Intraoperative Navigation Systems for Image-Guided Surgery

Recent technological advancements in medical imaging equipment have resulted in a dramatic improvement of image accuracy, now capable of providing useful information previously not available to clinicians. In the surgical context, intraoperative imaging provides a crucial value for the success of the operation. Many nontrivial scientific and technical problems need to be addressed in order to efficiently exploit the different information sources nowadays available in advanced operating rooms. In particular, it is necessary to provide: (i) accurate tracking of surgical instruments, (ii) real-time matching of images from different modalities, and (iii) reliable guidance toward the surgical target. Satisfying all of these requisites is needed to realize effective intraoperative navigation systems for image-guided surgery. Various solutions have been proposed and successfully tested in the field of image navigation systems in the last ten years; nevertheless several problems still arise in most of the applications regarding precision, usability and capabilities of the existing systems. Identifying and solving these issues represents an urgent scientific challenge. This thesis investigates the current state of the art in the field of intraoperative navigation systems, focusing in particular on the challenges related to efficient and effective usage of ultrasound imaging during surgery. The main contribution of this thesis to the state of the art are related to: Techniques for automatic motion compensation and therapy monitoring applied to a novel ultrasound-guided surgical robotic platform in the context of abdominal tumor thermoablation. Novel image-fusion based navigation systems for ultrasound-guided neurosurgery in the context of brain tumor resection, highlighting their applicability as off-line surgical training instruments. The proposed systems, which were designed and developed in the framework of two international research projects, have been tested in real or simulated surgical scenarios, showing promising results toward their application in clinical practice

Enabling technologies for MRI guided interventional procedures

This dissertation addresses topics related to developing interventional assistant devices for Magnetic Resonance Imaging (MRI). MRI can provide high-quality 3D visualization of target anatomy and surrounding tissue, but the benefits can not be readily harnessed for interventional procedures due to difficulties associated with the use of high-field (1.5T or greater) MRI. Discussed are potential solutions to the inability to use conventional mecha- tronics and the confined physical space in the scanner bore. This work describes the development of two apparently dissimilar systems that repre- sent different approaches to the same surgical problem - coupling information and action to perform percutaneous (through the skin) needle placement with MR imaging. The first system addressed takes MR images and projects them along with a surgical plan directly on the interventional site, thus providing in-situ imaging. With anatomical images and a corresponding plan visible in the appropriate pose, the clinician can use this information to perform the surgical action. My primary research effort has focused on a robotic assistant system that overcomes the difficulties inherent to MR-guided procedures, and promises safe and reliable intra-prostatic needle placement inside closed high-field MRI scanners. The robot is a servo pneumatically operated automatic needle guide, and effectively guides needles under real- time MR imaging. This thesis describes development of the robotic system including requirements, workspace analysis, mechanism design and optimization, and evaluation of MR compatibility. Further, a generally applicable MR-compatible robot controller is de- veloped, the pneumatic control system is implemented and evaluated, and the system is deployed in pre-clinical trials. The dissertation concludes with future work and lessons learned from this endeavor

Interactive Multi-Stage Robotic Positioner for Intra-Operative MRI-Guided Stereotactic Neurosurgery

Magnetic resonance imaging (MRI) demonstrates clear advantages over other imaging modalities in neurosurgery with its ability to delineate critical neurovascular structures and cancerous tissue in high-resolution 3D anatomical roadmaps. However, its application has been limited to interventions performed based on static pre/post-operative imaging, where errors accrue from stereotactic frame setup, image registration, and brain shift. To leverage the powerful intra-operative functions of MRI, e.g., instrument tracking, monitoring of physiological changes and tissue temperature in MRI-guided bilateral stereotactic neurosurgery, a multi-stage robotic positioner is proposed. The system positions cannula/needle instruments using a lightweight (203 g) and compact (Ø97 × 81 mm) skull-mounted structure that fits within most standard imaging head coils. With optimized design in soft robotics, the system operates in two stages: i) manual coarse adjustment performed interactively by the surgeon (workspace of ±30°), ii) automatic fine adjustment with precise (<0.2° orientation error), responsive (1.4 Hz bandwidth), and high-resolution (0.058°) soft robotic positioning. Orientation locking provides sufficient transmission stiffness (4.07 N/mm) for instrument advancement. The system's clinical workflow and accuracy is validated with lab-based (<0.8 mm) and MRI-based testing on skull phantoms (<1.7 mm) and a cadaver subject (<2.2 mm). Custom-made wireless omni-directional tracking markers facilitated robot registration under MRI

Image-Based Force Estimation and Haptic Rendering For Robot-Assisted Cardiovascular Intervention

Clinical studies have indicated that the loss of haptic perception is the prime limitation of robot-assisted cardiovascular intervention technology, hindering its global adoption. It causes compromised situational awareness for the surgeon during the intervention and may lead to health risks for the patients. This doctoral research was aimed at developing technology for addressing the limitation of the robot-assisted intervention technology in the provision of haptic feedback. The literature review showed that sensor-free force estimation (haptic cue) on endovascular devices, intuitive surgeon interface design, and haptic rendering within the surgeon interface were the major knowledge gaps. For sensor-free force estimation, first, an image-based force estimation methods based on inverse finite-element methods (iFEM) was developed and validated. Next, to address the limitation of the iFEM method in real-time performance, an inverse Cosserat rod model (iCORD) with a computationally efficient solution for endovascular devices was developed and validated. Afterward, the iCORD was adopted for analytical tip force estimation on steerable catheters. The experimental studies confirmed the accuracy and real-time performance of the iCORD for sensor-free force estimation. Afterward, a wearable drift-free rotation measurement device (MiCarp) was developed to facilitate the design of an intuitive surgeon interface by decoupling the rotation measurement from the insertion measurement. The validation studies showed that MiCarp had a superior performance for spatial rotation measurement compared to other modalities. In the end, a novel haptic feedback system based on smart magnetoelastic elastomers was developed, analytically modeled, and experimentally validated. The proposed haptics-enabled surgeon module had an unbounded workspace for interventional tasks and provided an intuitive interface. Experimental validation, at component and system levels, confirmed the usability of the proposed methods for robot-assisted intervention systems

AUGMENTED REALITY AND INTRAOPERATIVE C-ARM CONE-BEAM COMPUTED TOMOGRAPHY FOR IMAGE-GUIDED ROBOTIC SURGERY

Minimally-invasive robotic-assisted surgery is a rapidly-growing alternative to traditionally open and laparoscopic procedures; nevertheless, challenges remain. Standard of care derives surgical strategies from preoperative volumetric data (i.e., computed tomography (CT) and magnetic resonance (MR) images) that benefit from the ability of multiple modalities to delineate different anatomical boundaries. However, preoperative images may not reflect a possibly highly deformed perioperative setup or intraoperative deformation. Additionally, in current clinical practice, the correspondence of preoperative plans to the surgical scene is conducted as a mental exercise; thus, the accuracy of this practice is highly dependent on the surgeon’s experience and therefore subject to inconsistencies. In order to address these fundamental limitations in minimally-invasive robotic surgery, this dissertation combines a high-end robotic C-arm imaging system and a modern robotic surgical platform as an integrated intraoperative image-guided system. We performed deformable registration of preoperative plans to a perioperative cone-beam computed tomography (CBCT), acquired after the patient is positioned for intervention. From the registered surgical plans, we overlaid critical information onto the primary intraoperative visual source, the robotic endoscope, by using augmented reality. Guidance afforded by this system not only uses augmented reality to fuse virtual medical information, but also provides tool localization and other dynamic intraoperative updated behavior in order to present enhanced depth feedback and information to the surgeon. These techniques in guided robotic surgery required a streamlined approach to creating intuitive and effective human-machine interferences, especially in visualization. Our software design principles create an inherently information-driven modular architecture incorporating robotics and intraoperative imaging through augmented reality. The system's performance is evaluated using phantoms and preclinical in-vivo experiments for multiple applications, including transoral robotic surgery, robot-assisted thoracic interventions, and cocheostomy for cochlear implantation. The resulting functionality, proposed architecture, and implemented methodologies can be further generalized to other C-arm-based image guidance for additional extensions in robotic surgery

Novel Magnetic Resonance Imaging-Compatible Mechatronic Needle Guidance System for Prostate Focal Laser Ablation Therapy

Advances in prostate cancer (PCa) screening techniques have led to diagnosis of many cases of low-grade and highly localized disease. Conventional whole-gland therapies often result in overtreatment in such cases and debate still surrounds the optimal method of oncologic control. MRI-guided prostate focal laser ablation (FLA) is a minimally invasive treatment option, which has demonstrated potential to destroy localized lesions while sparing healthy prostatic tissue, thereby reducing treatment-related side effects. Many challenges still exist in the development of FLA, including patient selection; tumour localization, visualization, and characterization; needle guidance; and evaluation of treatment efficacy. The objective of this thesis work was to advance and enhance techniques for needle guidance in MRI-guided focal laser ablation (FLA) therapy of PCa. Several steps were taken in achieving this goal. Firstly, we evaluated the overlap between identified lesions and MRI-confirmed ablation regions using conventional needle guidance. Non-rigid thin-plate spline registration of pre-operative and intra-operative images was performed to align lesions with ablation boundaries and quantify the degree of coverage. Complete coverage of the lesion with the ablation zone is a clinically important metric of success for FLA therapy and we found it was not achieved in many cases. Therefore, our next step was to develop an MRI-compatible, remotely actuated mechatronic system for transperineal FLA of prostate cancer. The system allows physicians in the MRI scanner control room to accurately target lesions through 4 degrees of freedom while the patient remains in the scanner bore. To maintain compatibility with the MRI environment, piezoelectric motors were used to actuate the needle guidance templates, the device was constructed from non-ferromagnetic materials, and all cables were shielded from electromagnetic interference. The MR compatibility and needle placement accuracy of the device were evaluated with virtual and phantom targets. The system should next be validated for accuracy and usefulness in a clinical trial where more complex tissue properties and potential patient motion will be encountered. Future advances in modeling the tissue properties and compensating for deformation of the prostate, as well as predicting needle deflection, will further bolster the potential of FLA as option for the management of PCa

Intra-Operative Needle Tracking Using Optical Shape Sensing Technology

RÉSUMÉ Contexte : Les métastases hépatiques colorectales sont la principale cause de décès liée au cancer du foie dans le monde. Au cours de la dernière décennie, il a été démontré que l’ablation par radiofréquence (RFA, pour radiofrequency ablation) est une méthode de traitement percutané très efficace contre ce type de métastases. Cela dit, un positionnement précis de l’embout de l’aiguille utilisé en RFA est essentiel afin de se départir adéquatement de la totalité des cellules cancéreuses. Une technologie prometteuse pour obtenir la forme et la position de l’aiguille en temps réel est basée sur l’utilisation de réseaux de Bragg (FBG, pour fiber Bragg grating) à titre de senseur de contrainte. En effet, ce type de senseurs a une vitesse d’acquisition allant jusqu’à 20 kHz, ce qui est suffisamment rapide pour permettre des applications de guidage en temps réel. Méthode : Les travaux présentés au sein de ce mémoire décrivent le développement d’une technologie, compatible aux systèmes d’imageries par résonance magnétique (IRM), permettant d’effectuer le suivi de la forme de l’aiguille utilisée en RFA. Premièrement, trois fibres contenant une série de réseaux de Bragg ont été collées dans une géométrie spécifique et intégrées à l’intérieur d’une aiguille 20G-150 mm. Ensuite, un algorithme de reconstruction de forme tridimensionnelle a été développé, basé sur les mesures de translation spectrales des FBGs acquises en temps réel durant le guidage de l’aiguille. La position du bout de l’aiguille ainsi que la forme tridimensionnelle complète de celle-ci ont été représentées et comparées à la position de la zone ciblée à la suite d’une simple méthode de calibration. Finalement, nous avons validé notre système de navigation en effectuant une série d’expériences in vitro. La précision du système de reconstruction tridimensionnelle de la forme et de l’orientation de l’aiguille a été évaluée en utilisant deux caméras positionnées perpendiculairement de manière à connaitre la position de l’aiguille dans le système d’axes du laboratoire. L’évaluation de la précision au bout de l’aiguille a quant à elle été faite en utilisant des fantômes précisément conçus à cet effet. Finalement, des interventions guidées en IRM ont été testées et comparées au système de navigation électromagnétique NDI Aurora (EMTS, pour Electromagnétic tracking system) par le biais du FRE (fiducial registration error) et du TRE (target registration error). Résultats: Lors de nos premières expériences in vitro, la précision obtenue quant à la position du bout de l’aiguille était de 0,96 mm pour une déflexion allant jusqu’à ±10,68 mm. À titre comparatif, le système d’Aurora a une précision de 0.84 mm dans des circonstances similaires. Les résultats obtenus lors de nos seconds tests ont démontré que l’erreur entre la position réelle du bout de l’aiguille et la position fournie par notre système de reconstruction de forme est de 1,04 mm, alors qu’elle est de 0,82 mm pour le EMTS d’Aurora. Pour ce qui est de notre dispositif, cette erreur est proportionnelle à l’amplitude de déflexion de l’aiguille, contrairement à l’EMTS pour qui l’erreur demeure relativement constante. La dernière expérience a été effectuée à l’aide d’un fantôme en gélatine, pour laquelle nous avons obtenu un TRE de 1,19 mm pour notre système basé sur les FBG et de 1.06 mm pour le système de navigation par senseurs électromagnétiques (EMTS). Les résultats démontrent que l’évaluation du FRE est similaire pour les deux approches. De plus, l’information fournie par les caméras permet d’estimer la précision de notre dispositif en tout point le long de l’aiguille. Conclusion : En analysant et en interprétant les résultats obtenus lors de nos expériences in vitro, nous pouvons conclure que la précision de notre système de navigation basé sur les FBG est bien adaptée pour l’évaluation de la position du bout et la forme de l’aiguille lors d’interventions RFA des tumeurs du foie. La précision de notre système de navigation est fortement comparable avec celle du système basé sur des senseurs électromagnétiques commercialisé par Aurora. L’erreur obtenue par notre système est attribuable à un mauvais alignement des réseaux de Bragg par rapport au plan associé à la région sensorielle et aussi à la différence entre le diamètre des fibres et celui de la paroi interne de l’aiguille.----------ABSTRACT Background: Colorectal liver metastasis is the leading cause of liver cancer death in the world. In the past decade, radiofrequency ablation (RFA) has proven to be an effective percutaneous treatment modality for the treatment of metastatic hepatic cancer. Accurate needle tip placement is essential for RFA of liver tumors. A promising technology to obtain the real-time information of the shape of the needle is by using fiber Bragg grating (FBG) sensors at high frequencies (up to 20 kHz). Methods: In this thesis work, we developed an MR-compatible needle tracking technology designed for RFA procedures in liver cancer. At first, three fibers each containing a series of FBGs were glued together and integrated inside a 20G-150 mm needle. Then a three-dimensional needle shape reconstruction algorithm was developed, based on the FBG measurements collected in real-time during needle guidance. The tip position and shape of the reconstructed 3D needle model were represented with respect to the target defined in the image space by performing a fiducial-based registration. Finally, we validated our FBG-based needle navigation by doing a series of in-vitro experiments. The shape of the 3D reconstructed needle was compared to measurements obtained from camera images. In addition, the needle tip accuracy was assessed on the ground-truth phantoms. Finally, MRI guided intervention was tested and compared to an NDI Aurora EM tracking system (EMTS) in terms of fiducial registration error (FRE) and target registration error (TRE). Results: In our first in-vitro experiment, the tip tracking accuracy of our FBG tracking system was of 0.96 mm for the maximum tip deflection of up to ±10.68 mm, while the tip tracking accuracy of the Aurora system for the similar test was 0.84 mm. Results obtained from the second in-vitro experiment demonstrated tip tracking accuracy of 1.04 mm and 0.82 mm for our FBG tracking system and Aurora EMTS, respectively for the maximum tip deflection of up to ±16.83 mm. The tip tracking error in the developed FBG-based system reduced linearly with decreasing tip deflection, while the error was similar but randomly varying for the EMTS. The last experiment was done with a gel phantom, yielding a TRE of 1.19 mm and 1.06 mm for the FBG and EM tracking, respectively. Results showed that across all experiments, the computed FRE of both tracking systems was similar. Moreover, actual shape information obtained from the camera images ensured the shape accuracy of our FBG-based needle shape model. Conclusion: By analyzing and interpreting the results obtained from the in-vitro experiments, we conclude that the accuracy of our FBG-based tracking system is suitable for needle tip detection in RFA of liver tumors. The accuracy of our tracking system is nearly comparable to that of the Aurora EMTS. The error given by our tracking system is attributed to the misalignment of the FBG sensors in a single axial plane and also to the gap between the needle's inner wall and the fibers inside

Should patients with brain implants undergo MRI?

Patients suffering from neuronal degenerative diseases are increasingly being equipped with neural implants to treat symptoms or restore functions and increase their quality of life. Magnetic resonance imaging (MRI) would be the modality of choice for diagnosis and compulsory post-operative monitoring of such patients. However, interactions between the MR environment and implants pose severe health risks to the patient. Nevertheless, neural implant recipients regularly underwent MRI examinations, and adverse events were reported rarely. This should not imply that the procedures are safe. More than 300.000 cochlear implant recipients are excluded from MRI unless the indication outweighs excruciating pain. For 75.000 DBS recipients quite the opposite holds: MRI is considered essential part of the implantation procedure and some medical centres deliberately exceed safety regulations which they referred to as crucially impractical. MRI related permanent neurological dysfunctions in DBS recipients have occurred in the past when manufacturer recommendations were exceeded. Within the last decades extensive effort has been invested to identify, characterise, and quantify the occurring interactions. Today we are far from a satisfying solution to achieve a safe and beneficial MR procedure for all implant recipients. To contribute, we intend to raise awareness of a growing concern and want to summon the community to stop absurdities and instead improve the situation for the increasing number of patients. Therefore, we review implant safety in the MRI literature from an engineering point of view, with a focus on cochlear and DBS implants as success stories in clinical practice. We briefly explain fundamental phenomena which can lead to patient harm, and point out breakthroughs and errors made. We end with conclusions and strategies to avoid future implants from being contraindicated to MR examinations. We believe that implant recipients should enter MRI, but before doing so, we should make sure that the procedure is reasonable