SYSTEM AND METHOD FOR MONITORING AND CONTROLLING INTRAUTERINE PRESSURE USING A PRESSURE CUFF
20220361919 · 2022-11-17
Inventors
Cpc classification
A61M2205/3344
HUMAN NECESSITIES
A61M3/0233
HUMAN NECESSITIES
A61M3/0245
HUMAN NECESSITIES
A61B5/022
HUMAN NECESSITIES
A61B17/42
HUMAN NECESSITIES
International classification
Abstract
A method of determining a pressure of a body cavity with a controller of a fluid management system includes determining a pressure and a volume of a cuff disposed about a collapsible bag, determining a volume of the collapsible bag based on the pressure and the volume of the cuff, and determining a pressure of the collapsible bag based on the volume of the collapsible bag. The method also includes calculating a fluid flow from the collapsible bag into a body cavity from the collapsible bag and determining a pressure of the body cavity based on the fluid flow.
Claims
1. A method of determining a pressure of a body cavity with a controller of a fluid management system, the method comprising: determining a pressure and a volume of a cuff disposed about a collapsible bag; determining a volume of the collapsible bag based on the pressure and the volume of the cuff; determining a pressure of the collapsible bag based on the volume of the collapsible bag; calculating a fluid flow from the collapsible bag into a body cavity from the collapsible bag; and determining a pressure of the body cavity based on the fluid flow.
2. The method according to claim 1, wherein determining a pressure of the cuff includes measuring a pressure of the cuff with a pressure sensor disposed between an air pump and the cuff.
3. The method according to claim 1, wherein determining a volume of the cuff includes monitoring an airflow into the cuff over time.
4. The method according to claim 1, wherein calculating the fluid flow from the bag includes subtracting the volume of the collapsible bag at a first time from a volume of the collapsible bag at a second time and dividing the result by the amount of time between the first and second time.
5. The method according to claim 1, further comprising providing the pressure of the body cavity on a display of the controller.
6. The method according to claim 1, further comprising transmitting a control signal to the air pump to pump air into the cuff in response to determining a pressure of the body cavity.
7. A method of determining a pressure of a body cavity with a fluid management system, the method comprising: inflating a cuff to a predetermined pressure to apply pressure to a collapsible bag; monitoring a change in pressure of the cuff as fluid flows from the collapsible bag; determining a bag volume change of the collapsible bag using the change in pressure of the cuff; calculating a fluid flow from the collapsible bag into a body cavity from the collapsible bag; and determining a pressure of the body cavity based on the fluid flow.
8. The method according to claim 7, wherein inflating the cuff includes a controller activating an air pump to inflate the cuff to the predetermined pressure.
9. The method according to claim 7, wherein inflating the cuff includes manually pumping an air pump to inflate the cuff to the predetermined pressure.
10. The method according to claim 7, further comprising releasing fluid from the collapsible bag after inflating the cuff to the predetermined pressure and wherein monitoring the change in pressure of the cuff is in response to releasing the fluid from the collapsible bag.
11. The method according to claim 7, wherein a controller of the fluid management system determines the bag volume change from a memory of the controller.
12. The method according to claim 7, wherein inflating the cuff to a predetermined pressure includes measuring a pressure of the cuff with a pressure sensor disposed between an air pump and the cuff.
13. The method according to claim 7, wherein calculating the fluid flow from the collapsible bag includes subtracting the volume of the collapsible bag at a first time from a volume of the collapsible bag at a second time and dividing the result by the amount of time between the first and second time.
14. The method according to claim 7, further comprising providing the pressure of the body cavity on a display of a controller.
15. The method according to claim 7, further comprising transmitting a control signal to an air pump to pump air into the cuff in response to determining a pressure of the body cavity.
16. A fluid management system comprising: an air pump; a cuff configured to apply pressure to a collapsible bag; an air hose interconnecting the air pump with the cuff; a pressure sensor in communication with the air hose and configured to generate a signal indicative of a pressure of the cuff; and a controller configured to receive the signal and to determine a pressure of a body cavity in response to the signal.
17. The fluid management system according to claim 16, further comprising a collapsible bag, wherein the cuff is configured to apply pressure to the collapsible bag as the cuff is inflated.
18. The fluid management system according to claim 17, wherein the cuff includes a passage defined therethrough, the collapsible bag positioned within the passage of the cuff.
19. The fluid management system according to claim 17, wherein the air pump is a manual air pump.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0020] Various aspects of the present disclosure are described hereinbelow with reference to the drawings, which are incorporated in and constitute a part of this specification, wherein:
[0021]
[0022]
[0023]
[0024]
[0025]
[0026]
[0027]
[0028]
DETAILED DESCRIPTION
[0029] Embodiments of the present disclosure are described in detail with reference to the drawings in which like reference numerals designate identical or corresponding elements in each of the several views. As used herein, the term “clinician” refers to a doctor, a nurse, or any other care provider and may include support personnel. Throughout this description, the term “proximal” refers to the portion of the device or component thereof that is closer to the clinician and the term “distal” refers to the portion of the device or component thereof that is farther from the clinician.
[0030] Referring to
[0031] The compressible bag 20 includes a fluid reservoir 22 defined therein that is configured to hold a volume of fluid. The compressible bag 20 includes an output port 26 that is coupled to the output tube 30 such that a channel (not shown) of the output tube 30 is in fluid communication with the fluid reservoir 22 of the compressible bag 20. The compressible bag 20 may include a hanger 24 on an opposite side from the output port 26 that is configured to support the compressible bag 20, e.g., on a hook. The hanger 24 may include a scale integrated into the compressible bag 20.
[0032] The output tube 30 extends to an outlet 50 and may include a safety valve 40. The safety valve 40 may be an inline valve that prevents overpressurizing the output tube 30. For example, the safety valve 40 may be a relief valve that vents fluid to prevent overpressurizing the output tube 30.
[0033] The cuff 60 is disposed about the compressible bag 20 and is configured to compress the compressible bag 20 to reduce a volume of the fluid reservoir 22 and/or increase a pressure of the fluid reservoir 22. The cuff 60 is in fluid communication with the air pump 70 via the air hose 80. The air pump 70 is configured to inflate the cuff 60 to compress the compressible bag 20. The air pump 70 may be a compressible bulb that is squeezable by a clinician such that each squeeze pumps an amount of air from the environment into the air hose 80. In some embodiments, the air pump 70 is an electric air pump which pumps air from the environment through the air hose 80. The cuff 60 may form a ring about the compressible bag 20, similar to a blood pressure cuff on an arm, or the cuff 60 may completely surround the compressible bag 20. In embodiments, the cuff 60 is a bladder that is disposed on one side of the compressible bag 20 and is configured to press the compressible bag 20 against a fixed surface such that a volume of the fluid reservoir 22 is reduced and/or pressure within the fluid reservoir 22 is increased.
[0034] For a detailed description of a suitable compressible bag and cuff reference may be made to U.S. Patent Publication No. 2017/0000946 and U.S. Pat. No. 8,062,214, the entire contents of each of these publications are hereby incorporated by reference.
[0035] Referring to
[0036] During a medical procedure, the sheath 180 is inserted into a body cavity, e.g., a uterus, to provide access to the body cavity and the elongated member 124 is inserted through the tube 120 to access the body cavity. The outlet 50 is coupled to the output tube 30 to fluidly connect the fluid reservoir 22 with the hysteroscope 100 such that as air pressure increases in the cuff 60, fluid is expelled from the fluid reservoir 22, through the hysteroscope 100, and into the body cavity to increase the volume or distend the body cavity to improve visualization of an interior of the body cavity.
[0037] For a detailed description of an exemplary hysteroscope reference may be made to U.S. Pat. No. 8,062,214, the entire contents of which are hereby incorporated by reference.
[0038] With reference to
[0039] Referring to
[0040] Before determining a pressure of the body cavity, a relationship between a bag volume V.sub.CB of the compressible bag 20 from a cuff pressure P.sub.CUFF and a cuff volume V.sub.CUFF is determined empirically to form a reference graph for bag volume V.sub.CB as shown in
[0041] A bag pressure P.sub.CB within the compressible bag 20 can also be determined empirically for the cuff pressure P.sub.CUFF and cuff volume V.sub.CUFF as shown in
[0042] Initially to determine the uterine pressure P.sub.U, an air pump pressure P.sub.AP is determined using the pressure sensor 82 that is positioned in communication with the air hose 80 between the air pump 70 and the cuff 60 (Step 210). The air pump pressure P.sub.AP is determined in the first initial pumps of the air pump 70. When the pressure of the air pump P.sub.AP is static such that here is no instantaneous air flow within the air hose 80, the air pump pressure P.sub.AP is equal to the cuff pressure P.sub.CUFF. The controller 72 also monitors an air flow QA from the air pump 70 into the cuff 60 over time (Step 215) such that the control 72 determines the cuff volume V.sub.CUFF based on the cumulative air flow into the cuff 60 (Step 220).
[0043] With the cuff pressure P.sub.CUFF and the cuff volume V.sub.CUFF determined, the controller 72 utilizes a function as shown in
[0044] Once the bag volume V.sub.CB is determined, the controller 72 calculates a fluid flow Q.sub.F through the output tube 30 and into the uterus. The controller 72 determines the fluid flow Q.sub.F (Step 240) as follows:
[0045] Once the fluid flow Q.sub.F is calculated, the uterine pressure P.sub.U can be determined (Step 250) as follows:
P.sub.CB=P.sub.U+Q.sub.FR.sub.IN−pgΔh
which is solved for uterine pressure P.sub.U as:
P.sub.U=P.sub.CB−Q.sub.FR.sub.IN+pgΔh
where resistance R.sub.IN of the output tube 30 and the height Δh of the compressible bag 20 are known. The uterine pressure P.sub.U may be a quadratic function of the fluid flow Q.sub.F. The equations above show a simplification of this quadratic function to a linear function which estimates the uterine pressure P.sub.U within a low margin of error. However, a quadratic function may be used for increased accuracy.
[0046] The controller 72 may include a display 74 that displays the uterine pressure P.sub.U. In some embodiments, the display 74 may display an indication that the controller 72 is calibrating or determining a volume of the collapsible bag V.sub.CB such as “CAL” while the controller 72 is determining the cuff pressure P.sub.CUFF, the cuff volume V.sub.CUFF, and the bag volume V.sub.CB. In embodiments, the controller 72 is in wireless communication to a portable electronic device, e.g., a smart phone, a tablet, a computer, such that the uterine pressure and/or the calibrating of the controller 72 is provided on the display. The controller 72 may also track a fluid volume of the compressible bag 20 and provide an signal, e.g., an audible or visual signal, to a clinician when a fluid volume of the compressible bag 20 is below an acceptable volume, e.g, when the compressible bag 20 is empty. Additionally or alternatively, the controller 72 may be in communication with a scale integrated into the compressible bag 20, e.g., hook 24, to track a weight, and thus a volume, of fluid within the compressible bag 20.
[0047] The air pump 70 may be a powered pump, e.g., an electric air pump. In such embodiments, the controller 72 may be in communication with the air pump 72 such that when the uterine pressure P.sub.U is known, the controller 72 may increase, maintain, or decrease the air flow QA within the air hose 80 to increase, maintain, or decrease the uterine pressure P.sub.U in response to determining the uterine pressure P.sub.U to reach a desired uterine pressure P.sub.U (Step 260). The desired uterine pressure P.sub.U may be entered by a clinician or may be preselected for a selected organ which is inputted by the clinician.
[0048] With reference to
[0049] Before determining the pressure of the body cavity, a relationship between the bag pressure P.sub.CB of the compressible bag 20 and the cuff pressure P.sub.CUFF of the cuff 60 for combinations of cuff volumes V.sub.CUFF and bag volumes V.sub.CB are determined to empirically form a reference graph for bag volume V.sub.CB as a function of cuff pressure P.sub.CUFF as shown in
[0050] Initially to determine the uterine pressure P.sub.U, the air pump 70 is used to inflate the cuff 60 to a predetermined cuff pressure P.sup.1.sub.CUFF (Step 310). The cuff pressure P.sub.CUFF may be measured by the pressure sensor 82 which is positioned in communication with the air hose 80 between the air pump 70 and the cuff 60.
[0051] When the cuff 60 reaches the predetermined cuff pressure P.sup.1.sub.CUFF, fluid is allowed to flow from the compressible bag 20 and into the uterus (Step 320). As the fluid flows from the compressible bag 20, the cuff pressure P.sub.CUFF decays over time as the bag volume V.sub.CB of the compressible bag 20 decreases and the cuff pressure change ΔP.sub.CUFF is measured as fluid flows from the compressible bag 20 (Step 325).
[0052] Once the cuff pressure change ΔP.sub.CUFF is determined, the controller 72 uses a reference function, e.g., as shown in
[0053] Once the fluid flow Q.sub.F is calculated, the uterine pressure P.sub.U can be determined (Step 350) as follows:
P.sub.CB=P.sub.U+Q.sub.FR.sub.IN−pgΔh
which is solved for uterine pressure P.sub.U as:
P.sub.U=P.sub.CB−Q.sub.FR.sub.IN+pgΔh
where resistance R.sub.IN of the output tube 30 and the height Δh of the compressible bag 20 are known.
[0054] The controller 72 may include a display 74 that displays the uterine pressure P.sub.U. In some embodiments, the display 74 may display an indication that the controller 72 is calibrating or determining the fluid flow Q.sub.F such as “CAL” while the controller 72 is determining the fluid flow Q.sub.F. In embodiments, the controller 72 is in wireless communication to a portable electronic device, e.g., a smart phone, a tablet, a computer, such that the uterine pressure and/or the calibrating of the controller 72 is provided on the display.
[0055] In some embodiments, the air pump 70 is a powered pump, e.g., an electric air pump. In such embodiments, the controller 72 may be in communication with the air pump 72 such that when the uterine pressure P.sub.U is known, the controller 72 may increase, maintain, or decrease the air flow QA within the air hose 80 to increase, maintain, or decrease the uterine pressure P.sub.U in response to determining the uterine pressure P.sub.U to reach a desired uterine pressure P.sub.U (Step 360). The desired uterine pressure P.sub.U may be entered by a clinician or may be preselected for a selected organ which is inputted by the clinician.
[0056] While several embodiments of the disclosure have been shown in the drawings, it is not intended that the disclosure be limited thereto, as it is intended that the disclosure be as broad in scope as the art will allow and that the specification be read likewise. Any combination of the above embodiments is also envisioned and is within the scope of the appended claims. Therefore, the above description should not be construed as limiting, but merely as exemplifications of particular embodiments. Those skilled in the art will envision other modifications within the scope of the claims appended hereto.