Abstract: A system and a method for managing a clinical trial of patients. The method includes obtaining consents of the patients undergoing the clinical trial and storing consent data of the patients. Consent data of the patients is validated before progressing onto any stage of the clinical trial. Data associated with at least one clinical trial site is collected for performing the clinical trial. The patients are randomly grouped into two or more groups for performing one or more of a single blinded study and a double blinded study during the clinical trial. Clinical data and non-clinical data of the patients is collected during the clinical trial. Timelines, progress, compliance, and data associated with different stages of the clinical trial are managed.

Abstract: The present disclosure generally relates to user interfaces for managing sharing of health-related data. In some embodiments, user interfaces for establishing sharing of health-related data are described. In some embodiments, user interfaces for viewing and managing shared health-related data are described.

Abstract: A disclosed method includes receiving an emergency data request with a patient identifier; retrieving protected data from a database corresponding to the patient identifier; and displaying the protected data on an emergency responder device display.

Abstract: A method for improving a physician's workflow by optimizing the physician's access to patient data during a visit of patients to a medical facility includes an electronic medical record (EMR) processor implementing a Health Value Analytics (HVA) component and receiving inputs from EMR/HVA devices. In response, the EMR processor creates value baselines for patient visits, generates a health care value continuum based on a visit of a first patient to the medical facility, and generates a comparison of the health care value continuum to a value baseline, detects a location, on a display screen of the EMR/HVA device, of an EMR record for the first patient; provides the comparison for display in a location adjacent to the displayed EMR record for the first patient; detects replacement of the EMR record with an EMR record for a second patient; and in response to the replacement, discontinues display of the HVA page.

Abstract: Configuration output for use in configuring a patient care device for administration of a therapy to a patient. The configuration output may include at least one code. The code may be used in the verification and/or indication of at least one configuration data component used in the configuration of the patient care device to be used to administer a therapy to a patient. Additionally, a check code for validation of the entry of the code and/or check code may be provided.

Abstract: Systems and methods are disclosed hosting multiple visual assessments, evaluating user performance on the assessments, and providing recommendations to assess and improve user visual performance. One method includes hosting a plurality of visual assessments; presenting, via a web portal, a user interface for selecting one or more visual assessments of the hosted plurality of visual assessments; receiving, via a web portal, a request for a user to access a visual assessment, wherein the visual assessment is an assessment out of the hosted plurality of assessments; administering the visual assessment to the user; receiving user performance data associated with a user, in response to the administered visual assessment; comparing the user performance data with performance data associated with one or more other users; and generating a report of user visual performance based on the user performance data, wherein the report is accessible to the user via the web portal.

Abstract: An information processing apparatus that sends and receives data to and from an image storage apparatus that manages a medical file for each examination includes a first hardware processor. The first hardware processor generates image data from character information included in a non-image file related to examination, attaches examination information related to the non-image file to the generated image data, and creates a file converted to image. The first hardware processor further sends the created file converted to image to the image storage apparatus.

Abstract: An ingredient determining apparatus configured to determine nutritional ingredients in food provided for a user. The ingredient determining apparatus includes a processor configured to obtain a muscle index indicating a degree of muscle mass of the user and a fat index indicating a degree of fat mass of the user, and determine the nutritional ingredients based on the muscle index and the fat index.

Abstract: The present specification discloses systems and computer implemented assessment methods including a system and method of assigning an individual to a group participating in a clinical study regarding a psychotic disorder, a system and method of determine whether and what type of psychotic disorder an individual may be suffering from; and a system and method of recommending a therapy to treat an individual with a psychotic disorder. All disclosed systems and computer implemented assessment methods use a non-invasive computational device-based test that uses a graphical user interface to measure a latent inhibition response of an individual to calculate a latent inhibition score and assess working memory. The latent inhibition score determines whether the individual exhibits an attenuated latent inhibition response, a normal latent inhibition response or an enhanced latent inhibition response.

Abstract: Systems and methods for performing personalized cardiovascular analyses are provided. A method includes building, using a modeling and simulation computing device, a patient-specific model, storing, using the modeling and simulation computing device, the patient-specific model in a database, receiving, at the modeling and simulation computing device, remote monitoring data from at least one remote monitoring data source, and receiving, at the modeling and simulation computing device, clinical data from at least one clinical data source. The method further includes updating, using the modeling and simulation computing device, the patient-specific model using the remote monitoring data and the clinical data, performing, using the modeling and simulation computing device, at least one simulation on the updated patient-specific model, and outputting, from the modeling and simulation computing device, at least one output based on the at least one simulation.

Abstract: An apparatus and method for adjusting a user nourishment selection based on nutrient diversity, the apparatus comprising at least a processor and a memory communicatively connected to the at least a processor, the memory containing instructions configuring the at least a processor to receive a proposed user selection relating to nourishment, wherein the proposed user selection comprises a plurality of ingredients, evaluate each ingredient of the plurality of ingredients, wherein evaluating each ingredient includes extracting at least a nutrient from each ingredient of the plurality of ingredients and calculating a nutrient biodiversity score for the at least a nutrient, optimize the plurality of ingredients as a function of each nutrient biodiversity score, and adjust the plurality of ingredients as a function of the optimization of the plurality of ingredients.

Abstract: Methods and systems for transferring restricted distribution medical products to an over-the-counter general sales environment are provided. Methods and systems of dispensing non-prescription, behind-the-counter medical products from a vending machine in a general sales location are also provided. In some embodiments, methods and systems are provided for dispensing a medical product from a vending machine in a general sales location based, at least in part, on biometric data collected from the purchaser and, in some instances, based on self-selection and/or de-selection criteria, is provided. Further, methods and systems of switching prescription medical products to non-prescription, over-the-counter medical products are provided.

Abstract: Techniques are disclosed herein for generating personalized food guidance using predicted food responses. Using the technologies described herein, instead of providing food guidance that is generalized for a group of individuals, personalized food guidance is provided that takes into account an individual's personalized responses to foods, such as the individual's glucose and fat responses, the individual's micro biome, the individual's overall health, potential health risks for the individual, and/or other data associated with the individual. Providing an individual with personalized food guidance can make choosing food easier and healthier.

Abstract: A fabrication system and method for prosthetic appliances employs imaging of a contralateral skeletal structure for designing a matched, patient specific replacement appliance based on the patient's own skeletal structure. Many skeletal structures are disposed on opposed sides, i.e. left and right sides. A contralateral bone or skeletal member often accurately depicts the individual bone shape of a particular patient more accurately than a generalized approximation. A scan such as a CT or MRI is segmented to apportion a skeletal member for replacement and reconstructed into a 3D (3 dimensional) model. The 3D model is inverted to define the contralateral side, and augmented for surgical connection features and comparison with an anatomic ideal to mitigate imperfections. 3D printing and/or additive manufacturing techniques are invoked with biocompatible materials to render the replacement prosthetic appliance based on the model.

Abstract: Systems, methods, and GUIs are provided for visually communicating clinically relevant information in a manner that maintains context and trends across various sizes of user interfaces, such as smaller user interfaces on mobile devices. In an embodiment, a user interface may display a first timeline area with a first indication of a timespan that represents a portion of the timeline. The first indication of the timespan may be scrollable to change the portion of the timeline displayed. The first timeline area may further comprise a set of clinical diagnoses with corresponding duration indicators. The user interface may also display a second timeline area with a second indication of a timespan, which may mirror the first indication of the timespan. The second timeline area may further comprise a set of diagnostic parameters and associated measurements. The user interface may also present a medication area having lists of medications separated by classification.

Abstract: A computer-implemented method and system for modeling the pathophysiology of a human intervertebral disc may comprise an anatomic dataset and a biophysical model disposed in connection with a simulation program. The biophysical model may comprise a plurality of subsystems, including, without limitation, governing equations, constitutive equations, boundary conditions, initial conditions, and parameter values. By altering certain subsystems of the biophysical model, a user may selectively solve for certain pathophysiological metrics using at least one of a plurality of algorithms disposed within the simulation program.

Abstract: A system for use with a user interface system, a first data provider, a second data provider and a display device. The system comprises a data input component, a fishbone diagram generating component, an output component, a user interface component, and a data trend generating component. The data trend generating component can generate data trend image data based on a trends diagram instruction. The output component can further output the data trend image data to the display device to be displayed so as to include a first graphical function and a second graphical function, wherein the first graphical function corresponds to first patient laboratory test data, and wherein the second graphical function corresponds to second patient laboratory test data.

Abstract: Systems and methods for determining a predicted brain health of a first user and providing individualized health recommendations to the first user based at least in part on an artificial neural network trained on previously existing anatomical and functional neuroimaging information, behavioral information, self-reported information, and other types of information of a plurality of users. The artificial neural network may be capable of determining a predicted benchmark of brain health of the first user's information when compared with the previously existing users' information and storing the first user's anatomical and/or functional neuroimaging information, behavioral information, self-reported information, and other types of information in a database such that the artificial neural network can be re-trained based on the new information of the first user. The first user can be notified of his or her brain health and receive individualized health recommendations.

Abstract: A method for checking the quality of data content in a structured clinical record is disclosed. The method may include the steps of providing a data quality test that checks the content of at least a portion of the data content in the structured clinical record, applying the data quality test to the portion of the data content, and returning the results of the data quality test.

Abstract: In one example, an ambulatory medical device is provided. The ambulatory medical device includes a plurality of subsystems, at least one sensor configured to acquire data descriptive of a patient, a user interface and at least one processor coupled to the at least one sensor and the user interface. The at least one processor is configured to identify subsystem status information descriptive of an operational status of each subsystem of the plurality of subsystems and to provide a device health report for the ambulatory medical device via the user interface, the device health report being based on the operational status of each subsystem.