A heating system comprises a wearable sleeve, a first heating pad associated with a first portion of the wearable sleeve, a second heating pad associated with a second portion of the wearable sleeve, one or more temperature sensors associated with the wearable sleeve, and control circuitry communicatively coupled to the first heating pad, the second heating pad, and the one or more temperature sensors. The control circuitry is configured to receive one or more temperature signals from the one or more temperature sensors, determine a temperature associated with a patient based on the one or more temperature signals, determine that the temperature is less than a target temperature value, and at least partly in response to said determining that the temperature is less than the target temperature value, activate at least one of the first heating pad or the second heating pad.

A rapid contrast therapy system can provide cold, heat/hot/warm (hereafter referred to as “hot”), and/or rapid contrast therapy, which involves rapidly alternating between cold therapy and hot therapy. The system can circulate cold or hot fluid, such as water, through a hose, into a therapy wrap, and then back to the fluid reservoirs of the system. The system can utilize a vapor compression system or other chiller technology to cool the cold water reservoir, and immersion heaters can be used to heat the hot water reservoir.

The invention pertains to a method for operating a cryocabin arrangement 100 with an open-top cabin 10, a cooling unit 20 and a number of fluid circulation units 30. The method comprises receiving user-specific data comprising at least temperature indications measureable, by a number of sensor devices, at skin surface of the user upon delivery of cooling fluid 201 into the cabin via the cooling unit followed by intake and recirculation of said cooling fluid by fluid circulation units, which further return recirculated cooling fluid 301 inside said cabin, and based on said user-specific data, selectively adjusting distribution of said cooling fluid 201, 301 inside the cabin, in terms of at least speed and/or direction of a fluidic flow, to a predetermined level during an operation cycle.

A medical device for monitoring biological parameters through an Abreu Brain Thermal Tunnel (ABTT) is provided. By monitoring and analyzing the temperature of the ABTT, it is possible to diagnosis changes in a patient or subject under a variety of conditions, including predicting the course of medical conditions. Furthermore, since the ABTT is predictive, analysis of the ABTT may be used to control mechanisms for safety when an impending medical condition makes such operation hazardous.

A reconfigurable, foldable, and manually transportable infant radiant warmer. In a collapsed configuration, the warmer consumes a minimal amount of space and can be manually transported easily. In a deployed configuration, the warmer provides open access to an infant lying on a bed platform for receiving resuscitative therapy and warmth from a radiant heater disposed upon an adjacent mast. The reconfigurable infant radiant warmer includes mutually reconfigurable bed, mast, and suspension modules. The mast module and the suspension module may be selectively moved relative to the bed module to achieve the collapsed configuration.

Systems and methods for providing vibration and temperature therapy via a therapy device is disclosed. According to one embodiment, a therapy device includes a pad comprising an adhesive layer configured to adhere to a skin surface of a user. The therapy device includes a control unit coupled to the pad. The control unit is configured to provide temperature therapy to the skin surface of the user and provide vibration therapy to the skin surface of the user. The pad includes a coupling connector configured to removably couple the control unit. The pad can include a heat generation module comprising a resistive wire and a heat spreader. The pad can include one or more electrical stimulation modules, wherein each electrical stimulation module comprises a conductor and a pad. The pad includes a temperature sensor coupled to the heat generation module. The adhesive layer can be coupled to the heat spreader.

Disclosed are: a system comprising a gas circulation device capable of circulating hyperthermic gas in the peritoneal cavity and a temperature control device; and a system comprising a drug spray device for effectively spraying a drug in the peritoneal cavity together with gas. The systems of the present invention are used as systems for hyperthermic intraperitoneal chemotherapy and can maximize the anticancer therapy effect by more effectively delivering a small amount of an anticancer drug to cancer cells while maintaining the temperature of gas in the peritoneal cavity at a predetermined temperature.

A thermal device includes an inflatable non-perforated blanket, a conduit structure, and a recirculating assembly. The inflatable non-perforated blanket is configured to transport warm air internally. The conduit structure is configured to provide conduit to transport the warm air externally to the inflatable non-perforated blanket. The recirculating assembly is configured to inflate the inflatable non-perforated blanket with the warm air and: (1) to cause the warm air to flow from the first port to the second port in a first direction, and (2) to recirculate the warm air through the conduit structure to flow from the second port to the first port in the first direction. The inflatable non-perforated blanket includes first and second sheets. The first sheet faces ambient air and has a first thermal conductivity. The second sheet faces the subject body and has a second thermal conductivity higher than the first thermal conductivity.

Systems configured to acquire temperature signals from an Abreu Brain Thermal Tunnel (ABTT), to analyze the temperatures signals, and to determine a condition of a human body from the analysis, and a method for doing the same, are described. In addition, systems for application of thermal signals to the ABTT for treatment of conditions are described.

A catheter includes a first tubular portion provided with a first opening communicating with an interior of the first tubular portion; a second tubular portion passing through the first tubular portion, the second tubular portion having an extension extending from a leading end of the first tubular portion and provided with a second opening communicating with an interior of the second tubular portion; and a temperature sensor configured to measure temperature of a measuring unit placed in the extension of the second tubular portion, wherein the catheter is configured to collect fluid discharged from one of the first opening and the second opening from another one of the first opening and the second opening.