Apparatus and method for percutaneous catheterization

• US 4,411,655 A
• Filed: 11/30/1981
• Issued: 10/25/1983
• Est. Priority Date: 11/30/1981
• Status: Expired due to Fees

• Current Assignee: David M. Schreck
• Original Assignee: David M. Schreck
• Inventors: Schreck, David M.
• Primary Examiner(s): Pellegrino, Stephen C.
• Application Number:
  US06/325,848
• Time in Patent Office: 694 Days
• Field of Search: 128/214.4, 128/214 R, 128/343, 128/348-350, 285/381, 604/104, 604/164, 604/165, 604/281
• US Class Current: 604/165.01
• CPC Class Codes: A61B 17/3417 Details of tips or shafts, e.g. grooves, expandable, bendable; Multiple coaxial sliding cannulas, e.g. for dilating syringe needles A61M5/32; dilators A61M29/00
• CPC Class Codes: A61B 17/3439 with means for changing the inner diameter of the cannula, e.g. expandable A61B17/3423, A61B17/3431 take precedence; catheters A61M25/0662
• CPC Class Codes: A61M 2025/0687 having means for atraumatic insertion in the body or protection of the tip of the sheath during insertion, e.g. special designs of dilators, needles or sheaths
• CPC Class Codes: A61M 25/0662 Guide tubes

Abstract

An apparatus for percutaneous catheterization of a vascular or other body compartment employs a shape memory alloy cylindrical cannula which expands after introduction into the body compartment with sufficient radial force to dilate the vascular member. A cylindrical plastic sheath embracing the cannula facilitates introduction and insulates the vascular compartment from contact with the metal of the cannula.

Claims

1. A device for introducing a large bore diagnostic or therapeutic catheter into a body compartment or vessel, comprising a thin wall cannula of shape memory alloy having an inner diameter fashioned to embrace the shank of a hypodermic needle, said cannula exhibiting, in its martensitic phase, an outer diameter convenient for percutaneous puncture of a body compartment or vessel and exhibiting, in its austentitic beta-phase, an inner diameter to slidably accomodate the outer diameter of said large bore diagnostic or therapeutic catheter, and a dilatable elastomeric cylindrical sheath deployed over the surface of said cannula.

2. A device according to claim 1 wherein said cannula is fabricated of shape memory alloy exhibiting said martensitic phase in the temperature range of 28°

C. to 35°

C. and said austentitic phase in the range of 37°

C. to 41°

C.

3. A device according to claim 1 wherein said cannula is flared at its proximal end to form a hub having a lumen to accomodate the unrestricted passage of large bore diagnostic/therapeutic catheters, said hub having an outer surface which may be grasped to facilitate removal of the cannula from said body compartment or vessel after said large bore catheter has been inserted.

4. A device according to claim 1 further comprising a dilatable elastomeric cylindrical sheath, deployed over a surface of said cannula.

5. A device according to claim 3 wherein said sheath is flared at its proximal end to accomodate an intravenous tubing connection.

6. A device according to claim 1 wherein said cannula comprises a shape memory alloy cylinder in the form of a helical ribbon having a pitch substantially equal to its longitudinal dimension such that upon transformation from the martensitic to the austentitic phase said shape memory alloy cannula will effectively dilate to allow the unrestricted longitudinal passage of a large-bore diagnostic or therapeutic catheter.

7. A device according to claim 1 wherein said shape memory alloy cylinder comprises a hollow cylindrical mesh.

8. A device according to claim 1 wherein said shape memory alloy cannula is fabricated of helically-wound wire.

9. A device according to claim 1 wherein dilation will be achieved using the "two-way" shape memory effect such that the device will exist in its austentitic phase as a small bore needle-cannula combination so as to effect simple percutaneous insertion and, upon cooling to its martensitic phase, said device will effectively dilate.

10. A device according to any of claim 1 wherein said plastic sheath is fabricated of sufficiently rigid material to withstand premature dilational transformation prior to insertion in a body compartment which may occur as a result of unexpected high environmental temperatures encountered during shipping, storage, or sterilization.