Abstract: Filtering face mask 10 has a mask body 12 and an exhalation valve 14. The mask body 12 is adapted to fit over the nose and mouth of a person, and the exhalation valve 14 is attached to the mask body 12. The exhalation valve 14 has a valve seat 26 and a single flexible flap 24. The valve seat 26 includes a seal surface 31 and an orifice 32. The orifice 32 is circumscribed by the seal surface 31. The single flexible flap 24 has a fixed portion 28 and one free portion 38. The one free portion 38 has a free end, and the fixed portion 28 is located off-center of the flexible flap 24 away from the free end and is secured to the valve seat 26 outside the orifice 32. The one free portion 38 is pressed toward the seal surface 31 when the wearer is neither inhaling or exhaling. The free portion 38 can be lifted from the seal surface 31 during an exhalation.

Abstract: A microstructured filter for a fluid, the filter having an inlet for unfiltered fluid and an outlet for filtered fluid, the filter comprising: a plurality of projections (7) which are arranged in at least two rows (3) in mutually juxtaposed relationship and which project out of a base plate (1) and which are an integral component of the base plate, a plurality of passages (8) between the projections (7), and a cover plate which is securable to the base plate to cover the projections (7) and the passages (8), wherein the passages form a plurality of through paths from the inlet to the outlet, said inlet comprises an elongate inlet slot (5) for the unfiltered fluid, which extends over approximately the entire filter width and which is approximately as high as the projection (7) projecting out of the base plate, on the outlet side of the filter. The filter according to the invention remains operational, even if a part of the filter area is obstructed.

Abstract: A filtering face mask that comprises a mask body that is adapted to fit over the nose and mouth of a wearer, the mask body comprising a filtration layer through which inhaled air may pass before being inhaled by a wearer of the face mask; and an exhalation valve that is attached to the mask body, the exhalation valve allowing air exhaled by a wearer to pass from an interior of the mask body to its exterior without having to pass through the filtration layer, the exhalation valve comprising: a valve seat that comprises: a seal surface; and an orifice that is circumscribed by the seal surface; and a single flexible flap that has one fixed portion and one free portion and a circumferential edge, the circumferential edge having a first segment that is associated with the one fixed portion of the flap so as to remain at rest during an exhalation and having a second segment that is associated with the one free portion of the flexible flap so as to be lifted away from the seal surface during an exhalation, the secon

Abstract: Systems, methods and devices for performing pulmonary procedures, and in particular treating lung disease. A flow control element includes a valve that prevents airflow in the inhalation direction but permits airflow in the exhalation direction. The flow control element is guided to and positioned at the site by a bronchoscope that is introduced into the patient's trachea and used to view the lungs during delivery of the flow control element. The valve may include one, two or more valve elements, and it may be collapsible for easier delivery. A source of vacuum or suction may be used to increase the amount of fluid withdrawn from the lung tissue. A device for measuring hollow structures, such as bronchioles, and a device for removing a previously-placed flow control element are disclosed as well.

Abstract: The present invention relates to a ventilation system for a protective suit for use in hazardous environments. In a further aspect it concerns the protective suit itself. An air purifying respirator draws air from outside the protective suit through a filter, supplies filtered breathing air via a breathing hose to a space within the face piece, and supplies filtered ventilating air via a ventilating hose to the interior of the protective suit. A ventilation valve in the ventilating hose automatically closes only during periods of high breathing demand to counter a pressure drop inside the face piece.

Abstract: The present invention provides a metered dose inhaler including an ejection mechanism with at least one chamber for containing a medicament. The ejection mechanism is configured to effect controlled ejection of the medicament from the chamber. The inhaler further includes a controller configured to send electronic signals to the ejection mechanism to direct ejection of medicament from such chamber, and configured to selectively alter dosage of the medicament by selected changes in such electronic signal.

Abstract: Here is disclosed a snorkel comprising a mouthpiece section, an open end section, a tubular section being contiguous to the open end section and a connector section interposed between the mouthpiece section and the tubular section and provided with a check valve. First and second halves constituting the connector section are pressed against each other along respective peripheral edges of these halves and then covered with a belt-like section welded to the connector section from the outside.

Abstract: A travel mask that fits over the nose and mouth area of a wearer's face for filtration of air, particularly recycled air in the travel compartment of a common carrier, the travel mask having a face shield that preferably includes an aroma patch that emits a pleasant aroma and a retainer such as a head band for retaining the face shield against a user's head. The retainer has slidable ear plugs for blocking noise. The travel mask also has a foldable eye flap or flaps for blocking light when the flap or flaps are extended, the flap or flaps preferably having thermal gel packs for cooling or warming the eye lid area of the wearer during use.

Abstract: The present invention provides a vent assembly suitable for use with a respiratory mask of the type used in CPAP treatment. In one embodiment the vent is made of a thin air permeable membrane. Generally, the membrane is thinner than 0.5 mm. The membrane can be made of a hydrophobic material such as polytetrafluoroethylene (PTFE). The membrane can also be fabricated from expanded PTFE. The expanded PTFE membrane is mounted on a polypropylene scrim. The pores of the membrane have a reference pore size of 10 to 15 microns. In an alternative embodiment, the vent assembly includes a vent constructed from stainless steel. In another embodiment the membrane has a superficial cross-sectional area of approximately 500 mm2. In another embodiment the vent assembly comprises a membrane attached to a vent frame, the vent assembly forming an insert which can be removeably attached to a mask fame.

Abstract: A tracheal tube positioning apparatus is located relative to a patient's trachea by engaging the patient's Adam's apple. Indicia on relatively movable sections of the positioning apparatus provides an indication of the distance between the patient's mouth and the patient's larynx. A flexible guide rod is moved through a distance corresponding to the distance between the patient's mouth and larynx, as determined by the positioning apparatus. A magnet is utilized to attract a leading end portion of the guide rod. A plurality of emitters may be disposed in an array around the patient's Adam's apple. Outputs from the emitters are detected by a detector connected with the guide rod and by a detector connected with the tracheal tube. Alternatively, a plurality of detectors may be disposed in an array around the patient's Adam's apple to detect the output from an emitter connected with the guide rod and by an emitter connected with the tracheal tube.

Abstract: A process is provided for controlling at least one parameter of the breathing gas supply of a respirator with a patient connected to it as well as to a corresponding control device. The respiration pressure, the breathing gas flow generated by the respirator as well as the respiration rate may be used as parameters. The process presents the advantage that the control of the current respiration needs of the patient are taken into account by the muscle pressure (PMUS), i.e., the percentage of the airway pressure caused by the patient's own effort, being maintained at a value close to zero. An airway pressure (PAWC) is first calculated for this purpose from previously measured values for the airway pressure (PAW) and the breathing gas flow (d/dt V) and the mechanical parameters resistance (RL) and compliance (C) of the patient's lungs, which were determined therefrom, and this is subsequently compared with the actually measured value for the airway pressure (PAW).

Abstract: The invention concerns a method for open-loop regulation of a breathing aid apparatus which consists in constituting a compression chamber by dividing it into two compartments each connected to an intake of air or breathing mixture and to an outlet of compressed air, using an clastic floating diaphragm guiding said floating diaphragm by fixing its periphery to the wall of said chamber fixing a field coil at the center of said floating diaphragm, placing said field coil in an air gap which is oriented in the direction deforming said floating diaphragm, measuring the instantaneous flow rate of air leaving through said outlet and powering said field coil continuously calculating the instantaneous intensity and the direction of the supply current on the basis of the set pressure of compressed air, of said instantaneous flow rate and of the constants of said apparatus.

Abstract: The invention provides an apparatus for supplying a respiratory gas to a respiratory air way of a patient. The respiratory gas supplying apparatus 10 includes a cylinder 12 filled with a respiratory gas, a cart 14 having an accommodating portion for disposing the cylinder 12, a shut-off valve 18 attached to the cylinder 12, a flow regulating valve 40 attached to the shut-off valve 18, a conduit 22, attached to the flow regulating valve 40, for directing the respiratory gas to the inlet of the respiratory airway of the patient, a coupler 16, integrally connected to the flow regulator 40, for coupling the flow regulating valve 40 to the shut-off is valve 18, and a linkage 110 for disengaging the coupler 16 from the shut-off valve IS when the cylinder 12 is detached from the cart 14.

Abstract: Self-contained underwater re-breathing apparatus having a breathing circuit, an injection system for adding fresh breathable gas to the breathing circuit, and an automatic control system including a microcomputer for monitoring physical parameters in the breathing circuit and controlling the feeding of breathable gas to the breathing circuit in accordance with said physical parameters. The re-breathing apparatus has a bailout system automatically activated in an emergency, where the breathing circuit is shut off, and the diver starts inhaling directly from the breathable gas supply and exaling to the environment. With the system of the invention, a part of the existing closed circuit is used for bailout, and no separate bailout circuit is provided. Therefore, there is no need to incorporate in the mouthpiece means for switching from one breathing circuit to another, and the mouthpiece can be kept smaller and simpler.

Abstract: The apparatus provides for the determination of the instantaneous phase in the respiratory cycle, subject's average respiration rate and the provision of ventilatory assistance. A microprocessor (16) receives an airflow signal from a pressure transducer (18) coupled to a port (17) at a mask (11). The microprocessor (16) controls a servo (19), that in turn controls the fan motor (20) and thus the pressure of air delivered by the blower (10). The blower (10) is coupled to a subject's mask (ii) by a conduit (12). The invention seeks to address the following goals: while the subject is awake and making substantial efforts the delivered assistance should be closely matched in phase with the subject's efforts; the machine should automatically adjust the degree of assistance to maintain at least a specified minimum ventilation without relying on the integrity of the subject's chemoreflexes; and it should continue to work correctly in the pesence of large leaks.

Abstract: A respiratory mask assembly includes a rigid mask frame with a rim portion comprising a rearwardly projecting tongue and lateral flange and a cushion having a rim with a corresponding groove and a rearwardly facing shoulder. A clip in the form of a collar passes over the cushion, engaging behind the shoulder, and has securing tabs that engage recesses in the flange.

Abstract: A system for securing an endo-tracheal or other tube in position upon a patient includes a head pad and securing members which can be adjustably attached to the head pad. The head pad is configured to support the head of a patient in a supine position. The head pad includes a number of slits formed in each lateral side of the head pad, such that a securing member can be threaded through any one of the slits. The securing member is configured to be releasably and adjustably attachable to the lateral sides of the head pad by being secured to itself via hook and, loop fastener portions disposed upon the member. The opposite end of the securement member can include an adhesive layer or other mechanism for attachment of the end of the member to the endo-tracheal tube or other medical article.

Abstract: A first and second housing joined together and rotatable with respect to each other, each housing having a conduit integral with an exterior wall, the conduits each having passageways leading to an internal portion of the respective housings. An internal edge of each housing mounts a heat-moisture exchange material having a transverse opening axially aligned with the passageway of the closest conduit. The passageway in the respective conduits are offset permitting passage of air to and from the patient through the heat-moisture material. The housings are rotated with respect to each other to axially align the passageways in the two conduits to permit passage of aerosol medicine through the exchanger without passing through the heat-moisture material.

Abstract: A drug delivery device and method is disclosed which produces aerosolized particles of pharmaceutically active drug for delivery to a patient by inhalation. The device is comprised of a liquid feeding source such as a channel to which formulation is added at one end and expelled through an exit opening. The feeding channel is surrounded by a pressurized chamber into which gas is fed and out of which gas is expelled from an opening. The opening from which the gas is expelled is positioned directly in front of the flow path of liquid expelled from the feeding channel. Various parameters are adjusted so that pressurized gas surrounds liquid flowing out of the feeding channel in a manner so as to maintain a stable capillary microjet of liquid until the liquid exits the pressure chamber opening and is aerosolized. The aerosolized particles having a uniform diameter in the range of about 1 to 5 microns are inhaled into a patient's lungs and thereafter reach the patient's circulatory system.

Abstract: An inhalation device is described for use with a medicament pack in which at least one container for medicament in powder form is defined between two sheets peelably secured to one another. The device comprises means for peeling the sheets apart at an opening station to open the container; and an outlet, communicating with the opened container, through which a user can inhale medicament in powder form from the opened container.