Patent Application
20200016303
A portion of the disclosure of this patent contains material that is subject to copyright protection. The copyright owner has no objection to the reproduction by anyone of the patent document or the patent disclosure as it appears in the Patent and Trademark Office patent files or records, but otherwise reserves all copyright rights whatsoever.
The present invention relates to blood transfusions and devices for transfusions. In particular, it relates to a transfusion system that decreases the time it takes for a transfusion, especially in field (such as during military operations in the field) transfusions.
A transfusion is a traumatic event where blood is removed from one individual, animal, or human, and transfused to another in need. Since transfusion is a traumatic event, the longer it takes to complete the transfusion, the more traumatic the process is.
The current way blood is transfused, especially in the field, is first to remove blood from a donor into a “blood bag”. Typical blood bags hold about 450 to 500 ml of blood. After removal of the blood, the blood bag is connected to a “y” tubing along with a bag of saline or other appropriate solution. Both lines are then opened so that blood and saline travel to the recipient's veins. The process is completed once the blood bag is empty and the liquid solution has flushed the line. Typically this process takes about 30 to 40 minutes.
The more complex the transfusion process, the more complications can arise. The slower the process, likewise, is fraught with complications. With the bag, if more than 500 ml is necessary, the more complicated it gets with multiple bags being necessary. Accordingly, it would be of great use if the process could be made faster with less complexity. It would also be useful if in the field, transfusion could be done faster.
U.S. Pat. No. 2,102,523 issued on Dec. 14, 1937 to Ferrara teaches a transfusion system having an electric motor pump. However, Ferrara fails to disclose a device for setting the amount of blood to be transfused. It also does not disclose a device for stopping blood flow when a transfusion amount is reached, nor a blood counter. In U.S. Pat. No. 5,112,298 issued on May 12, 1992 to Prince, a system for separating blood into components and then return one or more of the components back to the donor is taught. There is no recipient in this case. And while there is a blood counter, it does not teach how that would be used in a transfusion.
The present invention involves a system and method that reduces the time to do a transfusion between two individuals to the 5 to 10 minute time frame from 30 to 40 minutes, or so. This is especially useful in the field such as in a military situation, a wilderness situation, a “buddy” transfusion, an emergency, and the like, where there is no medical facility close by, though the device can be used for any transfusion. A direct transfusion method with a blood counter which notifies the user that the transfer amount has been reached for manual stoppage or turns off automatically when the required amount of blood is transfused is disclosed.
Accordingly, in one embodiment, there is a system for transfusing blood from a donor to a recipient comprising:
In yet another embodiment, there is a method of transferring blood from a donor to a recipient comprising:
While this invention is susceptible to embodiment in many different forms, there is shown in the drawings, and will herein be described in detail, specific embodiments with the understanding that the present disclosure of such embodiments is to be considered as an example of the principles and not intended to limit the invention to the specific embodiments shown and described. In the description below, like reference numerals are used to describe the same, similar, or corresponding parts in the several views of the drawings. This detailed description defines the meaning of the terms used herein and specifically describes embodiments in order for those skilled in the art to practice the invention.
The terms “about” and “essentially” mean ±10 percent.
The terms “a” or “an”, as used herein, are defined as one or as more than one. The term “plurality”, as used herein, is defined as two or as more than two. The term “another”, as used herein, is defined as at least a second or more. The terms “including” and/or “having”, as used herein, are defined as comprising (i.e., open language). The term “coupled”, as used herein, is defined as connected, although not necessarily directly, and not necessarily mechanically.
The term “comprising” is not intended to limit inventions to only claiming the present invention with such comprising language. Any invention using the term comprising could be separated into one or more claims using “consisting” or “consisting of” claim language and is so intended.
Reference throughout this document to “one embodiment”, “certain embodiments”, “an embodiment”, or similar terms means that a particular feature, structure, or characteristic described in connection with the embodiment is included in at least one embodiment of the present invention. Thus, the appearances of such phrases or in various places throughout this specification are not necessarily all referring to the same embodiment. Furthermore, the particular features, structures, or characteristics may be combined in any suitable manner in one or more embodiments without limitation.
The term “or” as used herein is to be interpreted as an inclusive or meaning any one or any combination. Therefore, “A, B, or C” means any of the following: “A; B; C; A and B; A and C; B and C; A, B, and C”. An exception to this definition will occur only when a combination of elements, functions, steps, or acts are in some way inherently mutually exclusive.
The drawings featured in the figures are for the purpose of illustrating certain convenient embodiments of the present invention, and are not to be considered as limitation thereto. Term “means” preceding a present participle of an operation indicates a desired function for which there is one or more embodiments, i.e., one or more methods, devices, or apparatuses for achieving the desired function and that one skilled in the art could select from these or their equivalent in view of the disclosure herein and use of the term “means” is not intended to be limiting.
As used herein, the term “donor” refers to a human or animal donating blood.
As used herein, the term “recipient” refers to a corresponding human or animal receiving blood.
As used herein, the term “transfusing blood” refers to the process of taking blood from a donor (person or animal) and transferring it to a respective person or animal directly. Transfusions are used for various medical conditions to replace lost components of the blood. In the present invention, it refers only to whole blood transfusions since any intermediary steps have been eliminated. A filter may also be added to the system such that blood flows through the filter to remove any clots or other unwanted material. Typical filters are 170 to 260 microns and are well known in the art and are placed in line of the flow of blood. Transfusion is initiated when a venous device is in both donor and recipient, e.g., needle, PRN adapter, catheter in a vein, and is connected to the system. However, in some embodiments, hose clamps or other devices that block blood flow are used on the tubing to prevent the transfusion from starting before desired. Transfusion would then begin when the clamp or block is removed. Transfusion is accomplished by pressure flow between donor and recipient or by means of a pump.
As used herein, the term “venous device” refers to a sterile surgical needle standard for blood transfusions. Such needles are well known in the art. Needle size depends on the size and integrity of a donor's or recipient's vein. An 18-gauge needle is standard, but a needle or catheter as small as 23-gauge can be used for transfusion, if necessary. The smaller the gauge, the slower the flow rate and the higher the risk of clotting. Care must be taken to avoid excessive pressure resulting in hemolysis when very narrow needles are used. In addition to needles directly into a vein, other venous devices can be used to transfer from donor to recipient, e.g., connection to a PRN adapter and catheters already in a vein. Any coupling mechanism is then used, e.g., Luer Lock type attachment between the rest of the transfusion system and the venous device.
As used herein, the term “tubing” refers to medical tubing of the type generally accepted for use in doing blood transfusions. Such tubing is readily available. In the practice of the present invention, a first transfusion venous device attaches to one end of the tubing and a second transfusion venous device is attached to the second end with the first venous device inserted in the vein of the donor and the second venous device inserted in the vein of the recipient. In one embodiment, there is a single piece of tubing. In other embodiments, there can be multiple pieces of tubing connected together in fluid communication. In one embodiment, the blood counter is spliced into the tubing such that blood flows through the counter for measurement. The material and length of the tubing can be determined by one skilled in the art in view of this disclosure.
As used herein, the term “blood counter” refers to a device which can determine how much flowing blood is passing by a given point in the system from the donor to the recipient. It can do that by direct measure, mechanical or digital, of the blood flowing through the blood counter. In other embodiments, the blood counter is placed next to the tubing and can measure blood flow, such as by ultrasound. Since one needs to monitor the amount transfused, there is an input device on the blood counter to let the user set the amount to be transfused and to let the user know when that amount is reached. In one embodiment, wherein the blood flows through the counter, once the desired amount of blood is transfused, the flow of blood is then blocked automatically. In other embodiments, only an alarm sound or other notification initiates the user to then clamp or otherwise stop the flow of blood manually. Where the power is needed for the blood counter or the system, AC or DC power is included. In another embodiment, the blood counter detects back flow and either notifies user or blocks the blood flow or both. In one embodiment, it counts blood flow by precisely measured packets of blood by flowing through a device, e.g., a pump with chambers of known size, allowing the user to know precisely how much blood is transferred. Such pumps, when they are turned off, will stop the flow of blood. A notification device, e.g., alarm, light, etc. can be used to warn upon completion for manual blocking.
In the process of the present invention, the first transition venous device is inserted or has already been inserted into the vein of the donor. The second transfusion venous device is inserted or has already been inserted into the vein of the recipient. Blood flow is prevented, in one embodiment, by clamping the tubing which is connecting the two venous devices. The blood counter is positioned next to or flows through, such that the quantity of transfused blood is measured. In other embodiments, the blood counter can be set to have a notification when a designated amount of blood is transfused. In other embodiments, the blood counter can shut off the blood flow automatically. Blood flow commences and once completed, the needle venous devices can be removed from the donor and recipient, though other types of devices may remain in the recipient.
Now referring to the drawings,
In
Those skilled in the art to which the present invention pertains may make modifications resulting in other embodiments employing principles of the present invention without departing from its spirit or characteristics, particularly upon considering the foregoing teachings. Accordingly, the described embodiments are to be considered in all respects only as illustrative, and not restrictive, and the scope of the present invention is, therefore, indicated by the appended claims rather than by the foregoing description or drawings. Consequently, while the present invention has been described with reference to particular embodiments, modifications of structure, sequence, materials, and the like apparent to those skilled in the art still fall within the scope of the invention as claimed by the applicant.
This application is a continuation-in-part of U.S. non-provisional patent application number 15/938,768 filed on Mar. 28, 2018, and which is incorporated herein in its entirety by reference.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 15938768 | Mar 2018 | US |
| Child | 16580755 | US |
