Abstract: An intensity-based, micro-bending optical fiber sensor is disclosed herein, which is configured to acquire clean, stable, and reliable vital sign signals. Related systems and methods for vital sign monitoring are also provided herein. The sensor of various embodiments includes a multi-mode optical fiber, an LED light source, an LED driver, a receiver, and a single layer deformer structure. In various embodiments, the optical fiber and single layer deformer structure of the sensor are selected to meet specific parameters necessary to achieve a level of reliability and sensitivity needed to successfully monitor vital signs. In some embodiments, a specific sizing relationship exists between the optical fiber and the single layer deformer structure. In sonic embodiments, the sensor is configured to acquire ballistocardiograph waveforms.

Abstract: A method and system for diagnosing and treating infection or disease, in which an individual takes a photograph of an infected or diseased area of a body using a camera connected to a microprocessor. The photograph is sent to a diagnosing center having a server with a second microprocessor and a database of photographs correlated with different diseases and infections. The second microprocessor scans the image received from the camera and compares it to the photographs in the database. If a match is found, the second microprocessor then notes the disease or bacteria corresponding to the matching photograph. The second microprocessor then searches an additional database correlated to the match, to further refine the diagnosis. The second microprocessor then searches the second database for a treatment corresponding to the identified disease or bacteria. Once a treatment is identified, information regarding this treatment is automatically sent to the individual's microprocessor.

Abstract: A device combining magnetic resonance imaging and positron emission tomography for a breast examination is revealed herein to comprise an air pressure source, a servo flow control module, a pedestal disposed under a breast accommodating hole of a breast MRI bed and having a bearing platform for bearing a PET scanner ring thereon, a non-metallic and non-magnetic pneumatic actuator disposed on the pedestal and connected with the servo flow control module, and a movable pulley having a first nylon rope whose one end connects to the bearing platform and the other end connects to a counterweight unit, wherein the bearing platform connects to a displacement measurement unit by a second nylon rope for receipt of a location information thereof and transmission of the same to the servo flow control module for controlling the opening of the servo flow control valve to change gas flows entering into the pneumatic actuator.

Abstract: With respect to a forceps type treatment instrument including an ultrasound probe that protrudes from a treatment instrument main body at a position separated to a distal end side from a shaft portion, and a jaw that is displaceable between a closed state and an opened state by being linked with swing action of an clamp arm in a position separated to a distal end side from the shaft portion, stoppers are extendedly provided toward a clamp arm side from a treatment instrument main body side in a state in which edge portions at a distal end side are set to located at a distal end side from a locus of a proximal end of the jaw, and entry of a living body into a gap of the treatment instrument main body and the clamp arm is restricted.

Abstract: A method for determining, in real time, the probability that target biological tissue is opposite an ultrasonic transducer, the method including: transmitting, via an ultrasonic transducer, an ultrasonic signal into biological tissue; the ultrasonic transducer receiving the transmitted ultrasonic signal which has been backscattered by the biological tissue; calculating at least two instantaneous parameters of the backscattered ultrasonic signal; calculating a predictive value of the presence of an acoustic signature of target biological tissue, the predictive value being calculated via a statistical law using the at least two calculated instantaneous parameters; estimating the probability that the target biological tissue is opposite the ultrasonic transducer, the estimation depending on the calculated predictive value and/or on at least one strength condition based on at least one of the two calculated instantaneous parameters.

Abstract: Analysis of live beings is facilitated. According to an example embodiment of the present invention, a light-directing arrangement such as an endoscope is mounted to a live being. Optics in the light-directing arrangement are implemented to pass source light (e.g., laser excitation light) into the live being, and to pass light from the live being for detection thereof. The light from the live being may include, for example, photons emitted in response to the laser excitation light (i.e., fluoresced). The detected light is then used to detect a characteristic of the live being.

Abstract: An ultrasonic diagnostic imaging system is described which utilizes one or more transducer arrays affixed to the head of a patient to diagnose and treat stroke victims. The transducer headset produces a two or three dimensional image of the vasculature inside the cranium, preferably assisted by a microbubble contrast agent. A vascular flow map is produced by the system which may be diagnosed for signs of a blood clot. If a blood clot is detected, a therapeutic beam is transmitted while the contrast agent is present to break up the blood clot by the disruption of microbubbles. The headset may also be used in a monitoring application to detect the recurrence of blood clots in a stroke victim.

Abstract: An imaging catheter assembly is presented. The imaging catheter assembly includes an imaging catheter which includes an imaging catheter tip. Further, the imaging catheter assembly includes a fluid reservoir connected to the imaging catheter and configured to deliver fluid through a proximal end of the imaging catheter tip. The imaging catheter assembly also includes a release mechanism configured to cause delivery of the fluid to the imaging catheter tip when activated.

Abstract: An MRI-compatible tip assembly for an MRI-compatible medical device includes a first tubular member, a second tubular member, a ring electrode, and a tip electrode. The tip electrode proximal end is secured to the first tubular member distal end. The second tubular member distal end is inserted through the ring electrode and is secured to the first tubular member proximal end. When assembled, the tip assembly is a substantially rigid structure. Each tubular member has a recessed portion for a tracking coil.

Abstract: Methods of providing image-guided transendocardial injection of a therapeutic agent into a left ventricular wall of a heart. Some methods enable injections into heart tissue under visualization. The methods may include providing an endoventricular injection catheter having integrated echocardiographic capability. The endoventricular injection catheter may have an imaging core and an injection system carried on the elongated body with the imaging core. The method may include positioning the endoventricular injection catheter into the left ventricle of the heart, which inserts the imaging core into the heart. The method may also include transmitting ultrasonic energy via the imaging core, receiving reflected ultrasonic energy at the distal end, visualizing the left ventricular wall of the heart using the imaging core, identifying infarct regions of the left ventricle, and injecting a therapeutic agent into the visualized infarcted regions of the left ventricle using the injection system.

Abstract: A system and method for improved ultrasound strain imaging includes using data from a tracking system to enhance the quality of ultrasound strain image and to reduce the dependency of image quality of the user's expertise. The tracking information is synchronized with the RF frames and interpolated to find the transformation corresponding to each frame. The RF frames with their transformations are incorporated into calculation of ultrasound strain images. The tracking system may be an optical tracker, electromagnetic tracker, accelerometer, or a structured light system. The structured light system may also be used for probe calibration, by calibrating the surface of the probe pre-operatively. In addition, a relative Young's Modulus may be calculated using tracking information that is independent from the distribution of input force.

Abstract: A spatial position x? of each ultrasonic transducer is accurately obtained for each probe in consideration of each edge transducer gap, and a delay time T(x?(n)) and a weighting coefficient W(x?(n)) are calculated on the basis of the position of each ultrasonic transducer. A control unit executes ultrasonic transmission/reception by using the calculated delay times and weighting coefficients to realize a suitable acoustic field with high deflection angle accuracy, small sidelobes, and the like as compared with the prior art.

Abstract: A method of analyzing elastography of tissue using a one-dimensional (1D) ultrasound probe. The method includes: acquiring two-dimensional (2D) ultrasound images with respect to a region of interest (ROI) of an object to be diagnosed, to which a shear wave is induced, using the 1D ultrasound probe; measuring a displacement of the shear wave from the acquired 2D ultrasound images; estimating a change rate in the displacement of the shear wave along a y-axis direction orthogonal to a 2D plane on which the 2D ultrasound images are shown, using the measured displacement; and analyzing elastography information of tissue in the ROI using the measured displacement and the estimated displacement change rate.

Abstract: A method and apparatus for inserting and monitoring the placement of a cannula tip within a peripheral vein of a human body where the cannula includes a sensor located at predetermined location and mounted on the cannula for sensing the biological material of the body to guide the insertion of the cannula tip into the vein and alerts to the withdrawal of the cannula tip from the vein in the body.

Abstract: A device and method for detecting lameness in a standing animal uses at least one optical imaging device coupled to processing arrangement. The optical imaging device is arranged in a position to capture at least one image showing the lower portions of at least one leg of an animal and to forward the image to the processing arrangement, which, in turn, analyses the image to determine a condition of lameness when said at least one leg is held in a raised position on or above ground level. The system is particularly suited to detecting lameness in dairy animals and can be integrated in a milking or feeding stall or with an automatic or semi-automatic milking system.

Abstract: A device and method are disclosed for detecting and correcting unintended eye movements that may occur during an ultrasound scan by monitoring multiple position tracking sensors, examples being but not limited to ultrasound or optical position sensors. These position tracking sensors are in addition to the ultrasound imaging transducer and are in a fixed position on the scan head so as not to move during the scanning operation. These position tracking sensors can continuously monitor the distance to the cornea or other clearly defined anatomical features of the eye such as the posterior pigment layer of the iris during the movement of the scan head assembly and can provide continuous multi-dimensional correction for any unwanted motion of the eye relative to the scan head that may occur during the ultrasound scan.

Abstract: Insert devices that include a RF surface coil and gamma-ray photon detector array for enhancing PET and MRI images produced from integrated PET-MRI scanners are disclosed. Integrated PET-MRI scanners that include such insert devices as well of methods for scanning an object by use of such devices are also disclosed.

Abstract: A dual-mode closed-loop measurement system (100) for capturing a transit time, phase, or frequency of energy waves propagating through a medium (122) is disclosed. A first device comprises an inductor drive circuit (102), an inductor (104), a transducer (106), and a filter (110). A second circuit comprises an inductor (114) and a transducer (116). A parameter to be measured is applied to the medium (122). The medium (122) is coupled between the first device and the second device. The first device initiates the transmit inductor (104) to query via inductive coupling to a receive inductor (114) on the second device via a first path. The inductor (114) triggers a transducer (116) on the second device to emit an energy wave that is propagated in the medium (122) and detected by the first device. The transit time of energy waves is affected by the parameter by known relationship.

Abstract: According to one embodiment, a MRI apparatus includes an acquisition unit, a reference section information calculating unit, a positioning unit and an imaging unit. The acquisition unit acquires frames of section image data including a heart from an object with use of magnetic resonance. The reference section information calculating unit calculates spatial positional information of a reference section of the heart based on the frames of the section image data. The positioning unit displays a reference section image of the heart on a display unit and performs positioning of an imaging part for imaging through the displayed reference section image of the heart. The reference section image is calculated from the frames of the section image data based on the positional information of the reference section. The imaging unit images the imaging part set by the positioning.

Abstract: A fluorescence diagnosis system has a viewing system at least one light source and a camera system. The at least one light source can be operated in three modes, a first generating white light, a second with a first fluorescence excitation light of a first excitation wavelength and a third in which a second fluorescence excitation light of a second excitation wavelength is generated producing a fluorescence image in the NIR range. The camera system is sensitive at least in the visible and the NIR range. The system further comprises an image processing system for converting the fluorescence image in the NIR range into a visible image.