A method of determining the status of a fluid cooled microwave ablation system is provided including providing an electrical current to a pump to pump fluid through an ablation system along a fluid path to cool the ablation system, measuring an electrical current drawn by the pump, and determining a status of the ablation system based on the measured electrical current. In another aspect of the disclosure, an ablation system is provided including an ablation probe defining a fluid path for circulation of fluid therethrough, a generator configured to supply energy to the ablation probe for treating tissue, a pump configured to pump fluid through the fluid path of the ablation probe to cool the ablation probe, a sensor configured to measure an electrical current drawn by the pump, and a computing device configured to determine a status of the ablation system based on the measured electrical current.

A method, computer program product, and infusion pump assembly for determining a first rate-of-change force reading that corresponds to the delivery of a first dose of an infusible fluid via an infusion pump assembly. At least a second rate-of-change force reading is determined that corresponds to the delivery of at least a second dose of the infusible fluid via the infusion pump assembly. An average rate-of-change force reading is determined based, at least in part upon the first rate-of-change force reading and the at least a second rate-of-change force reading.

A device and method for controlling operation of an ambulatory infusion device drive. The drive may have a spindle drive with a stepper motor, a drive member operatively coupled to a rotary encoder, and a driver controller that executes several steps, including actuating the stepper motor to execute a requested number of steps in a current drive control sequence, receiving a drive member position that indicates an actual position of a drive member following the actuation, computing an executed steps number from the drive member position, computing a missed steps number for the current drive control sequence, which is the difference between the requested number of steps and the executed steps number, determining when the ambulatory infusion device drive is blocked based on a statistical evaluation of a time-distribution of the missed steps number over a history of drive control sequences, and generating a blockage alarm signal.

A patency device for catheter assemblies and other elongate tubular devices used for establishing access to an interior body portion of a patient is disclosed. The patency device establishes and preserves patency of one or more lumens defined by the catheter assembly by providing impulses of positive pressure to fluid disposed in the lumen of the catheter assembly. In one embodiment, the patency device comprises a fluid reservoir configured to provide a fluid path to at least one lumen of the catheter assembly, and a pressure input portion. The pressure input portion is configured to provide pressure for one or more impulses of positive pressure to a fluid disposed within the lumen. The impulses are configured to dislodge occlusions that may have formed in the lumen. A negative pressure can then be provided to the lumen to aspirate the occlusion.

Ambulatory infusion pumps, pump assemblies, and disposable assemblies, including cartridges, baseplates, cannulas, inserters, and related components therefor, as well as component combinations and related methods.

A dialysis machine (e.g., a peritoneal dialysis (PD) machine) can include a pressure sensor mounted at a proximal end of a patient line made of a distensible material that provides PD solution to a patient through a catheter. During treatment, an occlusion can occur at different locations in the patient line and/or the catheter. When an incremental volume of additional solution is provided to the patient line while the occlusion is present, a change in pressure results. The change in pressure depends on dimensions and a distensibility of a non-occluded portion of the patient line. If the change in pressure, the incremental volume, properties related to the distensibility of the patient line, and some of the dimensions of the patient line are known, a location of the occlusion can be inferred. An occlusion type can be inferred based on the location of the occlusion.

An occlusion detection device detects an occlusion of a flexible fluid path on either of upstream and downstream sides of a pump mechanism, the pump mechanism transporting a liquid through the fluid path by elastically deforming the fluid path. The occlusion detection device is provided with: an occlusion sensor that is disposed on the downstream side of the pump mechanism and detects an internal pressure of the fluid path during a liquid transporting operation of the pump mechanism; and a data processing circuit that analyzes on which side of the upstream and downstream sides of the pump mechanism the occlusion of the fluid path occurs, based on a change of the internal pressure of the fluid path detected by the occlusion sensor and outputs an analysis result.

A pump for pumping fluid includes a tube platen, a plunger, a bias member, inlet and outlet valves, an actuator mechanism, a position sensor, and a processor. The plunger is configured for actuation toward and away from the infusion-tube when the tube platen is disposed opposite to the plunger. The tube platen can hold an intravenous infusion tube. The bias member is configured to urge the plunger toward the tube platen.

A digital syringe is used with conventional polymer disposable syringe construction to be practical in the medical environment. Errors associated with the larger volumes of the syringes (which exacerbate minor errors in plunger position) and the flexibility and dimensional variations of the polymer plungers are accommodated by direct measurement of the syringe plunger position rather than indirect measurement of motor position and inference of syringe plunger position. This direct measurement eliminates mechanical tolerances (“stack up”) in the motor, gear train, and lead screw on plunger movement, an effect exacerbated by flexibility of the plunger and changes in syringe resistance and medicament viscosity, for example, with different medicaments or when the syringe is refrigerated. The digital syringe may be combined with the motor unit to provide additional versatility.

A removable power supply cover assembly (116) for an infusion pump is disclosed. The assembly includes a housing body configured to removably attach to an infusion pump, a conductor assembly (1020) attached to the housing body, a power supply contact assembly, and a spring (1002) attached to the power supply contact assembly and the conductor assembly. An electrical coupling between a power supply to the conductor assembly is formed through the spring.