Patent Application
20180360361
The subject matter disclosed herein relates to a system for collecting blood from an umbilical cord and the placenta and in particular to a system that is low in cost and rapidly collects cord blood.
The blood from a human umbilical cord, sometime referred to as “cord blood” is rich source of stem cells that have many therapeutic benefits. Cord blood has been used as a treatment for more than 70 different diseases, including cancers, blood disorders, and immune deficiencies. Further, there is a high probability that many therapeutic treatments that utilize cord blood have yet to be discovered. Despite these potential health benefits, only ˜5% of all parents chose to collect and store their newborn baby's cord blood. This is due to lack of availability to collection tools in the hospital, the time associated with collection after child birth and the expenses associated with long term storage.
Typically, the collection of cord blood is initiated after the umbilical cord stops pulsating and the cord is clamped and cut. There are two common collection procedures, known as the “bag method” and the “syringe method.” With the bag method, the placenta and cord are elevated, using the force of gravity to drain the blood from the placenta into the bag, but this method can take nearly 40 minutes to collect an adequate sample, delaying delivery of the placenta. With the syringe method, the procedure is similar to that of a blood draw, an empty syringe is inserted into the umbilical cord artery and is used to draw blood from within the vasculature of remaining cord, but only small volumes of blood can be collected with this method.
Accordingly, while existing cord blood collection techniques are suitable for their intended purpose the need for improvement remains, particularly in providing a system that rapidly collects the cord blood in a cost efficient manner.
According to one aspect of the disclosure a cord blood collection system is provided. The system includes a housing having an upper portion and a lower portion, the upper portion and lower portion defining a hollow interior. A peristaltic pump is disposed within the lower portion, the peristaltic pump having an input portion and an output portion. A reel member is disposed in the upper portion. A tubing member is movably coupled to the reel member, the tubing member being operably coupled to the peristaltic pump, the first end being configured to couple with a container, the second end being configured to couple with a needle.
According to another aspect of the disclosure a method of collecting cord blood is provided. The method includes coupling a tubing member to a reel member. Coupling the tubing member to a peristaltic pump. Coupling a first end of the tubing member to a container. Coupling the second end of the tubing member to a needle. The needle is inserted into a vasculature of an umbilical cord immediately after the delivery of a newborn infant. The peristaltic pump is activated and blood is transferred from the vasculature to the container in response to the activation of the peristaltic pump.
These and other advantages and features will become more apparent from the following description taken in conjunction with the drawings.
The subject matter, which is regarded as the disclosure, is particularly pointed out and distinctly identified in the claims at the conclusion of the specification. The foregoing and other features, and advantages of the disclosure are apparent from the following detailed description taken in conjunction with the accompanying drawings in which:
The detailed description explains embodiments of the disclosure, together with advantages and features, by way of example with reference to the drawings.
Embodiments of the invention provide advantages in the collection of cord blood from an umbilical cord and placenta in a rapid and cost effective manner. Referring now to
It should be appreciated that while embodiments herein refer to the storage container 30 as a bottle, vial or bag, the claims should not be so limited. In other embodiments, the storage container 30 may be any vessel suitable for receiving and holding the cord blood in accordance with standard bodily fluid handling procedures.
Referring now to
In an embodiment, the lower portion 42 includes a conically shaped outer surface 56 with a cylindrical portion 60 extending therefrom. An opening 62 extends through the cylindrical portion 60 into an opening 64 that extends from a top surface 66. The opening 64 is sized to receive a peristaltic pump 68 and an energy source, such as a battery 70. The switch 54 is electrically connected between the battery 70 and the peristaltic pump 68 to allow the operator to control the operation of the peristaltic pump 68.
In an embodiment shown in
In an embodiment, the motor portion 84 of the peristaltic pump 68 is positioned within a recession 86 of the system to allow the pump casing 88 to sit on a surface 90 within the opening 64. When positioned in this manner, the output port 74 may be approximately aligned with the opening 62. It be appreciated that the positioning of the motor 84 within the hole 86 along with the shape of the housing lower portion 42 also provides a center of gravity to improve stability of the housing assembly 26. In an embodiment, the input port 72 is fluidly coupled to the tubing second portion 36 and the output port 74 is fluidly coupled to the tubing first portion 34. In an embodiment, the flexible tube 76 and ports 72, 74 are replaceable and disposable to allow the pump 68 to be reused without having to use extensive sterilization or cleaning procedures between patients. In still another embodiment, the casement portion 88 (including the rotor 82, tube 76 and ports 72, 74) is removable and disposable allowing the motor 84 to be reused.
In an embodiment, the tubing second portion 36 may be extended from and retracted to the housing 38, this allows accessibility to the device from the table or the floor below to connect to the patient. In this embodiment, the reel member 58 is rotatably coupled to the housing upper portion 44 by a turning member 92. The turning member 92 may include a knob 94 and a threaded portion 96. A bottom surface of the knob 94 rests on the top surface 50 and the threaded portion 96 extends through the hole 54 and couples to a first end 98 of the reel member 58. In an embodiment, the reel member 58 includes a pair of opposing ends 98, 100 with a stem 102 (
Once the needle 28 is coupled to the first end 104, the operator may puncture the vasculature 22. By actuating the switch 54, the motor 84 is energized by the battery 70 causing the rotor 82 and lobes 80 to rotate and draw cord blood from the vasculature 22. The cord blood is drawn through the tubing 32 and deposited within the storage container 30. When the collection is completed, the operator actuates the switch 54 to de-energize the motor 84. To retract the tubing second portion 36, the operator rotates the knob 94 to rotate the reel member 58. The rotation of the reel member 58 cause the tubing 32 to be moved through the hole 46 and into the upper housing space 52.
It should be appreciated that while the switch 54 is illustrated as a toggle type switch, this is for exemplary purposes and the claims should not be so limited. In other embodiments, the switch 54 may include a rotary switch potentiometer that allows modulation of the voltage from the energy source to control pump speed.
It should also be appreciated that materials used in construction of the reusable components of the housing assembly 26, such as the housing 38, the reel member 58 and the turning member 92 may be selected to be sterilized using one or more common medical sterilization techniques, such as but not limited to steam sterilization, dry heat sterilization (autoclaving), chemical sterilization (ethylene oxide, sporicidal chemicals) and irradiation for example.
The term “about” is intended to include the degree of error associated with measurement of the particular quantity based upon the equipment available at the time of filing the application. For example, “about” can include a range of ±8% or 5%, or 2% of a given value.
The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting of the disclosure. As used herein, the singular forms “a”, “an” and “the” are intended to include the plural forms as well, unless the context clearly indicates otherwise. It will be further understood that the terms “comprises” and/or “comprising,” when used in this specification, specify the presence of stated features, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, integers, steps, operations, element components, and/or groups thereof.
While the disclosure is provided in detail in connection with only a limited number of embodiments, it should be readily understood that the disclosure is not limited to such disclosed embodiments. Rather, the disclosure can be modified to incorporate any number of variations, alterations, substitutions or equivalent arrangements not heretofore described, but which are commensurate with the spirit and scope of the disclosure. Additionally, while various embodiments of the disclosure have been described, it is to be understood that the exemplary embodiment(s) may include only some of the described exemplary aspects. Accordingly, the disclosure is not to be seen as limited by the foregoing description, but is only limited by the scope of the appended claims.
This application claims the benefit of U.S. Provisional Application Ser. No. 62/520,729, filed Jun. 16, 2017, the entire disclosure of which is incorporated herein by reference.
| Number | Date | Country | |
|---|---|---|---|
| 62520729 | Jun 2017 | US |
