Syringe assembly

• US 20030120255A1
• Filed: 02/07/2003
• Published: 06/26/2003
• Est. Priority Date: 04/14/1998
• Status: Active Grant

• Current Assignee: Alex S. Wallace, Lawrence J. Zach, Robert B. Odell
• Original Assignee: Alex S. Wallace, Lawrence J. Zach, Robert B. Odell
• Inventors: Zach, Lawrence J., Wallace, Alex S., Odell, Robert B.
• Granted Patent: US 6,743,216 B2
• Time in Patent Office: Days
• US Class Current: 604/500
• CPC Class Codes: A61M 2005/3104 Caps for syringes without needle
• CPC Class Codes: A61M 5/002 Packages specially adapted therefor, e.g. for syringes or needles, kits for diabetics needle protection, e.g. caps, A61M5/3202; for sharps A61B50/3001
• CPC Class Codes: A61M 5/3129 Syringe barrels A61M5/3205 and A61M5/50 take precedence
• CPC Class Codes: A61M 5/31525 Dosing burettes, pipettes B01L3/02
• CPC Class Codes: A61M 5/31535 Means improving security or handling thereof, e.g. blocking means, means preventing insufficient dosing, means allowing correction of overset dose
• CPC Class Codes: A61M 5/347 rotatable, e.g. bayonet or screw A61M5/344 takes precedence
• CPC Class Codes: A61M 5/5086 for indicating if defective, used, tampered with or unsterile

Abstract

A syringe assembly comprises a syringe barrel having an elongated body defining a chamber for retaining fluid, an open proximal end, a distal end and a frusto-conically shaped tip extending from the distal end and having a passageway therethrough in fluid communication with the chamber. The chamber has an inside diameter of at least 13.5 mm. A stopper is in fluid-tight engagement inside the barrel. An elongated plunger rod extends proximally from the stopper through the open proximal end of the barrel. A flange is positioned at the proximal end of the plunger rod. The flange is shaped and positioned to limit the distal motion of the plunger rod in the barrel by contacting the proximal end of the barrel. A tip cap is releasably connected to the tip for sealing the passageway and the chamber contains injectable liquid.

Claims

1. A method of flushing a catheter comprising the steps of:

(a) providing a syringe assembly including a syringe barrel having an elongated body defining a chamber for retaining fluid, an open proximal end, a distal end and a frusto-conically shaped tip extending from said distal end having a tip passageway therethrough in fluid communication with said chamber, said chamber having an inside diameter of at least 13.5 mm (0.53 inch), said chamber having a distal end defined by a distal wall through which said tip passageway passes, the length of said chamber being no more than 57 mm (2.25 inches);

a stopper in fluid-tight engagement inside said barrel;

an elongated plunger rod defining a longitudinal axis and extending proximally from said stopper through said open proximal end of said syringe barrel, a flange at a proximal end of said plunger rod;

a tip cap releasably connected to said tip for sealing said passageway; and

injectable liquid in said chamber;

(b) providing a catheter having a proximal end, a distal end and a passageway therethrough and a housing having a hollow interior in fluid communication with said passageway, said housing having a pierceable septum for allowing fluid communication with said hollow interior;

(c) providing a needle assembly including a cannula having a proximal end, a distal end, and a lumen therethrough, a hub having an open proximal end containing a cavity and a distal end attached to said proximal end of said cannula so that said lumen is in fluid communication with said cavity;

(d) placing said distal end of said catheter in a blood vessel;

(e) removing said tip cap from said syringe and attaching said needle assembly to said syringe so that said frusto-conically shaped tip of said barrel is in said cavity of said hub;

(f) piercing said septum with said distal end of said needle so that said lumen is in fluid communication with said hollow interior of said housing;

(g) applying force to said plunger rod to move said plunger rod in a distal direction with respect to said barrel so that said injectable liquid in said chamber flows through said lumen of said cannula into said hollow chamber of said housing and through said passageway of said catheter; and

(h) withdrawing said cannula from said septum.

2. The method of claim 1 wherein said septum is pre-slit and said distal end of said cannula includes a blunt tip.

3. The method of claim 1 wherein said injectable liquid is selected from the group consisting of saline flush solution and heparin lock flush solution.

4. The method of claim 1 wherein the volume of said injectable liquid in said chamber is no more than 3.3 ml.

5. The method of claim 1 wherein the volume of said injectable liquid in said chamber is no more than 4 ml.

6. The method of claim 1 wherein the length of said chamber is no more than 44.5 mm (1.75 inches).

7. A method of flushing a catheter comprising the steps of:

(a) providing a syringe assembly including a syringe barrel having an elongated body defining a chamber for retaining fluid, an open proximal end, a distal end and a frusto-conically shaped tip extending from said distal end having a tip passageway therethrough in fluid communication with said chamber, said chamber having an inside diameter of at least 13.5 mm (0.53 inch), said chamber having a distal end defined by a distal wall through which said tip passageway passes, the length of said chamber being no more than 57 mm (2.25 inches);

a stopper in fluid-tight engagement inside said barrel;

an elongated plunger rod defining a longitudinal axis and extending proximally from said stopper through said open proximal end of said syringe barrel, a flange at a proximal end of said plunger rod;

a tip cap releasably connected to said tip for sealing said passageway; and

injectable liquid in said chamber;

(b) providing a catheter having a proximal end, a distal end and a passageway therethrough and a housing having a hollow interior in fluid communication with said passageway, said housing having an access valve for allowing fluid communication with said hollow interior;

(c) placing said distal end of said catheter in a blood vessel;

(d) removing said tip cap from said syringe;

(e) engaging said frusto-conically shaped tip to said access valve so that said tip passageway is in fluid communication with said hollow interior of said housing;

(f) applying force to said plunger rod to move said plunger rod in a distal direction with respect to said barrel so that said injectable liquid in said chamber flows through said passageway into said hollow chamber of said housing and through said passageway of said catheter; and

(g) disengaging said tip from said access valve.

8. The method of claim 7 wherein said injectable liquid is selected from the group consisting of saline flush solution and heparin lock flush solution.

9. The method of claim 7 wherein the volume of said injectable liquid in said chamber is no more than 3.3 ml.

10. The method of claim 7 wherein the volume of said injectable liquid in said chamber is no more than 4 ml.

11. The method of claim 7 wherein the length of said chamber is no more than 44.5 mm (1.75 inches).