A computing system and/or a method may be provided for using a risk assessment to provide a notification. The computing system may comprise a processor. The processor may be configured to perform the method. A biomarker may be received for a patient from a sensing system. A data collection that includes pre-surgical data may be received for a patient. A probability of a patient outcome due to a surgery performed on the patient may be determined using the biomarker and the data collection. A notification may be sent to a user. The notification may indicate that the probability of the surgical complication may exceed a threshold.

A system for managing an alarm issued by a medical device being used to treat a patient is disclosed. The system includes a processor coupled to at least one of the medical device, a monitoring system being used to monitor the patient, and a hospital system. The system also includes a memory coupled to the processor. The memory contains data and instructions that, when loaded into the processor and executed, cause the processor to receive the alarm and retrieve information from one or more of the medical device, the monitoring system, and the hospital system. The information comprises a dynamic attribute associated with the patient. The system then assigns a sub-priority to the alarm based in part on evaluation of the dynamic attribute and provides an alert to a staff member.

A health monitoring system and corresponding method for monitoring a physiological condition of a user may include collecting, by a monitoring device, measurements representing physiological signals of the body, transmitting the measurements from the monitoring device to a local device, and receiving, at a remote server, the measurements and additional data from the local device. The remote server may include a processing module, a review portal and a clinician portal, such that the remote server may be arranged to automatically classify the measurements representing physiological signals of the body, verify the classifications, and provide the verified measurements at a clinician portal.

Disclosed are devices, systems and methods for in vivo monitoring of localized environment conditions within a patient user by measuring analytes, including glucose, oxygen, and/or other analytes. In some aspects, a sensor device includes a wafer-based substrate, at least one electrochemical sensor two-electrode contingent including a working electrode and a reference electrode on the substrate and configured to detect a target analyte in a body fluid when the sensor device is deployed within a subject's body, where the working electrode is functionalized by a chemical layer configured to facilitate a reaction involving the target analyte that produces an electrical signal; and an electronics unit in communication with the electrochemical sensor electrode contingent to transmit the electrical signal to an external processor.

Techniques related to temporary setpoint values are disclosed. The techniques may involve causing operation of a fluid delivery device in a closed-loop mode for automatically delivering fluid based on a difference between a first setpoint value and an analyte concentration value during operation of the fluid delivery device in the closed-loop mode. Additionally, the techniques may involve obtaining a second setpoint value. The second setpoint value may be a temporary setpoint value to be used for a period of time to regulate fluid delivery, and the second setpoint value may be greater than the first setpoint value. The techniques may further involve causing operation of the fluid delivery device for automatically reducing fluid delivery for the period of time based on the second setpoint value.

Disclosed herein is a medical system (100, 300, 500). The execution of machine executable instructions (112) causes a computational system (104) to: receive (200) a baseline anatomical measurement (114) descriptive of a clinical magnetic resonance image of a subject (318); receive (202) scan metadata (116) descriptive of the clinical magnetic resonance image of the subject; send (204) scan parameters via a network connection (350) to a low-field magnetic resonance imaging system (301); receive (206) subsequent k-space data (122) from the low-field magnetic resonance imaging system via the network connection in response to sending the scan parameters; reconstruct (208) a subsequent magnetic resonance image (124) from the subsequent k-space data; determine (210) a subsequent anatomical measurement (128) in response to inputting the subsequent magnetic resonance image into the segmentation module; and provide (212) a warning signal (132) if the subsequent anatomical measurement varies from the baseline anatomical measurement by more than a predetermined amount.

A monitoring device for monitoring a hypocortiolism patient, the monitoring device comprising:a needle for penetrating a skin of the patient, andan analysis module fluidly connected with the needle, the analysis module comprising: o a first sensor, for measuring an inflammation level representative for the patient; and/or o a second sensor, for measuring a stress level representative for the patient; and wherein the monitoring device is configured to automatically trigger a notification in response to the first sensor measuring an inflammation level exceeding a first pre-defined threshold and/or in response to the second sensor measuring a stress level exceeding a second pre-defined threshold.

A dry electrode and a physiological multi-parameter monitoring equipment are disclosed. The waterproof dry electrode comprises an encapsulation, extraction electrode and a contact surface layer, wherein the extraction electrode and the contact surface layer are connected with each other and disposed in the encapsulation; the contact surface layer comprises an exposed part and an embedded part encapsulation; the encapsulation comprises flexible silica gel and hard plastic portion, the embedded part being embedded into the hard plastic portion, and the hard plastic portion being packaged in the flexible silica gel. Through the above arrangement in the present invention, the dry electrode can reach a waterproof grade of IPX7, which is higher than living waterproof grade of an ordinary dry electrode. The PMPME can be a patch-type acquisition and monitoring equipment which is convenient for long time wearing and physiological multi-parameter monitoring, with excellent sealing and waterproofness, and the electrode is reusable.

In some embodiments, a self-monitoring intravenous catheter system is provided. An alarm controller is provided that receives signals representing a pH value, an oxygen saturation value, and a pressure value in proximity to the distal end of the catheter. By performing a fuzzy logic analysis of the values, the alarm controller is able to detect that the catheter is about to fail or has failed, and can cause alerts to be presented. In some embodiments, an intravenous catheter is provided that has a pH sensor and an oximeter disposed at a distal end of the catheter to obtain the pH value and oxygen saturation values analyzed by the alarm controller. Embodiments of the catheter and self-monitoring intravenous catheter system may be particularly useful in treating neonates, who are sensitive to catheter failure and are not capable of detecting the signs of failure themselves.

An alarm indicator (4) is provided with a light guiding member (41), a first light source (42) and a transmissive member (43). The light guiding member (41) extends in a first direction that is parallel to a display screen in which medical information is displayed. The first light source (42) faces an end face (41a) of the light guiding member (41) in the first direction. The transmissive member (43) covers the light guiding member (41) from a second direction intersecting with the first direction. The light guiding member (41) is provided with a light reflecting portion and an outer face (41d). The light reflecting portion extends in the first direction and reflects the light incident from the end face (41a) at least toward the second direction intersecting with the first direction. The light reflected by the reflecting portion is emitted from the outer face (41d) while being diffused.