Abstract: The disclosure relates to an actuation unit (16) for a medical instrument (10) and to a medical instrument (10) with a shaft (12) which extends between a proximal end (20) and a distal end (22), wherein the instrument (10) is designed at the distal end (22) to receive an end effector (14), an actuation unit (16, 216) which is assigned to the proximal end of the shaft (12), and which has a plurality of drives (50, 52, 54, 56), and with at least two control trains (100, 102, 104, 106, 108, 110, 112, 114) which extend through the shaft (12), wherein the at least two control trains (100, 102, 104, 106, 108, 110, 112, 114) can be used for controlling at least one degree of freedom of the instrument, in particular for deflecting the end effector (14), wherein the at least two control trains (100, 102, 104, 106, 108, 110, 112, 114) comprise a first control train (100, 104, 108, 112) and a second control train (102, 106, 110, 114), and wherein the first control train (100, 104, 108, 112) is coupled to a first carrier

Abstract: A medical device, comprising a housing, a combined modular structure which is formed by connecting a board card and an interface panel to a main bracket; a first opening arranged on the housing for the insertion of the combined modular structure; a first locking structure for locking and fixing the combined modular structure to the housing; a screen assembly; a second opening arranged on the housing for mounting the screen assembly, and a second locking structure for locking and fixing the screen assembly to the housing. The integral arrangement of a functional module of a medical device helps to improve the assembly precision between various components, and ensure the reliability of the connection between components. The housing adopts an integral structure, has good waterproof and dustproof effects as well as low production costs; the present disclosure facilitates the assembly of board card and other components, as well as module configuration and modular testing while also having good seismic performance.

Abstract: This invention is directed to a medical device having an elongate shaft having a distal end and a controller coupled to the shaft. A control member can extend through at least part of the elongate shaft and at least part of the controller, wherein the control member in a tensioned configuration can be moveable by the controller to control the distal end of the shaft and the control member can be slack in an untensioned configuration. A tensioning mechanism can be configured to move relative to at least one of the elongate shaft and the controller to tension the control member and automatically lock the control member in the tensioned configuration.

Abstract: A biological signal analysis device includes: an acquiring unit configured to acquire biological signals of a measurement target; a trigger information acquiring unit configured to acquire, from a stimulator configured to apply stimuli to the measurement target, trigger information indicating times at which the stimuli are generated; and a signal processing unit configured to process the biological signals. The signal processing unit is configured to calculate biological information on the measurement target based on the biological signals, maintain only pieces of trigger information corresponding to times at which it is determined that biological signals of the measurement target are generated, from the calculated biological information, delete another piece of trigger information, and use an averaged waveform that is obtained by performing an averaging process on the biological signals that are generated in synchronization with the stimuli based on the pieces of remaining trigger information.

Abstract: An illuminated microsurgical instrument comprises a distally projecting tubular member arranged to perform a medical procedure at an interventional site, a sheath member surrounding a portion of the tubular member, and an optical fiber extending along a length of the outer surface of the tubular member between the tubular member and the sheath member. A method of manufacturing an illuminated microsurgical instrument comprises placing an optical fiber on a positioning member, placing a sheath member around the optical fiber and positioning member and securing the sheath member to the optical fiber, removing material from a distal end of the sheath member and optical fiber at a non-perpendicular angle with respect to a longitudinal axis of the positioning member, removing the positioning member from within the sheath member, and placing the sheath member with the optical fiber secured thereto around a distally projecting tubular member.

Abstract: The disclosure provides an apparatus and methods for performing a piotomy on a mammal comprising: performing a craniotomy to remove the skull and expose dura mater; removing the dura mater and arachnoid mater to expose subarachnoid space; and performing a piotomy using a laser to create a hole and expose the cerebral cortex.

Abstract: Blood pressure information measurement device includes cuff including first and second fluid bag accommodated in first fluid bag, pressure increase/reduction mechanism configured to increase and decrease pressure in first fluid bag internal space and pressure in an internal space of second fluid bag, control unit configured to control operation of pressure increase/reduction mechanism, pressure detection device configured to detect first fluid bag internal pressure, and calculation unit configured to calculate blood pressure information.

Abstract: A surgical tool includes a drive housing having a shaft extending distally therefrom, first and second drive members extending distally from the drive housing along the shaft, and first and second translating gears rotationally fixed to the shaft within the drive housing and operatively coupled to the first and second drive members, respectively. First and second drive gears are rotatably mounted within the drive housing to act on the first and second translating gears, respectively. Rotating the first and second drive gears in opposite angular directions causes the first and second translating gears to move axially along the shaft in opposing directions and thereby move the first and second drive members. Rotating the first and second drive gears in a same angular direction causes the first and second translating gears to rotate the shaft about a longitudinal axis.

Abstract: An exemplary sound processor is configured to maintain data representative of a frequency allocation table that maps frequencies in an upper region of an audible frequency range to a plurality of electrodes located within a cochlea of the first ear, receive an audio signal, direct a cochlear implant to apply standard electrical stimulation representative of frequencies in the audio signal that are within the upper region to the cochlea of the first ear by way of the plurality of electrodes in accordance with the frequency allocation table, and direct the cochlear implant to apply phantom electrical stimulation representative of frequencies in the audio signal that are within a lower region of the audible frequency range to the cochlea of the first ear by way of a most apical electrode and one or more compensating electrodes included in the plurality of electrodes in accordance with a phantom electrode stimulation configuration.

Abstract: Systems and methods are provided for false alarm suppression in patient monitoring systems. In one embodiment, a method comprises inputting each electronic signal of a plurality of electronic signals into a corresponding predictor cloud of a plurality of predictor clouds, each predictor cloud comprising a long short-term memory neural network and a recurrent neural network, and responsive to an alarm generated based on at least one of the plurality of electronic signals, suppressing the alarm responsive to outputs of the plurality of predictor clouds indicating the alarm is false. In this way, patient monitors may be more reliable with fewer false alarms.

Abstract: An intraoral multisensor device includes a mouthpiece, a plurality of sensors at least one of attached to or integrated with the mouthpiece, and a data communications unit configured to receive signals from the plurality of sensors. The mouthpiece has a form to permit stable arrangement at least partially within a person's mouth such that it can remain for hands-free sensing of a plurality of biological parameters. Also, an intraoral multisensor system includes an intraoral multisensor device and a data processing device adapted to communicate with the intraoral multisensor device.

Abstract: A glove is described to simultaneously, non-invasively, and continuously, over a period of time, monitor physiological parameters (e.g., blood pressure, blood glucose, oxygen saturation level, electrical activity of the heart, and/or heart rate) of a patient. A computing server that is either communicatively coupled to the glove or is a part of the glove uses the monitored physiological parameters to determine whether the patient has a physiological condition (e.g., hypotension, hypertension, hypoglycemia, hyperglycemia, hypoxia, hyperoxia, arrhythmia, a strong form of tachycardia, a mild form of tachycardia, and/or bradycardia). Related apparatuses, systems, methods, techniques and articles are also described.

Abstract: A system for the treatment of targets under the skin of a patient comprising: a laser device for emitting a first series of laser pulses towards an area of the skin of a patient, where a target which must be reached by said laser pulses is located under said skin; a cooling system of said area of the skin by means of a cooling fluid; a first measurement sensor of a first temperature of said area of skin; a second measurement sensor of the temperature of said cooling fluid; said computer which receives the signals from said first and second temperature measurement sensor; said computer controls said laser device that emits a first series of laser pulses having predetermined power, duration and spacing; said temperature measurement sensor measures the temperature of said area of skin, following said first series of laser pulses; said computer calculates the predicted temperature reached of said area of the skin following the emission of a second series of pulses having said predetermined power, duration and spa

Abstract: An apparatus comprises an arrhythmia detection circuit configured to: receive a cardiac signal representative of cardiac activity of a subject; apply a first arrhythmia detection criteria to the received cardiac signal; apply, in response to the applied first arrhythmia detection criteria producing a positive indication of arrhythmia, a second arrhythmia detection criteria to the received cardiac signal, wherein the second arrhythmia detection criteria is more specific to detection of arrhythmia than the first detection criteria; detect, in response to the applied first and second arrhythmia detection criteria, a sensing event indicating one or both of the first and second arrhythmia detection criteria are susceptible to false indications of arrhythmia; and adjust, in response to a detected sensing event, sensitivity or specificity of one or both of the first and second arrhythmia detection criteria.

Abstract: Described herein is a monitoring system that includes a foot diagnostic device. The foot diagnostic device is shaped to receive one or both of a user's feet. The foot diagnostic device is equipped with a number of sensors that may work together or separately from each other, which are able to measure different diagnostic attributes of the feet. The system includes a mobile application and the ability to transmit information to the mobile application and other locations such as a physician's office.

Abstract: The present disclosure provides systems and methods for detecting cardiac activations of a patient. A system includes a data acquisition system (DAQ) communicatively coupled to an activation detection module. The DAQ detects an electrogram generated at an electrode disposed on or in the patient. The activation detection module is configured to receive the electrogram from the DAQ and compute an activation response. The activation detection module is further configured to determine a set of candidate detection time points (CDTPs) in the activation response. The activation detection module is configured to compute respective deflection characteristics for each CDTP. The activation detection module is configured to identify a group of final detection time points (FDTPs) among the set of CDTPs for a metric corresponding to the respective deflection characteristics. The group of FDTPs has similar deflection characteristics.

Abstract: A method of determining signal quality in a patient monitoring device includes acquiring one or more signals using the patient monitoring device. One or more signal quality metrics are determined based on the one or more acquired signals. A noise condition is detected based on the one or more signal quality metrics, and a determination is made whether the noise condition should be classified as intermittent or persistent. One or more actions are taken based on the classification of detected noise as intermittent or persistent.

Abstract: A treatment device for the surgical correction of hyperopia in the eye comprising a laser device controlled by a control device. The laser device separating corneal tissue by applying laser radiation. The control device controls the laser device for emitting the laser radiation into the cornea such that a lenticule-shaped volume is isolated. Removal thereof effects the desired correction. The control device predefines the volume such that a posterior surface and an anterior surface are connected via an edge surface that has a width in projection along the visual axis that is wider than the one which a straight line in the same projection, that is perpendicular at the edge of the posterior or the anterior surface would have relative to the associated surface and connects the anterior surface to the posterior surface or to the perceived extension thereof.

Abstract: A robotic microsurgery assembly (1) includes at least one master tool (2) to detect a manual command; at least one slave manipulator (3); and at least one surgical instrument (70) operated on by the one slave manipulator (3). At least one control unit (4) receives at least a first command signal including information about the manual command and sends a second command signal to at least one actuator to control the slave manipulator (3). The surgical instrument includes at least one jointed subassembly (5). The jointed subassembly (5) includes a first link (6), a second link (7), and a third link (8). The first link structural body (9) and the second link structural body (10) have at least one tendon contact surface (18), avoiding the at least one tendon contact surface (18) being a hole surface.

Abstract: Within examples, a wire clamping device includes a base. The base includes an indentation, a first attachment component at a first end of the base, and a second attachment component at a second end of the base that is opposite the first end. The wire clamping device further includes an arm that includes a protrusion and a third attachment component that is attached to the first attachment component. The arm is configured to rotate with respect to the first attachment component to a position at which the arm is restrained by the second attachment component against the base and at least a portion of the protrusion is within the indentation or aligned with the indentation. Additional examples include a method for using the wire clamping device, a tool for opening the wire clamping device, and a method for using the tool to open the wire clamping device.