Fluid Delivery System, Fluid Path Set, and Pressure Isolation Mechanism with Hemodynamic Pressure Dampening Correction

Abstract

The fluid delivery system includes a pressurizing device for delivering injection fluid under pressure, a low pressure fluid delivery system, and a pressure isolation mechanism. The pressure isolation mechanism includes a first lumen associated with the pressurizing device, a second lumen associated with the low pressure fluid delivery system, and a pressure isolation port. The first valve is in a normally open position permitting fluid communication between the first lumen and the second lumen and movable to a closed position when fluid pressure in the first lumen reaches a predetermined pressure level. The first valve isolates the pressure isolation port from the first lumen in the closed position. A second valve is associated with the second lumen and regulates fluid flow through the second lumen. The second valve may be a disk valve defining one or more passageways in the form of slits through the body of the disk valve.

Description

RELATED APPLICATIONS [0001] This application is a continuation in part of application Ser. No. 11 / 004,670, filed Dec. 3, 2004, entitled “Fluid Delivery System Including a Fluid Path Set with Sterile Check Valve Connector”, which is a continuation in part of application Ser. No. 10 / 826,149, filed Apr. 16, 2004, entitled “Fluid Delivery System, Fluid Path Set, Sterile Connector and Improved Drip Container and Pressure Isolation Mechanism”, which may contain subject matter that is related to that disclosed in the following co-pending applications: (1) application Ser. No. 10 / 818,748, filed on Apr. 6, 2004; (2) application Ser. No. 10 / 818,477, filed on Apr. 5, 2004; (3) application Ser. No. 10 / 326,582, filed on Dec. 20, 2002; (4) application Ser. No. 10 / 237,139, filed on Sep. 6, 2002; and (5) application Ser. No. 09 / 982,518, filed on Oct. 18, 2001, the disclosures of which are incorporated herein by reference.BACKGROUND OF THE INVENTION [0002] 1. Field of the Invention [0003] The presen...

AI Technical Summary

Benefits of technology

[0020] In one aspect, the manual control includes a first actuator providing control of flow rate of the first fluid by changing the force on the first actuator and a second actuator, the second actuator causing the injector to enter into a preprogrammed high pressure injection mode when placed in an on state. The system may further include a pressure sensor in fluid communication with the second fluid path via a pressure-activated isolator that isolates the pressure sensor from pressures in the second fluid path above a set pressure. In one embodiment, the per-patient disposable section may include a check valve in the second fluid path separating components of the per-patient disposable section from the multi-patient reusable section to reduce or eliminate flow of contaminated fluid into the multi-patient reusable section.

[0078] The first annular member may be adapted to coaxially receive the second annular member. The first annular member may be internally threaded and the second annular member may be externally threaded such that first and second annular members threadably engage to securely and releasably connect the first and second connector members. One of the first and second luer members may be formed as a male luer and the other may be formed as a female luer. The first annular member and first luer member may define an annular cavity therebetween such that the second annular member is at least partially received in the annular cavity when the first and second annular members are in operative engagement. When the second annular member is at least partially received in the annular cavity, the annular cavity may form a liquid-trapping chamber for inhibiting leakage of liquid between the first and second connector members.

Problems solved by technology

Manual sources of fluid pressure and flow used in medical applications such as syringes and manifolds thus typically require operator effort that provides feedback of the fluid pressure / flow generated to the operator.

The feedback is desirable, but the operator effort often leads to fatigue.

However, compliance in the system components, for example, expansion of the syringe, tubing, and other components under pressure, using such a manifold system can lead to a less than optimal injection bolus.

Moreover, the arrangement of the system components of U.S. Pat. No. 5,800,397 results in relatively large amounts of wasted contrast and / or undesirable injection of an excessive amount of contrast when the low pressure, typical saline system, is used.

Unlike manual injection systems, however, there is little if any feedback to the operator of system pressure in the systems disclosed in the U.S. Patents identified previously.

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