The present invention generally relates to device and system for facilitating vascular access into a vessel of a patient and to a method of using such a device or system. In one embodiment, the vessel is a vein and the device is used to facilitate obtaining a blood sample.
The Seldinger technique, also known as Seldinger wire technique, is a medical procedure to obtain safe access to vessels, for example blood vessels, or other hollow organs. The desired vessel or cavity is punctured with a sharp hollow needle called a trocar. A round-tipped guidewire is then advanced through the lumen of the trocar, and the trocar is withdrawn. A “sheath” or blunt cannula can now be passed over the guidewire into the cavity or vessel. Alternatively, drainage tubes are passed over the guidewire. After passing a sheath or tube, the guidewire is withdrawn.
A sheath can be used to introduce catheters or other devices to perform endoluminal (inside the hollow organ) procedures, such as angioplasty. Fluoroscopy may be used to confirm the position of the catheter and to maneuver it to the desired location. Injection of radiocontrast may be used to visualize organs. Interventional procedures, such as thermo-ablation, angioplasty, embolization or biopsy, may be performed. Upon completion of the desired procedure, the sheath is withdrawn. In certain settings, a sealing device may be used to close the hole made by the procedure.
Intravenous (IV) cannulation is a technique in which a cannula is placed inside a vein to provide venous access. Venous access allows sampling of blood as well as administration of fluids, medications, parenteral nutrition, chemotherapy, and blood products.
When performing the Seldinger technique to gain vessel access or provide therapy, two significant difficulties may arise. Initially, it may be difficult to find a vessel, for example a vein, that is distended enough to puncture with a needle or other access device. Furthermore, after removal of the access device, it may be difficult to control bleeding from the entry point.
One aspect of the present invention provides a device for facilitating vascular access into a vessel of a patient. One embodiment of the device includes a housing having an interior chamber and having a peripheral rim defining an opening. A fluid port is positioned in a wall of the housing and provides for fluid ingress and egress to the interior chamber. In addition, a cannula access port is also positioned in the wall of the housing. The device may also include a ring clamp attaching to the peripheral rim. In certain other embodiments, the device includes an adhesive coating on the peripheral rim.
In some embodiments, the device also includes a compliant gasket positioned on the peripheral rim. In other embodiments, the device includes a fastener attached to an exterior of the domed housing and sized and shaped to extend about a body part of the patient and to hold the peripheral rim against the patient. The device may have a viewing window positioned in the wall of the housing. In other embodiments, the housing is formed from a transparent material.
Another aspect of the invention provides a system for facilitating vascular access into a vessel of a patient. One embodiment of the system includes a device including a housing having a peripheral rim defining an opening and an interior chamber. A fluid port is positioned on a wall of the housing and provides fluid ingress and egress to the interior chamber. A cannula access port is also positioned on the wall of housing. The system also includes a pressure/vacuum source that is connectable to the fluid port.
In another embodiment, the system also includes an adhesive-backed tape having a size sufficient to cover the opening. In yet another embodiment, the system includes a ring clamp attaching to the peripheral rim.
Another aspect of the invention provides a method for facilitating vascular access into a vessel of a patient. One embodiment of the method includes placing the opening of a vascular access device as described herein against a body part of the patient and securing the device to the body part so as to position the opening over the vessel.
Once the device is in position, the pressure in the interior chamber is reduced for a time sufficient to distend the vessel and a cannula or other access device inserted through the cannula access port and into the vessel to provide for access to the vessel. After access is achieved, a procedure may be performed, for example, a sample may be obtained from the vessel. The cannula is then withdrawn from the vessel and from the cannula access port. The interior chamber may be subjected to an increased pressure for a time sufficient to constrict the vessel before the device is removed from the body part of the patient.
In one embodiment, the device also includes a ring clamp attaching to the peripheral rim. Securing the device to the body part of the patient includes attaching the adhesive side of an adhesive-backed tape to the body part and securing the adhesive-backed tape with the ring clamp. In another embodiment, the device includes a fastener attached to the exterior of the housing. Here, securing the device to the body part includes placing the fastener around the body part and tightening the fastener to hold the peripheral rim against the body part.
In various embodiments, accessing the vessel includes withdrawing a blood sample from the vessel through the cannula or introducing a wire guide or a catheter into the vessel. The vessel may be, for example, a vein.
For the purpose of promoting an understanding of the principles of the invention, reference will now be made to embodiments, some of which are illustrated in the drawings, and specific language will be used to describe the same. It will nevertheless be understood that no limitation of the scope of the invention is thereby intended. Any alterations and further modifications in the described embodiments, and any further applications of the principles of the invention as described herein are contemplated as would normally occur to one skilled in the art to which the invention relates. Each disclosed feature or features can be combined with the generalized features discussed herein, to form a disclosed embodiment of the present invention.
One aspect of the present invention provides a device for facilitating vascular access into a vessel, for example, an artery or a vein, of a human or veterinary patient. The vascular access device may assist in obtaining access into the vessel by helping to distend the vessel enough to allow for its puncture with a needle or other puncture device. The device may also assist in the constriction of the vessel and the control of bleeding from the entry point after vascular access is complete and the puncture device is removed. The vessel may be any vessel, typically an artery or a vein close to the surface of any part of the patient's body (“body part”.) In certain preferred embodiments, the vessel is a vein close to the surface of a limb of the patient.
In operation, the device allows for the surface overlaying the vessel to be subjected to a reduced pressure for a time sufficient to distend the vessel and hence provide for easier access to the vessel with a puncture device. The device may also assist in the closure of the access puncture site in the vessel by allowing the surface overlaying the vessel to be subjected to an increased pressure for a time sufficient to constrict the vessel, in particular, access puncture site.
Turning now to
Membrane 10 may be a self-sealing membrane allowing for the passage of the device through the port, while preventing the passage of gasses and/or liquid. Alternatively, the cannula access port may include a pneumostatic valve. Hence, the pressure at interior chamber 80 of the device may be maintained at a raised or lowered level with respect to the air pressure outside at the exterior of the device when opening 55 is positioned against the skin of a patient so as to form a fluid seal and the cannula device is passed through the port.
Housing 40 may include a viewing window 65 having sufficient transparency to allow the operator to observe the interior chamber, and the surface of the patient enclosed by the device, when the device is positioned against the skin of a patient. In other embodiments, all or part of housing 40 is formed from a material having sufficient transparency to allow the operator of the device to observe the interior of the device when it is positioned against the skin of the patient. For example, all or part of the housing may be formed from a transparent or translucent plastic material.
Compliant gasket 30 may be positioned around at least a portion of peripheral rim 45 of housing 40 and may provide for improved sealing of the rim against the skin of the patient. In certain embodiments, an adhesive coating may be applied to peripheral rim 45 or to gasket 30, if present, to assist in maintaining the device in position.
Turning how to
In those embodiments where the device is intended to be placed against the arm and/or leg of the patient, the base of the housing may have a curved or arched profile so as to match the contour of the limb of the patient. For example, in certain embodiments where the device is to be used to obtain and close access to the femoral vessels, the base of the housing may have an irregular shape in order to make a “seal” with specifically the left (or the right) groin area.
Typically, the device is sized such that the cross-sectional dimension of opening 55 is between, for example, 4 cm and 15 cm, or between 5 cm and 12 cm, or between 6 cm and 10 cm. The housing may be formed form any suitable material, for example a plastic material, and may be manufactured by, for example, a molding or vacuum-forming process. Preferably, the device is a disposable single use device. In one embodiment, the device housing is formed from a biodegradable plastic material.
Similarly, although
The housing may be rigid, or at least semi-rigid, having sufficiently rigidity to withstand collapse or puncture when the pressure of the interior of the housing is raised or lowered with respect to the air pressure at the outside exterior of the device. In one embodiment, the housing is sufficiently rigid to allow the pressure of the interior of the device to be raised or lowered by between 30 and 60 mm/Hg when the device is positioned against the surface of the patient's body to obtain a fluid seal at opening 55. In another embodiment, the housing may be rigid enough to withstand the vacuum/increased pressure extremes applied during the vascular procedure but flexible enough to allow the housing perimeter to confirm to the contours of the body of the patient.
In certain embodiments, the vascular access device may also include a fastener that assists in holding the device in place against the body of the patient. This may be particularly important when the internal pressure within chamber 80 is raised to constrict the vessel after the access procedure is complete and the operator wishes to constrict the puncture point.
After the device is positioned and a seal between peripheral rim 45 or gasket 30, if present, and the patient's body is obtained, a vacuum source is applied to fluid port 20 to draw air from the interior of the device.
Turning now to
In other embodiments of the method, a wire guide or a similar device many be inserted into the vessel to allow another procedure to be performed. In such embodiments, the device may be removed after access to the vessel is obtained and later re-attached and put under increased pressure to assist in sealing the access puncture after the wire guide or other device is removed.
As illustrated in
In any case, after the device is attached to the adhesive-backed tape, a vacuum source is applied to fluid port 20 to draw air from the interior chamber of the device, as is illustrated in
Turning now to
Although the invention has been described and illustrated with reference to specific illustrative embodiments thereof, it is not intended that the invention be limited to those illustrative embodiments. Those skilled in the art will recognize that variations and modifications can be made without departing from the true scope and spirit of the invention as defined by the claims that follow. It is therefore intended to include within the invention all such variations and modifications as fall within the scope of the appended claims and equivalents thereof.
This non-provisional patent application claims priority to U.S. Provisional Patent Application No. 62/254,256, filed Nov. 12, 2015, the contents of which are incorporated by reference in their entirety.
Number | Date | Country | |
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62254256 | Nov 2015 | US |