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| United States Patent | 4554929 |
| Link to this page | http://www.wikipatents.com/4554929.html |
| Inventor(s) | Samson; Wilfred J. (Saratoga, CA);
Solar; Ronald J. (Palo Alto, CA) |
| Abstract | Guide wire and method for insertion and use of a catheter. The guide wire
has a shaft of substantially smaller diameter than the luminal opening,
with a flexible coil at one end of the shaft. The guide wire is inserted
into the cardiovascular system, and the catheter is advanced along the
guide wire to the desired position, with the flexible coil outside the
distal end of the catheter. An annular passageway is formed between the
shaft and the wall of the luminal opening, and fluids are passed through
this passageway while the guide wire is within the catheter. A marker of
radio opaque material is provided at the distal end of the guide wire so
that the position of the wire can be accurately determined even though the
wire itself may be too small to be visible with a fluoroscope. |
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Title Information  |
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Drawing from US Patent 4554929 |
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Catheter guide wire with short spring tip and method of using the same |
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| Publication Date |
November 26, 1985 |
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| Filing Date |
July 13, 1983 |
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Title Information  |
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Claims  |
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We claim:
1. In a guide wire for use in the placement of a catheter in the
cardiovascular system, an elongated shaft of relatively rigid material
having proximal and distal ends and a cross-sectional area subtantially
smaller than the luminal opening in the catheter, a relatively flexible
helical coil having proximal and distal ends, said coil having an outer
diameter slightly smaller than the diameter of the luminal opening and a
length substantially less than the length of the shaft, the distal end
portion of the shaft extending into the coil but terminating short of the
distal end of the coil, the portion of the shaft extending into the coil
being tapered to provide a gradual transition in flexibility of the shaft,
means for bonding the proximal end of the coil to the shaft and a flexible
safety wire disposed interiorally of the coil and having one end bonded to
the distal extremity of the shaft and having the other end bonded to the
distal extremity of the coil.
2. A guide wire as in claim 1 wherein the safety wire is formed as a flat
ribbon having a generally rectangular cross section.
3. A guide wire as in claim 1 together with a relatively smooth rounded tip
disposed at the distal extremity of the coil.
4. A guide wire as in claim 1 together with a radio opaque marker formed of
radio opaque material carried by the shaft adjacent the distal end of the
shaft.
5. A guide wire of claim 4 wherein the radio opaque material has a density
of at least 13 gm/cm.sup.3.
6. A guide wire as in claim 5 wherein the radio opaque material includes an
element selected from the group consisting of gold, tantalumm, tungsten,
platinum, iridium, rhenium and alloys thereof.
7. A guide wire as in claim 6 wherein the radio opaque material comprises
an alloy containing on the order of 80% gold, 12% silver, and 8% copper
and zinc.
8. A guide wire as in claim 1 wherein the helical coil is formed of a radio
opaque material.
9. In apparatus for use in the cardiovascular system, an elongated,
relatively flexible catheter having a wall defining an axially extending
luminal opening and a guide wire extending through the luminal opening and
having a cross-sectional area substantially smaller than the luminal
opening so that fluids can pass freely between the guide wire and the wall
defining the luminal opening, said guide wire comprising an elongated
shaft of relatively rigid material having proximal and distal ends and a
cross-sectional area substantially smaller than the luminal opening in the
catheter, a relatively flexible helical coil having proximal and distal
ends, said coil having an outer diameter slightly smaller than the
diameter of the luminal opening and a length substantially less than the
length of the shaft, the distal end portion of the shaft extending into
the helical coil but terminating short of the distal end of the coil, the
portion of the shaft extending into the coil being tapered to provide a
gradual transition in flexibility of the shaft, means for bonding the
proximal end of the coil to the shaft and a flexible safety wire disposed
interiorally of the coil and having one end bonded to the distal extremity
of the shaft and having the other end bonded to the distal extremity of
the coil.
10. Apparatus as in claim 9 wherein the safety wire is formed as a flat
ribbon having a generally rectangular cross section.
11. Apparatus as in claim 9 wherein the luminal opening has a diameter on
the order of 0.020 inch, the guide wire shaft has a diameter on the order
of 0.008 inch, and the helical coil has a diameter on the order of 0.018
inch.
12. Apparatus as in claim 9 together with a radio opaque marker formed of
radio opaque material carried by the shaft adjacent the distal end of the
shaft.
13. Apparatus as in claim 12 wherein the radio opaque material has a
density of at least 13 gm/cm.sup.3.
14. Apparatus as in claim 12 wherein the radio opaque material includes an
element selected from the group consisting of gold, tantalum, tungsten,
platinum, iridium, rhenium and alloys thereof.
15. Apparatus as in claim 12 wherein the radio opaque material comprises an
alloy containing on the order of 80% gold, 12% silver, and 8% copper and
zinc.
16. The apparatus of claim 12 wherein the helical coil is formed of a radio
opaque material. |
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Claims  |
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Description  |
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This invention pertains generally to the insertion of catheters into the
cardiovascular system, and more particularly to a guide wire and method
for inserting and using a catheter.
Guide wires heretofore utilized in the insertion of catheters into the
cardiovascular system have included an elongated wire core surrounded by a
helically wrapped outer wire of smaller diameter than the luminal openings
of the catheters with which they are employed. With dilation catheters for
use in the coronary vessels and catheters of relatively small diameter
(e.g., 0.020 inch or less), the guide wire is only slightly smaller than
the luminal opening, and the guide wire must be removed before any fluid
is passed through the catheter. It has generally not been possible to make
the guide wire smaller because it might not have sufficient torsional
rigidity to permit it to be steered into the cardiovascular system. In
addition, the smaller wire might puncture the wall of the artery or other
surrounding tissue.
Another problem which catheters of relatively small diameter is determining
the position of the guide wire. Larger guide wires are generally visible
with a fluoroscope or other radiographic instrument, but with the smaller
catheters, the guide wires may be too small to be seen in this manner.
It is in general an object of the invention to provide a new and improved
guide wire and method for the insertion and use of catheters into the
cardiovascular system.
Another object of the invention is to provide a guide wire and method of
the above character in which the guide wire remains in the catheter while
the catheter is in use.
These and other objects are achieved in accordance with the invention by
providing a guide wire having an elongated shaft of relatively rigid
material and a helical coil at the distal end of the shaft. The guide wire
is inserted into the cardiovascular system, and the catheter is advanced
along the guide wire to the desired position, with the helical coil
outside the distal end of the catheter. The shaft of the guide wire is
substantially smaller than the luminal opening of the catheter, and fluids
are passed through the luminal opening while the guide wire is still in
place. A marker of radio opaque material is provided at the distal end of
the guide wire so that the position of the wire can be accurately
determined even though the wire itelf may be too small to be visible with
a fluoroscope.
FIG. 1 is a side elevational view of a catheter and a guide wire
incorporating the invention.
FIG. 2 is an enlarged fragmentary centerline sectional view of the distal
end portion of the guide wire in the embodiment of FIG. 1.
FIG. 3 is a fragmentary elevational view of the tip portion of the guide
wire of FIG. 1, illustrating the manner in which the tip can be shaped to
facilitate insertion into a given artery.
FIG. 4 is an enlarged, fragmentary centerline sectional view of another
embodiment of a guide wire incorporating the invention.
In FIG. 1, the guide wire 11 is illustrated in connection with a catheter
12 having a proximal end 13 and a distal end 14. The catheter comprises an
elongated tubular body of relatively flexible material having an axially
etending luminal opening or passageway 16, with a connector fitting 17 at
the proximal end of the tubular body. The catheter can be of any desired
type, for example, a dilation catheter having a inflatable balloon toward
the distal end thereof.
Guide wire 11 comprises an elongated, relatively rigid shaft 21 having a
proximal end 22 and a distal end 23, with a relatively flexible helical
coil or spring 24 extending axially from the distal end of the shaft. The
cross-sectional area of the shaft is substantially smaller than the
luminal opening of the catheter so that fluids can pass freely between the
shaft and the wall of the luminal opening, and the outer diameter of the
helical winding is greater than the diameter of the shaft but small enough
to pass through the luminal opening. In one presently preferred embodiment
for use with a catheter having a luminal opening of 0.020 inch, for
example, the shaft has a diameter on the order of 0.008 inch and the
helical coil has an outer diameter on the order of 0.018 inch. The coil is
relatively short compared to the overall length of the guide wire, and
shaft 21 is substantially longer than the coil. In one presently preferred
embodiment, for example, the guide wire has an overall length on the order
of 175 cm, and the helical coil has a length on the order of 4 cm.
Shaft 21 and helical coil 24 are each fabricated of a suitable material
such as stainless steel wire, and in the embodiment of FIG. 1 the distal
end portion of the shaft is tapered to provide a gradual transition in
flexibility between the very flexible coil and the stiffer shaft. In this
particular embodiment, the tapered portion of the shaft extends all the
way to the distal end of the coil, but it can terminate before the end, if
desired.
The coil and shaft are bonded together by suitable means such as brazing,
welding or soldering, as indicated at 29, in the region of the overlap. If
desired, the bond can be made with a radio opaque material to make the tip
of the wire visible to a fluoroscope or other conventional radiographic
instrument. The radio opaque material preferably has a density of at least
13 gm/cm.sup.3, and suitable materials include gold, tantalum, tungsten,
platinum, iridium, rhenium and alloys of these materials. One presently
preferred material is an alloy containing on the order of about 80% gold,
12% silver, and 8% copper and zinc. If desired, coil 24 itself can be
fabricated of a radio opaque material such as tungsten, tantalum,
platinum, gold or an alloy thereof to make the entire coil visible to a
fluoroscope.
A relatively smooth, rounded tip 31 is provided at the distal end of
helical coil to facilitate insertion of the wire into the cardiovascular
system without damage to the surrounding tissue. In the embodiment
illustrated, this tip comprises a plug which is inserted partially into
the distal end portion of coil 24 and heated to form a bond with the coil
and the tip of shaft 21. This plug can also be fabricated of a radio
opaque material to make the tip visible to a fluoroscope or other
radiographic instrument. Alternatively, the rounded tip can be formed by
fusing the distal end of the wire forming the helical coil into the
desired rounded shape.
In the embodiment of FIG. 1, connections to the proximal ends of guide wire
11 and catheter 12 are made through a side arm adapter 36 having an
axially extending body 37 and a side arm 38 which extends at an angle from
the body. The connector fitting 17 at the proximal end of the catheter is
connected to one end of the adapter body by suitable connector 39, and the
luminal opening of the catheter is in fluid communication with the chamber
formed within the adapter. The guide wire extends axially through the
adapter body, and a control knob 41 is affixed to the end of the wire
beyond the adapter. An O-ring assembly 42 provides a fluid-tight seal
about the guide wire at the rear of the adapter body while permitting the
wire to be rotated within the body. Communication with the passageway of
the catheter is provided through side arm 38, and suitable appliances can
be connected to the side arm for introducing fluids into or receiving
fluids from the catheter.
Operation and use of the guide wire, and therein the method of the
invention, are as follows. The guide wire is inserted into the luminal
opening of the catheter, and the guide wire and the catheter are inserted
together into the cardiovascular system, with helical coil 24 extending
from the distal end of the catheter. The guide wire and catheter can be
inserted either directly into the system or through a guiding catheter, as
desired. The torsional rigidity of shaft 21 permits the guide wire to be
turned or steered by rotating control knob 41, and the flexibility of coil
24 facilitates movement of the wire into the artery or other passageway in
the body without damage to the surrounding tissue. The position of the
wire is determined by monitoring the radio opaque marker or markers at the
distal end with a fluroscope or other radiographic instrument. The
catheter is advanced along the wire until it is in the desired position.
Because of the relatively small diameter of shaft 21 compared to the
cross-sectional area of the luminal opening, fluids can be passed through
the catheter without removing the guide wire. For example, a contrast
material or dye can be introduced through the annular passageway formed
between the shaft of the guide wire and the wall of the luminal opening,
and pressure measurements can be made through this same passageway.
As illustrated in FIG. 3, coil 24 can be bent in any suitable manner to
facilitate steering of the wire into a side branch of the cardiovascular
system. The angle of the bend can be chosen in accordance with the angle
of the branch into which the guide wire is to be inserted.
The embodiment of FIG. 4 is generally similar to the embodiment of FIGS.
1-2, and like reference numerals designate corresponding elements in the
two embodiments. In the embodiment of FIG. 4, the tapered end portion 23
of the shaft 21 terminates prior to the distal end of coil 24, and the
windings toward the distal end of the coil are spaced apart to provide a
tip which is substantially more flexible than the remainder of the guide
wire. A safety wire 36 extends between the distal end of shaft 21 and the
distal end of coil 24, and is fabricated of a material stronger than the
coil. This wire prevents the coil from being overstretched or broken in
use, and it also facilitates the shaping of coil 24 into various curves
for steering into side branches of the cardiovascular system. Suitable
materials for the safety wire include tungsten and other metals or alloys
stronger than stainless steel. In one presently preferred embodiment, the
wire comprises a flat tungsten ribbon having a generally rectanguar
cross-section, with a width of about 0.003 inch and a thickness of about
0.001 inch. This ribbon allows the coil to remain extremely flexible and
helps the coil retain a curvature to which it is formed. The safety wire
is bonded both to shaft 21 and to end plug 31, and in the embodiment
illustrated, the proximal end of the safety wire is secured by the same
bond 29 that affixes the coil to the shaft. Alternatively, if desired, the
proximal end of the safety wire can be affixed to the tapered portion of
the shaft. Operation and use of the embodiment of FIG. 4 is similar to
that described above.
It is apparent from the foregoing that a new and improved guide wire and
method of using the same have been provided. While only certain presently
preferred embodiments have been described in detail, as will be apparent
to those familiar with the art, certain changes and modifications can be
made without departing from the scope of the invention as defined by the
following claims.
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Description  |
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