A system includes a probe, a processor, and a bubble detector. The probe is configured for insertion into a lumen of a patient and is coupled to an irrigation pump. The processor is configured to control delivery of irrigation fluid to the probe by turning on and controlling the irrigation pump. The bubble detector is coupled to a proximal portion of the probe. In response to the irrigation pump being turned on, the bubble detector is configured to automatically start detection of gas bubbles in the irrigated fluid, and transmit fail-safe signals indicating fail-safe bubble detection is operational. The processor is further configured to monitor the fail-safe signals and, in absence of fail-safe signals, to automatically disable delivery of the irrigation fluid.

A medical device (10) includes a device housing (12). An in-line thermal mass flow sensor (26) includes a heater (28) and at least one temperature sensor (30). The in-line thermal mass flow sensor is vertically mounted on or in the device housing. The in-line thermal mass flow sensor is configured to measure a flow rate of the fluid through the medical device. At least one electronic processor (18) is programmed to: read the flow rate of the fluid measured by the in-line thermal mass flow sensor, and detect at least one bubble in the fluid based on the measured flow rate.

A method that includes receiving, in a medication delivery module, a command to start a medication delivery from a first control module coupled to the medication delivery module, is provided. The command to start the medication delivery is based on clinical information received at the first control module. The method includes recording, in a memory of the medication delivery module, an update of the medication delivery, receiving an indication that the medication delivery module was decoupled from the first control module, and receiving an indication that the medication delivery module has become coupled with a second control module. The method also includes communicating, in response, with the second control module, to update the clinical information. A system and a non-transitory, computer readable medium storing instructions to perform the above method are also provided.

An infusion pump includes a housing with a door pivotally mounted to the housing, a tube channel on the housing configured to hold a tube in the infusion pump, a pumping mechanism including a shuttle, and a slide clamp ejection device.

Improvements in an infusion unit are disclosed. The infusion unit is a portable pump that can be used with patient that have wrist access or decubital PICC/MID-LINES without the risk of line accidently getting pulled. The infusion unit is in the shape of a conveniently shell that has an appearance of an arm cast. There are no hoses that extend beyond the body of the infusion unit and any vein penetration is completely covered under the body of the infusion unit. The secure enclosed unit prevents unauthorized tampering and entry into the unit. The medication dosing can be remotely monitored, fusion resumed, changed by nursing and the patient. The infusion unit has a wireless connection to a network to adjust medication and monitor vital signs, namely heart rate, O2 level and blood pressure that can be monitored and recorded for review.

Sensors, methods, and computer program products for air bubble detection are provided. An example method includes determining a first moving average for a first period of time based upon first temperature data and determining a second moving average for the first period of time based upon second temperature data. The method includes determining a first air presence parameter based upon a comparison between the first temperature data and the first moving average and a comparison between the second temperature data and the second moving average. The method includes determining a second air presence parameter based upon a comparison between the first temperature data, the second temperature data, and calibrated air thresholds. The method includes determining a third air presence parameter based upon a comparison between a first temperature data entry and each second temperature data entry. An air bubble within a fluid flow system is detected based upon the parameters.

A repeater system may control a pump by using a repeater and a user interface. An adhesive patch system may be used for affixing a pump or other object to a human body. Such an adhesive patch system may include two sets of adhesive members, each member including an adhesive material on at least one side so as to attach to the body. The members of the first set are spaced to allow the members of the second set to attach to the body in spaces provided between the members of the first set, and the members of the second set are spaced to allow members of the first set to detach from the body without detaching the members of the second set. Also, fill stations and base stations are provided for personal pump systems.

A fluid injection system includes an injector housing, a sleeve, and a lighting assembly. The sleeve is coupled to the injector housing and is configured to receive and secure a fluid reservoir. The lighting assembly is coupled to the injector housing. The lighting assembly includes a light source configured to illuminate an interior of the fluid reservoir by directing light emitted by the light source into the fluid reservoir.

An infusion pump includes: a main body configured to have an infusion tube fixed thereto, wherein the main body includes: a first fixing unit, a second fixing unit that is movable between (i) a pressing position in which the infusion tube is pressed against the first fixing unit, and (ii) a release position in which the pressing of the infusion tube against the first fixing unit is released, by being rotated with respect to a rotary shaft, an urging unit configured to urge the second fixing unit toward the release position, the urging unit comprising an urging member mounted on the rotary shaft, a transmission unit configured to transmit a signal toward the infusion tube sandwiched between the first fixing unit and the second fixing unit, and a reception unit configured to receive the signal transmitted from the transmission unit.

A system and method for monitoring and delivering medication to a patient. The system includes a controller that has a control algorithm and a closed loop control that monitors the control algorithm. A sensor is in communication with the controller and monitors a medical condition. A rule based application in the controller receives data from the sensor and the closed loop control and compares the data to predetermined medical information to determine the risk of automation of therapy to the patient. A system monitor is also in communication with the controller to monitor system, remote system, and network activity and conditions. The controller then provides a predetermined risk threshold where below the predetermined risk threshold automated closed loop medication therapy is provided. If the predetermined risk threshold is met or exceeded, automated therapy adjustments may not occur and user/clinician intervention is requested.