Described is a process for performing radiotherapy treatment according to the invention comprising the following operations: S.1) providing a radiotherapy system (1) comprising a radiation head (3), a movement system (7), a diagnostics subsystem for images, in turn comprising a probe (13) and a position detection subsystem (11); S.2) by means of the at least one probe (13) acquiring a plurality of images (IM_1, IM_2, IMJ, IM_N) of internal sections of a body to be treated (P); S.3) by means of the position detection subsystem (11) detecting the position in space of the probe (13) whilst it acquires each of said images (IMJ, IMJ, IMJ, IM_N); S.4) on the basis of said images (IMJ, IMJ, IMJ, IM_N) and by means of the movement system (7) moving the radiation head (3) and performing a predetermined treatment on the body to be treated (P).

A surgical system includes a skull attachment device that includes a support base configured to seat against a skull of a patient and one or more pins extending from a bottom surface of the support base and configured to pierce the scalp to seat the skull attachment device against the skull. The surgical system also includes an interface disposed along a top surface of the support base and having a shape that compliments a profile of a mating feature of a stereotactic device for defining a position and an orientation of the stereotactic device with respect to the support base while the interface is engaged with the mating feature.

The present invention relates to a mixed reality system integrated with a surgical navigation system including a group of moveable position markers configured on a surgical instrument; a position sensor sensing the group of moveable position markers to acquire an instrument coordinate for the surgical instrument; a registered positioning marker configured in proximity to a surgical area to acquire a surgical area coordinate for the surgical area; a plurality of mixed reality sensors detecting the registered positioning marker and a plurality of mixed reality information; a computing unit module configured to receive the instrument coordinate, the surgical area coordinate, the plurality of mixed reality information, and a digital model of the surgical area, to render the digital model corresponded to the surgical area, and to add a digital instrument object into the digital model in accordance with the instrument coordinate; and a mixed reality display providing for a user to view and showing the digital model and the digital instrument object to the user upon the receipt thereof.

A surgical instrument for treating the tissue of a patient is disclosed. The surgical instrument comprises a housing including a handle, a housing frame comprising a housing connector, and a drive system comprising at least one electric motor. The surgical instrument further comprises a shaft assembly releasably assembled to the housing including a shaft frame comprising a proximal connector and a distal connector, wherein the proximal connector is releasably coupled to the housing connector and a shaft drive system comprising at least one rotatable shaft operably coupled to the electric motor. The surgical instrument further comprises an end effector releasably assembled to the shaft assembly including an end effector frame comprising an end effector connector releasably coupled to the distal connector of the shaft assembly, a plurality of staple cartridges removably stored in the end effector, and a plurality of end effector drivers operably coupled to the rotatable shaft.

An electromagnetic device includes a jig and multiple wires. The jig includes a center member and coil-separating blocks. The coil-separating blocks protrude from the center member and are separated from each other to provide a coil channels. Each of the wires is wrapped on the jig, around the center member, and in one of the coil channels to form one of a multiple coils. Each of the coils is configured to connect to an electromagnetic navigation system and generate respective electromagnetic fields to be emitted relative to a subject.

A registration fixture is configured for use with a medical imaging system. The registration fixture comprises a rigid internal structure comprising a plurality of fiducial markers arranged in a predefined pattern. The registration fixture further comprises a housing configured to surround the rigid internal structure. The registration fixture is configured to be mounted on a patient table.

A head stabilization device or HFD includes a plurality of integrated markers. The HFD may be in the form of a skull clamp, vacuum bag, combinations thereof, or other supporting structure. The integrated markers include MRI markers detectable by an MRI scanner and fiducial markers detectable by a registration tool of a navigation system. The markers provide a reference point relative to an operation site in a patient for use in a navigation guided procedure and aid in registering or calibrating the location of the patient with captured images used in the navigation guided procedure.

Example systems and techniques for denervation, for example, renal denervation. In some examples, a processor determines one or more tissue characteristics of tissue proximate a target nerve and a blood vessel. The processor may generate, based on the one or more tissue characteristics, an estimated volume of influence of denervation therapy delivered by a therapy delivery device disposed within the blood vessel. The processor may generate a graphical user interface including a graphical representation of the tissue proximate the target nerve and the blood vessel and a graphical representation of the estimated volume of influence.

An MR marker (501, 601, 803, 902) for magnetic resonance imaging (MRI) guided intervention and method of fabricating same. The tracking device can be integrated with an MRI-guided robotic system to provide precise positional tracking of the interventional tools and robotic components, allowing safe operation inside the human body. The MR tracking device includes a plurality of stacked flexible printed circuit boards; a plurality of flat planar spirals comprised of a non-ferromagnetic material and directly disposed on a top surface and a bottom surface side of each flexible printed circuit board, a biocompatible, non-ferromagnetic material encapsulating the flexible printed circuit boards; and an adhesive bonding the flexible printed circuit boards. In another aspect, an orientation-independent device is provided including three or more markers (501, 601, 803, 902) in an array around a cylindrical substrate.

This document relates to the apparatus and methods used in the minimally invasive creation of arteriovenous fistula (AVF). In particular, the invention relates to the creation of an AVF using catheters and an alignment methodology that is based upon detection of asymmetric electric fields. The invention finds particular application in vascular access (VA) in the hemodialysis (HD) population.