BAG FOR PROVIDING PATIENT-SPECIFIC DRUGS
20200237619 · 2020-07-30
Inventors
Cpc classification
A61M39/00
HUMAN NECESSITIES
A61M39/28
HUMAN NECESSITIES
International classification
Abstract
Bag for providing patient-specific, in particular oncological drugs, with an interior divided into a plurality of, preferably four, separate chambers interior, wherein in at least one, preferably three chambers an infusion solution can be provided and patient-specific active substances can be added.
Claims
1. A bag for providing patient-specific, in particular oncological drugs, with an interior divided into a plurality of, preferably four, separate chambers, wherein in at least one, preferably three chambers, an infusion solution can be provided and patient-specific active substances can be added.
2. The bag according to claim 1, wherein at least one chamber serves to provide a rinsing solution.
3. The bag according to claim 2, the interior of the bag having four chambers, of which three serve to provide an infusion solution and the addition of a patient-specific active ingredient and one serves to provide a rinse solution.
4. The bag according to claim 1, the bag comprising a tube, and the chambers are formed by at least one of a group including welds, gluing, and clamping means.
5. The bag according to claim 1, the chambers being multi-layered, wherein the layers include either the same materials as one another or different materials from one another.
6. The bag according to claim 1, the chambers being at least one of equal in their volume or dimensioned differently.
7. The bag according to claim 1, each chamber is being assigned at least one connecting piece for at least one of filling or emptying the chamber.
8. The bag according to claim 1, and on the container, a merging system is mounted.
9. The bag according to claim 8, the merging system having an injection port for adding further liquids.
10. The bag according to claim 8, at least one of the merging or the administration of the solutions being regulatable via tube clamps.
11. The bag according to claim 1, at least one of a group including the bag, the connecting pieces, and the merging system being produced based on polymer, the polymer comprising polyolefins (POF) selected from a group including polyethylene (PE), polypropylene (PP), polyvinyl chloride (PVC), and ethylene-vinyl acetate (EVA).
12. The bag according to claim 1, at least one of a group including the shape, the material, the surface structuring of the chambers, the connecting pieces, and the merging system is/are designed such that an at least almost complete administration of the solutions is feasible.
13. The bag according to claim 1, at least one of a group including the chambers, the at least one connecting piece, and the merging system are made of colored plastic which has a photoprotective effect.
14. The set for providing patient-specific oncological drugs, comprising a bag according to claim 1 and a merging system coupled with the bag for administering patient-specific oncological drugs to a patient, wherein the bag and the merging system are housed one of together or individually in a closed package.
15. The bag according to claim 4, the tube comprising a polymer tube
16. The bag according to claim 15, the polymer of the polymer tube comprising one or more polyolefins (POF) of a group including polyethylene (PE), polypropylene (PP), polyvinyl chloride (PVC), and ethylene vinyl acetate (EVA).
Description
[0027] There are now various possibilities for designing and developing the teaching of the present invention in an advantageous manner. For this purpose, reference is made on the one hand to the claims subordinate to claim 1 and on the other hand to the following explanation of preferred embodiments of the invention using the drawings. In conjunction with the explanation of the preferred exemplary embodiments of the invention with reference to the drawings, generally preferred embodiments and developments of the teaching are also explained. In the drawings,
[0028]
[0029]
[0030]
[0031] The tube outlet 6 is associated with a Luer-Lock tube connector 7, by means of which the bag 1 is connected to a merging system 8. The merging system 8 comprises individual tubes, each connected to a tube outlet 6, which are brought together on the ends opposite the tube outlets 6. In the region of the Luer-Lock tube connector 7, closing clips 9 made of plastic are arranged to regulate the flow. The leftmost outermost tube of the merging system 8 is assigned an injection port 10 for further injections during the treatment. At the end of the merging system 8 opposite the bag 1, an opening 11 or a port for administering the drug via an infusion line to the patient is provided.
[0032] The inside surface of the bag 1 is designed such that an almost complete emptying of the chambers 2a, 2a, 2a, 2b can be realized. Both the bag 1 and the merging system 8 are made of a photoprotective plastic to protect the drugs used from light. A clear plastic can also be used.
[0033]
[0034] The connecting piece 5, 6 is associated with a Luer-Lock tube connector 7, by means of which the bag 1 and the individual chambers are connected to a merging system 8. Other means of connection of the merging system 8 are conceivable. The merging system 8 comprises individual tubes, which are connected at one end to a connecting piece 5, 6 of a chamber 2a, 2a, 2a, 2b, and are merged at the end opposite the connecting piece 5, 6 into a single tube. In the area of the Luer-Lock tube connector 7 or in the area before the merger of the individual tubes, each tube is provided with plastic closing clips 9 for regulating or opening and closing the flow. The left-most tube of the merging system 8 is assigned an injection port 10 for further injections during a treatment. At the end of the merging system 8 opposite the bag 1, an opening 11 or a port for administering the drug via an infusion line to the patient is provided. In the opening 11, a silicone plug is provided.
[0035] Frequently, the tube system 8 is pre-filled before the administration of the liquids or active substances located in the chambers 2a, 2a, 2a through the opening 11 with saline, so that the patient is supplied with sufficient liquid/saline. Since the contents of the individual chambers 2a, 2a, 2a are generally not allowed to mix, they are administered to the patient one after the other. For this purpose, the administration of the liquids of the individual chambers 2a, 2a, 2a, 2b is controlled by the closing clips 9 and between the administration of two liquids or active substances at least the last section of the merging system 8, in which the individual tubes connected with the chambers 2a, 2a, 2a, 2b are merged in a tube, is rinsed with rinse solution, in particular with saline.
[0036] With regard to further advantageous embodiments of the bag according to the invention, reference is made to avoid repetition to the general part of the description and to the appended claims.
[0037] Finally, it should be expressly understood that the above-described embodiments of the bag according to the invention are merely for the purpose of discussion of the claimed teaching, but this is not limited to the exemplary embodiments.
REFERENCE SYMBOL LIST
[0038] 1 Bag [0039] 2a, 2a, 2a Chamber with infusion solution and active substance [0040] 2b Chamber with rinse solution [0041] 3 Weld seam [0042] 4 Walls of the chambers [0043] 5 Connecting piece, tube inlet [0044] 6 Connecting piece, tube outlet [0045] 7 Luer-Lock tube connector [0046] 8 Merging system [0047] 9 Closing clips [0048] 10 Injection port [0049] 11 Opening/port of the merging system