Abstract: A flow logging utility tracer (“FLUTE”) system can present a FLUTE user interface through which the FLUTE system can receive a trace request. The FLUTE system can interface, via a FLUTE controller, with a FLUTE adapter corresponding to a cloud environment associated with the trace request. The FLUTE adaptor can extract event log data from a log repository corresponding to the cloud environment. The FLUTE adapter can filter the event log data according to a logging specification. The FLUTE adapter can transform the filtered event log data for compatibility with a FLUTE stitcher. The FLUTE stitcher can generate tracing data based upon the event log data. The FLUTE stitcher can correlate the tracing data based upon a common identifier enforced by the logging specification, prepare the tracing data for publication to a distributed tracing system, and publish the tracing data to the distributed tracing system for storage.

Abstract: This present disclosure relates to compositions and methods useful in therapeutic embolisation and particularly in methods for bariatric arterial embolisation (BAE).

Abstract: This present disclosure relates to compositions and methods useful in therapeutic embolisation and particularly in methods for bariatric arterial embolisation (BAE).

Abstract: A method of treating CNS tumors such as gliomas is provided comprising delivering a ?-emitting radionuclide containing composition to the tumor via the cerebral vasculature.

Abstract: Sterile RF coil arrangements for use in magnetic resonance imaging are provided. The sterile coil arrangements can be formed by spraying or coating a curable liquid onto an RF coil housing and allowing the liquid to cure or dry to form a continuous sterile layer on the coil housing. The thickness of the sterile layer can be between 100 and 1000 micrometers. The curable liquid can include an antimicrobial or antibacterial agent, such as silver ions or triclosan, to better maintain sterility of the coil arrangement. The curable liquid can be selected such that it adheres to the housing when cured and is also removable without leaving residue behind.

Abstract: A configurable coil arrangement for use with MRI-guided procedures is provided that facilitates optimal imaging for both pre-procedure planning and imaging of the target sites during the procedure. The coil arrangement includes a plurality of connected coil elements. Spacers connecting the coil elements can be adjustable and/or deformable to provide one or more openings in the coil arrangement of optimal size for accessing the subject within the imaged region. Individual coil elements can also be removed to provide access openings during such procedures, or left in the array for improved pre- and post-procedure image quality. The MRI system can be configured to detect configurations of the coil arrangement and modify imaging parameters to optimize image quality.

Abstract: Sterile RF coil arrangements for use in magnetic resonance imaging are provided. The sterile coil arrangements can be formed by spraying or coating a curable liquid onto an RF coil housing and allowing the liquid to cure or dry to form a continuous sterile layer on the coil housing. The thickness of the sterile layer can be between 100 and 1000 micrometers. The curable liquid can include an antimicrobial or antibacterial agent, such as silver ions or triclosan, to better maintain sterility of the coil arrangement. The curable liquid can be selected such that it adheres to the housing when cured and is also removable without leaving residue behind.

Abstract: A configurable coil arrangement for use with MRI-guided procedures is provided that facilitates optimal imaging for both pre-procedure planning and imaging of the target sites during the procedure. The coil arrangement includes a plurality of connected coil elements. Spacers connecting the coil elements can be adjustable and/or deformable to provide one or more openings in the coil arrangement of optimal size for accessing the subject within the imaged region. Individual coil elements can also be removed to provide access openings during such procedures, or left in the array for improved pre- and post-procedure image quality. The MRI system can be configured to detect configurations of the coil arrangement and modify imaging parameters to optimize image quality.

Abstract: In a method for image guided prostate cancer needle biopsy, a first registration is performed to match a first image of a prostate to a second image of the prostate. Third images of the prostate are acquired and compounded into a three-dimensional (3D) image. The prostate in the compounded 3D image is segmented to show its border. A second registration and then a third registration different from the second registration is performed on distance maps generated from the prostate borders of the first image and the compounded 3D image, wherein the first and second registrations are based on a biomechanical property of the prostate. A region of interest in the first image is mapped to the compounded 3D image or a fourth image of the prostate acquired with the second modality.

Abstract: A device and method of the present invention provides application of low-energy acoustic waves to indwelling surfaces of a catheter in order to remove and prevent microbial biofilm formation. The low-energy acoustic waves are generated by an electrically activated piezo element. The device can take the form of a luer connector configured to couple to the hub of the indwelling catheter or can take the form of a catheter insert. The characteristics of the acoustic waves can be varied in order to inhibit bacterial adhesion to the indwelling surfaces of the catheter. Moreover, the characteristics of the acoustic waves must also be in a range so as to not induce bacterial adhesion to the indwelling catheter surfaces.

Abstract: Device to thermally affect delimited regions of the body of a patient, wherein it possesses at least one heating or cooling means that can be inserted into a blood vessel of the patient or can be attached to a blood vessel of the patient in order to heat or cool the blood in a portion of the blood vessel that leads into or away from a tissue to be treated.

Abstract: Device to thermally affect delimited regions of the body of a patient, wherein it possesses at least one heating or cooling means that can be inserted into a blood vessel of the patient or can be attached to a blood vessel of the patient in order to heat or cool the blood in a portion of the blood vessel that leads into or away from a tissue to be treated.

Abstract: A thermal ablation device for introduction of heat or cold into the body of a patient has a first heating or cooling device to heat or cool the tissue to be ablated, as well as at least one additional cooling or heating arrangement that serves to cool or heat tissue surrounding the tissue to be ablated, and that can be introduced into a natural or latent cavity of the patient.

Abstract: In a method for image guided prostate cancer needle biopsy, a first registration is performed to match a first image of a prostate to a second image of the prostate. Third images of the prostate are acquired and compounded into a three-dimensional (3D) image. The prostate in the compounded 3D image is segmented to show its border. A second registration and then a third registration different from the second registration is performed on distance maps generated from the prostate borders of the first image and the compounded 3D image, wherein the first and second registrations are based on a biomechanical property of the prostate. A region of interest in the first image is mapped to the compounded 3D image or a fourth image of the prostate acquired with the second modality.