A method for at least one of characterizing, diagnosing, and treating a condition associated with microbiome taxonomic features in at least a subject, the method comprising: receiving an aggregate set of biological samples from a population of subjects; generating at least one of a microbiome composition dataset and a microbiome functional diversity dataset for the population of subjects; generating a characterization of the condition based upon features extracted from at least one of the microbiome composition dataset and the microbiome functional diversity dataset; based upon the characterization, generating a therapy model configured to correct the condition; and at an output device associated with the subject, promoting a therapy to the subject based upon the characterization and the therapy model.

Embodiments herein relate to devices and related systems and methods for motion sickness prevention and mitigation. In an embodiment, a method of preventing or mitigating motion sickness in a subject is included, the method tracking motion of the subject using a first motion sensor; estimating a vestibular system input based on tracked motion of the subject; tracking head position of the subject using the first motion sensor; estimating a visual system input based on tracked head position of the subject; estimating consistency between the vestibular system input and the visual system input; and initiating a responsive measure if the estimated consistency crosses a threshold value. Other embodiments are also included herein.

There is provided a system for measuring impedance at multiple locations within a body of a patient, comprising: an elongated probe sized and shaped for being disposed within a cavity of the body of the patient or in an extracorporeal position, at least one pair of parallel transmission wires disposed along a length of the elongated probe, a plurality of impedance elements, each connected to the at least one pair of parallel transmission wires at a respective spaced apart location along the length of the elongated probe in a ladder arrangement, a transmitter configured for injecting an electrical signal to the at least one pair of parallel transmission wires, a receiver configured for measuring a plurality of reflections of the electrical signal from the plurality of impedance elements, and a processor configured for computing an impedance value for each of the impedance elements according to the measured plurality of reflections.

Apparatus and associated methods relate to diagnostic device and system including a proximal balloon disposed along a length of a catheter and a distal balloon disposed at a distal end of the catheter, with at least one camera disposed at the distal balloon and a pH sensor deployable via inflation of the proximal balloon and configured to engage a patient's esophagus wall to attach the pH sensor to the patient's esophagus wall. In an illustrative example, the pH sensor may be releasably retained to the catheter adjacent to the proximal balloon. The pH sensor may include a tissue engaging feature configured to engage a patient's esophagus wall to attach the pH sensor to the patient's esophagus wall. The diagnostic device may improve upon existing processes by providing a single device to perform a multi-purpose diagnostic procedure.

An esophageal device is used to recognize, diagnose, characterize, or relieve an impact of an abnormal or defective UES anatomy, physiology, or functionality. In one implementation, the esophageal device measures a UES response to esophageal fluid infusion to detect or characterize an abnormality or defective UES anatomy, physiology, or functionality. An Upper Esophageal Sphincter compression device is used to increase intra-luminal pressure within the Upper Esophageal Sphincter of a patient in order relieve an impact of an abnormal or defective UES anatomy, physiology, or functionality.

A computer-implemented method of treating a patient's and automated enteral feeding, comprising: monitoring a plurality of reflux-related parameters and at least one reflux event while the patient is automatically enterally fed by an enteral feeding controller according to a baseline feeding profile including a target nutritional goal, training a classifier component of a model for predicting likelihood of a future reflux event according to an input of scheduled and/or predicted plurality of reflux-related parameters, the classifier trained according to computed correlations between the plurality of reflux-related parameters and the at least one reflux event, feeding scheduled and/or predicted reflux-related parameters into the trained classifier component of the model for outputting risk of likelihood of a future reflux event, and computing, by the model, an adjustment to the baseline feeding profile for reducing likelihood of the future reflux event and for meeting the target nutritional goal.

There is provided a system for managing reflux during an enteral feeding, comprising: (i) a non-transitory memory having stored thereon a code for execution by at least one hardware processor of a computing device, the code comprising: code for receiving electrical signals outputted by at least one reflux event sensor disposed within a digestive system of a patient; code for determining a gastric reflux event based on an analysis of the electrical signals; code for outputting instructions to pause enteral feeding of the patient by a feeding controller that regulates enteral feeding of the patient using an enteral feeding tube positioned within the digestive system of the patient; and (ii) an evacuation controller that directs back-flow of digestive contents from the digestive system of the patient to an external evacuation reservoir through an evacuation tube.

An esophageal device is used to recognize, diagnose, characterize, or relieve an impact of an abnormal or defective UES anatomy, physiology, or functionality. In one implementation, the esophageal device measures a UES response to esophageal fluid infusion to detect or characterize an abnormality or defective UES anatomy, physiology, or functionality. An Upper Esophageal Sphincter compression device is used to increase intra-luminal pressure within the Upper Esophageal Sphincter of a patient in order relieve an impact of an abnormal or defective UES anatomy, physiology, or functionality.

A naso/orogastric device having backflow blocking means and comprises a naso/orogastric tube sized and shaped for being disposed within the esophagus so that at least a distal end thereof being placed in the stomach lumen of a patient, at least one elastic esophageal body, positioned along the naso/orogastric tube, having a pressure dependent volume, at least one esophageal sensor that detects fluid around at least one segment of the naso/orogastric tube, and a pressure regulator that regulates a pressure within the elastic esophageal body according to the detection.

A pH measuring device is disclosed. One aspect includes a body portion including a hollow portion therein and a through-portion formed in a first region so that the hollow portion communicates with the outside; an electrode unit including a reference electrode and a sensing electrode including different materials and configured to measure the pH in a living body by allowing a first end to be located in the hollow portion and a second end opposite to the first end to be exposed to the outside of the body portion through the through-portion; and a wireless communication unit configured to transmit a pH measurement value sensed by the electrode unit to the outside.