Abstract
Two dimensional pelvic intraoperative neuromonitoring (pIONM®) is based on electric stimulation of autonomic nerves under observation of electromyography of internal anal sphincter (IAS) and manometry of urinary bladder. The method provides nerve identification and verification of its’ functional integrity. Currently pIONM® is gaining increased attention in times where preservation of function is becoming more and more important. Ongoing technical and methodological developments in experimental and clinical settings require further analysis of the obtained signals. This work describes a postprocessing algorithm for pIONM® signals, developed for automated analysis of huge amount of recorded data. The analysis routine includes a graphical representation of the recorded signals in the time and frequency domain, as well as a quantitative evaluation by means of features calculated from the time and frequency domain. The produced plots are summarized automatically in a PowerPoint presentation. The calculated features are filled into a standardized Excel-sheet, ready for statistical analysis.
1 Introduction
Pelvic intraoperative neuromonitoring (pIONM®) has been introduced in rectal cancer surgery as a tool to electrophysiologically map the autonomic nerves in order to preserve urinary, sexual and anorectal function [1]. Ongoing technical and methodological developments enabled further application of pIONM® during laparoscopic [2], [3] and robotic-assisted low anterior resection [4].
The current pIONM® method is based on intracorporeal electric neurostimulation under needle electromyography (EMG) of internal anal sphincter (IAS) and manometry of urinary bladder. Within the BMBF-funded research project named “autoPIN”, new requirements arising from a more minimal invasive pIONM® are met by developing and evaluating a new generation of systems and accessories. This project aims for developments of non-invasive IAS-EMG recordings and extracorporeal neurostimulation approach.
A first evaluation of the novel systems and accessories was performed in an experimental setting. A standardized and reproducible approach produced numerous data sets which needed to be analyzed. In order to ensure systematic evaluation of this data, we established an automated postprocessing routine, which combined different analysis methods and provided adequate representation of the results. This contribution describes the developed routines for automatic analysis of data obtained from EMG recordings of IAS and manometry of urinary bladder.
2 Material and methods
Four male pigs underwent low anterior rectal resection. Animal care and experimental procedures were approved by the local ethics committee (approval code G 14-1-061). Anesthesia was carried out with intravenous thiopental sodium (Trapanal®, Nycomed, Germany) and Piritramid (Dipidolor®, Janssen-Cilag, Germany). The perioperative management has been described by Kauff et al. [5].
For EMG recording a bipolar needle electrode (Art.-No. 530227, inomed Medizintechnik GmbH, Emmendingen, Germany) was inserted into the IAS. Additional intra-anal surface EMG of IAS was realized with a newly developed electrode design. This electrode was equipped with two conductive silicone electrode contacts which were arranged circularly for recording [5].
Manometry of the urinary bladder was carried out via a transurethral catheter which was connected to a pressure sensor (Art.-Nr. 520332, inomed Medizintechnik GmbH, Emmendingen, Germany).
Intracorporeal stimulation of pelvic autonomic nerves (inferior hypogastric plexus and pelvic splanchnic nerves) was performed with a handheld bipolar stimulation probe (Art.-No. 522610, inomed Medizintechnik GmbH, Emmendingen, Germany). Monophasic cathodic pulse stimulation was performed in the range of 0.5–6 mA with 200 μs pulse width and a frequency of 30–40 Hz. Further extracorporeal stimulation was carried out via stainless steel surface electrode pads with a diameter of 1 cm (Fraunhofer IBMT, St. Ingbert, Germany). Ten electrodes were placed over the sacral foramina. Stimulation was carried out via a carbon anode (AAM GmbH, Triberg, Germany) which was placed in four positions. Stimulation parameters were 25 mA, 30 Hz and 200 μs pulse width with cathodic rectangular shape. The trigger output of the stimulator was additionally recorded parallel to EMG and bladder manometry acquisition in order to determine the exact stimulation intervals for later signal analysis. For data acquisition, a neuromonitoring device with the NeuroExplorer software (ISIS Xpress and NeuroExplorer Version 5.1, both inomed Medizintechnik GmbH, Emmendingen, Germany) was used. The device allowed to record and display up to 16 channels simultaneously with individual filter and measurement range settings. Additionally, the unfiltered raw data was stored with 20 kHz sampling frequency.
Offline data analysis was performed postoperatively using MATLAB (Version R2009b, The MathWorks, Inc., Natick, United States).
3 Results
The automatic analysis routine combined the following steps:
Converting the recorded data from the inomed NeuroExplorer format (.emg-files) to MATLAB
Identifying the stimulation intervals based on trigger information from the stimulator
Plotting single data sets of bladder manometry
Combining the plotted data sets in a PowerPoint presentation for reference (Figure 1)
Performing quantitative analysis of each data set of needle and non-invasive IAS-EMG and bladder manometry

Graphical flow chart of the analysis of experimental data.
To interpret the huge amount of data that the algorithm had produced, the plots required automatic annotation. In order to include certain parameters of interest (e.g. stimulation parameters) in the plots, a standardized Excel file had to be prepared. The table sheet contained the information regarding the whole set of performed recordings, the used stimulation parameters (current amplitude, frequency, used system, stimulation site), intraoperative observations regarding the IAS-EMG and bladder manometry, as well as further, additional remarks. A corresponding paper version of the Excel sheet served as a template to protocol the procedure of each study. The routine allowed the analysis of 10 stimulation intervals in one single recording file.
As Kauff et al. described in [6], stimulation of the autonomic pelvic nerves results in modulation of the IAS resting activity in terms of a shift of frequency components towards higher frequencies (5 – 20 Hz). As shown in Figure 2B, filtering in the time domain was focused on these frequencies. Also in FFT special attention was payed to this frequency range (Figure 3).

Graphical representation of the IAS EMG and bladder manometry. A: Raw Signal. B: Bandpass filtered signal between 5 and 20 Hz. (Note the different scales of plot A and B), C: Signal of bladder manometry.

Graphical representation of frequency analysis of the IAS EMG. A: In the resting state, B: During stimulation.
The quantitative analysis was based on the calculation of features from the signals in the time and frequency domain in order to compare these features between the resting state and during stimulation (see Figures 2 and 3). This enabled the statistical analysis of the data to identify the correlation between the electrical stimulation and the neuromodulatory response, which could be identified by an amplitude increase in the filtered time domain signal or an increased power between 5 and 20 Hz in the frequency domain. For each data set, an amplitude feature from the filtered signal and a frequency feature from the FFT of the IAS-EMG of both recording modalities were calculated for the resting state and each stimulation interval. These values were stored in the Excel table, where they could easily be correlated with the applied stimulation parameters. For bladder manometry, a mean pressure in the resting state and the maximal pressure in a stimulation interval were calculated and included in the Excel sheet.
The animal studies resulted in a total of 236 data sets (mean of 59 data sets per animal experiment). All in all, 1359 stimulation intervals were recorded and had to be analyzed. In average 5.8 stimulations were performed in one data set. This resulted in a total counting of 3826 plots of graphical representations of IAS-EMG in the time and frequency domain, as well as of bladder pressure. Regarding the quantitative analysis, the four animal experiments resulted in a total of 7798 calculated values for the described features of the IAS-EMG and 1595 values for the feature of bladder manometry.
4 Discussion
The major aim of this work was the development of a postprocessing algorithm which facilitates and automates the analysis of a high number of recordings obtained from the pIONM®.
Since our approach of a more minimal invasive pIONM® is completely new, the optimal parameters for this kind of stimulation and recording have not yet been described.
This is why in this project we needed to generate huge amounts of data, which then had to be analyzed in order to extract these parameters (like electrode placement, stimulation current, frequency, pulse with, etc.). Thus, an automatic data analysis is a crucial tool, which helps determining the usability of non-invasive EMG recordings and extracorporeal stimulation for pIONM®.
Like every automated algorithm, this method relies on a certain set of internal parameters and their quality, which have to be respected during recording. The number of recording channels can be varied. However, in order to be able to use the algorithm without any manual changes, the channel configuration summarized in Table 1 needs to be maintained.
Required channel assignment in recording scenario.
| Specification | Channel No. |
|---|---|
| IAS Needle Electrode | 2 |
| Trigger | 3 |
| Bladder Manometry | 4 |
| Non-Invasive IAS Electrode | 5 |
Another standard condition, which has to be prepared, is the Excel table from which the algorithm uses information from and also writes results to. This table has to be manually filled, since notes are usually taken by hand during the experiment. This table also limits the maximal number of stimulation intervals to 10. This restriction has to be taken into account during the experiment.
Since the quantitative analysis of the algorithm relies on comparing features from the resting state and during stimulation, the standardized procedure of each stimulation routine needs to ensure the recording of a sufficiently long time window of the resting signal. Care needs to be taken so that during this period the signal remains undisturbed by any movement or electrical artifacts.
The results of the algorithm are displayed as a graphical visualization of the data sets in different representations (raw signal, filtered signal and FFT). The quantitative evaluation currently includes the calculation of two different features for a time window of the resting state and during stimulation. An automatic interpretation, that is the classification of the signal as a reaction to the stimulation or no reaction, is currently not part of the signal analysis routine. Defining thresholds for the single calculated features, which indicate a reaction of the IAS to the performed stimulation, is nevertheless the next upcoming challenge, which should be approached by large-scale statistical analysis of the obtained data. At one point this could further facilitate the analysis of huge data sets obtained in experimental and clinical studies by including an automatic interpretation of the neuromodulatory response. In a further outlook, this work could also be the basis for facilitating the intraoperative online representation of stimulation results and supporting the surgeon’s decision by automated analysis and interpretation of the recorded signals.
Acknowledgement
The authors would like to thank the autoPIN consortium for their support.
Author’s Statement
Research funding: The autoPIN project was funded by the Federal Ministry of Education and Research (BMBF, Grand number 13GW0022C). Conflict of interest: Celine Wegner and Thilo Krueger are full-time employees of the research and development department of inomed Medizintechnik GmbH. Material and Methods: Informed consent has been obtained from all individuals included in this study. Ethical approval: Animal care and experimental procedures were approved by the local ethics committee (approval code G 14-1-061).
References
[1] Kauff DW, Koch KP, Somerlik KH, Hoffmann, KP, Lang H, Kneist W. Evaluation of two-dimensional intraoperative neuromonitoring for prediciting urinary and anorectal function after rectal cancer surgery. Int J Colorectal Dis. 2013;28:659–64.10.1007/s00384-013-1662-4Search in Google Scholar PubMed
[2] Kauff DW, Koch KP, Hoffmann KP, Lang H, Kneist W. Minimal Invasive Pelvic Neuromonitoring – Technical Demands and Requirements. Biomed Tech (Berl). 2013.10.1515/bmt-2013-4369Search in Google Scholar PubMed
[3] Kauff DW, Wachter N, Bettzieche R, Lang H, Kneist W. Electrophysiology-based quality assurance of nerve-sparing in laparoscopic rectal cancer surgery: is it worth the effort? Surg Endosc. 2016. [Epub ahead of print].10.1007/s00464-016-4787-zSearch in Google Scholar PubMed
[4] Grade M, Beham AW, Schúler P, Kneist W, Ghadimi BM. Pelvic intraoperative neuromonitoring during robotic-assisted low anterior resection for rectal cancer. J Robot Surg. 2016;10:157–60.10.1007/s11701-015-0556-6Search in Google Scholar PubMed PubMed Central
[5] Kauff DW, Wachter N, Heimann A, Krüger TB, Hoffmann KP, Lang H, et al. Surface electromyography reliably records electrophysiologically evoked internal anal sphincter activity: a more minimally invasive approach for monitoring extrinsic innervation. Eur Surg Res. 2016;57:81–8.10.1159/000445683Search in Google Scholar PubMed
[6] Kauff DW, Koch KP, Somerlik KH, Heiman A, Hoffmann KP, Lang H, et al. Online signal processing of internal anal sphincter activity during pelvic autonomic nerve stimulation: a new method to improve the reliability of intra-operative neuromonitoring signals. Colorectal Dis. 2011;13:1422–7.10.1111/j.1463-1318.2010.02510.xSearch in Google Scholar PubMed
©2016 Celine Wegner et al., licensee De Gruyter.
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.
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- From imaging to hemodynamics – how reconstruction kernels influence the blood flow predictions in intracranial aneurysms
- Flow optimised design of a novel point-of-care diagnostic device for the detection of disease specific biomarkers
- Improved FPGA controlled artificial vascular system for plethysmographic measurements
- Minimally spaced electrode positions for multi-functional chest sensors: ECG and respiratory signal estimation
- Automated detection of alveolar arches for nasoalveolar molding in cleft lip and palate treatment
- Control scheme selection in human-machine- interfaces by analysis of activity signals
- Event-based sampling for reducing communication load in realtime human motion analysis by wireless inertial sensor networks
- Automatic pairing of inertial sensors to lower limb segments – a plug-and-play approach
- Contactless respiratory monitoring system for magnetic resonance imaging applications using a laser range sensor
- Interactive monitoring system for visual respiratory biofeedback
- Development of a low-cost senor based aid for visually impaired people
- Patient assistive system for the shoulder joint
- A passive beating heart setup for interventional cardiology training