Systems and methods for blood flow control are described herein. In some variations, a blood flow control system may comprise a blood flow control device. The blood flow control device may be placed within a body of a patient and may comprise an expandable member and a sensor. The sensor may be configured to measure at least one of a physiologic condition of the patient and a pressure associated with the expandable member. The blood flow control system may include at least one controller communicably coupled to the sensor to: receive data indicative of at least one of the physiologic condition of the patient and the pressure associated with the expandable member from the sensor, compare the received data with target data, identify at least one error based on the comparison, and in response to identifying the error, inhibit at least one function of the blood flow control system.

Techniques are disclosed for automatically calibrating a reference orientation of an implantable medical device (IMD) within a patient. In one example, sensors of an IMD sense a plurality of orientation vectors of the IMD with respect to a gravitational field. Processing circuitry of the IMD processes the plurality of orientation vectors to identify an upright vector that corresponds to an upright posture of the patient. The processing circuitry classifies the plurality of orientation vectors with respect to the upright vector to define a sagittal plane of the patient and a transverse plane of the patient. The processing circuitry determines, based on the upright vector, the sagittal plane, and the transverse plane, a reference orientation of the IMD within the patient. As the orientation of the IMD within the patient changes over time, the processing circuitry may recalibrate its reference orientation and accurately detect a posture of the patient.

The present technology relates to intracardiac pressure monitoring devices, and associated systems and methods. In some embodiments, the present technology includes a device for monitoring pressure within a patient's heart. The device can include a pressure sensor configured to reside within a first chamber of a heart of a patient, and a pressure transmission element configured to extend from the first chamber through a septal wall to a second chamber of the heart of the patient. When the device is implanted in the patient's heart, the pressure transmission element is configured to transmit pressure from the second chamber to the pressure sensor residing within the first chamber.

A highly integrated analyte detection device, includes: a bottom case; a sensor including a signal output portion and a detection portion; a transmitter provided with at least two second electrical connection ends which are corresponding to the first electrical connection ends; and a connection member, arranged between the first electrical connection ends and the second electrical connection ends, including at least two conductive areas and at least one insulation area. The insulation area is provided between two adjacent conductive areas, and at least two first electrical connection ends are respectively electrically connected to the corresponding second electrical connection ends.

A sensor-retention structure includes a sensor-support strut and a means for securing a sensor device to the sensor-support strut. A sensor-support arm can be configured to have disposed thereon an at least partially cylindrical sensor device and be associated with one or more sensor-retention fingers projecting from the sensor-support arm and/or a cage structure configured to be secured to the sensor device.

The invention relates to a pressure sensor (100) comprising: a biocompatible housing (110), a biocompatible flexible membrane (120) covering an open portion in the housing (110), a pressure transferring medium, an attachment portion (130), an electrical connection (140), and a pressure sensitive sensor (150).

A catheter system includes an elongated tube structure configured for insertion into a luminal space, such as the vasculature, of a body. The catheter is conductive and configured to conduct electrical signals. The catheter includes one or more power and data coupling devices configured to send and receive power and/or data signals, such as from an underlying guidewire disposed within a lumen of the catheter. One or more sensors are coupled to a distal section of the catheter and are electrically connected to the one or more power and data coupling devices.

A catheter with three distinct compression resistance coils, including a body coil and two pull wire coils, is disclosed. The triple coil system can provide maximal resistance to compression of the catheter's proximal shaft, as well as maximization of the curve angle that the catheter tip can achieve. Additionally, the tri-coil catheter can allow for a lower initial compression load and a more flexible proximal shaft. A gap between the outer diameter of the pull wire and the inner diameter of the pull wire compression coil that is equal to about 10-30% of inner diameter of the pull wire compression coil can provide optimal catheter performance.

A ventricular support system including a light source, a fiber optic splitter, two or more filters, an intravascular blood pump having two or more sensor heads, and a photodetector is disclosed. At least some of the light transmitted by the light source is split by the fiber optic splitter such that a portion is transmitted to each of the two or more filters. Each portion of light is filtered by one of the two or more filters and transmitted to one of the two or more sensor heads. Light beams reflected from each of the two or more sensor heads are combined by the fiber optic splitter. At least some of the combined light beams are received by the photodetector. By only using a single light source and a single photodetector with the two or more sensor heads, the ventricular support system may have improved portability.

The application describes embodiments including, e.g., a measurement device comprising: a casing, a first magnet arranged within the casing such that it is rotatable out of an equilibrium orientation responsive to an external magnetic torque acting on the first magnet, a second magnet to provide a restoring torque to force the first magnet back into the equilibrium orientation responsive to an external magnetic torque rotating the first magnet out of the equilibrium orientation, allowing for a rotational oscillation of the first magnet, which is excited by the external magnetic torque, with a resonant frequency, and a temperature sensitive magnetic material to modify the resonant frequency.