Abstract:
The present invention relates to a catheter (6) comprising: a connector (65, 66) at a proximal side of the catheter for connecting the catheter to an external signal transmission/receiving unit (10) for transmitting and/or receiving signals, an electrode (63, 64) at a distal side of the catheter, and an electrical connection including an electrical wire (61, 62) for electrically connecting the electrode and the connector for the transmission of signals between the electrode and the connector, wherein the electrical connection has a high electrical resistance of at least 1 kOmega, in particular of at least 5 kOmega. Thus, the present invention provides a solution to prevent excessive heating during EP interventions under MR guidance by using highly resistive wires and or lumped resistors as connections within catheters.
Abstract:
A catheter comprising: -a transmission line (104, 106, 924, 1202, 1302, 1902,), wherein the transmission line comprises a plurality of radio frequency traps (118, 318, 418, 518, 618, 718, 818, 918, 1018, 1202, 1404,); and -a cooling line (104, 304, 1200, 1900) for cooling the plurality of radio frequency traps with a fluid.
Abstract:
The invention relates to electrophysiology catheter systems and their use, such as in an MRI environment, and in particular to analysis of electric signals from such. An electrophysiology (EP) catheter with a plurality of electrically isolated electrode segments arranged in longitudinally spaced bands around the catheter is used to detect electric signals. A workstation receives the electrical signals which are then processed by a processing unit. Electric signals from electrode segments can be used to determine roll angle information of the catheter in relation to patient anatomy by determining signals from electrode segments in contact with tissue. Also, electric signals can be used to extract a reference signal that can be used to correct for gradient induced artefacts.
Abstract:
A transmission cable for use in an elongate medical device (420) such as a catheter, guide wire, etc., wherein the transmission cable is capable of being switched to an MR-safe mode only when necessary, while retaining its optimal electrical transmission properties otherwise, is disclosed herein. The transmission cable comprises a transmission line including at least two electrically conductive line segments (104a, 104b) separated by a non-conductive gap (106a), a bridging unit comprising at least one electrically conductive bridge segment (108a) capable of bridging the non-conductive gap, and a switching unit (112) arranged to move the bridging unit and/or the transmission line to electrically connect the two line segments by closing the non-conductive gap using the bridge segment or to electrically disconnect the two line segments by opening the non-conductive gap.
Abstract:
The invention relates to a device for magnetic resonance imaging of a body (7), wherein the device (1) is arranged to a) generate a series of MR echo signals (20) by subjecting at least a portion of the body (7) to an MR imaging sequence comprising RF pulses and switched magnetic field gradients, b) acquire the MR echo signals for reconstructing an MR image (21) therefrom, c) calculate a susceptibility gradient map (22) from the MR echo signals or from the MR image (21), the susceptibility gradient map (22) indicating local susceptibility induced magnetic field gradients, d) determine the position of an interventional instrument (16) having paramagnetic or ferromagnetic properties from the susceptibility gradient map (22).
Abstract:
A magnetic resonance method comprises applying a radio frequency excitation in an examination region (14), measuring a magnetic resonance signal generated by the applied radio frequency excitation in a subject (16) in the examination region, monitoring a radio frequency parameter during the applying, and evaluating subject safety based on the monitoring. A magnetic resonance safety monitor (40) comprises an analyzer (42, 44, 46, 50) configured to (i) receive a radio frequency signal during magnetic resonance excitation, (ii) extract a radio frequency parameter from the received radio frequency signal, and (iii) evaluate subject safety based on the extracted radio frequency parameter, and a remediation module (54) configured to perform a remediation of the magnetic resonance excitation responsive to the evaluation (iii) indicating a potentially unsafe condition.