Disclosed is a method for determining an unworn state of a sensor system comprising a pair of sensors configured for mounting on first and second body parts either side of a joint. The method comprises: obtaining one or more measurements from each sensor; calculating a relative angle between the two sensors using one or more of the obtained one or more measurements; calculating, using one or more of the obtained one or more measurements, a joint angle between the first and second body parts, where the joint angle is defined in a plane of normal bending of the joint; and determining, based on the calculated angles, whether either of the sensors is not mounted and if so, determining that the system is in an unworn state. Also disclosed is a system for providing information about a joint.

A system includes a console assembly, a trocar assembly operably coupled to the console assembly, a camera assembly operably coupled to the console assembly having a stereoscopic camera assembly, and at least one rotational positional sensor configured to detect rotation of the stereoscopic camera assembly about at least one of a pitch axis or a yaw axis. The console assembly includes a first actuator and a first actuator pulley operable coupled to the first actuator. The trocar assembly includes a trocar having an inner and outer diameter, and a seal sub-assembly comprising at least one seal and the seal sub-assembly operably coupled to the trocar. The camera assembly includes a camera support tube having a distal and a proximal end, the stereoscopic camera operably coupled to the distal end of the support tube and a first and second camera module having a first and second optical axis.

The present disclosure relates a multi-leaf collimator. The multi-leaf collimator may include a plurality of leaves. At least two leaves of the plurality of leaves may be movable parallel to each another. For each leaf of at least some of the plurality of leaves, at least one portion of the leaf may have thicknesses varying along a longitudinal direction of the each leaf. The each leaf may have a first end and a second end along the longitudinal direction of the each leaf.

Systems, devices, and methods for electroporation ablation therapy are disclosed, with a protection device for isolating electronic circuitry, devices, and/or other components from a set of electrodes during a cardiac ablation procedure. A system can include a first set of electrodes disposable near cardiac tissue of a heart and a second set of electrodes disposable in contact with patient anatomy. The system can further include a signal generator configured to generate a pulse waveform, where the signal generator coupled to the first set of electrodes and configured to repeatedly deliver the pulse waveform to the first set of electrodes. The system can further include a protection device configured to selectively couple and decouple an electronic device to the second set of electrodes.

Disclosed is a breath sampling device comprising a buffer tube, sensor module and breath sampling port. The buffer tube has a proximal end into which a user exhales and a distal end opposite the proximal end, the sensor module is at the distal end and used for measuring parameters of a breath exhaled by the user into the buffer tube, and the breath sampling port is disposed between the proximal end and distal end. The used exhales into the distal end and a portion of the exhaled breath can be diverted into the sampling port substantially without contacting the sensor module.

A wearable cardiac monitoring and treatment device for improved skin interface contact and easy assembly and disassembly includes a garment including an inner surface and an outer surface, ECG sensing electrodes, and at least one stiffener forming a section of the garment in proximity to one or more of the ECG sensing electrodes. The at least one stiffener is configured to resist rotation or pulling away of the one or more of the ECG sensing electrodes from a patient's torso. The device includes therapy electrodes, at least one separate module including a therapy delivery circuit, and a controller. The device includes compartments configured to receive the therapy electrodes and at least one separate module, and retention loops configured to route external wires extending between at least the therapy electrodes and at least one separate module, where the compartments and retention loops are disposed on the outer surface of the garment.

The bioelectrical impedance measurement device mainly includes a portable casing, a control member inside the portable casing, and an electrode assembly joined to the portable casing and electrically connected to the control member. The control member includes current generation element, a current collection and processing element, and a current protection element. The electrode assembly includes a left-hand contact and a right-hand contact, both configured on the portable casing. The electrode assembly further includes a left-foot contact, and a right-foot contact, both extended from the portable casing. The left-hand contact, right-hand contact, left-foot contact, and right-foot contact are respectively connected to a user's left hand, right hand, left foot, and right foot. The current generation element generates an electrical current, which enters the user's body through the limbs and then collected to calculate various bioelectrical impedances and to determine a required biological information.

A detection system for detecting a loop and/or a knot in a catheter includes a first coil and a second coil in spaced positions on a catheter body of the catheter. A driver is coupled by a wired communication link to the first coil, wherein the driver is configured to transmit a first signal to the first coil. A receiver is coupled by a wired communication link to the second coil, wherein the receiver is configured to receive a second signal from the second coil indicative of a proximity of the first coil and the second coil. A signal analyzer is coupled by a wired or wireless communication link to the receiver that is configured to receive the second signal from the receiver and determine whether there is a change in the second signal indicative of a formation of the loop and/or the knot in the catheter.

An information generation device includes: a receiver configured to receive physiological information of a subject, from a terminal device configured to operate by power of a battery, and continuously acquire and transmit the physiological information; a determination unit configured to determine whether non-transmission time, during which the terminal device is not capable of transmitting the physiological information to the receiver since the power is not supplied to the terminal device, is equal to or longer than predetermined time; and a generator configured to generate first alert information indicating that the non-transmission time is equal to or longer than the predetermined time, when the determination unit determines that the non-transmission time is equal to or longer than the predetermined time.

A method of adaption of a medical computed tomography imaging process to an individual respiration behaviour of a patient comprises: recording a respiratory movement of a patient by monitoring a respiratory surrogate, and adapting the medical computed tomography imaging process based on the recorded respiratory movement of the patient. An adaption device and a medical computed tomography imaging system are also described.