Solution administration set

• US 4,521,212 A
• Filed: 08/03/1982
• Issued: 06/04/1985
• Est. Priority Date: 08/03/1982
• Status: Expired due to Term

• Current Assignee: Baxter Travenol Laboratories Incorporated
• Original Assignee: Baxter Travenol Laboratories Incorporated
• Inventors: Ruschke, Rick R.
• Primary Examiner(s): Pellegrino, Stephen C.
• Application Number:
  US06/404,810
• Time in Patent Office: 1,036 Days
• Field of Search: 604/251-256, 604/404, 604/246, 604/126, 73/293, 73/290, 73/323, 73/327, 116/227, 55/159
• US Class Current: 604/126
• CPC Class Codes: A61M 5/36 with means for eliminating or preventing injection or infusion of air into body dialysis systems, blood oxygenators A61M1/14; haemofiltration equipment A61M1/34; automatic tube cut-off A61M39/281

Abstract

In a parenteral solution administration set, the porous hydrophilic filter member which can control the liquid level and prevent the passage of gas downwardly through the set can be located adjacent the lower end of the drip chamber to control flow out of the lower end and to be submerged in liquid held in the drip chamber during operation thereof. Significant advantages are obtained. Particularly, the set becomes conveniently usable with parenteral solution pumps. Also the drip chamber may contain an elongated member projecting inwardly of the lower end of the chamber and carrying indicia along its length to indicate liquid volume in the chamber as a function of liquid level.

Claims

1. A parenteral solution administration set having tubular means for conveying solution from a supply source toward the vascular system of a patient, comprising:

a metering chamber measuring aliquots of solution for administration;

a drip chamber connected to said metering chamber and having upper and lower ends positioned below said metering chamber;

said drip chamber including, at its lower end, a porous, hydrophilic filter member having a pore size sufficiently small to prevent air at a predetermined maximum pressure from passing through said filter member when wet, while permitting the flow of parenteral solution therethrough, said filter member being operative at the lower end of the drip chamber to control flow out of said lower end and to be submerged by liquid held in the drip chamber during operation thereof;

said metering chamber and drip chamber being free of any air-blocking membrane therebetween, whereby back priming of the set is enabled.

2. The set of claim 1 in which said filter member exhibits a "bubble point" of at least 12 lb/in².

3. The set of claim 2 in which said filter member exhibits a nominal pore size of about 0.6 micron.

4. The set of claim 1, having means permitting use with a clinical pump for parenteral solution.

5. A filter for fluids which comprises a filter member and a base upon which said filter member is supported, said base defining a central flow port for receiving filtrate from the filter and conveying it away from the filter member, said base also defining substantially radial flow channels for receiving and conveying filtrate passing through the filter member to the central flow port, the improvement comprising, in combination:

said base defining a filter member-facing surface, peripheral portions of said surface being spaced from the filter member more than central portions thereof adjacent the flow port, said surface defining a slope upwardly and inwardly toward said central flow port to cause trapped air bubbles on priming spontaneously to migrate to the central flow port.

6. In a parenteral solution administration set having tubular means for conveying solution from a supply source to the vascular system of a patient, and including a metering chamber for measuring aliquots of solution for administration, plus a drip chamber having upper and lower ends positioned below said metering chamber, the improvement comprising, in combination:

a porous hydrophilic filter member having a pore size sufficiently small to prevent air at a predetermined maximum pressure from passing through said filter member when wet, while permitting the flow of parenteral solution therethrough, said filter member being positioned adjacent the lower end of the drip chamber to control flow out of said lower end then to be submerged by liquid held in the drip chamber during operation thereof;

said filter member being supported on a base, said base defining a central flow port for receiving filtrate from the filter and conveying it away from the filter member, said base also defining substantially radial flow channels for receiving and conveying filtrate passing through the filter member to the central flow port, said base defining a filter member-facing surface, peripheral portions of said surface being spaced from the filter member more than central portions thereof adjacent the flow port, said surface defining a slope upwardly and inwardly toward said central flow port to cause trapped air bubbles on priming spontaneously to migrate to the central flow port.

7. The set of claim 6 in which said filter member exhibits a "bubble point" of at least 12 pounds per square inch, and having means permitting use with a clinical pump for parenteral solution.

8. The filter of claim 7 in which said drip chamber carries at its lower end an elongated member projecting inwardly of said drip chamber, said elongated member carrying indicia along its length to indicate liquid volume in said drip chamber as a function of liquid level.

9. The solution administration set of claim 8 in which the indicia of said elongated member includes step members defined therein at predetermined positions.

10. The solution administration set of claim 9 in which said elongated member comprises a plurality of longitudinally extending vanes which project radially outwardly.

11. The solution administration set of claim 10 in which said filter member exhibits a nominal pore size of about 0.6 micron.

12. A parenteral solution administration set in integral, unitary form, having tubular means for conveying solution from a supply source toward the vascular system of a patient, comprising:

a metering chamber for measuring aliquots of solution for administration;

a drip chamber integrally connected to said metering chamber having upper and lower ends positioned below said metering chamber;

said drip chamber including, adjacent its lower end, a porous, hydrophilic filter member having a pore size sufficiently small to prevent air at a predetermined maximum pressure from passing through said filter member when wet, while permitting the flow of parenteral solution therethrough, said filter member being operative to control flow out of said lower end and to be submerged by liquid held in the drip chamber during operation thereof;

said metering chamber and drip chamber being free of any air-blocking membrane therebetween, whereby back priming of the set is enabled.

13. In a medical solution administration set having a spike, an end connector and tubular means connected to and between said spike and said end connector for conveying solution from a supply source toward the vascular system of the patient, the improvement comprising:

a chamber connected to said tubular means, between said spike and said end connector, said chamber including opposed ends;

an elongated member projecting inwardly of said chamber from adjacent one of said ends, and including a plurality of longitudinally extending vanes which project radially outwardly; and

indicia carried along the length of said elongated member to indicate liquid volume in said chamber as a function of liquid level when said one end is pointed downwardly, said indicia including step members carried by said elongated member.