Abstract: Embodiments disclose a blood pressure parameter detection method. The method includes: detecting, by user equipment UE, an electrocardiogram ECG signal of a user by using a first ECG contact and a second ECG contact that are connected to an ECG detection circuit of the UE; when determining that the detected ECG signal matches a pre-stored reference ECG signal, enabling, by the UE, a photoplethysmogram PPG detection circuit, and detecting a PPG signal of the user by using a PPG detection point connected to the PPG detection circuit; and when determining that the detected PPG signal matches a pre-stored reference PPG signal, enabling, by the UE, a blood pressure detection application, and processing the detected ECG signal and the detected PPG signal by using the blood pressure detection application to obtain a blood pressure parameter of the user.

Abstract: Embodiments of this invention generally relate to ophthalmic laser procedures and, more particularly, to systems and methods for lenticular laser incision. In an embodiment, an ophthalmic surgical laser system comprises a laser delivery system for delivering a pulsed laser beam to a target in a subject's eye, an XY-scan device to deflect the pulsed laser beam, a Z-scan device to modify a depth of a focus of the pulsed laser beam, and a controller configured to form a top lenticular incision and a bottom lenticular incision of a lens in the subject's eye, where each of the top and bottom lenticular incision includes a center spherical portion and an edge transition portion that is not located on the same spherical surface as the spherical portion but has a steeper shape.

Abstract: The embodiments of the present disclosure disclose a method and apparatus for establishing a blood pressure model. The method comprises: acquiring pulse wave data, electrocardiographic data, blood pressure data and body mass indexes of a plurality of subjects to be examined; determining pulse wave transit time and pulse wave intensity ratios based on the pulse wave data and the electrocardiographic data; establishing a blood pressure model based on the blood pressure data, the pulse wave transit time, the pulse wave intensity ratios, and/or the body mass index.

Abstract: Systems and methods for assessing sympathetic nervous system (SNS) tone for renal neuromodulation therapy are disclosed herein. A system configured in accordance with embodiments of the present technology can include, for example, a detector attached to or implanted in a patient and a receiver communicatively coupled to the detector. The detector can measure cardiac data and the receiver and/or a device communicatively coupled thereto can analyze the cardiac data to provide one or more SNS tone indicators. The SNS tone indicators can be used to determine whether a patient will be responsive to a neuromodulation therapy and/or whether a neuromodulation therapy was effective.

Abstract: A joint assembly including first and second supports, a spring cage, first and second drive shafts, and first and second cables. The spring cage having a first end fixed to the first support and a second end fixed to the second support and defining a spring channel between the first and second supports. The first drive shaft rotatably disposed along a first longitudinal axis defined by the first support and the second drive shaft rotatably disposed along a second longitudinal axis defined by the second support. The first and second cables extending through the first support and having an end secured to the second support. The first and second cables translatable in a direction parallel to the first longitudinal axis to articulated the second support relative to the first support such that the second longitudinal axis is disposed at a total joint angle relative to the first longitudinal axis.

Abstract: Devices, systems, kits and methods are provided, that simplify focused ultrasound treatment. Devices comprise a supporting structure and a focused ultrasound (FUS) transducer having a central axis that is affixed to the supporting structure. Devices may further comprise an imaging ultrasound transducer and/or an x-ray aim, that may be attached to the supporting structure along the central axis of the FUS transducer. The FUS transducer is connected to a controller configured to control application of focused ultrasound by the transducer and may be associated with an imaging unit for imaging the treatment region using ultrasound and/or x-ray image data. The devices are hand held and easy to manipulate and aim correctly, utilizing coupling member(s) as well as feedback from the concurrently imaged treatment region.

Abstract: A system and method for determining a patient's susceptibility to develop cardiorespiratory instability wherein physiological parameters are analyzed with respect to a dynamics systems model to produce and indicator associated with a probability that the patient will become unstable is provided.

Abstract: A personal sauna unit with an integrated chromotherapy unit. The sauna unit is configured for use by a single person lying generally prone on a surface. The sauna unit includes a cabin that is disposed to overlie the user and that includes a plurality of infrared heating elements that direct infrared energy toward the user's body. When using the sauna unit, the user's head extends from an open end of the cabin. A chromotherapy light unit is integrated with the cabin to extend along the perimeter of the open end of the cabin and to direct a selected spectrum of visible light toward the user's face for therapy. A pad with additional heating elements may be provided beneath the cabin to provide additional heating and comfort to the user. A control unit is provided to control the heating elements and the light element during a sauna session.

Abstract: Methods and apparatus for monitoring a subject are described. A monitoring device configured to be attached to a body of a subject includes a sensor that is configured to detect and/or measure physiological information from the subject and a motion sensor configured to detect and/or measure subject motion information. The physiological sensor and motion sensor are in communication with a processor that is configured to receive and analyze signals produced by the physiological sensor and motion sensor. The processor is configured to process motion sensor signals to identify an activity characteristic of the subject. Once an activity characteristic is determined, the processor is configured to select a biometric signal extraction algorithm or circuit in response to the activity characteristic of the subject, and then process physiological sensor signals via the biometric signal extraction algorithm or circuit to produce physiological information about the subject.

Abstract: In one implementation, a multi-vital-sign smartphone system detects multiple vital signs from sensors such as a digital infrared sensor, a photoplethysmogram (PPG) sensor and at least one micro dynamic light scattering (mDLS) sensor, and thereafter in some implementations the vital signs are transmitted to, and stored by, an electronic medical record system.

Abstract: A method and system for determining energy expenditure (EE) are disclosed. The method comprises determining a plurality of sensor streams using a plurality of detected physiological signals and processing the plurality of sensor streams to determine the EE. The system includes at least one sensor to detect a plurality of physiological signals, a processor coupled to the at least one sensor, and a memory device coupled to the processor, wherein the memory device includes an application that, when executed by the processor, causes the processor to determine a plurality of sensor streams using a plurality of detected physiological signals and to process the plurality of sensor streams to determine the EE.

Abstract: A surgical apparatus comprising: a mechanism that is configured to perform an operational motion of the surgical apparatus; and at least one transformation member having an original shape and a deformed shape, the at least one transformation member connecting the mechanism together, when the at least one transformation member is in the deformed shape so that the mechanism is capable of performing the operational motion; and wherein after the transformation member is subject a transition temperature, the at least one transformation member changes from the deformed shape to the original shape and disengages a portion of the mechanism so that the mechanism is prevented from performing the operational motion.

Abstract: An energy-based surgical system includes a light beam source and a probe defining a channel about a longitudinal axis thereof and a side opening near a distal end thereof. Methods of nerve detection using the system include positioning the probe adjacent targeted tissue, transmitting a beam of light from the light beam source through the channel of the probe and the side opening of the probe to the targeted tissue, measuring a response to determine the presence of a nerve within the targeted tissue, and delivering energy to the targeted tissue with the probe to treat tissue.

Abstract: The present invention discloses a connector for deploying an energy transmission medium, comprising a cylindrical tube and a telescopic arrangement comprising a fixed tube attached to and penetrating a sealed first end of the cylindrical tube, leaving a tunnel connecting an inner space of the cylindrical tube and the environment, and a sliding tube slidably engaged with the fixed tube and affixed with at least one energy transmission medium having a front end extending through out of the sliding tube towards a second end of the cylindrical tube and a tail end connected to an energy source coupler.

Abstract: Laser energy delivery devices and methods are provided. A laser energy delivery device for providing treatment to a subject may include a coupling adapted to couple to a laser energy generator. A sheath is coupled to the coupling, the sheath including a distal end adapted to be disposed in the subject. A plurality of transport members are carried by the coupling and the sheath, the plurality of transport members being adapted to receive laser energy at the coupling, transmit laser energy through the sheath, and deliver laser energy to the subject. A sensor is adapted to detect transmission of laser energy through at least one of the plurality of transport members.

Abstract: A combination therapy pad that includes a first layer and a second layer operatively coupled to the first layer. A fiber-optic array is disposed between the first layer and the second layer. A third layer is operatively coupled to the first layer. The third layer includes a vacuum tube in fluid communication with a vacuum source and a therapeutic fluid tube in fluid communication with a therapeutic fluid source. The third layer provides at least one of vacuum therapy and therapeutic fluid treatment to a wound area.

Abstract: In one implementation, a device detects multiple vital signs from sensors such as a digital infrared sensor, a photoplethysmogram (PPG) sensor and at least one micro dynamic light scattering (mDLS) sensor, and thereafter in some implementations the vital signs are transmitted to, and stored by, an electronic medical record system.

Abstract: Laser energy delivery devices and methods are provided. A laser energy delivery device may include a housing, and a coupling is carried by the housing and adapted to couple to a laser energy generator. A sheath is carried by the housing, and the sheath includes a distal end adapted to be disposed in the subject. A plurality of transport members are carried by the sheath, and the plurality of transport members are adapted to receive laser energy at the coupling, transmit laser energy through the sheath, and deliver laser energy to the subject. A fluid-driven motor is carried by the housing and adapted to be driven upon receiving a fluid from a fluid source. A drive wire is carried by the sheath and eccentrically coupled to the distal end of the sheath, and the drive wire is adapted to be rotatably driven by the fluid-driven motor and rotates to eccentrically rotate the distal end of the sheath.

Abstract: A biomarker detector used to detect and notify a user of a biological substance. More specifically, a biomarker detector coating layered on a surgical instrument that enables a user of the surgical instrument to know when a critical bodily fluid, such as cerebrospinal fluid, or critical tissue, such as nerve tissue, has been reached by the surgical instrument, thereby allowing the user to react accordingly and avoid iatrogenic injury.

Abstract: A phototherapeutic system for providing phototherapy inside a user's mouth comprises a housing; and a plurality of radiation sources disposed in the housing, wherein the plurality of radiation sources is configured to provide to the user's mouth a plurality of beams, wherein at least two beams of the plurality of beams have different wavelengths, and wherein a portion of the housing is configured to receive a pressure resulting from the user's mouth so as to prevent the housing from moving during the phototherapy.