Abstract: A portable air purifier and method includes a collapsible first tube; a perforated firm second tube that houses the first tube; a fan that brings air into a first end of the first tube and pushes the air through the first tube; a multi-part filter arranged in a concentric configuration inside the first tube; an outlet at a second end of the first tube; and a breathing mask coupled to the outlet. The filter filters the air as the air proceeds through the first tube and the outlet discharges filtered air from the first tube to the breathing mask. The first tube and the second tube may be semi-circular to fit around the neck of a user. The filter may be a corrugated filter. The portable air purifier may include a power source electrically connected to the fan.

Abstract: In one embodiment, the present invention provides a system to deliver at least one therapeutic gas to a spontaneously breathing patient, wherein the rate of delivery of the at least one therapeutic gas exceeds the patient's inspiratory flow rate, and the amount of the at least one therapeutic gas that is wasted is minimized or eliminated.

Abstract: Disclosed is a waterseal virus-killing mask, including a mask body, a liquid virus-killing assembly, and two elastic ear loops. A breather valve is disposed on an outer surface of the mask body. The two elastic ear loops are disposed on two sides of the mask body, respectively. The liquid virus-killing assembly includes a U-shaped tube within which disinfectant is provided. A disinfectant replenishing tube is vertically disposed at an upper end in the middle of the U-shaped tube. A first horizontal straight tube and a second horizontal straight tube are separately disposed at two ends of the U-shaped tube. A left end of the first horizontal straight tube is in communication with an opening of the breather valve. A first filter mesh used to separate water and air is disposed at a right end of the first horizontal straight tube.

Abstract: The oxygen delivery device is a portable structure. The oxygen delivery device contains a plurality of oxygen canisters. The plurality of oxygen canisters contain oxygen under pressure. The oxygen delivery device stores the plurality of oxygen canisters. The oxygen delivery device dispenses the oxygen contained in the plurality of oxygen canisters. The oxygen delivery device comprises a housing, a distribution apparatus and the plurality of oxygen canisters. The housing contains the plurality of oxygen canisters and the distribution apparatus. The housing: a) stores the plurality of oxygen canisters; and, b) forms a fluidic connection between the plurality of oxygen canisters and the distribution apparatus. The distribution apparatus delivers the oxygen received from the plurality of oxygen canisters for consumption.

Abstract: Various embodiments of a respirator (10) that includes a harness (13, 16), a mask body (12), and an exhalation valve (14) are disclosed. The exhalation valve (14) can include a valve seat (20) and a flexible flap (22) that is in engagement with the valve seat. The flexible flap can have one or more materials that can cause the flap to flash (26) when moving from a closed position to an open position or vice versa. The flashing valve can make it easier for a user to ascertain whether the valve is operating properly.

Abstract: Systems and methods for triggering inspiration and/or cycling exhalation with a ventilator are described herein. In particular, systems and methods for synchronizing ventilator breath delivery with patient breath demand utilizing a digital sample counting trigger mode are described herein. The digital sample counting triggering mode characterizes digital samples taken from a measured or estimated parameter during the patient inhalation/exhalation period to synchronize breath delivery with patient breath demand.

Abstract: In one embodiment, a nasal cannula is shaped to fit within a user's nares, where the nasal cannula includes at least one prong allowing high flow delivery of humidified gases and creates positive airway pressure in the patient's airway. The prongs have angled ends such that, in use, gases flowing through the prongs are directed to the user's nasal passages. The nasal cannula body is partially swivelling and preferably has a ball joint connector. In another embodiment the nasal cannula may have at least one flared end prong that preferably seals within a patient's nare.

Abstract: An apparatus for respirating a patient has a gas circulation device for circulating a gas in one direction in a line system, a pressure varying device suitable for varying a pressure of the gas in the line system in accordance with the desired respirating the pattern, a measurement sensor cooperative with the gas in the line system so as to measure a flow rate and composition of the gas, an absorber device suitable for withdrawing carbon dioxide as exhaled by the patient, a bypass line having a closing device suitable for completely or partially leading the respiratory gas outside of the line system, and a circulation blower cooperative with the line system so as to provide a continuous flow of gas in one direction through the line system.

Abstract: A user interface has a non-sealing nasal cannula and a mask arranged about the nasal cannula, the mask including a seal configured with a user's face to allow the interface to be pressurized, the cannula configured to deliver breathing gases to the nares of a user at a flow rate exceeding the intended user's peak inspiratory flow requirements so that the mask and the user's pharynx are flushed continuously with fresh breathing gases to reduce dead space.

Abstract: A regulator is disclosed that controls fluid flow through a control valve via a linkage including a lever that is acted upon by a spring cylinder acting in a direction perpendicular to the direction of fluid flow through pipes connected to the control valve. The closure performance of the control valve of the regulator is optimized by the direction the spring cylinder acts and the mechanical advantage the lever provides. The regulator further includes a diaphragm and diaphragm cover, and the regulator is configured to allow the diaphragm cover to be stamped rather than cast.

Abstract: [Subject] A test substance application system for animal experiment capable of administering a required amount of a test substance uniformly and reliably from a nose or a mouth into a nasal cavity or into a lung of an experimental animal is provided. [Means for Solution] The system includes a respiration monitoring device 2 that monitors a respiration state of an experimental animal detected by a respiration pick-up device 1 to thereby measure a timing upon switching from an expiratory phase to an inhalatory phase and outputs a trigger signal T at that timing, and an application device 3 that sprays a predetermined amount of a test substance into a nasal cavity or an oral cavity of the experimental animal when the trigger signal T is outputted from the device 2.

Abstract: This invention relates to a treatment device (10) and method of use, and in particular to a treatment device adapted to assist the clearance of bronchial secretions in persons whose cough function is impaired. The invention provides a treatment device having a pump (12) with a negative pressure inlet side (22) and a positive pressure outlet side (24). The device has a breathing tube (14) for connection to a patient, and a pressure sensor (18) adapted to determine the pressure within the breathing tube. A valve (16) selectively connects the breathing tube to the inlet side or the outlet side of the pump whereby to provide cycles of positive and negative pressure within the breathing tube. A controller (26) is provided to control the valve. An indicator (20) alerts the patient to an operational status of the device so that the patient can breathe in time with the device and in particular can seek to cough at the same time as the pressure within the breathing tube is rapidly reduced.

Abstract: Wastegated turbochargers all use actuators to manipulate the wastegate valve which controls turbine wheel bypass of exhaust gas energy. The diaphragms in these actuators are susceptible to foreign material damage. This damage is minimized by the addition of a boot around the actuator shaft, preventing ingress of foreign materials and fluids which could be detrimental to actuator life.

Abstract: A gas generating system for health use is provided, including a hydrogen-oxygen gas generator and an atomized/volatile gas generator. The hydrogen-oxygen gas generator has a first casing. The first casing accommodates an electrolysis device for electrolyzing water in order to produce a gas mixture of hydrogen and oxygen. The atomized/volatile gas generator has a second casing, the second casing accommodates a gas mixing camber coupled to the electrolysis device to receive and combine the gas mixture of hydrogen and oxygen with water vapor, an atomized medicine, a volatile essential oil or any combination thereof in order to produce a healthy gas for a user to inhale.

Abstract: A CPAP apparatus in which the swing in pressure at the patient interface is adjusted by regulating the air flow from the flow generator through an air delivery conduit taking into account a pressure drop representative of the inertance of the airflow in the air delivery conduit during the increase of air flow from the flow generator.

Abstract: A manual emergency resuscitator uses a volume control system having pre-defined setting to accommodate patients of different sizes. An upper plate 305 is attached to a front hinge assembly 103 and a lower housing assembly is attached to the front hinge assembly. The lower housing assembly defines the lower portions of an accordion chamber 206. A selection void 300 is defined within the upper plate 305, with the selection void further defined by voids indexed to a closed position, infant position, child position and an adult position. A volume selector cord 201 has a first end attached to a volume selector, with the volume selector contained within the selection void. Placing the volume selector into one of the predefined positions regulates the amount of air delivered by the resuscitator.

Abstract: A breathable gas supply apparatus for a patient features a breathable gas supply system and a respiratory mask assembly in communication with the breathable gas supply system. The breathable gas supply system provides a supply of breathable gas to the respiratory mask assembly and removes a supply of exhaled gas from the respiratory mask assembly. The breathable gas supply system includes a housing having an inspiration chamber and an exhalation chamber and a movable structure in communication with the inspiration and exhalation chambers. The movable structure moves in phase with a respiratory cycle of a patient. In one preferred embodiment, the breathable gas supply system includes a second movable structure, which moves in response to a phase of the respiratory cycle of the patient. In another one preferred embodiment, the breathable gas supply system is powered to assist the patient's respiratory effort.

Abstract: A method and apparatus for providing ventilatory assistance to a spontaneously breathing patient An error signal (56) is computed that is the difference between a function of respiratory airflow (54) over a period of time and a target value (52). Using a servo loop, air is delivered to the patient at a pressure that is a function of the error signal, the phase of the current breathing cycle, and a loop gain that varies depending on the magnitude of the error signal. The loop gain increases with the magnitude of the error signal, and the gain is greater for error signals below a ventilation target than for error signals above the ventilation target value. The target value (52) is an alveolar ventilation that takes into account the patient's physiologic dead space.

Abstract: A breathing circuit for sequential gas delivery of a first gas set (FGS) and a second gas set (SGS) employs an arrangement of conduits and active or passive valves to prevent mixing of the FGS and SGS including a valve triggered by depletion of FGS that makes the SGS available for inspiration after the FGS is depleted.

Abstract: A device for automatically squeezing and releasing an AMBU-bag is disclosed. A device has a housing and a mechanical compression squeezer in the housing. There are openings in the housing for inlet tubes and outlet tubes of AMBU-bag to pass in and out of the housing. A powered actuator powers the compression squeezer. Alarms and signals provide information regarding excessive pressure and regarding bag cycling.

Abstract: Oxygen breathing masks, as well as methods of providing oxygen to persons, are detailed. The devices may include mechanisms for supplying either oxygen or ambient air to a person depending on inspiration pressure applied by the person to a first volume to which the person's mouth and/or nose is connected.

Abstract: An adjustable volume control manual resuscitation bag assembly includes a resuscitation bag, a volume control knob, a traction assembly operating in response to adjustment of the control knob, and a follower assembly including a bag compression limiting member and a follower which are moved in response to operation of the traction assembly to adjust and limit the volume of gas delivered by compression of the bag.

Abstract: In one embodiment, the invention provides a medical method for treating a person and comprises repeatedly compressing the person's chest. While repeatedly compressing the person's chest, the method further includes repeatedly delivering a positive pressure breath to the person and extracting respiratory gases from the person's airway using a vacuum following the positive pressure breath to create an intrathoracic vacuum to lower pressures in the thorax and to enhance blood flow back to the heart.

Abstract: A rebreather system for aircrew that includes a double counter lung having a void between inner and outer bladders that allows selective pressurization of the inner bladder.

Abstract: An apparatus (1) for non-invasive mechanical ventilation comprises a fan (2) of Bi-level type, or BiPAP, for generating an air flow according to a succession of inspiration steps, or IPAP, and exhalation steps, or EPAP. The flow is conveyed in the aerial ducts of a patient (25) by means of a flexible tube (3) connected to a nasal mask (4). A flexible air reservoir (5) is provided pneumatically connected to the duct (3) and the nasal mask (4) in order to subtract from the inspiration flow a certain air amount before that it reaches the patient (25) at the beginning of an IPAP step. During the exhalation EPAP step, since the air flow pressure decreases automatically, there is the emptying at least partial of the flexible air reservoir (5), whereas the air exhaled by the patient exits through an opening (14) made on the nasal mask (4).

Abstract: The multitask medical treatment respiratory apparatus may have a mask defining a chamber wherein the mask may have a first port, a second port and a venting valve. A reservoir bag having a first opening may be in communication with the first port or there may be a venturi device may be in communication with a second opening of the reservoir bag. One or more gas sources may be in communication with the venturi device. A medicant device may be mounted in the second port wherein the medicant device having a mouthpiece that may be inserted and retracted relative to the mask chamber and a patients mouth. The medicant device having a medicant chamber formed therein.

Abstract: An apparatus and method for supplying a breathing gas for a respiration. The apparatus includes a reciprocating unit configured to receive an inspiration gas flow and adapted to control respiratory movements. The apparatus also includes a gas mixer for supplying a fresh gas flow. The apparatus also includes a breathing circuit configured to conduct an expiration gas flow to the reciprocating unit and to conduct the fresh gas flow from the gas mixer for the respiration and to conduct the gas flow from the reciprocating unit for an inspiration, the breathing circuit comprising a CO2 remover configured to remove carbon dioxide from the gas. The apparatus also includes a first bypass passage configured to permit bypassing the reciprocating unit and connecting the breathing circuit to the inspiration gas flow upstream from the reciprocating unit.

Abstract: In one embodiment, the invention provides a device for decreasing intracranial or intraocular pressures. The device comprises a housing having an inlet opening and an outlet opening that is adapted to be interfaced with a person's airway. The device further includes a valve system that is operable to regulate respiratory gas flows through the housing and into the person's lungs during spontaneous or artificial inspiration. The valve system assists in lowering intrathoracic pressures during each inspiration to repetitively lower pressures in the venous blood vessels that transport blood out of the head to thereby reduce intracranial or intraocular pressures.

Abstract: Described herein are nasal respiratory devices, in particular, nasal respiratory devices configured to achieve positive end-expiratory pressure (PEEP) in a subject wearing the device. PEEP devices may have a threshold pressure for opening during expiration. In some variations, these devices have a threshold pressure for closing during expiration.

Abstract: A portable semi-closed breathing apparatus for divers, having a circuit comprising a breathing bellows (1) connected to a pressure gas source (2) for the supply of breathing gas, a demand-controlled breathing valve (20), an actuator (4) for expansion and contraction of the breathing bellows (1) in step with the diver's breathing pattern, a means (5) for compensation of consumed oxygen, and a means (6) for removal of CO2 from the breathing gas. The actuator (4) is a cylinder/piston unit (9, 10) having a first chamber (11) connected to a source (13) for compensation gas, and a second chamber (12) connected to a valve means (5). During the diver's exhalation phase the valve means (5) is arranged to supply compensation gas to said second chamber (12) under control of the breathing valve (20), so that the breathing bellows (1) expands and absorbs exhaled gas from the diver.

Abstract: A combination of a bellows structure (12), volume restrictor, and pressure restrictor for use on a hand-operated resuscitator is provided to enable delivery of ventilation within specific volume and pressure limitations specified by the operator. The bellows structure (12) consistently provides predictable and uniform generation of gas flow for ventilation without regard to one or two-handed technique, hand placement, or hand size. The volume restrictor, primarily comprising of an inflow obturator (20), outflow obturator (22), and placement cam (34), enables the physician to specify a specific tidal volume to be delivered, which constitutes a volume-controlled cycling capability of the invention. The pressure restrictor, primarily comprising of an outer housing (40), stopper housings (41), and a stopper (50), enables the physician to specify a specific maximum airway pressure to be exposed to the patient, which constitutes a pressure-controlled cycling capability of the invention.

Abstract: An oxygen therapy face mask has a face engaging portion and a valve assembly connected thereto. The valve assembly has a first passage communicating with the interior of the face engaging portion from which gas can flow into the face engaging portion and into a patient's mouth and nose and which can also receive gas from a patient's mouth and nose and the interior of the face engaging portion. A first one-way valve is associated with the first passage and a second passage connectable to an oxygen reservoir bag and to an external source of pressurized oxygen. The first one-way valve is operable to permit flow of gas from the second passage to the first passage and to prevent flow of gas from the first passage to the second passage. A second one-way valve is associated with the first passage and is operable to permit flow of gas from the first passage to the external atmosphere and to prevent flow of gas from the external atmosphere to the first passage.

Abstract: An anaesthetic device has a manual ventilation bag, a mechanical ventilator and a user interface for setting an operating mode, including mechanical ventilation via the mechanical ventilator and manual ventilation via the manual ventilation bag, and for setting parameter values for the operating mode that has been set. The anaesthetic device further has a remote control for wireless transmission of commands to the user interface. The user interface is adapted to carry out the commands from the remote control only when the anaesthetic device is set for manual ventilation.

Abstract: A breathing gas feed assembly for the flight crew of an airplane comprises an emergency breathing mask and a stowage box for the mask. The box is adapted to receive the mask diagonally and it is closed by two doors hinged about respective hinge axes situated on two adjacent edges of the box.

Abstract: A self contained breathing apparatus (SCBA) served by a source of breathing gas with a mask and a demand regulator connected to the mask. The regulator has a flexible diaphragmatic member having a side exposed to pressure differentials to cause a valve mechanism to introduce breathing gas to the mask. An expanding and contracting member and a chamber fluidically connected to the diaphragm compensates for movement of the diaphragm while shielding the diaphragm from ambient contaminants.

Abstract: A device for manipulating intrathoracic pressures comprises a compressible bag structure, and an interface member coupled to the bag structure. A one way forward valve is coupled to the bag structure to permit respiratory gas to flow to the patient when the bag structure is compressed. A one way exit valve is employed to allow respiratory gases to be pulled from the person's airway upon decompression of the bag structure to produce a negative intrathoracic pressure.

Abstract: An apparatus (1) for administering a gas to a person or an animal, is provided with a chamber (9) for receiving a quantity of gas to be administered. The chamber is provided with a gas line (3) for supplying gas from a source to the chamber (9) and elements for pressurizing the gas in the chamber. The chamber (9) is connected to a breathing tube (5) for supplying pressurized gas from the chamber (9) to the person or the animal, wherein the breathing tube (5) connects to a discharge channel (26), for discharging gas exhaled by the person or the animal, via a valve (11), which restricts the flow of exhaled gas from the breathing tube (5) to the discharge channel (26) in order to build up gas pressure in the breathing tube (5) during exhalation.

Abstract: A combination of a bellows structure (12), volume restrictor, and pressure restrictor for use on a hand-operated resuscitator is provided to enable delivery of ventilation within specific volume and pressure limitations specified by the operator. The bellows structure (12) consistently provides predictable and uniform generation of gas flow for ventilation without regard to one or two-handed technique, hand placement, or hand size. The volume restrictor, primarily comprising of an inflow obturator (20), outflow obturator (22), and placement cam (34), enables the physician to specify a specific tidal volume to be delivered, which constitutes a volume-controlled cycling capability of the invention. The pressure restrictor, primarily comprising of an outer housing (40), stopper housings (41), and a stopper (50), enables the physician to specify a specific maximum airway pressure to be exposed to the patient, which constitutes a pressure-controlled cycling capability of the invention.

Abstract: In one embodiment, the invention provides a device for decreasing intracranial or intraocular pressures. The device comprises a housing having an inlet opening and an outlet opening that is adapted to be interfaced with a person's airway. The device further includes a valve system that is operable to regulate respiratory gas flows through the housing and into the person's lungs during spontaneous or artificial inspiration. The valve system assists in lowering intrathoracic pressures during each inspiration to repetitively lower pressures in the venous blood vessels that transport blood out of the head to thereby reduce intracranial or intraocular pressures.

Abstract: An apparatus and method for humidification of inspired gases, wherein the present invention utilizes moisture from condensed expiratory gases deposited within the outer expiratory tube of a conventional unilimb breathing circuit to humidify oxygen gas (or any other inspiratory gas) for subsequent patient inhalation, and wherein the oxygen gas may be directed through the outer expiratory tube via a novel reverse flow adapter coupled to an oxygen gas source. The present invention preferably functions to effectively eliminate prior art methods of oxygen gas humidification that depend upon the wasteful utilization of bottles of sterile water, corrugated tubing, nebulizer adapters and excess consumption of oxygen gas; thus, effectuating a cost savings for the patient and contributing to overall environmental conservation efforts.

Abstract: A device for manipulating intrathoracic pressures comprises a compressible bag structure, and an interface member coupled to the bag structure. A one way forward valve is coupled to the bag structure to permit respiratory gas to flow to the patient when the bag structure is compressed. A one way exit valve is employed to allow respiratory gases to be pulled from the person's airway upon decompression of the bag structure to produce a negative intrathoracic pressure.

Abstract: A respirator with a tidal volume-measuring device (6) between a respiration bag (8) and a patient adapter (2) provides accurate metering of the tidal volume. The device includes a first pressure-measuring device (4) and a breathing gas interruptor (5) in series sequence between the patient adapter (2) and the tidal volume-measuring device (6). A second pressure-measuring device (7) is provided between the tidal volume-measuring device (6) and the respiration bag (8). A control unit (20) is connected with the tidal volume-measuring device (6) and the pressure-measuring devices (4, 7) and sends control signals in such a way that when a predetermined tidal volume is reached, the breathing gas interrupter (5) is switched to the closed position, and that the closed position is eliminated when the pressure p2 measured with the second pressure-measuring means (7) has dropped below the pressure p1 determined with the first pressure-measuring means (4).

Abstract: A life support system has a semi-closed rebreather supplying oxygen for multiple users, such as high altitude parachutists. A first tank supplies oxygen to initially purge the system, and a second, larger tank supplies oxygen at prescribed amounts for the duration of a mission. Users are connected by hoses to an inlet hose manifold on a scrubber body of the rebreather. The inlet hose manifold has an inlet port boss to receive exhaled gas from each user and an overpressure valve vents excessive amounts of exhaled gas. A CO2 absorbent in the scrubber body scrubs CO2 from the exhaled gas. An outlet hose manifold is connected to the scrubber body and has an inlet fitting to supply oxygen and at least one outlet port boss to feed the oxygen and the CO2 scrubbed gas to the users. This reliable system is lighter-weight and smaller than contemporary systems.

Abstract: A combination of a bellows structure (12), volume restrictor, and pressure restrictor for use on a hand-operated resuscitator is provided to enable delivery of ventilation within specific volume and pressure limitations specified by the operator. The bellows structure (12) consistently provides predictable and uniform generation of gas flow for ventilation without regard to one or two-handed technique, hand placement, or hand size. The volume restrictor, primarily comprising of an inflow obturator (20), outflow obturator (22), and placement cam (34), enables the physician to specify a specific tidal volume to be delivered, which constitutes a volume-controlled cycling capability of the invention. The pressure restrictor, primarily comprising of an outer housing (40), stopper housings (41), and a stopper (50), enables the physician to specify a specific maximum airway pressure to be exposed to the patient, which constitutes a pressure-controlled cycling capability of the invention.

Abstract: A manual ventilation bag has a first opening and a second opening, a first soft bag connected to the first opening and a second soft bag connected to the second opening. The manual ventilation bag is advantageously used in combination with a breathing apparatus.

Abstract: The invention relates to a device for performing artificial respiration on a patient, comprising a container (1) which defines an inner volume relative to the ambient and has a first opening accommodating a valve arrangement (2, 14) which allows inflow of air or gases from the outer area to the inner area, and a second opening in connection with which there is provided a valve arrangement (3, 16) which allows outflow from the container and prevents inflow to the container through the second opening. An expansible means (7) is provided in the container and adapted to expand upon action from the outer area to displace air and/or other gases in the container (1) out through the second opening. This improves the certainty that oxygen and/or other gas finds its way to the patient's air passages.

Abstract: A manual inexsufflator including a standard mechanical ventilator, a medical suction unit, and a piston-like sliding valve mechanism which connects a patient ventilation interface with either the ventilator or the suction unit. By sliding the valve mechanism in and out the user selectively connects the patient to either the ventilator, for purposes of insufflation, or the suction unit, for purposes of exsufflation. The ventilator may generate expiratory positive airway pressure between inexsufflation cycles.

Abstract: A variable volume ratio compound counterlung is disclosed for use with a semi-closed circuit breathing apparatus. The compound counterlung generally comprises a flexible bag member disposed within and attached to an outer counterlung member. A pair of depth sensors are provided to vary the volume of said flexible bag member with changes in depth. The flexible bag member is driven by the outer counterlung to discharge gas stored within the flexible bag member depending on the diver's respiratory minute volume. The volumetric capacity of the inner counterlung is controlled by one or more ambient pressure sensing devices with an outer bellows-type counterlung that drives the inner counterlung's contents overboard with each breathing cycle.

Abstract: A device and method for movement and measurement of fluid volumes involves defining a fluid volume in a measuring chamber of a rotation vessel by at least first and second pistons movable within the measuring chamber, with the first and second pistons separating and indicating the volume of fluid moved into and out of the measuring chamber via flow-regulating valves. A holding means alternately holds the first and second pistons at fixed positions within the measuring chamber while the other piston rotates. A device and method of respiration involves a respirator including a plurality of flexible gas bags and a stiff gas tank with a first flexible gas bag positioned inside a second flexible gas bag and both gas bags being positioned inside the stiff tank. The respirator is connected to the device for the movement and measurement of fluid volumes via respirator valves.

Abstract: The Pediatric Prepatory and Induction Anesthesia Device (“PPIAD”) is designed to aid anesthetists in effectively administering anesthetic gas to young patients. The PPIAD has a toy-like appearance, which calms the fears of children. The PPIAD also incorporates toy-like devices such as whistles and balloons. When the PPIAD is given to children prior to treatment, the child can play with it as a toy. During this play time, the PPIAD actually teaches the child proper breathing for the administration of anesthetic gas because the whistle and balloon are only activated by deep breathing. Thus, when the child is administered anesthetic gas with the PPIAD, the application of anesthetic gas is much more effective. In addition, as the anesthetic gas is applied with the PPIAD, the child is encouraged to breathe deeply to activate the toy-like devices, enhancing the application of anesthetic gas to the child.