CA1336059C - Catheters - Google Patents
CathetersInfo
- Publication number
- CA1336059C CA1336059C CA000586844A CA586844A CA1336059C CA 1336059 C CA1336059 C CA 1336059C CA 000586844 A CA000586844 A CA 000586844A CA 586844 A CA586844 A CA 586844A CA 1336059 C CA1336059 C CA 1336059C
- Authority
- CA
- Canada
- Prior art keywords
- catheter
- tip portion
- curvature
- coronary artery
- right coronary
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/01—Introducing, guiding, advancing, emplacing or holding catheters
- A61M25/0105—Steering means as part of the catheter or advancing means; Markers for positioning
- A61M25/0108—Steering means as part of the catheter or advancing means; Markers for positioning using radio-opaque or ultrasound markers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/0021—Catheters; Hollow probes characterised by the form of the tubing
- A61M25/0041—Catheters; Hollow probes characterised by the form of the tubing pre-formed, e.g. specially adapted to fit with the anatomy of body channels
Abstract
An angiographic catheter includes a relatively soft, tip portion having a preformed curvature, and a resilient body portion extending therefrom having a preformed curvature in the opposite direction. A lumen extends through the catheter for the injection of angiographic dye therethrough to the right coronary artery. The part of the body portion of the catheter which it in the aortic arch of the patient during use has an amount of curvature which is less than the amount of curvature of the aortic arch, so that the body portion of the catheter is resiliently deformed where it passes through the aortic arch. The deformation results in the biassing of the tip portion of the catheter into the ostium of the right coronary artery. Upon insertion into the aorta the preformed catheter is oriented so that the curvature of the body portion of the catheter corresponds in direction to the curvature of the aortic arch. the tip portion of the catheter being disposed above the ostium of the right coronary artery with the distal end of the tip portion touching the wall of the ascending aorta. The tip portion of the catheter is moved down the wall of the ascending aorta until it reaches the ostium of the right coronary artery.
Description
, I ' 1 336059 CATHETERS
This invention relates to catheters useful in cardiac angiography and more particularly to such catheters especially suited for the injection of a radiopaque dye into the right coronary artery.
Coronary angiography or arteriography involves the insertion of a hollow catheter into an artery at a remote point such as an arm or leg. The catheter is typically guided to the heart itself by a guide wire over which the catheter rides. The guide wire is removed before use of the catheter. Once the catheter is properly placed, a radiopaque dye is injected through the lumen of the catheter so that an x-ray machine or fluoroscope may be used to determine the physical condition of the particular part of the heart under study.
The exact placement of the tip of the catheter in the heart depends upon the type of coronary angiography to be performed. For example, in non-selective angiography the tip of the catheter is positioned in the aorta itself so that both the left and right coronary arteries can be simultaneously injected with radiopaque dye. In selective angiography, on the other hand, the tip of the catheter is actually placed in the ostium of the coronary artery which one wishes to study, in this case the right coronary artery, and the radiopaque dye is injected directly into that artery.
Selective angiography produces pictures having sharp images which are extremely helpful in diagnosing and treating coronary diseases.
Heretofore, some catheters used for selective right coronary artery angiography have not always retained their positions in the ostium of the right coronary artery during the procedure. As a result the radiopaque dye was not wholly injected i.nto the right coronary artery and the images obtained were not as satisfactory as could be desired. While some catheters fall or pop out of the ostium, others are di.fficult to i.nsert properly i.nto the ostium initially. In addition, some pri.or catheters have been known to dive too far into the right coronary artery itself, which can cause a spasm of the artery.
It is also important that the catheter be made of the proper materials. Although a certain hardness and rigidity is desi.red to maintain the catheter in position in the ostium once the tip is inserted therein, a catheter which is too rigid is difficult to position properly. Moreover, a relatively hard tip on the catheter can result in the di.slodging of plaque from the vessel walls, which is not desirable.
Several catheters have been proposed or developed to solve some of the above difficulties. For example, US
Patent 3,935,857 to Co discl-oses a cardiac catheter whi.ch i.s alleged to be useful in both right coronary and left coronary selective arteriography. On the other hand, Dr Melvin P Judkins in Chapter 7 of Coronary Arteriography and Angioplasty (McGraw-Hill) discloses differently shaped catheters for right coronary and left coronary selective arteriography.
The Judkins right coronary catheter has a preformed curvature which i.s designed to assist in the placement of the catheter tip in the ostium of the right coronary artery and to help hold the tip in place during the procedure. Because of the particular configuration chosen for the Judkins right coronary catheter, it is necessary for the catheter to be made in a number of different sizes to accommodate di.fferent patients. It is also necessary in usi.ng the Judkins right coronary l 3 3 6 0 5 q S-7482 catheter to physically rotate the catheter approximately 180 degrees once the catheter is in the heart to make it assume the proper position to enter the ostium of the right coronary artery. As Dr Judkins points out in the aforementioned chapter, this rotation must be done very slowly and commonly gives rise to error in placement of the catheter.
The present invention relates to a catheter particularly suited for use in selective arteriography of the right coronary artery.
A preferred embodiment of the catheter of the present invention has an improved ability to stay in place in the ostium once placed there. Also it may be easy to manipulate, may reduce the possibility of spasm of the right coronary artery and may minimize trauma to the heart itself. The catheter may reduce or eliminate the need to select the proper size catheter to use with a particular patient. The catheter may be less dependent upon operator technique for proper placement of the 2~ catheter in the ostium of the right coronary artery and may be less prone to error in placement.
According to the invention there is provided a right coronary artery angiographic catheter characterised in that it comprises:
a relatively soft, distal tip portion (45), the tip portion having a preformed curvature in a first direction;
a body portion extending proximally from the tip portion, the body portion having a preformed curvature in a second direction, opposite the direction of curvature of the tip portion, the body portion being resilient so that it tends to assume its preformed curvature;
a lumen extending from the distal end of the tip portion through at least a substantial part of the body portion, the lumen being sui.table for the i.njection of angiographic dye therethrough to exit from the distal end of the tip portion of the catheter;
the body portion having an amount of curvature in a second segment which is less than the amount of curvature of the aortic arch of a human being, the second segment being that part of the body portion disposed i.n the aortic arch when the tip portion is disposed in the ostium of the right coronary artery so that the body portion of the catheter is resiliently deformed where it passes through the aortic arch, the deformation resultinq in the biassing of the ti.p porti.on of the catheter into the ostium of the right coronary artery when in use.
The shape of the tip portion is preferably such as to prevent spasm of the ri.ght coronary artery when the tip portion is i.nserted in the ostium thereof. The tip portion of the catheter may extend in the direction of the right coronary artery approximately ten millimeters when in use. The tip portion curvature preferably includes an approximately ninety degree bend which can have an i.nner radius of approximately fi.ve millimeters.
Preferably the radius of curvature for the body portion exceeds by at least an order of magnitude, eg by a factor of approximately twenty, the radius of curvature of the tip portion.
The method of using the catheter of the present invention includes the steps of inserting the preformed, hollow catheter through the aorta to a predetermined position above the ostium of the right coronary artery and orienting the preformed catheter so that the curvature of the body portion of the catheter corresponds in directi.on to the curvature of the aortic arch with the tip porti.on of the cathet~r disposed above the ostium of the right coronary artery and the distal end of the tip portion touching the wall of the ascending aorta. Then the tip portion of the catheter is moved down the wall of the ascending aorta (eg in a rotatory manner using the catheter torque and applying small injections of radiopaque dye) until the ostium of the right coronary artery is located and reached.
There the tip portion of the catheter is biassed into the ostium of the right coronary artery as a result of ~he tendency of the body portion of the catheter to assume its preformed curvature from which it has been deformed in passing through the aortic arch. Once the catheter is placed, an arteriographic dye is injected through the hollow catheter i.nto the right coronary artery.
In the above method the catheter is preferably i.nserted into the ascending aorta in its oriented position with the curvature of the body portion corresponding in direction to the curvature of the aortic arch and the distal end of the tip portion touching the wall of the ascending aorta so that the tip portion may enter the ostium of the right coronary artery without being substantially rotated from i.ts initial ori.ented position.
In the inserti.ng step the catheter may be guided along the aorta with a guide wire disposed in the lumen of .
the hollow catheter until the catheter reaches the ~ -6- 1 336~5`9 vicinity of the top of the aortic arch, and then the guide wire may be removed before the tip portion of the catheter moves down the wall of the ascending aorta.
The invention also relates to a method of performing a selective coronary arteriography on the ri.ght coronary artery of a human being comprising the steps of:
i.nserting a catheter through the aortic arch into the ascending aorta of the human being such that a tip porti.on of the catheter is disposed above the ostium of the right coronary artery;
orienting the catheter so that an open distal end of the catheter tip portion is pointed toward and in contact with the inner wall of the ascending aorta;
advancing the catheter tip portion toward the ostium of the right coronary artery by moving the distal end along and contacting the inner wall while biassi.ng the tip portion of the catheter toward the inner wall of the ascending aorta with resilience of the catheter body; and inserting the distal open end of the tip portion in the ostium of the right coronary artery responsive to the advancing and biassing steps.
The invention is described by way of example only in the following description of a preferred embodiment shown with reference to the accompanying drawings in which Figure 1 is a perspective view of the human heart illustrating the relative placement of the right coronary artery, the ascending aorta, and the aortic arch;
` _7_ l 336059 Figure 2 is a side elevation of the catheter of the present invention illustrating the overall configuration thereof;
Figure 3 is a cross-sectional view of the catheter of the present invention; and Figure 4A - 4C are semidiagrammatic view of the catheter of the present invention in the process of being placed in the ostium of the right coronary artery.
Similar reference characters indicate similar parts throughout the several views of the drawings.
Description of the Preferred Embodiment A typical human heart 11 (Fig 1) includes a right ventricle 13, a right atrium 15, and a left ventricle and left atrium (not shown). The aorta, labelled 17, arises from the aortic opening of the left ventricle and consists of three parts: the ascending aorta 19, the aortic arch 21, and the descending aorta 23. At the base of the ascending aorta is located the ostia for the right coronary artery 25 and the left coronary artery 27. At the top of the aortic arch the brachiocephalic trunk 29, the left common carotid artery 31, and the left subclavian artery 33 branch off from the aorta.
Also shown in Fig 1, although of no special relevance to the present invention, are the superior vena cava 35, the inferior vena cava 37, the left pulmonary veins 39, and the left auricle 41.
-8- 1 336~59 A catheter 43 (Figs 2 and 3) of the present invention is specially configured to be inserted through aorta 17 into the ostium of right coronary artery 25. More particularly, catheter 43 is inserted into a suitable artery, such as the femoral artery (not shown) and is directed by means of a conventional guide wire (not shown) to a position in the ascending aorta somewhat above the ostium of right coronary artery 25. The guide wire is then withdrawn and the tip of catheter 43 is moved into the ostium as described below in detail.
As can be seen from Fig 2, catheter 43 includes a tip portion 45 having a preformed curvature formed therein in a conventional manner. This curvature is represented by the angle alpha between the two legs of tip portion 45. This angle in Fig 2 is 84.5 degrees, although an angle of approximately ninety degrees is also acceptable. Thi.s angle is chosen so that the tip porti.on 45 of catheter 43 will remain securely in the ostium of right coronary artery 25 once the catheter is placed. It is a function of the angle made between the ascending aorta 19 and the right coronary artery 25.
Proxi.mal from ti.p portion 45 of catheter 43 is a body portion 47 extending from the tip portion of the proximal end of the catheter. Body porti.on 47 also has a preformed curvature formed therein by conventional means. As can be seen in Figs 2 and 3, the radius of curvature of the preformed curvature of body portion 47 is much larger than that of tip portion 45. Moreover, the angle beta formed by the legs of body portion 47 is also larger than the corresponding angle alpha of the tip portion. For example, the angle beta is approximately 125 degrees. The curvature of the normal ascendi.ng aorta 19 i.n humans (although the present i.nventi.on also works well with abnormal ascendi.ng ~ S-7482 -aortas) and i.s in the opposi.te direction from the curvature of tip portion 45.
It is preferred that tip portion 45 may be relatively soft in comparison to body portion 47. This may be accomplished by making catheter 43 in accordance with the teachings of US Patent 4,385,635 to Ruiz.
As can be seen in Fig 3, catheter 43 has a lumen 49 extending axially through the catheter and terminati.ng at the open di.stal tip of the catheter. This lumen allows radiopaque dye to be injected through the catheter into the right coronary artery once the catheter is properly placed.
The angle alpha in Fig 3 is measured at right angles to the legs of tip portion 45 and is taken with respect to a generating circle having a radius R1 which defines the curvature of tip portion 45. Radius R1 is preferably five millimeters and the maxi.mum distance tip portion 45 can extend into the right coronary artery with this catheter configuration is approximately ten millimeters. These dimensions are chosen to ensure firm retention of the tip portion in the ostium of the right coronary artery without unduly increasing the possibility of spasm of the artery caused by ~diving in~, or over-insertion, of tip portion 45. The length and configuration of tip portion 45, as well as the opposite curvature of the body portion from the curvature of the tip portion permits insertion of the tip portion 45 into the ostium 25A only to the desired extent. Moreover, this configuration ensures that the distal end of tip portion 45 remains generally perpendicular to body porti.on 47 and that the catheter will not ~roll-up~
during placement.
-'- 1 336059 The segment of body portion 47 immediately proximate tip porti.on 45 has a radius of curvature R2 of, for example, approximately 100 millimeters. This curvature smoothly changes as one moves proximally away from the tip portion to one having a radius of curvature of approximately 150 millimeters. This curvature ends a distance Dl (approximately 130 millimeters) from the distal end of the catheter, and the remaining portion of the catheter over a distance D2 is generally straight. For a catheter 43 designed for femoral entry, distance D2 may be, for example, approximately ninety centimeters.
The actual placement of catheter 43 is illustrated in Figs 4A - 4C. As shown in Fig 4A, the ti.p portion 45 of catheter 43 is inserted through the aorta to a position within the ascending aorta 19 where the distal ti.p of the catheter is disposed above the ostium 25A of right coronary artery 25 with the end of the tip touching the inner wall of ascending aorta 19 above the ostium. This insertion is preferably performed using a gui.de wire that straightens the preformed curvature of tip portion 45 during inserti.on through the descending aorta and aortic arch into the ascending aorta. The guide wire is retracted to allow tip portion 45 to assume its preformed curvature. The tip portion 45 is then oriented so that the end of the tip portion is pointed toward and in contact with the right inner wall 20 of the ascending aorta, as shown in Fig 4A for example. The tip portion is then moved downwardly as shown in Figs 4B and 4C, contacting the right inner wall 20 of the ascending aorta, by physically applying a torque to the proximal end of the catheter to cause the catheter tip to rotate somewhat, while injecti.ng small amounts of radiopaque dye, until the rotatory moti.on and injections reveal that the ti.p portion 45 --"- 1 336059 has reached the osti.um 25A (Fig 4C). At this point, tip portion 45 is biassed into the ostium by the body portion of catheter 43. More particularly, body portion 47 includes a first segment 51 and a second segment 53. As can be seen by examining Figs 3 and 4C, second segment 53 as shown in Fig 4C is deformed because no part of body portion 47 has a curvature as great as that of the aortic arch in which second segment 53 is disposed. Body porti.on 47 is resilient, however, so the deformation caused by aortic arch 21 causes tip portion 45 to be forced to the left as shown in Fig 4C so that it remains firmly in place in ostium 25A.
Note that with catheter 43, there is no need for the user to accurately rotate the catheter to ensure proper placement. Nor is there any significant danger of the catheter diving into the ri.ght coronary artery since the configuration of the tip portion prevents over-insertion of the catheter.
iNumerous variations, within the scope of the appended claims, wi.ll be apparent to those skilled in the art in light of the foregoing description and accompanying drawings. These variations are merely illustrati.ve.
This invention relates to catheters useful in cardiac angiography and more particularly to such catheters especially suited for the injection of a radiopaque dye into the right coronary artery.
Coronary angiography or arteriography involves the insertion of a hollow catheter into an artery at a remote point such as an arm or leg. The catheter is typically guided to the heart itself by a guide wire over which the catheter rides. The guide wire is removed before use of the catheter. Once the catheter is properly placed, a radiopaque dye is injected through the lumen of the catheter so that an x-ray machine or fluoroscope may be used to determine the physical condition of the particular part of the heart under study.
The exact placement of the tip of the catheter in the heart depends upon the type of coronary angiography to be performed. For example, in non-selective angiography the tip of the catheter is positioned in the aorta itself so that both the left and right coronary arteries can be simultaneously injected with radiopaque dye. In selective angiography, on the other hand, the tip of the catheter is actually placed in the ostium of the coronary artery which one wishes to study, in this case the right coronary artery, and the radiopaque dye is injected directly into that artery.
Selective angiography produces pictures having sharp images which are extremely helpful in diagnosing and treating coronary diseases.
Heretofore, some catheters used for selective right coronary artery angiography have not always retained their positions in the ostium of the right coronary artery during the procedure. As a result the radiopaque dye was not wholly injected i.nto the right coronary artery and the images obtained were not as satisfactory as could be desired. While some catheters fall or pop out of the ostium, others are di.fficult to i.nsert properly i.nto the ostium initially. In addition, some pri.or catheters have been known to dive too far into the right coronary artery itself, which can cause a spasm of the artery.
It is also important that the catheter be made of the proper materials. Although a certain hardness and rigidity is desi.red to maintain the catheter in position in the ostium once the tip is inserted therein, a catheter which is too rigid is difficult to position properly. Moreover, a relatively hard tip on the catheter can result in the di.slodging of plaque from the vessel walls, which is not desirable.
Several catheters have been proposed or developed to solve some of the above difficulties. For example, US
Patent 3,935,857 to Co discl-oses a cardiac catheter whi.ch i.s alleged to be useful in both right coronary and left coronary selective arteriography. On the other hand, Dr Melvin P Judkins in Chapter 7 of Coronary Arteriography and Angioplasty (McGraw-Hill) discloses differently shaped catheters for right coronary and left coronary selective arteriography.
The Judkins right coronary catheter has a preformed curvature which i.s designed to assist in the placement of the catheter tip in the ostium of the right coronary artery and to help hold the tip in place during the procedure. Because of the particular configuration chosen for the Judkins right coronary catheter, it is necessary for the catheter to be made in a number of different sizes to accommodate di.fferent patients. It is also necessary in usi.ng the Judkins right coronary l 3 3 6 0 5 q S-7482 catheter to physically rotate the catheter approximately 180 degrees once the catheter is in the heart to make it assume the proper position to enter the ostium of the right coronary artery. As Dr Judkins points out in the aforementioned chapter, this rotation must be done very slowly and commonly gives rise to error in placement of the catheter.
The present invention relates to a catheter particularly suited for use in selective arteriography of the right coronary artery.
A preferred embodiment of the catheter of the present invention has an improved ability to stay in place in the ostium once placed there. Also it may be easy to manipulate, may reduce the possibility of spasm of the right coronary artery and may minimize trauma to the heart itself. The catheter may reduce or eliminate the need to select the proper size catheter to use with a particular patient. The catheter may be less dependent upon operator technique for proper placement of the 2~ catheter in the ostium of the right coronary artery and may be less prone to error in placement.
According to the invention there is provided a right coronary artery angiographic catheter characterised in that it comprises:
a relatively soft, distal tip portion (45), the tip portion having a preformed curvature in a first direction;
a body portion extending proximally from the tip portion, the body portion having a preformed curvature in a second direction, opposite the direction of curvature of the tip portion, the body portion being resilient so that it tends to assume its preformed curvature;
a lumen extending from the distal end of the tip portion through at least a substantial part of the body portion, the lumen being sui.table for the i.njection of angiographic dye therethrough to exit from the distal end of the tip portion of the catheter;
the body portion having an amount of curvature in a second segment which is less than the amount of curvature of the aortic arch of a human being, the second segment being that part of the body portion disposed i.n the aortic arch when the tip portion is disposed in the ostium of the right coronary artery so that the body portion of the catheter is resiliently deformed where it passes through the aortic arch, the deformation resultinq in the biassing of the ti.p porti.on of the catheter into the ostium of the right coronary artery when in use.
The shape of the tip portion is preferably such as to prevent spasm of the ri.ght coronary artery when the tip portion is i.nserted in the ostium thereof. The tip portion of the catheter may extend in the direction of the right coronary artery approximately ten millimeters when in use. The tip portion curvature preferably includes an approximately ninety degree bend which can have an i.nner radius of approximately fi.ve millimeters.
Preferably the radius of curvature for the body portion exceeds by at least an order of magnitude, eg by a factor of approximately twenty, the radius of curvature of the tip portion.
The method of using the catheter of the present invention includes the steps of inserting the preformed, hollow catheter through the aorta to a predetermined position above the ostium of the right coronary artery and orienting the preformed catheter so that the curvature of the body portion of the catheter corresponds in directi.on to the curvature of the aortic arch with the tip porti.on of the cathet~r disposed above the ostium of the right coronary artery and the distal end of the tip portion touching the wall of the ascending aorta. Then the tip portion of the catheter is moved down the wall of the ascending aorta (eg in a rotatory manner using the catheter torque and applying small injections of radiopaque dye) until the ostium of the right coronary artery is located and reached.
There the tip portion of the catheter is biassed into the ostium of the right coronary artery as a result of ~he tendency of the body portion of the catheter to assume its preformed curvature from which it has been deformed in passing through the aortic arch. Once the catheter is placed, an arteriographic dye is injected through the hollow catheter i.nto the right coronary artery.
In the above method the catheter is preferably i.nserted into the ascending aorta in its oriented position with the curvature of the body portion corresponding in direction to the curvature of the aortic arch and the distal end of the tip portion touching the wall of the ascending aorta so that the tip portion may enter the ostium of the right coronary artery without being substantially rotated from i.ts initial ori.ented position.
In the inserti.ng step the catheter may be guided along the aorta with a guide wire disposed in the lumen of .
the hollow catheter until the catheter reaches the ~ -6- 1 336~5`9 vicinity of the top of the aortic arch, and then the guide wire may be removed before the tip portion of the catheter moves down the wall of the ascending aorta.
The invention also relates to a method of performing a selective coronary arteriography on the ri.ght coronary artery of a human being comprising the steps of:
i.nserting a catheter through the aortic arch into the ascending aorta of the human being such that a tip porti.on of the catheter is disposed above the ostium of the right coronary artery;
orienting the catheter so that an open distal end of the catheter tip portion is pointed toward and in contact with the inner wall of the ascending aorta;
advancing the catheter tip portion toward the ostium of the right coronary artery by moving the distal end along and contacting the inner wall while biassi.ng the tip portion of the catheter toward the inner wall of the ascending aorta with resilience of the catheter body; and inserting the distal open end of the tip portion in the ostium of the right coronary artery responsive to the advancing and biassing steps.
The invention is described by way of example only in the following description of a preferred embodiment shown with reference to the accompanying drawings in which Figure 1 is a perspective view of the human heart illustrating the relative placement of the right coronary artery, the ascending aorta, and the aortic arch;
` _7_ l 336059 Figure 2 is a side elevation of the catheter of the present invention illustrating the overall configuration thereof;
Figure 3 is a cross-sectional view of the catheter of the present invention; and Figure 4A - 4C are semidiagrammatic view of the catheter of the present invention in the process of being placed in the ostium of the right coronary artery.
Similar reference characters indicate similar parts throughout the several views of the drawings.
Description of the Preferred Embodiment A typical human heart 11 (Fig 1) includes a right ventricle 13, a right atrium 15, and a left ventricle and left atrium (not shown). The aorta, labelled 17, arises from the aortic opening of the left ventricle and consists of three parts: the ascending aorta 19, the aortic arch 21, and the descending aorta 23. At the base of the ascending aorta is located the ostia for the right coronary artery 25 and the left coronary artery 27. At the top of the aortic arch the brachiocephalic trunk 29, the left common carotid artery 31, and the left subclavian artery 33 branch off from the aorta.
Also shown in Fig 1, although of no special relevance to the present invention, are the superior vena cava 35, the inferior vena cava 37, the left pulmonary veins 39, and the left auricle 41.
-8- 1 336~59 A catheter 43 (Figs 2 and 3) of the present invention is specially configured to be inserted through aorta 17 into the ostium of right coronary artery 25. More particularly, catheter 43 is inserted into a suitable artery, such as the femoral artery (not shown) and is directed by means of a conventional guide wire (not shown) to a position in the ascending aorta somewhat above the ostium of right coronary artery 25. The guide wire is then withdrawn and the tip of catheter 43 is moved into the ostium as described below in detail.
As can be seen from Fig 2, catheter 43 includes a tip portion 45 having a preformed curvature formed therein in a conventional manner. This curvature is represented by the angle alpha between the two legs of tip portion 45. This angle in Fig 2 is 84.5 degrees, although an angle of approximately ninety degrees is also acceptable. Thi.s angle is chosen so that the tip porti.on 45 of catheter 43 will remain securely in the ostium of right coronary artery 25 once the catheter is placed. It is a function of the angle made between the ascending aorta 19 and the right coronary artery 25.
Proxi.mal from ti.p portion 45 of catheter 43 is a body portion 47 extending from the tip portion of the proximal end of the catheter. Body porti.on 47 also has a preformed curvature formed therein by conventional means. As can be seen in Figs 2 and 3, the radius of curvature of the preformed curvature of body portion 47 is much larger than that of tip portion 45. Moreover, the angle beta formed by the legs of body portion 47 is also larger than the corresponding angle alpha of the tip portion. For example, the angle beta is approximately 125 degrees. The curvature of the normal ascendi.ng aorta 19 i.n humans (although the present i.nventi.on also works well with abnormal ascendi.ng ~ S-7482 -aortas) and i.s in the opposi.te direction from the curvature of tip portion 45.
It is preferred that tip portion 45 may be relatively soft in comparison to body portion 47. This may be accomplished by making catheter 43 in accordance with the teachings of US Patent 4,385,635 to Ruiz.
As can be seen in Fig 3, catheter 43 has a lumen 49 extending axially through the catheter and terminati.ng at the open di.stal tip of the catheter. This lumen allows radiopaque dye to be injected through the catheter into the right coronary artery once the catheter is properly placed.
The angle alpha in Fig 3 is measured at right angles to the legs of tip portion 45 and is taken with respect to a generating circle having a radius R1 which defines the curvature of tip portion 45. Radius R1 is preferably five millimeters and the maxi.mum distance tip portion 45 can extend into the right coronary artery with this catheter configuration is approximately ten millimeters. These dimensions are chosen to ensure firm retention of the tip portion in the ostium of the right coronary artery without unduly increasing the possibility of spasm of the artery caused by ~diving in~, or over-insertion, of tip portion 45. The length and configuration of tip portion 45, as well as the opposite curvature of the body portion from the curvature of the tip portion permits insertion of the tip portion 45 into the ostium 25A only to the desired extent. Moreover, this configuration ensures that the distal end of tip portion 45 remains generally perpendicular to body porti.on 47 and that the catheter will not ~roll-up~
during placement.
-'- 1 336059 The segment of body portion 47 immediately proximate tip porti.on 45 has a radius of curvature R2 of, for example, approximately 100 millimeters. This curvature smoothly changes as one moves proximally away from the tip portion to one having a radius of curvature of approximately 150 millimeters. This curvature ends a distance Dl (approximately 130 millimeters) from the distal end of the catheter, and the remaining portion of the catheter over a distance D2 is generally straight. For a catheter 43 designed for femoral entry, distance D2 may be, for example, approximately ninety centimeters.
The actual placement of catheter 43 is illustrated in Figs 4A - 4C. As shown in Fig 4A, the ti.p portion 45 of catheter 43 is inserted through the aorta to a position within the ascending aorta 19 where the distal ti.p of the catheter is disposed above the ostium 25A of right coronary artery 25 with the end of the tip touching the inner wall of ascending aorta 19 above the ostium. This insertion is preferably performed using a gui.de wire that straightens the preformed curvature of tip portion 45 during inserti.on through the descending aorta and aortic arch into the ascending aorta. The guide wire is retracted to allow tip portion 45 to assume its preformed curvature. The tip portion 45 is then oriented so that the end of the tip portion is pointed toward and in contact with the right inner wall 20 of the ascending aorta, as shown in Fig 4A for example. The tip portion is then moved downwardly as shown in Figs 4B and 4C, contacting the right inner wall 20 of the ascending aorta, by physically applying a torque to the proximal end of the catheter to cause the catheter tip to rotate somewhat, while injecti.ng small amounts of radiopaque dye, until the rotatory moti.on and injections reveal that the ti.p portion 45 --"- 1 336059 has reached the osti.um 25A (Fig 4C). At this point, tip portion 45 is biassed into the ostium by the body portion of catheter 43. More particularly, body portion 47 includes a first segment 51 and a second segment 53. As can be seen by examining Figs 3 and 4C, second segment 53 as shown in Fig 4C is deformed because no part of body portion 47 has a curvature as great as that of the aortic arch in which second segment 53 is disposed. Body porti.on 47 is resilient, however, so the deformation caused by aortic arch 21 causes tip portion 45 to be forced to the left as shown in Fig 4C so that it remains firmly in place in ostium 25A.
Note that with catheter 43, there is no need for the user to accurately rotate the catheter to ensure proper placement. Nor is there any significant danger of the catheter diving into the ri.ght coronary artery since the configuration of the tip portion prevents over-insertion of the catheter.
iNumerous variations, within the scope of the appended claims, wi.ll be apparent to those skilled in the art in light of the foregoing description and accompanying drawings. These variations are merely illustrati.ve.
Claims (11)
1. A right coronary artery angiographic catheter characterised in that it comprises:
a relatively soft, distal tip portion, the tip portion having a preformed curvature in a first direction;
a body portion extending proximally from the tip portion, the body portion having a preformed curvature in a second direction, opposite the direction of curvature of the tip portion, the body portion being resilient so that it tends to assume its preformed curvature;
a lumen extending from the distal end of the tip portion through at least a substantial part of the body portion, the lumen being suitable for the injection of angiographic dye therethrough to exit from the distal end of the tip portion of the catheter;
the body portion having an amount of curvature in a second segment which is less than the amount of curvature of the aortic arch of a human being, the second segment being that part of the body portion disposed in the aortic arch when the tip portion is disposed in the ostium of the right coronary artery so that the body portion of the catheter is resiliently deformed where it passes through the artic arch, the deformation resulting in the biassing of the tip portion of the catheter into the ostium of the right coronary artery when in use.
a relatively soft, distal tip portion, the tip portion having a preformed curvature in a first direction;
a body portion extending proximally from the tip portion, the body portion having a preformed curvature in a second direction, opposite the direction of curvature of the tip portion, the body portion being resilient so that it tends to assume its preformed curvature;
a lumen extending from the distal end of the tip portion through at least a substantial part of the body portion, the lumen being suitable for the injection of angiographic dye therethrough to exit from the distal end of the tip portion of the catheter;
the body portion having an amount of curvature in a second segment which is less than the amount of curvature of the aortic arch of a human being, the second segment being that part of the body portion disposed in the aortic arch when the tip portion is disposed in the ostium of the right coronary artery so that the body portion of the catheter is resiliently deformed where it passes through the artic arch, the deformation resulting in the biassing of the tip portion of the catheter into the ostium of the right coronary artery when in use.
2. A right coronary artery angiographic catheter as claimed in Claim 1 wherein the shape of the tip portion is such as to prevent spasm of the right coronary artery when the tip portion is inserted in the ostium thereof.
3. A right coronary artery angiographic catheter as claimed in Claim 1 or 2 wherein the tip portion of the catheter extends in the direction of the right coronary artery approximately ten millimeters when in use.
4. A right coronary artery angiographic catheter as claimed in Claim 2 wherein the tip portion curvature includes an approximately ninety degree bend.
5. A right coronary artery angiographic catheter as claimed in Claim 4 wherein the ninety degree bend has an inner radius of approximately five millimeters.
6. A right coronary artery angiographic catheter as claimed in Claim 1 wherein the radius of curvature for the body portion exceeds by at least an order of magnitude the radius of curvature of the tip portion.
7. A right coronary artery angiographic catheter as claimed in Claim 6 wherein the radius of curvature for the body portion exceeds the radius of curvature of the tip portion by at least a factor of approximately twenty.
8. The use of a preformed, hollow catheter having a relatively soft, distal tip portion, the tip portion having a curvature in a first direction, the catheter further having a body portion proximal the tip portion, the body portion having a curvature in a second direction, opposite the direction of the curvature of the tip portion, the body portion being resilient so that it tends to assume its preformed curvature, the inserting step including orienting the preformed catheter so that the curvature of the body portion of the catheter corresponds in direction to the curvature of the aortic arch, and the tip portion of the catheter being disposed above the ostium of the right coronary artery with the distal end of the tip portion biassed into contact with the wall of the ascending aorta for performing a selective coronary arteriography on the right coronary artery of a human being by (i) inserting the catheter through the aorta to a predetermined position above the ostium of the right coronary artery;
(ii) moving the tip portion of the catheter down the wall of the ascending aorta until it reaches the ostium of the right coronary artery, the body portion having an amount of curvature where it passes through the aortic arch which is less than the curvature of the aortic arch so that the body portion is resiliently deformed where it passes through the aortic arch due to the greater curvature of the aortic arch;
(iii) biassing the tip portion of the catheter into the ostium of the right coronary artery, the biassing resulting from the tendency of the body portion of the catheter to assume its preformed curvature from which it has been deformed in passing through the aortic arch; and (iv) inserting an arteriographic dye through the hollow catheter into the right coronary artery.
(ii) moving the tip portion of the catheter down the wall of the ascending aorta until it reaches the ostium of the right coronary artery, the body portion having an amount of curvature where it passes through the aortic arch which is less than the curvature of the aortic arch so that the body portion is resiliently deformed where it passes through the aortic arch due to the greater curvature of the aortic arch;
(iii) biassing the tip portion of the catheter into the ostium of the right coronary artery, the biassing resulting from the tendency of the body portion of the catheter to assume its preformed curvature from which it has been deformed in passing through the aortic arch; and (iv) inserting an arteriographic dye through the hollow catheter into the right coronary artery.
9. The use of a catheter as claimed in Claim 8, wherein the catheter is inserted into the ascending aorta in its oriented position with the curvature of the body portion corresponding in direction to the curvature of the aortic arch and the distal end of the tip portion touching the wall of the ascending aorta so that the tip portion may enter the ostium of the right coronary artery without being substantially rotated from its initial oriented position.
10. The use of a catheter as claimed in Claim 8, wherein the inserting step includes the step of guiding the catheter along the aorta with a guide wire disposed in the lumen of the hollow catheter until the catheter reaches the vicinity of the top of the aortic arch, and then removing the guide wire before the tip portion of the catheter moves down the wall of the ascending aorta.
11. The use of a right coronary artery angiographic catheter as defined in claim 1 or claim 2 for performing a selective coronary arteriography on the right coronary artery of a human being, by (i) inserting a catheter through the aortic arch into the ascending aorta of the human being such that a tip portion of the catheter is disposed above the ostium of the right coronary artery;
(ii) orienting the catheter so that an open distal end of the catheter tip portion is pointed toward and in contact with the inner wall of the ascending aorta;
(iii) advancing the catheter tip portion toward the ostium of the right coronary artery by moving the distal end along and contacting the inner wall while biassing the tip portion of the catheter toward the inner wall of the ascending aorta with resilience of the catheter body; and (iv) inserting the distal open end of the tip portion in the ostium of the right coronary artery responsive to the advancing and baissing steps.
(ii) orienting the catheter so that an open distal end of the catheter tip portion is pointed toward and in contact with the inner wall of the ascending aorta;
(iii) advancing the catheter tip portion toward the ostium of the right coronary artery by moving the distal end along and contacting the inner wall while biassing the tip portion of the catheter toward the inner wall of the ascending aorta with resilience of the catheter body; and (iv) inserting the distal open end of the tip portion in the ostium of the right coronary artery responsive to the advancing and baissing steps.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US141,208 | 1988-01-06 | ||
| US07/141,208 US4883058A (en) | 1988-01-06 | 1988-01-06 | Right coronary angiographic method |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1336059C true CA1336059C (en) | 1995-06-27 |
Family
ID=22494662
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000586844A Expired - Fee Related CA1336059C (en) | 1988-01-06 | 1988-12-22 | Catheters |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US4883058A (en) |
| EP (1) | EP0323738B1 (en) |
| JP (1) | JPH01238872A (en) |
| AT (1) | ATE96682T1 (en) |
| CA (1) | CA1336059C (en) |
| DE (1) | DE3885439T2 (en) |
| ES (1) | ES2047564T3 (en) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4973306A (en) * | 1988-01-06 | 1990-11-27 | Sherwood Medical Company | Method of performing right coronary artery angiography |
| US5348545A (en) * | 1990-08-21 | 1994-09-20 | Advanced Cardiovascular Systems, Inc. | Guiding catheter for the right coronary artery |
| US5445625A (en) * | 1991-01-23 | 1995-08-29 | Voda; Jan | Angioplasty guide catheter |
| WO1992012754A1 (en) * | 1991-01-23 | 1992-08-06 | Jan Voda | Guide catheter construction |
| WO1992019307A1 (en) * | 1991-04-24 | 1992-11-12 | Myers Gene E | Aortic branch internal thoracic artery catheter |
| US5195990A (en) * | 1991-09-11 | 1993-03-23 | Novoste Corporation | Coronary catheter |
| WO1993014802A1 (en) * | 1992-01-28 | 1993-08-05 | Nesto Richard W | Left coronary guiding catheter |
| US5215540A (en) * | 1992-01-31 | 1993-06-01 | St. Jude Medical, Inc. | Right coronary catheter |
| US5306263A (en) * | 1992-05-01 | 1994-04-26 | Jan Voda | Catheter |
| US5538512A (en) * | 1993-02-25 | 1996-07-23 | Zenzon; Wendy J. | Lubricious flow directed catheter |
| US5336205A (en) * | 1993-02-25 | 1994-08-09 | Target Therapeutics, Inc. | Flow directed catheter |
| US5536247A (en) * | 1993-06-10 | 1996-07-16 | Scimed Life Systems, Inc. | Method of treating cardiac conduction defects |
| US5643231A (en) * | 1993-08-13 | 1997-07-01 | Daig Corporation | Coronary sinus catheter |
| US5984909A (en) * | 1993-08-13 | 1999-11-16 | Daig Corporation | Coronary sinus catheter |
| US5423772A (en) * | 1993-08-13 | 1995-06-13 | Daig Corporation | Coronary sinus catheter |
| US6001085A (en) * | 1993-08-13 | 1999-12-14 | Daig Corporation | Coronary sinus catheter |
| US5814027A (en) * | 1993-11-03 | 1998-09-29 | Daig Corporation | Guiding introducer used for medical procedures within the right ventricle associated with the right ventricular outflow track |
| US5722400A (en) * | 1995-02-16 | 1998-03-03 | Daig Corporation | Guiding introducers for use in the treatment of left ventricular tachycardia |
| US5427119A (en) * | 1993-11-03 | 1995-06-27 | Daig Corporation | Guiding introducer for right atrium |
| US5497774A (en) * | 1993-11-03 | 1996-03-12 | Daig Corporation | Guiding introducer for left atrium |
| US5628316A (en) * | 1993-11-03 | 1997-05-13 | Swartz; John F. | Guiding introducer system for use in the right atrium |
| US5846223A (en) * | 1993-11-03 | 1998-12-08 | Daig Corporation | Diagnosis and treatment of atrial flutter in the right atrium |
| US5656028A (en) * | 1993-11-03 | 1997-08-12 | Daig Corporation | Process for the nonsurgical mapping and/or treatment of ectopic atrial tachycardia using a guiding introducer |
| US5564440A (en) * | 1993-11-03 | 1996-10-15 | Daig Corporation | Method for mopping and/or ablation of anomalous conduction pathways |
| US5640955A (en) * | 1995-02-14 | 1997-06-24 | Daig Corporation | Guiding introducers for use in the treatment of accessory pathways around the mitral valve using a retrograde approach |
| US5575766A (en) * | 1993-11-03 | 1996-11-19 | Daig Corporation | Process for the nonsurgical mapping and treatment of atrial arrhythmia using catheters guided by shaped guiding introducers |
| FR2715827B1 (en) * | 1994-02-07 | 1996-04-19 | Braun Celsa Sa | Implantable medical device in the body of a patient, with axially stabilized rod, rod and curved part for this purpose and their production method. |
| US5833673A (en) * | 1994-11-02 | 1998-11-10 | Daig Corporation | Guiding introducer system for use in the treatment of left ventricular tachycardia |
| US5814029A (en) * | 1994-11-03 | 1998-09-29 | Daig Corporation | Guiding introducer system for use in ablation and mapping procedures in the left ventricle |
| CA2153178A1 (en) * | 1995-02-14 | 1996-08-15 | John D. Ockuly | Guiding introducer system for use in the treatment of accessory pathways around the mitral valve using a retrograde approach |
| US6540755B2 (en) | 1995-02-14 | 2003-04-01 | Daig Corporation | Guiding introducers for use in the treatment of accessory pathways around the mitral valve using a retrograde approach |
| US5730733A (en) * | 1995-06-01 | 1998-03-24 | Scimed Life Systems, Inc. | Flow assisted catheter |
| US5603704A (en) * | 1995-06-30 | 1997-02-18 | Medtronic, Inc. | Multi-purpose curve |
| US5971974A (en) * | 1995-09-06 | 1999-10-26 | Schneider ( Usa ) Inc | Left coronary artery catheter |
| ATE248621T1 (en) * | 1996-01-19 | 2003-09-15 | Scimed Life Systems Inc | CATHETER WITH AN INCREASING RADIUS CURVE |
| US5846229A (en) * | 1996-05-31 | 1998-12-08 | Scimed Life Systems, Inc. | Catheter for the right coronary artery |
| US5899892A (en) * | 1996-05-31 | 1999-05-04 | Scimed Life Systems, Inc. | Catheter having distal fiber braid |
| US5938660A (en) * | 1997-06-27 | 1999-08-17 | Daig Corporation | Process and device for the treatment of atrial arrhythmia |
| US6251109B1 (en) * | 1997-06-27 | 2001-06-26 | Daig Corporation | Process and device for the treatment of atrial arrhythmia |
| WO1999025411A1 (en) | 1997-11-18 | 1999-05-27 | Daig Corporation | Catheter guiding introducers for use in pediatric hearts |
| US6200315B1 (en) | 1997-12-18 | 2001-03-13 | Medtronic, Inc. | Left atrium ablation catheter |
| US5916209A (en) | 1997-12-24 | 1999-06-29 | Mick; Matthew J. | Coronary catheters for use in a transradial catheterization |
| US6193705B1 (en) | 1998-10-28 | 2001-02-27 | Scimed Life Systems, Inc. | Flow assisted catheter |
| US6595983B2 (en) | 2000-12-07 | 2003-07-22 | Jan K. Voda | Guide or diagnostic catheter for right coronary artery |
| US20040015152A1 (en) * | 2002-05-20 | 2004-01-22 | Day Ronald W. | Reducing torque needed to perform a cardiovascular procedure |
| WO2004091710A1 (en) | 2003-04-14 | 2004-10-28 | Cook Incorporated | Large diameter delivery catheter/sheath |
| DK1872820T3 (en) | 2003-04-28 | 2015-09-07 | Cook Medical Technologies Llc | Flexible insertion sheath with varying durometer |
| US7789877B2 (en) | 2003-07-02 | 2010-09-07 | St. Jude Medical, Atrial Fibrillation Division, Inc. | Ablation catheter electrode arrangement |
| US7234225B2 (en) | 2003-09-22 | 2007-06-26 | St. Jude Medical, Atrial Fibrillation Division, Inc. | Method for manufacturing medical device having embedded traces and formed electrodes |
| US7229437B2 (en) * | 2003-09-22 | 2007-06-12 | St. Jude Medical, Atrial Fibrillation Division, Inc. | Medical device having integral traces and formed electrodes |
| US8147486B2 (en) | 2003-09-22 | 2012-04-03 | St. Jude Medical, Atrial Fibrillation Division, Inc. | Medical device with flexible printed circuit |
| US7867218B1 (en) | 2004-02-24 | 2011-01-11 | Voda Heart Technology, Llc | Steerable catheter for right coronary artery |
| EP2001542B1 (en) | 2006-03-31 | 2010-02-10 | C.R.Bard, Inc. | Catheter including arcuate transition region |
| US10252023B2 (en) | 2013-01-11 | 2019-04-09 | C. R. Bard, Inc. | Curved catheter and methods for making same |
| US11027093B2 (en) * | 2016-12-08 | 2021-06-08 | Sanford Health | Slide guide catheter and methods for use thereof |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3419010A (en) * | 1966-01-17 | 1968-12-31 | Cordis Corp | Catheter |
| CA930636A (en) * | 1970-04-29 | 1973-07-24 | Cardinal Roland | Catheters and method and mold for making same |
| US3935857A (en) * | 1974-07-31 | 1976-02-03 | Co Eddy D | Cardiac catheter |
| SE390886B (en) * | 1975-06-23 | 1977-01-31 | Siemens Elema Ab | CATHETER FOR SELECTIVE CORONAR ARTERIOGRAPHY OF LEFT CORONAR SPECIES |
| US4033331A (en) * | 1975-07-17 | 1977-07-05 | Guss Stephen B | Cardiac catheter and method of using same |
| US4292976A (en) * | 1979-08-08 | 1981-10-06 | Banka Vidya S | Right ventricular injection catheter; right ventricular angiographic method; and method of monitoring septal wall motion |
| US4279252A (en) * | 1979-08-24 | 1981-07-21 | Martin Michael T | X-ray scaling catheter |
| JPS56124449U (en) * | 1980-02-20 | 1981-09-22 | ||
| US4385635A (en) * | 1980-04-25 | 1983-05-31 | Ruiz Oscar F | Angiographic catheter with soft tip end |
| US4430083A (en) * | 1981-03-06 | 1984-02-07 | American Hospital Supply Corporation | Infusion catheter |
| US4563181A (en) * | 1983-02-18 | 1986-01-07 | Mallinckrodt, Inc. | Fused flexible tip catheter |
| EP0273618A3 (en) * | 1986-12-23 | 1989-09-13 | BAXTER INTERNATIONAL INC. (a Delaware corporation) | Soft tip catheter |
| US4784639A (en) * | 1987-07-06 | 1988-11-15 | Patel Piyush V | Catheter and method of inserting catheter |
-
1988
- 1988-01-06 US US07/141,208 patent/US4883058A/en not_active Expired - Lifetime
- 1988-12-22 ES ES88312198T patent/ES2047564T3/en not_active Expired - Lifetime
- 1988-12-22 CA CA000586844A patent/CA1336059C/en not_active Expired - Fee Related
- 1988-12-22 DE DE88312198T patent/DE3885439T2/en not_active Expired - Lifetime
- 1988-12-22 EP EP88312198A patent/EP0323738B1/en not_active Expired - Lifetime
- 1988-12-22 AT AT88312198T patent/ATE96682T1/en not_active IP Right Cessation
- 1988-12-28 JP JP63332685A patent/JPH01238872A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| EP0323738B1 (en) | 1993-11-03 |
| ATE96682T1 (en) | 1993-11-15 |
| DE3885439T2 (en) | 1994-03-17 |
| DE3885439D1 (en) | 1993-12-09 |
| EP0323738A3 (en) | 1990-05-23 |
| JPH01238872A (en) | 1989-09-25 |
| ES2047564T3 (en) | 1994-03-01 |
| JPH0459916B2 (en) | 1992-09-24 |
| EP0323738A2 (en) | 1989-07-12 |
| US4883058A (en) | 1989-11-28 |
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Legal Events
| Date | Code | Title | Description |
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| MKLA | Lapsed |