A respiratory system is configured to pressurize and deliver a flow of respiratory gas to a patient's airways. The respiratory system includes a cushion configured to sealingly engage the patient's face and a blower mounted to the cushion and configured to pressurize a flow of respiratory gas. An interface structure is attached to an outlet of the blower and an aperture in the cushion. The interface structure forms a gas flow path between the cushion and the blower. The gas flow path is configured to deliver the pressurized respiratory gas from the blower through the aperture in the cushion. The gas flow path is also configured to vent exhaled gas from the aperture in the cushion to atmosphere. The respiratory system also includes headgear configured to support the cushion and the blower on the patient's face.

A coordination unit for a group of medical devices, which is configured to execute the following steps: receiving sensor data from at least one of the medical devices the sensor data being associated with a patient, receiving a medical data set which is associated with the patient, and initiating an evaluation of the sensor data and/or the at least one medical data set to derive a treatment scheme. Also provided is a treatment system comprising the coordination unit and at least one medical device, the coordination unit being coupled to the medical device (3) via a data connection.

Methods and apparatus involve generation of an anti-infection therapy. The method/apparatus may include a controller controlling setting of a respiratory flow therapy device for the therapy. The controller may compute a target flow rate profile for a patient using a margin function, such that the target flow rate profile, according to the margin function, exceeds a minimum inspiratory flow rate profile of the patient's inspiration. The controller may control setting the respiratory flow therapy device to generate a flow of air to a patient interface according to the target flow rate profile, where the generation may be in synchrony with a sensed parameter that is indicative of a breathing cycle of the patient.

The present invention relates to the art of automatic regulation of pulmonary devices for assisting and/or enforcing the breathing process by converting Bag-Valve-Mask (BVM) apparatus are also known as manual resuscitators to automatic system by pneumatic matter with the goal to enhance both phases of breathing: inhalation and exhalation. It also replaces a mechanical chest compression for automatic pneumatic compression, could be complimented with the use of the TENs unit and can be used for extended periods of time with a high level of reliability, simplicity, efficacy and low cost.

This portable and light device is recommended to be used as a resuscitator attached to the patients with mild to extremely suppressed or without respiratory drive.

The source of power can be electrical, battery operated, manual or a combination thereof.

That feature is extremely critical for its use in a combat zone or during a power failure.

A system and method to configure a rule set used in connection with a medical monitoring system for monitoring patients and patient care equipment, especially medication delivery pumps, based on a variety of conditions and parameters associated with monitored biometric information and equipment information and for providing user-defined responses to those conditions and parameters.

A system and methods for the delivery of oxygen through a body cavity of a subject using oxygen microbubbles. Through circulation of oxygen microbubbles through the body cavity, oxygen and carbon dioxide exchange may occur. Overall improvement in extending survival rate time during emergency situations caused by pulmonary or similar oxygen-intake restricting injury and/or failure may be achieved through use of the invented system and methods.

A system (1000) for a feeding of substances to a patient (30) with ventilation and oxygenation of the patient. The system (1000) includes a ventilation system (1), an oxygenation system (2), a breathing gas dispensing path (3), a purge gas dispensing path (4), a breathing gas connection system (5), an oxygenation connection system (6), a dispensing system (7), a switching unit (8), and at least one control unit (9). The switching unit (8) is configured for a distribution or splitting of a quantity of a drug or anesthetic active ingredient, which quantity was dispensed into a gas mixture by means of the dispensing system (7), between the ventilation system (1) and the oxygenation system (2). The at least one control unit (9) is configured to control the switching unit (8).

A blower includes a housing including a proximal opening and a distal opening that are co-axially aligned, a stator component provided to the housing, an impeller positioned between the proximal opening of the housing and the stator component, and a motor adapted to drive the impeller. The impeller includes a plurality of impeller blades. The stator component includes a plurality of air directing grooves along its exterior surface. The leading edge of the air directing grooves extend tangentially outwards from the outer tips of the impeller blades and are configured to collect the air exiting the impeller blades and direct it from a generally tangential direction to a generally radial direction by dividing the air from the impeller and directing the air along a curved path towards the distal opening so that airflow becomes substantially laminar.

A sample cell (10) for a respired gas sensor has a single-piece injection molded main body (40) defining a gas flow path including an optical sampling bore (42), a gas inlet lumen (50) connected with the inlet end (44) of the optical sampling bore, and a gas outlet lumen (52) connected with the outlet end (46) of the optical sampling bore. The gas flow path includes at least two curved walls (100, 102, 104, 106). The sample cell may be manufactured by assembling mold pins (120, 122, 124, 126, 128) for defining the gas flow path wherein at least two mold pins (122, 124) have curved surfaces for defining the at least two curved walls of the gas flow path, and injection molding the single piece injection molded main body including removing the mold pins after defining the gas flow path including the at least two curved walls.

A sleep-inducing device, including: 1) a probe including a heart rate sensor detecting a heart rate of an infant's mother; 2) a sampling module collecting data with regard to the heart rate detected by the probe; 3) a first microcontroller unit (MCU) calculating the data transmitted from the sampling module and outputting a heart rate signal; 4) a second microcontroller unit (MCU) receiving and processing the heart rate signal transmitted from the first MCU; 5) a keyboard inputting, controlling and adjusting parameters of the second MCU; 6) a display displaying an operation/control state of the device; 7) a loudspeaker playing audio data of the heart rate signal processed by and transmitted from the second MCU; 8) a first memory storing the audio data of the heart rate signal; 9) a low dropout regulator (LDO) providing a constant voltage to the second MCU; and 10) a power supply.