A bi-directional perfusion cannula is provided that includes an elongate tube for insertion into an artery. The elongate tube has a first aperture at a distal end of the tube which is forward during insertion and configured so that blood can flow into the artery in the direction of insertion, an elbow formed in the elongate tube, and a second aperture formed in or slightly rearward of the elbow and configured for supplying blood into the artery in a second direction which is generally opposite to the insertion direction.

A fabric-based item may be provided with a stretchable band. The stretchable band may be formed from a ring-shaped strip of stretchable fabric having an opening configured to fit around a body part of a user. Circuitry may be coupled to strands of material in the stretchable band. The circuitry may include sensor circuitry for making measurements on the body part such as electrocardiogram measurements, blood pressure measurements, and respiration rate measurements. Wireless communications circuitry in the fabric-based item may be used to communicate wirelessly with external electronic equipment. A wireless power transmitting device may transmit wireless power. A coil formed from conductive strands in the fabric-based item may be used by wireless power receiving circuitry in the fabric-based item to receive the wireless power. The coil may have one or more turns that run around the ring-shaped strip of stretchable fabric.

The blood pressure measuring device (1) is designed as a photoplethysmographic measuring system which functions according to the “vascular unloading technique”. Metrological components and a pressure generating and pressure control system are accommodated in the base part (3). The fitted cuff part (2) has an ergonomic palm support (4), two finger supports (6) divided from one another by a web (5), and also a receiving part (7) which comprises two receiving tubes (9) for fingers. The cuff part (2) projects beyond the base part (3), both towards the front and also towards the rear, and covers the base part (3) almost completely, i.e. by more than 90%. The lateral attachment of the cable (8) facing in the direction of the forearm has the advantage that the cable can be guided along the patient's arm, the wrist does not rub against the cable (8), and in particular the carpal tunnel is also protected.

The two inflatable sleeve cushions (10) which can be arranged in the receiving tubes (9) are each connected by means of a connection (11) at the interface between sleeve part (2) and base part (3) to the pressure generation and pressure control system in the base part (3). A valve device is preferably provided on the connection (11). The channels (19) that connect the respective connection (11) to the respective sleeve cushion (20) are formed in the main body (21) of the receiving body, said main body being produced from plastic by means of injection moulding, and are covered towards the outside by means of a cover (20). The connections (11) are disposed one behind the other in the direction parallel to the axial direction of the receiving tubes (9). From there, each channel (19) is first guided upwards, then diagonally to the side, and finally downwards to the fluid access opening (22) of the respective sleeve cushion (10).

The present disclosure relates to a device, method and system for calculating, estimating, or monitoring the blood pressure of a subject based on physiological features and personalized models. At least one processor, when executing instructions, may perform one or more of the following operations. A first signal representing a pulse wave relating to heart activity of a subject may be received. A plurality of second signals representing time-varying information on a pulse wave of the subject may be received. A personalized model for the subject may be designated. Effective physiological features of the subject based on the plurality of second signals may be determined. A blood pressure of the subject based on the effective physiological features and the designated model for the subject may be calculated.

A blood flow stimulator may help encourage blood flow in a limb of a patient. The blood flow stimulator may include a housing configured for sealing about the limb of the patient. The housing may include a sealable volume, and the sealable volume may receive the limb of the patient. The blood flow stimulator may include a seal, and the seal may be coupled with the housing. The seal may engage with at least a portion of the limb, for instance to segregate the sealable volume from a surrounding environment of the blood flow stimulator. The blood flow stimulator may include a conduit extending through the housing. The conduit mat help provide access to the sealable volume, for instance from the surrounding environment. In some examples, an adjustable stent is utilized to enhance blood flow within vasculature of a patient. A stent operator may change a size of the stent.

A catheter, such as a fractional flow reserve catheter, includes an elongate shaft having a pressure sensing wire extending to the distal portion of the elongate shaft. The wire has a pressure sensor mounted on the distal end for measuring a pressure of a fluid within lumen of vessel. The pressure sensor wire is disposed within a pocket formed adjacent to the pressure sensor thereby minimizing the profile of the catheter. Bending stresses experienced by a pressure sensor mounted to a fractional flow reserve catheter when tracking the catheter through the vasculature creates a distortion of the sensor resulting in an incorrect pressure reading or bend error. In order to isolate the sensor from bending stresses, the sensor is spaced apart from the pressure sensor wire to allow the pressure sensor and the pressure sensor wire to move independently from one another.

The present invention relates to a positioning and exposure device (1) for the defined arrangement on at least one body part (2, 3) of a living being (4) and for exposing the body part (2, 3) to radiation for determining at least one vital parameter of the living being (4). The positioning and exposure device (1) here comprises at least: a guiding and support structure (6) for delimiting an examination area (8), wherein the body part (2) can be positioned during exposure in the examination area (8), wherein the guiding and support structure (6) in a section (10) bounding the examination area (8) forms at least one radiation input area (12), wherein radiation can be introduced through the radiation input area (12) into the examination area (8) and wherein the guiding and support structure (6) forms a radiation exit area (16) in a further portion (14) delimiting the examination area (8), wherein at least part of the radiation which can be introduced through the radiation input area (12) into the examination area (8) can be guided out of the examination area (8) through the radiation exit area (16), and wherein a first elongate optical guide (18) is arranged in the path (20) of the radiation at least before entry into the examination area (8), wherein the first optical guide (18) is curved at least in sections for at least one deflection of the path (20) of the radiation which can be introduced into the first optical guide (18).

An electronic device for measuring blood pressure includes a measurement assembly, an airbag, and a fluid pipeline, where a fluid pump and a pressure sensor in the measurement assembly are connected to the airbag through a first fluid pipeline and a second fluid pipeline respectively, a first nozzle in the first fluid pipeline and a second nozzle in the second fluid pipeline are located on a same side of the airbag, and an opening direction of one of the first nozzle and the second nozzle is away from that of the other, so that the first nozzle and the second nozzle are away from each other. This reduces impact on the pressure sensor caused by airflow in the airbag, and improves blood pressure measurement accuracy.

A belt used in an electrocardiographic measurement apparatus includes a belt body to be wrapped around a living body, three or more base electrodes disposed in a longitudinal direction of the belt body, and two or more cap electrodes detachable and attachable to the base electrodes and smaller in number than the number of base electrodes.