Provided herein are systems and methods for monitoring one or more health or physiological parameters in a subject. The systems and methods may comprise a patch coupled to an injector. Data may be transmitted to a mobile device or remote server, where the data may be processed. Processed data may be used to inform a subject on a health or physiological condition.

The disclosure relates to a method for prognosis management based on medical information of a patient, a device, and a medium. The method includes acquiring, by a processor, medical information of the patient at a first time. The method further includes receiving the medical information of the patient at a first time. The method may further include predicting, by a processor, a progression condition of an object associated with the patient at a second time based on the acquired medical information of the first time. The progression condition is indicative of a prognosis risk, and the second time is after the first time. The method may also include outputting the predicted progression condition to an information management system. The method is helpful for users to understand the potential prognosis risk of the object at the second time to aid users in making treatment decisions.

A yarn has a first conductive yarn having conductivity, a first insulating section covering the first conductive yarn and formed of an insulating material having absorbency, and a second conductive yarn having conductivity and disposed on an outer circumferential side of the first insulating section.

A medical capsule is equipped with a sensor device having light emitting and light receiving elements. The sensor device can detect blood on the basis of light absorption properties of the blood. The capsule has a casing forming a recess or gap at its outer surface. The recess has a pre-selected width which represents a fixed measuring track between the light emitting and light receiving elements being arranged at opposing sides of the recess or gap when seen in its width direction. The medical capsule also has a shielding plate/layer/membrane arranged at least at or near the bottom of the recess or gap and extending along the width direction of the recess or gap preferably to exceed the recess at both sides into its width direction to prohibit emitted light from bypassing the recess via the casing material of the capsule.

An electronic endoscope system includes an image processing unit that uses a numerical value to evaluate an appearance feature appearing in a biological tissue by using an images captured by an electronic endoscope. The image processing unit calculates a first pixel evaluation value indicating a degree of a first feature, which is featured by a first color component or a first shape appearing in an attention area in the biological tissue, and which relates to the first color component or the first shape, for each pixel from the image, and calculates a first representative evaluation value relating to the first feature by integrating the first pixel evaluation value. Furthermore, the image processing unit evaluates a degree of a second feature that shares the first color component or the first shape with the first feature.

Disclosed are methods, materials and devices for approximation of blood volume in a fluid, such as in a biological fluid collected during a surgical procedure. In particular applications, methods of estimating blood loss from a subject are provided. The method and devices may include a RBC flocculant, such as polyDADMAC, and provide for an approximate blood hematocrit for a selected type of animal, as well as provide for a calculated RBC packing ratio corresponding to the collection device receiving the fluid. Also provided is a Blood Indicator Panel (BIP), comprising a series of markings calculated from an observed red blood cell sedimentation volume, the average animal type hematocrit, and a calculated RBC packing ratio “η” value for the collection device. Pediatric (about 200 ml or 250 ml size container), adult human (about 1,000 ml-1,500 ml) and veterinary (about 500 ml-2,500 ml) collection containers are also disclosed, that may include a RBC flocculant, for use in approximating blood volume in a fluid. Methods of detecting blood in a sample, such as a fluid sample, and kits for performing the methods, are also provided.

Embodiments of the present disclosure relate to a system and method for determining a risk, onset, or presence of hypovolemia based on one or more features of a plethysmographic waveform during a patient breathing cycle. For example, a hypovolemic patient may exhibit characteristic changes in pulse amplitude or stroke volume during inhalation and exhalation relative to a healthy patient. Further, a trend or pattern of such features may be used to assess the patient's fluid condition.

Novel tools and techniques for assessing, predicting and/or estimating effectiveness of hydration of a patient and/or an amount of fluid needed for effective hydration of the patient, in some cases, noninvasively.

A system for evaluating a status of a fistula of a subject includes a radio device that emits a carrier radio wave toward the fistula, and that receives a return wave signal formed through reflection of the carrier radio wave by the fistula, and an evaluating device that performs a time-frequency transform on a digitized detection signal related to the return wave signal to result in frequency spectrum information, that calculates a magnitude ratio based on the frequency spectrum information, that generates an evaluation result by using a machine learning model based on the magnitude ratio, and that outputs the evaluation result which indicates the status of the fistula.

Systems and methods for Endovascular Perfusion Augmentation for Critical Care (EPACC) are provided. The system may include a catheter having an expandable aortic blood flow regulation device disposed on the distal end of the catheter for placement within an aorta of a patient. The system may also include a catheter controller unit that causes the expandable aortic blood flow regulation device to expand and contract to restrict blood flow through the aorta. The system may also include one or more sensors for measuring physiological information indicative of blood flow through the aorta, and a non-transitory computer readable media having instructions stored thereon, wherein the instructions, when executed by a processor coupled to the one or more sensors, cause the processor to compare the measured physiological information with a target physiological range associated with blood flow through the aorta such that the catheter controller unit automatically adjusts expansion and contraction of the expandable aortic blood flow regulation device to adjust an amount of blood flow through the aorta if the measured physiological information falls outside the target physiological range.