Abstract: A home therapy machine is configured to perform a home therapy on a patient at a home or dwelling of the patient. The home therapy machine includes at least one processor operating a connectivity agent having an activated mode and a deactivated mode. When the connectivity agent is in the activated mode, the at least one processor is able to send data to and receive data from a system hub. When the connectivity agent is in the deactivated mode, the at least one processor is not able to send data to or receive data from the system hub. The home therapy machine further includes a user interface configured to receive a patient selection of a device program received from the system hub and at least one pump under control of the at least one processor for performing the home therapy according to the selected device program.

Abstract: An ultra-low noise sensor for magnetic fields comprises a mechanically resonant structure having a magnetized proof mass. The displacement of the proof mass due to a magnetic field provides a high resolution and highly amplified measurement of magnetic field fluctuations near the resonance frequency. A flux modulator may be used with the resonant structure to amplify magnetic fluctuations in a non-resonant frequency band. The resonant structure, combined with a high resolution readout device and a frequency-compensating numerical processor, can amplify magnetic fluctuations in a broad range of frequencies. A solenoid coil surrounding the resonant structure may be used to null the quasi-static earth's magnetic field and thereby increase the dynamic range of the sensor. Cryogenically cooling the resonant structure can improve the resolution of the sensor. A magnetometer that embodies features of the present invention is miniaturized and has improved amplification and resolution at room temperature.

Abstract: A renal therapy machine with a blood pressure monitor is disclosed. In an example, a renal therapy machine includes a dialysis fluid pump a control processor for controlling a treatment performed by the dialysis fluid pump, and a user interface in operable communication with the control processor. The renal therapy machine also includes a blood pressure monitor in operable communication with the control processor. The blood pressure monitor includes a blood pressure cuff positioned and arranged to receive air pressurized from within the renal therapy machine for the purpose of taking a patient's blood pressure.

Abstract: A peritoneal dialysis system includes (i) a reusable fill container; (ii) a reusable drain container; and (iii) a reusable continuous ambulatory peritoneal dialysis (“CAPD”) set configured and arranged to be fluidly connected to at least one of the reusable fill container or the reusable drain container.

Abstract: A home therapy machine is configured to perform a home therapy on a patient at a home or dwelling of the patient. The home therapy machine includes at least one processor operating a connectivity agent having an activated mode and a deactivated mode. When the connectivity agent is in the activated mode, the at least one processor is able to send data to and receive data from a system hub. When the connectivity agent is in the deactivated mode, the at least one processor is not able to send data to or receive data from the system hub. The home therapy machine further includes a user interface configured to receive a patient selection of a device program received from the system hub and at least one pump under control of the at least one processor for performing the home therapy according to the selected device program.

Abstract: A dialysis system includes at least one source of fluid for dialysis, a fluid line in fluid communication with the at least one source of fluid, at least one pump positioned and arranged to pump fluid from the at least one source of fluid through the fluid line, a first patient connector configured to be removably placed in fluid communication with the fluid line to allow a blood treatment to be performed using the at least one source of fluid, and a second patient connector configured to be removably placed in fluid communication with the fluid line to allow a peritoneal dialysis treatment to be performed using the at least one source of fluid.

Abstract: A dialysis system includes: a dialysis fluid pump receptacle actuated by a dialysis fluid pump actuator; a dialysis fluid line; a blood filter in fluid communication with the dialysis fluid pump receptacle via the dialysis fluid line; an extracorporeal circuit; a blood pump receptacle actuated by a blood pump actuator and in fluid communication with the blood filter via the extracorporeal circuit; and a control unit that (i) in a first treatment pumps peritoneal dialysis fluid through the dialysis fluid pump receptacle, the dialysis fluid line, the blood filter, the extracorporeal circuit and the blood pump receptacle to the patient's peritoneum operating the dialysis fluid pump actuator and the blood pump actuator at a first pressure, and (ii) in a second treatment pumps blood through the extracorporeal circuit, the blood pump receptacle and the blood filter operating the blood pump actuator at a second, different pressure.

Abstract: A MEMS gyroscope is provided. A substrate can be formed with a substantially planar surface, a substantially hemispherical cavity extending into the surface, an actuation electrode, and a plurality of sensing electrodes. A resonator formed from a substantially hemispherical shell can be suspended within the cavity by a stem coupling the center of the bottom of the cavity to the center of the bottom of the shell. An electronic processor can be configured to cause a voltage to be applied to the actuation electrode, receive signals from the sensing electrodes, and process the received signals to determine rotation of the MEMS gyroscope.

Abstract: A method for performing renal therapy at a home or dwelling of a patient using a renal therapy machine includes electronically retrieving a doctor's prescription for renal therapy and based on the doctor's prescription, enabling electronic selection of supplies, including a dialyzer, at a first location other than the patient's home or dwelling by a person other than the patient. The method further includes electronically initiating a sending of the supplies and the renal therapy machine to the patient's home or dwelling.

Abstract: A computer readable medium stores instructions configured to cause a home therapy machine to allow an at home patient selection of a device program from a plurality of device programs stored on the home therapy machine and perform an at home treatment using fluid flow equipment provided by the home therapy machine according to the selected device program. The instructions are further configured to receive data generated during the at home treatment and generate at least one log file based upon the received data.

Abstract: A home therapy entry, modification and reporting system includes a website configured to display therapy entry, modification and reporting information and a system hub configured to manage a flow of the information between the website and a plurality of home therapy machines. The website specifically includes a therapy prescription screen configured to specify supplies needed at the patient's home or dwelling for operation with one of the home therapy machines, a device program screen configured to set parameters by which at least one of the home therapy machines operates to perform the home therapy on the patient, and a clinician dashboard screen including a list of patients and a notification associated with at least one of the listed patients, the notification indicating whether a predefined treatment condition or alert occurred during the home therapy.

Abstract: An item stabilizer configured to prevent lateral movement of an item (such as a product-supporting pallet) in a transport container. The item stabilizer includes a first item side engager, a second item side engager, and a connector attached to each of the item side engagers such that an item can be positioned on the connector between the item side engagers. The item stabilizer is configured to prevent movement of the item by engaging opposite sides of the item while the weight of the item and any products thereon or therein rest on the connector, thereby preventing the connector and the item side engagers themselves from moving laterally. Each item side engager respectively extends between one side of the item and one of the side walls of the transport container to limit the lateral movement of the item. Multiple item stabilizers can work together to hold an item in place.

Abstract: A shipping container load securer including a pallet and a box connected to the pallet and filled with a filler, wherein the pallet and the box are substantially the same size and shape as a standardized crate used to package goods for transport in shipping containers. The load securer fills voids in partially filled shipping containers, enabling the shipping container to be tightly packed and preventing the movement of goods-filled crates during transport to minimize damage to the goods in the crates in the shipping container, while not substantially increasing the weight of the container.

Abstract: Electronic images of a video stream are programmatically analyzed and metadata associated with the images automatically populated with contextually relevant tags and markers for later referencing the images for curated entertainment. Specifically, a user can specify parameters for a video montage that leverages the metadata for automatic video montage creation based on the metadata.

Abstract: A consumer electronics (CE) device receives, from an imager and/or a microphone, an emotion signal representing an expression of a user of the CE device. Also, a biometric sensor generates a biometric signal representing a biometric parameter of the user of the CE device. Based on the emotion signal and biometric signal, a rating is determined that is related to content presented on the CE device at or near the time the emotion signal and biometric signal were generated.

Abstract: A peritoneal dialysis system includes (i) a fill container, and (ii) an energizing unit that removably accepts the fill container, the energizing unit including a sterilization source so configured and arranged relative to the fill container when accepted by the energizing unit to place fluid within the fill container in a physiologically safe condition for delivery to the peritoneal cavity of a patient.

Abstract: A system and method is provided to allow multiple patients to receive peritoneal dialysis treatment at a walk-in facility without having to keep fresh dialysis solution on hand themselves. The walk-in facility is enabled to receive a peritoneal dialysis prescription from a patient, verify the prescription, determine the appropriate treatment for the patient, provide the patient with the appropriate dialysis solution in the appropriate amount, and enable the patient to undergo a dialysis treatment at the facility. The walk-in facility can also be enabled to monitor the patient's home dialysis treatment and to adjust the patient's treatment at the facility accordingly. The facility can be enabled to produce dialysis solution on demand by manufacturing the solution from solution components according to a patient's prescription. Moreover, the facility can use a sorbent system to regenerate effluent dialysis solution into fresh dialysis solution.

Abstract: A peritoneal dialysis system includes (i) a reusable fill container; (ii) a reusable drain container; and (iii) a reusable continuous ambulatory peritoneal dialysis (“CAPD”) set configured and arranged to be fluidly connected to at least one of the reusable fill container or the reusable drain container.

Abstract: A dialysis system includes: a dialysis fluid pump receptacle actuated by a dialysis fluid pump actuator; a dialysis fluid line; a blood filter in fluid communication with the dialysis fluid pump receptacle via the dialysis fluid line; an extracorporeal circuit; a blood pump receptacle actuated by a blood pump actuator and in fluid communication with the blood filter via the extracorporeal circuit; and a control unit that (i) in a first treatment pumps peritoneal dialysis fluid through the dialysis fluid pump receptacle, the dialysis fluid line, the blood filter, the extracorporeal circuit and the blood pump receptacle to the patient's peritoneum operating the dialysis fluid pump actuator and the blood pump actuator at a first pressure, and (ii) in a second treatment pumps blood through the extracorporeal circuit, the blood pump receptacle and the blood filter operating the blood pump actuator at a second, different pressure.

Abstract: A shock absorption and restraint apparatus including a plurality of co-acting cushioned pads which create a protective shock absorbing barrier for a load in a railroad car (or other shipping container) and a set of straps which are employed to restrain the cushioned pads and the load. In certain embodiments, the cushioned pads include one or more central or connector cushioned pads and one or more side or cooperating cushioned pads. In certain embodiments, the cushioned pads include strap engaging mechanisms which are configured to be engaged by the straps. The cushioned pads are preferably lightweight, easy to handle and install, recyclable, and readily reusable. In certain embodiments, the cushioned pads are configured, sized, and constructed in such a way to protect the specific load in the railroad car.