Procedures for the treatment of chronic diseases often require repeated and prolonged access to the vascular system. The more often these procedures are repeated, the more impractical and dangerous it becomes to insert and remove a needle at every session. Thus, patients requiring frequent sessions are often fitted with a semi-permanent catheter with a distal end opening into a vein and an accessible proximal end which is sealed when the catheter is not in use.
The proximal end is often sealed by a valve such as a Pressure Actuated Safety Valve (PASV) designed to open only when a fluid pressure in the catheter exceeds a preselected threshold pressure. PASV's often include a slitted membrane which flexes open when a fluid pressure above the threshold value is applied and which closes as soon as the pressure drops below the threshold to prevent fluid from leaking from the catheter and to prevent contaminants from entering therein.
The proximal end of the catheter may extend through the skin to remain accessible outside the body and may include provisions for connection to external devices. For example, a connector may be attached to the catheter, or may be formed at the proximal end of the catheter so that an external medical device may be placed in fluid connection thereto. These connectors may include the flow control valves (e.g., PASV's) described above in a housing to permit fluids to enter and/or exit the catheter only under predefined conditions. The flow control valve housing may either be part of the catheter or may be a separate component connected to the catheter body when the device is implanted. One type of such catheter is the peripherally inserted central catheter (PICC) which allows access to portions of the vascular system deep inside the body. A relatively long portion of the catheter is tunneled into the body while a proximal end remains accessible at a convenient location.
Most therapeutic procedures infuse fluids at a slow flow rate and a low injection pressure. For example, chemotherapy agents, drugs and blood products are typically delivered at low flow rates and pressures. In certain procedures, however, fluids are administered at higher pressures. For example, contrast media used in the visualization of blood vessels and other biological structures require special injection procedures including flow rates and pressures which are often higher than those which the flow control valves can withstand without damage. These procedures, commonly referred to as power injection procedures, typically require a separate, more robust catheter than those used for conventional infusion techniques.
The present invention is directed to a bypass for power injection, comprising a housing defining a lumen extending from a proximal end to a distal end coupled to a catheter and a membrane valve mounted within the lumen, the membrane valve having an opening extending therethrough sized to tightly receive therethrough and seal around a power injection device in combination with a flapper valve extending across the lumen distally of the membrane valve, the flapper valve including a flap biased toward a closed position in which the lumen is sealed, the flap being rotatable away from the closed position when contacted by a power injection device to permit the device to extend therethrough.
The present invention may be further understood with reference to the following description and the appended drawings, wherein like elements are referred to with the same reference numerals. The invention relates to devices used to connect a source of pressurized fluid to a valved catheter without damaging a valve of the catheter. More specifically, the invention relates to a bypass for a PICC catheter allowing power injections thereto without damaging a valve of the catheter and preventing back flow of fluids through the bypass.
Exemplary embodiments of the present invention provide for a catheter and, in particular, a bypass portion of a valved catheter enabling the catheter to be used for both low pressure infusions and power injections. The exemplary device prevents damage to the safety valve by employing a bypass lumen for power injections which isolates a valve of the catheter from the high pressures and flow rates of the power injections. The bypass lumen according to the present invention seals around the power injection device to prevent back flow and, when the bypass lumen is not in use, it is reliably sealed preventing leaks and contamination, even after repeated insertion of a power injection nozzle therethrough.
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After completion of the power injection procedure and the device 130 is withdrawn from the lumen 108, the flap 124 of the flapper valve 120 closes and seals the lumen 108 and the membrane valve 110 is left with the opening 112, but is no longer necessary to close the bypass 100 because that function is now performed by the flapper valve 120. The low pressure/low flow rate port of the catheter may then be used in its conventional manner as the bypass 100 is sealed against back flow.
The present invention has been described with reference to specific exemplary embodiments. Those skilled in the art will understand that changes may be made in details, particularly in matters of shape, size, material and arrangement of parts. Accordingly, various modifications and changes may be made to the embodiments. The specifications and drawings are, therefore, to be regarded in an illustrative rather than a restrictive sense.
This application claims the priority to the U.S. Provisional Application Ser. No. 61/014,959, entitled “FLAPPER VALVE WITH MEMBRANE BYPASS FOR POWER PICC,” filed Dec. 19, 2007. The specification of the above-identified application is incorporated herewith by reference.
Number | Date | Country | |
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61014959 | Dec 2007 | US |