US 6,029,660 AGrant
Substance Delivery Apparatus
Issue Date:2000-02-29
•23 Claims
•7 Drawing Sheets
Abstract
A substance delivery apparatus (10) for use with a system (12) for supplying breathable gas to a human or animal. The apparatus includes a mechanism (22) to measure the pressure of the supplied breathable gas (22) to detect inhalation by the human or animal; and elements (54, 56, 58, 60) to deliver the substance (52) to the human or animal during inhalation at a pressure higher than the supplied pressure of the breathable gas. A method of delivering a substance (52) is also disclosed.
Metadata
Assignee
- ResMed Limited
Inventors
- Michel Calluaud
- Victor Yerbury
Application Information
Application Number:US 9891501
Filing Date:1997-12-12
Priority Date:1996-12-12
Art Unit:371
Classifications
IPC:
A61M 1500A61M 1610
Field of Search:
128200.21;203.12;203.16;203.22;203.25;204.18;204.22;204.23
Patent Drawings (7 sheets)
Description
Field of the Invention
The present invention relates to a substance delivery apparatus for use with a system for supplying breathable gas to a human or animal.
Background of the Invention
Treatment of Obstructive Sleep Apnea (OSA) with Continuous Positive Airway Pressure (CPAP) flow generator systems involves the continuous delivery of a breathable gas (generally air) pressurised above atmospheric pressure to a patient's airways via a conduit and a mask. CPAP pressures of 4 cm H.sub.2 O to 22 cm H.sub.2 O are typically used for treatment of OSA, depending on patient requirements. Treatment pressures for assisted ventilation can range of up to 32 cm H.sub.2 O and beyond, again depending on patient requirements.
For either the treatment of OSA or the application of assisted ventilation or similar, the pressure of the gas delivered to patients can be constant level, bi-level (in synchronism with patient infpiration) or auto setting in level. Throughout the specification reference to CPAP is intended to incorporate a reference to any one of, or combinations of, these forms of pressurised gas supply.
It is difficult to administer substances such as medicines to patients undergoing CPAP treatment without interrupting the treatment by removing the gas supply mask.
It is an object of the present invention to ameliorate the above disadvantage.
Summary of the Invention
In a first aspect, the present invention provides a substance delivery apparatus for use with a system for supply breathable gas to a human or animal, the apparatus including:
means to measure the pressure of the supplied breathable gas;
means to detect inhalation by the human or animal; and
means to deliver the substance to the human or animal during inhalation at a pressure higher than the supplied pressure of the breathable gas.
In a second aspect the invention provides a method of delivering a substance to a human or animal being supplied with breathable gas, the method includes the steps of:
measuring the pressure of the supplied breathable gas;
detecting inhalation by the human or animal; and
delivering the substance to the human or animal during inhalation at a pressure higher than the supplied pressure of the breathable gas.
The substance is preferably a medicinal substance and, desirably, in the form of a gas, mist, aerated suspension, jet, spray, gas mixture or the like.
The substance is preferably delivered to the respiratory system of the human or animal and, in particular, to the nasal airways.
The supplied breathable gas is preferably pressurised above atmospheric pressure.
The system for supplying the breathable gas preferably includes a pressurized gas flow generator in fluid communication with a mask worn by the human or animal via a flexible conduit, and the inhalation detection means includes an airflow sensor adapted to measure the volumetric flow rate of the breathable gas passing through the conduit and generate a first input signal indicative of the breathable gas flow rate. The term mask is herein understood to include facemasks, nosemasks, mouthmasks, apenditures in the vicinity of any of these masks and the like.
The first signal is preferably simplified by a first amplifier into a second input signal also indicative of the gas flow rate. A derivative of the first signal is also generated by a differentiating filter to determine the acceleration or deceleration of the gas, which is indicative of inhalation or exhalation respectively, and is represented by a third input signal.
When the airflow sensor is disposed downstream of the mask's vent to atmosphere then inhalation can be detected by sensing a reversal of the direction of the gas flow through the vent. Inhalation can also be detected by sensing an interruption of the gas flow.
The apparatus preferably also includes means to measure the volume of the substance to be delivered to the human or animal.
the pressure measuring means is preferably a pressure transducer connected to the conduit which is adapted to generate a fourth input signal indicative of the pressure of the gas in the conduit. The fourth input signal is preferably amplified by a second amplifier into a fifth input signal also indicative of the gas pressure.
The substance delivery means is preferably a positive displacement pump, most preferably a diaphragm pump. The diaphragm pump is desirably in fluid communication with a substance reservoir via a one-way valve adapted to allow the substance to only pass from the reservoir to the pump. The pump is preferably also in fluid communication with the gas supply conduit via a one-way valve adapted to allow the substance to only pass from the pump to the conduit.
The diaphragm of the pump is desirably displaced by a linear drive means which, in one form, may take the form of an electromagnet. In other forms, a rotary drive means such as an electric DC motor, an electric AC motor, a stepper motor, or a brushless motor are used with a rotary to linear converter interposed between the rotary drive means and the diaphragm pump.
The apparatus preferably also includes a first control system adapted to receive the second, third and fourth input signals. The control system preferably also includes input means adapted to allow the input of a predetermined sixth input indicative of the volume of the substance to be delivered and a predetermined seventh input signal indicative of the amount by which the pressure of the delivered substance should exceed the pressure of the supplied breathable gas. The first control system is preferably adapted to receive the second, third, fifth, sixth and seventh input signals to calculate and generate a first output signal indicative of the amount of displacement of the linear or rotary drive means and a second output signal indicative of the direction of the displacement required to produce negative or positive pumping pressure.
The first and second output signals are preferably sent to a second control system which converts them into third and fourth output signals indicative of drive means displacement and direction respectively, the third and fourth output signals being compatible with the linear or rotary drive means.
Preferably, the first and second output signals are sent to a second control system adapted to convert them into third and fourth output signals indicative of drive means displacement and direction respectively, the third and fourth output signals being compatible with the linear or rotary drive means.
The input and output signals can be analog, digital or the like.
The described embodiments have been developed primarily for use in delivering medicinal substances to patients using Continuous Positive Airway Pressure (CPAP) gas delivery systems in, for example, the treatment of Obstructive Sleep Apnea (OSA) or similar sleep disorder breathing conditions.
The invention will be described hereinafter with reference to these applications. However, it will be appreciated that the invention is not limited to this particular field of use. As examples, the invention may also be used in conjunction with suitable mask and gas delivery systems for other treatments such as assisted ventilation, assisted respiration or mechanical ventilation.
Brief Description of the Drawings
Preferred embodiments of the invention will now be described, by way of example only, with reference to the accompanying figures in which:
FIG. 1 is a schematic diagram of a substance delivery apparatus according to a first embodiment of the invention;
FIG. 2 is a schematic diagram of a substance delivery apparatus according to a second embodiment of the invention;
FIG. 3 is a schematic diagram of a substance delivery apparatus according to a third embodiment of the invention;
FIG. 4 is a schematic diagram of the apparatus of FIG. 3 during inhalation;
FIG. 5 is a schematic diagram of the apparatus shown in FIG. 3 during exhalation;
FIG. 6 is a partial schematic diagram of a substance delivery apparatus according to a fourth embodiment of the invention; and
FIGS. 7a, 7b and 7c are partial schematic diagrams of a substance delivery apparatus according to a fifth embodiment of the invention.
Description of the Preferred Embodiments
Referring firstly to FIG. 1, there is shown a first embodiment of a substance delivery apparatus 10 according to the invention. The apparatus 10 is used with a system, indicated generally at 12, for supplying air, indicated by arrow 14, to a human patient (not shown). The system 12 includes a pressurised gas flow generator 16 in fluid communication with a mask 18 via conduit 20.
The apparatus 10 includes a means to measure the pressure of the air 14 and to detect patient inhalation, in the form of an air flow sensor 22. The sensor 22 is interposed in the conduit 20 between the mask 18 and the pressurised gas flow generator 16. The airflow sensor 22, in the form of a fixed orifice, is connected to an electronic flow transducer 24. A variable orifice, venturi tube, Pitot tube or tubes bundle can also be used to sense airflow. The transducer 24 generates a first electrical input signal 26 indicative of the flow rate of the air 14 passing through the conduit 20 which is sent to a first flow signal processing amplifier and differentiating filter 28 which in turn generates second and third input signals 30 and 32 respectively.
The second input signal 30 is an amplified version of the first input signal 26. The third input signal 32 is the derivative of the first signal 26, with acceleration and deceleration being respectively indicative of inhalation or exhalation. When a patient inhales they apply suction to the air being delivered thus causing acceleration. Upon exhalation the air being delivered is obstructed by the exhaled air flowing in the opposite direction thus causing deceleration.
An air pressure transducer 34 is also connected to the conduit 20 and generates a fourth electrical input signal 36 indicative of the pressure in the conduit. The fourth signal 36 is delivered to an air pressure processing amplifier 38 which generates a fifth input signal 40 also indicative of the pressure in the conduit 20.
The second, third and fifth input signals 30, 32 and 40 are fed to a first control system 42. The first control system 42 also receives sixth and seventh predetermined input signals 44 and 46 from manual inputs 48 and 50 in the form of potentiometers accessible by a system operator. Variable resistors can also be used as the manual inputs. The sixth input signal 44 is indicative of the volume of substance to be delivered to the mask during each inhalation cycle of the patient. The seventh signal 46 is indicative of the amount by which the delivery pressure of the substance is to exceed the measured pressure of the air 14 in the conduit 20.
The means to deliver a substance 52 to the mask 18 includes a substance reservoir 54 connected by conduit 56 to diaphragm pump 58 having a flexible diaphragm 60. A one way valve 62 is interposed between the reservoir 54 and pump 58 and permits the substance 52 to only enter the pump 58. The pump 58 is in fluid communication with the conduit 20 by virtue of conduit branch 64 and one way valve 66 which allows the substance 52 to pass from the pump 58 to the conduit 20.
The stroke of the diaphragm 60 is controlled by an electromagnet drive means 68, in the form of a magnet 70 connected to the centre of the diaphragm 60 and surrounded by electrical windings 72. The drive means 68 are controlled by a second control system 74.
In response to receiving the second, third, fifth, sixth and seventh input signals, the first control system 42 generates first and second output signals 76 and 78, respectively indicative of the electromagnet displacement magnitude and direction. Displacement in the direction of arrow 80 draws the substance 52 into the pump 58. Displacement in the direction of arrow 82 causes the substance 52 to be pumped into the conduit branch 64 and thereafter the conduit 20. The output signals 76 and 78 are received by the second control system 74 which issues third and fourth output signals 84 and 86 respectively, which are compatible with the drive means 68. The third output signal 84 is indicative of the amount of displacement of the electromagnet 68 and the fourth signal 86 is indicative of the displacement direction.
In use, when the system is switched on, breathable air 14 is supplied by the gas flow generator 16 to the mask 18 via the conduit 20 so the patient may breathe.
As the patient inhales, an analogue to digital converter (not shown) in the control system 42 samples the air flow information of the first input signal 30 over a few breaths and stores it in a memory (not shown). The stored values are integrated with respect to the time of the inhalation portion of their respective breathing cycle. The integrated value is the tidal volume of each breath and is also stored in the memory. The stored values of the tidal volume are averaged over a small number of breaths to provide an average value of the tidal volume.
From the average value of the tidal volume and the setting of the manual input 48 the volume of the substance 52 (ie, the drug or gas) to be delivered for each breath is calculated. The control system 42 also calculates the magnitude of the current to be applied to the windings 72 of the diaphragm pump 58.
When the third input signal 32 indicates exhalation, the control systems 42 and 74 calculate and issue the third and fourth output signals 84 and 86 to the windings 72. The direction of the current applied to the windings 72 causes the magnet 70 and the diaphragm 60 to be displaced in the direction of the arrow 80 to the position shown by phantom line 87. This movement of the diaphragm 60 draws the substance 52 past the one way valve 63 and into the pump 58. The magnitude of the current applied to windings 72 is proportional to the displacement of the diaphragm 60 and also therefore the volume of gas drawn into the pump 58 which is delivered to the patient during the next inhalation cycle. At the end of the patient exhalation cycle the current applied to the windings 72 remains constant and the magnet 70 and diaphragm 60 remain as indicated by line 87.
When the third input signal 32 indicates inhalation, the control systems 42 and 74 reverse the current flowing into the windings 72, thereby displacing the magnet 70 and the diaphragm 60 in the direction indicated by the arrow 82 to the position shown by phantom line 89. This movement forces the substance 52 from the pump 58 through the one way valve 68 and conduit branch 64 into the mask 18.
The air pressure of the gas 14 in the conduit 20 is exceeded by the pressure of the substance pumped through conduit branch 64. The supply pressure of the substance 52 is calculated by the control system 42 and is the sum of the pressure measured by pressure transducer 34 in conduit 20 and the pressure increment set by manual input 48. The substance 52 is then delivered to the patient via the conduit 64 and the mask 18.
A second embodiment of the present invention is shown in FIG. 2, in which like reference numerals are used to indicate like features.
The first control system 42 of the second embodiment incorporates a microcontroller 92 and a linear position transducer 94 connected to the magnet 70 to provide a feedback signal 96 indicative of the position of the magnet 70 and the diaphragm 60, to which it is connected.
The two manual inputs 48 and 50 are replaced by a digital control panel 98 with: a three digit digital display 100; three push buttons: Mode 102, "+" 104, "-" 106; and three LEDs to indicate the mode selected: Volume 108, Delivery Pressure 110 and Run 112.
The operation of this system is generally similar to the description above except where indicated below.
Successive depression of the Mode push button 102 cycles through the three modes of operation: Volume, Delivery Pressure and Run.
When Volume or Delivery Pressure is selected, the digital display 100 indicates the current setting of that parameter. This value may be modified if required by operating either of the two push buttons "+" 104 or "-" 106.
When Run is selected, the parameters stored in the memory of the microcontroller 90 calculate the desired position of the magnet 70. This is then compared with the actual magnet position indicated by the linear position transducer 94. Any difference produces an error signal that is used to correct the position of the magnet 70 to the desired position.
A third embodiment of the present invention is shown in FIGS. 3 to 5, in which like reference numerals are again used to indicate like features. In this embodiment, the flow processing amplifier and differentiating filter 28 again detects the onset of inhalation by sensing a change in the rate of flow (ie. the acceleration or deceleration) of the gas flowing past the sensor 22.
The output signal 120 from the amplifier filter 28 of this embodiment is active when the onset of inhalation is detected and remains active for the duration of the inhalation portion of the breathing cycle. The output signal 120 from the amplifier filter 28 is not active for the exhalation portion of the breathing cycle.
The output signal 120 is supplied to a driver stage 122 and an inverter stage 124.
When the output signal 120 is active, during inhalation, the driver stage 122 is active and applied power to an electromagnetic winding 126 through a connection 128. When the output signal 120 is inactive, during exhalation, the inverter stage 124 supplies a drive signal 130 to a driver stage 132. The driver stage 132 is activated and supplies power to an electromagnetic winding 134 through a connection 136.
A magnetic core 138 is located within the electromagnetic winding 126. Similarly, a magnetic core 140 is located within the electromagnetic winding 134.
The magnetic core 138 and the magnetic core 140 are connected by a connecting rod 142 which is also connected to a sliding spool valve 144.
When the winding 126 is energised through the connection 128 the magnetic core 138 is displaced in the direction of arrow 150 and pulls with it the spool valve 144 and core 140.
When winding 134 is energised through connection 136 the magnetic core 140 is displaced in the direction of arrow 152 and pulls with it the spool valve 144 and core 138.
The body 154 of the spool valve 144 is connected to the gas flow generator 16 through a branch conduit 156 connected to the conduit 20.
A diaphragm motor 157 is comprised of housing halves 158 and 160 separated by a diaphragm 162 which defines cavities 164 and 166. A diaphragm pump 168 is comprised of housing halves 170 and 172 separated by a diaphragm 174 which defines cavities 176 and 178. The cavity 164 is connected to the spool valve body 154 by a conduit 182. The cavity 166 is connected to the spool valve body 154 by a conduit 184. The cavity 176 is open to atmosphere. The cavity 178 is connected to the source 54 of the substance 52 to be delivered by the conduit 56 and the one-way valve 62. The cavity 178 is also connected to the mask 18 by the conduit 64 and the one-way valve 66.
The motor diaphragm 162 and the pump diaphragm 174 are connected by a connecting rod 186. The connecting rod 186 passes through an air sealed bearing (not shown) between cavities 166 and 176.
An adjusting screw 188 is located on the top of housing halve 158.
With reference to FIG. 4, the operation of the apparatus will be described during the inahlation portion of the breathing cycle.
As the patient start to inhale, the second output signal 120 from the flow processing amplifier 28 is set to active and activates the driver stage 122. The inverter stage 124 is inactive and magnetic core 140 is free to move. The driver stage 122 supplies power to the electromagnetic winding 126 through connection 128. The magnetic core 138 is forced in the direction of the arrow 150 and with it the spool valve 144. The air 14 now flows from the branch conduit 156 into the spool valve body 154 and is diverted by the spool valve 144 through the conduit 182 and into the cavity 164. The pressure of the air entering the cavity 164 forces the motor diaphragm 162 in the direction of arrow 190 and with it the pump diaphragm 174. The cavity 178 is already filled with the substance 52 to be delivered to the mask 18.
The displacement of the pump diaphragm 174 into the cavity 178 increases the substance pressure, closes the one-way valve 62, opens the one-way valve 66, and forces the substance 52 into the conduit 64. The conduit 64 is in fluid communication with the conduit 20 and the mask 18 and the substance 52 is thereby delivered to the mask 18 and the patient.
With reference to FIG. 5, the operation of the apparatus will be described during the exhalation portion of the breathing cycle.
As the patient start to exhale, the second output signal 120 from the flow processing amplifier 28 is set to inactive. The driver stage 122 is not activated and power is not supplied to the electromagnetic winding 126 through connection 128. The magnetic core 138 is therefore free to move. As the output signal 120 from the flow processing amplifier 28 is not inactive, the inverter stage 124 turns its output signal 130 to active and activates the driver stage 132. The driver stage 132 supplies power to the electromagnetic winding 134 through the connection 136 and the magnetic core 140 is forced in the direction of the arrow 152 and with it the spool valve 144. The air flows from the branch conduit 156 into the spool valve body 154 and is diverted by the spool valve 144 through the conduit 184 into the cavity 166. The pressure of the air in the cavity 166 forces the motor diaphragm 162 in the direction of arrow 192 and with it the pump diaphragm 174. The displacement of pump diaphragm 174 into cavity 176 produces a vacuum in cavity 178, closes the one-way valve 66, opens the one-way valve 62, and draw the substance 52 through the conduit 56 into the cavity 178.
The movement of the motor diaphragm 162 and pump diaphragm 174 is limited by the adjusting screw 188. The setting of the screw 188 governs the maximum displacement of the motor diaphragm 162 and pump diaphragm 174 in direction of the arrow 192, therefore controlling the volume of the substance 52 able to be drawn into the cavity 178 for delivery to the patient during the next inhalation.
The pump diaphragm 174 is smaller in area than the motor diaphragm 162. Accordingly, a given pressure supplied to motor diaphragm 162 will produce a greater pressure from the pump diaphragm 174. Therefore, the pressure delivered by the pump diaphragm 174 into the conduit 64 and the patient mask 18 will always exceed the pressure of the gas in the conduit 20. The ratio between the pressure in the conduit 20 and the conduit 64 is proportional to the ratio between the area of the diaphragms 174 and 162.
In another embodiment (not shown) the motor diaphragm 157 is replaced by an electric motor, such as a stepper motor, controlled by a control system to provide more accurate delivery of the substance 52.
A fourth embodiment of the present invention is shown in FIG. 6, in which like reference numerals are again used to indicate like features. This embodiment is for use in conjunction with a bi-level CPAP flow generator (not shown) that delivers breathable gas at a relatively high treatment pressure to the mask during patient inhalation and at a relatively low treatment pressure during exhalation. The applicant markets such a bi-level system under the trade mark VPAP.
This embodiment includes a motor cylinder 200 having a slidable piston 202 which defines cavities 204 and 206. A pump cylinder 208 is also provided having a slidable piston 210 which defines cavities 212 and 214. The pistons 202 and 210 are connected by a connecting rod 216 which passes through an air sealed bearing 218.
The cavity 204 is connected to the conduit 20 by the branch conduit 156. The cavities 206 and 212 are open to atmosphere. The cavity 214 is connected to the source 54 of the substance 52 by the conduit 56 via the one-way valve 62. The cavity 214 is also connected to the mask 18 by the conduit 64 and the one-way valve 66.
The pistons are biased in the direction of arrow 220 by a spring 222.
The operation of the apparatus shown in FIG. 6 will now be described. During exhalation, relatively low pressure gas is passing through conduit 20 which generates only a small amount of force on the piston 202. The spring 222 overcomes this force and drives the pistons 202 and 210 in the direction of the arrow 220 thereby creating a vacuum in cavity 214. The vacuum draws the substance 52 past the one-way valve 62 and in the cavity 214.
During exhalation, relatively high pressure gas is passing through the conduit 20 which generates enough force on the piston 202 to overcome the spring 222 and drive the pistons 202 and 210 in the direction of arrow 224. This forces the substance in the cavity 214 past the one-way valve 66 and into the mask 18 via the conduit 64.
The surface area of the piston 202 is larger than that of the piston 210 and the pressure generated by the piston 210 will therefore exceed that applied to the piston 202. Accordingly, the substance delivery pressure will always exceed the pressure produced by the flow generator during the inhalation phase of the breathing cycle. The ratio between the surface areas of the pistons 202 and 210 is proportional to the ratio between the breathable gas pressure and the substance delivery pressure.
A fifth embodiment of the present invention is shown in FIGS. 7a, 7b and 7c. The fifth embodiment is essentially a modification of the fourth embodiment so it will work with a constant pressure flow generator.
The fifth embodiment includes a control valve 230 interposed between the conduit 20 and the motor cylinder 200. The valve 230 includes an inlet 232 connected to the conduit 20, a first outlet 234 connected to the cavity 204 and a second outlet 236 open to atmosphere.
The valve 232 is controlled by an electronic valve controller 238 which receives a signal 240 indicative of inhalation or exhalation, as discussed with respect to earlier embodiments.
When the signal 240 indicates inhalation, the controller 238 causes the valve 230 to move to the position indicated in FIG. 7b. In this position, the air 14 is diverted into the cavity 204 causing the pistons to move in the direction of the arrow 224 and the substance 52 to be pumped into the mask 18, as previously described.
When the signal 240 indicates exhalation, the controller 238 causes the valve 230 to move to the position shown in FIG. 7c. In this position, the air in the cavity 204 is vented to atmosphere as the pistons move in the direction of the arrow 220 under the influence of the spring 222. As previously described, this movement also causes the substance 52 to be drawn into the cavity 214.
The present invention, at least in preferred forms, provides a measured substance dose to a human or animal during inspiration only, thereby greatly reducing drug wastage.
The preferred apparatus also allows the substance to be delivered to the patient without interrupting CPAP, or similar treatment, or sleep, thereby increasing patient comfort and convenience.
The preferred apparatus also obviates the need for a patient to remember to take medicine.
The invention has been described with reference to specific examples. However, it will be appreciated by those skilled in the art that the invention may be embodied in many other forms.
Claims
We claim:
1. A substance delivery apparatus for use with a system for supplying breathable gas to a human or animal, said system including a pressurized gas flow generator in fluid communication with a mask worn by the human or animal via a flexible conduit, the apparatus including: an airflow sensor adapted to measure the volumetric flow rate of the breathable gas passing through the conduit and generate a first signal indicative of the breathable gas flow rate; a first amplifier to amplify the first input signal into a second input signal also indicative of the breathable gas flow rate; a differentiating filter to derive the first input signal into a third input signal indicative of acceleration or deceleration of the breathable gas and inhalation or exhalation respectively; a linear drive means; a positive displacement diaphragm pump displaced by the linear drive means to deliver the substance to the human or animal during inhalation at a pressure higher than the supplied pressure of the breathable gas; a pressure transducer connected to the conduit, the transducer being adapted to generate a fourth input signal indicative of the pressure of the supplied breathable gas; a second amplifier to amplify the fourth input signal into a fifth input signal also indicative of the breathable gas pressure; a first control system having input means adapted to allow the input of a predetermined sixth input signal indicative of the volume of the substance to be delivered and a predetermined seventh input signal indicative of the amount by which the pressure of the delivered substance is to exceed the pressure of the supplied breathable gas, wherein said first control system is adapted to receive the second, third, fifth, sixth and seventh input signals and calculate and generate a first output signal indicative of the amount of displacement of the linear drive means and a second output signal indicative of the direction of the displacement required to produce a negative or positive pumping pressure.
2. An apparatus as claimed in claim 1, wherein the substance is a medicinal substance.
3. An apparatus as claimed in claim 1, wherein the substance is in the form of a gas, mist, aerated suspension, jet, spray, gas mixture.
4. An apparatus as claimed in claim 1, wherein the substance is delivered to the respiratory system of the human or animal.
5. An apparatus as claimed in claim 4, wherein the substance is delivered to the nasal airways of the human or animal.
6. An apparatus as claimed in claim 1, further including means to measure the volume of the substance to be delivered to the human or animal.
7. An apparatus as claimed in claim 1, wherein the diaphragm pump is in fluid communication with a substance reservoir via a one-way valve adapted to allow the substance to only pass from the reservoir to the diaphragm pump.
8. An apparatus as claimed in claim 1, wherein the diaphragm pump is in fluid communication with the gas supply conduit via a one-way valve adapted to allow the substance to only pass from the diaphragm pump to the conduit.
9. An apparatus as claimed in claim 1, wherein the linear drive means is an electromagnet.
10. An apparatus as claimed in claim 1, wherein a negative pumping pressure draws the substance from the substance reservoir into the pump and a positive pumping pressure expels the substance from the pump to the conduit and so to the human or animal.
11. An apparatus as claimed in claim 10, wherein the first and second output signals are sent to a second control system adapted to convert them into third and fourth output signals indicative of drive means displacement and direction respectively, the third and fourth output signals being compatible with the linear drive means.
12. An apparatus as claimed in claim 11, wherein the input and output signals are analog or digital.
13. A method of delivering a substance to a human or animal being supplied with breathable gas, the method including the steps of: measuring the volumetric flow rate of the supplied breathable gas with an air flow sensor adapted to generate a first input signal indicative of the volumetric flow rate of the supplied breathable gas; amplifying the first input signal into a second input signal also indicative of the volumetric flow rate of the supplied breathable gas; differentiating the first input signal into a third input signal indicative of breathable gas acceleration or deceleration to detect inhalation or exhalation respectively; measuring the pressure of the supplied breathable gas with a pressure transducer adapted to generate a fourth input signal indicative of the pressure of the supplied breathable gas; amplifying the fourth input signal into a fifth input signal also indicative of the pressure of the supplied breathable gas; inputting the second, third, fourth, fifth input signals and a predetermined sixth input signal indicative of the volume of the substance to be delivered and a predetermined seventh input signal indicative of the amount by which the pressure of the delivered substance should exceed the pressure of the breathable gas into a first control system, the first control system adapted to generating a first output signal indicative of the amount of displacement of a linear drive means and a second output signal indicative of the direction of the displacement required to produce negative or positive pumping pressure; and delivering the substance to the human or animal during inhalation at a pressure higher than the supplied pressure of the breathable gas using a positive displacement diaphragm pump driven by the linear drive means.
14. A method as claimed in claim 13, wherein the substance is a medicinal substance.
15. A method as claimed in claim 14, wherein the substance is in the form of a gas, mist, aerated suspension, jet, spray, gas mixture.
16. A method as claimed in claim 13, wherein the substance is delivered to the respiratory system of the human or animal.
17. A method as claimed in claim 16, wherein the substance is delivered to the nasal airways of the human or animal.
18. A method as claimed in claim 13, wherein the supplied breathable gas is pressurised above atmospheric pressure.
19. A method as claimed in any one of claim 13, wherein the diaphragm pump is in fluid communication with a substance reservoir via a one-way valve adapted to allow the substance to only pass from the reservoir to the diaphragm pump.
20. A method as claimed in claim 13, wherein the diaphragm pump is in fluid communication with the gas supply conduit via a one-way valve adapted to allow the substance to only pass from the diaphragm pump to the conduit.
21. A method as claimed in claim 13, wherein the linear drive means is an electromagnet.
22. A method as claimed in claim 13, wherein a negative pumping pressure draws the substance from the substance reservoir into the pump and a positive pumping pressure expels the substance from the pump to the conduit and so to the human or animal.
23. A method as claimed in claim 22, further including the steps of inputting the first and second output signals into a second control system and the second control system adapted converting them into third and fourth output signals indicative of drive means displacement length and direction respectively, the third and fourth output signals being compatible with the linear or rotary drive means.
Patent Citations (439)
| Patent | Date | Inventor | Cited By |
|---|---|---|---|
| USRe35295 | 1996-07-01 | Estes et al. | |
| USRe35339 | 1996-10-01 | Rapoport | |
| USD188084 | 1960-05-01 | Garelick | |
| USD231803 | 1974-06-01 | Huddy | |
| USD250131 | 1978-10-01 | Lewis et al. | |
| USD262322 | 1981-12-01 | Mizerak | |
| USD293613 | 1988-01-01 | Wingler | |
| USD310431 | 1990-09-01 | Bellm | |
| USD323908 | 1992-02-01 | Hollister et al. | |
| USD334633 | 1993-04-01 | Rudolph | |
| USD362061 | 1995-09-01 | McGinnis et al. | |
| USD377089 | 1996-12-01 | Starr et al. | |
| US781516 | 1905-01-01 | Guthrie | |
| US812706 | 1906-02-01 | Warbasse | |
| US1081745 | 1913-12-01 | Johnston et al. | |
| US1192186 | 1916-07-01 | Greene | |
| US1653572 | 1927-12-01 | Jackson | |
| US1926027 | 1933-09-01 | Biggs | |
| US2123353 | 1938-07-01 | Catt | |
| US2248477 | 1941-07-01 | Lombard | |
| US2254854 | 1941-09-01 | O'Connell | |
| US2317608 | 1943-04-01 | Heidbrink | |
| US2371965 | 1945-03-01 | Lehmberg | |
| US2376871 | 1945-05-01 | Fink | |
| US2415846 | 1947-02-01 | Randall | |
| US2438058 | 1948-03-01 | Kincheloe | |
| US2578621 | 1951-12-01 | Yant | |
| US2904033 | 1959-09-01 | Shane | |
| US2931356 | 1960-04-01 | Schwarz | |
| US2939458 | 1960-06-01 | Lundquist | |
| US3013556 | 1961-12-01 | Galleher | |
| US3099985 | 1963-08-01 | Wilson et al. | |
| US3189027 | 1965-06-01 | Bartlett | |
| US3238943 | 1966-03-01 | Holley | |
| US3315674 | 1967-04-01 | Bloom et al. | |
| US3330273 | 1967-07-01 | Bennett | |
| US3362420 | 1968-01-01 | Blackburn et al. | |
| US3363833 | 1968-01-01 | Laerdal | |
| US3556122 | 1971-01-01 | Laerdal | |
| US3559638 | 1971-02-01 | Potter | |
| US3580051 | 1971-05-01 | Blevins | |
| US3595228 | 1971-07-01 | Simon et al. | |
| US3611801 | 1971-10-01 | Paine et al. | |
| US3700000 | 1972-10-01 | Hesse et al. | |
| US3720235 | 1973-03-01 | Schrock | |
| US3741208 | 1973-06-01 | Jonsson et al. | |
| US3783893 | 1974-01-01 | Davison | |
| US3796216 | 1974-03-01 | Schwarz | |
| US3799164 | 1974-03-01 | Rollins | |
| US3802417 | 1974-04-01 | Lang | |
| US3817246 | 1974-06-01 | Weigl | |
| US3882847 | 1975-05-01 | Jacobs | |
| US3903875 | 1975-09-01 | Hughes | |
| US3914994 | 1975-10-01 | Banner | |
| US3932054 | 1976-01-01 | McKelvey | |
| US3985467 | 1976-10-01 | Lefferson | |
| US3989037 | 1976-11-01 | Franetzki | |
| US3992598 | 1976-11-01 | Welsh et al. | |
| US3995661 | 1976-12-01 | Van Fossen | |
| US4006634 | 1977-02-01 | Billette et al. | |
| US4077404 | 1978-03-01 | Elam | |
| US4083245 | 1978-04-01 | Osborn | |
| US4109749 | 1978-08-01 | Sweet | |
| US4167185 | 1979-09-01 | Lewis | |
| US4226234 | 1980-10-01 | Gunderson | |
| US4245632 | 1981-01-01 | Houston | |
| US4249527 | 1981-02-01 | Ko et al. | |
| US4301833 | 1981-11-01 | Donald, III | |
| US4304229 | 1981-12-01 | Curtin | |
| US4312235 | 1982-01-01 | Daigle | |
| US4322594 | 1982-03-01 | Brisson | |
| US4328797 | 1982-05-01 | Rollins, III et al. | |
| US4347205 | 1982-08-01 | Stewart | |
| US4354488 | 1982-10-01 | Bartos | |
| US4381788 | 1983-05-01 | Douglas | |
| US4387722 | 1983-06-01 | Kearns | |
| US4396034 | 1983-08-01 | Cherniak | |
| US4402316 | 1983-09-01 | Gadberry | |
| US4412537 | 1983-11-01 | Tiger | |
| US4414982 | 1983-11-01 | Durkan | |
| US4433693 | 1984-02-01 | Hochstein | |
| US4448058 | 1984-05-01 | Jaffe et al. | |
| US4449525 | 1984-05-01 | White et al. | |
| US4467799 | 1984-08-01 | Steinberg | |
| US4499914 | 1985-02-01 | Schebler | |
| US4506666 | 1985-03-01 | Durkan | |
| US4522639 | 1985-06-01 | Ansite et al. | |
| US4530334 | 1985-07-01 | Pagdin | |
| US4550615 | 1985-11-01 | Grant | |
| US4550726 | 1985-11-01 | McEwen | |
| US4558710 | 1985-12-01 | Eichler | |
| US4570631 | 1986-02-01 | Durkan | |
| US4579114 | 1986-04-01 | Gray et al. | |
| US4580575 | 1986-04-01 | Birnbaum et al. | |
| US4595016 | 1986-06-01 | Fertig et al. | |
| US4602644 | 1986-07-01 | DiBenedetto et al. | |
| US4616647 | 1986-10-01 | McCreadie | |
| US4622964 | 1986-11-01 | Flynn | |
| US4630614 | 1986-12-01 | Atlas | |
| US4648396 | 1987-03-01 | Raemer | |
| US4648407 | 1987-03-01 | Sackner | |
| US4655213 | 1987-04-01 | Rapoport et al. | |
| US4665213 | 1987-05-01 | Rapoport et al. | |
| US4665570 | 1987-05-01 | Davis | |
| US4671271 | 1987-06-01 | Bishop et al. | |
| US4677975 | 1987-07-01 | Edgar et al. | |
| US4677977 | 1987-07-01 | Wilcox | |
| US4686974 | 1987-08-01 | Sato et al. | |
| US4686999 | 1987-08-01 | Snyder et al. | |
| US4738266 | 1988-04-01 | Thatcher | |
| US4739755 | 1988-04-01 | White et al. | |
| US4770169 | 1988-09-01 | Schmoegner et al. | |
| US4773411 | 1988-09-01 | Downs | |
| US4774941 | 1988-10-01 | Cook | |
| US4777963 | 1988-10-01 | McKenna | |
| US4782832 | 1988-11-01 | Trimble et al. | |
| US4795314 | 1989-01-01 | Prybella et al. | |
| US4799477 | 1989-01-01 | Lewis | |
| US4802485 | 1989-02-01 | Bowers et al. | |
| US4803471 | 1989-02-01 | Rowland | |
| US4809692 | 1989-03-01 | Nowacki et al. | |
| US4819629 | 1989-04-01 | Jonson | |
| US4819962 | 1990-01-01 | Jonson | |
| US4821713 | 1989-04-01 | Bauman | |
| US4823788 | 1989-04-01 | Smith et al. | |
| US4825802 | 1989-05-01 | Le Bec | |
| US4827922 | 1989-05-01 | Champain et al. | |
| US4838258 | 1989-06-01 | Dryden et al. | |
| US4841953 | 1989-06-01 | Dodrill | |
| US4844085 | 1989-07-01 | Gattinoni | |
| US4848334 | 1989-07-01 | Bellm | |
| US4848366 | 1989-07-01 | Aita et al. | |
| US4856506 | 1989-08-01 | Jinotti | |
| US4860766 | 1989-08-01 | Sackner | |
| US4870960 | 1989-10-01 | Hradek | |
| US4870963 | 1989-10-01 | Carter | |
| US4907584 | 1990-03-01 | McGinnis | |
| US4910806 | 1990-03-01 | Baker et al. | |
| US4913401 | 1990-04-01 | Handke | |
| US4915103 | 1990-04-01 | Visveshwara et al. | |
| US4919128 | 1990-04-01 | Kopala et al. | |
| US4938210 | 1990-07-01 | Shene | |
| US4938212 | 1990-07-01 | Snook et al. | |
| US4944310 | 1990-07-01 | Sullivan | |
| US4957107 | 1990-09-01 | Sipin | |
| US4960118 | 1990-10-01 | Pennock | |
| US4971051 | 1990-11-01 | Toffolon | |
| US4971065 | 1990-11-01 | Pearce | |
| US4972842 | 1990-11-01 | Korten et al. | |
| US4982738 | 1991-01-01 | Griebel | |
| US4986269 | 1991-01-01 | Hakkinen | |
| US4989599 | 1991-02-01 | Carter | |
| US5005568 | 1991-04-01 | Loescher et al. | |
| US5005571 | 1991-04-01 | Dietz | |
| US5009635 | 1991-04-01 | Scarberry | |
| US5024219 | 1991-07-01 | Dietz | |
| US5038776 | 1991-08-01 | Harrison et al. | |
| US5042473 | 1991-08-01 | Lewis | |
| US5042478 | 1991-08-01 | Kopala et al. | |
| US5046200 | 1991-09-01 | Feder | |
| US5052400 | 1991-10-01 | Dietz | |
| US5063922 | 1991-11-01 | Hakkinen | |
| US5065756 | 1991-11-01 | Rapoport | |
| US5069205 | 1991-12-01 | Urso | |
| US5105354 | 1992-04-01 | Nishimura | |
| US5109839 | 1992-05-01 | Blasdell et al. | |
| US5109840 | 1992-05-01 | Daleiden | |
| US5117819 | 1992-06-01 | Servidio et al. | |
| US5121745 | 1992-06-01 | Israel | |
| US5133347 | 1992-07-01 | Huennebeck | |
| US5134995 | 1992-08-01 | Gruenke et al. | |
| US5140982 | 1992-08-01 | Bauman | |
| US5148802 | 1992-09-01 | Sanders et al. | |
| US5159938 | 1992-11-01 | Laughlin | |
| US5161525 | 1992-11-01 | Kimm et al. | |
| US5161541 | 1992-11-01 | Bowman et al. | |
| US5170798 | 1992-12-01 | Riker | |
| US5174287 | 1992-12-01 | Kallok et al. | |
| US5178138 | 1993-01-01 | Walstrom et al. | |
| US5183983 | 1993-02-01 | Knop | |
| US5190048 | 1993-03-01 | Wilkinson | |
| US5195528 | 1993-03-01 | Hok | |
| US5199424 | 1993-04-01 | Sullivan et al. | |
| US5203343 | 1993-04-01 | Axe et al. | |
| US5230330 | 1993-07-01 | Price | |
| US5231979 | 1993-08-01 | Rose et al. | |
| US5231983 | 1993-08-01 | Matson et al. | |
| US5233978 | 1993-08-01 | Callaway | |
| US5239995 | 1993-08-01 | Estes et al. | |
| US5243971 | 1993-09-01 | Sullivan et al. | |
| US5245995 | 1993-09-01 | Sullivan et al. | |
| US5259373 | 1993-11-01 | Gruenke et al. | |
| US5265595 | 1993-11-01 | Rudolph | |
| US5271391 | 1993-12-01 | Graves | |
| US5279289 | 1994-01-01 | Kirk | |
| US5280784 | 1994-01-01 | Kohler | |
| US5293864 | 1994-03-01 | McFadden | |
| US5303700 | 1994-04-01 | Weismann et al. | |
| US5305787 | 1994-04-01 | Thygesen | |
| US5311862 | 1994-05-01 | Blasdell et al. | |
| US5311875 | 1994-05-01 | Stasz | |
| US5313937 | 1994-05-01 | Zdrojkowski | |
| US5322057 | 1994-06-01 | Raabe et al. | |
| US5335654 | 1994-08-01 | Rapoport | |
| US5343878 | 1994-09-01 | Scarberry et al. | |
| US5353788 | 1994-10-01 | Miles | |
| US5357951 | 1994-10-01 | Ratner | |
| US5360008 | 1994-11-01 | Campbell, Jr. | |
| US5372130 | 1994-12-01 | Stern et al. | |
| US5388571 | 1995-02-01 | Roberts et al. | |
| US5394882 | 1995-03-01 | Mawhinney | |
| US5398673 | 1995-03-01 | Lambert | |
| US5404871 | 1995-04-01 | Goodman et al. | |
| US5413111 | 1995-05-01 | Wilkinson | |
| US5419318 | 1995-05-01 | Tayebi | |
| US5429126 | 1995-07-01 | Bracken | |
| US5429683 | 1995-07-01 | Le Mitouard | |
| US5431158 | 1995-07-01 | Tirotta | |
| US5433193 | 1995-07-01 | Sanders et al. | |
| US5438981 | 1995-08-01 | Starr et al. | |
| US5441046 | 1995-08-01 | Starr et al. | |
| US5443061 | 1995-08-01 | Champain et al. | |
| US5443075 | 1995-08-01 | Holscher | |
| US5458137 | 1995-10-01 | Axe et al. | |
| US5477852 | 1995-12-01 | Landis et al. | |
| US5479920 | 1996-01-01 | Piper et al. | |
| US5483969 | 1996-01-01 | Testerman et al. | |
| US5488948 | 1996-02-01 | Dubruille et al. | |
| US5490502 | 1996-02-01 | Rapoport et al. | |
| US5492113 | 1996-02-01 | Estes et al. | |
| US5492116 | 1996-02-01 | Scarberry et al. | |
| US5501214 | 1996-03-01 | Sabo | |
| US5503146 | 1996-04-01 | Froehlich et al. | |
| US5507282 | 1996-04-01 | Younes | |
| US5509404 | 1996-04-01 | Lloyd et al. | |
| US5509904 | 1996-04-01 | Lloyd | |
| US5513631 | 1996-05-01 | McWilliams | |
| US5517983 | 1996-05-01 | Deighan et al. | |
| US5517986 | 1996-05-01 | Starr et al. | |
| US5522382 | 1996-06-01 | Sullivan et al. | |
| US5526805 | 1996-06-01 | Lutz et al. | |
| US5535738 | 1996-07-01 | Estes et al. | |
| US5535739 | 1996-07-01 | Rapoport et al. | |
| US5537997 | 1996-07-01 | Mechlenburg et al. | |
| US5538000 | 1996-07-01 | Rudolph | |
| US5540219 | 1996-07-01 | Mechlenburg et al. | |
| US5540220 | 1996-07-01 | Gropper | |
| US5540223 | 1996-07-01 | Starr et al. | |
| US5540733 | 1996-07-01 | Testerman et al. | |
| US5542128 | 1996-08-01 | Lomas | |
| US5546933 | 1996-08-01 | Rapoport et al. | |
| US5546952 | 1996-08-01 | Erickson | |
| US5549106 | 1996-08-01 | Gruenke et al. | |
| US5549655 | 1996-08-01 | Erickson | |
| US5551418 | 1996-09-01 | Estes et al. | |
| US5551419 | 1996-09-01 | Froehlich et al. | |
| US5558099 | 1996-09-01 | Bowman et al. | |
| US5560354 | 1996-10-01 | Berthon-Jones et al. | |
| US5567127 | 1996-10-01 | Wentz | |
| US5570682 | 1996-11-01 | Johnson | |
| US5570689 | 1996-11-01 | Starr et al. | |
| US5588439 | 1996-12-01 | Hollub | |
| US5592938 | 1997-01-01 | Scarberry et al. | |
| US5598838 | 1997-02-01 | Servidio et al. | |
| US5605151 | 1997-02-01 | Lynn | |
| US5608647 | 1997-03-01 | Rubsamen et al. | |
| US5617846 | 1997-04-01 | Graetz et al. | |
| US5630411 | 1997-05-01 | Holscher | |
| US5632269 | 1997-05-01 | Zdrojkowski | |
| US5642730 | 1997-07-01 | Baran | |
| US5645053 | 1997-07-01 | Remmers et al. | |
| US5645054 | 1997-07-01 | Cotner et al. | |
| US5647351 | 1997-07-01 | Weismann et al. | |
| US5647355 | 1997-07-01 | Starr et al. | |
| US5647357 | 1997-07-01 | Barnett et al. | |
| US5649532 | 1997-07-01 | Oren | |
| US5649533 | 1997-07-01 | Griffiths | |
| US5655520 | 1997-08-01 | Howe et al. | |
| US5655522 | 1997-08-01 | Mechlenburg et al. | |
| US5655527 | 1997-08-01 | Scarberry et al. | |
| US5657493 | 1997-08-01 | Ferrero et al. | |
| US5660171 | 1997-08-01 | Kimm et al. | |
| US5662101 | 1997-09-01 | Ogden et al. | |
| US5666946 | 1997-09-01 | Langenback | |
| US5682878 | 1997-11-01 | Ogden | |
| US5685296 | 1997-11-01 | Zdrojkowski et al. | |
| US5687715 | 1997-11-01 | Landis et al. | |
| US5701883 | 1997-12-01 | Hete et al. | |
| US5704345 | 1998-01-01 | Berthon-Jones | |
| US5715812 | 1998-02-01 | Deighan et al. | |
| US5715814 | 1998-02-01 | Ebers | |
| US5730121 | 1998-03-01 | Hawkins | |
| US5746201 | 1998-05-01 | Kidd | |
| US5794615 | 1998-08-01 | Estes | |
| US5797852 | 1998-08-01 | Karakasoglu et al. | |
| US5803066 | 1998-09-01 | Rapoport et al. | |
| US5813423 | 1998-09-01 | Kirchgeorg | |
| US5823187 | 1998-10-01 | Estes et al. | |
| US5832918 | 1998-11-01 | Pantino | |
| US5845636 | 1998-12-01 | Gruenke et al. | |
| AUXB-59270/90 | 1990-12-01 | ||
| AUXA-62221/90 | 1991-03-01 | ||
| AUX91/77110 | 1991-11-01 | ||
| AUXA-33877/93 | 1993-04-01 | ||
| AUXA-38508/93 | 1993-07-01 | ||
| AUXA-48748/93 | 1993-09-01 | ||
| AUXA-4874893 | 1993-12-01 | ||
| AUXA-52628/93 | 1994-07-01 | ||
| AUX94/64816 | 1994-12-01 | ||
| AUXB79174/94 | 1995-06-01 | ||
| AUX95/16178 | 1995-07-01 | ||
| AUXA-34471/95 | 1996-02-01 | ||
| AUXA32914/95 | 1996-02-01 | ||
| AUX9459430 | 1996-02-01 | ||
| AUXA-40711-95 | 1996-04-01 | ||
| AUXB34354/95 | 1996-05-01 | ||
| AUXA39130/95 | 1996-06-01 | ||
| AUXA41018/97 | 1998-04-01 | ||
| AUXA89312/98 | 1999-01-01 | ||
| EPX62166A2 | 1982-10-01 | ||
| EPX66451A1 | 1982-12-01 | ||
| EPX88761 | 1983-09-01 | ||
| EPX164500A2 | 1985-03-01 | ||
| EPX178925A2 | 1986-04-01 | ||
| EPX185980 | 1986-07-01 | ||
| EPX252052A1 | 1988-01-01 | ||
| EPX872643A2 | 1988-03-01 | ||
| EPX264772A1 | 1988-04-01 | ||
| EPX298367A2 | 1989-01-01 | ||
| EPX425092A1 | 1989-09-01 | ||
| EPX452001A2 | 1990-03-01 | ||
| EPX388525A1 | 1990-09-01 | ||
| EPX427474A2 | 1991-05-01 | ||
| EPX462701A1 | 1991-12-01 | ||
| EPX461281A1 | 1991-12-01 | ||
| EPX481459A1 | 1992-04-01 | ||
| EPX481459A1 | 1992-04-01 | ||
| EPX549299A2 | 1993-06-01 | ||
| EPX606687A2 | 1994-07-01 | ||
| EPX608684A1 | 1994-08-01 | ||
| EPX651971A1 | 1995-05-01 | ||
| EPX656216A2 | 1995-06-01 | ||
| EPX697225 | 1995-07-01 | ||
| EPX178925A2 | 1996-04-01 | ||
| EPX714670A2 | 1996-06-01 | ||
| EPX747078A2 | 1996-12-01 | ||
| EPX765631A2 | 1997-04-01 | ||
| EPX788805A2 | 1997-08-01 | ||
| EPX821978 | 1998-02-01 | ||
| EPX839545A1 | 1998-05-01 | ||
| FRX2682042A1 | 1993-04-01 | ||
| DEX3537507A1 | 1987-04-01 | ||
| DEX29810846U1 | 1998-08-01 | ||
| JPX60-212607 | 1985-10-01 | ||
| JPX62-103297 | 1987-04-01 | ||
| JPX2-173397 | 1988-12-01 | ||
| JPX8019610 | 1996-01-01 | ||
| SEX1710064A1 | 1992-02-01 | ||
| SEXSE467041 | 1992-05-01 | ||
| GBX1395391 | 1975-05-01 | ||
| GBX1432572 | 1976-04-01 | ||
| GBX1444053 | 1976-07-01 | ||
| GBX1467828 | 1977-03-01 | ||
| GBX1583273 | 1981-01-01 | ||
| GBX2077444 | 1981-12-01 | ||
| GBX2145335 | 1985-03-01 | ||
| GBX2147506 | 1985-05-01 | ||
| GBX2147506 | 1985-05-01 | ||
| GBX3402603A1 | 1985-08-01 | ||
| GBX2164569 | 1986-03-01 | ||
| GBX2166871 | 1986-05-01 | ||
| GBX2205167 | 1988-11-01 | ||
| GBX2221302 | 1990-01-01 | ||
| GBX2254700 | 1992-10-01 | ||
| GBX2261290 | 1993-05-01 | ||
| GBX2267648 | 1993-12-01 | ||
| GBX2271811 | 1994-04-01 | ||
| GBX2294400 | 1996-05-01 | ||
| WOXWO80/01044 | 1980-05-01 | ||
| WOXWO82/03326 | 1982-10-01 | ||
| WOXWO82/03548 | 1982-10-01 | ||
| WOXWO86/05965 | 1986-10-01 | ||
| WOXWO86/06969 | 1986-12-01 | ||
| WOXWO87/01950 | 1987-04-01 | ||
| WOXWO87/02577 | 1987-05-01 | ||
| WOXWO88/10108 | 1988-12-01 | ||
| WOXWO90/14121 | 1990-01-01 | ||
| WOXWO91/03277 | 1991-03-01 | ||
| WOXWO91/12051 | 1991-08-01 | ||
| WOXWO92/11054 | 1992-07-01 | ||
| WOXWO92/15353 | 1992-09-01 | ||
| WOXWO92/20395 | 1992-11-01 | ||
| WOXWO92/22244 | 1992-12-01 | ||
| WOXWO93/01854 | 1993-02-01 | ||
| WOXWO93/09834 | 1993-05-01 | ||
| WOXWO93/08857 | 1993-05-01 | ||
| WOXWO93/21982 | 1993-11-01 | ||
| WOXWO93/24169 | 1993-12-01 | ||
| WOXWO94/02190 | 1994-02-01 | ||
| WOXWO94/04071 | 1994-03-01 | ||
| WOXWO94/16759 | 1994-08-01 | ||
| WOXWO94/20018 | 1994-09-01 | ||
| WOXWO94/20051 | 1994-09-01 | ||
| WOXWO94/22517 | 1994-10-01 | ||
| WOXWO94/23780 | 1994-10-01 | ||
| WOXWO95/02428 | 1995-01-01 | ||
| WOXWO95/32016 | 1995-11-01 | ||
| WOXWO96/17643 | 1996-06-01 | ||
| WOXWO96/16688 | 1996-06-01 | ||
| WOXWO96/25983 | 1996-08-01 | ||
| WOXWO96/32055 | 1996-10-01 | ||
| WOXWO96/36279 | 1996-11-01 | ||
| WOXWO96/40337 | 1996-12-01 | ||
| WOXWO96/41571 | 1996-12-01 | ||
| WOXWO96/39206 | 1996-12-01 | ||
| WOXWO97/05824 | 1997-02-01 | ||
| WOXWO97/10019 | 1997-03-01 | ||
| WOXWO97/07847 | 1997-03-01 | ||
| WOXWO97/15343 | 1997-05-01 | ||
| WOXWO97/18752 | 1997-05-01 | ||
| WOXWO97/20499 | 1997-06-01 | ||
| WOXWO97/22377 | 1997-06-01 | ||
| WOXWO97/28838 | 1997-08-01 | ||
| WOXWO97/41812 | 1997-11-01 | ||
| WOXWO97/41911 | 1997-11-01 | ||
| WOXWO98/06449 | 1998-02-01 | ||
| WOXWO98/11930 | 1998-03-01 | ||
| WOXWO98/18514 | 1998-05-01 | ||
| WOXWO98/24499 | 1998-06-01 | ||
| WOXWO98/25662 | 1998-06-01 | ||
| WOXWO98/26829 | 1998-06-01 | ||
| WOXWO98/26830 | 1998-06-01 | ||
| WOXWO98/36245 | 1998-08-01 | ||
| WOXWO98/36338 | 1998-08-01 | ||
| WOXWO98/35715 | 1998-08-01 | ||
| WOXWO98/33433 | 1998-08-01 | ||
| WOXWO98/47554 | 1998-10-01 | ||
| WOXWO98/48878 | 1998-11-01 | ||
| WOXWO98/57691 | 1998-12-01 |
Non-Patent Literature (54)
- Mark Kantrowitz, Erik Horskotte and Cliff Joslyn; "Answers to Frequently Asked Questions about Fuzzy Logic and Fuzzy Expert Systems" Version 1.24 last Modified 20 2 96.
- Mask 1 Photographs, Respironics Inc., Reusable Full Mask (small) Part #452033 Lot #951108.
- Mask 2 Photographs, Puritan--Bennett, Adam Curcuit, Shell Part #231700. Swivel Part #616329-00, Pillows (medium) Part #616324.
- Mask 3, Photographs, DeVilbiss Healthcare Inc., DeVilbiss Seal-Ring and CPAP Mask Kit (medium), Part 73510-669.
- Mask 4 Photographs, Respironics Inc., Monarch Mini Mask with Pressure Port. Part # 572004, Monarch Headgear, Part #572011.
- Mask 5 Photographs, Healthdyne Technologies, Nasal CPAP Mask (medium narrow), Part #702510.
- Mask 6 Photographs, Healthdyne Technologies, Soft Series Nasal CPAP Mask, Part #702020.
- Mask 7 Photographs, DeVilbiss Healthcare Inc., Small Mask and Seal Rings, Part #73510-668.
- Mask 8 Photographs, Respironics Inc., Reusable Contour Mask (medium), Part #302180.
- Mask 9 Photographs, Healthdyne Technologies, Healthdyne Large Headgear.
- Mask 10 Photographs, Respironics Inc., Soft Cap (medium), Part #302142.
- Mask 11 Photographs, Weinmann: Hamburg, Nasalmaskensystem mit Schalldampfer (medium), Part #WN 23105.
- Mask 12 Photographs, Life Care.
- Mask 13 Photographs, Healthdyne Technologies.
- Mask 14 Photograph, King System.
- Mask 15 Photographs, Respironics Inc., Paediatric Mask.
- Mask 16 Photographs, Hans Rudolph Inc., Hans Rudolph Silicone Rubber Face Mask/8900.
- New! Breas PV 100 CPAP First Class Quality and Function. At the right Price; Jul. 4, 1998, pp. 1-2.
- PV 101 Bi Level CPAP and PV 102 Bi-Level Time; pp. 1-3.
- Puritan Bennett; Companion 318 Nasal CPAP System; May 1993.
- Nellcor Puritan Bennett; Announcing the Goodnight 314 and GoodKnight 318 Nasal CPAP Systems.
- Puritan Bennett; Clean, Quiet, and Comfortable . . . The Companion's 515 Nasal CPAP System; Jun. 1988.
- DeVilbiss Night Guard Nasal CPAP for the Treatment of Obstructive Sleep Apnea.
- Sunrise; DeVilbiss Horizon LT 8001 Nasal CPAP Therapy Small in Size, big features.
- Devilbiss; Revitalizer Soft Start; The Facts Speak for Themselves.
- Tranquility; Performance CPAP Advantage.
- Healthdyne International; Tranquility Plus.
- Respironics Inc.; Respironics' Solo CPAP System Provides Simplified OSA Therapy at an Outstanding value; Sep. 19, 1996.
- Respironics Inc.; The First Family of OSA Therapy; 1991.
- Fisher & Paykel Healthcare; HC200 Series Nasal CPAP Blower & Heated Humidifier.
- Puritan Bennett; 515a Part of Our Blueprint for the Future; Mar. 1990.
- Puritan Bennett; Companion 320 I/E Bi-Level Respiratory System; Apr. 1993.
- ResMed; Sullivan VPAP II & II ST.
- ResMed; The Sullivan V Family of CPAP Systems.
- ResMed; The AutoSet Portable II.
- ResMed; Sullivan Nasal CPAP System.
- ResMed; The Sullivan IIID.
- ResMed; The Sullivan Comfort.
- DeVilbiss a Division of Sunrise Medical; Expand your Horizons With The Horizons.
- Healthdyne Technologies; Home Health Care Dealer; The Journal of Home Medical Equipment and Services/Supplier; Nov. and Dec. 1997.
- Healthdyne International; Tranquility Quest, The Compact CPAP for Greater patient comfort.
- AirStep; Medical Products . . . Stand the Test of Time.
- MAP Medical Progress for Physician und Patient; The Gentle Therapy for Sleep-Related Breathing Disorders.
- Taema; Ventilation CP 90.
- DPAP; Breath, by breath, by breath.
- Lifecare; Smallest. Quietest. Smartest.
- Lifecare; Quiet CPAP Sytem for Maximum Compliance; 1991.
- Lifecare; Software Nasal Mask, Custom Nasal Masks; 1991.
- Nidek Medical; Silenzio.
- Weinmann; Just to Fell Well, Sensitive Sleep Apnoea Therapy with Somnotron 3 and Somno-Mask System.
- Respironics Inc.; Aria CPAP System.
- Respironics Inc.; SleepEasy III A New Dawn in Patient Compliance.
- Respironics Inc.; Mulitple Choice REMstar Choice Nasal CPAP System.
- MaxII nCPAP and Moritz II Bi-Level Brochure.