Abstract: A computing system for determining a systematic training strategy for the user is provided. The computing system includes a user device that uses one or more sensors to obtain partial pressure of oxygen (PO2) levels of a user over a period of time. The user device provides previous PO2 levels to a personalized erythropoiesis model generation computing platform. The computing platform obtains individualized user data for the user indicating or more previous hematocrit and/or hemoglobin measurements for the user. The computing platform determines an individualized erythropoiesis model for the user based on the one or more previous hematocrit and/or hemoglobin measurements and the previous PO2 information, and employs the individualized erythropoiesis model to determine predicted hematocrit and/or hemoglobin measurements. The computing platform performs one or more actions based on the one or more predicted hematocrit and/or hemoglobin measurements.

Abstract: An apparatus for preparing a dialysis solution has a dialyzate line for conducting a dialysis solution and means configured to discontinuously convey a dialysis solution in the dialyzate line. The apparatus has a conductivity sensor that is arranged to measure the conductivity of the dialysis solution, a concentrate line opening into the dialyzate line upstream of the conductivity sensor at an addition point, a concentrate pump, and a concentrate container from which the concentrate pump conveys concentrate into the concentrate line, and from there, into the dialyzate line. The apparatus has a controller that is connected to the conductivity sensor and to the concentrate pump, and that is configured to control the concentrate pump such that the conductivity fluctuations over time in the dialysis solution downstream of the addition point are reduced with respect to a continuous concentrate conveying.

Abstract: The present invention relates to a blood treatment device, preferably a dialysis machine, that is configured to be used with a disposable, preferably with a cassette system, and that has a coupling region for the disposable and a control unit that is configured to carry out a plurality of pressure measurements at different times during a coupling procedure of the disposable to the blood treatment device, with a quality of the coupling of the disposable to the blood treatment device being able to be determined with reference thereto. The present invention further relates to a method of monitoring a coupling procedure of a disposable to a blood treatment device.

Abstract: The invention relates to a medical apparatus designed to receive a detachable fluid-conducting first line portion (3). The medical apparatus comprises a second line portion (2) designed to be connected to the first line portion (3), wherein a movable element (38) is situated in the second line portion (2), by means of which movable element the second line portion (2) is separated into a first sub-portion (2a) and a second sub-portion (2b).

Abstract: The invention relates to a device for discharging wastewater, in particular used or spent dialysate, comprising a plurality of line connections 3, 4, 5 for connecting wastewater lines, in particular wastewater lines of dialysis machines. The device according to the invention is designed as a part which can stand on the bottom of a basin. Sufficient stability can be achieved on account of the weight (gravitational force) of the device alone, without it being necessary to secure the device. Recontamination is prevented effectively in that the line connections 3, 4, 5 are in fluid connection with at least one inflow line, the lower end of which is arranged so as to be spaced apart from the bottom, such that a free-fall distance is formed. In a preferred embodiment, a casing 1 surrounds the at least one inflow line 6, 7, 8. The casing 1 forms a splash guard in the form of a hood such that the wastewater, which emerges from the inflow lines 6, 7, 8 under relatively high pressure, cannot reach the surroundings.

Abstract: The present invention relates to a method of disinfecting a region, in particular a skin region of a patient, wherein the method comprises the following steps: a) Application of an optically effective substance to the region; and b) Application of a disinfectant to the region, wherein the optically effective substance and the disinfectant are configured such that the optically effective substance is removed by the disinfectant or its optical properties are changed by the disinfectant.

Abstract: The invention relates to a device and a method for producing a hollow fibre membrane bundle consisting of hollow fibre membranes, wherein, in the claimed device, a sheaf of hollow fibre membranes is received in a lower semitubular shell and bundled together to form a hollow fibre membrane bundle by a complementary upper semitubular shell.

Abstract: An infusion site for a blood tubing set, comprises a first (102) and a second (104) connection sites for connecting a first and a second tubing portion of the blood tubing set to the infusion site (100), and suitable to let a first and a second liquid enter the infusion site (100); and a third connection site (103) for connecting a third tubing portion of the blood tubing set to the infusion site (100) and suitable to let a third liquid exit the infusion site (100).

Abstract: The disclosure relates to a medical device with a display and with a processing unit and method therefor. The processing unit is suitable for detecting states of one or more technical units of the medical device. The processing unit is further set up to control the display on the basis of detected states in order to output states of the medical device. The display is an autostereographic display. The processing unit, based on an evaluation of detected states, drives the display in such a way that a first state is visually highlighted with respect to a 3D representation, while a second state is visually not highlighted with respect to a 3D representation.

Abstract: The present invention relates to an apparatus (1) for holding a disposable medical item, in particular a dialyzer (2), plasma filter or adsorbent, for treating blood, a system (10) comprising such an apparatus, and a method for operating a disposable medical item for treating blood. A bearing device (4) is thereby configured to rotatably support the disposable item, and a drive device (5) is thereby configured to rotate the rotatably mounted disposable item around a longitudinal axis (L) extending substantially in a direction in which the blood flows through the disposable item when the disposable item is in operation. Alternatively or additionally, a sensor device (6) is configured to detect a rotation of the rotatably mounted disposable item around at least one rotational axis (L, Q), in particular around the longitudinal axis (L) and/or around a transverse axis (Q) running perpendicular to the longitudinal axis (L) and output corresponding sensor data.

Abstract: The present disclosure relates to a method for determining an actual pump rate and/or for calibrating a blood pump of a blood treatment apparatus connected to an extracorporeal blood circuit. The method includes providing a blood pump of a blood treatment apparatus or establishing a signal communication to a blood pump. The blood pump comprises, or is connected to at least a first source for a fluid and at least a first line of an extracorporeal blood circuit which is connected to the first source downstream. Furthermore, the blood pump comprises, or is connected to, a reception unit for receiving fluids of the first source wherein the reception unit is in fluid communication with the first line. The reception unit is arranged on or at a first weighing device such that the weight of the reception unit or of its content is determined using the weighing device.

Abstract: Coupling device (1), which comprises at least two connectable elements in the form of a sleeve (2) and a sleeve holder (3), and the sleeve (2) has, at a first side (a), a recess (4) which is configured on both sides as hooks (5) and is provided with bevelled edges (6), and the sleeve holder (3) has, at a second side (c), a horizontally extending through-pin (7).

Abstract: A system and method for failsafe storage of real-time data, for example, relating to a hemodialysis or peritoneal dialysis treatment, includes: temporarily storing the real-time data in a ring buffer memory; pre-allocating a set of storage units of a storage medium, which is supplied with an operating voltage, for storing the real-time data in a file system; and based on the operating voltage of the storage medium being within a predefined reference range, transferring the real-time data from the ring buffer memory to the storage medium and storing the real-time data on a storage unit of the storage medium. In case of error, the integrity, authenticity, and availability of the stored real-time data are ensured.

Abstract: The present disclosure relates to a blood hose set, or to an extracorporeal blood circuit, for a single-needle treatment. In some embodiments, the set includes: a patient hose line and a Y-shaped connector or three-way connecter, which is connected to the patient hose line. In some embodiments, the blood hose set does not include any single-needle chamber in a blood path or on a blood side, nor is it connected to any single-needle chamber provided in a blood path or on a blood side. The present disclosure further relates to a control device or closed-loop control device, a blood treatment apparatus, a method for the single-needle treatment, a digital storage medium, a computer program product and a computer program.

Abstract: The present disclosure relates to a medical condensate trap for use in external blood treatment by means of a blood treatment apparatus. The condensate trap comprises an interior; a first connection for connecting the interior in fluid communication to a gas outlet of the blood treatment apparatus; a second connection for connecting the interior in fluid communication to a gas inlet of the blood treatment apparatus; and a third connection for connecting the interior to an air port of a blood treatment device. The blood treatment device may be, for example, a blood tubing set or a blood cassette.

Abstract: A water source, an acid source, an electrolyte tank containing a mixture of electrolytes in exactly the quantity needed for the manufacture of the liquid acid concentrate, and a sodium chloride source are connected to a mixing tank. A quantity of water needed for the manufacture of the batch of liquid acid concentrate is introduced into the mixing tank. A quantity of acid needed for manufacture of the liquid acid concentrate is introduced into the mixing tank, the solution is stirred until a homogeneous solution is obtained. Part of the solution contained in the mixing tank is transferred into the electrolyte tank, then the solution contained in the electrolyte tank is transferred into the mixing tank. A quantity of sodium chloride needed to manufacture the liquid acid concentrate is introduced into the mixing tank. The solution is stirred and recirculated until a homogeneous liquid acid concentrate is obtained.

Abstract: The invention relates to a communications device for non-electric communication between fluidically interconnected devices, the communications device being designed to be mounted in a position in a fluidic overall system formed by the fluidically interconnected devices and to receive and/or emit non-electric signals, in particular in the form of pressure or sound signals, the non-electric signals being transmitted via a line that fluidically interconnects the devices. The invention further relates to a method for non-electric communication between fluidically interconnected devices, the non-electric communication taking place preferably by means of pressure and/or sound signals via at least one line that fluidically interconnects the devices.

Abstract: The invention relates to a filter device for the exchange of substances, comprising a pipe section-shaped housing with a center of gravity and with two housing ends, in which housing a hollow fiber bundle consisting of semi-permeable membranes is arranged, comprising, furthermore, an end cap having a first and second opening, wherein the housing and the end cap configure a first sealing surface which connects the housing and the end cap sealingly, and wherein the first sealing surface is spaced apart further from the center of gravity of the housing than the aperture, and wherein a first fluid chamber is formed between the first sealing surface and the first opening of the end cap, via which first fluid chamber the first opening is connected to the first flow chamber, wherein the housing and the one end cap configure a second sealing surface, wherein the first and second sealing surface are not configured by way of a sealant.

Abstract: A pumping device for pumping liquids includes a centrifugal pump with a radially pumping pump wheel having a hollow center, and is configured to remove accumulations of gas from the interior of the pump. The pumping device includes a detecting device for detecting a first operating parameter, a sensor for measuring a second operating parameter, and a control unit for controlling the pump. The control unit is configured to control the operation of the pump so as to remove accumulations of gas from the hollow center of the pump during liquid pumping operation.

Abstract: The present invention relates to a dialysis machine comprising a balancing system that has at least one balancing chamber for a volumetrically exact supply and removal of dialysis solution to and from a dialyzer fluidically connected to the balancing system in operation; a water inlet system connected to the balancing system for the supply of fresh dialysis liquid, with the water inlet system having an apparatus for degassing water that is connected to an air separator of the dialysis machine, with a first subsection of the air separator serving as a mixing chamber and being connectable to at least one concentrate source via at least one concentrate line and being in fluid communication with the balancing system via at least one dialysate line, wherein the filling volume of a balancing chamber corresponds to or exceeds the sum of the volume of the mixing chamber and the inner volume of the dialysate line.