US20030045872A1 - Instrument for interrupting conduction paths within the heart - Google Patents
Instrument for interrupting conduction paths within the heart Download PDFInfo
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- US20030045872A1 US20030045872A1 US10/277,144 US27714402A US2003045872A1 US 20030045872 A1 US20030045872 A1 US 20030045872A1 US 27714402 A US27714402 A US 27714402A US 2003045872 A1 US2003045872 A1 US 2003045872A1
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- Prior art keywords
- instrument
- electrode
- probe
- physiologically acceptable
- handle
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
- A61B18/04—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating
- A61B18/12—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating by passing a current through the tissue to be heated, e.g. high-frequency current
- A61B18/14—Probes or electrodes therefor
- A61B18/1402—Probes for open surgery
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/00234—Surgical instruments, devices or methods, e.g. tourniquets for minimally invasive surgery
- A61B2017/00238—Type of minimally invasive operation
- A61B2017/00243—Type of minimally invasive operation cardiac
- A61B2017/00247—Making holes in the wall of the heart, e.g. laser Myocardial revascularization
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
- A61B2018/00315—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body for treatment of particular body parts
- A61B2018/00345—Vascular system
- A61B2018/00351—Heart
- A61B2018/00392—Transmyocardial revascularisation
Definitions
- the invention relates to an instrument for making at least one transmural lesion in one or more walls of the atria of the heart, which lesion essentially blocks the electrical impulse conduction in a direction crosswise to the transmural lesion.
- a known surgical procedure was designed to eliminate atrial fibrillation permanently.
- incisions are made with a scalpel in the walls of the atria, in order to block electrical impulse conduction in a direction crosswise to the incisions, by the interruption of the tissue continuity.
- these electrical blocks acquire a permanent character.
- the duration of the operation, and in particular the cross-clamp time (x-clamp) is so long that there is a great risk of damage to the heart muscle.
- the object of the present invention is to provide an instrument of the above-mentioned type which eliminates the abovementioned disadvantages, and which in particular shortens the time required for the operation and reduces the risk of bleeding and damage, therefore reducing the risk for the patient in open-heart surgery.
- the instrument indicated is characterized in that the instrument is a probe in which the end which during the operation comes into contact with the wall to be treated is a closed electrode which can interact with an RF power source, while the probe is of a relatively rigid type.
- the instrument according to the invention is a probe by means of which in open-heart surgery it is possible to make a permanent change in an atrial wall which is transmural, i.e. it extends over the entire thickness of the wall.
- the electrode at the end of the probe is brought into contact with the atrial wall to be treated and is moved along it in a linear pattern.
- RF dielectric
- the probe In order to be able to work well with it, the probe must be of a relatively rigid type, so that the electrode can be accurately positioned on and moved along the atrial wall. In the operation no disintegration of the tissue of the atrial wall occurs, and there is no risk of subsequent bleeding. The operation can be carried out on the outside or the inside of the atrium as desired.
- Methods of RF heating or dielectric heating are based on the use of heat generated in materials which are relatively poor electrical conductors when they are placed in high-frequency electromagnetic fields.
- the heat is generated as a result of dielectric losses occurring in a material situated between metal electrodes which form a capacitor which is connected to a high-frequency (RF) generator.
- RF high-frequency
- Such heating is highly uniform and therefore extremely suitable for use of the instrument, the probe, according to the invention.
- one of the capacitor “plates” is formed by the electrode at the end of the probe, while the other “plate” is a counter-electrode which is stuck on, for example, the patient's back; when the latter electrode is being placed, it is preferable to use a contact gel which has electrical conductance.
- the counter-electrode can also be placed on the outside of the atrial wall of the heart, for example if the electrode of the probe is being brought into contact with the inside of said wall.
- WO 95/03742 discloses a catheter comprising at the distal a metal electrode by means of which tissue erosion, also known as ablation, can be carried out.
- Such a catheter typically has a length of approximately 1 meter, a diameter of approximately 2 mm, and has an electrode of approximately 2 mm diameter, and its low thickness makes it very flexible, so that it can follow a blood vessel without any problems.
- This catheter is suitable for local punctate ablation.
- Such a catheter is not suitable for use as a probe for making stripe-shaped transmural lesions in an atrial wall.
- the probe according to the invention has at least a handle; an end; a relatively rigid member, such as a shaft, between the handle and the end, and connecting and conduction means for connecting the end of the probe to an RF power source.
- a temperature recorder is advantageously present near the end of the probe, which temperature recorder, operating in a feedback system with the RF power source, can regulate the temperature of the end of the probe to a preset value.
- the temperature recorder can regulate the temperature of the end of the probe to a preset value.
- the temperature of the end of the probe will generally rise; feedback with the RF power source makes it possible to ensure that the temperature of the end does not exceed a predetermined value.
- the probe can interact with means for supplying a physiologically acceptable liquid to the end thereof.
- a physiologically acceptable liquid is supplied near the electrode of the probe by way of a line which does not form part of the probe.
- the function of the liquid is, on the one hand, to cool the electrode and, on the other, to prevent the occurrence of electrically insulating air gaps which adversely affect the efficiency of the RF action.
- the probe according to the invention itself to have means for discharging a physiologically acceptable liquid near the end of the probe.
- Said liquid will generally preferably have a certain degree of electrical conduction, and is expediently a physiological salt solution.
- the instrument has between the handle of the probe and the shaft inlet means for introducing the physiologically acceptable liquid, which inside the shaft remains electrically insulated from the connecting and conduction means present in the shaft, while near the end it has outflow means for the physiologically acceptable liquid.
- the functioning of the probe can be improved yet further, and it can be ensured that the greatest RF energy effect is concentrated in the wall of the atrium to be treated, forming the desired transmural lesion.
- the conduction and connecting means of the probe according to the invention comprise a connector connected thereto, with contact means for connection of the electrode to the end of the probe and the temperature recorder present therein to the RF power source.
- the connector is preferably of the rapid coupling type, so that easy coupling to the RF power source is permitted.
- the shaft of the probe in the form of a probe, as easy as possible for the operating surgeon during an open-heart operation, preferably has an intrinsic curvature, which is expediently approximately 140 degrees.
- FIG. 1 shows a schematic picture of the transmural lesions which can be made with the instrument according to the invention, and which can block electrical impulses in directions crosswise to said lesions;
- FIG. 2 shows an instrument according to the invention in a first embodiment
- FIG. 3 shows an instrument according to the invention in a second embodiment.
- FIG. 1 shows diagrammatically in a two-dimensional view the two atria of a human heart, in which the transmural lesions are indicated by reference letter C, the undisturbed electrical impulses by A, and the blocked electrical impulses by B.
- the lesions C are in the nature of scar tissue which is formed after treatment using the probe according to the invention.
- the atria as viewed epicardially, include the left atrium 100 and the right atrium 101 .
- Structural features of the atria include the pulmonary veins 110 , the inferior vena cava 120 , the superior vena cava 130 , the left atrial appendage 140 and the right atrial appendage 150 .
- a first lesion 160 is a curved lesion that is joined end-to-end such that it encircles the pulmonary veins 110 , and is between the pulmonary veins 110 and conductive pathways in the left atrium 100 and between the pulmonary veins 110 and conductive pathways in the right atrium 101 .
- a second lesion 165 extends between the superior vena cava 130 and the inferior vena cava 120 and blocks a first conductive pathway 167 .
- a third lesion 170 extends across the left atrium 100 from an intersection 171 with a portion of the first lesion 160 toward the left atrial appendage 140 and blocks a second conductive pathway 172 .
- a fourth lesion 175 extends along the right atrium 101 laterally from an intersection 176 with a portion of the second lesion 165 .
- a fifth lesion 180 extends from a portion of the first lesion 160 along the left atrium 100 and blocks a third conductive pathway 182 .
- a sixth lesion 185 extends along the right atrium 101 toward the right atrial appendage 150 .
- FIG. 2 shows a probe according to the invention in a first embodiment, and shows a handle 1 , an active metal end 2 as a closed electrode with indication of the position of a temperature sensor 3 .
- the shaft of the probe 5 has a curvature 4 of approximately 140 degrees, and inside the shaft run the electrical wires 6 for exciting the closed electrode-type end 2 and wire 7 for connecting the temperature sensor which is fitted at the position of reference number 3 .
- FIG. 3 shows a particularly advantageous embodiment of the probe according to the invention, which is identical to the probe of FIG. 2, but in which reference number 11 indicates a Y-connector which makes it possible to supply a physiologically acceptable liquid by way of a port 12 into the shaft 5 , said physiologically acceptable liquid being guided through the shaft 5 without contact with the conduction means 6 and 7 .
- the physiologically acceptable solution flows by way of the port 12 to an inner shaft 13 , and from there by way of the shaft 5 to the outflow ports 14 which are disposed in the vicinity of the metal end 2 .
- the physiologically acceptable liquid is expediently a physiological salt solution which is readily tolerated by the body.
- the physiological salt solution achieves cooling of the closed electrode 2 and, on the other hand, lowers the electrical resistance between the closed electrode of the end 2 and the atrial wall. Extremely good and reproducible results are obtained with the probe shown in the figure.
- the source of RF power is typically a generator which can deliver a power of, for example, maximum 50 watt at a frequency of 500 kHz.
- the power supplied is a function of the temperature set and the tissue contact of the electrode forming the end of the probe.
- the desired temperature can be set at the generator, and in general lies in the range 50 to 70 degrees C. If temperatures higher than the given range are permitted, burning of the tissue (coagulation) will occur, with the result that an insulating layer is formed; said layer will make further action of the RF energy difficult, with the result that underlying tissue is not treated fully, if at all.
- the end 2 of the probe expediently comprises platinum and is typically a cylindrical shape with a diameter of 4 mm.
- the diameter can generally lie between 3 and 6 mm.
- the total length of the probe without connection means is typically approximately 35 cm, the handle being approximately 20 cm long, the shaft approximately 10 cm, and the end approximately 2 cm.
- the length of the shaft 5 lies between 8 and 15 cm, and the shaft has a diameter between 3 and 6 mm and is made of a physiologically acceptable plastic. Suitable plastics are nylon 66, polypropylene and high-density polyethylene.
Abstract
A probe for making transmural lesions in one or more walls of the atria of the heart in open-heart surgery. The lesion blocks electrical impulses in a direction crosswise to the lesion. The probe has a handle (1), a closed electrode (2) at an end of the probe, a relatively rigid member (5) of physiologically acceptable plastic connecting the probe and the electrode, and means (6, 7) for coupling the probe to an RF power source.
Description
- This is a continuation of application Ser. No. 09/583,303, filed May 30, 2000, which is a divisional of application Ser. No. 09/180,124 filed Nov. 2, 1998, which is the U.S. national phase of PCT application No. PCT/NL97/00223 filed Apr. 25, 1997, which claims priority from Netherlands application No. 1003021, filed May 3, 1996.
- The invention relates to an instrument for making at least one transmural lesion in one or more walls of the atria of the heart, which lesion essentially blocks the electrical impulse conduction in a direction crosswise to the transmural lesion.
- All kinds of heart arrhythmias, and in particular chronic and paroxysmal atrial fibrillation, can currently be treated by surgery.
- A known surgical procedure (MAZE) was designed to eliminate atrial fibrillation permanently. In this procedure incisions are made with a scalpel in the walls of the atria, in order to block electrical impulse conduction in a direction crosswise to the incisions, by the interruption of the tissue continuity. As a result of the subsequent scarring, these electrical blocks acquire a permanent character.
- This known technique is as yet performed only to a limited extent worldwide, owing to the complexity of the operation. The increased risk is particularly associated with the duration of the operation and the way in which the operation has to be carried out.
- The duration of the operation, and in particular the cross-clamp time (x-clamp) is so long that there is a great risk of damage to the heart muscle.
- The cross-clamp time required for the MAZE procedure alone is currently still an average of 68 min. (range 50-102 min.), and the necessary time on the heart-lung machine is on
average 182 min. (range 130-256 min.). For further data you are referred to Atrial Fibrillations: Mechanisms and Therapeutic Strategies, Futura Publishing Co. Inc. Armonk, N.Y. 1994. J. L. Cox: Surgical Interruption of Atrial Reentry as a Cure for Atrial Fibrillation. The way in which the operation is performed with the scalpel produces an increased risk of vascular suture leaks and subsequent bleeding, due to the large number and location of the vascular sutures involved. - The object of the present invention is to provide an instrument of the above-mentioned type which eliminates the abovementioned disadvantages, and which in particular shortens the time required for the operation and reduces the risk of bleeding and damage, therefore reducing the risk for the patient in open-heart surgery.
- According to the invention, the instrument indicated is characterized in that the instrument is a probe in which the end which during the operation comes into contact with the wall to be treated is a closed electrode which can interact with an RF power source, while the probe is of a relatively rigid type.
- The instrument according to the invention is a probe by means of which in open-heart surgery it is possible to make a permanent change in an atrial wall which is transmural, i.e. it extends over the entire thickness of the wall.
- As will be discussed at a later stage, during the performance of the operation the electrode at the end of the probe is brought into contact with the atrial wall to be treated and is moved along it in a linear pattern. On excitation of the electrode with RF power, dielectric (RF) heating of the wall tissue occurs. The RF treatment produces a change in the cell structure of the atrial wall, with the result that electrical impulse conduction in a direction crosswise to the transmural lesion is blocked.
- In order to be able to work well with it, the probe must be of a relatively rigid type, so that the electrode can be accurately positioned on and moved along the atrial wall. In the operation no disintegration of the tissue of the atrial wall occurs, and there is no risk of subsequent bleeding. The operation can be carried out on the outside or the inside of the atrium as desired.
- Methods of RF heating or dielectric heating are based on the use of heat generated in materials which are relatively poor electrical conductors when they are placed in high-frequency electromagnetic fields. The heat is generated as a result of dielectric losses occurring in a material situated between metal electrodes which form a capacitor which is connected to a high-frequency (RF) generator. Such heating is highly uniform and therefore extremely suitable for use of the instrument, the probe, according to the invention. During use of the probe, one of the capacitor “plates” is formed by the electrode at the end of the probe, while the other “plate” is a counter-electrode which is stuck on, for example, the patient's back; when the latter electrode is being placed, it is preferable to use a contact gel which has electrical conductance. Of course, the counter-electrode can also be placed on the outside of the atrial wall of the heart, for example if the electrode of the probe is being brought into contact with the inside of said wall.
- In connection with the invention, reference is made to WO 95/03742, which discloses a catheter comprising at the distal a metal electrode by means of which tissue erosion, also known as ablation, can be carried out.
- Such a catheter typically has a length of approximately 1 meter, a diameter of approximately 2 mm, and has an electrode of approximately 2 mm diameter, and its low thickness makes it very flexible, so that it can follow a blood vessel without any problems. This catheter is suitable for local punctate ablation. Such a catheter is not suitable for use as a probe for making stripe-shaped transmural lesions in an atrial wall.
- In particular, the probe according to the invention has at least a handle; an end; a relatively rigid member, such as a shaft, between the handle and the end, and connecting and conduction means for connecting the end of the probe to an RF power source.
- In the instrument according to the invention a temperature recorder is advantageously present near the end of the probe, which temperature recorder, operating in a feedback system with the RF power source, can regulate the temperature of the end of the probe to a preset value. Through input of the RF power, the temperature of the end of the probe will generally rise; feedback with the RF power source makes it possible to ensure that the temperature of the end does not exceed a predetermined value.
- With use of RF power it is extremely important that the fewest possible electrical blockages should be present in the body section between the end of the probe and the counter-electrode on the outside of the body. On account of this, it is preferable to ensure that the probe can interact with means for supplying a physiologically acceptable liquid to the end thereof. In its simplest form, such a liquid is supplied near the electrode of the probe by way of a line which does not form part of the probe. The function of the liquid is, on the one hand, to cool the electrode and, on the other, to prevent the occurrence of electrically insulating air gaps which adversely affect the efficiency of the RF action.
- It is very advantageous for the probe according to the invention itself to have means for discharging a physiologically acceptable liquid near the end of the probe. Said liquid will generally preferably have a certain degree of electrical conduction, and is expediently a physiological salt solution.
- In a very attractive embodiment, the instrument has between the handle of the probe and the shaft inlet means for introducing the physiologically acceptable liquid, which inside the shaft remains electrically insulated from the connecting and conduction means present in the shaft, while near the end it has outflow means for the physiologically acceptable liquid. With this embodiment, the functioning of the probe can be improved yet further, and it can be ensured that the greatest RF energy effect is concentrated in the wall of the atrium to be treated, forming the desired transmural lesion.
- At the side of the handle facing away from the end of the probe, the conduction and connecting means of the probe according to the invention comprise a connector connected thereto, with contact means for connection of the electrode to the end of the probe and the temperature recorder present therein to the RF power source.
- The connector is preferably of the rapid coupling type, so that easy coupling to the RF power source is permitted.
- In order to make handling of the instrument according to the invention, in the form of a probe, as easy as possible for the operating surgeon during an open-heart operation, the shaft of the probe preferably has an intrinsic curvature, which is expediently approximately 140 degrees.
- The invention will now be explained with reference to the drawing, in which:
- FIG. 1 shows a schematic picture of the transmural lesions which can be made with the instrument according to the invention, and which can block electrical impulses in directions crosswise to said lesions;
- FIG. 2 shows an instrument according to the invention in a first embodiment;
- FIG. 3 shows an instrument according to the invention in a second embodiment.
- FIG. 1 shows diagrammatically in a two-dimensional view the two atria of a human heart, in which the transmural lesions are indicated by reference letter C, the undisturbed electrical impulses by A, and the blocked electrical impulses by B. The lesions C are in the nature of scar tissue which is formed after treatment using the probe according to the invention. The atria, as viewed epicardially, include the
left atrium 100 and theright atrium 101. Structural features of the atria include thepulmonary veins 110, theinferior vena cava 120, thesuperior vena cava 130, the leftatrial appendage 140 and the rightatrial appendage 150. Afirst lesion 160 is a curved lesion that is joined end-to-end such that it encircles thepulmonary veins 110, and is between thepulmonary veins 110 and conductive pathways in theleft atrium 100 and between thepulmonary veins 110 and conductive pathways in theright atrium 101. Asecond lesion 165 extends between thesuperior vena cava 130 and theinferior vena cava 120 and blocks a firstconductive pathway 167. Athird lesion 170 extends across theleft atrium 100 from anintersection 171 with a portion of thefirst lesion 160 toward the leftatrial appendage 140 and blocks a secondconductive pathway 172. Afourth lesion 175 extends along theright atrium 101 laterally from anintersection 176 with a portion of thesecond lesion 165. Afifth lesion 180 extends from a portion of thefirst lesion 160 along theleft atrium 100 and blocks a thirdconductive pathway 182. Asixth lesion 185 extends along theright atrium 101 toward the rightatrial appendage 150. - FIG. 2 shows a probe according to the invention in a first embodiment, and shows a
handle 1, anactive metal end 2 as a closed electrode with indication of the position of atemperature sensor 3. The shaft of theprobe 5 has acurvature 4 of approximately 140 degrees, and inside the shaft run theelectrical wires 6 for exciting the closed electrode-type end 2 andwire 7 for connecting the temperature sensor which is fitted at the position ofreference number 3. - Inside the
handle 1 are electrical switch means 10 (not shown in any further detail) for permitting connection of the probe to the RF generator (not shown).Reference numbers 8 and 9 also indicate a connector making it possible to couple the probe to the RF generator. - FIG. 3 shows a particularly advantageous embodiment of the probe according to the invention, which is identical to the probe of FIG. 2, but in which
reference number 11 indicates a Y-connector which makes it possible to supply a physiologically acceptable liquid by way of aport 12 into theshaft 5, said physiologically acceptable liquid being guided through theshaft 5 without contact with the conduction means 6 and 7. The physiologically acceptable solution flows by way of theport 12 to aninner shaft 13, and from there by way of theshaft 5 to the outflow ports 14 which are disposed in the vicinity of themetal end 2. The physiologically acceptable liquid is expediently a physiological salt solution which is readily tolerated by the body. - The physiological salt solution, on the one hand, achieves cooling of the
closed electrode 2 and, on the other hand, lowers the electrical resistance between the closed electrode of theend 2 and the atrial wall. Extremely good and reproducible results are obtained with the probe shown in the figure. The source of RF power is typically a generator which can deliver a power of, for example, maximum 50 watt at a frequency of 500 kHz. The power supplied is a function of the temperature set and the tissue contact of the electrode forming the end of the probe. The desired temperature can be set at the generator, and in general lies in the range 50 to 70 degrees C. If temperatures higher than the given range are permitted, burning of the tissue (coagulation) will occur, with the result that an insulating layer is formed; said layer will make further action of the RF energy difficult, with the result that underlying tissue is not treated fully, if at all. - The
end 2 of the probe expediently comprises platinum and is typically a cylindrical shape with a diameter of 4 mm. The diameter can generally lie between 3 and 6 mm. - The total length of the probe without connection means is typically approximately 35 cm, the handle being approximately 20 cm long, the shaft approximately 10 cm, and the end approximately 2 cm. In general, the length of the
shaft 5 lies between 8 and 15 cm, and the shaft has a diameter between 3 and 6 mm and is made of a physiologically acceptable plastic. Suitable plastics are nylon 66, polypropylene and high-density polyethylene.
Claims (14)
1. An instrument for supplying RF energy to body tissue, the instrument comprising a probe having:
a handle;
a closed electrode at one end of said probe, the instrument being adapted to allow said electrode to be accurately positioned on and moved along an atrium wall during open heart surgery and to make at least one transmural conduction blocking lesion in the atrium wall;
a connection and conduction means electrically communicating with said electrode and adapted for connecting said electrode to an RF power source;
a substantially rigid member connecting said handle and said electrode, said member formed of a physiologically acceptable plastic; and
means for supplying a physiologically acceptable liquid to said electrode, wherein said means for supplying the liquid is connected to said member,
wherein said probe is sufficiently rigid such that an operator grasping said handle of the instrument can accurately position and move said electrode along an atrium wall to be treated, whereby the instrument can be used in an open-heart operation to make at least one transmural conduction blocking lesion in the atrium wall.
2. The instrument of claim 1 , wherein said member has an intrinsic curvature.
3. The instrument of claim 2 , wherein said curvature of said member is approximately 140 degrees.
4. The instrument of claim 1 , wherein said member has a length between approximately 8 and 15 cm.
5. The instrument of claim 1 , wherein said physiologically acceptable liquid is a salt solution.
6. The instrument of claim 1 , wherein said member is a shaft.
7. The instrument of claim 6 , wherein said shaft has a diameter between approximately 3 and 6 mm.
8. The instrument of claim 6 , wherein said means for supplying the physiologically acceptable liquid comprises an inner shaft located within said shaft connecting said handle and said electrode.
9. The instrument of claim 8 , wherein said shaft connecting said handle and said electrode further comprises an inlet port for introducing the physiologically acceptable liquid into said inner shaft.
10. The instrument of claim 8 , wherein said inner shaft comprises at least one outflow port disposed in the vicinity of said electrode.
11. The instrument of claim 1 , wherein said electrode comprises platinum.
12. The instrument of claim 1 , wherein said electrode is generally cylindrical.
13. The instrument of claim 12 , wherein said electrode has a diameter between approximately 3 mm and 6 mm.
14. The instrument of claim 12 , wherein said electrode has a length of approximately 2 cm.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/277,144 US20030045872A1 (en) | 1996-05-03 | 2002-10-21 | Instrument for interrupting conduction paths within the heart |
US10/405,392 US7128740B2 (en) | 1996-05-03 | 2003-04-02 | Method for interrupting conduction paths within the heart |
US11/133,989 US20060084967A1 (en) | 1996-05-03 | 2005-05-20 | Instrument for interrupting conduction paths within the heart |
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL1003024A NL1003024C2 (en) | 1996-05-03 | 1996-05-03 | Stimulus conduction blocking instrument. |
NL1003024 | 1996-05-03 | ||
US09/180,124 US6165174A (en) | 1996-05-03 | 1997-04-25 | Instrument for interrupting conduction paths within the heart |
US09/583,303 US6502575B1 (en) | 1996-05-03 | 2000-05-30 | Instrument for interrupting conduction paths within the heart |
US10/277,144 US20030045872A1 (en) | 1996-05-03 | 2002-10-21 | Instrument for interrupting conduction paths within the heart |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US09/583,303 Continuation US6502575B1 (en) | 1996-05-03 | 2000-05-30 | Instrument for interrupting conduction paths within the heart |
Related Child Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/405,392 Continuation US7128740B2 (en) | 1996-05-03 | 2003-04-02 | Method for interrupting conduction paths within the heart |
US11/133,989 Continuation US20060084967A1 (en) | 1996-05-03 | 2005-05-20 | Instrument for interrupting conduction paths within the heart |
Publications (1)
Publication Number | Publication Date |
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US20030045872A1 true US20030045872A1 (en) | 2003-03-06 |
Family
ID=19762795
Family Applications (5)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US09/180,124 Expired - Lifetime US6165174A (en) | 1996-05-03 | 1997-04-25 | Instrument for interrupting conduction paths within the heart |
US09/583,303 Expired - Lifetime US6502575B1 (en) | 1996-05-03 | 2000-05-30 | Instrument for interrupting conduction paths within the heart |
US10/277,144 Abandoned US20030045872A1 (en) | 1996-05-03 | 2002-10-21 | Instrument for interrupting conduction paths within the heart |
US10/405,392 Expired - Lifetime US7128740B2 (en) | 1996-05-03 | 2003-04-02 | Method for interrupting conduction paths within the heart |
US11/133,989 Abandoned US20060084967A1 (en) | 1996-05-03 | 2005-05-20 | Instrument for interrupting conduction paths within the heart |
Family Applications Before (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US09/180,124 Expired - Lifetime US6165174A (en) | 1996-05-03 | 1997-04-25 | Instrument for interrupting conduction paths within the heart |
US09/583,303 Expired - Lifetime US6502575B1 (en) | 1996-05-03 | 2000-05-30 | Instrument for interrupting conduction paths within the heart |
Family Applications After (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/405,392 Expired - Lifetime US7128740B2 (en) | 1996-05-03 | 2003-04-02 | Method for interrupting conduction paths within the heart |
US11/133,989 Abandoned US20060084967A1 (en) | 1996-05-03 | 2005-05-20 | Instrument for interrupting conduction paths within the heart |
Country Status (6)
Country | Link |
---|---|
US (5) | US6165174A (en) |
EP (1) | EP0918490B1 (en) |
AU (1) | AU2410097A (en) |
DE (1) | DE69704363T2 (en) |
NL (1) | NL1003024C2 (en) |
WO (1) | WO1997041793A1 (en) |
Cited By (72)
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US20040015106A1 (en) * | 2000-01-19 | 2004-01-22 | Coleman R. Glen | Focused ultrasound ablation devices having selectively actuatable emitting elements and methods of using the same |
US20040015219A1 (en) * | 2002-05-16 | 2004-01-22 | Francischelli David E. | Device and method for ablation of cardiac tissue |
US20040049179A1 (en) * | 2001-04-26 | 2004-03-11 | Francischelli David E. | Ablation system |
US20040078069A1 (en) * | 2001-12-11 | 2004-04-22 | Francischelli David E. | Method and system for treatment of atrial tachyarrhythmias |
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Also Published As
Publication number | Publication date |
---|---|
NL1003024C2 (en) | 1997-11-06 |
EP0918490B1 (en) | 2001-03-21 |
US6165174A (en) | 2000-12-26 |
US6502575B1 (en) | 2003-01-07 |
WO1997041793A1 (en) | 1997-11-13 |
EP0918490A2 (en) | 1999-06-02 |
DE69704363D1 (en) | 2001-04-26 |
DE69704363T2 (en) | 2001-07-12 |
AU2410097A (en) | 1997-11-26 |
US7128740B2 (en) | 2006-10-31 |
US20030191462A1 (en) | 2003-10-09 |
US20060084967A1 (en) | 2006-04-20 |
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