Methods and apparatus for aspiration and priming of inflatable structures in catheters
An aspiration baffle comprises an outer tube and an inner core wire. Microholes are provided in the outer tubular member to permit passage of gas but inhibit the passage of liquids. The aspiration baffle is used in a catheter having a balloon or other inflatable structure to assist in priming of the structure. After evacuating the inflatable structure by applying a vacuum, the aspiration baffle can collect and trap residual gas which remains during the priming of the inflatable structure.
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This application is a divisional of U.S. patent application Ser. No. 10/447,676 (Attorney Docket No. 021621-0011US), filed on May 28, 2003, which claimed the benefit of Provisional Application No. 60/384,894 (Attorney/Docket No. 21621-001100US), filed on May 28, 2002, the full disclosures of which are incorporated herein by reference.
BACKGROUND OF THE INVENTION1. Field of the Invention
The present invention relates generally to medical devices and methods. More particularly, the present invention relates to apparatus and methods for removing air from vascular and other medical catheters having chambers which are filled with liquid.
Balloon angioplasty, stent treatment, and numerous other intravascular procedures employ catheters which are introduced to the vasculature and advanced intravascularly to a target location, often in the coronary vasculature. Many such intravascular catheters have inflatable balloons and other structures intended to effect or assist in performing a therapeutic procedure, e.g. balloon angioplasty, stent placement, and/or drug delivery. Such expandable structures can take a variety of forms, including non-distensible balloons of the type typically used for performing angioplasty, elastomeric balloons of the type often used for vessel occlusion, and driving structures of the type used for advancing needles and manipulating other tools.
Because of the dangers of the release of air into the bloodstream, such expandable structures are typically inflated with a liquid, such as saline, in order to achieve inflation within the vasculature. In order to purge the inflatable structures prior to use, the catheters are typically primed with liquid immediately prior to use. A common method of priming relies on vacuum aspiration of air from the inflatable structure through a lumen in the catheter, typically the inflation lumen which is subsequently used to introduce the liquid inflation medium. Thus, a vacuum is typically applied through the inflation lumen to lower the air pressure within the inflatable structure to a fraction of atmospheric pressure, typically 15 mm Hg or below. A liquid inflation medium is then introduced into the inflatable structure while preventing the reintroduction of air and other gasses.
While this procedure significantly limits the presence of air and other gasses within the inflatable structure, it will be appreciated that there will usually be a small residual amount of gas within the inflatable structure since the vacuum drawn is not complete. In order to even further enhance the safety, it is desirable to reduce or eliminate such residual gas amount within the inflatable structure.
The most common method for eliminating such residual gas in the balloon or other inflatable structure is to provide a vent tube or hole from the interior of the inflatable structure to the atmosphere. In this way, as the balloon or other inflatable structure is primed with liquid inflation medium, the residual air or gas will migrate toward the vent and be released into the atmosphere. The release of liquid medium is reduced or eliminated by providing vent tubes or holes having small or capillary dimensions. Thus, the vent tubes or holes will allow gas to pass but will inhibit the passage of the liquid inflation medium at the priming pressures and subsequent therapeutic pressures used in the procedures.
While the use of vent tubes and holes has been generally successful, the need to provide a passage from the interior of the inflatable structure to the atmosphere can compromise the integrity and design of the inflatable structure. Thus, it would be desirable to provide alternative and improved structures for removing or sequestering residual gas inside an inflatable structure on a vascular or other catheter prior to use. In particular, it would be desirable if the apparatus and methods did not require significant alteration in the structure of the balloon or other inflatable structure on the catheter. Some of these objectives will be met by the invention described herein below.
2. Description of the Background Art
Vascular catheters having balloons with vent structures are described in U.S. Pat. Nos. 4,638,805; 4,692,200; 4,715,378; 4,810,455; 4,821,722; 5,035,705; 5,049,130; 5,100,385; 5,176,698; and 5,256,143.
BRIEF SUMMARY OF THE INVENTIONThe present invention provides apparatus and methods for purging gas from inflatable structures on intravascular and other medical catheters while said structures are being primed with a liquid inflation medium. While the inflatable structures will typically be angioplasty balloons, stent delivery balloons, elastomeric isolation balloons, embolectomy balloons, occlusion balloons, and like, there may also be other inflatable structures intended for distinct purposes. In particular, the purging apparatus and methods of the present invention may find particular use with inflatable structures intended for driving needles, cutting blades, and other tools and implements intended for intravascular and other therapeutic procedures.
In a first aspect of the present invention, an aspiration baffle for purging gas from a liquid-filled chamber in a catheter comprises a tubular member having a distal end, a proximal end, and an interior volume extending between said ends. The tubular member will be sealed over its entire surface except for a plurality of “microholes.” The microholes have dimensions selected to permit the passage of gas under the differential pressures expected during the priming process. Such selected dimensions, however, will also inhibit or prevent the flow of liquid inflation medium through the microholes under the both the priming pressures as well as the inflation pressures expected during use of the catheter and vasculature. In angioplasty procedures, such inflation pressures can be as high as 10 atmospheres, 20 atmospheres, or even higher in some circumstances. Particular dimensions for the microholes are set forth below.
The tubular member of the aspiration baffle, will be adapted to be disposed axially in the catheter so that the microholes are present in the interior of the chamber which is first purged of gas and later filled with liquid inflation medium. Thus, the microholes will initially allow residual gas present in the inflatable chamber after initial vacuum aspiration to pass into the interior of the tubular member as a priming liquid is introduced, typically at atmospheric pressure or higher. While the inflatable chamber is being primed with the liquid inflation medium, the residual gas will thus be able to pass into the interior of the tubular member which remains at or close to the vacuum which had been achieved during the initial vacuum step. Thus, the aspiration baffle acts as a low-pressure reservoir or “sponge” for drawing and trapping the residual gas volume present in the inflatable chamber after the initial vacuum aspiration. The near-vacuum pressure is maintained since the gas volume is very low and the entrance of liquid into the interior of the tubular member (which liquid would quickly relieve the vacuum) is prevented by the small size of the microhole.
In a preferred construction, the aspiration baffle further comprises a core wire or other interior structure to provide mechanical strength. For example, the core wire may be coaxially disposed within the interior volume of the tubular member, running axially over at least a portion of the length of the tubular member, usually over the entire length. The exterior surface of the core wire and interior surface of the tubular member thus define an annular flow path or volume for receiving the residual gas through the microholes.
Typically, the tubular member will have a length in the range 12 cm to 200 cm, often from 20 cm to 150 cm. The tubular member will have an outside diameter usually in the range from 0.1 mm to 1 mm, and the microholes will have a maximum width, usually a diameter in the case of circular microholes, in the range of 0.001 mm to 0.1 mm. The microholes may extend over the entire length of the exterior of the tubular member, or may optionally extend over only a portion of the length, e.g. in the range from 1 cm to 20 cm. The microholes may be arranged axially in one or more rows, may be arranged spirally, or may be arrange in any other random or regular pattern. The number of microholes may range from 2 to 1,000, typically being from 5 to 500. The core wire may extend the entire length of the tubular member or, alternatively, may only extend through a portion thereof, typically from 1 cm to 100 cm.
In a second aspect of the present invention, a catheter comprises a catheter body having a proximal end, a distal end, and an inflation lumen therethrough. An inflatable chamber is disposed on the catheter body to receive inflation medium from the inflation lumen, and an aspiration baffle is disposed in the catheter body. The aspiration baffle defines a sealed interior volume open to an interior of the inflatable chamber through a plurality of microholes. Thus, by applying a vacuum to the interior of the inflatable chamber, typically through the inflation lumen, the interior volume of the aspiration baffle is initially evacuated to a sub atmospheric pressure. After such initial evacuation, the inflatable chamber is primed with a liquid inflation medium, typically at atmospheric pressure or higher, such that residual gas remaining after the initial evacuation passes from the inflatable chamber into the interior volume of the aspiration tube.
Depending on the desired use, the inflatable chamber may be an angioplasty balloon, may be adapted to carry an expandable tubular prosthesis, such as a stent, graft, or the like, or may carry a needle in order to effect extraluminal drug delivery. Optionally, the catheter body may also include a guide wire lumen. The aspiration lumen may optionally be held within yet another lumen within the catheter body. In some embodiments, the additional catheter body lumen may actually form part of the aspiration baffle, e.g. an end of the tubular member may be opened into a volume defined by the additional lumen in the catheter body. So long as said additional lumen were otherwise sealed, the luminal volume would then form part of the interior volume of the aspiration baffle. Other aspects of the aspiration baffle forming part of the catheter of the present invention have been described above with respect to the aspiration baffle embodiments.
In a third aspect of the present invention, a method for priming an inflatable chamber on a catheter with liquid comprises drawing a vacuum in the chamber through an inflation lumen in the catheter to remove gas from the chamber. Depending on the level of vacuum which is drawn, a residual amount of gas will be left in the inflatable chamber. The chamber is then filled or “primed” with a liquid, typically the same liquid which will be used for inflating the chamber during use. An aspiration baffle is disposed in the catheter body such that microholes are in communication with the interior of the inflatable chamber. The aspiration baffle is able to draw and sequester at least a major portion of the residual air or gas volume which remains in the inflatable chamber after the initial vacuum aspiration step. Typically, the initial vacuum will be drawn down to a pressure of about 15 mm Hg or lower, and the inflatable chamber will then be filled with liquid at a pressure of at least one atmosphere, and often two atmospheres or greater. Particular aspects of the aspiration baffle used in these methods are generally as described above in connection with the aspiration baffle itself.
BRIEF DESCRIPTION OF THE DRAWINGS
An aspiration baffle 10 constructed in accordance with the principles of the present invention comprises an outer tubular member 12 and, optionally, an inner core wire 14 (
Note that while the tubular member 12 is shown in
Referring now to
Referring now to
The catheter 20 may be prepared for use in a patient as follows. A conventional balloon catheter vacuum and inflation device, such as those available from Guidant Corporation, Johnson & Johnson, Boston Scientific, and the like, is used to first draw a vacuum through the inflation lumen or tube 24/26 to a desired low pressure, typically about 15 mm of Hg. After the pressure has been achieved, the balloon 22 is then primed with saline or other inflation medium to a conventional pressure, typically one atmosphere, two atmospheres, or higher.
In the initial vacuum aspiration step, air or other gas from the interior of the aspiration baffle 28 is withdrawn through the microhole 16 together with the other air or gasses which are present in the balloon 22. When the liquid inflation medium is introduced into the balloon 22, however, the liquid is prevented from entering the interior of aspiration baffle 28 as the flow through individual microholes 16 is blocked, generally shown in
Catheter 20 of
Claims
1. A method for priming an inflatable chamber on a catheter with liquid, said method comprising:
- drawing a vacuum in the chamber through the inflation lumen to remove gas, wherein a residual amount of gas is left; and
- filling the chamber with liquid;
- wherein an aspiration baffle is disposed in the catheter body said baffle defining a sealed interior volume open to an interior of the inflatable chamber through a plurality of microholes only;
- wherein the interior volume of the aspiration baffle is evacuated through the microholes as the vacuum is drawn in the interior of the inflatable chamber through the inflation lumen so that the residual amount of gas may pass from the inflatable chamber into the interior volume of said aspiration tube.
2. A method as in claim 1, wherein the vacuum is drawn to a pressure of 15 mmHg or lower.
3. A method as in claim 2, wherein the chamber is filled with liquid at a pressure of at least one atmosphere.
4. A method as in claim 3 wherein the chamber is filled with liquid at a pressure of at least two atmospheres.
5. A method as in claim 1 wherein the aspiration baffle further comprises a core wire disposed coaxially within the interior volume of the tubular member, wherein an annular gas flow path is formed between an interior wall of the tubular member and an exterior surface of the core wire.
6. A method as in claim 5, wherein the tubular member has a length in the range from 10 cm to 200 cm and an outer diameter in the range from 0.1 mm to 1 mm, and wherein the microholes have a maximum width in the range from 0.001 mm to 0.1 mm.
7. A method as in claim 6, wherein the microholes are disposed over only a distal length of the tubular member in the range from 1 cm to 20 cm.
8. A method as in claim 7, wherein the core wire extends from the distal end of the tubular member over a distance in the range from 1 cm to 100 cm.
Type: Application
Filed: Jan 4, 2006
Publication Date: May 25, 2006
Applicant: MERCATOR MEDSYSTEMS, INC. (San Leandro, CA)
Inventor: Kirk Seward (Dublin, CA)
Application Number: 11/325,896
International Classification: A61M 1/00 (20060101);