Abstract: A hair cutting device for cutting hair on a body of a subject includes a laser light source, and a light guiding element for guiding light from the light source to the cutting element. The cutting element includes an optical waveguide for receiving light from the light guiding element. The light guiding element has a tapered section in which a diameter of the light guiding element reduces from a light source side diameter to a cutting element side diameter. A portion of a sidewall of the optical waveguide of the cutting element forms a cutting face for contacting hair.

Abstract: A medical apparatus is provided that includes an implantable element, in particular a heart pump, and a control unit for the implantable element, which control unit is connected to the implantable element by means of a first connection. The problem of arranging an antenna of a radio module on the control unit expediently and favourably is solved in that the control unit is configured for arrangement outside the patient's body and has a predetermined orientation relative to the patient's body and has a radio module, wherein an antenna of the radio module is arranged in such a way that the region in which the patient's body is intended to be positioned, as considered from the control unit, is shielded from the antenna at least in part by electromagnetically shielding, in particular electrically conductive parts of the control unit or housing thereof.

Abstract: [Object] To provide an ablation system capable of suppressing heat damages to the lumen intima. [Solution] An ablation system 10 has an ablation device 11 in which a balloon 21 is provided on the distal end side of a shaft 22 and an in-side tube 27 causing a fluid to flow into the balloon 21, the internal space of the shaft 22 causing a fluid to flow out of the balloon 21, and an optical fiber 29 guiding laser light into the balloon 21 are individually provided along the shaft 22, a laser light generating unit 12 emitting laser light to the optical fiber 29, and a fluid returning unit 13 returning a fluid into the internal space of the balloon 21. The ablation device 11 has a reflector 33 reflecting laser light emitted from the optical fiber 29 in the balloon 21, in which the reflector 33 is movable along the axial direction 191 in the balloon 21 and is rotatable in the axial direction 101 as the axis line.

Abstract: Harvested stem cells are activated by treating them with an amplitude modulated laser beam having a wavelength lying in the range of 405 to 980 nanometers. The frequency of the laser beam is modulated within a range of 8 to 12 MHz. Using the activated stem cells, tissue can be repaired and regenerated by preparing the unactivated stem cells, treating the unactivated stem cells with an amplitude modulated laser beam having a pre-determined frequency for obtaining activated stem cells, administering the activated stem cells into a body containing the tissue, and using a homing beam to guide the activated stem cells within the body to the location of the tissue.

Abstract: A circuit for non-contact electrocardiography monitoring according to an embodiment of the present invention includes a non-contact monitoring unit for acquiring and outputting plus or minus monitoring signal of signal source with non-contact; an amplification control unit for amplifying the monitoring signal to output to output terminal; and an input impedance calibration circuit for being connected to input terminal and output terminal of the amplification control unit to process calibration of input impedance in calibration mode.

Abstract: The present disclosure pertains to a system configured to detect slow wave sleep and/or non-slow wave sleep in a subject during a sleep session based on a predicted onset time of slow wave sleep and/or a predicted end time of slow wave sleep that is determined based on changes in cardiorespiratory parameters of the subject. Cardiorespiratory parameters in a subject typically begin to change before transitions between non-slow wave sleep and slow wave sleep. Predicting this time delay between the changes in the cardiorespiratory parameters and the onset and/or end of slow wave sleep facilitates better (e.g., more sensitive and/or more accurate) determination of slow wave sleep and/or non-slow wave sleep.

Abstract: The present invention describes a system and method for continuous monitoring of central (aortic) and peripheral Blood Pressure. The system includes a fully mobile, non-invasive, continuous blood pressure monitoring system that includes one or more Biostrip devices affixed on a user, coupled with an application running on a computing device, which is further connected to a web server in the cloud. The system performs various computations on the Biostrip device, or on the gateway device (Smartphone or Smartwatch), or on the Cloud, and provides the user and authorized third parties with various insights about the blood pressure levels of the user. Further, the system enables the user to receive biofeedback training for controlling hypertension, and schedule online appointments, pay online for such appointments, share data the data securely to obtain insights.

Abstract: Methods are disclosed for determining an efficacy of a stimulus based on one or more measurable physiological responses to one or more stimuli including one or more stimulus features. Data is acquired on physiological responses of a group of one or more subjects to presentation of one or more stimuli including one or more stimulus features. The data on the one or more physiological responses of the one or more subjects is correlated with the presentation of the one or more stimulus features included in the one or more stimuli. The correlated data on the one or more physiological responses are associated with a separately-determined efficacy of the one or more stimuli to form a stimulus efficacy model. From this information, a projected efficacy of a stimulus is determinable by comparing one or more subsequently-measured physiological responses to the stimulus with the stimulus efficacy model.

Abstract: A ventricular assist system including an implantable rotary pump, a pump drive circuit for supplying power to the pump, and a signal processing circuit receiving one or more electrophysiological signals and one or more physiological signals of the subject. The signal processing circuit is operable to receive inputs from the one or more electrophysiological sensors and the physiological sensor, and determine the presence or absence of a non-normal sinus cardiac rhythm condition based on the input from the electrophysiological sensors. In the presence of a non-normal sinus rhythm, the circuit operates the pump in a modified mode of operation. In the absence of a non-normal sinus rhythm, the circuit operates the pump in a normal mode of operation. In either case, the circuit controls the power to the pump and/or speed of the pump based on the input from the physiological sensor and the mode of operation.

Abstract: An apparatus, system, and method for monitoring a person suffering from a chronic medical condition predicts and assesses physiological changes which could affect the care of that subject. Examples of such chronic diseases include (but are not limited to) heart failure, chronic obstructive pulmonary disease, asthma, and diabetes. Monitoring includes measurements of respiratory movements, which can then be analyzed for evidence of changes in respiratory rate, or for events such as hypopneas, apneas and periodic breathing. Monitoring may be augmented by the measurement of nocturnal heart rate in conjunction with respiratory monitoring. Additional physiological measurements can also be taken such as subjective symptom data, blood pressure, blood oxygen levels, and various molecular markers. Embodiments for detection of respiratory patterns and heart rate are disclosed, together with exemplar implementations of decision processes based on these measurements.

Abstract: Systems, methods, and computer program products are provided for the administration of ablation profiles during refractive surgery treatments. Basis data framework techniques enable the implementation of ablation profiles having various shapes, resulting in increased ablation accuracy when treating certain vision conditions. Exemplary basis data architecture approaches are configured to efficiently operate with annular, elliptical, and slit laser beam shapes.

Abstract: The invention relates to treatment apparatus (10) for correcting a refractive error of an eye (12) that includes a laser device (14) for separating corneal tissue by means of laser radiation (16); a control device (18) designed to control the laser device (14) to emit the laser radiation (16) for cutting out and/or ablating a volume (24) out of the surface (26) of the cornea (22) of the eye (12) in dependency on a measured pachymetry of the cornea (22) and the refractive error of the eye (12), whereby the cut-out and/or ablated volume (24) in the surface (20) of the cornea (22) results in a shape of a closed ring, a partial ring, a crescent or a crescent shaped closed ring. A method for controlling such an apparatus for correcting a refractive error of an eye, and to a protective mask for an eye are also provided.

Abstract: The present invention pertains to devices and methods for increasing the ease of data gathering and efficiency of information flow in a clinical setting. The devices of the present invention comprise medical examination tables, dental examination chairs and vital signs monitors, all of which further comprise integrated hardware and software that allow these devices to effectively collect and communicate data in a manner that allows for greater ease of use of these devices and subsequent increased efficiency in the clinical space on the part of the clinician. The medical examination tables and dental examination chairs of the present invention preferably include at least one load sensor for measuring a subject's weight when the subject is seated thereon. The methods of the present invention are directed at using the aforementioned devices to increase ease of data collection and efficiency of care delivery within a space in which the devices are used.

Abstract: An ophthalmological laser treatment system comprising a laser source (2) for producing laser radiation, a light projector (3) for focusing the laser radiation onto a focus (F) and a scanner system (5) for moving the focus (F) along a work line (p) comprises a monitoring system (6), which comprises a light detector (60) and is configured to monitor, by way of a light path (r), a monitored region (m) moving together with the focus (F). The monitoring system (6) is configured to monitor a monitored region (m), which moves together with the focus (F) with a fixed geometric assignment to the focus (F) and is for example disposed upstream of the focus (F) in the work direction and not yet worked on by laser radiation.

Abstract: A method for treating a patient's heart is provided. The method includes providing a light source which emits light having an initial power density. The method further includes positioning the light source relative to the patient's heart with intervening tissue of the patient between the light source and the patient's heart. The method further includes directing light onto cardiac tissue of the patient's heart from the light source through the intervening tissue without damaging the intervening tissue. The cardiac tissue is irradiated by an efficacious power density of light for an efficacious period of time.

Abstract: Provided are dermatological medical devices and methods comprising a distal end for positioning at a region proximal a target therapeutic region of tissue, an output port at the distal end, an energy source that generates optical energy, which is output from the output port to the target therapeutic region of tissue, and a control device that controls the optical energy at the target therapeutic region of tissue for increasing a temperature of the target therapeutic region of tissue for a period of time to a temperature that is less than an injuring temperature and induces an expression of heat shock proteins (HSPs) at the target therapeutic region of tissue.

Abstract: There is provided a light treatment device (1). The device (1) comprises a carrier (11) having an opening (5) for positioning over and viewing a treatment area and a light emitter (6) for providing treatment light to the treatment area. There is also provided an attachment (3) for attaching the carrier to a patient. The device is useful as the opening can be positioned over an area where light therapy is desired, whilst viewing the area, and then held in position with the attachment. Light therapy can then be administered to the area and treatment of areas where light therapy is not desired can be avoided.

Abstract: An intracranial treatment apparatus comprises an outer shaft having a proximal end and a distal end for positioning within the tissue region of the brain. The outer shaft defines a lumen extending between the proximal end and the distal end of the outer shaft and having at least one aperture adjacent the distal end of the outer shaft. An inner light-delivery element having a distal end and a proximal end is adapted to be operatively connected to the light source. The light-delivery element is configured to be received within the lumen and extend from the proximal end of the shaft to adjacent the distal end of the shaft. The light-delivery element is adapted to deliver light from the light source through the at least one aperture of the outer shaft to the tissue region of the brain in proximity to the distal end of the outer shaft.

Abstract: The present invention is directed to a self-contained hand-held device that obtains vital signs accurately, simultaneously, comfortably, and quickly. Unlike currently used devices that require trained personnel and the attachment of sensors to the different parts of the patient's body, this device can obtain all vital signs +ECG and pulse-ox by being held by the patient for approximately half a minute. The device contains sensors on the hand-held unit as well as on the individual/disposable mouthpiece. The method of the present invention includes simultaneously acquiring the following measurements: temperature, pulse rate, breathing rate, blood pressure, electrocardiogram, and pulse-ox waveform and blood oxygen level.

Abstract: A surgical laser system includes a laser source configured to generate laser energy, a laser fiber optically coupled to the laser source and configured to discharge the laser energy and collect electromagnetic energy feedback from a treatment site a photodetector configured to generate an output signal in response to the electromagnetic energy collected from the treatment site, a display, and a controller configured to produce an image or indication about the temperature at the treatment site on the display based on the output signal.