Abstract: A medication delivery monitoring device is disclosed. The device includes a user interface configured to receive input information, and a sensor configured to measure a plurality of fluid state parameters of a fluid delivery channel through which the medication is delivered by a vascular access device (VAD) to an infusion site region of the patient. The device also includes a processor configured to determine a state of the infusion site region based on the plurality of measured fluid state parameters and the input information, and an output device configured to provide a communication regarding the state of the infusion site region. Methods and computer-readable mediums for monitoring medication delivery are also disclosed.

Abstract: An infusion data communication system provides a communication link among a fluid container, an infusion pump, and a patient through which identification data may be communicated. Data devices are located at the fluid container and the patient and conduct low frequency RF energy at a low power level containing the data into the medical fluid. The data-laden RF energy propagates through the medication fluid to data readers at the infusion pump which receives the RF energy and reads the data. A comparison is made to verify that the right medication is mounted to the infusion pump for administration to the right patient. RFID devices may be used for the data devices and readers. Pump programming data may also be propagated to the infusion pump from the container RFID tag. The RFID device at the patient may be writable and may be used to store a patient MAR.

Abstract: Systems and methods of measuring pressure of fluid in a disposable IV set connected to a fluid supply pump is disclosed. At least one sensing arrangement coupled to the fluid supply pump is provided. A chamber having a movable element is provided, the movable element configured to move in response to changes in fluid pressure within the disposable IV set and thereby cause a change in a sensed measurement variable associated with the sensing arrangement without contacting the sensing arrangement. A measuring signal indicative of the sensed measurement variable is generated. The fluid pressure within the disposable IV set is determined based on the measuring signal.

Abstract: A pump having a disposable fluid contacting portion which defines a fluid inlet and outlet and a fluid path there between. The pump includes a drive portion configured to engage the disposable portion to cause fluid to be moved from the fluid inlet to the fluid outlet. The disposable portion is configured to be selectively coupled to the drive portion. The disposable portion includes a driven membrane which forms a portion of the fluid path, and the drive portion includes a drive membrane. The two membranes are vacuum coupled to each other, whereby movement of the drive membrane causes the driven membrane to move, causing fluid to be pumped through the disposable portion. The pump has particular utility in the medical field for moving fluid from a source to a patient. The pump may include features such as an air-trap, bubble detection, fluid flow controls, and pressure detection.

Abstract: The concentration of air or other agents in a fluid delivery line is determined by monitoring agent signals and processing those agent signals along with information regarding the age of each agent signal. The processor determines a primary agent concentration value based on the received agent signal values, with the primary agent concentration value determined by giving greater weight to more recent agent signal values. Where the primary agent concentration value exceeds a primary threshold value, an alarm signal may be activated. The processor also may determine a secondary agent concentration value, which may be determined from the actual agent signal values instead of the weighted agent signal values. Where the secondary agent concentration value exceeds a secondary threshold value, an alarm signal may be activated.

Abstract: An infusion data communication system provides a communication link among a fluid container, an infusion pump, and a patient through which identification data may be communicated. Data devices are located at the fluid container and the patient and conduct low frequency RF energy at a low power level containing the data into the medical fluid. The data-laden RF energy propagates through the medication fluid to data readers at the infusion pump which receives the RF energy and reads the data. A comparison is made to verify that the right medication is mounted to the infusion pump for administration to the right patient. RFID devices may be used for the data devices and readers. Pump programming data may also be propagated to the infusion pump from the container RFID tag. The RFID device at the patient may be writable and may be used to store a patient MAR.

Abstract: Systems and methods of measuring pressure of fluid in a disposable IV set connected to a fluid supply pump is disclosed. At least one sensing arrangement coupled to the fluid supply pump is provided. A chamber having a movable element is provided, the movable element configured to move in response to changes in fluid pressure within the disposable IV set and thereby cause a change in a sensed measurement variable associated with the sensing arrangement without contacting the sensing arrangement. A measuring signal indicative of the sensed measurement variable is generated. The fluid pressure within the disposable IV set is determined based on the measuring signal.

Abstract: In a patient controlled analgesia (PCA) system, physiological data is processed and alarms are provided by the controller of the physiological module sensing the data according to a first rule. The physiological data is also processed by a second, separate controller according to a second rule independent from the first controller. According to the second rule, the physiological data may be filtered, processed with physiological data and non-physiological data obtained from another source, such as a remote server, and the PCA delivery device controlled to prevent delivery of medication accordingly. The provided system of multiple processors and rules enables normal alarming by physiological sensor modules while the pausing or prevention of the PCA delivery is controlled by a separate controller. Through this means, not only are false pauses and alarms for PCA delivery reduced, but the normal alarms of the monitors are permitted to function normally.

Abstract: A system and method for monitoring changes in the pressure of a fluid line upstream of an infusion pump to determine when a fluid container has emptied, and to provide a signal indicating that the container needs replacement or replenishment. The difference between averaged pressures over separate time periods is monitored to determine when the fluid container is empty. The system and method are applicable to primary and secondary fluid container setups and can detect the point where the secondary has been emptied and the primary flow has resumed.

Abstract: A pump having a disposable fluid contacting portion which defines a fluid inlet and outlet and a fluid path there between is presented. The pump includes a drive portion configured to engage the disposable portion to cause fluid to be moved from the fluid inlet to the fluid outlet. The disposable portion is configured to be selectively coupled to the drive portion. The disposable portion includes a driven membrane which forms a portion of the fluid path, and the drive portion includes a drive membrane. The two membranes are vacuum coupled to each other, whereby movement of the drive membrane causes the driven membrane to move, causing fluid to be pumped through the disposable portion. The pump has particular utility in the medical field for moving fluid from a source to a patient. The pump may include features such as an air-trap, bubble detection, fluid flow controls, and pressure detection.

Abstract: The concentration of air or other agents in a fluid delivery line is determined by monitoring agent signals and processing those agent signals along with information regarding the age of each agent signal. The processor determines a primary agent concentration value based on the received agent signal values, with the primary agent concentration value determined by giving greater weight to more recent agent signal values. Where the primary agent concentration value exceeds a primary threshold value, an alarm signal may be activated. The processor also may determine a secondary agent concentration value, which may be determined from the actual agent signal values instead of the weighted agent signal values. Where the secondary agent concentration value exceeds a secondary threshold value, an alarm signal may be activated.

Abstract: A system and method for processing keystrokes made while operating a medical device to prevent keypad entry errors. The key press-to-press time is monitored and a subsequent key press rejected if the actual key press-to-press time is shorter than a key press-to-press limit. The actual key inactive time between the release of a key and the subsequent press of a key is compared to an inactive time limit. The subsequent key press is rejected if the actual inactive time is shorter than the inactive time limit. Alerts are provided and further key presses are ignored until the operator presses a CLEAR key. The active time of a key press is monitored and compared to an active time limit. If the actual key press active time exceeds the key press active time limit, an alert is provided but the key press is recognized. An adaptive approach is disclosed in which key presses of an operator are monitored and timing limits modified in accordance with the keying patterns of that operator.

Abstract: A thermometer system and method that rapidly predict body temperature based on the temperature signals received from a temperature sensing probe when it comes into contact with the body. A nonlinear, multi-parameter curve fitting process is performed and depending on the errors in the curve fit, parameters are changed or a prediction of the temperature is made. Criteria exist for the differences between the curve fit and the temperature data. The processor switches to a Continuous Monitor State if the curve fit over a limited number of time frames is unacceptable. Determining the start time on which the measurement time frame for prediction is based is performed by tissue contact threshold coupled with a prediction time delay.

Abstract: A system and method for determining whether the pressure in a fluid line upstream of an infusion pump is becoming lower as pumping draws fluid from the fluid line and fluid container due to a lack of proper venting. An initial pressure is sensed by an upstream pressure sensor at the start of an infusion. After a period of time, which may be determined either by monitoring infusion time or the number of pump cycles completed, a second pressure is sampled and compared to the initial pressure. Various analytical methods may be applied to the sensed pressures to determine upstream pressures or trends. Where an upstream pressure reading indicates a lack of proper venting, an alert signal is provided. Continuous monitoring may occur in which succeeding samples are compared to preceding samples to determine upstream pressures or trends.

Abstract: A system and method for monitoring changes in the pressure of a fluid line upstream of an infusion pump to determine when a fluid container has emptied, and to provide a signal indicating that the container needs replacement or replenishment. The difference between averaged pressures over separate time periods is monitored to determine when the fluid container is empty. The system and method are applicable to primary and secondary fluid container setups and can detect the point where the secondary has been emptied and the primary flow has resumed.

Abstract: The concentration of air in a fluid delivery line is determined by monitoring output signals corresponding to the amount of air detected in the fluid and processing those signals along with information as to the time or total volume of fluid dispensed since each signal was produced. The processor determines an air concentration value based on the received signal values, with the air concentration value determined by giving greater weight to more recent signal values. Where the air concentration value exceeds a predetermined value, an alarm signal may be activated or fluid delivery may be stopped. The processor also may determine a secondary air concentration value, which may be determined from the raw signal values instead of the weighted signal values. Where the secondary air concentration value exceeds a second predetermined threshold, an alarm signal may be activated or fluid delivery may be stopped.

Abstract: An infusion data communication system provides a communication link among a fluid container, an infusion pump, and a patient through which identification data may be communicated. Data devices are located at the fluid container and the patient and conduct low frequency RF energy at a low power level containing the data into the medical fluid. The data-laden RF energy propagates through the medication fluid to data readers at the infusion pump which receives the RF energy and reads the data. A comparison is made to verify that the right medication is mounted to the infusion pump for administration to the right patient. RFID devices may be used for the data devices and readers. Pump programming data may also be propagated to the infusion pump from the container RFID tag. The RFID device at the patient may be writable and may be used to store a patient MAR.

Abstract: The concentration of air or other agents in a fluid delivery line is determined by monitoring agent signals and processing those agent signals along with information regarding the age of each agent signal. The processor determines a primary agent concentration value based on the received agent signal values, with the primary agent concentration value determined by giving greater weight to more recent agent signal values. Where the primary agent concentration value exceeds a primary threshold value, an alarm signal may be activated. The processor also may determine a secondary agent concentration value, which may be determined from the actual agent signal values instead of the weighted agent signal values. Where the secondary agent concentration value exceeds a secondary threshold value, an alarm signal may be activated.

Abstract: A system for controlling fluid flow through multiple conduits for use in a fluid administration device. The system includes a housing, a cam, and a control element used to move the cam to selectively occlude the conduits. When used with a medical burette, the cam is located between the vent and supply conduits and rotates to alternately occlude one or the other conduits or to leave both conduits patent. Depending on the rotational position of the cam, the continuous flow mode, the intermittent flow mode, and the priming mode are all obtained with a single control lever. The housing secures the conduits in predetermined, fixed positions both above and below the contact location of the cam to the conduit. A positive locking device is included to assist in locating the cam in the desired position. Clear visual indicators are included on the housing for viewing the present flow operating state.

Abstract: A system for controlling fluid flow through multiple conduits for use in a fluid administration device. The system includes a housing, a cam, and a control element used to move the cam to selectively occlude the conduits. When used with a medical burette, the cam is located between the vent and supply conduits and rotates to alternately occlude one or the other conduits or to leave both conduits patent. A cam lobe occludes the conduits by pressing the conduit against a pressure surface until occlusion is obtained. Depending on the rotational position of the cam, the continuous flow mode, the intermittent flow mode, and the priming mode are all obtained with a single control lever. The housing secures the conduits in predetermined, fixed positions both above and below the contact location of the cam to the conduit. A positive locking device is included to assist in locating the cam in the desired position.