Abstract: Techniques for administering a care plan for a patient. A monitoring device is selected, at a care plan management system based on a care plan, to use in administering the care plan. The care plan specifies biometric data to monitor for a patient. The monitoring device is configured to collect the biometric data, based on the care plan. The biometric data collected using the monitoring device is received at the care plan management system. The biometric data includes a first event initially classified as a first type of event using the monitoring device. The first event is selected for reclassification, based on the initial classification, and in response the first event is reclassified as a second type of event using the care plan management system. The patient is treated based on the care plan and the reclassified first event.

Abstract: A surgical instrument, has an end effector that includes an ultrasonic blade, and a clamp arm that moves relative to the ultrasonic blade from an opened position toward an intermediate position and a closed position. The clamp arm is offset from the ultrasonic blade to define a predetermined gap in the intermediate position between the opened position and the closed position. A clamp arm actuator connects to the clamp arm and moves from an opened configuration to a closed configuration to direct the clamp arm from the opened position toward the intermediate position and the closed position. A spacer connects with the clamp arm to inhibit movement of the clamp arm from the intermediate position toward the closed position for maintaining the predetermined gap between the clamp arm and the ultrasonic blade.

Abstract: A neuromodulation therapy is delivered via at least one electrode implanted subcutaneously and superficially to a fascia layer superficial to a nerve of a patient. In one example, an implantable medical device is deployed along a superficial surface of a deep fascia tissue layer superficial to a nerve of a patient. Electrical stimulation energy is delivered to the nerve through the deep fascia tissue layer via implantable medical device electrodes.

Abstract: A neuromodulation therapy is delivered via at least one electrode implanted subcutaneously and superficially to a fascia layer superficial to a nerve of a patient. In one example, an implantable medical device is deployed along a superficial surface of a deep fascia tissue layer superficial to a nerve of a patient. Electrical stimulation energy is delivered to the nerve through the deep fascia tissue layer via implantable medical device electrodes.

Abstract: An example power tool includes a battery pack receiving portion including a battery pack compartment including a battery pack support structure configured to receive and support a battery pack including battery terminals. The power tool further includes a terminal block located in the battery pack receiving portion and including tool terminals. At least two terminals of the tool terminals are configured to electrically and physically couple to the battery terminals. The power tool further includes an insertable device compartment located in the battery pack receiving portion and configured to receive an insertable wireless communication device including a first electronic processor, a transceiver, and device terminals. At least one device terminal is configured to electrically and physically couple to at least one shared terminal of the at least two terminals of the tool terminals. The insertable wireless communication device is configured to wirelessly communicate with an external device.

Abstract: Devices, systems and/or methods for repairing soft tissue adjacent a soft tissue repair site. In one embodiment, a repair device configured to couple to soft tissue is provided. The repair device includes a capture portion and an anchor portion. The capture portion configured to extend with radial portions. The anchor portion includes a base with multiple legs extending therefrom. The multiple legs are configured to move from a linear position to a formed position such that, in the formed position, the multiple legs couple to structure of the capture portion.

Abstract: A computer system displays a representation of a field of view of the one or more cameras, including a representation of a portion of a three-dimensional physical environment that is in the field of view of the one or more cameras. The computer system receives a request to add a first virtual effect to the displayed representation of the field of view of the one or more cameras. In response to receiving the request to add the first virtual effect to the displayed representation of the field of view of the one or more cameras and in accordance with a determination that the first virtual effect requires a scan of the physical environment, the computer system initiates a scan of the physical environment to detect one or more features of the physical environment and displays a user interface that indicates a progress of the scan of the physical environment.

Abstract: A therapy system includes a patient support apparatus and a pneumatic therapy device that is coupleable to the patient support apparatus. The therapy device may receive power and air flow from the patient support apparatus.

Abstract: A system for transmitting power and data between two circuit boards may include a fixed circuit board having a primary coil and a rotatable circuit board having a secondary coil. The system may further include a sensor in communication with the secondary coil of the rotatable circuit board. The fixed circuit board's primary coil may be inductively coupled to the secondary coil and may provide power and receive data from the sensor when inductively coupled to the secondary coil.

Abstract: Biometric data is measured by at least one remote monitoring device, and the biometric data includes electrocardiogram (ECG) data relating to a patient. The ECG data includes a plurality of critical rhythms, and one of the plurality of critical rhythms is identified as an onset event. The ECG data is modified, based on the identified onset event.

Abstract: Techniques for identifying onset of a cardiac event. Embodiments receive biometric data measured by at least one remote monitoring device, the biometric data comprising an electrocardiogram (ECG) data relating to a patient. It is determined that the ECG data includes a plurality of critical rhythms, and one of the plurality of critical rhythms is identified as an onset event. The ECG data is modified, based on the identified onset event. The modified ECG data facilitates treatment of the patient related to the identified onset event.

Abstract: Techniques for administering a care plan for a patient. A monitoring device is selected, at a care plan management system based on a care plan, to use in administering the care plan. The care plan specifies biometric data to monitor for a patient. The monitoring device is configured to collect the biometric data, based on the care plan. The biometric data collected using the monitoring device is received at the care plan management system. The biometric data includes a first event initially classified as a first type of event using the monitoring device. The first event is selected for reclassification, based on the initial classification, and in response the first event is reclassified as a second type of event using the care plan management system. The patient is treated based on the care plan and the reclassified first event.

Abstract: Techniques for administering a care plan for a patient. A monitoring device is selected, at a care plan management system based on a care plan, to use in administering the care plan. The care plan specifies biometric data to monitor for a patient. The monitoring device is configured to collect the biometric data, based on the care plan. The biometric data collected using the monitoring device is received at the care plan management system. The biometric data includes a first event initially classified as a first type of event using the monitoring device. The first event is selected for reclassification, based on the initial classification, and in response the first event is reclassified as a second type of event using the care plan management system. The patient is treated based on the care plan and the reclassified first event.

Abstract: Techniques for voice control of a patient care device are described. A patient care device receives an audio request from a user. The patient care device records the audio request. The patient care device transmits the audio request over a communication network to a speech recognition service, and in response receives, from the speech recognition service, a textual representation of the audio request. The patient care device matches the textual representation, using the computer processor, to a first command in a vocabulary of available commands, and in response performs the first command.

Abstract: A method includes retrieving a plurality of indications of cardiac events in a patient, heart rates of the patient during the cardiac events, and durations of the cardiac events. The method also includes selecting a subset of indications from the plurality of indications based on the heart rates of the patient during the cardiac events and the durations of the cardiac events and sorting the subset of indications based on heart rates of the patient during the cardiac event indicated by the subset of indications and based on durations of the cardiac events indicated by the subset of indications to produce a sorted list of indications. The method further includes communicating, from the sorted list, an indication that is first in the sorted list for clinical review.

Abstract: Techniques for administering a care plan. Biometric data collected by a monitoring device is received at a care plan management system using a communication network. The biometric data includes a first event classified by a remote device as a first type of event. A relative processing priority for the first event is determined, at the care plan management system, based on the first type. The first event is processed, at the care plan management system, based on the relative processing priority. The processing includes re-classifying the first event as a second type of event. The re-classification is more computationally intensive than the classification by the remote device. At least one treatment task specified in the care plan is initiated, using a computer processor, and based on the re-classified first event.

Abstract: Embodiments presented herein provide a dynamically adaptive care plan. More specifically, embodiments presented herein describe techniques for modifying a care plan assigned to a patient based on data observed from the patient. According to one embodiment of the present disclosure, data corresponding to one or more types of biometric data for the patient is received. One or more reported symptoms for the patient is received. The care plan includes one or more conditions corresponding to the one or more reported symptoms. Upon determining that at least one of the received data satisfy at least one of the biometric thresholds and the one or more reported symptoms satisfy at least one of the conditions, an event rule for modifying the care plan is identified. The care plan is modified based on the event rule.

Abstract: Embodiments provide techniques for authenticating and configuring a care plan device in a care plan environment. Embodiments receive, from the care plan device, a care plan device identifier written to a memory of the care plan device by a manufacturer. The care plan device is authenticated with a remote server, based on matching a reference identifier within a patient care plan with the care plan device identifier. Upon authenticating the care plan device, embodiments receive, from the remote server, the configuration information for the care plan device. The care plan device is configured in accordance with the patient care plan, based on the received configuration information.

Abstract: One or more described embodiments relate to techniques for generating a care plan tailored for an individual. A care plan for treatment of one or more medical conditions for a patient is generated based on care protocol templates. The generating includes identifying a first patient task that conflicts with a second patient task, in the care protocol templates. The care protocol templates are parsed to identify a conflict resolution rule, pre-defined in a respective template, and the conflict is resolved by generating a patient task based on the conflict resolution rule and including the patient task in the care plan. The care plan is transmitted to a client device for the patient. The client device is configured to use the care plan to configure one or more sensor devices to collect biometric data as part of the treatment of the one or more medical conditions for the patient.

Abstract: Techniques for administering a care plan for a patient. A monitoring device is selected, at a care plan management system based on a care plan, to use in administering the care plan. The care plan specifies biometric data to monitor for a patient. The monitoring device is configured to collect the biometric data, based on the care plan. The biometric data collected using the monitoring device is received at the care plan management system. The biometric data includes a first event initially classified as a first type of event using the monitoring device. The first event is selected for reclassification, based on the initial classification, and in response the first event is reclassified as a second type of event using the care plan management system. The patient is treated based on the care plan and the reclassified first event.