A medical face mask is provided which includes a mask body having a mask interior and contoured to fit against the face of a patient. A permanently-open nasal aperture is provided in the mask body to facilitate insertion of an equipment, instrument or device into the mask interior and into the nose of the patient. A permanently-open oral aperture is provided in the mask body to facilitate insertion of an equipment, instrument or device into the mask interior and into the mouth of the patient. A one-way oxygen port is provided in the mask body to facilitate introduction of oxygen and/or medical gases into the mask interior of the mask body. A one-way valve port is provided in the mask body to facilitate discharge of carbon dioxide from the mask interior. A capnography or gas sampling port may be provided in the mask body to capture gases for analysis.

A medical face mask is provided which includes a mask body having a mask interior and contoured to fit against the face of a patient. A permanently-open nasal aperture is provided in the mask body to facilitate insertion of an equipment, instrument or device into the mask interior and into the nose of the patient. A permanently-open oral aperture is provided in the mask body to facilitate insertion of an equipment, instrument or device into the mask interior and into the mouth of the patient. A one-way oxygen port is provided in the mask body to facilitate introduction of oxygen and/or medical gases into the mask interior of the mask body. A one-way valve port is provided in the mask body to facilitate discharge of carbon dioxide from the mask interior. A capnography or gas sampling port may be provided in the mask body to capture gases for analysis.

Various implementations include a CPAP alarm system that generates an alarm when the concentration of CO.sub.2 is less than a certain threshold. The threshold may represent a minimum concentration of CO.sub.2 that is expected to be expelled from the patient. Other implementations are directed to a CPAP apparatus that can couple the CPAP alarm system to a CPAP air delivery device. The CPAP apparatus includes a support body that can be coupled to the CPAP air delivery device and that supports the CPAP alarm system outside of the air delivery device. A CO.sub.2 concentration sensor of the CPAP alarm system can be disposed on the apparatus such that the flow of CO.sub.2 from a breathing patient is directed toward the CO.sub.2 concentration sensor when the CPAP air delivery device is in use and is in the proper position for the patient.

Various implementations include a CPAP alarm system that generates an alarm when the concentration of CO.sub.2 is less than a certain threshold. The threshold may represent a minimum concentration of CO.sub.2 that is expected to be expelled from the patient. Other implementations are directed to a CPAP apparatus that can couple the CPAP alarm system to a CPAP air delivery device. The CPAP apparatus includes a support body that can be coupled to the CPAP air delivery device and that supports the CPAP alarm system outside of the air delivery device. A CO.sub.2 concentration sensor of the CPAP alarm system can be disposed on the apparatus such that the flow of CO.sub.2 from a breathing patient is directed toward the CO.sub.2 concentration sensor when the CPAP air delivery device is in use and is in the proper position for the patient.

The present invention relates to the diagnosis and treatment of urinary incontinence. Th diagnosis and treatment involves the use of a multiple sensor-enabled catheter capable of providing real-time data regarding the patient's physiology, such as urinary flow and muscular function of the bladder sphincter, as well as the position and movement of the catheter within the patient.

A system for performing an endoscopic surgical procedure in a surgical cavity of a patient that includes a multi-lumen tube set including a dual lumen portion having a pressurized gas line and a return gas line for facilitating gas recirculation relative to the surgical cavity of the patient, and a single lumen portion having a gas supply and sensing line for delivering insufflation gas to the surgical cavity of the patient and for periodically sensing pressure within the surgical cavity of the patient, a first gas sealed single lumen access port communicating with the dual lumen portion of the tube set and a second valve sealed single lumen access port communicating with the single lumen portion of the tube set.

The present disclosure relates to non-hemolytic adsorbent compositions useful for isolating, enumerating, accounting, and removing the disease-causing toxic constituents in the blood. The said compositions are useful in identifying the disease, disease status, and validating the efficacy of the therapeutic treatment being administered for the treatment of the disease. Methods for isolating, enumerating, accounting, and removing disease-causing toxic constituents in the blood as well as monitoring the disease status and validating the efficacy of the therapeutic treatment being administered for the treatment of the disease are disclosed.

The mucus-removing device is adapted for use with a patient. The patient is further defined with a tracheostomy tube. The mucus-removing device is configured for use with the tracheostomy tube. The mucus-removing device generates a vacuum at the tracheostomy tube such that mucus is withdrawn from the pulmonary system through the tracheostomy tube and into the mucus-removing device. The mucus-removing device generates the vacuum at the tracheostomy for a fixed period of time. The periodic nature of the generation of the vacuum allows the patient to breath comfortably during the removal process. The mucus-removing device comprises a pump, a hose, a tracheostomy tube connector, and a control system. The hose attaches the pump to the tracheostomy tube connector. The tracheostomy tube connector attaches the mucus-removing device to the tracheostomy tube of the patient. The control system regulates the operation of the pump.

The mucus-removing device is adapted for use with a patient. The patient is further defined with a tracheostomy tube. The mucus-removing device is configured for use with the tracheostomy tube. The mucus-removing device generates a vacuum at the tracheostomy tube such that mucus is withdrawn from the pulmonary system through the tracheostomy tube and into the mucus-removing device. The mucus-removing device generates the vacuum at the tracheostomy for a fixed period of time. The periodic nature of the generation of the vacuum allows the patient to breath comfortably during the removal process. The mucus-removing device comprises a pump, a hose, a tracheostomy tube connector, and a control system. The hose attaches the pump to the tracheostomy tube connector. The tracheostomy tube connector attaches the mucus-removing device to the tracheostomy tube of the patient. The control system regulates the operation of the pump.

A mask is disclosed that has a gas outlet which is quiet and provides for a diffused outlet flow of gases. The outlet is preferably a slot formed between a hollow body and cover over said hollow body. The mask also preferably extends and seals under a user's chin in use.