摘要:
A patient monitor system is configured to measure and display a hemoglobin concentration measurement to assist caregivers in providing care or treatment and/or to automatically control a fluid, blood, medicine, or dialysis administration system. The patient monitor can analyze the displayed hemoglobin concentration measurement and provide alarms and feedback to assist caregivers. Additional measurement can be combined with the hemoglobin concentration measurement to provide combined displays helpful to caregivers, such as, for example, a plethysmograph variability index v. SpHb display.
摘要:
A modular patient monitor has a docking station configured to accept a handheld monitor. The docking station has standalone patient monitoring functionality with respect to a first set of parameters. At least some of the first parameter set are displayed simultaneously on a full-sized screen integrated with the docking station. The handheld monitor also has standalone patient monitoring functionality with respect to a second set of parameters. At least some of the second set of parameters are displayed simultaneously on a handheld-sized screen integrated with the handheld monitor. The docking station has a port configured to accept the handheld monitor. While the handheld monitor is docket in the port, the docking station functionally combines the first set of parameters and the second set of parameters, and at least some of the combined first and second sets of parameters are displayed simultaneously on the full-sized screen.
摘要:
A modular patient monitor has a docking station configured to accept a handheld monitor. The docking station has standalone patient monitoring functionality with respect to a first set of parameters. At least some of the first parameter set are displayed simultaneously on a full-sized screen integrated with the docking station. The handheld monitor also has standalone patient monitoring functionality with respect to a second set of parameters. At least some of the second set of parameters are displayed simultaneously on a handheld-sized screen integrated with the handheld monitor. The docking station has a port configured to accept the handheld monitor. While the handheld monitor is docket in the port, the docking station functionally combines the first set of parameters and the second set of parameters, and at least some of the combined first and second sets of parameters are displayed simultaneously on the full-sized screen.
摘要:
A non-invasive electronic patient monitor tracks one or more physiological parameters of a patient, such as intravascular volume index (IVI), extravascular volume index (EVI), total hemoglobin (SpHb), impedance, and/or weight. The patient monitor determines if one or more of the physiological parameters are within a predetermined range. The patient monitor activates an alarm if one or more of the physiological parameters are outside the predetermined range and indicates a patient can be experiencing edema and/or heart failure, or sepsis.
摘要:
A non-invasive electronic patient monitor tracks one or more physiological parameters of a patient, such as intravascular volume index (IVI), extravascular volume index (EVI), total hemoglobin (SpHb), impedance, and/or weight. The patient monitor determines if one or more of the physiological parameters are within a predetermined range. The patient monitor activates an alarm if one or more of the physiological parameters are outside the predetermined range and indicates a patient can be experiencing edema and/or heart failure, or sepsis.
摘要:
A control solution packet for calibrating a bodily fluid sampling device includes a container, a control solution pressurized within the container, and a membrane for covering and sealing the container. The control solution can be pressurized before or during calibration so as to ensure the appropriate amount of control solution is delivered to the bodily fluid sampling device. The control solution is manufactured to have a viscosity that controls delivery of the control solution to the device. The membrane is permeable by a piercing device of the bodily fluid sampling device and seals around the piercing device during calibration. In another aspect, the container is in the form of a capsule or dosing attachment that contains the control solution along with a sponge-like material.
摘要:
A piston compressor with at least one compression cylinder having a piston, and with one suction port and one pressure port is described. The suction port and the pressure port are arranged at one end face of the compression cylinder.
摘要:
A medical device is provided, comprising a data management unit for providing patient data regarding a patient's health and/or treatment status, a display for displaying the patient data provided by the data management unit, and an actuator configured to cause one or both of activation and deactivation of the device. The patient data is displayed on the display in response to the initiation of activation and/or deactivation of the device.
摘要:
A control solution packet for calibrating a bodily fluid sampling device includes a container, a control solution pressurized within the container, and a membrane for covering and sealing the container. The control solution can be pressurized before or during calibration so as to ensure the appropriate amount of control solution is delivered to the bodily fluid sampling device. The control solution is manufactured to have a viscosity that controls delivery of the control solution to the device. The membrane is permeable by a piercing device of the bodily fluid sampling device and seals around the piercing device during calibration. In another aspect, the container is in the form of a capsule or dosing attachment that contains the control solution along with a sponge-like material.
摘要:
Analysis device for analyzing samples, in particular of body liquids, with respect to components contained therein. It comprises a plurality of liquid handling (LH) stations. At at least a part of the LH stations there is a production of liquid waste whereby said LH-station form liquid waste sources. The liquid waste is evacuated, with at least one pump, from the liquid waste sources, with different proportions of air, via a liquid waste conducting system, into a liquid waste container. A substantial reduction of foam production is obtained by connecting at least two liquid waste sources to the liquid waste container via at least two liquid waste lines leading separately into the liquid waste container, whereas liquid waste sources with a higher average air proportion are connected to a first liquid waste line and liquid waste sources with a lower average air proportion are connected to a second liquid waste line.