Patent classifications
A61F2007/0096
AIR WARMER
An air blower has an inlet muffler and an outlet muffler to reduce the noise of the air blower during operation. Each of the mufflers may have two sections. One section is configured to attenuate high frequency noise and the other section is configured to attenuate lower frequency noise. A tubular internal wall in each of the mufflers defines the through passage for each of the mufflers. A noise absorbent material may be fitted about the tubular wall within each muffler. A plurality of holes are formed along the tubular wall of each through passage to expose the through passage to the noise absorbent material. A heater plenum may be interposed between the blower plenum and the outlet muffler to heat the air from the blower plenum. A filter at the input muffler filters the air sucked into the air blower.
SYSTEMS AND METHODS FOR PROVIDING A CARDIAC ASSISTANCE ECOSYSTEM
Disclosed is a cooling device, including a housing having a wall; a reservoir within the housing; a cooling material such as a liquid or gel in the reservoir; a pump within the housing; and a conduit passing adjacent the wall and through which the material is circulated by the pump from the reservoir back to the reservoir.
Controllable heated mask
A heated mask comprises a user-operated control providing a number of different parameters including temperature and duration of heat application. At least one area contains a heater element. The heated mask covers an upper portion of a face and has areas positioned to be in registration with sinuses of a user. The heating element in one form comprises a serpentine conductor having a path through each area and having a preselected resistance in each area. In another form, a plurality of separate electrodes are provided, each in one selected area. Each electrode section is separately controlled to provide a preselected level of heat. It has been found that selected temperatures for a heater provide relief for sinus congestion, and that particular combinations of relative setting of a plurality of electrodes are associated with enhanced therapeutic results.
Temperature Control System
A temperature control system (300) comprising a first peripheral fluid circuit (312) for the passage of a first heat exchanger fluid. The first peripheral fluid circuit (312) comprises a first fluid connection (314) for fluidly connecting a first peripheral heat exchanger (310) in series with a first peripheral-evaporator heat exchanger (316). There is also provided a first peripheral pump (318) for pumping the first heat exchanger fluid around the first peripheral fluid circuit (312). There is also provided a first evaporator circuit (320) for the passage of an evaporator heat exchanger fluid through the first peripheral-evaporator heat exchanger (316). The first evaporator circuit (320) comprises a first evaporator pump (322) for pumping the evaporator heat exchanger fluid around the first evaporator circuit (320). The first evaporator circuit (320) is fluidly isolated from the first peripheral fluid circuit (312). The first peripheral-evaporator heat exchanger (316) is configured to permit heat exchange between the heat exchanger fluids.
Target heating method and system within a designated space
A heating system includes a sensing and tracking module to sense length in at least one dimension of an object to-be-heated in a previously determined area. A light source module has at least one light source that can change its lighting direction and can also change its beam angle e along the at least one dimension. A control module is provided for regulating light emitted by the light source module onto the to-be heated object along the at least one dimension to match with the length of the to-be-heated object based on the length sensed by the sensing and tracking module. The heating system described above and a bed incorporated having this kind of heating system may automatically adjust its output power according to the physical characteristics of the object to-be-heated to avoid heating unrelated object, area or space so as to ensure high energy efficiency.
Therapeutic Room Thermostat
The purpose of the disclosed thermostat is to prevent age-related diseases, induced by long term cool indoor temperatures. As people age, the body produces progressively less heat while aging-impaired vasoconstriction results in progressively more heat being lost. This age-induced cold stress requires ever greater use of vasoconstriction or behavior to maintain the body's heat balance. When behavioral regulation becomes diminished with age, vasoconstriction becomes progressive throughout life. In at risk elderly, an ongoing mild indoor cold stress can unknowingly maximize negative feedback vasoconstriction leaving it unable to further defend core body temperature. Before hypothermia occurs, positive feedback vasoconstriction activates as a defense mechanism. Like inflammation and fever, this beneficial defense mechanism can also cause harm when its use becomes excessive. The therapeutic function of this medical device is to sense skin temperature and use it to modify the indoor environment, keeping thermoregulation within the effective range of negative feedback vasoconstriction.
METHOD FOR DETERMINING GASES PROPORTIONS IN AN INHALABLE MEDICAL GASEOUS COMPOSITION AND INHALATION TEMPERATURE OF SUCH INHALABLE MEDICAL GASEOUS COMPOSITION
A method for determining gases proportions to obtain an inhalable medical gaseous composition consisting of a first noble gas, a second noble gas, and oxygen, in order to reach a body temperature value, including determining a proportion of first or second noble gas depending on predetermined parameters, such as the body temperature value and an inhalation temperature value, the determining further including determining, for the inhalation temperature value, two body temperature theoretical values for the first and second noble gas modeled by reference regression lines, calculating a difference between both body temperature theoretical values, calculating a difference between body temperature value and any one of the body temperature theoretical values, calculating a ratio representing proportion of first or second noble gas in the inhalable medical gaseous composition.
APPARATUS AND METHOD FOR ESOPHAGEAL COOLING
A balloon catheter is used in a closed-loop heat exchange system for manipulating the temperature of a patient. The balloon catheter is positioned in the stomach of the patient, and then expanded with a heat exchange fluid delivered through a lumen formed in the shaft of the catheter. The balloon catheter comes into contact with the wall of the stomach, and the stomach substantially conforms around the expanded balloon catheter. The heat exchange fluid is allowed to flow continuously into and out of the balloon catheter. Heat is exchanged between the balloon catheter and the stomach so as to controllably alter the temperature of at least a portion of the patient. Anti-shivering mechanisms and automatic control based on temperature feedback from the patient may be used in connection with the heat exchange system.
MULTI-APPLICATOR SYSTEM AND METHOD FOR BODY CONTOURING
Systems, methods, and devices for treating a subject are described herein. In some embodiments, an applicator for selectively affecting a subject's subcutaneous tissue is provided. The applicator can include: a housing; a treatment cup mounted in the housing, wherein the treatment cup defines a tissue-receiving cavity and includes a temperature-controlled surface; at least one thermal device coupled to the treatment cup and configured to receive energy via a flexible connector coupled to the applicator and to cool the temperature-controlled surface; an at least one vacuum port coupled to the treatment cup and configured to provide a vacuum to draw the subject's tissue into the tissue-receiving cavity and against at least a portion of a treatment area of the temperature-controlled surface to selectively damage and/or reduce the subject's subcutaneous tissue.
STIMULATION APPLICATION APPARATUS
A stimulation application apparatus includes a substrate, a stimulation application member provided on one surface of the substrate to apply a stimulation to a site, and a stimulation imposition layer provided on another surface of the substrate opposed to the first surface to impose the stimulation. The site includes at least one area selected from a group of (F) site that intersects the perpendicular line of the medial malleolus on an extension line of the medial margin on os metatarsale primam 1 and 2 in foot sole, and (L) incisurasive foramen supraorbitalis site, and (K) site where the lintersection of the line connecting an augulus oculi medialis of eye and L site, and perpendicular of an augulus oculi lateralis of eye is located, and (M) site of augulus oculi lateralis located above 1 horizontal finger from center of the line where connect the inner end of left and right eyebrow.