Tunneling guidewire
A medical device tunneling system, and a method of using the same, to subcutaneously route trocars, also commonly referred to as tunnelers, or introducers, having a cannula, stylet, and a guidewire stylet, inside a patient during a surgical procedure, such as a ventriculoperitoneal hydrocephalus shunt implantation, from a proximal entry point to a distal end point, in order to subcutaneously route and implant a medical device, such as shunt tubing, in a patient.
1. A method of subcutaneously routing tubing within a human patient as part of a surgical procedure for cerebrospinal fluid diversion, comprising:
in a torso area of the patient;
inserting at least a portion of a stylet into a cannula, wherein the cannula comprises a hollow passage;
inserting at least a portion of the cannula and stylet into the patient subcutaneously through the first skin incision;
extravascularly routing the cannula and stylet from the first skin incision to an area adjacent an external surface of the patient's skull;
inserting a guidewire through the hollow passage of the cannula;
steering the guidewire around the area and to a second skin incision located proximate the external surface of the patient's skull, wherein said steering is achieved without the use of a third incision;
attaching tubing to the guidewire, the attached tubing comprising drainage tubing for allowing flow of cerebrospinal fluid therethrogh; and
retracting the guidewire and attached tubing, wherein the attached tubing is disposed subcutaneously and extends between the first and second skin incisions.
2. The method of claim 1 , further comprising inserting the guidewire through a passage defined through the stylet.
3. The method of claim 2 , further comprising bending the guidewire before inserting the guidewire through the passage of the stylet.
4. The method of claim 1 , further comprising removing the stylet from the cannula, wherein inserting the guidewire comprises inserting a combination guidewire-stylet into the cannula.
5. The method of claim 1 , wherein attaching the tubing comprises securing the tubing to a blunt tip of the guidewire.
6. The method of claim 1 , wherein the guidewire is pre-bent such that a portion of the guidewire comprises a minimum bend radius of about one centimeter.
7. The method of claim 1 , wherein the guidewire is pre-bent to a bend radius that substantially matches the parietal bone radius of the patient's skull.
8. The method of claim 1 , wherein the guidewire comprises a tensile strength range from about 300 mega-pascals to about 3,500 mega-pascals.
9. The method of claim 1 , wherein the guidewire comprises a Young's modulus of at least 30 giga-pascals.
10. The method of claim 1 , wherein the cannula comprises a first end, a second end, a first portion associated with the first end, and a second portion associated with the second end, wherein the second portion comprises a bend such that the second end is located at a point between 0 degrees and 45 degrees from an axis aligned with the first portion.
11. The method of claim 1 , wherein attaching the tubing comprises securing the tubing to an endpoint loop.
12. The method of claim 1 , further comprising bending the guidewire before inserting the guidewire through the hollow passage.