摘要:
The present invention relates to a monitoring apparatus (101) for monitoring an ablation procedure. The monitoring apparatus (101) comprises an ultrasound signal providing unit for providing an ultrasound signal that depends on received echo series of an object (4) that is ablated. The monitoring apparatus (101) further comprises an ablation depth determination unit (103) for determining an ablation depth from the provided ultrasound signal. The ablation depth can be determined directly from the ultrasound signal and is an important parameter while performing an ablation procedure. For example, it can be used for determining the progress of ablation within the object (4) and for determining when the ablation has reached a desired progression.
摘要:
The present invention relates to a monitoring apparatus (101) for monitoring an ablation procedure. The monitoring apparatus (101) comprises an ultrasound signal providing unit for providing an ultrasound signal that depends on received echo series of an object (4) that is ablated. The monitoring apparatus (101) further comprises an ablation depth determination unit (103) for determining an ablation depth from the provided ultrasound signal. The ablation depth can be determined directly from the ultrasound signal and is an important parameter while performing an ablation procedure. For example, it can be used for determining the progress of ablation within the object (4) and for determining when the ablation has reached a desired progression.
摘要:
A catheter apparatus (100, 2000, 3000, 4000, 540) includes an elongated body (110) having proximal (112) and distal (114) ends, an acoustic transducer (130, 2300, 5 3300, 4300, 544), disposed proximate the distal end (114) of the elongated body (110), and a variably-refracting acoustic lens (140, 2200, 3200, 4200, 542) adapted to dynamically adjust a direction associated with an acoustic wave coupled to the acoustic transducer in response to one or more control signals provided thereto.
摘要:
In a medical therapy or diagnostic system, magnetic resonance (MR) techniques are used in order to determine the position of the focal point of an ultrasound wave with respect to a patient's body. Therefore, it is an object of the present invention to provide an ultrasound waveguide which could be used within a magnetic resonance environment. To better address these concerns, it is an aspect of the present invention to provide an ultrasound waveguide comprising an electrically conducting section and an electrically isolating section. A reduction of the length of an electrically isolating section possibly decreases the electromagnetic coupling of the high frequency electromagnetic field in the MR environment to the electrically conducting section.
摘要:
A catheter apparatus includes an elongated body having proximal and distal ends, and an acoustic transducer disposed proximate the distal end of the elongated body. A variably-refracting acoustic lens is provided to dynamically adjust a direction associated with an acoustic wave coupled to the acoustic transducer in response to one or more control signals provided thereto.
摘要:
A display panel includes pixels with a light emissive layer and an electrode layer deposited on the light emissive layer. A first pixel is determined by a first barrier structure and a second pixel, adjacent to the first pixel, is determined by a second barrier structure. The first and second barrier structures are separated by an electrically conductive structure in electrical contact with the electrode layer. Accordingly, space is available between the barrier structures for electrical shunting of the electrode layer.
摘要:
The application relates to an ingestible capsule and method for in vivo imaging and/or treatment of one or more diseased areas of interest within the gastrointestinal tract of an animal or human being. The capsule comprises an image sensor; a lens system for focusing images onto the image sensor; at least one light source for illumination of the tissue area of interest, the at least one light source optionally being capable of providing optical therapeutic treatment to the diseased areas; a variable lens system located in front of the at least one light source, wherein the variable lens system comprises beam steering means and focusing means for directing and focusing the light beams from the at least one light source onto the diseased tissue areas, —a control unit in communication with the image sensor, the at least one light source, and variable lens system, a power source for powering the image sensor, the at least one light source and the control unit; and a non-digestible, transparent outer protective shell configured to pass through the gastrointestinal tract, housing within the image sensor, the lens system, the at least one light source, the variable lens system, the control unit and the power source.
摘要:
The invention relates to a method of determining in vitro the amount of nuclear DNA within a human or animal cell using UV absorption measurement with UV light. The invention also relates to a method for detecting in vitro cancerous cells in a biological sample relying on the aforementioned principles. The invention also relates to an in vitro method of diagnosing or predicting the likely occurrence of cancer in a human or animal subject.
摘要:
A system for imaging of prostate cancer in a prostate in vivo is provided. The system utilizes Diffuse Optical Tomography (DOT) for creating a 3D image for the detection of suspicious prostate tissue. The DOT image may be used to guide the biopsy, thereby reducing the number of false negatives. A method, computer-readable medium and use are also provided.
摘要:
A method of displaying an input signal (IV) on a full color LED display is discussed wherein the display has pixels (11) comprising at least four LED's (PLi) which respectively emit light with four primary colors. The method comprises converting (SC) the input signal (IV) into drive signals for the at least four LED's (PLi). The converting (SC) comprises: (i) determining (RD) valid ranges (VRi) of at least two of the drive signals (DSi) to obtain a color of the combined light emitted which fits the input signal (IV), (ii) determining (LD) a gradation or lifetime indication (LTi) of the at least two LED's (PLi) for associated ones of the drive signals (DSi) within the valid ranges (VRi), and (iii) determining (CD) a combination (DCi) of values of drive signals (DSi) providing substantially the minimum degradation, or the maximum lifetime, of a combination of the at least two LED's (PLi) based on the degradation or lifetime indications (LTi).