Over-the-needle guidewire vascular access system
Systems and methods for accessing body tissue are disclosed. The systems and methods can include an introducer assembly for percutaneous access to a body lumen. The assembly can include a needle and an over-the-needle guidewire. The needle and the guidewire can be inserted into body tissue and the guidewire advanced into the body tissue relative to the needle. The needle can be removed after advancing the guidewire.
1. A vascular access system comprising:
a needle having a proximal end, a sharpened distal end, a tubular body, and a central lumen therethrough;
an over-the-needle guidewire configured to fit over the outside diameter of the needle, the guidewire comprising a proximal section and a distal section,
wherein the proximal section comprises a first cross-sectional profile in the proximal section,
wherein the distal section comprises an outer tubular sidewall, a skive in the outer tubular sidewall configured for passage of the needle therethrough, the guidewire having the first cross-sectional profile proximally and a second cross-sectional profile distally, and a transition zone between the first cross-sectional profile and the second cross-sectional profile, wherein the second cross-sectional profile is smaller than the first cross-sectional profile; and
a luer connector operably connected to the needle having at least one input port fluidly connected to the central lumen of the needle, and a guidewire lumen not fluidly connected to the central lumen of the needle, the guidewire lumen configured to slidably house the guidewire therethrough, the guidewire lumen having a longitudinal axis that forms an acute angle with respect to a longitudinal axis of the luer connector.
2. A vascular access system comprising:
a needle having a proximal end, a sharpened distal end, a tubular body, and a central lumen therethrough;
an over-the-needle guidewire configured to fit over the outside diameter of the needle, the guidewire comprising a first proximal section, a second middle section, and a third distal section,
wherein the first proximal section comprises a first cross-sectional profile in the first proximal section,
wherein the second middle section comprises an outer tubular sidewall, a skive in the outer tubular sidewall configured for passage of the needle therethrough, the guidewire having the first cross-sectional profile proximally and a second cross-sectional profile distally, and a transition zone between the first cross-sectional profile and the second cross-sectional profile, wherein the second cross-sectional profile is smaller than the first cross-sectional profile, and
wherein the third distal section comprises the outer tubular sidewall having the second cross-sectional profile; and
a luer connector operably connected to the needle having at least one input port fluidly connected to the central lumen of the needle, and a guidewire lumen not fluidly connected to the central lumen of the needle, the guidewire lumen configured to slidably house the guidewire therethrough, the guidewire lumen having a longitudinal axis that forms an acute angle with respect to a longitudinal axis of the luer connector.
3. The system of claim 2 , wherein the first proximal section further comprises a coil disposed at least partially over a core wire.
4. They system of claim 3 , wherein the core wire at least partially occludes the skive.
5. The system of claim 3 , wherein the coil of the first proximal section comprises a wire circumferentially wound about a central coil axis to form the coil, wherein the wire has an outer diameter of 0.006 inches, and wherein the coil formed from the wound wire has an outer diameter of about 0.035 inches.
6. The system of claim 2 , wherein the longitudinal axis of the luer connector is parallel to a longitudinal axis of the needle, wherein when the guidewire slides through the guidewire lumen, the guidewire in the guidewire lumen is positioned at the acute angle relative to the longitudinal axis of the needle.
7. The system of claim 6 , wherein the acute angle of the guidewire is formed at the skive in the second middle section of the guidewire.
8. The system of claim 2 , wherein the acute angle is between about 5 to 45 degrees.
9. The system of claim 8 , wherein the acute angle is about 15 degrees.
10. The system of claim 2 , wherein the outer tubular wall of the second middle section and the third distal section extends from the skive through the guidewire lumen when the guidewire is positioned over the needle.
11. The system of claim 2 , wherein the guidewire covers a majority of an overall length of the needle when the guidewire is positioned over the needle.
12. The system of claim 2 , wherein an outer diameter of the needle is about 0.022 inches and an inner diameter of the guidewire at the third distal section is about 0.024 inches.
13. The system of claim 12 , wherein the inner diameter of about 0.024 inches extends through second middle section and the first proximal section.
14. The system of claim 2 , wherein the guidewire has an entire length of about 45 centimeters.
15. A vascular access system comprising:
a needle having a proximal end, a sharpened distal end, a tubular body, and a central lumen therethrough;
an over-the-needle guidewire configured to fit over the outside diameter of the needle, the guidewire comprising a first proximal section, a second middle section, and a third distal section,
wherein the first proximal section comprises a core wire and a coil disposed over the core wire, the core wire having a first cross-sectional profile in the first proximal section,
wherein the second middle section comprises an outer tubular sidewall, a skive in the outer tubular sidewall configured for passage of the needle therethrough, and the core wire disposed within the outer tubular sidewall, the core wire having the first cross-sectional profile proximally and a second cross-sectional profile distally, and a transition zone between the first cross-sectional profile and the second cross-sectional profile, wherein the second cross-sectional profile is smaller than the first cross-sectional profile, and
wherein the third distal section comprises the outer tubular sidewall, and the core wire having the second cross-sectional profile, the core wire extending at least partially through the outer tubular sidewall in the third section; and
a luer connector operably connected to the needle having at least one input port fluidly connected to the central lumen of the needle, and a guidewire lumen not fluidly connected to the central lumen of the needle, the guidewire lumen configured to slidably house the guidewire therethrough, the guidewire lumen having a longitudinal axis that forms an acute angle with respect to a longitudinal axis of the luer connector.
16. The system of claim 15 , wherein the longitudinal axis of the luer connector is parallel to the a longitudinal axis of the needle, wherein when the guidewire slides through the guidewire lumen, the guidewire in the guidewire lumen is positioned at the acute angle relative to the longitudinal axis of the needle.
17. The system of claim 16 , wherein the acute angle of the guidewire is formed at the skive in the second middle section of the guidewire.
18. The system of claim 15 , wherein an outer diameter of the guidewire tapers substantially to an outer diameter of the needle at the third distal section proximate to the sharpened distal end of the needle.
19. The system of claim 15 , wherein a cross-sectional profile of the transition zone of the core wire between the first cross-sectional profile and the second cross-sectional profile is about 0.010 inches in a dimension of the cross-sectional profile of the transition zone.
20. The system of claim 15 , wherein a combined length of the second middle section and the third distal section is less than about 30% of an entire length of the guidewire.