, require pre-booking, and are costly. In addition, such monitoring is fraught with difficulties due to the small size of potentials and ongoing noise which make recognizing significant changes, and alerting of these changes, difficult. In current systems that are used to generate alerts automatically, substantial noise and variability can cause false alerts.


Embodiments described herein relate to improved, systems, methods and devices for accurately detecting changes in electrophysiological evoked potentials. Improvements to existing systems include reduction in false positive/false negative alerts due to signal noise. Accordingly, the improved systems, methods, and devices generate more accurate alerts. Reducing the number of false positive alerts also creates more efficient systems, methods, and devices compared to known systems.


SUMMARY OF THE INVENTION

Embodiments described herein relate to methods, devices, systems, apparatuses, and/or means to automatically detect and display changes to the evoked potential waveforms (EPs) in real time while showing incremental changes between completed ensemble averages. Embodiments described herein also relate to producing alerts with reduced or eliminated influence of variable noise and bias, while minimizing or eliminating false negative and false positive errors. The present disclosure generally relates to the computer signal processing and display algorithms for the characterization and classification of changes to EPs in real-time. The disclosed embodiments can be used in lieu of expert analysis typically provided by the technologist and physician. Further, various embodiments can be used in conjunction with other equipment. For example, upon detecting a change in EPs, an operating room table can be moved or adjusted. Such movement allows the patient to be automatically moved to ameliorate or avoid patient injury. Thus various embodiments herein extend the benefit of such equipment by automatically controlling the equipment based upon the EPs.


When seeking to accurately monitor or detect somatosensory evoked potentials (SSEPs), the waveforms can require acquisition at specific frequencies and/or averaging together to help eliminate random and cyclical noise. Even a few aberrant waveforms heavily affected by noise can markedly change the apparent amplitude (height) or latency (time of onset) of a waveform of interest when averaged together. While this is partly avoided by careful choice of stimulation frequencies and filtering of the waveforms, such methods cannot be complete as the waveforms of interest fall within the frequency range of the background noise and the cyclical background noise varies somewhat in frequency. In addition, these methods require producing a complete average (Ensemble Average or EA) of 100-300 stimulations and resultant waveforms, and then confirming any suspected change based on comparison with another EA, each taking up to 3 minutes to collect.


There is presently no way of observing slow onset incremental changes or discounting aberrant epochs affected by noise. The cost of having professionals fully engaged in interpreting these waveforms results in limiting of the service to only the most high risk surgeries. In addition, interpretation may be biased by human factors such as prior negative patient outcomes.


Thus, embodiments herein generally relate to systems, methods, devices and computer algorithms for measuring, displaying, and accurately detecting changes in electrophysiological evoked potentials. In some aspects the embodiments can automatically detect and display changes to the EPs in real time, including while showing incremental changes between completed ensemble averages. Also, in some aspects the embodiments can provide alerts free of the influence of variable noise and bias, including while minimizing or eliminating false negative and false positive errors. Embodiments described herein generally relate to the computer signal processing and display algorithms for the characterization and classification of changes to EPs in real-time implemented on specialized devices and systems. This systems and devices utilizing the algorithms may substitute for the expert analysis typically provided by the technologist and physician.


In an exemplary embodiment of the present invention a system, method, and computer algorithm for measuring, displaying and accurately detecting changes in electrophysiological evoked potentials is disclosed. In this disclosure, an EP is defined as a voltage versus time signal obtained by ensemble averaging of the electrophysiological responses to repetitive stimulation of a specific neural system, detected using suitable electrodes. Examples of EPs are somatosensory, auditory or visual EPs. The algorithms are applied to a time sequence of EPs acquired over the course of an ongoing clinical procedure. The algorithms establish changes to the characteristics of an EP relative to the baseline/normal EP, as well as to any previous EPs to determine if the functioning of the underlying neural system has been significantly affected by the ongoing clinical procedure. The algorithms communicate with ancillary hardware and algorithms developed to acquire the sequence of EPs and provide suitable feedback to ensure a safe and effective clinical workflow. The algorithms provide the basis for a clinically effective application such that false positives and false negatives are minimized.


Further features and advantages of the invention, as well as the structure and operation of various embodiments of the invention, are described in detail below with reference to the accompanying drawings.





BRIEF DESCRIPTION OF DRAWINGS

The foregoing and other features and advantages of the invention will be apparent from the following, more particular description of a preferred embodiment of the invention, as illustrated in the accompanying drawings.



FIG. 1 illustrates the traditional method evoked potential waveform (EP) acquisition and display.



FIG. 2 illustrates a sliding window method of EP acquisition, display, and alerting, according to an exemplary embodiment of the present invention.



FIG. 3 is a block diagram of a model EP analysis apparatus according to an exemplary embodiment.





DETAILED DESCRIPTION

Various exemplary embodiments of the invention including preferred embodiments are discussed in detail below. While specific exemplary embodiments are discussed, it should be understood that this is done for illustration purposes only. A person skilled in the relevant art will recognize that other components and configurations can be used without parting from the spirit and scope of the invention.



FIG. 1. illustrates a traditional way in which EPs are acquired and displayed. Using this method, a series of stimulations are applied and the resultant individual waveforms are displayed either as each is acquired, or as an evolving average of the ongoing average until a final ensemble average is acquired and displayed. The clinical interpretation is based on this ensemble average. If the user is satisfied with the average they may set that average as the ‘baseline’ to which all others are compared, or repeat it to confirm the presence and morphology of the waveform of interest. The whole process is then repeated with the next series of stimulations. Comparison of that series is then made to the preceding one that is chosen to be the baseline.


Since as few as five or six noisy individual waveforms that escape filtering can cause the waveform morphology, amplitude, and latency to widely vary, applying this method in an electrically noisy environment may lead to erroneous alerting of potential, imminent injury if an automated alerting system is used. This generally requires expert interpretation of the individual waveforms that takes into account the clinical situation, expected waveform and general trend in the waveform pattern over time.


An embodiment of the present invention relates to the computer signal processing and algorithms for the display of EP waveforms, calculation of alerts to waveform changes, and minimization of false positive and false negative alerts. This algorithm may substitute for the expert analysis typically provided by the technologist and physician. The computer algorithm running in software installed on an EP machine may be used in any surgery or situation where a patient is at risk, in order to detect, alert, and ameliorate positioning effect, or any nerve injury or abnormality.



FIG. 2. illustrates an exemplary depiction of a sliding window of analysis and alerting using metadata from automatically calculated alerts that takes into consideration variation in noise and automatically looks back at the trend of the waveform over time, according to the present invention.


After collection of one or more sets of EPs, an Ensemble Average (EA) is created and a baseline of the waveform of interest is calculated. The baseline waveform may be identified by any standard technique including for example wavelet analysis, curve fitting etc.


For the next “n” number of stimulations, a new EA is created using similar waveforms as the previous one but from which a number of EPs are removed from the beginning of the average and a similar number is added to the end. For example, as shown on FIG. 2, EP2 does not incorporate the first two EPs of EP1, and includes two additional EPs at the end. Thus achieving a “sliding window” selection of EP data on which to create the new EA for the ongoing stimulation series. In certain preferred embodiments, a new EA is created for every epoch, i.e. the “window” slides forward only one EP, eliminating the first and adding an additional one to the end, relative to the previous EP selection for the previous EA.


The overall average can be updated and displayed with every overlapping epoch allowing a slow change in the morphology to evolve for the viewer. In this way, the viewer observes a real-time, incremented change in the EP waveform morphology over time, similar to viewing a live event or motion picture. In an exemplary embodiment of the invention, the generated overlapping EAs allows display of the effect of incremental consequence on the baseline average caused by newly collected waveforms in between non-overlapping EAs.


Each new EA waveform is identified and the salient characteristic (for example amplitude or latency) is measured and recorded. The new values are compared to the baseline value of the characteristic and it is determined whether an alert vote is to be generated. An alert vote is generated if the characteristic reaches a change threshold, i.e., a degree of change the user has set to trigger an alert. This process is repeated. Each new EA generates a vote as to whether an alert should be triggered or not. When the number of EAs reaches a specific number (n), typically when the initial stimuli of the EA no longer overlap the baseline EA, the votes are tallied and, in preferred embodiments, only then can an alert be triggered depending upon the ratio of yes to no (Y/N) alert votes required to trigger an alert. The user may alter the ratio of alert votes (Y/N) required depending upon their wish for specificity of the alerting process. In other embodiments, the votes may be continuously tallied and an alert triggered once the yes (Y) votes reach a certain predetermined number, or the ratio reaches a predetermined value.


In an exemplary embodiment of the invention, since the voting process may be asymmetrical, different ratios of voting may be used for triggering (onset) and releasing (offset) a final alert to the user that nerve injury to the patient is possible or imminent.


The alerting process examines the meta-data (the alerting vote) for the individual overlapping epochs. Since any real change in data will be sustained and always eventually deliver 100% (or close) Y/N votes for alert, the specificity of the alerting process can now be manipulated independent of the sensitivity of the system on the basis of the voting. For example, the user may alter the ratio to be less specific, requiring only 30% or 50% of votes vs 80% of votes for more specificity. In this way, there can be a reduction in the number of false alerts without really altering the sensitivity of the process to detecting real sustained change. In currently used systems, substantial noise and variability can cause false alerts, whereas the voting ratio used according to the present invention lessens the impact of the noisy signals. In an exemplary embodiment of the invention, EAs with wildly variant waveform values can be discarded from the voting process, eliminating intermittent noise that escapes the frequency filters. Thus, embodiments have an improved way of handling the effects of noise in EPs. The effect of this noise is further nullified by the voting process itself


Going forward the process is repeated, the voting using the last ‘n’ number of EAs to decide if an alert is triggered and displaying each EA or an averaged group of EAs as a progressively changing waveform which can easily be compared to baseline visually. In various embodiments, when an alert is triggered other actions can also occur. For example, information leading to the alert trigger can be sent to other equipment. As another example, a command to move a portion of an operating room table can be sent to the operating room table. Upon receipt, the operating room table can move and thus move the position of the patient. The movement reduces the patient's risk of nerve injury.


In an exemplary embodiment of the invention, once the process is established, a smooth ongoing generation of overlapping EAs can identify gradual changes that are due to processes such as cooling or depth of anesthesia that are not due to more abrupt onset injuries.


Referring to FIG. 3, according to an exemplary embodiment, the EP analysis described above is implemented with an EP analysis apparatus 30. The EP analysis apparatus 30 includes hardware and software for operation and control of the system. According to an exemplary embodiment, the EP analysis apparatus 30 includes a computing system 31, an input device 36, and a display device 37. The computing system comprises a processing circuit 32 having a processor 33 and memory 34. Processor 33 can be implemented as a general purpose processor, an application specific integrated circuit (ASIC), one or more field programmable gate arrays (FPGAs), a group of processing components, or other suitable electronic processing components. Memory 34 (e.g., memory, memory unit, storage device, etc.) is one or more devices (e.g., RAM, ROM, Flash-memory, hard disk storage, etc.) for storing data and/or computer code for completing or facilitating the various processes described in the present application. Memory 34 may be or include volatile memory or non-volatile memory. Memory 34 may include database components, object code components, script components, or any other type of information structure for supporting the various activities described in the present application. According to an exemplary embodiment, memory 34 is communicably connected to processor 33 and includes computer code for executing one or more processes described herein. The memory 34 may contain a variety of modules, each capable of storing data and/or computer code related to specific types of functions.


Referring still to FIG. 3, the computing system 31 further includes a communication interface 35. The communication interface 35 can be or include wired or wireless interfaces (e.g., jacks, antennas, transmitters, receivers, transceivers, wire terminals, etc.) for conducting data communications with external sources via a direct connection or a network connection (e.g., an Internet connection, a LAN, WAN, or WLAN connection, etc.).

Claims
  • 1. An automated evoked potential analysis apparatus for monitoring, detecting, and identifying changes to a patient's physiological system, wherein the apparatus comprises: an input device for obtaining electrical potential data from the patient's physiological system after application of stimulation to a nerve of the patient;a computing system for receiving and analyzing the electrical potential data, and comprising a processing circuit configured to: generate a series of evoked potential waveforms (EPs) based on the electrical potential data;calculate a series of ensemble average waveforms (EAs) as the EPs are generated where each EA represents a subset of the plurality of EPs with each new EA including the most recent EP while omitting at least the earliest EP contained in the immediately preceding EA;identify a characteristic in each EA;determine an alert vote for each subset, representative of changes to the physiological system generating the EPs, the determining the alert vote comprising: creating a positive alert vote if the characteristic of a particular EA reaches a change threshold compared to the characteristic of a preceding EA; andcreating a negative alert vote if the characteristic of the particular EA does not reach the change threshold compared to the preceding EA;determine, after calculating at least one subsequent EA that does not overlap with at least one preceding EA, whether a ratio of positive alert votes to negative alert votes exceeds a threshold value; andtrigger, upon determining that the ratio exceeds the threshold value, an alert.
  • 2. The apparatus of claim 1, wherein each EA contains the same number of EPs.
  • 3. The apparatus of claim 1, wherein the processing circuit is further configured to display each calculated EA so as to display incremental changes between each sequential subset of EPs.
  • 4. The apparatus of claim 1, wherein said apparatus is further configured to integrate into other devices in a surgical environment.
  • 5. The apparatus of claim 4, wherein said computing system is further configured to feed information to other devices in the surgical environment that allows these devices to manually or automatically ameliorate or mitigate the physiological changes and improve subsequently acquired EP waveforms.
  • 6. The apparatus of claim 5, further comprising an operating table, wherein the operating table is configured to be adjustable to ameliorate or mitigate the physiological changes by causing an adjustment of the patient's position, in response to the information from the computing system.
  • 7. The apparatus of claim 1, wherein said apparatus computing system is further configured to identify gradual changes that are due to cooling or depth of anesthesia.
  • 8. The apparatus of claim 1, wherein the characteristic in each EA comprises a latency, an amplitude, or a morphology.
  • 9. The apparatus of claim 1, wherein said apparatus computing system is further configured to identify gradual changes that are due to cooling of the patient.
  • 10. A method of automatically identifying potential injury to peripheral nerve structures, the method comprising: stimulating, by an output device of an automated evoked potential analysis apparatus, a peripheral nerve with electrical pulses;recording, by an input device of the automated evoked potential analysis apparatus, resultant electrical waveforms (EPs) generated by the nervous system, wherein the input device comprises electrodes placed over a nerve pathway;measuring, by a computing system of the automated evoked potential analysis apparatus, changes in acquired EPs utilizing a sliding window of analysis, the computing system comprising a processing circuit, wherein utilizing the sliding window of analysis comprises: calculating, by the computing system, a series of ensemble average waveforms (EAs), each EA comprising a subset of the plurality of EPs with each new EA including the latest EP while excluding at least the earliest EP contained in the last EA, displaying, by the computing system, a second EA to display incremental changes between a first and a second subset of EPs; andidentifying, by the computing system, a characteristic in each EA;determining, by the computing system, an alert vote for each subset, representative of changes to the physiological system generating the EPs, the determining the alert vote comprising: creating, by the computing system, a positive alert vote if the characteristic of a particular EA reaches a change threshold compared to the characteristic of a preceding EA; andcreating, by the computing system, a negative alert vote if the characteristic of the particular EA does not reach the change threshold compared to the preceding EA;determining, by the computing system and after calculating at least one EA that does not overlap with at least one preceding EA, whether a ratio of positive alert votes to negative alert votes exceeds a threshold value;triggering, by the computing system, upon determining that the ratio exceeds the threshold value, an alert; andalerting, by the computing system, a user to the changes.
  • 11. The method of claim 10, wherein the sliding window analysis further comprises displaying, by the computing system, each EA so as to display incremental changes between each subsequent subset of EPs.
  • 12. The method of claim 10, wherein the characteristic in each EA comprises a latency, an amplitude, or a morphology.
  • 13. The method of claim 10, further comprising passing, by the computing system, information related to alerts to an automated operating room table and readjusting patient position through adjustment of the table.
  • 14. The method of claim 13, wherein adjustment of the operating room table is performed, by the computing system, automatically or semi automatically.
  • 15. The method of claim 10, further comprising passing, by the computing system, information related to alerts to other devices or processes.
  • 16. The method of claim 10, wherein the electrodes are placed at the neck or head of a patient.
  • 17. The method of claim 10, wherein the method further comprises identifying gradual changes that are due to cooling or depth of anesthesia.
RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No. 15/569,367, filed Oct. 25, 2017, and entitled “SYSTEM, METHOD, AND COMPUTER ALGORITHM FOR MEASURING, DISPLAYING, AND ACCURATELY DETECTING CHANGES IN ELECTROPHYSIOLOGICAL EVOKED POTENTIALS,” which is a national stage entry of International Application No. PCT/US2016/030605, filed May 3, 2016, and entitled “SYSTEM, METHOD, AND COMPUTER ALGORITHM FOR MEASURING, DISPLAYING, AND ACCURATELY DETECTING CHANGES IN ELECTROPHYSIOLOGICAL EVOKED POTENTIALS,” which claims priority from Provisional Application U.S. Application 62/156,874, filed May 4, 2015, entitled “SYSTEM, METHOD, AND COMPUTER ALGORITHM FOR MEASURING, DISPLAYING, AND ACCURATELY DETECTING CHANGES IN ELECTROPHYSIOLOGICAL EVOKED POTENTIALS,” each of which is incorporated herein by reference in its entirety. This application is also related to U.S. patent application Ser. No. 13/874,867 (published as U.S. Patent Publication 2014/0020178), filed May 1, 2013, entitled “SYSTEM, METHOD, AND COMPUTER ALGORITHM AND CHARACTERIZATION AND CLASSIFICATION OF ELECTROPHYSIOLOGICAL EVOKED POTENTIALS,” which is hereby incorporated by reference in its entirety.

US Referenced Citations (157)
Number Name Date Kind
4161945 Grossman Jul 1979 A
4305402 Katims Dec 1981 A
4863265 Flower et al. Sep 1989 A
4934377 Bova et al. Jun 1990 A
5284154 Raymond et al. Feb 1994 A
5313956 Knutsson et al. May 1994 A
5662105 Tien Sep 1997 A
5797854 Hedgecock Aug 1998 A
5825936 Clarke et al. Oct 1998 A
5827195 Lander Oct 1998 A
5916179 Sharrock Jun 1999 A
6067467 John May 2000 A
6304772 Taha et al. Oct 2001 B1
6391024 Sun et al. May 2002 B1
6535767 Kronberg Mar 2003 B1
6556861 Prichep Apr 2003 B1
6634043 Lamb et al. Oct 2003 B2
6725086 Marinello Apr 2004 B2
6985833 Shambroom et al. Jan 2006 B2
7174206 Frei et al. Feb 2007 B2
7216001 Hacker et al. May 2007 B2
7234180 Horton et al. Jun 2007 B2
7512439 Farazi Mar 2009 B1
7522953 Kaula et al. Apr 2009 B2
7620453 Propato et al. Nov 2009 B1
7628757 Koh Dec 2009 B1
7628761 Gozani et al. Dec 2009 B2
7806862 Molnar Oct 2010 B2
7904160 Brodnick et al. Mar 2011 B2
8055349 Gharib et al. Nov 2011 B2
8108039 Saliga et al. Jan 2012 B2
8255045 Gharib et al. Aug 2012 B2
8386025 Hoppe Feb 2013 B2
8515530 Warner et al. Aug 2013 B2
8538512 Bibian et al. Sep 2013 B1
8538539 Gharib et al. Sep 2013 B2
8568331 Bertagnoli et al. Oct 2013 B2
8591431 Calancie et al. Nov 2013 B2
8731654 Johnson et al. May 2014 B2
8740783 Gharib et al. Jun 2014 B2
8903487 Fischell et al. Dec 2014 B1
8965520 Botros et al. Feb 2015 B2
8989866 Gharib et al. Mar 2015 B2
9084551 Brunnett et al. Jul 2015 B2
9211074 Johnson et al. Dec 2015 B2
9332918 Buckley et al. May 2016 B1
9579037 Brunnett et al. Feb 2017 B2
9585618 Leschinsky Mar 2017 B2
9681880 Neubardt et al. Jun 2017 B2
9700228 Gharib et al. Jul 2017 B2
9743853 Kelleher Aug 2017 B2
9743884 Rasmussen Aug 2017 B2
9744356 Botros et al. Aug 2017 B2
10342443 Johnson et al. Jul 2019 B2
10376167 Mahon et al. Aug 2019 B2
10391012 Stashuk et al. Aug 2019 B2
11083387 Mahon et al. Aug 2021 B2
11197640 Johns et al. Dec 2021 B2
11684533 Stashuk et al. Jun 2023 B2
20020042563 Becerra et al. Apr 2002 A1
20020183605 Devlin et al. Dec 2002 A1
20030052775 Shambroom et al. Mar 2003 A1
20030083719 Shankar et al. May 2003 A1
20030125777 Ding et al. Jul 2003 A1
20030176799 Beatty et al. Sep 2003 A1
20040010303 Bolea Jan 2004 A1
20040122482 Tung et al. Jun 2004 A1
20050075578 Gharib et al. Apr 2005 A1
20050085866 Tehrani Apr 2005 A1
20050101878 Daly et al. May 2005 A1
20050119711 Cho et al. Jun 2005 A1
20050228306 Kurtz Oct 2005 A1
20050228654 Prieto et al. Oct 2005 A1
20050261559 Mumford et al. Nov 2005 A1
20060025702 Sterrantino et al. Feb 2006 A1
20060052845 Zanella Mar 2006 A1
20060173510 Besio et al. Aug 2006 A1
20060178593 Neubardt et al. Aug 2006 A1
20060241562 John et al. Oct 2006 A1
20060276704 McGinnis et al. Dec 2006 A1
20070016097 Farquhar et al. Jan 2007 A1
20070135722 Lin Jun 2007 A1
20070192960 Jackson Aug 2007 A1
20070225674 Molnar et al. Sep 2007 A1
20070282217 Mcginnis et al. Dec 2007 A1
20080033511 Dobak Feb 2008 A1
20080051844 Brodnick et al. Feb 2008 A1
20080167574 Farquhar Jul 2008 A1
20080221473 Calancie et al. Sep 2008 A1
20080269835 Carlson et al. Oct 2008 A1
20080300655 Cholette Dec 2008 A1
20090033486 Costantino Feb 2009 A1
20090048531 McGinnis et al. Feb 2009 A1
20090054758 Dunseath Feb 2009 A1
20090054804 Gharib et al. Feb 2009 A1
20090069027 Brock et al. Mar 2009 A1
20090124869 Hu et al. May 2009 A1
20090143693 Ye et al. Jun 2009 A1
20090177112 Calancie et al. Jul 2009 A1
20090247893 Lapinlampi et al. Oct 2009 A1
20100010367 Foley et al. Jan 2010 A1
20100036211 La Rue et al. Feb 2010 A1
20100042012 Alhussiny Feb 2010 A1
20100130834 Vertio-Oja et al. May 2010 A1
20100144200 Holliday Jun 2010 A1
20100156376 Fu et al. Jun 2010 A1
20100198099 Murphy et al. Aug 2010 A1
20100274144 Hu et al. Oct 2010 A1
20100312124 Johnson et al. Dec 2010 A1
20100317989 Gharib et al. Dec 2010 A1
20110054346 Hausman et al. Mar 2011 A1
20110224570 Causevic Sep 2011 A1
20110224988 Mahajan et al. Sep 2011 A1
20110230785 Higgins et al. Sep 2011 A1
20110279676 Terada et al. Nov 2011 A1
20110295142 Chakravarthy et al. Dec 2011 A1
20120065536 Causevic et al. Mar 2012 A1
20120095360 Runney et al. Apr 2012 A1
20120136276 Johnson et al. May 2012 A1
20120150063 Rea Jun 2012 A1
20120165690 Chen et al. Jun 2012 A1
20120197153 Kraus et al. Aug 2012 A1
20120313757 Volpi et al. Dec 2012 A1
20130024524 Graff et al. Jan 2013 A1
20130035606 Wichner Feb 2013 A1
20130190599 Wyeth et al. Jul 2013 A1
20130204156 Hampton et al. Aug 2013 A1
20130245424 Decharms Sep 2013 A1
20130245722 Ternes et al. Sep 2013 A1
20140020178 Stashuk Jan 2014 A1
20140121555 Scott et al. May 2014 A1
20140148725 Cadwell May 2014 A1
20140275926 Scott Sep 2014 A1
20140276195 Papay et al. Sep 2014 A1
20140288389 Gharib et al. Sep 2014 A1
20140324118 Simon et al. Oct 2014 A1
20150061758 Hsu Mar 2015 A1
20150088030 Taylor Mar 2015 A1
20150148683 Hermanne May 2015 A1
20150208934 Sztrubel et al. Jul 2015 A1
20150257700 Fu Sep 2015 A1
20150313512 Hausman et al. Nov 2015 A1
20160106994 Crosby et al. Apr 2016 A1
20160113587 Kothe et al. Apr 2016 A1
20160128620 Iriki et al. May 2016 A1
20160213268 Kim et al. Jul 2016 A1
20160228018 Mahon et al. Aug 2016 A1
20160270679 Mahon et al. Sep 2016 A1
20170347955 Rasmussen Dec 2017 A1
20180078210 Snow et al. Mar 2018 A1
20180078220 Johns et al. Mar 2018 A1
20180140843 Kent et al. May 2018 A1
20180310849 Johns et al. Nov 2018 A1
20180360336 O'Brien et al. Dec 2018 A1
20200315478 Mahon et al. Oct 2020 A1
20220096022 Johns et al. Mar 2022 A1
20220287619 Cleveland et al. Sep 2022 A1
Foreign Referenced Citations (19)
Number Date Country
101137332 Mar 2008 CN
101309419 Nov 2008 CN
201185940 Jan 2009 CN
102481107 May 2012 CN
104411234 Mar 2015 CN
20090118969 Jun 2009 JP
2012529344 Nov 2012 JP
2001074248 Oct 2001 WO
2003000128 Jan 2003 WO
2003005887 Jan 2003 WO
2006072050 Jul 2006 WO
2006084193 Aug 2006 WO
2010144200 Dec 2010 WO
2011045936 Apr 2011 WO
2013166157 Nov 2013 WO
2015048822 May 2015 WO
2016179191 Nov 2016 WO
2018232365 Dec 2018 WO
2022192569 Sep 2022 WO
Non-Patent Literature Citations (37)
Entry
AMSCO 3085 SP Surgical Table Sales Brochure, STERIS Corporation, Apr. 2006, 16 pages.
Warner et al. (Dec. 1994) “Ulnar Neuropathy. Incidence, Outcome, and Risk Factors in Sedated or Anesthetized Patients” Anesthesiology, 81(6):1332-1340.
Winfree et al. (Jan. 2005) “Intraoperative Positioning Nerve Injuries” Surgical Neurology, 63(1):5-18.
IOM and Neurophysiological Monitoring Software, NeuroStream, Apr. 21, 2010, 1 page.
Intraoperative Monitoring Document Management, NeuroStream, Apr. 21, 2010, 1 page.
Intraoperative Monitoring Interpreting Physician Access, NeuroStream, Apr. 21, 2010, 1 page.
Software for Intraoperative Monitoring Scheduling, NeuroStream, Apr. 21, 2010, 1 page.
Baumann et al. (Jan. 2000) “Intraoperative SSEP Detection of Ulnar Nerve Compression or Ischemia in an Obese Patient: A Unique Complication Associated with a Specialized Spinal Retraction System” Archives of Physical Medicine and Rehabilitation, 81(1):130-132.
Ben-David et al. (Oct. 1997) “Prognosis of Intraoperative Brachial Plexus Injury: A Review of 22 Cases” British Journal of Anaesthesia, 79(4):440-445.
Bizzarri et al. (Jan. 2001) “Iatrogenic Injury to the Long Thoracic Nerve”, Texas Heart Institute Journal, 28(4):315-317.
Chung et al. (Apr. 2009) “Upper-limb somatosensory evoked potential monitoring in lumbosacral spine surgery: a prognostic marker for position-related ulnar nerve injury” The spine journal: official journal of the North American Spine Society, 9(4):287-295.
Fishel et al. (Jun. 1990) “Postoperative Injuries of Upper Limb Nerves” The Clinical Journal of Pain, 6(2):128-130.
Graham et al. (Jul. 1981) “Brachial Plexus Injury After Median Sternotomy” Journal of Neurology, Neurosurgery, and Psychiatry, 44(7):621-625.
Hickey et al. (Jan. 1993) “Intraoperative Somatosensory Evoked Potential Monitoring Predicts Peripheral Nerve Injury During Cardiac Surgery” Anesthesiology, 78(1):29-35.
Jellish et al. (Feb. 1997) “Hands-up Positioning During Asymmetric Sternal Retraction for Internal Mammary Artery Harvest: A Possible Method to Reduce Brachial Plexus Injury” Anesthesia & Analgesia, 84(2):260-265.
Kamel et al. (May 2006) “The Use of Somatosensory Evoked Potentials to Determine the Relationship Between Patient Positioning and Impending Upper Extremity Nerve Injury During Spine Surgery: A Retrospective Analysis” Anesthesia & Analgesia, 102(5):1538-1542.
Labrom et al. (Sep. 15, 2005) “Clinical Usefulness of Somatosensory Evoked Potentials for Detection of Brachial Plexopathy Secondary to Malpositioning in Scoliosis Surgery” Spine, 30(18):2089-293.
Makarov et al. (Mar.-Apr. 1996) “Intraoperative SSEP Monitoring During External Fixation Procedures in the Lower Extremities” Journal of Pediatric Orthopaedics, 16(2):155-160 (1-8 pages).
Makarov et al. (Sep.-Oct. 1997) “Monitoring Peripheral Nerve Function During External Fixation of Upper Extremities” Journal of Pediatric Orthopaedics, 17(5):663-667 (1-8 pages).
Nagda et al. (May-Jun. 2007) “Neer Award 2005: Peripheral Nerve Function During Shoulder Arthroplasty Using Intraoperative Nerve Monitoring” Journal of Shoulder and Elbow Surgery, 16(3 Suppl):7 pages.
Posta et al. (Dec. 1997) “Neurologic Injury in the Upper Extremity After Total Hip Arthroplasty” Clinical Orthopaedics and Related Research, 345:181-186.
Prielipp et al. (Aug. 1999) “Ulnar Nerve Pressure: Influence of Arm Position and Relationship to Somatosensory Evoked Potentials” Anesthesiology, 91(2):345-354.
Crum, et al. “ Peripheral nerve stimulation and monitoring during operative procedures.” Muscles & nerve 35.2: 159-170. (Year: 2007).
Crum, et al. “intraoperative peripheral nerve stimulation and recording.” Handbook of Clinical Neurophysiology 8: 364-370. (Year: 2008).
Doemges, et al., “Changes in the Stretch Reflex of the Human First Dorsal Interosseous Muscle During Different Tasks,” Journal of Physiology, 1992, pp. 563-573, vol. 447.
European Patent Office acting as International Searching Authority, “ Search Report and Written Opinion,” International Application No. PCT/US2022/019798, Jul. 6, 2022.
European Patent Office, “Communication Pursuant to Article 94(3) EPC,” European Application No. 18771706.1, mailed Jul. 4, 2023.
European Patent Office, “Extended European Search Report,” European Application No. 23188630.0, Sep. 5, 2023.
Hongxuan Zhang et al., “Intraoperative Neurological Monitoring,” vol. 25, No. 4, Jul. 1, 2006 (Jul. 1, 2006), pp. 39-45.
International Search Report and Written Opinion for PCT Application No. PCT/US2010/034076, dated Jul. 9, 2010, 8 pages.
International Search Report and Written Opinion, PCT/US16/30605, dated Aug. 8, 2016.
Japan Patent Office, “Office Action,” Japanese Application No. 2022191709, mailed Nov. 14, 2023.
Makeig, et al., Mining event-related brain dynamics, Trends in Cognitive Sciences. vol. 8, No. 5, May 2004, pp. 204-210.
Extended European Search Report issued in European Application No. 16789949.1, mailed on Dec. 4, 2018, 7 pages.
Extended European Search Report issued in European Application No. 13784125.0, mailed on Dec. 9, 2015, 8 pages.
International Search Report and Written Opinion received for PCT Application No. PCT/US2016/030605, mailed on Aug. 8, 2016, 8 pages.
International Search Authority, “Search Report and Written Opinion,” International Application No. PCT/US/2023/029024, Dec. 15, 2023.
Related Publications (1)
Number Date Country
20220096022 A1 Mar 2022 US
Provisional Applications (1)
Number Date Country
62156874 May 2015 US
Continuations (1)
Number Date Country
Parent 15569367 US
Child 17549764 US