Abstract: A fetal movement information processing device and method for accurately grasping and predicting the healthy development state of a fetus, namely, the well-being state of the fetus by adequately detecting and recording information on the fetal movement of a pregnant woman.

Abstract: A biopsy device includes a body, a needle, and a cutter. A motor is operable to both move the cutter relative to the needle and actuate a needle firing assembly to retract and fire the needle relative to the body. The biopsy device also includes a needle rotation assembly that is configured to substantially prevent rotation of the needle about the longitudinal axis when the needle is in a proximal position yet permit rotation of the needle about the longitudinal axis when the needle is in a distal position. A valve assembly of the biopsy device includes a slider that selectively couples a secondary lumen in the needle with either atmospheric air or saline based on the longitudinal position of the slider. The cutter passes through the slider.

Abstract: A photoplethysmograph device includes a light source for illuminating a target object. A modulator drives the light source such that the output intensity varies as a function of a modulation signal at a modulation frequency. A detector receives light from the target object and generates an electrical output as a function of the intensity of received light. A demodulator with a local oscillator receives the detector output and produces a demodulated output, insensitive to any phase difference between the modulation signal and the oscillator, indicative of blood volume as a function of time and/or blood composition. A number of demodulators may be provided to derive signals from multiple light sources of different wavelengths, or from an array of detectors. The plethysmograph may operate in a transmission mode or a reflectance mode. When in a reflectance mode, the device may use the green part of the optical spectrum and may use polarizing filters.

Abstract: A disposable tissue removal device comprises a “tube within a tube” cutting element mounted to a handpiece. The inner cannula of the cutting element defines an inner lumen and terminates in an inwardly beveled, razor-sharp cutting edge. The inner cannula is driven by both a rotary motor and a reciprocating motor. At the end of its stroke, the inner cannula makes contact with the cutting board to completely sever the tissue. An aspiration vacuum is applied to the inner lumen to aspirate excised tissue through the inner cannula and into a collection trap that is removably mounted to the handpiece. The rotary and reciprocating motors are hydraulically powered through a foot pedal operated hydraulic circuit. The entire biopsy device is configured to be disposable. In one embodiment, the cutting element includes a cannula hub that can be connected to a fluid source, such as a valve-controlled saline bag.

Abstract: A patient assessment apparatus, such as for balance assessment, includes an elongated member having a length and first, second and third positions along the length, a first receiving member situated at the first position, and a second receiving member situated at the third position, the second position situated between the first and third positions. The first and second receiving members are each arranged to receive a marker from a patient. Reach characteristic data is collected from a patient using the balance assessment apparatus, and the reach characteristic data is analyzed to determine whether the patient has a balance deficit.

Abstract: A hearing test method and apparatus are provided for improving a measuring accuracy and a test speed in finding the auditory threshold that is the audibility limit of discriminating a sound. In the method, after outputting a test sound relevant to a selected test frequency and a selected test sound pressure, the apparatus determines whether a user hears the test sound, then the test sound pressure zone is divided into an auditory threshold presence region and an auditory threshold absence region according to the result of determination. Thereafter, the test sound pressure zone is redefined using the auditory threshold presence region and this process of hearing test is repeated using the redefined test sound pressure zone to finally determine an auditory threshold for the selected test frequency.

Abstract: According to various embodiments, a system, method, and sensor are provided that is capable of monitoring electrical impedance of oral or nasal mucosal tissue. Such sensors may be appropriate for assessing gut hypoperfusion, gut ischemia, or the onset of shock. The electrical impedance of the oral mucosa or other tissues in the upper respiratory tract may be used to non-invasively assess the clinical state of gastrointestinal tissue.

Abstract: A device for accessing a hollow organ comprises an elongated body sized for insertion into an entrance passage to the hollow organ, the elongated body including an outer sealing surface engaging an inner surface of the entrance passage and a working channel extending therethrough from a proximal port which, when the elongated body is in the operative position is proximal to a proximal opening of the entrance passage, to a distal port which, when the elongated body is in the operative position, extends distally past a distal opening of the entrance passage into the hollow organ and a plurality of suction holes formed through an outer wall of the elongated body, disposed around a circumference of a portion of the elongated body which, when the elongated body is in the operative position, is located within the entrance passage in combination with a vacuum channel formed in the elongated body for transferring a negative pressure to the suction holes to increase a sealing force applied by tissue of the entrance pa

Abstract: A method of collecting a specimen sample and simultaneously dividing the sample into separate portions is presented. The method of the instant invention is comprised of providing a specimen collector comprised of a collection receptacle attached by a connector to at least 2 tubes which lead to at least 2 conduits which in turn empty into separate collection containers; expelling a biological specimen into the collection receptacle of the specimen collection device; and allowing the biological specimen to flow downward through the device and into separate specimen containers.

Abstract: Among other things, a vestibular prosthesis includes a wearable motion sensing system, the motion sensing system generating a motion signal indicative of a motion thereof, wherein the motion includes rotation about two distinct axes; a signal processor in communication with the motion sensing system, the signal processor being configured to generate an estimate of a tilt of the motion sensing system; and an actuator responsive to the estimate of the tilt made by the signal processor.

Abstract: The present invention relates to a biopsy needle, a sample extracting unit, a biopsy apparatus, and a biopsy needle control method. The biopsy needle includes an outer tube and an inner tube movably disposed within the outer tube. The inner tube has a plurality of inner openings defined in a side wall thereof. The outer tube has at least one outer opening defined in a side wall thereof. In response to movement of the inner tube, the outer opening selectively overlaps one of the inner openings thereby to define a communication port which communicates with an interior of the inner tube. The biopsy needle is incorporated in the sample extracting unit and the biopsy apparatus, and is controlled by the biopsy control method.

Abstract: A system for remotely controlling the positioning within the body of a patient of an elongated medical device optionally having a control handle, comprises a robotic system and a remote controller configured to control the robotic device. The robotic system comprises a handle controller; a sled member coupled to the handle controller, the sled member being configured to position the medical device within the body of the patient; and a sled base configured to advance the sled member towards the body of a patient, the sled bed being coupled to a sterile barrier effective to maintain sterility inside the sled base. A medical device introducer is effective to guide the elongated medical device into a patient's body.

Abstract: A biopsy device includes a coring cannula, a retract stylet, and a localization needle. The coring cannula has a longitudinal axis and a shaft centered on the axis. The stylet has a tip containing at least one blade and a central passage. The localization needle has a channel and is slidably disposed within the central passage. A drive mechanism rotates the cannula and moves the cannula in a direction parallel to the longitudinal axis of the cannula. A guide element has a first end and a second end and is slidably disposed within the channel of the localization needle. The guide element is movable from a first position to a second position within the localization needle.

Abstract: A biopsy apparatus includes a biopsy region positional information calculator for calculating a three-dimensional position of a biopsy region, a biopsy needle moving mechanism for moving a biopsy needle along three axes and/or turning the biopsy needle obliquely to an object to be examined, a biopsy needle positional information calculator for calculating a three-dimensional position of the biopsy needle, and a traveled distance calculator for calculating a distance over which the biopsy needle moves with respect to the biopsy region based on the three-dimensional position of the biopsy needle and the three-dimensional position of the biopsy region.

Abstract: A guidewire has a coil with a side of the coil winds having solid physical connections between the coil winds to prevent the connected coil wind side from expanding resulting from the application of force by an actuating member. The application of longitudinal force to the coil causes the unconnected coil wind side to expand while the connected side does not expand, resulting in the guidewire assuming a different configuration.

Abstract: The present invention provides for exemplary embodiments of a single-insertion, multiple sample biopsy device. Exemplary embodiments of a single-insertion, multiple sampling device with integrated marker release.

Abstract: An apparatus comprising a blood vessel measuring device is disclosed. The blood vessel measuring device may comprise a handle. A measuring member may be attached to the handle. The measuring member may be dimensioned to wrap around a blood vessel to measure a size of the blood vessel. The blood vessel measuring device may comprise an extension, and a first end of the extension may be attached to the handle. The blood vessel measuring device may comprise a connector attached to a second end of the extension. A method is also disclosed. The method may comprise inserting a measuring device into an incision in a patient. The measuring device may comprise a measuring member. The method may also comprise wrapping the measuring member around a blood vessel of the patient and measuring a dimension of the blood vessel with the measuring member.

Abstract: The present invention provides for exemplary embodiments of a single-insertion, multiple sample biopsy device. Exemplary embodiments of a single-insertion, multiple sampling device with integrated marker release.

Abstract: A continuous Glomerular Filtration Rate (GFR) estimation system may include a Foley catheter, a continuous urine creatinine sensor, and a urine output monitor. The continuous GFR estimation system computes creatinine clearance as CrCl=(Ucr×Uvol)/Pcr×Tmin), where Ucr is urine creatinine in mg/dL, Uvol is urine volume in mL, Pcr is plasma (serum) creatinine in mg/dL, and Tmin is time in minutes. A Foley catheter may be used to withdraw urine from the bladder. The urine may be delivered to a urine output monitor that provides the Uvol value over a time Tmin. Attached to the catheter is the flow-through continuous urine creatinine sensor for providing the Ucr value. The remaining parameter is Pcr. Because serum creatinine levels do not change rapidly over time, a blood sample may be withdrawn prior to the start of the continuous GFR to obtain the Pcr value.

Abstract: A method of monitoring or assessing the motion of the limbs of a body when performing repetitive cyclic activity uses inertial measurement units secured to each of the limbs to be monitored. The operation of all of the IMUs is synchronized by way of a pulse from a computer. On performing the repetitive cyclic activity such as walking, running, trotting or galloping, the outputs of the IMUs are assembled and analyzed in realtime, to determine the relative phase of the limb movements, from which an assessment of the gait may be made.