Surgery – Container for blood or body treating material – or means used... – Bag type
Reexamination Certificate
2000-02-01
2003-09-02
Sykes, Angela D. (Department: 3762)
Surgery
Container for blood or body treating material, or means used...
Bag type
C604S403000, C604S410000, C604S415000, C206S438000, C206S828000, C383S067000, C383S113000
Reexamination Certificate
active
06613036
ABSTRACT:
BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates to a light-protective container assembly for a light-sensitive fluid and, particularly, is directed to an intravenous flexible bag having a light-protective sleeve connected thereto so as to inhibit or prevent degradation of a light-sensitive solution contained within the flexible bag.
2. Description of Related Art
A variety of fluids are sensitive to at least a certain amount of electromagnetic energy within certain wavelengths, such as within the spectrum of visible light. Upon extended exposure, these fluids, hereinafter referred to generally as light-sensitive fluids, are susceptible to a chemical or photo-chemical reaction often resulting in degradation of the fluid. Depending upon the fluid, such reactions can take place within a matter of minutes or hours, while other fluids may require days or weeks before such degradation occurs. Light-sensitive fluids can be protected against such reactions by using a container made of a suitable material capable of blocking the transmission of detrimental electromagnetic energy. For example, the use of an opaque material is often preferred to protect against visible light. Certain situations or applications, however, preclude the use of opaque materials because visual inspection of the fluid is required. One such situation involves the use of intravenous or I.V. systems.
Flexible Intravenous (I.V.) bags are commonly used to store and administer medical agents to patients. The I.V. bags can contain a variety of fluids, such as water or saline, containing therapeutic agents including nutritional supplements, diagnostic substances, therapeutic substances, pharmaceuticals, medicaments and other drugs. A problem with such agents is that many are sensitive to electromagnetic energy, and particularly to light. Exposing such agents to light may cause a chemical or photo-chemical response, which often results in a loss of paternity and other undesirable impurities. Depending on the agent, this degradation can occur within 20 minutes of exposure to light or the like.
Furthermore, I.V. bags are typically flexible and made from a translucent or see-through material to allow visual inspection. In use, a caregiver hangs the I.V. bag on a pole. A delivery tube extends from the bottom of the bag to a needle that is inserted into the patient. The agent then gradually flows into the patient's body, usually over a 1- to 24-hour period. As such, the contents of the I.V. bag, as well as the I.V. bag itself, is potentially exposed to damaging amounts of light.
One way to prevent exposure of an agent to light would be to make the I.V. bag of an opaque material. However, there is a risk that the pigment or dye that constitutes the opaque material will leach from the bag and contaminate the fluid. This risk is especially significant if the agent in the I.V. bag is expected to have a long shelf life. Additionally, making the bag opaque prevents visual inspection of its contents. Visual inspection of the bag is beneficial both during the manufacturing process and during use to ensure that the fluid in the I.V. bag is clean and free of particulates and precipitates, and to verify the amount of fluid remaining within the reservoir.
Another way to prevent exposure of an agent to light is to enclose the I.V. bag in a sealed overwrap that is opaque. However, these overwraps generally are configured to be torn off and discarded when the I.V. bag is to be used. Thus, the bag and its contents are exposed to light during use.
To protect the fluid from light or similar electromagnetic energy, caregivers may cover the I.V. bag with a separate cover that is made of translucent material such as that available from Medipak of Winchester, VA. The use of such separate cover, however, involves an additional step in the administration of an agent. That is, when the overwrap has been torn from the I.V. bag, the translucent cover, if provided, must be removed from the overwrap and manually placed in proper position over the I.V. bag prior to administration. However, caregivers tend to use such separate covers inconsistently, while more often, the cover is merely discarded with the overwrap and not used at all. This failure can be detrimental to some fluids, especially those containing agents that react quickly to electromagnetic energy, such as light. Additionally, such covers generally are configured such that one size is intended to fit all applications. As a result, such covers tend to be ill fitting and allow ambient light to pass onto the I.V. bag.
Alternatively, caregivers may merely attempt to cover the I.V. bag with a towel, linen, or some other shroud. These make-shift shrouds commonly fail to completely shield the I.V. bag from light and often fall from the I.V. bag. Another problem is that these attempts to shroud the I.V. bag do not easily permit visual inspection of the I.V. bag and its contents. Typically, the caregiver must remove the shroud from the I.V. bag, which again exposes the agent to potentially harmful light. Each time that a caregiver removes such a cover or shroud, there is an increased likelihood that the I.V. bag will not be properly recovered and the agent will be exposed to damaging light. As such there remains a need for an improved light-protective container assembly, as well as a method of making the same.
SUMMARY OF THE INVENTION
The purpose and advantages of the present invention will be set forth in and apparent from the description that follows, as well as will be learned by practice of the invention. Additional advantages of the invention will be realized and attained by the methods and systems particularly pointed out in the written description and claims hereof, as well as from the appended drawings.
To achieve these and other advantages and in accordance with the purpose of the invention, as embodied and broadly described, the invention includes a light-protective container assembly for a light-sensitive fluid. The container assembly generally includes a translucent container, although more preferably transparent, and a flexible sleeve connected to the container. The container has an inner reservoir defined therein to contain the fluid. The sleeve, which is configured to substantially cover the container, is made of a material capable of substantially preventing the transmission of an identified range of wavelengths from the electromagnetic spectrum.
To connect the sleeve, the container preferably has at least one passageway defined therethrough, wherein the passageway is isolated from the inner reservoir. The sleeve has a first portion, which is positioned on one side of the container, and a second portion, which is positioned on an opposite side of the container. The first portion of the sleeve is attached to the second portion through the passageway to connect indirectly the sleeve to the container. Preferably, a plurality of passageways are provided, with the first and second portions of the sleeve being attached to each other through each passageway. Although a separate fastener, such as a snap, button, clip or adhesive, may be used, a heat stake or similar thermal weld is preferred.
The container is translucent, and more preferably transparent, to allow visual inspection selectively of the fluid contained therein and, in accordance with one aspect of the invention, the container is a flexible intravenous supply bag having a port structure at one end. As such, the sleeve is configured to extend at least over the reservoir of the container, and preferably over the port structure. Furthermore, and in accordance with a preferred embodiment, the first portion of the sleeve is a first side wall having opposite lateral edge portions, and the second portion of the sleeve is a second side wall having opposite lateral edge portions. In this manner, the lateral edge portions of the first side wall are integral with the lateral edge portions of the second side wall to define a tubular structure having at least one opened end to allow the sleeve to be disp
Daniels Marc M.
Farmer Randall M.
Garcia Lysander R.
Bianco Patricia
Sykes Angela D.
Vrioni Beth A.
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