Patent classifications
A61M1/1692
System, method, and apparatus for electronic patient care
A method, related system and apparatus are disclosed. The method is implemented by an operative set of processor executable instructions configured for execution by a processor. The method includes the acts of: determining if a monitoring client is connected to a base through a physical connection; establishing a first communications link between the monitoring client and the base through the physical connection; updating, if necessary, the interface program on the monitoring client and the base through the first communications link; establishing a second communications link between the monitoring client and the base using the first communications link; and communicating data from the base to the monitoring client using the second communications link.
Manifold Diaphragms
The specification discloses a portable dialysis machine having a detachable controller unit and base unit. The controller unit includes a door having an interior face, a housing with a panel, where the housing and panel define a recessed region configured to receive the interior face of the door, and a manifold receiver fixedly attached to the panel. The manifold includes diaphragms adapted to minimize the dead space between the dialysis machine pins and improve responsivity. The base unit has a planar surface for receiving a container of fluid, a scale integrated with the planar surface and a heater in thermal communication with the container. Embodiments of the disclosed portable dialysis system have improved structural and functional features, including improved modularity, ease of use, and safety features.
Precision recharging of sorbent materials using patient and session data
The invention relates to devices, systems, and methods for recharging zirconium phosphate and/or zirconium oxide in reusable sorbent modules. The devices, systems, and methods provide for precision recharging of the zirconium phosphate and/or zirconium oxide to avoid the need of excess recharge solutions. The devices systems and methods also provide for calculation of the volumes of recharge solution needed for fully recharging the zirconium phosphate and zirconium oxide modules.
HEMODIALYSIS SYSTEM WITH ULTRAFILTRATION CONTROLLER
The hemodialysis system includes a closed loop dialysate flow path which includes a dialyzer and a reservoir for storing dialysate, and a closed loop blood flow path which passes through the dialyzer in the opposite direction as the dialysate flow path. In addition, the hemodialysis system includes pumps for pumping dialysate and blood through their respective flow paths, a flow sensor for measuring the flow rate of dialysate in the dialysate flow path, and a level sensor for measuring the level of dialysate in the dialysate reservoir. A processor is connected to the flow sensor, reservoir level sensor and pumps to provide a first closed loop control system including the processor, flow sensor and a first dialysate pump, and a second closed loop control system including the processor, level sensor and a second dialysate pump which enable the processor to initiate, monitor and maintain ultrafiltration.
Medical device leak sensing devices, methods and systems
Features for protecting against leaks in a fluid circuit are disclosed. In an embodiment, a first indicator of a leak is used to trigger confirmation by blood flow reversal and air detection in the blood circuit. A method for performing a blood treatment includes, at blood treatment machine, pumping blood to a patient through a first blood line. Further, at a controller of the blood treatment machine, a first signal is received, indicating a probability of a leak in the first blood line. Responsively to the first signal, the controller commands a leak verification operation and receives a second signal indicating whether a leak in the first blood line is verified. Further, a leak indicating signal is generated if the second signal indicates a leak is verified.
DIALYSIS DEVICES AND SENSOR CAPS AND SYSTEMS AND METHODS INCORPORATING THE SAME
Dialysis devices include a frame defined by a plurality of sidewalls that are impermeable to a sample being dialyzed, a pair of dialysis membranes that are each associated with an opposing face of the plurality of sidewalls such that the plurality of sidewalls and the pair of dialysis membranes define a sample chamber, an outer shell surrounding at least a portion of the pair of dialysis membranes, and a cap selectively associated with the sample chamber. The cap can be selectively associated with the sample chamber via an attachment mechanism that is configured to provide aural and/or haptic feedback when the cap forms a tight association with the sample chamber. The cap can be a sensor cap having one or more probes for measuring at least one property of fluid inside and/or outside the sample chamber and a transmitter for transmitting data captured at the probe(s) to a destination device.
Method And System For The Calibration Of Devices For Identifying Blood Or Blood Constituents In A Fluid
The invention relates to a method and to an assembly for calibrating devices 11 for detecting blood or blood components in a liquid, in particular dialysate, which devices comprise a light transmitter 17 and a light receiver 18, and an evaluation unit 20 that receives the signal from the light receiver 18 and is designed such that blood or blood components in the liquid are detected on the basis of the weakening of radiation passing through the liquid. The method according to the invention is based on the fact that the calibration of the devices 11 for detecting blood or blood components is carried out without the use of blood. The calibration is carried out using an absorption standard 30, which has predetermined optical properties in relation to the absorption of the light in blood, the absorption standard 30 being arranged in the beam path 19 between the light transmitter 17 and the light receiver 18. The absorption standard 30 makes it possible to identify defined spectral weakening in the light depending on the components of the blood, in particular haemoglobin. Since, by contrast with blood, the absorption standard 30 does not bring about any scattering, meaning that the beam path is influenced in a different way from blood, the calibration is also carried out using a scattering standard 36, which has predetermined optical properties in relation to the scattering of the light in blood. The assembly also comprises a beam deflection unit 22 for coupling out light for a spectral measurement of the light transmitter 17 using a spectrometer 27.
SMART PERITONEAL DIALYSIS DEVICE
A device for monitoring and/or modifying a peritoneal dialysis treatment, including: a memory which stores at least one treatment protocol; a control circuitry connected to the memory, wherein said control circuitry generates a report and/or modifies the treatment if an outcome of the treatment is not a desired outcome of the treatment protocol.
Extracorporeal blood treatment device and method for monitoring the integrity of a dialyzer of an extracorporeal blood treatment device
The invention relates to an extracorporeal blood treatment device for carrying out an extracorporeal blood treatment, in which blood flows in an extracorporeal blood circuit A through the blood chamber 2 of a dialyser 1 which is divided by a semi-permeable membrane 4 into the blood chamber 2 and a dialysate chamber 3. The invention further relates a method for monitoring the integrity of a dialyser 1. The blood treatment device provides a preparation mode in preparation for the blood treatment, in which the dialysate chamber 3 of the dialyser 1 (filter) is filled with a liquid, while the blood chamber 2 is not filled with blood, and a treatment mode following the preparation mode, in which blood is conveyed through the blood chamber 2. For monitoring the integrity of the dialyser 1, in the preparation mode the fluid system B including the dialysate chamber 3, or a portion of the fluid system including the dialysate chamber, is filled with a liquid. At this time, however, the blood chamber 2 is not filled with blood. After the membrane of the dialyser 1 has been wetted with liquid, liquid is removed from the fluid system B including the dialysate chamber 3 such that a low pressure p is established in the fluid system. The control and arithmetic unit 29 of the blood treatment device is so configured that the increase in the amount of the low pressure p, measured by means of a pressure measuring apparatus 34, in a given time interval is determined, and the leakage rate LR of the fluid system is determined from the increase in the amount of the low pressure in a given time interval and the compliance C of the fluid system B including the dialysate chamber 3. A lack of integrity of the dialyser is then concluded on the basis of the determined leakage rate LR.
Blood treatment device comprising a functional unit for carrying out the blood treatment and method for monitoring the functionality and/or the operating state of the functional unit
The invention relates to a blood treatment device comprising an attachment unit 7 for attaching a functional unit 1 intended for single use for carrying out the blood treatment. The blood treatment device according to the invention is characterised by a monitoring unit 8 for monitoring the operability and/or the operating state of the functional unit 1, which functional unit comprises at least one light transmitter 17A, 18A and at least one light receiver 17B, 18B. The light transmitter and light receiver are arranged in the monitoring unit 8 according to the invention on one side of the functional unit 1. The arrangement of the light transmitter and light receiver on the same side has the advantage that the monitoring unit 8 can be integrated into the attachment unit 7 of the blood treatment device without any major structural modifications. The monitoring of the functional unit 1 is based on an optical measurement method in which the light reflected on a part of the functional unit 1 or a part of the attachment unit 7 is detected. A calculation- and evaluation unit 13 is configured such that conclusions can be drawn as to a defective state and/or a certain operating state of the functional unit 1 based on the intensity of the light falling on the functional unit and the light reflected on the functional unit or the attachment unit.