Patent classifications
A61M1/3403
SYSTEMS AND METHODS FOR ESTIMATING ULTRAFILTRATION RATES
Systems and methods for estimating the post-treatment ultrafiltration rate of a patient are provided. A medical device can be configured to determine an estimated post-treatment ultrafiltration rate based on one or more values associated with a patient prepared to undergo treatment with the medical device. The medical device can also be configured to compare the estimated post-treatment ultrafiltration rate with one or more threshold values. The medical device can be configured to have an alert module, which can be activated when the estimated post-treatment ultrafiltration rate exceeds the one or more threshold values.
BLOOD FILTRATION SYSTEMS
A blood filtration system can reduce the amount of plasma constituents (e.g., water and/or electrolytes) in the blood of the patient, and accordingly increase the hematocrit value of the patient. The blood filtration system (e.g., a controller, or the like) can determine a hematocrit value of a patient. The blood filtration system can determine a venous pressure of vasculature of a patient. The blood filtration system can compensate for pressure head in a component of a blood circuit (e.g., a withdrawal line of a catheter), for example to improve the accuracy of the venous pressure determination. The blood filtration system can determine one or more resistance characteristics of a blood circuit for the blood filtration system. The resistance characteristics can correspond to a resistance to a flow of blood through a component of the blood circuit.
APPARATUS FOR EXTRACORPOREAL BLOOD TREATMENT AND METHOD FOR ADMINISTERING NUTRITIONAL PRODUCTS IN AN APPARATUS FOR EXTRACORPOREAL BLOOD TREATMENT
An apparatus for extracorporeal blood treatment for chronic therapy comprises a nutritional bag (33) containing a nutritional solution, a weighing device (36) configured to determine a weight (W) of the nutritional bag (33), a nutritional line (34) for infusing the nutritional solution into either a blood return line (7) or into the patient vascular system. An ultrafiltration device (30) is configured to achieve a fluid removal from the patient through a semi- permeable membrane (5) of a filtration unit (2) and a sensor (31, 32) is configured to determine an ultrafiltration rate (UFR). A control unit (100) connected to the ultrafiltration device (30), to the weighing device (33) and to the sensor (31, 32) is programmed for receiving a patient prescription and for controlling the ultrafiltration device (30) to achieve the patient prescription based on the weight (W) and on ultrafiltration rate (UFR).
Method for Identifying the Type of a Medical Filter, and Apparatuses
The present disclosure relates to a method for identifying a type of filter, a class of filters, or a feature of a filter, wherein the filter includes a first filter compartment and a second filter compartment, which are separated by a filter medium. The method includes generating a pressure in a fluid on a first side of the filter medium via a first pressure source, measuring the pressure profile on the first side of the filter medium using a first pressure sensor as a first pressure profile and on the second side of the filter medium using a second pressure sensor as a second pressure profile, over time, evaluating both the first pressure profile and the second pressure profile to obtain an evaluation result, and assigning the filter to a type of filter, a class of filters, or identifying a feature of the filter.
ULTRAFILTRATION CONTROL IN EXTRACORPOREAL BLOOD PROCESSING
A control system operates (201) an apparatus for extracorporeal blood processing to extract, process and return the blood of an individual while removing fluid from the blood in accordance with a set value for ultrafiltration rate, UFR. The control system further obtains (202) sensor data representing one or more physiological parameters of the individual, and intermittently performs an optimization procedure (203) to generate the set value based on the sensor data. The optimization procedure comprises: evaluating (203A) the sensor data for detection of a limiting physiological status, LPS, sequentially controlling (203B) the apparatus in accordance with a test sequence of UFRs until the LPS is detected for a current UFR, and updating (203C) the set value based on the current UFR for use in operating the apparatus subsequent to the optimization procedure. The control system may perform a series of temporally separated optimization procedures during a treatment session to adapt the UFR to the individual.
Treatment fluid multi-stream blood warmer
The disclosed subject matter relates to extracorporeal blood processing or other processing of fluids. A blood treatment system treats blood with multiple fluids and performs fluid balancing on a patient's blood compartment. Multiple streams influence the patient temperature but only a subset of the fluids are dynamically temperature regulated. The system regulates a temperature of the flow, for example, of dialysate in order to regulate the return temperature of blood, in such a way that the temperature effect of the multiple streams is compensated.
METHOD AND APPARATUS FOR MEASUREMENT OF AN ULTRAFILTRATION RATE IN A RENAL REPLACEMENT THERAPY DEVICE
A system of identifying an ultrafiltration rate in a renal replacement therapy device is provided, wherein the system includes a controller connected to a first flow sensor obtaining flow rate data from a blood withdrawal line and a second sensor obtaining flow rate data from a blood delivery line. The controller calibrates, such as matches, the first flow sensor and the second flow sensor from flow measurements during periods of known ultrafiltration by the renal replacement therapy device. The controller is further configured to perform periodic equalization of the flow sensors, at a known ultrafiltration rate during the treatment session. The controller can employ flow rate data from the calibrated or equalized first flow sensor and the second flow sensor to calculate an ultrafiltration rate of the renal replacement therapy device based on the measured blood flow into and out of the renal replacement therapy device. The calibration can be performed before, during, or after blood treatment in a treatment session.
Flow Balancing Devices, Methods, and Systems
The disclosed subject matter relates to extracorporeal blood processing or other processing of fluids. Volumetric fluid balance, a required element of many such processes, may be achieved with multiple pumps or other proportioning or balancing devices which are to some extent independent of each other. This need may arise in treatments that involve multiple fluids. Safe and secure mechanisms to ensure fluid balance in such systems are described.
Methods And Systems For High-Throughput Blood Component Collection
Described are embodiments that include methods and devices for separating components from multi-component fluids. Embodiments may involve use of separation vessels and movement of components into and out of separation vessels through ports. Embodiments may involve the separation of plasma from whole blood. Also described are embodiments that include methods and devices for positioning portions, e.g., loops, of disposables in medical devices. Embodiments may involve use of surfaces for automatically guiding loops to position them into a predetermined position.
Treatment Fluid Multi-Stream Blood Warmer
The disclosed subject matter relates to extracorporeal blood processing or other processing of fluids. A blood treatment system treats blood with multiple fluids and performs fluid balancing on a patient's blood compartment. Multiple streams influence the patient temperature but only a subset of the fluids are dynamically temperature regulated. The system regulates a temperature of the flow, for example, of dialysate in order to regulate the return temperature of blood, in such a way that the temperature effect of the multiple streams is compensated.