US20020030002A1 - Filter bag and connector cartridge - Google Patents

Filter bag and connector cartridge Download PDF

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Publication number
US20020030002A1
US20020030002A1 US09/951,555 US95155501A US2002030002A1 US 20020030002 A1 US20020030002 A1 US 20020030002A1 US 95155501 A US95155501 A US 95155501A US 2002030002 A1 US2002030002 A1 US 2002030002A1
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United States
Prior art keywords
connector
fluid
filter
sheets
cavity
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US09/951,555
Inventor
Wesley Verkaart
James Ellsworth
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Haemonetics Corp
Original Assignee
Verkaart Wesley H.
Ellsworth James R.
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Filing date
Publication date
Application filed by Verkaart Wesley H., Ellsworth James R. filed Critical Verkaart Wesley H.
Priority to US09/951,555 priority Critical patent/US20020030002A1/en
Publication of US20020030002A1 publication Critical patent/US20020030002A1/en
Assigned to HAEMONETICS CORPORATION reassignment HAEMONETICS CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: HARVEST TECHNOLOGIES CORPORATION, TURESKI, GARY D., VERKAART, WESLEY H.
Assigned to HAEMONETICS CORPORATION reassignment HAEMONETICS CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: HARVEST TECHNOLOGIES CORPORATION, TURESKI, GARY D., VERKAART, WESLEY H.
Abandoned legal-status Critical Current

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61JCONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
    • A61J1/00Containers specially adapted for medical or pharmaceutical purposes
    • A61J1/05Containers specially adapted for medical or pharmaceutical purposes for collecting, storing or administering blood, plasma or medical fluids ; Infusion or perfusion containers
    • A61J1/10Bag-type containers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/60Containers for suction drainage, adapted to be used with an external suction source
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/60Containers for suction drainage, adapted to be used with an external suction source
    • A61M1/63Containers for suction drainage, adapted to be used with an external suction source with means for emptying the suction container, e.g. by interrupting suction
    • A61M1/631Emptying the suction container without interrupting suction
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/71Suction drainage systems
    • A61M1/79Filters for solid matter
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M39/00Tubes, tube connectors, tube couplings, valves, access sites or the like, specially adapted for medical use
    • A61M39/10Tube connectors; Tube couplings
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D29/00Filters with filtering elements stationary during filtration, e.g. pressure or suction filters, not covered by groups B01D24/00 - B01D27/00; Filtering elements therefor
    • B01D29/01Filters with filtering elements stationary during filtration, e.g. pressure or suction filters, not covered by groups B01D24/00 - B01D27/00; Filtering elements therefor with flat filtering elements
    • B01D29/03Filters with filtering elements stationary during filtration, e.g. pressure or suction filters, not covered by groups B01D24/00 - B01D27/00; Filtering elements therefor with flat filtering elements self-supporting
    • B01D29/036Filters with filtering elements stationary during filtration, e.g. pressure or suction filters, not covered by groups B01D24/00 - B01D27/00; Filtering elements therefor with flat filtering elements self-supporting ring shaped
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D29/00Filters with filtering elements stationary during filtration, e.g. pressure or suction filters, not covered by groups B01D24/00 - B01D27/00; Filtering elements therefor
    • B01D29/88Filters with filtering elements stationary during filtration, e.g. pressure or suction filters, not covered by groups B01D24/00 - B01D27/00; Filtering elements therefor having feed or discharge devices
    • B01D29/90Filters with filtering elements stationary during filtration, e.g. pressure or suction filters, not covered by groups B01D24/00 - B01D27/00; Filtering elements therefor having feed or discharge devices for feeding
    • B01D29/908Filters with filtering elements stationary during filtration, e.g. pressure or suction filters, not covered by groups B01D24/00 - B01D27/00; Filtering elements therefor having feed or discharge devices for feeding provoking a tangential stream
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D36/00Filter circuits or combinations of filters with other separating devices
    • B01D36/001Filters in combination with devices for the removal of gas, air purge systems
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F04POSITIVE - DISPLACEMENT MACHINES FOR LIQUIDS; PUMPS FOR LIQUIDS OR ELASTIC FLUIDS
    • F04BPOSITIVE-DISPLACEMENT MACHINES FOR LIQUIDS; PUMPS
    • F04B43/00Machines, pumps, or pumping installations having flexible working members
    • F04B43/0009Special features
    • F04B43/0054Special features particularities of the flexible members
    • F04B43/0072Special features particularities of the flexible members of tubular flexible members
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F04POSITIVE - DISPLACEMENT MACHINES FOR LIQUIDS; PUMPS FOR LIQUIDS OR ELASTIC FLUIDS
    • F04BPOSITIVE-DISPLACEMENT MACHINES FOR LIQUIDS; PUMPS
    • F04B43/00Machines, pumps, or pumping installations having flexible working members
    • F04B43/12Machines, pumps, or pumping installations having flexible working members having peristaltic action
    • F04B43/1253Machines, pumps, or pumping installations having flexible working members having peristaltic action by using two or more rollers as squeezing elements, the rollers moving on an arc of a circle during squeezing
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F04POSITIVE - DISPLACEMENT MACHINES FOR LIQUIDS; PUMPS FOR LIQUIDS OR ELASTIC FLUIDS
    • F04BPOSITIVE-DISPLACEMENT MACHINES FOR LIQUIDS; PUMPS
    • F04B43/00Machines, pumps, or pumping installations having flexible working members
    • F04B43/12Machines, pumps, or pumping installations having flexible working members having peristaltic action
    • F04B43/1253Machines, pumps, or pumping installations having flexible working members having peristaltic action by using two or more rollers as squeezing elements, the rollers moving on an arc of a circle during squeezing
    • F04B43/1284Means for pushing the backing-plate against the tubular flexible member
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61JCONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
    • A61J1/00Containers specially adapted for medical or pharmaceutical purposes
    • A61J1/14Details; Accessories therefor
    • A61J1/1475Inlet or outlet ports
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/36Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits
    • A61M1/3621Extra-corporeal blood circuits
    • A61M1/3626Gas bubble detectors
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/36Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits
    • A61M1/3621Extra-corporeal blood circuits
    • A61M1/3627Degassing devices; Buffer reservoirs; Drip chambers; Blood filters
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/71Suction drainage systems
    • A61M1/78Means for preventing overflow or contamination of the pumping systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M39/00Tubes, tube connectors, tube couplings, valves, access sites or the like, specially adapted for medical use
    • A61M39/10Tube connectors; Tube couplings
    • A61M2039/1044Verifying the connection, e.g. audible feedback, tactile feedback, visual feedback, using external light sources
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00General characteristics of the apparatus
    • A61M2205/14Detection of the presence or absence of a tube, a connector or a container in an apparatus
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00General characteristics of the apparatus
    • A61M2205/33Controlling, regulating or measuring
    • A61M2205/3379Masses, volumes, levels of fluids in reservoirs, flow rates
    • A61M2205/3393Masses, volumes, levels of fluids in reservoirs, flow rates by weighing the reservoir
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00General characteristics of the apparatus
    • A61M2205/75General characteristics of the apparatus with filters
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2206/00Characteristics of a physical parameter; associated device therefor
    • A61M2206/10Flow characteristics
    • A61M2206/16Rotating swirling helical flow, e.g. by tangential inflows
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M60/00Blood pumps; Devices for mechanical circulatory actuation; Balloon pumps for circulatory assistance
    • A61M60/10Location thereof with respect to the patient's body
    • A61M60/104Extracorporeal pumps, i.e. the blood being pumped outside the patient's body
    • A61M60/109Extracorporeal pumps, i.e. the blood being pumped outside the patient's body incorporated within extracorporeal blood circuits or systems
    • A61M60/113Extracorporeal pumps, i.e. the blood being pumped outside the patient's body incorporated within extracorporeal blood circuits or systems in other functional devices, e.g. dialysers or heart-lung machines

Definitions

  • This invention relates to the art of systems for the collection of fluids.
  • the invention relates to a bag for receiving fluids and a connector for connecting the bag to a supply pump.
  • a novel bag includes an internal filter, and a connector for attaching the bag to a fluid supply ensures that the bag is properly connected prior to operation of the pump.
  • the bag for receiving physiological fluids that have been recovered from a patient includes a filter for removing particles that are larger than a predetermined size.
  • the filter is a 40 ⁇ mesh.
  • the bag is made of two layers of flexible plastic with the filter held between the two layers.
  • the inlet to the bag is placed between the filter and one of the outer layers, and the outlet is placed between the filter and the other of the outer layers.
  • the flexible plastic layers and the filter are bonded together by heat, radio frequency (RF), or ultrasonic welding at the edges.
  • edges are bonded in two locations. First, the filter and the outer layers are bonded completely around the bag inward of the outer edge of the bag, except for the locations where the inlet and outlet are secured. Then, the two outer layers and inlet and outlet conduits are bonded without the filter between them.
  • the bond of all three layers positions the filter to separate the bag into two compartments, and the outer bond acts as a safeguard to ensure that the contents are not spilled even if the inner bond fails.
  • a fluid supply line is connected to one or more lines, preferably inlet lines to the bag described above, by a verification connector.
  • the verification connector includes means for verifying that the lines are properly connected and for controlling an interlock that prevents operation of the fluid pumps if the lines are not connected.
  • the verification elements are easily attached to a base unit for cooperation with verification elements on the base unit to verify that the supply line is properly connected to the outlet lines. In the absence of such verification, operation of the fluid supply pump is inhibited.
  • the verification connectors preferably include known Luer connectors for connecting the supply line to the inlet lines. Other types of connectors may, of course, be used.
  • the verification elements are optical.
  • a light emitting diode, preferably infrared, and a photo detector, also preferably infrared, are contained in the base unit and are located with respect to the verification elements such that a beam from the light emitting diode will enter a transparent, conducting, portion of the verification elements when properly installed.
  • the inlet line verification element will refract the light through an angle that will cause it to impinge on a detector in the base unit. Reflecting surfaces may be used to direct the incident and refracted beams to desired locations in the base unit. Signals from the photo detector are supplied to a control circuit that allows operation of a fluid supply pump only when the outlet lines are properly connected.
  • FIG. 1 is a front view of a filter bag, partially broken away, in accordance with the invention.
  • FIG. 2 is a cross-section taken along line 2 - 2 of FIG. 1.
  • FIG. 3 is a cross-section taken along line 3 - 3 of FIG. 1.
  • FIG. 4 is a cross-section taken along line 4 - 4 of FIG. 2.
  • FIG. 5 is a cross-section taken along line 5 - 5 of FIG. 4.
  • FIG. 6 is a perspective of a male Luer connector with a mounting key attached.
  • FIG. 7 is a perspective of a base element having verification components in accordance with the invention.
  • FIGS. 8A and 8B are front views of the base element illustrating attachment of the mounting key to the base element.
  • FIGS. 9 a and 9 B illustrate the operation of the verification elements.
  • FIG. 10 is a perspective showing the fluids lines properly connected and attached to the base element.
  • a filter bag 200 is constructed of respective outer sheets 202 and 204 . These sheets are preferably flexible and may be made of known plastic material.
  • An inner sheet 206 is a filter, which is preferably a 40 ⁇ mesh of plastic material that can be easily bonded to the outer sheets.
  • the bag includes an opening 208 to allow it to be hung from a variety of locations, such as a known I.V. stand.
  • the bag includes an inlet line 210 and an outlet port 212 .
  • the inlet line 210 includes a Luer connector 214 for attaching the line to a source of the physiological fluid, such as the supply line shown in FIG. 6.
  • This connector is preferably designed to connect with other Luer connectors of standard size but also includes means for verifying whether the line is connected to a source of supply. While this verification element may take various forms, both electrical and mechanical, in the preferred embodiment the verification means is a cylindrical optical element 216 .
  • the cylinder is transparent to light, for example, infrared light from a light emitting diode. When the Luer connector is properly attached to the source of supply, the light passes through the cylinder and is refracted thereby to impinge on a detector.
  • An electronic control circuit senses the presence of light on the detector and, in response, allows activation of a supply pump. This ensures that the line is connected to the source of supply, preventing inadvertently spilling the physiological fluids.
  • the preferred construction of the filter bag is more clearly shown in FIG. 2.
  • the three layers of material, the two outer sheets 202 , 204 and the filter 206 are bonded together at an inner bond 218 .
  • This bond which may be produced by heating, radio frequency (RF), ultrasound, or other known methods, secures the three layers together to form two chambers 220 and 222 separated by the filter 206 .
  • a second, outer bond 220 is formed at the outer edge of the bag. This outer bond is between only the two outer sheets and excludes the filter material.
  • the outer bond 220 provides an additional measure of safety to prevent separation of the two sheets and accidental discharge of the contents of the bag, should the inner bond fail. This is important in situations, such as pressure infusion, where the contents of the bag are subjected to pressures as high as 300 mmHg to increase the flow rate.
  • FIGS. 4 and 5 show how the sheets 202 and 204 and the filter 206 are secured to the inlet line 210 and the outlet 212 .
  • the inlet and outlet could as well be attached by a variety of means. For example, these could be provided by a known sidewall connector in each of the sheets 202 and 204 .
  • physiological fluid such as blood obtained from a surgical site
  • a pump not sown
  • This fluid first flows through the inlet line 210 into the chamber 222 .
  • the filter removes unwanted particles.
  • an appropriate outlet line (not shown), such as an l.V. line is attached to the outlet 212 to permit fluid to flow out of the bag.
  • outlet 212 is a known spikeport that has a removable cover 226 and receives a spike in known fashion.
  • the spikeport includes a flange 228 , which may be used to support the bag while it is being filled.
  • a flange 228 which may be used to support the bag while it is being filled.
  • a male Luer connector 302 is attached to a tube 304 , as known in the art.
  • a mounting key 306 according to the invention is attached to the Luer connector, as by welding or cement. The key is used to secure the male connector to the base element shown in FIGS. 7 through 10.
  • the base element 308 is attached to, or is a part of, apparatus for pumping fluids into a bag, such as bag 200 .
  • the base element includes a face plate 310 for receiving the key 306 and the Luer connector.
  • the face plate includes an opening 312 , which is of a shape that will allow the key to be inserted.
  • a narrower notch 314 is located below the opening 312 , and a slot 316 is formed between the front of the faceplate and a rear wall thereof. Slot 316 extends vertically from the bottom of the opening 312 to just above the bottom of the faceplate. While the key has been shown to be square, other shapes are possible.
  • FIGS. 8A and 8B The installation of the key will be explained with reference to FIGS. 8A and 8B.
  • the key 306 with the male Luer connected is first inserted in the opening 312 as shown in FIG. 8A. Then, the key is slid downward as illustrated in FIG. 8B, whereby the edges of the key engage the slot 316 to thereby secure the male Luer and key in the faceplate 310 .
  • the key is preferably retained in the position shown in FIG. 8B by gravity; as well the position may be maintained by friction or other mechanisms.
  • base element 308 includes a source 318 of electromagnetic energy, such as infrared energy from a light emitting diode.
  • the base also includes a window 320 for allowing refracted energy to impinge on a detector 322 .
  • the detector is shown located behind the window, but it could be placed in the element 308 as well. Also, reflectors cold be employed to direct the beams as desired to detectors located elsewhere.
  • FIG. 9A illustrates the situation when the female Luer connector 214 is attached to the male Luer connector 302 , and the key 306 is secured in the faceplate 310 .
  • the light beam 324 is refracted by the optical element 216 on the female Luer.
  • the light path is as shown in FIG. 9A where is passes through window 320 and impinges on detector 322 .
  • the detector 322 supplies a signal to a control circuit allowing the pumps to operate.
  • FIG. 9B illustrates the situation where the female Luer is not properly connected. In this situation, the required refraction does not occur, and the beam does not pass through the window 322 . Accordingly, the detector 322 does not detect the impingement, and the control circuit does not enable operation of the pumps.
  • FIG. 10 shows the male and female Luer connectors attached to each other and installed on the base element.
  • the base element provides an opening at the bottom for receiving the line 304 from the source of fluid, such as a pump.
  • the line 304 and key may be installed from the front of the base element prior to connection of the line 210 . Or, the two lines may be attached and then installed in the base element.
  • One advantage of the key is that the connector 214 may be easily attached to the connector 302 with one hand when the key is secure in the base element.
  • inlet lines 210 may be used, only one is illustrated in the figures.
  • supply line 304 may be connected to a Y-connector (not shown), which is in turn connected to the supply pump
  • each of the inlet lines 210 includes a female Luer connector 214 that has been modified to include a verification element.
  • the verification element in the preferred embodiment is the optical element 216 that cooperates with the light source and detector in the base element to verify that the connector 214 is properly in place.
  • the described verification system is fail-safe because it requires a predetermined signal to be received by the photo detectors before connection is verified. If the Luer connectors are not in place, the light from the source in the base unit will not be refracted to the photo detectors, and verification will be precluded. Modifications within the scope of the claims will be apparent to those of skill in the art.

Abstract

A filter bag (200) and connector cartridge are used for collection of physiological fluids. The bag (200) includes an internal filter (206) and two seals (218, 220) on the perimeter. An inner seal (218) bonds the outer sheets (202, 204) of the bag and the filter, while the outer seal (220) bonds only the two outer sheets (202, 204) and acts as a safety seal. The bag includes a verification element that cooperates with a verification connector to ensure that the bag is properly attached to the fluid supply line before a fluid pump is enabled.

Description

    FIELD OF THE INVENTION
  • This invention relates to the art of systems for the collection of fluids. In particular, the invention relates to a bag for receiving fluids and a connector for connecting the bag to a supply pump. [0001]
  • BACKGROUND
  • It is known to collect fluids in containers such a flexible bags. For example, it is known to collect blood and other physiological fluids during surgery by pumping the blood into flexible bags. The fluids are then redelivered to the patient after processing. The fluids generally include debris that must be removed, and filters are used for this. Prior bags that include filters have not been effective, however, and are often expensive. Moreover, because the bags are disposable, the fluid lines are detachable, and it is necessary to provide an effective means for ensuring that the lines are properly connected before the pumping operation begins. [0002]
  • SUMMARY OF THE INVENTION
  • In accordance with the invention, a novel bag includes an internal filter, and a connector for attaching the bag to a fluid supply ensures that the bag is properly connected prior to operation of the pump. [0003]
  • The bag for receiving physiological fluids that have been recovered from a patient includes a filter for removing particles that are larger than a predetermined size. In the preferred embodiment, the filter is a 40μ mesh. The bag is made of two layers of flexible plastic with the filter held between the two layers. The inlet to the bag is placed between the filter and one of the outer layers, and the outlet is placed between the filter and the other of the outer layers. The flexible plastic layers and the filter are bonded together by heat, radio frequency (RF), or ultrasonic welding at the edges. [0004]
  • The edges are bonded in two locations. First, the filter and the outer layers are bonded completely around the bag inward of the outer edge of the bag, except for the locations where the inlet and outlet are secured. Then, the two outer layers and inlet and outlet conduits are bonded without the filter between them. By this construction, the bond of all three layers positions the filter to separate the bag into two compartments, and the outer bond acts as a safeguard to ensure that the contents are not spilled even if the inner bond fails. [0005]
  • In accordance with another aspect of the invention, a fluid supply line is connected to one or more lines, preferably inlet lines to the bag described above, by a verification connector. The verification connector includes means for verifying that the lines are properly connected and for controlling an interlock that prevents operation of the fluid pumps if the lines are not connected. The verification elements are easily attached to a base unit for cooperation with verification elements on the base unit to verify that the supply line is properly connected to the outlet lines. In the absence of such verification, operation of the fluid supply pump is inhibited. The verification connectors preferably include known Luer connectors for connecting the supply line to the inlet lines. Other types of connectors may, of course, be used. [0006]
  • In the preferred embodiment, the verification elements are optical. A light emitting diode, preferably infrared, and a photo detector, also preferably infrared, are contained in the base unit and are located with respect to the verification elements such that a beam from the light emitting diode will enter a transparent, conducting, portion of the verification elements when properly installed. The inlet line verification element will refract the light through an angle that will cause it to impinge on a detector in the base unit. Reflecting surfaces may be used to direct the incident and refracted beams to desired locations in the base unit. Signals from the photo detector are supplied to a control circuit that allows operation of a fluid supply pump only when the outlet lines are properly connected. [0007]
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 is a front view of a filter bag, partially broken away, in accordance with the invention. [0008]
  • FIG. 2 is a cross-section taken along line [0009] 2-2 of FIG. 1.
  • FIG. 3 is a cross-section taken along line [0010] 3-3 of FIG. 1.
  • FIG. 4 is a cross-section taken along line [0011] 4-4 of FIG. 2.
  • FIG. 5 is a cross-section taken along line [0012] 5-5 of FIG. 4.
  • FIG. 6 is a perspective of a male Luer connector with a mounting key attached. [0013]
  • FIG. 7 is a perspective of a base element having verification components in accordance with the invention. [0014]
  • FIGS. 8A and 8B are front views of the base element illustrating attachment of the mounting key to the base element. [0015]
  • FIGS. 9[0016] a and 9B illustrate the operation of the verification elements.
  • FIG. 10 is a perspective showing the fluids lines properly connected and attached to the base element.[0017]
  • DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
  • With reference to FIG. 1, a [0018] filter bag 200 is constructed of respective outer sheets 202 and 204. These sheets are preferably flexible and may be made of known plastic material. An inner sheet 206 is a filter, which is preferably a 40μ mesh of plastic material that can be easily bonded to the outer sheets. The bag includes an opening 208 to allow it to be hung from a variety of locations, such as a known I.V. stand.
  • The bag includes an [0019] inlet line 210 and an outlet port 212. The inlet line 210 includes a Luer connector 214 for attaching the line to a source of the physiological fluid, such as the supply line shown in FIG. 6. This connector is preferably designed to connect with other Luer connectors of standard size but also includes means for verifying whether the line is connected to a source of supply. While this verification element may take various forms, both electrical and mechanical, in the preferred embodiment the verification means is a cylindrical optical element 216. The cylinder is transparent to light, for example, infrared light from a light emitting diode. When the Luer connector is properly attached to the source of supply, the light passes through the cylinder and is refracted thereby to impinge on a detector. An electronic control circuit senses the presence of light on the detector and, in response, allows activation of a supply pump. This ensures that the line is connected to the source of supply, preventing inadvertently spilling the physiological fluids.
  • The preferred construction of the filter bag is more clearly shown in FIG. 2. The three layers of material, the two [0020] outer sheets 202, 204 and the filter 206, are bonded together at an inner bond 218. This bond, which may be produced by heating, radio frequency (RF), ultrasound, or other known methods, secures the three layers together to form two chambers 220 and 222 separated by the filter 206. A second, outer bond 220 is formed at the outer edge of the bag. This outer bond is between only the two outer sheets and excludes the filter material. The outer bond 220 provides an additional measure of safety to prevent separation of the two sheets and accidental discharge of the contents of the bag, should the inner bond fail. This is important in situations, such as pressure infusion, where the contents of the bag are subjected to pressures as high as 300 mmHg to increase the flow rate.
  • FIGS. 4 and 5 show how the [0021] sheets 202 and 204 and the filter 206 are secured to the inlet line 210 and the outlet 212. It will be appreciated that the inlet and outlet could as well be attached by a variety of means. For example, these could be provided by a known sidewall connector in each of the sheets 202 and 204.
  • In operation, physiological fluid, such as blood obtained from a surgical site, is supplied to the [0022] inlet line 210 by a pump (not sown). This fluid first flows through the inlet line 210 into the chamber 222. As the fluid passes through the filter into chamber 220, the filter removes unwanted particles. As the bag continues to fill, some of the fluid will remain in chamber 222, while the remainder will pass through the filter to chamber 220. When it is desired to use the fluid in the bag, an appropriate outlet line (not shown), such as an l.V. line is attached to the outlet 212 to permit fluid to flow out of the bag. Preferably, outlet 212 is a known spikeport that has a removable cover 226 and receives a spike in known fashion.
  • The spikeport includes a [0023] flange 228, which may be used to support the bag while it is being filled. When the fluid in the bag is withdrawn, the bag is hung from the opening 208, and the inlet line 210 is closed with a slide clamp, metal crimp, Luer cap, or the like. Thus, the bag is filled in an orientation opposite from the orientation from which it is emptied. This increases efficiency by providing even usage of the filter layer; the in-flowing fluid will pass continuously through one end of the filter as it is filling and the out-flowing fluid will continuously pass through the opposite end of the filter as it is being discharged.
  • With reference to FIG. 6, a [0024] male Luer connector 302 is attached to a tube 304, as known in the art. A mounting key 306 according to the invention is attached to the Luer connector, as by welding or cement. The key is used to secure the male connector to the base element shown in FIGS. 7 through 10. The base element 308 is attached to, or is a part of, apparatus for pumping fluids into a bag, such as bag 200. The base element includes a face plate 310 for receiving the key 306 and the Luer connector. The face plate includes an opening 312, which is of a shape that will allow the key to be inserted. A narrower notch 314 is located below the opening 312, and a slot 316 is formed between the front of the faceplate and a rear wall thereof. Slot 316 extends vertically from the bottom of the opening 312 to just above the bottom of the faceplate. While the key has been shown to be square, other shapes are possible.
  • The installation of the key will be explained with reference to FIGS. 8A and 8B. The key [0025] 306 with the male Luer connected is first inserted in the opening 312 as shown in FIG. 8A. Then, the key is slid downward as illustrated in FIG. 8B, whereby the edges of the key engage the slot 316 to thereby secure the male Luer and key in the faceplate 310. The key is preferably retained in the position shown in FIG. 8B by gravity; as well the position may be maintained by friction or other mechanisms.
  • The purpose of this structure is to provide verification of the proper installation of the Luer connectors. Thus, [0026] base element 308 includes a source 318 of electromagnetic energy, such as infrared energy from a light emitting diode. The base also includes a window 320 for allowing refracted energy to impinge on a detector 322. The detector is shown located behind the window, but it could be placed in the element 308 as well. Also, reflectors cold be employed to direct the beams as desired to detectors located elsewhere.
  • FIG. 9A illustrates the situation when the [0027] female Luer connector 214 is attached to the male Luer connector 302, and the key 306 is secured in the faceplate 310. In this configuration, the light beam 324 is refracted by the optical element 216 on the female Luer. Thus, the light path is as shown in FIG. 9A where is passes through window 320 and impinges on detector 322. The detector 322 supplies a signal to a control circuit allowing the pumps to operate.
  • FIG. 9B illustrates the situation where the female Luer is not properly connected. In this situation, the required refraction does not occur, and the beam does not pass through the [0028] window 322. Accordingly, the detector 322 does not detect the impingement, and the control circuit does not enable operation of the pumps.
  • FIG. 10 shows the male and female Luer connectors attached to each other and installed on the base element. The base element provides an opening at the bottom for receiving the [0029] line 304 from the source of fluid, such as a pump. The line 304 and key may be installed from the front of the base element prior to connection of the line 210. Or, the two lines may be attached and then installed in the base element. One advantage of the key, however, is that the connector 214 may be easily attached to the connector 302 with one hand when the key is secure in the base element.
  • While any number of [0030] inlet lines 210 may be used, only one is illustrated in the figures. Thus, supply line 304 may be connected to a Y-connector (not shown), which is in turn connected to the supply pump As described above, each of the inlet lines 210 includes a female Luer connector 214 that has been modified to include a verification element. The verification element in the preferred embodiment is the optical element 216 that cooperates with the light source and detector in the base element to verify that the connector 214 is properly in place.
  • It will be appreciated that the described verification system is fail-safe because it requires a predetermined signal to be received by the photo detectors before connection is verified. If the Luer connectors are not in place, the light from the source in the base unit will not be refracted to the photo detectors, and verification will be precluded. Modifications within the scope of the claims will be apparent to those of skill in the art. [0031]

Claims (15)

We claim:
1. A container for a fluid comprising first and second outer sheets forming a cavity and a filter between said sheets dividing said cavity into first and second chambers in communication with each other through said filter, fluid inlet means communicating with said first chamber for conducting fluid into said cavity, and fluid outlet means communicating with said second chamber for conducting fluid out of said cavity, wherein said sheets and filter are bonded together at a first peripheral bond and only said sheets are bonded together at a second peripheral bond.
2. A container according to claim 1 wherein said first peripheral bond lies radially inward of said second peripheral bond.
3. A container according to claim 1 wherein said fluid inlet means is secured between a first of said sheets on one side of said inlet means and the other of said sheets and said filter on the other side of said inlet means.
4. A container according to claim 1 wherein said filter comprises a 40μ mesh.
5. A container according to claim 1 wherein one of said fluid inlet and fluid outlet means comprises a first connector element and means for verifying proper attachment of said first connector element to a second connector element.
6. A container according to claim 5 wherein said means for verifying comprises an optical element.
7. A container according to claim 6 wherein said optical element comprises a transparent cylinder.
8. In combination, a first connector element and means for verifying whether said first connector is connected to a second connector element, wherein said means for verifying comprises an optical element.
9. A combination according to claim 8 wherein said connector is a Luer connector and said optical element comprises a transparent cylinder.
10. A combination according to claim 9 in further combination with a fluid container and wherein said connector is part of an inlet or outlet line for said container.
11. A combination according to claim 10 wherein said container comprises first and second outer sheets forming a cavity and a filter between said sheets dividing said cavity into first and second chambers in communication with each other through said filter, fluid inlet means communicating with said first chamber for conducting fluid into said cavity, and fluid outlet means communicating with said second chamber for conducting fluid out of said cavity, wherein said sheets and filter are bonded together at a first peripheral bond and only said sheets are bonded together at a second peripheral bond.
12. Apparatus for connecting two fluid lines, comprising a housing having means for removably engaging a mounting element on a base unit, a first connector means in fluid communication with a first fluid line and adapted to be removably attached to a second connector means on a second fluid line, and means for verifying that said first connector means is connected to said second connector means.
13. Apparatus according to claim 12 wherein said means for verifying is adapted to cooperate with verifying means on said base unit when said apparatus is attached to said base unit.
14. Apparatus according to claim 13 wherein said means for verifying comprises means forming at least one optical channel for directing a beam of light toward said second connector means when said second connector means is attached to said first connector means.
15. Apparatus according to claim 14 wherein said at least one optical channel comprises an inlet channel positioned to align with a light source on said base unit and an outlet channel positioned to align with a light detector when said apparatus is received on said base unit.
US09/951,555 1995-10-20 2001-09-14 Filter bag and connector cartridge Abandoned US20020030002A1 (en)

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US812795P 1995-10-20 1995-10-20
US577295P 1995-10-20 1995-10-20
US812895P 1995-10-20 1995-10-20
US60/008127 1995-10-20
US60/008128 1995-10-20
US60/005772 1995-10-20
US2075496P 1996-06-28 1996-06-28
US60/020754 1996-06-28
US09/051,481 US6325422B1 (en) 1995-10-20 1996-10-18 Filter bag and connector cartridge
US09/951,555 US20020030002A1 (en) 1995-10-20 2001-09-14 Filter bag and connector cartridge

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US09/051,481 Continuation US6325422B1 (en) 1995-10-20 1996-10-18 Filter bag and connector cartridge
PCT/US1996/016772 Continuation WO1997014493A1 (en) 1995-10-20 1996-10-18 Filter bag and connector cartridge

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JP (1) JP3537145B2 (en)
CN (1) CN1200052A (en)
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US11559619B2 (en) 2018-04-30 2023-01-24 Smith & Nephew Asia Pacific Pte. Limited Systems and methods for controlling dual mode negative pressure wound therapy apparatus
US11955829B2 (en) 2018-04-30 2024-04-09 Smith & Nephew Asia Pacific Pte. Limited Power source charging for negative pressure wound therapy apparatus
US11744932B2 (en) 2018-05-23 2023-09-05 T.J.Smith And Nephew, Limited Systems and methods for determining blockages in a negative pressure wound therapy system

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EP1738782A1 (en) 2007-01-03
CA2235218A1 (en) 1997-04-24
CN1200052A (en) 1998-11-25
CA2235218C (en) 2007-02-13
EP0883430A4 (en) 2000-04-26
JP3537145B2 (en) 2004-06-14
EP0883430B1 (en) 2007-01-03
DE69636816T2 (en) 2007-10-04
DE69636816D1 (en) 2007-02-15
ATE350078T1 (en) 2007-01-15
JP2001519680A (en) 2001-10-23
US6325422B1 (en) 2001-12-04
EP0883430A1 (en) 1998-12-16
WO1997014493A1 (en) 1997-04-24

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