Abstract: A two-photon imaging system capable of imaging of an image region in real time is presented. The imaging system comprises a source of excitation light that provides the excitation light as a plurality of laser beamlets. The plurality of laser beamlets is collectively scanned by a single-axis scanner along a first direction in the focal plane of the image region and oriented such that neither the rows nor columns are aligned with the first direction. As a result, each laser beamlet scans a different sub-region of the image region and the plurality of sub-regions are simultaneously scanned. As a result, the entirety of the image region is scanned in the same amount of time required to scan one image sub-region.

Abstract: An imager for in vivo viewing of diseased tissue by way of fluorescently conjugated molecules. A generally planar imaging surface with a microlens array. The imager may be modular, such that a plurality of generally planar imaging surfaces can be used to image various aspects of disease tissue simultaneously. Certain implementations include an angle-selective imager, wherein light from substantially perpendicular to the plane of the imager is received, while incident light is selectively eliminated.

Abstract: An observation device includes a light source unit capable of adjusting a quantity of 390-490 nm illuminating light according to a B1 range and a B2 range having a longer wavelength than the B1 range, and an imaging element that images reflected light from a subject irradiated with illuminating light. The light source unit changes the light quantity ratio of the B1 range to the B2 range depending on whether white light imaging is conducted or narrow band imaging is conducted. The imaging element includes RGB color filters arranged according to pixels and the R color filter transmits more light in an R range and the B1 range than light in the second B range and has a spectral characteristic that satisfies a predetermined conditional formulae.

Abstract: Systems and methods for spectral analysis of a tissue mass using an instrument, an optical probe, and a Monte Carlo algorithm or a diffusion algorithm are provided. According to one method, an instrument is inserted into a tissue mass. A fiber optic probe is applied via the instrument into the tissue mass. Turbid spectral data of the tissue mass is measured using the fiber probe. The turbid spectral data is converted to absorption, scattering, and/or intrinsic fluorescence spectral data via a Monte Carlo algorithm or diffusion algorithm. Biomarker concentrations in the tissue mass are quantified using the absorption, scattering, and/or intrinsic fluorescence spectral data.

Abstract: The invention pertains to the establishment, implementation and management of a personalized information system pertinent to a user's general health, wellness and/or sport performance. Disclosed is a system capable of transcutaneous measurement of a subject including at least one light source, at least one light detector, and at least one component for generating or storing at least one value of VC02 or at least one value of V02 from the detected signal. Further, disclosed is a portable device for analyzing the composition of the respired gasses of a subject including at least one air flow conduit through which the subject can inspire or expire air through the body of the device, at least one sampling portal, an oxygen sensor, and at least one flow sensor. A dual-battery system is also provided by which an uninterrupted power supply can be provided for electronic components.

Abstract: A wireless system for a person includes a wearable appliance with an accelerometer; a wireless device in communication with the wearable appliance; and a remote computer coupled to the wireless device to provide information to an authorized remote user.

Abstract: A medical system includes a network; one or more medical data collection appliances coupled to the network, each appliance transmitting data conforming to an interoperable format; and a server coupled to the network to store data for each individual in accordance with the interoperable format.

Abstract: A monitoring device with a pedometer function preferably comprises an article, an optical sensor, an accelerometer and processor. The optical sensor preferably comprises a photodetector and a plurality of light emitting diodes. A sensor signal from the optical sensor is processed with a filtered accelerometer output signal from the accelerometer to generate a pedometer function.

Abstract: Embodiments of the present disclosure are configured to assess the severity of a blockage in a vessel and, in particular, a stenosis in a blood vessel. In some particular embodiments, the devices, systems, and methods of the present disclosure are configured to assess the severity of a stenosis in the coronary arteries without the administration of a hyperemic agent. In some embodiments, the devices, systems, and methods of the present disclosure are configured to optimize proximal and distal pressure measurements utilized to assess the vessel.

Abstract: A biological information detection apparatus includes a detection unit which has a light receiving unit receiving light from a subject, a light transmitting member which is provided on a housing surface side in contact with the subject of the biological information detection apparatus, transmits light from the subject, and has a convex portion in contact with the subject to give a pressing force when measuring biological information of the subject, and a pressing force suppression unit which is disposed in periphery of the convex portion on or above the housing surface and suppresses the pressing force given to the subject by the convex portion. A groove portion is provided between the convex portion of the light transmitting member and the pressing force suppression unit.

Abstract: Catheter systems and methods for determining blood flow rates based on light reflection measurements. The catheter may include a lumen extending between a proximal end of the catheter and a distal end of the catheter. The catheter may include fluid infusion openings at the distal end region of the catheter that are configured to permit the indicator fluid to exit the catheter from the lumen. The catheter system may include an optical fiber having one or more sensors thereon for sensing light reflected by blood particles in a body vessel lumen. A blood flow rate may be determined based on the sensed light reflected by blood particles in the body vessel lumen.

Abstract: Methods of analysis to extract and assess brain data collected from subject animals, including humans, to detect intentional and unintentional brain activity and other unexpected signals are disclosed. These signals are correlated to higher cognitive brain functions or unintended, potentially adverse events, such as a stroke or seizure, and to translation of those signals into defined trigger events or tasks.

Abstract: A catheter adapted or high density mapping and/or ablation of tissue surface has a distal electrode matrix having a plurality of spines arranged in parallel configuration on which a multitude of electrodes are carried in a grid formation for providing uniformity and predictability in electrode placement on the tissue surface. The matrix can be dragged against the tissue surface upon deflection (and/or release of the deflection) of the catheter. The spines generally maintain their parallel configuration and the multitude of electrodes generally maintain their predetermined relative spacing in the grid formation as the matrix is dragged across the tissue surface in providing very high density mapping signals. The spines may have free distal ends, or distal ends that are joined to form loops for maintaining the spines in parallel configuration.

Abstract: A remotely-interfaceable extended wear electrocardiography and physiological sensor monitor recorder is provided. A sealed housing forms on a bottom surface a cavity shaped to accommodate an upward projection of a battery compartment formed on a non-conductive receptacle of a disposable extended wear electrode patch and includes a set of electrical contacts that protrude from the bottom surface and are arranged in alignment with electrical pads provided on the non-conductive receptacle. Electronic circuitry is provided within the sealed housing and includes an externally-powered micro-controller operable to execute under micro programmable control. An electrocardiographic front end circuit is electrically interfaced to the micro-controller. A wireless transceiver electrically interfaces with the micro-controller and externally-powered flash memory is electrically interfaced with the micro-controller and operable to store samples of the electrocardiographic signals.

Abstract: A method can include analyzing non-invasive electrical data for a region of interest (ROI) of a patient's anatomical structure to identify one or more zones within the ROI that contain at least one mechanism of distinct arrhythmogenic electrical activity. The method also includes analyzing invasive electrical data for a plurality of signals of interest at different spatial sites within each of the identified zones to determine intracardiac signal characteristics for the plurality of sites within each respective zone. The method also includes generating an output that integrates the at least one mechanism of distinct arrhythmogenic electrical activity for the one or more zones with intracardiac signal characteristics for the plurality of sites within each respective zone.

Abstract: There is a method and system for detecting heartbeat irregularities comprising the steps of receiving a dataset representative of at least one waveform, the at least one waveform indicative of a subject's heart activity over a predetermined period of time; identifying from the data representative of at least one waveform, a plurality of peaks, each peak corresponding to a heartbeat; identifying from the predetermined period of time the time occurrence of each peak; calculating the difference (duration) between the time occurrence of each peak with its adjacent peak; determining the difference between each duration; classifying the absolute value of the difference into one of at least three intermediate categories; wherein each intermediate category comprises a specified range such that the absolute value is categorized into the intermediate category if it falls between the range; the intermediate categories further providing an indication of whether the subject has heartbeat irregularity.

Abstract: An elongated device adapted for insertion, including self-insertion, through the body, especially the skull is disclosed. The device has at least one effector or sensor and is configured to permit implantation of multiple functional components through a single entry site into the skull by directing the components at different angles. The device may be used to provide electrical, magnetic, and other stimulation therapy to a patient's brain. The lengths of the effectors, sensors, and other components may completely traverse skull thickness (at a diagonal angle) to barely protrude through to the brain's cortex. The components may directly contact the brain's cortex, but from there their signals can be directed to targets deeper within the brain. Effector lengths are directly proportional to their battery size and ability to store charge. Therefore, longer angled electrode effectors not limited by skull thickness permit longer-lasting batteries which expand treatment options.

Abstract: Systems and methods for determining brain health of a subject include or employ an electrical stimulator configured to apply a current to at least one pair of electrodes, and the electrodes are positioned on a skull of the subject to apply the current and to receive brain activity of the subject. The electrical stimulator is configured to apply a current having a waveform according to a Stochastic Gabor Function (SGF). A signal processor is configured to record the brain activity of the subject in the form of spectral electrical impedance data, and a computer system having non-transient computer readable media is programmed and configured to process the spectral electrical impedance data and indicate an impedance change within the brain of the subject.

Abstract: An electrode carrier system includes one or more electrode assemblies having an electrode body. One or more tubular members extend from the electrode body and define a lumen terminating in a distal opening. The electrode assemblies carry a reservoir containing a conductive fluid or gel. The reservoir is in fluid communication with the lumens in the tubular members, and the electrode assemblies are typically supported on a backing which may optionally be configured as a headband. Systems are for tracking patient movement may be used in combination with the electrode carrier system.

Abstract: Described herein are methods of detecting the presence or progression of neuromuscular disorders (including ALS) based at least in part on diaphragm EMG signals taken at different points in time from the same implanted electrode(s). Signals may be used to diagnose or to monitor progression of a disorder or to track a treatment. Thus, diaphragm EMG signal may be used as a marker (e.g., a “biomarker”) for the detection or progression of a neurological disorder such as ALS. The characteristics or parameters of diaphragm EMG signals may be used to create an activity index, which may be output or compared and further analyzed. These signals may also be analyzed to show a difference between the left and right sides of the diaphragm.

Abstract: A method for colon screening and collecting data by using Magnetic Particle Imaging wherein an imaging magnetic field is generated with a spatial distribution of the magnetic field strength such that the area of examination in the colon consists of a first sub-area with lower magnetic field strength, where the magnetization of a magnetic particle which was pre-delivered to the colon is not saturated, and a second sub-area with a higher magnetic field strength, where the magnetization of said magnetic particle is saturated. The spatial location of both sub-areas in the area of examination is modified so that the magnetization of said particles changes locally. Signals are acquired and are evaluated to obtain information about the spatial distribution of the signals in the area of examination. The method may be carried out during an entire peristaltic cycle in a colon portion or segment.

Abstract: An implanted device for an organ of a patient including a housing. The device includes a detector having electrodes that have a varying distance over time between them which produces a detector signal based on electrical signals derived from the organ. The device includes a signal processor disposed in the housing in communication with the detector which determines admittance from the detector signal based on the varying distance over time between the electrodes. The device includes a drive circuit disposed in the housing to cause the electrodes to generate emitted electrical signals. A method for monitoring a patient's organ.

Abstract: An apparatus for determining cardiac performance in the patient includes a plurality of electrodes adapted to be placed in the patient and in communication with a heart chamber of the patient for measuring conductance and blood volume in the heart chamber of the patient; and a processor for determining instantaneous volume of the ventricle based on measurement of complex admittance at a plurality of frequencies to identify mechanical strength of the chamber, the processor in communication with the electrodes. A method for determining cardiac performance in a patient.

Abstract: An encapsulatable life support mechanism (ELSM) for an analyzed animal, including: a cradle or bed adapted by means of size and shape to accommodate the animal; an anesthetization gas mask (AGM) characterized by a cup with conic cross section, comprising a plurality of apertures located at the outer circumference of the cup; a fluid supplying mechanism (FSM) in which the AGM is placed, the FSM is in a continuous fluid communication with (i) an anesthetization gas inlet positioned outside the ELSM and an outlet located within the ELSM; (ii) an air suction scavenging device positioned outside the ELSM and a mask and an air suction outlet located within the ELSM; and a plurality of (iii) air conditioning tubes; and an airtight shell enveloping the same. The airtight ELSM prevent leakage of anesthetization gas.

Abstract: Apparatus and method for imaging a patient in an MRI system. This includes a frame, and at least one assembly that includes a patient-interface positioner connected to a reference position on the frame, a first lockable joint on the positioner; and a patient interface connected to a patient-proximal end of the positioner by a second joint, wherein the first patient-interface is moveably positioned to a selected pitch angle, a selected yaw angle, and a selected one of a plurality of distances relative to the reference position on the frame. The first lockable joint is configured to be tightened to yieldably hold the first patient-interface at the selected pitch and yaw angles, and at the selected one of the plurality of distances, relative to the reference position. Optionally a second substantially similar patient-interface and assembly are provided. The earpiece(s) optionally include audio transducer(s) and/or RF coil(s).

Abstract: A system and method for determining a position of a medical device within a body are provided. The system includes an electronic control unit that receives position signals from position sensors of a first type and a second type disposed on the device and applies a filter to each of the position signals to obtain filtered estimated positions for each sensor. The unit computes a spline connecting the position sensors of the first type responsive to the filtered estimated positions for the sensors and estimates a spline position for the sensor of the second type along the spline. The unit generates maps between the spline position and filtered and unfiltered estimated positions for the sensor of the second type and determines actual positions for the sensors of the first type responsive to the filtered estimated position for the sensors and a composite map of the two maps.

Abstract: A system is disclosed herein for providing a kinetic assessment and preparation of a prosthetic joint comprising one or more prosthetic components. The system comprises a prosthetic component including sensors and circuitry configured to measure load, position of load, and joint alignment. The system further includes a remote system for receiving, processing, and displaying quantitative measurements from the sensors. The kinetic assessment measures joint alignment under loading that will be similar to that of a final joint installation. The kinetic assessment can use trial or permanent prosthetic components. Furthermore, adjustments can be made to the applied load magnitude, position of load, and joint alignment by various means to fine-tune an installation. The kinetic assessment increases both performance and reliability of the installed joint by reducing error that is introduced by elements that load or modify the joint dynamics not taken into account by prior assessment methods.

Abstract: A measurement device and method for measuring a portion of an animal's leg to more accurately and fairly determine the height setting required for a jump apparatus to be jumped by the animal. The device, which is particularly useful for measuring dogs for Flyball competitions, comprises an elongated body member and a sliding mechanism slidably attached thereto. The preferred body member has a curved cross-section. A preferred sliding mechanism comprises a slot disposed in the body member and a slide member that slidably engages the slot. In use, the body member is placed against the ulna of the dog's front leg with the first end of the body member positioned at the intersection of the ulna and the accessory carpal bone so a contact plate of the slide member can be slid against the elbow. A color coded and labeled chart on the body member provides the jump height setting.

Abstract: The present invention relates to a system and method for determining sleep, sleep stage and/or sleep stage transition of a person, including heart rate detecting means configured for detecting a heart rate of the person, movement detecting means configured for detecting a movement of a part of the body of the person, where the detected movement is caused by a skeletal muscle of the body, recording means configured for recording the detected heart rate and the detected movement of the part of the body, heart rate classifying means configured for classifying the recorded heart rate of the person into at least one heart rate class at least one heart rate variability class, movement classifying means configured for classifying the recorded movement into at least one movement class, and determining means configured for determining sleep, a sleep stage, a sleep stage transition and/or a sleep event of the person based at least partially on the at least one heart rate class and the at least one movement class.

Abstract: Embodiments disclosed herein may describe systems and methods for reducing nuisance alarms using probability and/or accuracy of a measured physiological parameter, such as the pulse rate or SpO2 measurement generated by a pulse oximeter. Embodiments may include methods for adjusting a predetermined alarm threshold based on the probability distribution of the estimated pulse rate and/or oxygen saturation of a patient's blood.

Abstract: Blood sample optimization systems and methods are described that reduce or eliminate contaminates in collected blood samples, which in turn reduces or eliminates false positive readings in blood cultures or other testing of collected blood samples. A blood sample optimization system can include a blood sequestration device located between a patient needle and a sample needle. The blood sequestration device can include a sequestration chamber for sequestering an initial, potentially contaminated aliquot of blood, and may further include a sampling channel that bypasses the sequestration chamber to convey likely uncontaminated blood between the patient needle and the sample needle after the initial aliquot of blood is sequestered in the sequestration chamber.

Abstract: An apparatus and a method for measuring a property of a blood sample is shown. The apparatus comprises of a housing having an aperture; a shaft mounted inside the housing; a testing member rotatably mounted on the shaft; an actuating member coupled to the housing and configured to exert a force against the testing member; and a lancet for eliciting a blood sample fixedly coupled to and protruding substantially radially from the testing member and configured to co-rotate with the testing member. The apparatus is further configured such that the lancet is aligned with the aperture in the housing when the testing member is in a first position. The testing member is configured, in the presence of a force exerted against the testing member by the actuator member, to translate to a second position in which the lancet is in a skin penetrating position.

Abstract: Methods and apparatus are provided for manufacturing an analyte detecting device. In one embodiment, the apparatus comprises a housing; a penetrating member driver; a cartridge containing a plurality of penetrating members; a display on the cartridge; a linear slider on the housing, the slider coupled to a rod; and the rod moving with the slider, the rod having at least one roller. The device uses the linear motion of the slider to rotate the cartridge, punch open a new cavity and load a new penetrating member.

Abstract: The invention concerns a measurement device to capture at least one vital parameter of a person in a motor vehicle with a steering wheel. The measurement device includes a finger sensor device with an optical sensor device, where the finger sensor device is attached to the steering wheel in the transition zone between a steering wheel spoke and the hub of the steering wheel.

Abstract: A method for determining a drowsiness value that represents the drowsiness of a driver of a motor vehicle and is determined cyclically over defined time intervals on the basis of at least one drowsiness characteristic, includes the task of determining a drowsiness value of a time interval to be assessed, in addition to the drowsiness characteristic, at least one drowsiness base value is taken into account.

Abstract: An illuminating wire medical device may include an elongate flexible housing and an illuminating fiber and a core wire extending through at least part of the housing, the core wire providing desired pushability and torquability. The illuminating device may further include a connector assembly cooperating with the illuminating fiber to accommodate changes in length and to absorb forces applied during use of the device.

Abstract: Providing an indication of a state of awareness for a patient includes acquiring an EEG signal; filtering the EEG signal to generate a first frequency band of signals; and filtering the EEG signal to generate a second frequency band of signals. Providing the indication also includes concurrently displaying the first and second frequency bands of signals in a single display window such that at least a first portion of the first frequency band overlaps, spatially the second frequency band.

Abstract: A wearable device includes a mount to mount the wearable device on a living body and a detector to detect an analyte response signal transmitted from tissue in the living body. The tissue contains a biologically active agent in an inactive state and functionalized particles. The biologically active agent can be converted to an active state that can affect a biological state of the living body. The functionalized particles are configured to bind with a target analyte, the presence or absence or concentration or abundance of which is correlated with the biological state. The analyte response signal is related to interaction of the target analyte with the functionalized particles. A source can apply directed energy into the tissue that is sufficient to convert the biologically active agent from the inactive state to the active state. A processor can determine a presence or absence or concentration or abundance of the analyte based on the analyte response signal.

Abstract: A fluid titration system has an optical sensor, a physiological monitor, a titration controller and an infusion device. The optical sensor transmits multiple wavelengths of light into a tissue site of a person and detects the optical radiation after attenuation by pulsatile blood flowing within the tissue site. The physiological monitor receives a resulting sensor signal and derives a plethysmograph that corresponds to the pulsatile blood flow. The monitor also calculates a plethysmograph variability measure that is responsive to changes in perfusion at the tissue site. A titration controller generates a fluid control output according to the variability measure. The infusion device administers a liquid solution via an intravenous (IV) connection to the person according to the fluid control output so as to regulate at least one of a fluid flow start, rate and stop.

Abstract: Methods, structures, devices and systems are disclosed for fabricating and implementing electrochemical biosensors and chemical sensors. In one aspect, a method of producing an epidermal biosensor includes forming an electrode pattern onto a coated surface of a paper-based substrate to form an electrochemical sensor, the electrode pattern including an electrically conductive material and an electrically insulative material configured in a particular design layout, and attaching an adhesive sheet on a surface of the electrochemical sensor having the electrode pattern, the adhesive sheet capable of adhering to skin or a wearable item, in which the electrochemical sensor, when attached to the skin or the wearable item, is operable to detect chemical analytes within an external environment.

Abstract: An information processing apparatus includes a retaining unit, an image acquisition unit, an image processor, a comparator, and an image generator. The retaining unit is configured to retain a defined attachment position being an attachment position of a biological detection sensor with respect to a body site of a user, the defined attachment position being defined in advance. The image acquisition unit is configured to acquire a capture image captured by an imaging unit. The image processor is configured to extract, from the capture image, a body shape of the user. The comparator is configured to compare the body shape with the defined attachment position. The image generator is configured to generate, based on a comparison result by the comparator, a display image to be displayed on a display unit.

Abstract: A system includes a sensor device having a body configured to be inserted into an airway of a patient and one or more sensors mounted in or on the body. The one or more sensors are configured to collect sensor data associated with the airway of the patient. The system also includes a signal analyzer configured to analyze the sensor data. The one or more sensors could include one or more microphones. The signal analyzer could identify volume and/or pitch characteristics of the sensor data, perform pattern recognition to identify one or more patterns using the volume and/or pitch characteristics, and use the one or more patterns to identify a type, a location, and/or a degree of airway obstruction. This could be done, for instance, to determine if the patient suffers from obstructive sleep apnea or other condition that affects his or her airway.

Abstract: A method for detecting when a tool contacts a wall of a region of interest includes the steps of: tracking the motion of the tool and creating a tool motion profile; calculating a correlation value representative of the correlation between the tool motion profile and a wall motion profile indicative of the motion of the wall; and determining when the correlation value exceeds a threshold indicative of contact of the tool with the wall of the region of interest.

Abstract: A method and system for determining blood pressure are disclosed. The method comprises determining a plurality of heart sounds using a microphone of a handheld device and determining a pulse wave using a camera of the handheld device, wherein the plurality of heart sounds and the pulse wave are utilized to determine the blood pressure. The system includes a processor, a memory device coupled to the processor, and an application coupled to the memory device. The system further comprises a microphone coupled to the processor, wherein the microphone is utilized to determine a plurality of heart sounds and a camera coupled to the processor, wherein the camera is utilized to determine a pulse wave, further wherein the application, when executed by the processor, causes the processor to determine the blood pressure using the plurality of heart sounds and the pulse wave.

Abstract: A lesion determination apparatus includes: a number-of-images acquiring unit configured to acquire and record, on occurrence of a direction change that is either a first state in which a second operation instruction is received immediately after receipt of a first operation instruction or a second state in which the first operation instruction is received immediately after a receipt of the second operation instruction, a number of one-directionally viewed images that is either a number of tomography images continuously viewed in response to continuous first operation instructions including the first operation instruction in the first state or a number of tomography images continuously viewed in response to continuous second operation instructions including the second operation instruction in the second state; and a locality determining unit configured to determine whether the object part is a focal lesion or a diffuse lesion based on a change in the number of one-directionally viewed images.

Abstract: An actigraphy method includes receiving a physiological parameter signal as a function of time for a physiological parameter other than body motion (such as electrocardiography or a respiration monitor), computing a body motion artifact (BMA) signal as a function of time from the physiological parameter signal (for example, using a local signal power signal, a local variance signal, a short-time Fourier transform, or a wavelet transform over epochs of duration on order a few minutes or less), and computing an actigraphy signal as a function of time from the BMA signal, for example by applying a linear transform to the BMA signal and optionally applying filtering such as median removal and/or high-pass filtering.

Abstract: A system (100) is provided for processing status information of a medical device (020-023). The medical device performs a medical function at a bedside of a patient and is arranged for generating an alarm signal (030) to alert a caregiver of the patient to an occurrence of an event which is associated with the performing of the medical function. A status interface (120) acquires a device signal (024) of the medical device, the device signal comprising status information which is indicative of a current status of the performing of the medical function. Moreover, an analysis subsystem (140) analyzes the status information to estimate an imminent occurrence of the event based on said current status, and a notification subsystem notifies the caregiver of the imminent occurrence away from the bedside of the patient of the event by a generating a notification signal (162) for a notification device (060-064). The priority of notifying the caregiver is based on an estimate of whether the patient is asleep.

Abstract: An apparatus comprising a radiation source, coincident positron emission detectors configured to detect coincident positron annihilation emissions originating within a coordinate system, and a controller coupled to the radiation source and the coincident positron emission detectors, the controller configured to identify coincident positron annihilation emission paths intersecting one or more volumes in the coordinate system and align the radiation source along an identified coincident positron annihilation emission path.

Abstract: The present invention relates to an X-ray targeting device which includes a frame installed at an X-ray generator of an X-ray imaging device which outputs X-rays toward a patient to be measured, and a light radiation unit installed at the frame, and radiating guide light in accordance with a direction in which the X-rays are output to display a radiated position or radiated range of the X-rays with respect to the patient. According to the present invention, since an X-ray targeting device includes a light radiation unit radiating guide light in accordance with a radiated direction of X-rays, a worker can easily identify the radiated direction or the radiated range of the X-rays, thereby saving time and effort required for X-ray imaging.

Abstract: An extendable shield apparatus for reducing radiation exposure of medical personnel to be used especially in hospitals is provided that comprises a base capable of being connected to a patient table of an X-ray fluoroscopy bed and a pole connected substantially vertically to the base. A dispenser for X-ray opaque blanket is supported by the pole, and a self-supporting X-ray opaque blanket capable of being extended from the dispenser.