A yarn has a first conductive yarn having conductivity, a first insulating section covering the first conductive yarn and formed of an insulating material having absorbency, and a second conductive yarn having conductivity and disposed on an outer circumferential side of the first insulating section.

A system and method for identifying a disruption of a flow from an extracorporeal circuit to a patient circulatory system is based on flow rate data, such as from a venous line of the extracorporeal circuit. A patient contribution to the flow rate data is identified and monitored to assess a disruption of the extracorporeal circuit and the patient circulatory system, or access device. A spectrum analysis can be performed on the flow rate data to identify a harmonic corresponding to the patient contribution, wherein a change in or disappearance of the identified harmonic can be used to identify a disruption of the flow.

A system and method for identifying a disruption of a flow from an extracorporeal circuit to a patient circulatory system, such as a venous needle dislodgement or an access-bloodline separation, is based on flow rate data of the extracorporeal circuit. A patient contribution to the flow rate data can be identified as a harmonic and monitored to assess the presence of the disruption. The system can identify an inharmonic change, such as a spike, in the flow rate in the extracorporeal circuit, wherein the inharmonic change can be used alone or in conjunction with the identified harmonic to assess the existence of the disruption. The system can employ the spike in a blood flow rate as well as a spike in a dialysate flow rate fluidly connected to the extracorporeal circuit, wherein the spike can be used to identify the disruption.

A dialysis access site monitoring system may generate a treatment recommendation for treating a condition of an access site based on a video of the access site. The dialysis access site monitoring system may include an apparatus having a processor and a memory coupled to the processor. The memory may include instructions that, when executed by the processor, may cause the processor to generate video information based on a video of a dialysis access site of a patient, determine change in the number of pixels (CNP) information of the video information, the CNP information associated with movement of a skin surface of the patient due to blood flow through the dialysis access site, determine frequency domain information of the CNP information, determine a maximum-to-median power (M2) value of the frequency domain information, and determine at least one access site characteristic based on the M2 value.

Various smart medical connection embodiments of the present disclosure encompass a magnetic connectivity manager energizing ferromagnet(s) in response to a powering on the magnetic connectivity manager and a sensing of a connection strain on a medical base (21) and/or a patient base (31) of the device, whereby a magnetic connectivity interface (22, 32) activates a magnetic connectivity between metallic module(s) and the ferromagnet(s) for interfacing the conduit channels of the bases. The various smart medical connection embodiments of the present disclosure further encompass the magnetic connectivity manager deenergizing the ferromagnet(s) in response to a powering down of the magnetic connectivity manager and/or a sensing of a disconnection strain on the base(s), whereby the magnetic connectivity interface (22, 32) deactivates the magnetic connectivity between the metallic module(s) and the ferromagnet(s) for interfacing the conduit channels of the bases.

The invention relates to a device for extracorporeal blood treatment, comprising a blood treatment unit 1 that comprises at least one compartment 4. The invention further relates to a method for determining a hemodynamic parameter during an extracorporeal blood treatment by means of an extracorporeal blood treatment device. In order to determine the hemodynamic parameter, the conveying direction of the blood pump 10 is reversed from a “normal” blood flow to a “reversed” blood flow. In practice, it has been found that reversing the conveying direction of the blood pump for a measurement for determining a hemodynamic parameter carries the risk of blood clots reaching the patient, despite the dialyser holding back blood clots. The blood treatment device comprises an input unit 23 for inputting a time interval which can be specified by the user, taking into account the patient-specific and system-specific factors. The control and evaluation unit 12 of the blood treatment device is configured such that the operation of the blood pump 10 in the operating mode involving a reversed blood flow is only enabled during the time interval input by means of the input unit, the start of the time interval being determined from the point at which the blood treatment starts.

A dialysis fluid system includes a dialysis fluid inlet; a dialysis fluid outlet; a pump positioned and arranged to pump dialysis fluid through the dialysis fluid inlet and the dialysis fluid outlet; and an inductive heater located between the dialysis fluid inlet and the dialysis fluid outlet, the inductive heater including a fluid flowpath positioned and arranged to receive non-heated dialysis fluid from the dialysis fluid inlet and to output heated dialysis fluid to the a dialysis fluid outlet, a conductive heater element located within the fluid flowpath so as to be or act as a secondary coil of a transformer, and a primary coil of the transformer located outside of the fluid flowpath and positioned so as to magnetically induce a current into the conductive heater element, causing the conductive heater element and surrounding fluid to heat.

Methods and devices are disclosed that enable safe, rapid and relatively short and straight access to the cerebral arteries for the introduction of interventional devices to treat acute ischemic stroke. In addition, the disclosed methods and devices provide means to securely close the access site to the cerebral arteries to avoid the potentially devastating consequences of a transcervical hematoma.

In examples described herein, a system includes an elongate member configured to be introduced into vasculature of a patient. The elongate member includes a pressure sensor configured to generate a pressure signal indicative of pressure in the vasculature adjacent the needle. The system includes processing circuitry configured to receive the pressure signal from the pressure sensor, detect, based on the pressure signal, dislodgment of the elongate member from the vasculature, and generate an output in response to detecting the dislodgment of the elongate member from the vasculature.

A detector assembly configured for use in a dialysis (e.g., a hemodialysis) system is disclosed herein. The detector assembly including a wetness detector configured to detect blood, fluid, a leak, etc. The detector assembly being operatively coupled to, and more preferably, including an inertial measurement unit (IMU). Thus arranged, the detector assembly is configured to measure, read, obtain, provide, etc. additional information or data during a dialysis treatment, which information or data can be transmitted and/or used to, for example, provide greater insight into the system and/or to make better decisions. In one embodiment, the detector assembly can be used to determine when and how a patient is moving and feed that information back to the dialysis machine. In use, the information or data can be used in combination with other information to make an improved determination as to the requirement for an alert and/or stoppage of the dialysis treatment.