The disclosure relates to the field of medical instruments, and discloses a control device and method for a ventilation therapy equipment, and ventilation therapy equipment. The ventilation therapy equipment has multiple working modes. The control device includes an identification device used for identifying a type of an accessory of the ventilation therapy equipment; and a controller used for determining and controlling, according to the identified type of the accessory, the ventilation therapy equipment to switch to a working mode corresponding to the type of the accessory. The control device can automatically switch the corresponding working modes according to different types of accessories, and is more convenient and intelligent, so that a lot of time can be saved for a doctor and a patient.

Methods and system for treating obstructive sleep apnea and snoring are disclosed. The system generally comprises a mask for delivering pressurized air to patient's breathing orifice, a sensing mechanism for continuously assessing the state of patient's breathing and a pressure generator for generating the pressurized air in the mask. The pressurized air is applied to the breathing orifice only during selected portions of the breathing cycle, when such pressure might be required to prevent occlusion of the airway or to restore patency of the airway after such occlusion occurs.

A respiratory acoustic device is provided that is easy to operate and transport. The device delivers vibrations artificially to the lungs and airways to fluidize mucus adhering to the airways and promote its discharge. A respiratory acoustic device 1 is provided with a housing 10, and a mouthpiece 20 that is in communication with the housing 10. The housing 10 has a reflecting end 12 for reflecting air that has been blown in from the mouthpiece 20 and an open end 13 through which air that has been blown in from the mouthpiece 20 can escape. If a sudden exhalation such as a cough is blown into the housing 10 through the mouthpiece 20, the device causes the noise due to said exhalation to resonate with the oral and lower airway cavities, and vibrate the user's lungs and airways with the low frequency acoustic shock waves generated therein.

Various control methods can indirectly determine incorrect connections between components in a respiratory therapy system. For example, incorrect connections can occur between a patient interface, a humidifier and/or a gases source. The methods can indirectly detect if reverse flow conditions or other error conditions exist. A reverse flow condition can occur when gases flows in a direction different from an intended direction of flow. The methods can be implemented at the humidifier side, at the gases source side, or both.

A breathing tube system includes a gas receiving tube, an output tube and a flame arrester. The gas receiving tube is configured to receive a breathing gas. The output tube is coupled to the gas receiving tube to form a supply pipeline. The output tube is configured for a user to wear and to output the breathing gas from the supply pipeline to the user. The flame arrester is configured in the supply pipeline. Accordingly, the safety of the breathing equipment could be improved.

Various exemplary drug delivery devices with a spinning nozzle, drug products utilizing the same, and methods of using drug delivery devices with a spinning nozzle are provided. In general, a nasal drug delivery device configured to dispense a drug therefrom includes a spinning nozzle configured to facilitate the drug's ejection into a patient's nose. The spinning nozzle is located between a drug holder containing the drug to be dispensed and an opening of the drug delivery device through which the drug exits the drug delivery device. The spinning nozzle is configured to spin during the drug's delivery as the drug travels from the drug holder and out of the drug delivery device. The spinning nozzle includes a plurality of perforations therein through which the drug as a liquid is configured to pass. The spinning of the spinning nozzle causes the drug to exit the drug delivery device as a fine mist.

Apparatus and methods for providing controlled pressure-flow pulses which purge a catheter system with turbulent flow flushing. Accomplishment of such controlled pressure-flow pulses is provided by a variety of inventive devices including a special plunger rod for a conventional syringe, other interactive parts for conventional syringes, an in-line catheter attachable device which automatically generates the controlled pressure-flow pulses and also single pulse, digitally operated devices.

The invention provides an intraventricular pulsating blood pump fixedly disposed at the ventricularapex inside the ventricle to generate pulsation action. The pulsating blood pump is substantially jellyfish-shaped and includes a bell-shaped pump body and a driving source, an opening of the bell-shaped pump body faces to the outlet of the ventricle, the driving source drives the bell-shaped pump body to contract or relax, and the contraction or relaxation of the bell-shaped pump body drives the blood in the ventricle to eject directionally to the artery and form a convoluted blood flow field between the inner wall of the bell-shaped pump body and the inner wall of the ventricle. The invention not only provides assist to ventricular by pulsating blood flow, but also optimizes the flow field and pressure distribution in the ventricle, the blood pump of the invention is better in biocompatibility than the blood pumps in prior art.

A system and method for increasing the speed of blood and wall shear stress (WSS) in a peripheral vein for a sufficient period of time to result in a persistent increase in the overall diameter and lumen diameter of the vein is provided. The method includes pumping blood at a desired rate and pulsatility. The pumping is monitored and adjusted, as necessary, to maintain the desired blood speed, WSS and pulsatility in the peripheral vein in order to optimize the rate and extent of dilation of the peripheral vein.

A venous air capture chamber for use in dialysis, includes an upwardly extending fluid inlet terminating in first and second fluid inlet ports (102). The first and second fluid inlet ports (102) are opposedly positioned on the fluid inlet at an angle of about 180°. The venous air capture chamber also includes a fluid outlet (104) at the bottom of the chamber body. The venous air capture chamber provides improved fluid dynamics, reducing both stagnant flow and turbulence. The venous air capture chamber also provides for bidirectional flow of fluid through the chamber.