Abstract
Minimally invasive and robotic surgery changes the capacity for surgical mentors to guide their trainees with the control customary to open surgery. This neuroergonomic study aims to assess a “Collaborative Gaze Channel” (CGC); which detects trainer gaze-behavior and displays the point of regard to the trainee. A randomized crossover study was conducted in which twenty subjects performed a simulated robotic surgical task necessitating collaboration either with verbal (control condition) or visual guidance with CGC (study condition). Trainee occipito-parietal (O-P) cortical function was assessed with optical topography (OT) and gaze-behavior was evaluated using video-oculography. Performance during gaze-assistance was significantly superior [biopsy number: (mean ± SD): control = 5.6 ± 1.8 vs. CGC = 6.6 ± 2.0; p < 0.05] and was associated with significantly lower O-P cortical activity [ΔHbO2 mMol × cm [median (IQR)] control = 2.5 (12.0) vs. CGC 0.63 (11.2), p < 0.001]. A random effect model (REM) confirmed the association between guidance mode and O-P excitation. Network cost and global efficiency were not significantly influenced by guidance mode. A gaze channel enhances performance, modulates visual search, and alleviates the burden in brain centers subserving visual attention and does not induce changes in the trainee’s O-P functional network observable with the current OT technique. The results imply that through visual guidance, attentional resources may be liberated, potentially improving the capability of trainees to attend to other safety critical events during the procedure.
Highlights
A randomized crossover study assessing the impact of trainer visual guidance upon trainee visual cognition, occipito-parietal (O-P) brain function and technical performance.
Visual guidance is associated with enhanced gaze behavior, improved technical accuracy and attenuated activity across O-P cortices.
Parameters of network performance such as cost and global efficiency are not detrimentally effected by visual guidance.
Introduction
In high-risk industry, collaboration between operators is integral to performing goal-orientated tasks successfully (e.g., pilots, air-traffic controller, surgeons, etc). Regarding surgery, collaboration is necessary between surgeons and their assistant(s), theatre nurse(s) and occasionally members of allied specialties. Recent developments in technologies for robotic surgery such as dual console systems (e.g., da Vinci® Si) enable two surgeons to operate simultaneously, facilitating both high-level co-operation and mentorship as well as potentially streamlining the operators’ cognitive resources towards improved safety. However, in this scenario, it is important that communication between both surgeons is effective to enable a seamless flow of information between the two operators and ensure an efficient workflow. Similarly, excellent communication facilitates technical skills training in surgery. During “open” surgery, expert trainers’ employ a variety of methods for communication with trainees that include a combination of verbal instruction, physical pointing or actual demonstration(s). However, during robotic minimally invasive surgery (MIS), there may be circumstances in which the trainee or collaborating surgeon is using both instruments simultaneously within the operative field of view, constraining the trainer/master surgeon and rendering them reliant solely on verbal communication.
Within MIS and robotic surgery, techniques exist such as telestration that aid information transfer between surgeons and/or between trainer and trainee. Telestration allows information to be “drawn” onto a monitor at a remote site by the surgeon guiding the procedure. This information is then displayed on the operator’s screen with the aim of guiding performance and may be undertaken either remotely or locally (Ferguson and Stack, ). Remote guidance or telementoring enables surgeons to be guided by a mentor at a location remote from the operation. This form of instruction has been applied to better enable regional experts to guide surgeons at local centers and to provide assistance and mentoring from surgical experts in other countries (Micali et al., ; Schlachta et al., ).
There has been interest in the role that gaze behavior may have in improving the flow of communication between collaborating subjects. For example, it has been demonstrated that shared gaze during visual collaboration enables a more efficient search strategy when compared to verbal collaboration alone (Brennan et al., ). Therefore, it is anticipated that observing a guiding surgeon’s point of regard instead of, or in conjunction with their verbal instruction(s) will significantly improve the performance of the operating surgeon by providing supplementary cues critical to task success. Based on this concept, a new system referred to as “collaborative gaze control” (CGC) was developed to enable an operating surgeon to be directed by visual guidance as opposed to or in conjunction with verbal instruction(s) from an expert (Kwok et al., ). With CGC enabled, the trainer’s gaze behavior is extracted in real-time. Their point of regard is subsequently relayed to the trainee’s screen, which may be in a remote location. Therefore, the trainee’s operative manoeuvres can be directed more precisely, potentially obviating the dependence on verbal instruction(s). Importantly, in manipulating target salience, visual search is modulated leading to enhanced behavioral performance (Avraham et al., ).
More recently, there is evidence that workload can be inferred from saccadic eye movements (Tokuda et al., ), pupillary responses (Zheng et al., ) and blink frequency (Zheng et al., ). Challenging, effortful visual search results in greater visual cortical (V1) excitation (Kojima and Suzuki, ). Evaluating the impact that technological manipulation of visual search has on an operator’s cortical function helps to determine whether performance enhancement is offset by the need for greater attentional demands at brain level. This is encompassed by “neuroergonomics” which concerns the investigation of the brain behavior at work (Parasuraman, ), a paradigm that has been applied to surgery in order to investigate how recruited brain regions may be modulated by novel performance-enhancing tools (James et al., , ).
In order to examine this effect, functional Near Infrared Spectroscopy (fNIRS) a non-invasive neuroimaging modality is utilized to measure task-evoked fluctuations in oxygenated and deoxygenated hemoglobin (HbO2 and HHb respectively) within cortical tissues that reflects the magnitude of cortical activation (Jöbsis, ). This is based upon the principle that neuronal activity and the associated increased metabolic demand within the brain leads to local hemodynamic changes, so termed “neurovascular coupling” (Roy and Sherrington, ). Unlike functional magnetic resonance imaging (fMRI), fNIRS is relatively resistant to motion artifact and can be used in conjunction with ferromagnetic instruments and has been successfully applied to monitor the cortical responses in surgeons (Leff et al., ,,; Ohuchida et al., ; James et al., , ). Broadly, these studies highlight the importance of the prefrontal cortex (PFC) in supporting “cognitive phases” of skill learning (Leff et al., ), evolution in PFC excitation with technical skills training (Leff et al., ), and relative PFC redundancy amongst expert surgeons (Ohuchida et al., ). More recently, investigators have demonstrated the impact of the type of learning (e.g., implicit vs. explicit) and the influence of technology to stabilize performance and enhance neuronal efficiency amongst surgeons (Zhu et al., ; James et al., ).
Functional brain connectivity captured in coherence or cross-correlation between different brain regions can be used to investigate efficiency in brain networks (Zhu et al., ; James et al., ). Graph Theory, a popular method for interrogating brain networks, can model the organization, development and function of complex networks (Sporns et al., ; Bullmore and Sporns, ; Sporns, ) and has been successfully employed to networks derived from fNIRS data (Niu et al., ; James et al., ). In this regard, studies investigating graph topology such as the number of connections, cost and efficiency have demonstrated associations between task performance and brain network efficiency or cost-efficiency (Bassett et al., ). Despite the above, there have been no studies investigating the influence of varying trainer/mentor guidance on brain function or network architectures amongst trainees.
The aim of this paper is to investigate the influence of a gaze channel on changes in visual search strategies, technical performance, and brain behavior in a group of task naïve subjects being instructed to perform simulated biopsy using robotic MIS. Therefore, it is anticipated that compared to verbal guidance technical procedural skills may be superior during gaze-assistance owing to the improved perceptual flow of information to the trainee. The primary hypothesis is that increased target saliency will lead to a “bottom-up” search strategy, reflected in a more focused pattern of V1 activation and a reduction in the need for recruitment of extra-striatal visual association areas. Conversely, verbal communication (gold standard) is anticipated to lead to a more effortful “top down” visual search strategy, necessitating recruitment of additional cortical regions outside V1, manifest as greater excitation in centers of visual attention. The secondary hypothesis is that collaborative gaze may facilitate the flow of information transfer in the visual-parietal network manifest as reduced network costs, improved efficiency and reduced network burden.
Materials and Methods
Subjects
The study was carried out in accordance with the recommendations of the Local Regional Research Ethics Committee (LREC 05/Q0403/142) with written informed consent from all subjects. All subjects gave written informed consent in accordance with the Declaration of Helsinki. Following ethical approval a randomized control trial was conducted in which 20 subjects (1 female) were recruited from Imperial College London (mean age, years ± SD = 28.9 ± 1.5). Left-handed subjects and those with a history of neuropsychiatric illness or previous exposure to the task were excluded (Orihuela-Espina et al., ). Subjects were included on the basis that they were task naïve. The task was performed under both guidance conditions (order randomized) such that subjects served as their own controls and bias associated with learning or ordering effects was minimized.
Task Paradigm
The robotic surgical task entailed the subject (“trainee”) and an expert (“trainer”) collaborating in taking virtual biopsies from a simulated gastric mucosa in a shared surgical environment as depicted in Figure 1. Haptic manipulators (Phantom, Omni, SensAble Technologies, USA) were used to control robotic graspers in the virtual scene. The task necessitated the trainee take a virtual biopsy and pass the specimen to the guiding trainer. Both the trainee’s and the trainer’s graspers were visible within the same field of view with the former located inferiorly and the latter superiorly as depicted in Figure 1 (panels i–iv). Within the operative field, seven nodules were visible to the trainee. The choice of nodule for biopsy was randomly determined and this selection was available only to the trainer. Therefore, the appropriate biopsy site had to be conveyed to the trainee either visually or verbally by the trainer. Once the biopsy was taken by the trainee, the specimen was passed towards the trainer’s graspers and when successfully transferred to the trainer, it disappeared from the field of view. This process was repeated as many times as possible during the allotted task periods.
Figure 1
Prior to commencing the study, all subjects received a standardized period of task familiarization. All subjects performed the simulated biopsy task under verbal (control) and visual instruction (CGC; Kwok et al.,
Cortical Activity
Brain activation was assessed using a commercially available 24-channel Optical topography (OT) system (ETG-4000, Hitachi Medical Corp., Japan). Sixteen optodes (8 emitters and 8 detectors) were positioned in a 4 × 4 array over the O-P cortices as displayed in Figure 1. A “channel” represents a banana-shaped volume of cortex where changes in absorption of near infrared light from the optode emitters are interpreted as changes in HbO2 and HHb. The array was centered on “Oz” of the International 10–20 system (Jurcak et al.,
Technical Performance
The number of nodules that the trainee was able to successfully biopsy and transfer to the trainer’s graspers across the task period and the trainee’s instrument pathlength (metres) were recorded and used as objective metrics of technical performance. This was preferred to restricting the overall number of moves towards calculating time/nodule biopsied, and helped to ensure that subjects were focusing on the task quality and not the procedural time, or perceiving the number of movements.
Gaze Behavior
Subject and trainer gaze behavior was recorded throughout the study with portable eyetracking technology (×50 eyetracker, Tobii Technologies, Sweden) situated beneath the task monitor (as displayed in Figure 1). The gaze behavior of the trainer was interrogated to derive their fixation point in order to display this as a cross on the trainee’s monitor thereby facilitating gaze-guidance in CGC (study condition). The trainer’s fixation point was not visible to the trainee during episodes of verbal guidance (control condition). The trainee’s fixation points were recorded to determine the time taken, termed “gaze latency” (GL, seconds), to fixate on the same area of the surgical scene as the expert.
Heart Rate Monitoring
A portable band electrocardiogram (Bioharness v2.3.0.5; Zephyr Technology Limited, USA) was used to acquire continuous heart rate data, from which heart rate variability (HRV) was derived and used to infer subject stress (Task Force of the European Society of Cardiology the North American Society of Pacing Electrophysiology,
Data Analysis
Cortical Hemodynamics
Cortical hemodynamic data and network graph econometrics were observed to be non-Gaussian and therefore analyzed using non-parametric tests of significance. Channel-wise cortical activation was determined as a task-evoked statistically significant increase in HbO2 coupled to a significant decrease in HHb from baseline rest (Wilcoxon Rank Sign, p < 0.05). For each channel of data and hemoglobin species a variable ΔHb was computed (Hb task–Hb rest). To investigate the influence of the mode of guidance (CGC vs. control) and stress on cortical hemodynamics (i.e., ΔHbO2 and ΔHHb) random effects models (REM) were generated (Intercooled Stata, v10.0 for windows, Stata Corporation, USA).
Cortical hemodynamic data was subsequently used to construct a task-evoked network of the 24 channels using graph theory (Bullmore and Sporns,
Econometric data from these networks was then calculated to derive: (a) the number of network connections; (b) the maximum global efficiency (Achard and Bullmore,
Performance and Gaze Behavior
The number of nodules biopsied by each subject during the allotted task time and the instrument pathlength (metres) were determined. GL (seconds) was derived from the eye-tracking data stream. Behavioral performance and GL data was observed to be Gaussian and therefore analyzed using paired t-tests. These data were subsequently incorporated into the REM analysis in order to assess whether the guidance mode (control vs. CGC) was a predictor of performance accuracy and efficiency in visual search.
Heart Rate Analysis
HRV as calculated by the standard deviation of the R to R interval (SDRR) was derived from the HR data stream (Task Force of the European Society of Cardiology the North American Society of Pacing Electrophysiology,
Results
Technical Performance
Biopsy number and instrument pathlength was analyzed to determine whether CGC improved trainees’ technical performance. As illustrated in Figure 2A, gaze-guidance under the influence of CGC resulted in enhanced technical performance. Table 1 highlights the differences in technical performance according to the mode of guidance. With gaze-assistance, trainees’ biopsied a significantly greater number of nodules [biopsy number (mean ± SD): control = 5.6 ± 1.8 vs. CGC = 6.6 ± 2.0, p < 0.05] using significantly shorter instrument pathlength (metres) [mean ± SD: control = 0.6 ± 0.1 vs. CGC = 0.3 ± 0.7, p < 0.001]. This implies that trainees were faster, more productive and used virtual instruments more economically when operating from the CGC mode.
Figure 2

(A) Technical performance as indexed by the number of biopsies retrieved (I) and instrument path length (II). Box plots indicate mean and error bars represent 95% confidence interval. (B) Gaze plots from a representative subject under control (I) and gaze guidance (II) demonstrate more focussed fixations during gaze-assistance.
Table 1
| Outcome variable | Control condition (Mean ± SD) | CGC condition (Mean ± SD) | t-value | p-value |
|---|---|---|---|---|
| Technical lerformance | ||||
| Biopsy number | 5.6 ± 1.8 | 6.6 ± 2.0 | −3.394 | 0.003 |
| Instrument path length (m) | 0.6 ± 0.1 | 0.3 ± 0.7 | 11.765 | 0.000 |
| Visual search | ||||
| Gaze latency (s) | 1.4 ± 0.3 | 0.8 ± 0.2 | 7.292 | 0.000 |
| Outcome variable | Control condition median (IQR) | CGC condition median (IQR) | z-value | p-value |
| Cortical hemodynamics | ||||
| ΔHbO2 (mMol × cm) | 2.5 (12.0) | 0.6 (11.2) | −4.049 | 0.000 |
| ΔHHb (mMol × cm) | −1.4 (5.0) | −1.0 (4.5) | −1.098 | 0.272 |
| ΔHbT (mMol × cm) | 3.6 (13) | 1.1 (11.6) | −6.064 | 0.000 |
| Cortical network | ||||
| Normalized cost (a.u.) | 0.10 (0.13) | 0.19 (0.43) | −0.722 | 0.470 |
| Global efficiency (a.u.) | 0.03 (0.05) | 0.02 (0.08) | −0.220 | 0.826 |
| Network burden (a.u.) | 0.09 (0.14) | 0.18 (0.46) | −0.847 | 0.397 |
| Network edges (a.u.) | 56.0 (304.0) | 81.0 (120.0) | −0.589 | 0.556 |
| Systemic effect | ||||
| Heart rate (beatsmin-1) | 71.2 (10.0) | 73.4 (8.1) | −0.392 | 0.695 |
| SDNN | 57.7 (42.0) | 47.2 (36.9) | −0.784 | 0.433 |
The influence of guidance mode on technical performance, visual search behavior, changes in cortical hemodynamics, network topological properties and systemic effects.
p < 0.05 = bold, p < 0.001 = bold italic.
Gaze Behavior
GL which represents the temporal delay between trainer and trainee gaze fixation was analyzed to determine whether gaze guidance streamlined trainee visual search. Figure 2B depicts the visual search pattern acquired from a representative trainee under both guidance conditions. It is apparent that whilst operating under gaze guidance, trainee fixations appear to be more localized to the nodule to be biopsied. GL was significantly shorter in CGC mode [GL seconds (mean ± SD): control = 1.4 ± 0.3 vs. CGC = 0.8 ± 0.2, p < 0.001]. This suggests that gaze assistance manifests as more rapid fixation on the appropriate target nodule to be biopsied.
Cortical Activation
Cortical hemodynamic change was analyzed to compare trainee brain responses between verbal and gaze-assisted modes of operation, with the hypothesis that verbal guidance would induce higher amplitude and spatially broader O-P hemodynamic changes. Topograms of a representative subject depicting the average change in HbO2 overlying the O-P cortices are displayed in Figure 3. Table 1, depicts cortical hemodynamic change as ΔHbO2 (mMol × cm) averaged across the O-P cortices for both verbal and gaze-guidance. Cortical hemodynamic change evoked by verbal guidance was more diffuse as illustrated in Figure 4 (CGC: 11/24 channels active vs. verbal: 19/24 channels active), more likely to involve bilateral parietal as well as bilateral visual cortices and was greater in magnitude than the response evoked by gaze guidance (ΔHbO2 mMol × cm [median (IQR)]: control = 2.5 (12.0) vs. CGC = 0.63 (11.2), p < 0.001; ΔHbT mMol × cm [median (IQR)]: control = 3.6. (13.0) vs. CGC = 1.1 (11.6), p < 0.001). Overall, this data supports the primary hypothesis that training in CGC mode evokes an attenuated O-P brain response. The mode of guidance did not significantly influence the magnitude of ΔHHb [ΔHHb mMol × cm [median (IQR)]: control = −1.4 (5.0) vs. CGC = −1.0 (4.5), p = 0.27]. Similarly, as highlighted in Table 2, REM analysis revealed that guidance mode was a predictor of ΔHbO2 (p < 0.001) but not of ΔHHb (p = 0.19).
Figure 3

Topograms derived from task averaged HbO2 response of a representative subject for verbal (left) and gaze guidance (right) conditions, depicting spatially broader task-evoked oxygenated hemoglobin change during verbal guidance.
Figure 4

Figure depicting group averaged (O-P) channel activation for verbal (left) and gaze guidance (right). Magnitude of statistical changes in cortical hemodynamics reflect intensity of brain activation as follows: (A) statistically significant (p < 0.05) increase in HbO2 coupled to statistically significant (p < 0.05) decrease in HHb (red circles); (B) increase HbO2 and decrease HHb with one species reaching statistical significance, p < 0.05 (spots); (C) increase HbO2 and decrease HHb with neither species reaching statistical significance (stripes); and (D) no coupled increase HbO2 and decrease HHb (clear circles). Verbal guidance resulted in a greater number of activating channels (control vs. CGC = 19/24 vs. 11/24).
Table 2
| Dependent variable | Coefficient | S.E. | p > z | 95% C.I. |
|---|---|---|---|---|
| Biopsy number | 0.090 | 0.040 | 0.025 | 0.011 to −0.168 |
| Instrument pathlength (m) | −3.20 | 0.312 | 0.000 | −3.808 to −2.586 |
| Gaze latency (s) | −0.761 | 0.118 | 0.000 | −0.992 to −0.530 |
| ΔHbO2 (mMol × cm) | −1.294 | 0.326 | 0.000 | −1.933 to −0.654 |
| ΔHHb (mMol × cm) | −0.198 | 0.151 | 0.188 | −0.494 to −0.097 |
| ΔHbT (mMol × cm) | −1.094 | 0.303 | 0.000 | −1.689 to −0.500 |
| No. of connections | −0.000 | 0.000 | 0.754 | −0.002 to −0.001 |
| Normalized cost (a.u.) | −0.036 | 0.101 | 0.720 | −0.234 to −0.161 |
| Network burden (a.u.) | −0.333 | 0.097 | 0.732 | −0.244 to −0.157 |
| Global efficiency (a.u.) | −0.106 | 0.282 | 0.706 | −0.659 to −0.446 |
| Mean HR (beatsmin-1) | 0.008 | 0.009 | 0.353 | −0.009 to −0.025 |
| SDNN | −0.002 | 0.003 | 0.595 | −0.008 to −0.004 |
Results of univariate random effect models (REM), evaluating the influence of the independent variable (mode of guidance) on dependent variables including performance, changes in cortical hemodynamics, cortical network metrics, heart rate (HR) and heart rate variability (HRV).
(p < 0.05 = bold, p < 0.001 = bold italic).
Cortical Networks
Graph theoretical econometric data were computed and compared between guidance modes with the hypothesis that the performance of functional network in CGC mode would be associated with less cost and greater efficiency. Figure 5 depicts the activated cortical network under control and CGC conditions for a representative subject. Table 1 represent results of econometric analysis delineating the number of cortical connections, normalized cost, maximum global efficiency and cognitive burden. Differences in these network topological properties between modes guidance did not reach statistical threshold. Additionally, even when subject-level clustering was considered (Table 2) guidance mode was not found to predict network properties (e.g., cost, efficiency, etc). This suggests that CGC does not induce changes in the trainee’s O-P functional network observable with the current OT technique.
Figure 5

Activity-guided cortical networks for a representative subject during the control condition (A) and study condition (B). Approximate channel locations (black circles) are overlain onto reference MRI atlas. The strength of functional associations between nodes in the network is represented by the boldness of network edges.
Heart Rate Data
HR and SDRR were monitored to determine the influence of guidance mode on stress-related change in systemic responses (Table 1). Between-condition differences in HR and SDRR were not statistically significant [Median HR (IQR): control = 71.2 (10.0) vs. CGC = 73.4 (8.1) p = 0.70; Median SDRR (IQR): control = 57.7 (42.0) vs. CGC = 47.2 (36.9), p = 0.43). Additionally, upon REM analysis, neither HR nor SDRR were observed to be predictors for changes in cortical hemodynamics.
Harms
No harms occurred in the study.
Discussion
In this study, performance on a simulated surgical task has been improved by modulating the manner in which collaborating surgeons interact with one another. Communicating through collaborative gaze-driven control leads to a greater number of successful biopsies and a reduction in instrument path length, the latter being a measure of dexterity previously shown to reflect skill level in laparoscopic and open surgery (Bann et al.,
The current paper offers a potential mechanistic explanation for improvements observed in novices’ performance when training under the influence of expert visual cues (Wilson et al.,
There is evidence from functional neuroimaging studies that streamlined visual search strategies lead to reduced activation in the visual cortex (Kojima and Suzuki,
Parietal cortical activity is also associated with oculomotor intention and attention and may be important in planning eye movements (Kanwisher and Wojciulik,
Here, as well as investigating connectivity (i.e., correlations), network topology has been explored with graph theory, which provides a powerful method for quantitatively describing the topology of brain connectivity (He and Evans,
Intuitively verbal instructions about target location are time consuming to deliver, more complex to interpret and harder to translate into the “visual” workspace, ultimately relying therefore on greater cognitive work as evidenced by enhanced task performance when visual guidance is employed (Chetwood et al.,
Conclusion
To summarize, this study demonstrates that capitalizing on visual behavior enhances communication between collaborating surgeons, and improves operator performance. This may be achieved through a bottom up allocation of resources within the visual cortex of the surgeon being instructed. It is plausible that trainees instructed in this fashion will be better able to devote neural resources to other safety critical aspects of the procedure. In investigating these hypotheses, fNIRS technology is well placed to make an impact, as it overcomes the limitations of traditional scanning environments (Cutini et al.,
Funding
This work was funded in part by research grants from the Academy of Medical Sciences (Lecturer Starter Grant) and Cancer Research UK (Academic Lecturership).
Statements
Author contributions
Study design and protocols were conceived by DRCJ, DRL, FO-E, LWS, K-WK, GM, G-ZY, and AWD. Data collection was performed by DRCJ, DRL, FO-E, LWS and K-WK. Data analysis was performed by DRCJ, FO-E, DRL, K-WK, LWS, GM and TA. The manuscript was written by DRCJ, DRL and FO-E and final critical editing was performed by DRL, LWS, GM, TA, G-ZY and AWD.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
References
1
AchardS.BullmoreE. (2007). Efficiency and cost of economical brain functional networks. PLoS Comput. Biol.3:e17. 10.1371/journal.pcbi.0030017
2
AvrahamT.YeshurunY.LindenbaumM. (2008). Predicting visual search performance by quantifying stimulus similarities. J. Vis.8:9. 10.1167/8.4.9
3
BannS. D.KhanM. S.DarziA. W. (2003). Measurement of surgical dexterity using motion analysis of simple bench tasks. World. J. Surg.27, 390–394. 10.1007/s00268-002-6769-7
4
BassettD. S.BullmoreE. T.Meyer-LindenbergA.ApudJ. A.WienbergerD. R.CoppolaR. (2009). Cogntive fitness of cost-efficient functional networks. Proc. Natl. Acad. Sci. U S A106, 11747–11752. 10.1073/pnas.0903641106
5
BetzT.WilmingN.BoglerC.HaynesJ. D.KönigP. (2013). Dissociation between saliency signals and activity in the early visual cortex. J. Vis.13:6. 10.1167/13.14.6
6
BrennanS. E.ChenX.DickinsonC. A.NeiderM. B.ZelinskyG. J. (2008). Coordinating cognition: the costs and benefits of shared gaze during collaborative search. Cognition.106, 1465–1477. 10.1016/j.cognition.2007.05.012
7
BullmoreE.SpornsO. (2009). Complex brain networks: graph theoretical analysis of structural and functional systems. Nat. Rev. Neurosci.10, 186–198. 10.1038/nrn2575
8
BullmoreE. T.BassettD. S. (2011). Brain graphs: graphical models of the human brain connectome. Ann. Rev. Clin. Psychol.7, 113–140. 10.1146/annurev-clinpsy-040510-143934
9
CutiniS.Basso MoroS.BiscontiS. (2012). Functional near infrared optical imaging in cognitive neuroscience: an introductory review. J. Near Infrared Spectrosc.20, 75–92. 10.1255/jnirs.969
10
ChetwoodA. S.KwokK. W.SunL. W.MylonasG. P.ClarkJ.DarziA.et al. (2012). Collaborative eye tracking: a potential training tool in laparoscopic surgery. Surg. Endosc.26, 2003–2009. 10.1007/s00464-011-2143-x
11
DayanE.CohenL. G. (2011). Neuroplasticity subserving motor skill learning. Neuron.72, 443–445. 10.1016/j.neuron.2011.10.008
12
DehaisF.PeysakhovichV.ScanellaS.FongueJ.GateauT. (2015). ““Automation suprise” in aviation: real-time solutions,” in CHI’15 Proceedings of the 33rd Annual ACM Conference on Human Factors in Computing Systems (Seoul: Republic of Korea), 2525–2534.
13
Di NoceraF.CamilliM.TerenziM. (2007). A random glance at the Flight Deck: Pilots’ scanning strategies and real-time assessment of mental workload. J. Cogn. Eng. Decis. Mak.1, 271–285. 10.1518/155534307X255627
14
DuratinG.GagnonJ. F.TremblayS.DehaisF. (2014). Using near infrared spectroscopy and heart rate variability to detect mental overload. Behav. Brain Res259, 16–23. 10.1016/j.bbr.2013.10.042
15
EinhäuserW.KönigP. (2010). Getting real-sensory processing of natural stimuli. Curr. Opin. Neurobiol.20, 389–395. 10.1016/j.conb.2010.03.010
16
FergusonS.StackB. C. (2010). Addition of a telestrator for teaching during video-based procedures. Otolaryngol. Head Neck Surg.143, 159–160. 10.1016/j.otohns.2009.12.043
17
FittsP. M.PosnerM. I. (1967). Learning and Skilled Performance in Human Performance.Belmont, CA: Brooks/Cole.
18
HeY.EvansA. (2010). Graph theoretical modeling of brain connectivity. Curr. Opin. Neurol.23, 341–350. 10.1097/wco.0b013e32833aa567
19
JamesD. R.LeffD. R.Orihuela-EspinaF.KwokK. W.MylonasG. P.AthanasiouT.et al. (2013). Enhanced frontoparietal network architectures following “gaze-contingent” versus “free-hand” motor learning. Neuroimage.64, 267–276. 10.1016/j.neuroimage.2012.08.056
20
JamesD. R. C.Orihuela-EspinaF.LeffD. R.SodergrenM. H.AthanasiouT.DarziA. W.et al. (2011). The ergonomics of Natural Orifice Translumenal Endoscopic Surgery (NOTES) in terms of performance, stress and cognitive behaviour. Surgery.149, 525–533. 10.1016/j.surg.2010.11.019
21
JamesD. R. C.Orihuela-EspinaF.LeffD. R.MylonasG. P.KwokK. W.DarziA. W.et al. (2010a). Cognitive burden estimation for visuomotor learning with fNIRS. Med. Image Comput. Comput. Assist. Interv.13, 319–326. 10.1007/978-3-642-15711-0_40
22
JamesD. R. C.Orihuela-EspinaF.LeffD. R.MylonasG. P.KwokK. W.DarziA. W.et al. (2010b). Neuroergonomic assessment of the robotic enhancement of surgery. Surg. Endosc.24, 192–269.
23
JöbsisF. F. (1977). Noninvasive, infrared monitoring of cerebral and myocardial oxygen sufficiency and circulatory parameters. Science.198, 1264–1267. 10.1126/science.929199
24
JurcakV.TsuzukiD.DanI. (2007). 10/20, 10/10 and 10/5 systems revisited: their validity as relative head-surface-based positioning systems. Neuroimage.34, 1600–1611. 10.1016/j.neuroimage.2006.09.024
25
KanwisherN.WojciulikE. (2000). Visual attention: insights from brain imaging. Nat. Rev. Neurosci.1, 91–100. 10.1038/35039043
26
KojimaH.SuzukiT. (2010). Hemodynamic change in occipital lobe during visual search: visual attention allocation measured with NIRS. Neuropsychologia.48, 349–352. 10.1016/j.neuropsychologia.2009.09.028
27
KwokK. W.SunL. W.MylonasG. P.JamesD. R.Orihuela-EspinaF.YangG. Z. (2012). Collaborative gaze channelling for improved cooperation during robotic assisted surgery. Ann. Biomed. Eng.40, 2156–2167. 10.1007/s10439-012-0578-4
28
LeffD. R.ElwellC. E.Orihuela-EspinaF.AtallahL.DelpyD. T.DarziA. W.et al. (2008a). Changes in prefrontal cortical behaviour depend upon familiarity on a bimanual co-ordination task: an fNIRS study. Neuroimage.39, 805–813. 10.1016/j.neuroimage.2007.09.032
29
LeffD. R.LeongJ. J.AggarwalR.YangG. Z.DarziA. (2008b). Could variations in technical skills acquisition in surgery be explained by differences in cortical plasticity?Ann. Surg.247, 540–543. 10.1097/sla.0b013e31815fa42e
30
LeffD. R.Orihuela-EspinaF.AtallahL.AthanasiouT.LeongJ. J.DarziA. W.et al. (2008c). Functional prefrontal reorganization accompanies learning-associated refinements in surgery: a manifold embedding approach. Comput. Aided Surg.13, 325–339. 10.3109/10929080802531482
31
LeongJ. H.AtallahL.MylonasG. P.LeffD. R.EmeryR. J.DarziA. W.et al. (2008). “Investigation of partial directed coherence for hand-eye coordination in laparoscopic training,” in Lecture Notes in Computer Science. eds DohiT.SakumaI.LiaoH. (Berlin Heidelberg: Springer-Verlag), 270–278.
32
MicaliS.VirgiliG.VannozziE.GrassiN.JarrettT. W.BauerJ. J.et al. (2000). Feasibility of telementoring between Baltimore (USA) and Rome (Italy): the first five cases. J. Endourol.14, 493–496. 10.1089/end.2000.14.493
33
MolholmS.SehatpourP.MehtaA. D.ShpanerM.Gomez-RamirezM.OrtigueS.et al. (2006). Audio-visual multisensory integration in superior parietal lobule revealed by human intracranial recordings. J. Neurophysiol.96, 721–729. 10.1152/jn.00285.2006
34
NiuH.WangJ.ZhaoT.ShuN.HeY. (2012). Revealing topological organization of human brain functional networks with resting-state functional near infrared spectroscopy. PLoS One7:e45771. 10.1371/journal.pone.0045771
35
OhuchidaK.KenmotsuH.YamamotoA.SawadaK.HayamiT.MorookaK.et al. (2009). The frontal cortex is activated during learning of endoscopic procedures. Surg. Endosc.2310, 2296–2301. 10.1007/s00464-008-0316-z
36
Orihuela-EspinaF.LeffD. R.JamesD. R. C.DarziA. W.YangG. Z. (2010). Quality control and assurance in functional near infrared spectroscopy (fNIRS) experimentation. Phys. Med. Biol.55, 1–24. 10.1088/0031-9155/55/13/009
37
ParasuramanR. (2003). Neuroergonomics: research and practice. Theor. Issues Erg.4, 5–20. 10.1080/14639220210199753
38
RoyC. S.SherringtonC. S. (1890). On the regulation of the blood-supply of the brain. J. Physiol.11, 85–158. 10.1113/jphysiol.1890.sp000321
39
SchlachtaC. M.LefebvreK. L.SorsdahlA. K.JayaramanS. (2010). Mentoring and telementoring leads to effective incorporation of laparoscopic colon surgery. Surg. Endosc.24, 841–844. 10.1007/s00464-009-0674-1
40
SpornsO.ChialvoD. R.KaiserM.HilgetagC. C. (2004). Organization, development and function of complex brain networks. Trends Cogn. Sci.8, 418–425. 10.1016/j.tics.2004.07.008
41
SpornsO. (2011). Networks of the Brain.Cambridge: MIT Press.
42
Task Force of the European Society of Cardiology the North American Society of Pacing Electrophysiology (1996). Heart rate variability. Standards of measurement, physiological interpretation and clinical use. Task Force of the European Society of Cardiology and the North American Society of Pacing and Electrophysiology. Eur. Heart J.17, 354–381. 10.1161/01.cir.93.5.1043
43
TheeuwesJ. (2010). Top-down and bottom-up control of visual selection. Acta Psychologica.135, 77–99. 10.1016/j.actpsy.2010.02.006
44
TokudaS.ObinataG.PalmerE.ChaparroA. (2011). Estimation of mental workload using saccadic eye movements in a free-viewing task. Conf. Proc. IEEE Eng. Med. Biol. Soc.2011, 4523–4529. 10.1109/iembs.2011.6091121
45
van den HeuvelM. P.MandlR. C.KahnR. S.Hulshoff PolH. E. (2009). Functionally linked resting-state networks reflect the underlying structural connectivity architecture of the human brain. Hum. Brain Mapp.30, 3127–3141. 10.1002/hbm.20737
46
van der StigchelS.BelopolskyA. V.PetersJ. C.WijnenJ. G.MeeterM.TheeuwesJ. (2009). The limits of top-down control of visual attention. Acta. Psychologica.132, 201–212. 10.1016/j.actpsy.2009.07.001
47
van WijkB. C.StamC. J.DaffertshoferA. (2010). Comparing brain networks of different size and connectivity density using graph theory. PLoS One5:e13701. 10.1371/journal.pone.0013701
48
VinjeW. E.GallantJ. L. (2000). Sparse coding and decorrelation in primary visual cortex during natural vision. Science.287, 1273–1276. 10.1126/science.287.5456.1273
49
WilsonM. R.VineS. J.BrightE.MastersR. S.DefriendD.McGrathJ. S. (2011). Gaze training enhances laparoscopic technical skill acquisition and multi-tasking performance: a randomized, controlled study. Surgi. Endosc.25, 3731–3739. 10.1007/s00464-011-1802-2
50
XeroulisG.DubrowskiA.LeslieK. (2009). Simulation in laparoscopic surgery: a concurrent validity study for FLS. Surg. Endosc.23, 161–165. 10.1007/s00464-008-0120-9
51
ZhangD.SnyderA. Z.ShimonyJ. S.FoxM. D.RaichleM. E. (2010). Noninvasive functional and structural connectivity mapping of the human thalamocortical system. Cereb. Cortex.20, 1187–1194. 10.1093/cercor/bhp182
52
ZhengB.JiangX.TienG.MengeghettiA.PantonO. N.AtkinsM. S. (2012). Workload assessment of surgeons: correlation between NASA TLX and blinks. Surg. Endosc.26, 2746–2750. 10.1007/s00464-012-p2268-6
53
ZhengB.JiangX.AtkinsM. S. (2015). Detection of changes in surgical difficulty: Evidence from pupil responses. Surg. Innov. [Epub ahead of print]. 10.1177/1553350615573582
54
ZhuF. F.PooltonJ. M.WilsonM. R.HuY.MaxwellJ. P.MastersR. S.et al. (2011). Implicit motor learning promotes neural efficiency during laparoscopy. Surg. Endosc.25, 2950–2955. 10.1007/s00464-011-1647-8
Summary
Keywords
functional near infrared spectroscopy, optical topography, neuroergonomics, graph theory, collaborative gaze, visual attention, skills assessment, mentoring
Citation
Leff DR, James DRC, Orihuela-Espina F, Kwok K-W, Sun LW, Mylonas G, Athanasiou T, Darzi AW and Yang G-Z (2015) The impact of expert visual guidance on trainee visual search strategy, visual attention and motor skills. Front. Hum. Neurosci. 9:526. doi: 10.3389/fnhum.2015.00526
Received
28 July 2015
Accepted
10 September 2015
Published
14 October 2015
Volume
9 - 2015
Edited by
Klaus Gramann, Berlin Institute of Technology, Germany
Reviewed by
Peter König, University of Osnabrück, Germany; Frederic Dehais, Institut Supérieur de l’Aéronautique et de l’Espace, France
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Copyright
© 2015 Leff, James, Orihuela-Espina, Kwok, Sun, Mylonas, Athanasiou, Darzi and Yang.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution and reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Guang-Zhong Yang, Hamlyn Centre for Robotic Surgery, Imperial College London, Level 4, Bessemer Building, South Kensington Campus, London, SW7 2AZ, UK g.z.yang@imperial.ac.uk
†These authors have contributed equally to this work.
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