This patent is directed to a pump controller that is configured to and control method that includes determination of compliance in an associated pump or pump system, and optionally is directed to such a pump controller and control method that integrates temperature measurements at various positions in the system.
Pump controllers and control methods are subject to the sensitivity of associated measuring instruments (e.g., sensors) and to factors such as compliance in the associated infusion or pump system. Compliance may be referred to as a measurement of the degree to which a component deforms under force. When referencing a pump, one may refer to the compliance of the structures of the pump as well as the compliance of the associated infusion or administration set (tubing). The compliance of the pump and the infusion set may affect the ability of the measuring instruments to provide signals that are fully representative of the conditions within the pump and/or set.
Pump controllers and control methods that rely on gas law calculations may be subject to additional factors as well. For example, the ideal gas law equation includes not only pressure and volume, but temperature as well. As such, a pump controller or control method that relies on the ideal gas law equation, but does not take into account temperature variations, may experience unaccounted for variations because of temperature fluctuations in the system.
It would be advantageous to provide a pump controller and pump control method that includes the compliance of the associated pump and/or infusion set in its determinations of fluid movement. It also would be advantageous, either separately or in combination with the preceding, to provide a pump controller and pump control method that includes temperatures within the associated pump and/or its infusion set in its determinations of fluid movement.
According to one aspect of the present disclosure, a method includes applying a positive gauge pressure from a common volume to a diaphragm in a pumping chamber to empty a fluid from the pumping chamber, measuring the temperature and pressure of the common volume and the pumping chamber, wherein optionally the pressure is measured using a pressure sensor and the temperature is measured using a temperature sensor that measures the temperature of the pressure sensor, and calculating a volume of fluid in the pumping chamber based on ideal gas law and the pressure and temperature measurements.
According to another aspect of the present disclosure, an infusion system includes a common volume, a pumping chamber including a diaphragm, a fluid inlet coupled to a fluid source, and a fluid outlet, the pumping chamber coupled to the common volume, a pressure sensor and a temperature sensor associated with each of the common volume and the pumping chamber, and a controller coupled to the pressure sensors and temperature sensors. The controller is configured to apply a positive gauge pressure from a common volume to the diaphragm in the pumping chamber to empty a fluid from the pumping chamber, measure the temperature and pressure of the common volume and the pumping chamber, wherein the pressure is measured using a pressure sensor and the temperature is measured optionally using a temperature sensor that measures the temperature of the pressure sensor, and calculate a volume of fluid in the pumping chamber based on ideal gas law and the pressure and temperature measurements.
According to a further aspect of the present disclosure, a method including applying a negative gauge pressure from a common volume to a diaphragm in a pumping chamber to fill the pumping chamber with a fluid from a fluid source, applying the negative gauge pressure to the diaphragm with the pumping chamber filled with the fluid to define a negative full-volume state, and measuring temperature and pressure of the common volume and the pumping chamber during the negative full-volume state, and applying a positive gauge pressure to the diaphragm with the pumping chamber filled with the fluid to define a positive full-volume state, and measuring the temperature and pressure of the common volume and the pumping chamber during the positive full-volume state. The method also includes applying the positive gauge pressure to the diaphragm with the pumping chamber empty to define an empty-volume state, and measuring the temperature and pressure of the common volume and the pumping chamber during the empty-volume state, and calculating a volume of fluid in the pumping chamber when the chamber is not full or empty based on the pressure and temperature measurements taken during the negative full-volume state, the positive full-volume state, and the empty-volume state.
According to yet another aspect of the present disclosure, an infusion system includes a common volume, a pumping chamber including a diaphragm, a fluid inlet coupled to a fluid source, and a fluid outlet, the pumping chamber coupled to the common volume, a pressure sensor and a temperature sensor associated with each of the common volume and the pumping chamber, and a controller coupled to the pressure sensors and temperature sensors. The controller is configured to apply a negative gauge pressure from the common volume to the diaphragm in the pumping chamber to fill the pumping chamber with a fluid from the fluid source, apply the negative gauge pressure to the diaphragm with the pumping chamber filled with the fluid to define a negative full-volume state, and measure temperature and pressure of the common volume and the pumping chamber during the negative full-volume state, apply a positive gauge pressure to the diaphragm with the pumping chamber filled with the fluid to define a positive full-volume state, and measure the temperature and pressure of the common volume and the pumping chamber during the positive full-volume state, and apply the positive gauge pressure to the diaphragm with the pumping chamber empty to define an empty-volume state, and measure the temperature and pressure of the common volume and the pumping chamber during the empty-volume state. The controller is also configured to calculate a volume of fluid in the pumping chamber when the chamber is not full or empty based on the pressure and temperature measurements taken during the negative full-volume state, the positive full-volume state, and the empty-volume state.
It is believed that the disclosure will be more fully understood from the following description taken in conjunction with the accompanying drawings. Some of the figures may have been simplified by the omission of selected elements for the purpose of more clearly showing other elements. Such omissions of elements in some figures are not necessarily indicative of the presence or absence of particular elements in any of the exemplary embodiments, except as may be explicitly delineated in the corresponding written description. None of the drawings is necessarily to scale.
The pumping chamber 110 has a wall 112 that encloses, at least partially, a volume 114. Supported within the volume 114 is a flexible diaphragm (or membrane) 116 that divides the volume 114 into at least two spaces, first and second spaces 118, 120. According to some embodiments, the volume 114 is bifurcated by the flexible diaphragm 116. In such an embodiment, the first and second spaces 118, 120 are roughly of equal size (or volume). An example of such a chamber may be found for example, in U.S. patent Ser. No. 10/156,231, which is incorporated by reference in its entirety herein.
The first space 118 is connected to a pumping system to move a fluid, for example a gas such as air, into and out of the first space 118. The first space 118 may be referred herein to as the air side of the chamber 110. The second space 120 is connected to a fluid source via at least a valve Vi, and to a recipient via at least a valve Vo. The fluid source may be, for example, a container of a medical fluid such as a medication or a nutritional fluid, which may also be referred to as a liquid infusate, and the recipient may be, for example, a patient or another container. The second space 120 may be referred to herein as the fluid side of the chamber 110.
The chamber 110 may be defined by structures of an administrative set, which may be disposable. The administrative set may include, for example, a cassette with the chamber 110 defined by structures of the cassette. Non-limiting examples of such a cassette may be found in U.S. Pat. Nos. 9,433,734, 9,849,231, 9,616,172, 10010686, 10444770, 10881785, 11285262, which patents are incorporated by reference in their entirety herein. As such, the structures of the chamber 110 may be referred to as the set side, although it will be recognized that this is for ease of reference as the structures of the chamber should not be limited only to an embodiment where the chamber is defined by a disposable cassette of an administration set.
The first space 118 may be coupled (i.e., directly or indirectly connected) to reusable pumping equipment that moves the air into and out of the first space 118. Such a system is illustrated in part in
In a broad sense, one may refer to an air side volume to that includes a relatively fixed volume on a pump side and a variable volume on the set side (up to the diaphragm 116). Likewise, one may refer to a fluid side or liquid side volume (on the other side of the diaphragm 116). The fluid side volume varies as the medical fluid or liquid infusate is delivered or infused.
According to a method of operating the system 100, a negative gauge pressure and a positive gauge pressure are applied cyclically (via the common volume 130) to the first space 118. When a negative gauge pressure is applied to the space 118, the size of the space 120 expands and draws fluid from the fluid source into the pumping chamber 110. When a positive gauge pressure is applied to the space 118, the size of the space 120 decreases expelling fluid from the pumping chamber 110 to the recipient.
The total volume of the pumping chamber 110 is substantially constant regardless of the position of the diaphragm 116. As such, if the volume of air in the first space 118 can be determined, one is able to determine in a general sense the corresponding volume of fluid in the second space 120. For example, if the total volume is Vtotal and the volume of the first space 118 is Vair, the volume of fluid in the second space 120 can be determined by subtracting Vair from Vtotal. Moreover, by determining the volume of fluid in the second space 120 at different times, the delivery or infusion rate of the medical fluid may be determined.
It is desirable to improve the precision of the determination of the volume of air in the first space 118, and thereby improve the precision of the determination of the volume of fluid delivered and the determination of the delivery or infusion rate. As such, it is desirable to take into consideration the compliance of the system 100, that is how easily the components of the system 100 deform under force. For example, elastic compliance and deformation may occur because of the pressure changes in the pumping chamber 110, both on the pump side and the set side. In addition, it may be desirable to improve the precision of the determination of the volume of fluid on the fluid side by taking into consideration fluid side air bubbles that may existing the second space 120.
It is believed that the precision of the volume determinations may be improved by performing two different sets of measurements with the pumping chamber 110 in the full state, i.e., with the second space 120 filled with fluid, and a set of measurements taken with the pumping chamber 110 in the empty state, i.e., with the second space 120 emptied of fluid either by delivery downstream or regurgitation upstream. The former measurements (full-volume measurements) are conducted with the second space 120 filled with fluid and with a negative gauge pressure applied to the first space 118 (
Once these full- and empty-volume measurements have been performed, the information may be combined with pressure and temperature measurements taken while positive gauge pressure is applied to the first space 118 to determine intermediate volumes delivered or infused. The intermediate volumes may be combined with timing information to determined flow rates, which information can be used to vary the operation of the pumping chamber to achieve a desired flow rate.
Having discussed the system 100, pumping chamber 110 and other equipment (e.g., common volume 130) in a general sense, a specific embodiment is now discussed with reference to
As illustrated in
As mentioned above, the infusion system 100 may be operated to infuse the medical fluid (or liquid infusate) according to one or more pump cycles in accordance with a non-limiting exemplary embodiment. A pump cycle may be defined as at least partially moving the membrane 116 of the pumping chamber 110 from a first extreme (e.g., with the medical fluid expelled from the second space 120, an “empty” state) to a second extreme (e.g., with the second space 120 filled with medical fluid, a “full” state), and from the second extreme back to the first extreme. To do this, the infusion system 100 includes equipment in addition to the common volume 130 to move air into and out of the first space 118 of the pumping chamber 110.
As illustrated in
The tanks 142, 144 are coupled to the common volume (tank) 130 via valves V1 and V4. When valve V1 is opened, the pressure in the negative tank 142 is applied to the common volume 130. When the valve V4 is opened, the pressure in the positive tank 144 is applied to the common volume 130. It is also possible to vent the common volume 130 to ambient pressure via valve V3, as may be useful at different times during a pump cycle as explained below. As mentioned above, the common volume 130 is coupled to the first space 118 of the pumping chamber 110 via the valve V2.
The infusion system 100 may include a plurality of pressure sensors disposed at various places throughout the system 100 to determine the gauge pressures of, for example, the negative tank 142 (pressure sensor PS1), the positive tank (pressure sensor PS4), the common volume 130 (pressure sensor PS3) and the first space 118 (pressure sensor PS2). According to one embodiment, each of these pressure sensors PS1 to PS4 may have a temperature sensor associated therewith, which temperature sensor provides a reading of (or measures) the temperature of the pressure sensor itself, not necessarily of the air volume to which the pressure sensor. As one example, the pressure sensors PS1 to PS4 may be Honeywell ABP pressure transducers.
In addition, the sensors PS1 to PS4 may be mounted on a single board, and a further pressure sensor PSA and a temperature sensor TSA may also be mounted thereon. The pressure sensor PSA is capable of measuring the ambient (or atmospheric) pressure, and can be used to convert the other gauge pressures into absolute pressures, which absolute pressures are used in the calculations below. The temperature sensor TSA and the sensor board may be designed to improve its ability to read the temperature outside the infusion system 100. For example, the board may be relatively thin (e.g., 0.030 inches) to reduce the thermal path from the top-side mounted sensor and the bottom of the sensor board. The electrical contacts may be designed to maximize their cross-sectional thickness. The bottom side of the board may include a thermal pad to increase surface area contact. Further, the top side of the board, including and surrounding the sensor, may be covered with an insulating foam to shield this sensor from the internal temperature of the infusion system 100.
According to one embodiment, the temperature measurement used in calculating, for example, the air side pumping chamber volume is an average air side temperature, and more particularly a mass-weighted average (although optionally other averages, such as a volume-weighted average may be used). The average, and specifically the mass-weighted average, may be calculated using temperature measurements of the pressure sensor/temperature sensors and the ambient sensor board temperature sensor. That is, while the temperature sensors do not necessarily provide the temperature of the air volume to which the pressure sensor is connected (or ported), the temperature readings provide a collection of temperatures for the pneumatic subsystem because of the physical connection of the sensors to the pneumatic manifold. In particular, the sensor board, which may be located at the base of the pump 140 near the administrative set loading mechanism and coupled to the pump housing, has been shown to provide temperature readings that closely track the set side pumping chamber temperature.
Mass-weighted average pumping chamber temperatures may be calculated according to the following equations (Eqn. 1 and 2):
where
The equations are based on a constant volume region, v, within the pumping chamber 110 being at the average temperature of the temperature sensors (also referred to as the average pneumatic manifold temperature) TM, with the remaining portion of the air side pumping chamber volume taken to be at the administration set temperature TS.
The average pneumatic-manifold temperature TM is calculated according to the temperature measurements from the temperature sensors associated with pressure sensors PS1 to PS4. According to certain embodiments, TM may be calculated based on the temperature measurements from a subset of the temperature sensors. For example, an outlier-detection technique may be used to determine if any of the temperature measurements represents a temperature measurement that differs strongly from the other temperature measurements in the population that includes all the temperature measurements from all the temperature sensors. If no outliers are detected or if no outlier-detection technique is used, the average may be calculated, for example, as the average of the three temperature measurements closest to each other out of the four temperature measurements taken from the temperature sensors associated with pressure sensors PS1 to PS4.
The administrative set temperature TS is calculated based on TM and TA, which is the temperature measurement of ambient temperature sensor TSA. In particular, according to certain embodiments, TS is an interpolated value between TA and TM. For example, the calculation may be performed according to the following equation (Eqn. 3):
where β is a parameter. During an initialization, the set side of the pumping chamber will generally be close to room temperature. Accordingly, β may be set to zero at such times. After initialization, β may be set to a non-zero positive value (e.g., 0.125) to account for pre-heating of the set side pumping chamber volume by the warmer pump side pumping chamber air.
The second space 120 of the pumping chamber 110 is coupled to a fluid source (e.g., a flexible bag or rigid/semi-rigid walled container) 150 via the valve Vi. The second space 120 of the pumping chamber is also coupled to a recipient 160 (e.g., a patient or a container) via the valve Vo. As illustrated, the recipient 160 may be coupled to the pumping chamber 110 via a filter 170 and a fluid resistor 180, such as an adjustable fluid resistor (for example, an incrementally adjustable fluid resistor) that may be configured to vary the in-line fluid resistance. According to other embodiments, further equipment may also be coupled between the pumping chamber 110 and the recipient 160.
To control all of the valves Vi, Vo, and V1 to V4 and the air pump 140, a controller 190 is provided that is coupled to the valves Vi, Vo, and V1 to V4 and the air pump 140. The controller 190 may also be coupled to the fluid resistor 180 to vary the in-line fluid resistance. In addition, the controller 190 may also be coupled to the pressure sensors PS1 to PS4 and PSA and temperature sensor TSA, and may receive signals therefrom representative of pressure (P1 to P4 and PA) and of temperature (T1 to T4 and TA). Furthermore, the controller 190 may be coupled to additional equipment, including input devices (e.g., touch screens, keyboards, buttons, etc.) and/or output devices (e.g., electronic display devices, light emitting diodes, audio output devices such as speakers, etc.).
The controller 190 may include for example a processor and memory (or storage device), electrical circuits, or a combination of a processor and memory and electrical circuits. The controller 190 may be configured according to any of the methods of operating the system 100 discussed herein. Where the controller 190 includes a processor and memory, the controller 190 may be programmed to perform any of the methods of operating the system 100 discussed herein, and the memory may include a non-transitory computer readable medium on which the instructions executed by the controller 190 are stored.
In particular, the controller 190 may be configured to carry out one or more of the following non-limiting exemplary embodiments of a method for operating the infusion system 100.
To perform a pump cycle, the controller 190 sets the valves V1 to V4 to a closed state or position. The controller 190 then activates the air pump 140 (sets air pump 140 to the ON state) to bring the positive and negative tanks 142, 144 to the desired drive pressures.
Next, the controller 190 sets valves V1 and V2 to an open state or position to apply the pressure in negative tank 142 to the pumping chamber 110. The negative gauge pressure draws the diaphragm 116 towards the pump side, allowing the second space 120 to fill with medical fluid from the fluid source 150. With the second space 120 filled with medical fluid, the controller 190 sets valve V1 to the closed state, and sets valves V2 and V4 to an open state or position to apply the pressure in the positive tank 144 to the pumping chamber 110. The positive gauge pressure pushes the diaphragm 116 towards the set side, expelling the medical fluid from the second space 120 to flow towards the recipient.
At this point, the controller 190 may reset the pressures in the tanks 142, 144, and repeat the pump cycle.
In addition to performing one or more pump cycles, the controller 190 may perform volume calculations at one or more times after the first space 118 of the pumping chamber 110 is brought to positive gauge pressure. See
Based on the calculated flow rate, the controller may adjust the one or both of the target drive pressure in the positive tank 144 and the in-line resistance as determined by the fluid resistor 180. In general terms, increasing the pressure of the gas in the space 118 of the pumping chamber 110 increases the rate of fluid delivery, and decreasing the pressure decreases the rate of fluid delivery. On the other hand, increasing the in-line fluid resistance decreases the rate of fluid delivery to the recipient 160, while decreasing the in-line fluid resistance increases the rate of fluid delivery to the recipient 160.
In addition to performing one or more pump cycles and performing volume and flow rate calculations, the controller 190 may perform additional calculations to compensate for compliance on pump side and set side, as well as for air bubbles present on the fluid side of the pumping chamber 110. These calculations may be advantageously improved by the use of the pressure sensors with associated temperature sensors described above.
Returning to
As discussed above, by measuring the air side volume of the pumping chamber the fluid side volume may be determined, and by measuring the air side volume of the pumping chamber at multiple times the infusate flow out of the pump may be determined. That is, the change in air side pumping chamber volume may be used to calculate the amount of liquid delivered between the measurements, and thus the infusate flow.
In a general sense, the air side volume measurements are performed in the following manner. To begin, the pumping chamber 110 and the common volume 130 are at different pressures. Next, the pumping chamber 110 and the common volume 130 are combined by opening valve V2, with all other valves (V1, V3, V4) closed. Then, the pumping chamber air side volume is calculated using pressure and temperatures measurements, taking into account conservation of mass, the ideal gas law, and the known, calibrated reference volume of the common volume 130 (which serves as a reference point). The temperatures may be determined according to Equations 1 and 2, above.
As stated above, once the air side volume is known, the amount of liquid delivered between measurements can be calculated. According to the present disclosure, the calculation of the amount of liquid delivered is performed after compensating for compliance in the system. In particular, the compensation addresses liquid side air bubbles, as well as elastic compliance and deformation caused by pressure changes in the pumping chamber 110, both on the pump and set sides.
To compensate, additional measurements are taken with the pumping chamber in a full state and in an empty state. See, for example,
As noted above, the combination of the negative full volume and the positive full volume measurements permit the volume of air on the fluid or liquid side of the pumping chamber 110 to be calculated. Each of the measurements, negative and positive, calculates a particular volume, and may be independent of certain compliances while dependent on other compliances. Thus, before continuing, we discuss each of the full volume measurements separately.
The negative full volume measurements are used to calculate the pump side pumping chamber volume. During the negative full volume measurements, the air side of the pumping chamber is at a lower pressure than the hydrostatic fluid pressure throughout the measurement sequence. Consequently, after a complete fill, the diaphragm 116 will rest against a portion of the wall 112 of the pumping chamber 110 closest to the common volume 130 (the near wall). See
The positive full volume measurements are used to calculate the total volume of air in the pumping chamber (air side and fluid side). During the positive full volume measurements, the air side of the pumping chamber 110 is at a higher pressure than the hydrostatic fluid pressure through the measurement sequence. Consequently, the diaphragm will be pushed off the near wall. See
Like the other measurements made herein, the negative full volume and positive full volume measurements are performed in following manner. To begin, the pumping chamber 110 and the common volume 130 are at different pressures. A first, or initial, set of pressure and temperature measurements are taken. Next, the pumping chamber 110 and the common volume 130 are combined by opening valve V2, with all other valves (V1, V3, V4) closed. A second, or final, set of pressure and temperature measurements are taken. The two sets of measurements are then used to calculate the volume.
So, with respect to the negative full volume measurements, the controller 190 brings the pumping chamber 110 to a target pressure of around −6 psig. The valve V2 is then closed, and the common volume 130 is vented to ambient pressure by opening V3. After valve V3 is closed, an initial set of pressure and temperature measurements are taken in the pumping chamber 110 (PS2) and the common volume 130 (PS3) and by the ambient sensors (PSA, TSA). Then the valve V2 is opened, and the two air volumes (pumping chamber 110, common volume 130) are merged and allowed to equilibrate. A final set of pressure and temperature measurements are taken again in each chamber and by the ambient sensors.
Similarly, with respect to the positive full volume measurements, the controller 190 brings the pumping chamber 110 to the target drive pressure. The valve V2 is the closed, and the common volume 130 is vented to ambient pressure by opening V3. After valve V3 is closed, an initial set of pressure and temperature measurements are taken in the pumping chamber 110 (PS2) and the common volume 130 (PS3) and by the ambient sensors (PSA, TSA). Then the valve V2 is opened, and the two air volumes (pumping chamber 110, common volume 130) are merged and allowed to equilibrate. A final set of pressure and temperature measurements are taken again in each chamber and by the ambient sensors.
In the same way that a similar method is used for taking the measurements, the equations used to determine the desire volumes are based on conversation of air mass, the ideal gas law, and the temperature equations (Eqn. 1 and 2) above. A negative sign (−) is used in subscripts to denote negative full-volume measurements, and a positive sign (+) is used in subscripts to denote positive full-volume measurements.
Starting with the negative full volume measurements, the sum of moles of air in the volumes (pumping chamber 110 and common volume 130) is the same before and after the volumes are merged, and may be represented by the following equation (Eqn. 4):
where
Additionally, the ideal gas law may be used to relate the pressure, temperature, and volume before and after the volumes are merged, as expressed in the following equation (Eqn. 5):
where
As reflected in Eqn. 5, the volume of the common volume is the same both initially and finally (because of its high stiffness) and the temperature is the same both initially and finally. It is believed that the pump side pumping chamber volume, on the other hand, will vary with measurement pressure because of compliance of the passage (e.g., tubing material). Similarly, the mass-weighted temperature used for the pumping chamber (see Eqn. 1 and 2, above) can vary with pressure because of the compliance of the passage. All pressure and temperature terms are absolute.
It will be recognized that the nominal (unpressurized) pump side pumping chamber volume is equal to the volume of the measurement pressure less the volume change caused by membrane compliance. The volume may be expressed either in terms of the initial or final measurement volumes and pressures as follows (Eqn. 6):
where
Combining the foregoing equations, the nominal (unpressurized) pump side pumping chamber volume is obtained from the following equation, which combines the previous expressions and takes into account membrane compliance (Eqn. 7):
where
where
The dimensionless pressure ratio and the temperature-corrected pressure ratio implicitly assume that negative gauge pressures lower than hydrostatic liquid pressure are used for the initial and final pumping chamber temperatures. To minimize the effect of thermal transients during venting and merging of the air volumes, the system is allowed to equilibrate before air pressures are recorded.
Having discussed the negative full volume calculations, it will be recognized that much of the foregoing can be used in regard to the positive full volume calculations, as far as the conservation of air mass and ideal gas law equations would be the same as Equations 4 and 5, above, except that the negative signs (−) would be replaced with positive signs (+). Further, It will be recognized that the nominal (unpressurized) air volume in the pumping chamber is equal to the volume of the measurement pressure less the volume change caused by membrane compliance. The volume may be expressed either in terms of the initial or final measurement volumes and pressures as follows (Eqn. 10):
where
Combining the foregoing equations, the total amount of air in the pumping chamber (air side and fluid side) is obtained from the following equation, which combines the previous expressions and takes into account membrane compliance (Eqn. 11):
where
where
The dimensionless pressure ratio and the temperature-corrected pressure ratio implicitly assume that positive gauge pressures higher than hydrostatic liquid pressure are used for the initial and final pumping chamber temperatures. As above, to minimize the effect of thermal transients during venting and merging of the air volumes, the system is allowed to equilibrate before air pressures are recorded.
As noted above, empty volume measurements are used to determine the total pumping chamber volume (both on air and fluid sides). The total pumping chamber volume can be converted to a pumping chamber stroke volume, corresponding to the fluid delivered during a full pumping chamber stroke, by taking the difference of this volume and the volume calculated according to the negative full volume measurement.
Like the other measurements made herein, and most like the positive full volume measurements, the empty volume measurements are performed in following general manner. To begin, the pumping chamber 110 and the common volume 130 are at different pressures. A first, or initial, set of pressure and temperature measurements are taken. Next, the pumping chamber 110 and the common volume 130 are combined by opening valve V2, with all other valves (V1, V3, V4) closed. A second, or final, set of pressure and temperature measurements are taken. The two sets of measurements are then used to calculate the volume.
In particular, the controller 190 brings the pumping chamber 110 to the target drive pressure. The valve V2 is the closed, and the common volume 130 is vented to ambient pressure by opening V3. After valve V3 is closed, an initial set of pressure and temperature measurements are taken in the pumping chamber 110 (PS2) and the common volume 130 (PS3) and by the ambient sensors (PSA, TSA). Then the valve V2 is opened, and the two air volumes (pumping chamber 110, common volume 130) are merged and allowed to equilibrate. A final set of pressure and temperature measurements are taken again in each chamber and by the ambient sensors.
As for calculations, the conservation of mass, the application of the ideal gas law, and the calculation of mass-weighted average temperatures are the same as for the full volume measurements above. As such the total nominal pumping chamber volume may be calculated as follows (Eqn. 14):
Moreover, the total nominal (unpressurized) pumping chamber stroke volume may be calculated by taking the difference between the total nominal pumping chamber volume and the nominal pump side pumping chamber volume (Eqn. 15):
The terms with the positive sign (+) and the pressure ratio rPP correspond to the positive empty volume measurements. The terms with the negative sign (−) and the pressure ratio rPN refer to the negative full volume measurements, above.
The stroke volume may be periodically updated during an infusion, or may be determined once during the initialization of the system 100. For example, during an infusion with a high flow, the stroke volume may be periodically updated. During an infusion with a low flow rate, the stroke volume may be determined during system initialization, and may not be updated until the infusion system 100 is rebooted.
The amount of liquid that can be delivered during a pumping chamber stroke VIPC,fluid is calculated according to the following calculation (Eqn. 16):
With this information, the controller 190 can calculate the amount of volume delivered from the start of the pump stroke according to the following equation (Eqn. 17):
In addition, the amount of liquid delivered during a pump stroke between times, t1 and t2 may be calculated according to the following equation (Eqn. 18):
where ΔVIPC,partial is the amount of liquid delivered (or change in volumes);
To reflect this in the foregoing the equations, the volume Vair may be replaced by an effective air volume Vair,eff according to the following (Eqn. 19):
Similarly, the amount of liquid that can be delivered during a pumping chamber stroke VIPC,fluid may be calculated according to the following calculation (Eqn. 21):
Moreover, because Vair,eff is calculated after every pumping chamber fill, the active version of VIPC,fluid is updated after every pumping chamber fill even if VIPC,stroke is not.
Although the preceding text sets forth a detailed description of different embodiments of the invention, it should be understood that the legal scope of the invention is defined by the words of the claims set forth at the end of this patent. The detailed description is to be construed as exemplary only and does not describe every possible embodiment of the invention since describing every possible embodiment would be impractical, if not impossible. Numerous alternative embodiments could be implemented, using either current technology or technology developed after the filing date of this patent, which would still fall within the scope of the claims defining the invention.
where TS is the administrative set temperature;
where TS is the administrative set temperature;
where TS is the administrative set temperature;
where TS is the administrative set temperature;
This application claims the benefit of U.S. Provisional Patent App. No. 63/494,458, filed Apr. 5, 2023, which is expressly incorporated herein by reference in its entirety.
Number | Date | Country | |
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63494458 | Apr 2023 | US |