CA2280719A1 - Blood evacuating system and method of use thereof - Google Patents
Blood evacuating system and method of use thereof Download PDFInfo
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- CA2280719A1 CA2280719A1 CA002280719A CA2280719A CA2280719A1 CA 2280719 A1 CA2280719 A1 CA 2280719A1 CA 002280719 A CA002280719 A CA 002280719A CA 2280719 A CA2280719 A CA 2280719A CA 2280719 A1 CA2280719 A1 CA 2280719A1
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES 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
- A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
- A61M1/60—Containers for suction drainage, adapted to be used with an external suction source
- A61M1/62—Containers comprising a bag in a rigid low-pressure chamber, with suction applied to the outside surface of the bag
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Abstract
The invention relates to an apparatus and method for a blood evacuation system (14) comprising an inner flexible blood evacuation bag (38) inside an outer rigid container (16) for reinfusing sheld blood drawn from the collection chamber of a chest drainage unit (12). The outer rigid container (16) includes a suction port connected to a source of vacuum for applying a negative pressure within the interstitial space (46) between the interior surface of the rigid container (16), and the outside of the inner flexible blood evacuation bag (38). The negative pressure inside the interstitial space (46) draws blood from the collection chamber of the chest drainage unit (12) into the blood evacuation bag (38). Once the blood evacuation bag (38) is filled to a desired level, the inner flexible bag (38) is removed from the outer rigid container (16), and suspended using a suspension means (19) within the vicinity of a patient (10) for reinfusion. During reinfusion another blood evacuation bag (38) can replace the blood evacuation bag (38) being used for reinfusion.
Description
Blood Evacuating System and Method of Use Thereof TECHNIC.'AL FIELD
The present invention re:Lates generally to an apparatus and method for collecting fluids and the reinfusion of the fluids to a patient, and particularly to a blood evacuation system adapted for' autotransfusion. More specifically, the present invention is directed to a blood evacuation system that permits a disposable inner evacuation bag to be separated from an outer container for reinfusion so that another evacuation bag may be inserted inside the container to continue blood evacuation.
BACKGROUND ART
Blood evacuating apparatuses are commonly used in autotransfusion to evacuate and collect autologous blood from the collectic>n chamber of a chest drainage unit.
Autotransfusion refers to the reinfusion of a patient's own blood, known as autologous blood. Autotransfusion is the preferred method of reinfused since the blood being transfused is the patient's own blood, therefore eliminating problems over blood type incompatibility and exposure to blood carrying diseases such as hepatitis, AIDS, etc.
Moreover, autologous blood is more fresh than stored blood supplied by a donor and also contains the patient's own antibodies.
One type of autotransfusion, referred to as "post-operative" autotransfusion, is the transfusion of the patient's own shed blood following surgery where drained blood is collected and reinfused into the patient. Post-operative autotransfusion is limited in use since there are strict guidelines for the kind of blood which can be reinfused. Currently, the only post-operative blood believed suitable for autotransfusion is mediastinal blood, i.e. the blood which comes from the anatomical space or cavity in the chest.
Presently, chest drainage units are commonly used in the post-operative care of patients having surgery involving the chest cavity. Chest drainage units remove fluids and air from inside the chest cavity using tubing connected to the patient's chest cavity which drains the fluid and air into a collection chamber of the chest drainage unit. The chest drainage unit is attached to a source of vacuum which applies a suction to the tubing and draws the trapped fluid and air from the chest cavity and into the collection chamber. Once collected, the blood may be evacuated from the collection chamber using an autotransfusion pump or blood evacuation bag.
The use of a blood evacuation bag in autotransfusion is well known in the art. For example, U.S. Patent No.
5,380,314 to Herweck et al. discloses a blood collection bag having an internal spring that resiliently biases the bag into a fixed shape prior to use while concurrently inducing a negative pressure therein in order to manually draw blood from the collection chamber of the chest drainage unit.
However, one disadvantage with the '314 apparatus is that reinfusion must be accomplished using gravity means, whereby the bag is suspended in the vicinity of the patient and gravity is allowed to drain the collected blood from the bag for reinfusion to the patient. Unfortunately, the '314 apparatus will not properly drain unless the user first takes the extra step of bleeding in ambient air into the blood collection bag prior to reinfusion. This bleeding step is necessary in order to ford? collected blood inside the rigid blood collection bag to drain, otherwise the force of gravity alone will prove insufficient to draw blood from the bag during reinfusion.
Another example of a blo~~d evacuation system is found in U.S. Patent No.5,201,703 t~~ Gentelia et al. which discloses an apparatus for collecting blood from a chest drainage unit and reinfusion of the blood to the patient.
The '703 patent i~: directed to a self-contained, totally disposable apparatus comprising an rigid outer container housing an integrally attached flexible bag for use with a chest drainage unit. Negative pressure is applied or maintained inside the interstitial space between the rigid container and the inner flexible bag for causing blood stored in the collection chamber to be drawn into the bag.
As drawn blood travels through tubing connecting the '703 apparatus to the chest drainage unit, it begins to fill the flexible inner back. Once the bag is filled to a desired level with blood t:he entire apparatus, including the outer rigid container and the blood-filled inner baq, are disconnected from the chest drainage unit and suspended from a suitable suspen~~ion means in the vicinity of a patient for reinfusion of the collected blood.
WO 98/35718 PC't/US98/02586 -However, a disadvantage with the '703 apparatus is that the entire apparatus must be employed during reinfusion.
Specifically, both the outer rigid container and the inner flexible bag are utilized during the reinfusion process since the '703 apparatus has a unitary design wherein the inner flexible bag cannot be separated from the outer rigid container. As a result, another entire apparatus - a container and evacuation bag - must replace the used apparatus in order to continue the autotransfusion procedure on the same patient. Accordingly, the cost to the user is higher since the entire apparatus must be replaced after each transfusion.
Another disadvantage to the '703 apparatus is that the conventional means for attaining higher rates of reinfusion with the above noted blood evacuation systems are sometimes not possible. A prior art blood evacuation bag that fixedly attaches the evacuation bag to the outer rigid container or is made of a unitary, rigid container design are not adapted to employ high reinfusion rate techniques. For example, it is well known in the art that pressure cuffs wrapped around a flexible blood evacuation bag. can generate higher reinfusion rates by applying pressure to a bladder of the pressure cuff surrounding the container. However, if the evacuation container is of a rigid design a pressure cuff surrounding the container is unable to exert sufficient pressure to collapse the inner flexible bag and generate a higher rate of reinfusion. In view of these disadvantages regarding cost and performance, it is desirable to have a blood evacuation system in which only the inner flexible bag is used to reinfu~>e blood while the rigid outer container remains connected to a vacuum source for further collection T of blood from the chest drainage unit.
Accordingly, a need exists in the art for a blood evacuation system that permits detachment of the inner flexible bag from the outer rigid container before reinfusion so that. another flexible bag may be used inside the same container in order to collect further blood from the collection chamber. Moreover, there also exists a need in the art for a blood evacuation system that provides a cost effective means of reinfusing blood to a patient using multiple, detachable evacuation bags to continue blood evacuation while reinfusion takes place.
DISCLOSURE OF INVENTION
A principle object of the present invention is to provide a cost-effective means of reinfusing blood to a patient.
Another object of the present invention is to provide an efficient method of reinfusing autologous blood to a patient.
A further object of the present invention is to provide a blood evacuation system that includes an inner flexible bag that is separable from its outer container during reinfusion.
Another further object of the present invention is to provide a separab7_e evacuation bag that is adapted to receive a pressure cuff for generating a higher rate of reinfusion.
These and other objects of the present invention are realized in a presently preferred embodiment thereof, described by way of example and not by way of limitation, which provides for an apparatus and related method for evacuating and reinfusing blood to a patient using a blood evacuation system comprising a separable, flexible inner bag inside an outer rigid container for reinfusing shed blood drawn from the collection chamber of a chest drainage unit.
The outer rigid container includes a suction port connected to a source of vacuum for applying a negative pressure within the interstitial space between rigid container and the inner flexible bag disposed therein. The negative pressure maintained within the interstitial space inside the container causes blood to be drawn into the bag from the collection chamber of the chest drainage unit through tubing which maintains fluid flow communication between the bag and the collection chamber. Once the bag is filled to a desired level, the inner flexible bag is removed from the outer rigid container and suspended within the vicinity of a patient for reinfusion of the collected blood.
BRIEF DESCRIPTION OF DRAWINGS
FIG. 1 is a simplified block diagram showing the blood evacuation system according to the present invention;
FIG. 2 is a perspective view of the rigid outer container and transfer tubing according to the present invention;
FIG. 3 is a partial cross section view of the rigid outer container showing the blood evacuation bag according to the present invention; and FIG. 4 is a pE=_rspective view of the blood evacuation bag according to the present invention.
MODE ( S ) FOR CARRYII\fG OUT THE INVENTION
Referring to FIG. 1, a simplified block diagram of an autotransfusion sy:~tem 11 is illustrated showing the constituent element=s of system 11. The autotransfusion system 11 comprise; a patient 10 in fluid flow communication with a drainage device 12 using transfer tubing 24 to maintain fluid flow therebetween in direction A. The autotransfusion system 11 further includes a blood evacuation system 14 according to the present invention that is in fluid flow communication with the drainage device 12 using the same type' of transfer tubing 24 used between the patient 10 and the device 12. Preferably, the transfer tubing 24 is made of a flexible plastic material, although any flexible material suitable for transporting fluid, such as blood, is felt t=o fall within the scope of the present invention.
Referring to FIGS. 2 and 3, the blood evacuation system 14 according to the present invention is shown. The blood evacuation system 14 comprises a rigid canister 16 with a flexible blood evacuation bag 38 disposed therein.
Preferably, the canister 16 has a generally round shape, although any shaped container suitable for storing fluid is felt to fall within the scope of the present invention. The canister 16 includes a lid 18 that is attached to a canister body 21 by hinges 34 which permits the lid 18 to swing freely about the hinges 34 when opening and closing the canister 16. The canister 16 also includes a labeling area 20 on the outer surface. Preferably, the labeling area 20 includes a surface area for displaying instructions on the use of the blood evacuation system 14 for the user. The lid 18 of canister 16 has a dome-like shape with a suction port 32 in communication with the interior space 46 inside the canister 16. The lid 18 further includes a tubing groove 22 along the rim of lid 18 and a spike cover nest 28 formed in the middle of lid 18 for storing a spike cover (not shown) therein. The tubing groove 22 provides an opening whereby the transfer tubing 24 attached to the blood evacuation bag 38 is inserted therethrough and connected to the blood evacuation bag 38 to establish fluid flow communication with the collection chamber of drainage device 12. Although the tubing groove 22 does not maintain a hermetic seal inside the canister 16, sufficient negative pressure is maintained inside the interstitial space 50 between the canister 16 and the blood evacuation bag 28 to generate enough negative pressure inside the bag 28 for drawing blood into the blood evacuation bag 38.
The blood evacuation bag 38 disposed inside the canister 16 has a plurality of ports located at the top portion of the bag 38. One port, a reinfusion port 42, is closed and covered with a cap 52 and provides a site for draining collected blood from the blood evacuation bag 38 after the bag 38 is separated from the canister 16 during the reinfusion procedure. Another port, a collection port c, 40, is provided for attachment to the transfer tubing 24 leading from the drainage device 12 for the evacuation of blood therefrom.
Referring to FIG. 4, the blood evacuation bag 38 shall be discussed in greater detail. The blood evacuation bag 38 includes an expandable interi«r space 46 used for the evacuation of shed blood from the drainage device 12. As shed blood is collected inside the interior space 46 of the blood evacuation bag 38, the :pace 46 expands until the bag 38 is filled to the desired lc=vel. A hole 44 located at the bottom portion of the blood evacuation bag 38 below the interior space 46 serves as a site for suspending the bag 38 from a suitable suspension me<~ns (not shown) during reinfusion. A clamp 30 is also provided to prevent fluid flow through the transfer tub=ing 24 when the user wishes to stop the flow of blood into the blood evacuation bag 38 and to also prevent fluid flow from the bag 38 prior to reinfusion. Preferably, the blood evacuation bag 38 according to the present invention may be manufactured from any clear, flexible plastic material, although any material suitable for collecting and reinfusing fluid, like blood, is felt to fall within the scope of the present invention.
In establishing fluid flow communication between the blood evacuation bag 38 and tile drainage device 12, a user engages a spike port (not shown) leading from the collection chamber of the drainage device 12 with a blood spike 26. The blood spike 26 is attached to a spike port (not shown) attached to the distal end of the transfer tubing 24 leading from the blood evacuation bag 38. Prior to engaging the spike port, a dust cover 56 that caps the blood spike 26 during storage and transportation after manufacture is removed. Once the user engages the blood spike 26 to the spike port, a source of vacuum is applied to the suction 5 port 32. When vacuum is applied to the inside of canister 16, negative pressure builds inside the interstitial space 50 between the inner surface of canister 16 and the outside surface of blood evacuation bag 38 inside the canister 16.
With sufficient pressure decrease, blood collected inside 10 the drainage device 12 flows through the transfer tubing 24 and fills the interior space 46 of the blood evacuation bag 38.
Once the blood evacuation bag 38 is filled to a desired level reinfusion of the blood may take place. The reinfusion procedure begins by the user applying the clamp 30 to the transfer tubing 24 and turning off the source of vacuum to the canister 16, thereby preventing fluid flow therethrough from the drainage device 12. After the transfer tubing 24 is clamped, the blood spike 26 is disengaged from the spike port and properly encapsulated using a spike cover (not shown) stored inside the nest 2$ of the canister 16 to protect the contaminated pointed end 31 of the spike 26 after use. After encapsulating the blood spike 26, the lid 18 is opened and the blood evacuation bag 38 is removed from the canister 16 and suspended in the vicinity of the patient using suitable suspension means, for example an IV pole.
Once suspended, the user establishes fluid flow communication between the patient and the blood evacuation bag 38 by removing the cap 48 from the reinfusion port 42 17_ and connecting transfer tubing 24 between the patient and the port 42.
Reinfusion may occur by one of several methods.
Preferably, the blood evacuatuon bag 38 is suspended above the patient and the shed blood allowed to drain from the bag 38 using the force of gravity alone to draw the blood through transfer tubing 24 anc~ into patient 10. An alternative method of reinfus~_on is to apply a pressure cuff (not shown) around the blood evacuation bag 38 as it is suspended. As the user applies pressure through a bladder of the pressure cuff, blood inside the blood evacuation bag 38 is forced out and a higher rage of reinfusion is attained due to the increased pressure. Preferably, a suspension means 19 is provided on the outer surface of canister body 21 and includes a :hook integrally formed at the top portion for suspending the blood evacuation system 14.
Alternatively, a VELCRO support and corresponding VELCRO
loop can be provided at the bottom portion of canister body 21 for suspending the blood evacuation bag 38 from a suitable suspension means.
While reinfus.ion is occurring, the user may continue evacuating blood from the drainage device 12 by inserting another blood evac~sation bag ?.8 into the canister 16 and reestablishing fluid flow comrtrunication between the bag 38 and the drainage d~=vice 12 as noted above. In this manner, "batch" autotransfusion takes place by simply replacing the blood evacuation bag 38 inside the canister 16 every time a bag 38 is removed for reinfusi.on.
It should be understood from the foregoing that, while particular embodiments of the invention have been illustrated and described, various modifications can be made thereto without departing from the spirit and scope of the invention. Therefore, it is not intended that the invention be limited by the specification; instead, the scope of the present invention is intended to be limited only by the appended claims.
The present invention re:Lates generally to an apparatus and method for collecting fluids and the reinfusion of the fluids to a patient, and particularly to a blood evacuation system adapted for' autotransfusion. More specifically, the present invention is directed to a blood evacuation system that permits a disposable inner evacuation bag to be separated from an outer container for reinfusion so that another evacuation bag may be inserted inside the container to continue blood evacuation.
BACKGROUND ART
Blood evacuating apparatuses are commonly used in autotransfusion to evacuate and collect autologous blood from the collectic>n chamber of a chest drainage unit.
Autotransfusion refers to the reinfusion of a patient's own blood, known as autologous blood. Autotransfusion is the preferred method of reinfused since the blood being transfused is the patient's own blood, therefore eliminating problems over blood type incompatibility and exposure to blood carrying diseases such as hepatitis, AIDS, etc.
Moreover, autologous blood is more fresh than stored blood supplied by a donor and also contains the patient's own antibodies.
One type of autotransfusion, referred to as "post-operative" autotransfusion, is the transfusion of the patient's own shed blood following surgery where drained blood is collected and reinfused into the patient. Post-operative autotransfusion is limited in use since there are strict guidelines for the kind of blood which can be reinfused. Currently, the only post-operative blood believed suitable for autotransfusion is mediastinal blood, i.e. the blood which comes from the anatomical space or cavity in the chest.
Presently, chest drainage units are commonly used in the post-operative care of patients having surgery involving the chest cavity. Chest drainage units remove fluids and air from inside the chest cavity using tubing connected to the patient's chest cavity which drains the fluid and air into a collection chamber of the chest drainage unit. The chest drainage unit is attached to a source of vacuum which applies a suction to the tubing and draws the trapped fluid and air from the chest cavity and into the collection chamber. Once collected, the blood may be evacuated from the collection chamber using an autotransfusion pump or blood evacuation bag.
The use of a blood evacuation bag in autotransfusion is well known in the art. For example, U.S. Patent No.
5,380,314 to Herweck et al. discloses a blood collection bag having an internal spring that resiliently biases the bag into a fixed shape prior to use while concurrently inducing a negative pressure therein in order to manually draw blood from the collection chamber of the chest drainage unit.
However, one disadvantage with the '314 apparatus is that reinfusion must be accomplished using gravity means, whereby the bag is suspended in the vicinity of the patient and gravity is allowed to drain the collected blood from the bag for reinfusion to the patient. Unfortunately, the '314 apparatus will not properly drain unless the user first takes the extra step of bleeding in ambient air into the blood collection bag prior to reinfusion. This bleeding step is necessary in order to ford? collected blood inside the rigid blood collection bag to drain, otherwise the force of gravity alone will prove insufficient to draw blood from the bag during reinfusion.
Another example of a blo~~d evacuation system is found in U.S. Patent No.5,201,703 t~~ Gentelia et al. which discloses an apparatus for collecting blood from a chest drainage unit and reinfusion of the blood to the patient.
The '703 patent i~: directed to a self-contained, totally disposable apparatus comprising an rigid outer container housing an integrally attached flexible bag for use with a chest drainage unit. Negative pressure is applied or maintained inside the interstitial space between the rigid container and the inner flexible bag for causing blood stored in the collection chamber to be drawn into the bag.
As drawn blood travels through tubing connecting the '703 apparatus to the chest drainage unit, it begins to fill the flexible inner back. Once the bag is filled to a desired level with blood t:he entire apparatus, including the outer rigid container and the blood-filled inner baq, are disconnected from the chest drainage unit and suspended from a suitable suspen~~ion means in the vicinity of a patient for reinfusion of the collected blood.
WO 98/35718 PC't/US98/02586 -However, a disadvantage with the '703 apparatus is that the entire apparatus must be employed during reinfusion.
Specifically, both the outer rigid container and the inner flexible bag are utilized during the reinfusion process since the '703 apparatus has a unitary design wherein the inner flexible bag cannot be separated from the outer rigid container. As a result, another entire apparatus - a container and evacuation bag - must replace the used apparatus in order to continue the autotransfusion procedure on the same patient. Accordingly, the cost to the user is higher since the entire apparatus must be replaced after each transfusion.
Another disadvantage to the '703 apparatus is that the conventional means for attaining higher rates of reinfusion with the above noted blood evacuation systems are sometimes not possible. A prior art blood evacuation bag that fixedly attaches the evacuation bag to the outer rigid container or is made of a unitary, rigid container design are not adapted to employ high reinfusion rate techniques. For example, it is well known in the art that pressure cuffs wrapped around a flexible blood evacuation bag. can generate higher reinfusion rates by applying pressure to a bladder of the pressure cuff surrounding the container. However, if the evacuation container is of a rigid design a pressure cuff surrounding the container is unable to exert sufficient pressure to collapse the inner flexible bag and generate a higher rate of reinfusion. In view of these disadvantages regarding cost and performance, it is desirable to have a blood evacuation system in which only the inner flexible bag is used to reinfu~>e blood while the rigid outer container remains connected to a vacuum source for further collection T of blood from the chest drainage unit.
Accordingly, a need exists in the art for a blood evacuation system that permits detachment of the inner flexible bag from the outer rigid container before reinfusion so that. another flexible bag may be used inside the same container in order to collect further blood from the collection chamber. Moreover, there also exists a need in the art for a blood evacuation system that provides a cost effective means of reinfusing blood to a patient using multiple, detachable evacuation bags to continue blood evacuation while reinfusion takes place.
DISCLOSURE OF INVENTION
A principle object of the present invention is to provide a cost-effective means of reinfusing blood to a patient.
Another object of the present invention is to provide an efficient method of reinfusing autologous blood to a patient.
A further object of the present invention is to provide a blood evacuation system that includes an inner flexible bag that is separable from its outer container during reinfusion.
Another further object of the present invention is to provide a separab7_e evacuation bag that is adapted to receive a pressure cuff for generating a higher rate of reinfusion.
These and other objects of the present invention are realized in a presently preferred embodiment thereof, described by way of example and not by way of limitation, which provides for an apparatus and related method for evacuating and reinfusing blood to a patient using a blood evacuation system comprising a separable, flexible inner bag inside an outer rigid container for reinfusing shed blood drawn from the collection chamber of a chest drainage unit.
The outer rigid container includes a suction port connected to a source of vacuum for applying a negative pressure within the interstitial space between rigid container and the inner flexible bag disposed therein. The negative pressure maintained within the interstitial space inside the container causes blood to be drawn into the bag from the collection chamber of the chest drainage unit through tubing which maintains fluid flow communication between the bag and the collection chamber. Once the bag is filled to a desired level, the inner flexible bag is removed from the outer rigid container and suspended within the vicinity of a patient for reinfusion of the collected blood.
BRIEF DESCRIPTION OF DRAWINGS
FIG. 1 is a simplified block diagram showing the blood evacuation system according to the present invention;
FIG. 2 is a perspective view of the rigid outer container and transfer tubing according to the present invention;
FIG. 3 is a partial cross section view of the rigid outer container showing the blood evacuation bag according to the present invention; and FIG. 4 is a pE=_rspective view of the blood evacuation bag according to the present invention.
MODE ( S ) FOR CARRYII\fG OUT THE INVENTION
Referring to FIG. 1, a simplified block diagram of an autotransfusion sy:~tem 11 is illustrated showing the constituent element=s of system 11. The autotransfusion system 11 comprise; a patient 10 in fluid flow communication with a drainage device 12 using transfer tubing 24 to maintain fluid flow therebetween in direction A. The autotransfusion system 11 further includes a blood evacuation system 14 according to the present invention that is in fluid flow communication with the drainage device 12 using the same type' of transfer tubing 24 used between the patient 10 and the device 12. Preferably, the transfer tubing 24 is made of a flexible plastic material, although any flexible material suitable for transporting fluid, such as blood, is felt t=o fall within the scope of the present invention.
Referring to FIGS. 2 and 3, the blood evacuation system 14 according to the present invention is shown. The blood evacuation system 14 comprises a rigid canister 16 with a flexible blood evacuation bag 38 disposed therein.
Preferably, the canister 16 has a generally round shape, although any shaped container suitable for storing fluid is felt to fall within the scope of the present invention. The canister 16 includes a lid 18 that is attached to a canister body 21 by hinges 34 which permits the lid 18 to swing freely about the hinges 34 when opening and closing the canister 16. The canister 16 also includes a labeling area 20 on the outer surface. Preferably, the labeling area 20 includes a surface area for displaying instructions on the use of the blood evacuation system 14 for the user. The lid 18 of canister 16 has a dome-like shape with a suction port 32 in communication with the interior space 46 inside the canister 16. The lid 18 further includes a tubing groove 22 along the rim of lid 18 and a spike cover nest 28 formed in the middle of lid 18 for storing a spike cover (not shown) therein. The tubing groove 22 provides an opening whereby the transfer tubing 24 attached to the blood evacuation bag 38 is inserted therethrough and connected to the blood evacuation bag 38 to establish fluid flow communication with the collection chamber of drainage device 12. Although the tubing groove 22 does not maintain a hermetic seal inside the canister 16, sufficient negative pressure is maintained inside the interstitial space 50 between the canister 16 and the blood evacuation bag 28 to generate enough negative pressure inside the bag 28 for drawing blood into the blood evacuation bag 38.
The blood evacuation bag 38 disposed inside the canister 16 has a plurality of ports located at the top portion of the bag 38. One port, a reinfusion port 42, is closed and covered with a cap 52 and provides a site for draining collected blood from the blood evacuation bag 38 after the bag 38 is separated from the canister 16 during the reinfusion procedure. Another port, a collection port c, 40, is provided for attachment to the transfer tubing 24 leading from the drainage device 12 for the evacuation of blood therefrom.
Referring to FIG. 4, the blood evacuation bag 38 shall be discussed in greater detail. The blood evacuation bag 38 includes an expandable interi«r space 46 used for the evacuation of shed blood from the drainage device 12. As shed blood is collected inside the interior space 46 of the blood evacuation bag 38, the :pace 46 expands until the bag 38 is filled to the desired lc=vel. A hole 44 located at the bottom portion of the blood evacuation bag 38 below the interior space 46 serves as a site for suspending the bag 38 from a suitable suspension me<~ns (not shown) during reinfusion. A clamp 30 is also provided to prevent fluid flow through the transfer tub=ing 24 when the user wishes to stop the flow of blood into the blood evacuation bag 38 and to also prevent fluid flow from the bag 38 prior to reinfusion. Preferably, the blood evacuation bag 38 according to the present invention may be manufactured from any clear, flexible plastic material, although any material suitable for collecting and reinfusing fluid, like blood, is felt to fall within the scope of the present invention.
In establishing fluid flow communication between the blood evacuation bag 38 and tile drainage device 12, a user engages a spike port (not shown) leading from the collection chamber of the drainage device 12 with a blood spike 26. The blood spike 26 is attached to a spike port (not shown) attached to the distal end of the transfer tubing 24 leading from the blood evacuation bag 38. Prior to engaging the spike port, a dust cover 56 that caps the blood spike 26 during storage and transportation after manufacture is removed. Once the user engages the blood spike 26 to the spike port, a source of vacuum is applied to the suction 5 port 32. When vacuum is applied to the inside of canister 16, negative pressure builds inside the interstitial space 50 between the inner surface of canister 16 and the outside surface of blood evacuation bag 38 inside the canister 16.
With sufficient pressure decrease, blood collected inside 10 the drainage device 12 flows through the transfer tubing 24 and fills the interior space 46 of the blood evacuation bag 38.
Once the blood evacuation bag 38 is filled to a desired level reinfusion of the blood may take place. The reinfusion procedure begins by the user applying the clamp 30 to the transfer tubing 24 and turning off the source of vacuum to the canister 16, thereby preventing fluid flow therethrough from the drainage device 12. After the transfer tubing 24 is clamped, the blood spike 26 is disengaged from the spike port and properly encapsulated using a spike cover (not shown) stored inside the nest 2$ of the canister 16 to protect the contaminated pointed end 31 of the spike 26 after use. After encapsulating the blood spike 26, the lid 18 is opened and the blood evacuation bag 38 is removed from the canister 16 and suspended in the vicinity of the patient using suitable suspension means, for example an IV pole.
Once suspended, the user establishes fluid flow communication between the patient and the blood evacuation bag 38 by removing the cap 48 from the reinfusion port 42 17_ and connecting transfer tubing 24 between the patient and the port 42.
Reinfusion may occur by one of several methods.
Preferably, the blood evacuatuon bag 38 is suspended above the patient and the shed blood allowed to drain from the bag 38 using the force of gravity alone to draw the blood through transfer tubing 24 anc~ into patient 10. An alternative method of reinfus~_on is to apply a pressure cuff (not shown) around the blood evacuation bag 38 as it is suspended. As the user applies pressure through a bladder of the pressure cuff, blood inside the blood evacuation bag 38 is forced out and a higher rage of reinfusion is attained due to the increased pressure. Preferably, a suspension means 19 is provided on the outer surface of canister body 21 and includes a :hook integrally formed at the top portion for suspending the blood evacuation system 14.
Alternatively, a VELCRO support and corresponding VELCRO
loop can be provided at the bottom portion of canister body 21 for suspending the blood evacuation bag 38 from a suitable suspension means.
While reinfus.ion is occurring, the user may continue evacuating blood from the drainage device 12 by inserting another blood evac~sation bag ?.8 into the canister 16 and reestablishing fluid flow comrtrunication between the bag 38 and the drainage d~=vice 12 as noted above. In this manner, "batch" autotransfusion takes place by simply replacing the blood evacuation bag 38 inside the canister 16 every time a bag 38 is removed for reinfusi.on.
It should be understood from the foregoing that, while particular embodiments of the invention have been illustrated and described, various modifications can be made thereto without departing from the spirit and scope of the invention. Therefore, it is not intended that the invention be limited by the specification; instead, the scope of the present invention is intended to be limited only by the appended claims.
Claims (24)
1. An evacuation system (14) for the collection of fluid from a drainage device (12) and reinfusion of those fluids to a patient comprising:
a container (16), said container (16) including an open top and lid (18) for sealing said open top of said container (16), said lid (18) including a port (32) located at the top portion thereof, said port (32) being adapted for connection to a source of vacuum for applying and maintaining a negative pressure inside said container (16) for causing fluid to be drawn into said container (16), and a flexible bag (38) disposable within said container (16) and separable from said container (16), said flexible bag (38) having a plurality of ports (42, 40, 54), one of said plurality of ports (40) being in fluid flow communication with a drainage device (12) for drawing in fluid from said drainage device (12) when said source of vacuum is applied and collecting fluid into said flexible bag (38), another one of said ports (42) being adapted for reinfusion of said collected fluid to a patient, wherein said flexible back (38) is removable from said container (16) for reinfusion of fluid to a patient.
a container (16), said container (16) including an open top and lid (18) for sealing said open top of said container (16), said lid (18) including a port (32) located at the top portion thereof, said port (32) being adapted for connection to a source of vacuum for applying and maintaining a negative pressure inside said container (16) for causing fluid to be drawn into said container (16), and a flexible bag (38) disposable within said container (16) and separable from said container (16), said flexible bag (38) having a plurality of ports (42, 40, 54), one of said plurality of ports (40) being in fluid flow communication with a drainage device (12) for drawing in fluid from said drainage device (12) when said source of vacuum is applied and collecting fluid into said flexible bag (38), another one of said ports (42) being adapted for reinfusion of said collected fluid to a patient, wherein said flexible back (38) is removable from said container (16) for reinfusion of fluid to a patient.
2. The evacuation system (14) according to claim 1, wherein said negative pressure is applied to an interstitial space between an interior surface of said container (16) and an exterior surface of said flexible bag (38), said negative pressure causing fluid to be drawn from the drainage device (12) and into the flexible back (38).
3. The evacuation system (14) according to claim 1, wherein one of said plurality of ports (40, 42, 54) is adapted for use as a gravity drain for draining fluid from said flexible bag (38) during reinfusion.
4. The evacuation system (14) according to claim 4, wherein said port (32) is formed on said lid (18), said port (32) communicating with the inside of said container (16).
5. The evacuation system (14) according to claim 4, wherein said lid (18) is hingeable to said container (16).
6. The evacuation system (14) according to claim 1, wherein said fluid flow communication between the drainage device (12) and one of said plurality of ports (40, 42, 54) is maintained by tubing (29) attached therebetween.
7. A method of reinfusing fluid back to a patient (10), the steps of the method comprising:
a) establish fluid flow communication between a receptacle (38) housed in a container (16) and a source of fluid for the collection of said fluid into said receptacle (38) to a predetermined level;
b) close off fluid flow communication between said receptacle (38) and said source of fluid once the predetermined level of fluid is collected inside said receptacle (38);
c) disengage said receptacle (38) from said source of fluid and open a lid (18) of said container (16);
d) remove said receptacle (38) from said container (16) and suspend said receptacle (38) in the vicinity of the pat lent (10); and e) establish fluid flow communication between the patient (10) and said receptacle (38) and reinfuse said fluid back into the patient (10).
a) establish fluid flow communication between a receptacle (38) housed in a container (16) and a source of fluid for the collection of said fluid into said receptacle (38) to a predetermined level;
b) close off fluid flow communication between said receptacle (38) and said source of fluid once the predetermined level of fluid is collected inside said receptacle (38);
c) disengage said receptacle (38) from said source of fluid and open a lid (18) of said container (16);
d) remove said receptacle (38) from said container (16) and suspend said receptacle (38) in the vicinity of the pat lent (10); and e) establish fluid flow communication between the patient (10) and said receptacle (38) and reinfuse said fluid back into the patient (10).
8. The method according to claim 7, wherein said step of establishing fluid flow communication between said receptacle (38) and said source of fluid further includes applying a source of vacuum within the interior space (46) separating said receptacle (38) from said container (16).
9. The method according to claim 7, wherein said step of establishing fluid flow communication between said receptacle (38) and said source of fluid further includes engaging a tube (24) connected to said receptacle (38) with a tube (24) connected to said source of fluid.
10. The method according to claim 7, wherein said step of disengaging said receptacle (38) from said source of fluid further includes sealing off a free end of a tube (24) connected to said receptacle (38) after disengagement occurs.
11. The method according to claim 10, wherein sealing said free end of said tube (24) connected to said receptacle (38) further includes encapsulating a spike (26) attached to said free end of said tube (24) connected to said receptacle (38).
12. The method according to claim 7, wherein said step of disengaging further includes disengaging a spike (26) attached to a free end of a tube (24) connected to said receptacle (38) from a port attached to a free end of a tube (24) connected to said source of fluid.
13. The method according to claim 7, wherein said step of disengaging further includes disengaging a spike (26) attached to a free end of a tube (24) connected to said source of fluid from a port attached to a free end of a tube (24) connected to said receptacle (38).
14. The method according to claim 7, wherein said step of establishing fluid flow communication between the patient (10) and said receptacle (38) further includes engaging a free end of a tube (24) connected to said receptacle (38) with a free end of a tube (38) connected to the patient (10).
15. The method according to claim 14, wherein said step of establishing fluid flow communcation further includes applying a pressure means around the outside of said receptacle (38) for forcing fluid from said receptacle (38) and into the patient (10) during reinfusion.
16. A method of reinfusing fluid back to a patient (10), the steps of the method comprising:
a) establish fluid flow communication between a first receptacle (38) housed in a container (16) and a source of fluid for the collection of said fluid into said first receptacle (38) to a predetermined level;
b) close off fluid flow communication between said first receptacle (38) and said source of fluid once the predetermined level of said fluid is collected inside said first receptacle (38);
c) disengage said first receptacle (38) from said source of fluid and open a lid (18) of said container (16);
d) remove said first receptacle (38) from said container (16) and suspend said first receptacle (38) in the vicinity of the patient (10);
e) establish fluid flow communication between the patient (10) and said first receptacle (38) and reinfuse said fluid back into the patient (10);
f) insert a second receptacle (38) into said container (16) and close said lid (18);
g) establish fluid flow communication between said second receptacle (38) and said source of fluid for the collection of said fluid into said second receptacle (38) to a predetermined level; and h) repeat said steps (a) - (g) for as many receptacles (38) that are desired for reinfusion of fluid back to the patient (10).
a) establish fluid flow communication between a first receptacle (38) housed in a container (16) and a source of fluid for the collection of said fluid into said first receptacle (38) to a predetermined level;
b) close off fluid flow communication between said first receptacle (38) and said source of fluid once the predetermined level of said fluid is collected inside said first receptacle (38);
c) disengage said first receptacle (38) from said source of fluid and open a lid (18) of said container (16);
d) remove said first receptacle (38) from said container (16) and suspend said first receptacle (38) in the vicinity of the patient (10);
e) establish fluid flow communication between the patient (10) and said first receptacle (38) and reinfuse said fluid back into the patient (10);
f) insert a second receptacle (38) into said container (16) and close said lid (18);
g) establish fluid flow communication between said second receptacle (38) and said source of fluid for the collection of said fluid into said second receptacle (38) to a predetermined level; and h) repeat said steps (a) - (g) for as many receptacles (38) that are desired for reinfusion of fluid back to the patient (10).
17. The method according to claim 16, wherein said steps of establishing fluid flow communication between said as many receptacles (38) that are desired and said source of fluid further includes applying a source of vacuum within the interior space (46) separating said as many receptacles (38) that are desired from said container (16).
18. The method according to claim 16, wherein said steps of establishing fluid flow communication between said as many receptacles (38) that are desired and said source of fluid further includes engaging a tube (24) connected to said as many receptacles (38) that are desired with a tube (24) connected to said source of fluid.
19. The method according to claim 16, wherein said steps of disengaging said as many receptacles (38) that are desired from said source of fluid further includes sealing off a free end of a tube (24) connected to respective said as many receptacles (38) that are desired after disengagement occurs.
20. The method according to claim 19, wherein sealing said free end of said tube (24) connected to said as many receptacles (38) that are desired further includes encapsulating a spike (26) attached to said free end of said tube (24) connected to each of said as many receptacles (38) that are desired.
21. The method according to claim 16, wherein said step of disengaging further includes disengaging a spike (26) attached to a free end of a tube (24) connected to said as many receptacles (38) that are desired from a port attached to a free end of a tube (24) connected to said source of fluid.
22. The method according to claim 16, wherein said step of disengaging further includes disengaging a spike (26) attached to a free end of a tube (24) connected to said source of fluid from a port attached to a free end of a tube (24) connected to said as many receptacles (38) that are desired.
23. The method according to claim 16, wherein said step of establishing fluid flow communication between the patient (10) and said as many receptacles (38) that are desired further includes engaging a free end of a tube (24) connected to said as many receptacles (38) that are desired with a free end of a tube (24) connected to the patient (10).
24. The method according to claim 14, wherein said step of establishing fluid flow communcation further includes applying a pressure means around the outside of said as many receptacles (38) that are desired for forcing fluid from said as many receptacles (38) that are desired and into the patient during reinfusion.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US3836197P | 1997-02-13 | 1997-02-13 | |
| US60/038,361 | 1997-02-13 | ||
| PCT/US1998/002586 WO1998035718A1 (en) | 1997-02-13 | 1998-02-12 | Blood evacuating system and method of use thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2280719A1 true CA2280719A1 (en) | 1998-08-20 |
Family
ID=21899491
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002280719A Abandoned CA2280719A1 (en) | 1997-02-13 | 1998-02-12 | Blood evacuating system and method of use thereof |
Country Status (6)
| Country | Link |
|---|---|
| EP (1) | EP1007145A4 (en) |
| JP (1) | JP2001512343A (en) |
| CN (1) | CN1251537A (en) |
| AU (1) | AU6323198A (en) |
| CA (1) | CA2280719A1 (en) |
| WO (1) | WO1998035718A1 (en) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6183453B1 (en) * | 1997-11-20 | 2001-02-06 | Sherwood Services, Ag | Blood evacuation container with blood spike nesting feature |
| JP4550751B2 (en) * | 2006-03-08 | 2010-09-22 | 日本シャーウッド株式会社 | Medical suction collector |
| CN101121056A (en) * | 2007-09-07 | 2008-02-13 | 周泰立 | Medical negative pressure suction device using disposable collecting bag |
| KR101169783B1 (en) | 2010-04-13 | 2012-07-31 | 이희영 | Fat harwesting and storing equipment using pressure and storing method of fat |
| US11413378B2 (en) * | 2018-05-08 | 2022-08-16 | Biomagnetic Solutions Llc | Rigid chamber for cell separation from a flexible disposable bag |
| CN113509180B (en) * | 2021-05-26 | 2024-06-04 | 青岛市胶州中心医院 | Be applicable to clinical laboratory's quick device of drawing blood |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3680560A (en) * | 1968-11-26 | 1972-08-01 | Voys Inc Le | Vacuum drainage collecting apparatus with disposable liner |
| US4060107A (en) * | 1976-10-26 | 1977-11-29 | Henry Naftulin | Method and apparatus for collecting fluids |
| DE3172813D1 (en) * | 1980-05-20 | 1985-12-12 | Haemonetics Corp | Suction liquid collection assembly and flexible liquid collection bag suitable for use therein |
| DE3150500A1 (en) * | 1981-12-21 | 1983-06-30 | Friedrich Gerd 5000 Köln Lauterjung | SUCTION BOTTLE FOR MEDICAL PURPOSES |
| US4516973A (en) * | 1983-03-14 | 1985-05-14 | Becton, Dickinson And Company | One-piece disposable collection bag having a rigid cover for a suction canister unit |
| US4675010A (en) * | 1985-10-04 | 1987-06-23 | American Omni Medical, Inc. | Thoracic drainage collection system and method |
| US4775360A (en) * | 1986-11-07 | 1988-10-04 | Lantech, Inc. | Autologus blood methods and apparatus |
| FR2677254A1 (en) * | 1991-06-10 | 1992-12-11 | Gadrat Francis | Medical device for recovery and retransfusion of blood |
| CH686027A5 (en) * | 1991-07-26 | 1995-12-15 | Elp Rochat | Unit of recovery and blood filtration. |
| DE9403245U1 (en) * | 1994-02-26 | 1994-05-05 | Metec A. Schneider GmbH, 77866 Rheinau | Device for collecting and roughly cleaning blood accumulated during operations at the operating site |
| US5713879A (en) * | 1994-02-26 | 1998-02-03 | Metec A. Schneider Gmbh | Device for collecting and filtering blood |
-
1998
- 1998-02-12 EP EP98907419A patent/EP1007145A4/en not_active Withdrawn
- 1998-02-12 CN CN98802547A patent/CN1251537A/en active Pending
- 1998-02-12 AU AU63231/98A patent/AU6323198A/en not_active Abandoned
- 1998-02-12 WO PCT/US1998/002586 patent/WO1998035718A1/en not_active Application Discontinuation
- 1998-02-12 CA CA002280719A patent/CA2280719A1/en not_active Abandoned
- 1998-02-12 JP JP53585598A patent/JP2001512343A/en active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| EP1007145A4 (en) | 2001-06-06 |
| CN1251537A (en) | 2000-04-26 |
| AU6323198A (en) | 1998-09-08 |
| JP2001512343A (en) | 2001-08-21 |
| WO1998035718A1 (en) | 1998-08-20 |
| EP1007145A1 (en) | 2000-06-14 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FZDE | Discontinued |