|
Claims  |
|
|
I claim:
1. A method for detecting the site of origin of ventricular arrhythmias
during a single heartbeat, comprising the steps of:
providing a catheter having a distal end portion with a continuous outer
surface on which a series of sensor electrodes are distributed, and a
series of insulated electrical conductors located within said catheter and
connecting said sensor electrodes to means for receiving and processing
signals picked up by said sensor electrodes, said distal end portion on
which the sensor electrodes are located having a volume less than the
volume of a cardiac chamber into which said distal end portion is to be
inserted,
introducing said distal end portion into the cardiac chamber with the heart
closed, while maintaining the outer surface of said distal end portion
spaced apart from the wall of said cardiac chamber, so that normal cardiac
functions can be maintained, and
detecting at least once during a single heartbeat the electric potentials
picked up by said sensor electrodes on said outer surface, identifying
thereby the site of origin of the arrhythmia as the portion of the heart
closest to the electrode which has detected the most negative value of
electric potential.
2. A method according to claim 1 wherein the distal end portion of the
catheter is introduced into the cardiac chamber through the circulatory
system, with the thorax closed.
3. A method according to claim 1 wherein the distal end portion of the
catheter is introduced in the cardiac chamber through the circulatory
system, with the thorax open.
4. A method according to claim 1 wherein said distal end portion of the
catheter on which the sensor electrodes are loaded has a volume of between
1/5th and 1/10th of the volume of the cardiac chamber.
5. A method of according to claim 1 wherein said distal end portion of the
catheter on which the sensor electrodes are located has an ellipsoidal
shape.
6. A method according to claim 5 wherein said ellipsoidal end portion of
the catheter has a major axis of about 40 mm and minor axis of about 18
mm.
7. A method according to claim 5 wherein the sensor electrodes are
distributed on a series of circumferences lying in planes spaced from each
other and perpendicular to the major axis of said ellipsoidal end portion,
and wherein at least two further sensor electrodes are provided, each of
said further sensor electrodes being adjacent to a respective ends of said
major axis.
8. A method according to claim 7 wherein there are four of said
circumferences, and eight of said sensor electrodes are equiangularly
spaced apart on each of said circumferences.
9. A method according to claim 1, wherein said distal end portion of the
catheter on which the sensor electrodes are located is an inflatable body. |
|
|
|
|
Claims  |
|
|
Description  |
|
|
The present invention relates to a method for the detection of intracardiac
electrical potential fields, by means of a catheter having a distal end
portion provided with a series of sensor electrodes distributed over its
surface and connected to insulated electrical conductors intended for
connection to means for receiving and processing the signals picked up by
the sensor electrodes.
A method of the type specified above is described in the Article
"Endocardial mapping by simultaneous recording of endocardial electrograms
during cardiac surgery for ventricular aneurysm" by Jacques M. T. de
Bakker et al, JACC Vol. 2, No. 5, November 1983, pages 947-953. This known
method is used to record a plurality of endocardial electrograms
simultaneously during cardiac surgery on patients subject to
aneurismectomy and/or endocardial resection. The object of endocardial
resection is to prevent the occurrence of serious ventricular tachycardia,
this often being present in these subjects and not always being
correctable by medical care. The distal end portion of the said catheter
is constituted by an inflatable balloon carrying the aforementioned sensor
electrodes. In use, the balloon, after having been inserted into a
ventricle, is inflated so as to bring the sensor electrodes into contact
with the wall of the cardiac chamber. Obviously this operation is carried
out after extracorporeal circulation has been started so as to empty the
heart of blood. After the beginning of tachycardia, which is induced by
programmed stimulation should it not be present naturally at the time of
the operation, the signals picked up by the sensor electrodes are stored
and analysed so as to determine the electrode which was activated first.
The operation takes between 2 and 5 minutes.
Although the method carried out with the catheter described above has
advantages over methods previously used for the detection of the point of
origin of potentially lethal ventricular arrhythmia, it has, however, the
disadvantage, as mentioned above, of being useable only during surgery of
the type with extracorporeal circulation, with the heart empty. Use during
cardiac catheterization is excluded. Furthermore, when the heart is open,
it may not be possible to induce tachycardia or its characteristics may be
changed.
The object of the present invention is to provide a method of the type
specified at the beginning of the present description which allows the
point of origin of ventricular arrhythmia to be detected during normal
cardiac function, for example in a catheterization theatre or during
surgery, without extracorporeal circulation, and which requires a single
cardiac beat to provide the required result.
In order to achieve this object, the invention provides a new method for
detecting intracardiac electrical potential fields of the type specified
at the beginning of the present description, the main characteristic of
which lies in the fact that the method includes the steps of introducing
the distal end portion of the catheter into one of the ventricles, with
the heart closed, while maintaining normal cardiac function, and effecting
the detection with the sensor electrodes substantially spaced from the
wall of the cardiac chamber.
A further object of the present invention is that of providing a catheter
which allows the said method to be carried out.
This object is achieved by virtue of the fact that the said distal end
portion is so shaped that when it is inserted in a cardiac chamber, the
sensor electrodes are generally spaced substantially from the wall of the
cardiac chamber.
Preferably the said distal end portion has a volume of between 1/5th and
1/10th of the volume of the cardiac chamber, whereby the catheter
according to the invention may be used, as mentioned above, during normal
functioning of the heart. This is not, however, possible with the solution
used in the known method mentioned previously which, in the operative
condition, assumes a volume equal to that of the cardiac chamber. In the
case of the present invention, the blood present in the cardiac chamber
acts as a conductive medium and allows the electrodes distributed over the
distal end portion of the catheter to detect the electrical potential
present on the surface of the end portion itself. At any instant after the
start of tachycardia, possibly caused by programmed cardiac stimulation,
the sensor electrodes signal the instantaneous electrical potential field
relative to the cardiac beat. The potential field has a minimum in
correspondence with the electrode which faces the zone of origin of the
tachycardia.
In a preferred embodiment, the said distal end portion of the catheter is
substantially ellipsoidal in shape. The sensor electrodes are distributed
on a series of circumferences lying in planes spaced from each other and
perpendicular to the major axis of the said ellipsoidal end portion. At
least two further sensor electrodes are also provided adjacent the ends of
the major axis. There may for example be four of the said circumferences
and eight sensor electrodes equiangularly spaced from each other may be
arranged on each of these circumferences. In one embodiment, the major
axis of the ellipsoidal end portion of the catheter is about 40 mm and the
minor axis is about 20 mm.
Preferably the said ellipsoidal end portion is constituted by an inflatable
body. It is, however, possible to make the end portion of the catheter in
the form of a rigid body.
The catheter according to the invention has the basic advantage of being
usable during normal functioning of the heart.
Further characteristics and advantages of the method and of the catheter
according to the invention will become apparent from the description which
follows with reference to the appended drawings, provided purely by way of
non-limiting example, in which:
FIG. 1 is a schematic perspective view of part of a catheter according to
the present invention illustrated adjacent a portion of a cardiac wall,
FIG. 2 is a schematic view illustrating the principle of operation of the
catheter according to the invention,
FIG. 3 is a schematic diagram illustrating the distribution of the sensor
electrodes over the surface of the distal end portion of the catheter of
FIG. 1, and
FIG. 4 illustrates an example of a map of electrical potential on the
surface of the distal end portion of the catheter which can be obtained by
means of the catheter according to the invention during a closed heart
operation.
In the example illustrated in FIG. 1, the catheter according to the
invention has a distal end portion 1 constituted by an inflatable body
which, in the expanded condition illustrated in FIG. 1, assumes an
ellipsoidal shape. The structure of this body and the material forming it
may, for example, be of the type illustrated for the known catheter
described in the technical article mentioned in the introduction to the
present description.
A series of sensor electrodes 2 is distributed over the outer surface of
the body constituting the end portion 1 of the catheter. FIG. 3
illustrates one possible disposition of these sensor electrodes. In this
example, the electrodes are disposed on four imaginary circumferences L
lying in four planes spaced from each other and perpendicular to the major
axis X of the ellipsoidal end portion 1. Eight sensor electrodes 2 are
equiangularly spaced from each other on each circumference L. Two further
sensor electrodes 2 are also provided adjacent the ends of the major axis
X.
In one practical embodiment, the length of the major axis X was about 40 mm
and that of the minor axis Y (see FIG. 3) was about 18 mm, a size suitable
for an adult heart.
For childrens' hearts the dimensions are reduced in proportion. The sensor
electrodes 2 are constituted by silver plates of, for example, flat
circular shape of about 0.5 mm diameter. In the embodiment illustrated,
the catheter also has a tube 3 terminating in the distal end portion 1 and
containing a series of electrical conductor wires 4, preferably of silver,
insulated from each other and connected to the respective sensor
electrodes 2. The conductor wires 4 are not illustrated for reasons of
clarity in FIG. 3.
Obviously, the conformation and disposition of the sensor electrodes 2
could be different from that explained above purely by way of example.
The electrical conductor wires 4 are intended for connection at their
opposite ends from the sensor electrodes 2 to means for receiving and
processing the signals picked up by the sensor electrodes. These means may
be constituted by a conventional instrument for recording cardiac maps
such as for example the apparatus marketed by the Italian company
Battaglia Rangoni di Casalecchio di Reno, under the name "Cardimap 2".
In use, the catheter described above may be introduced without surgery in a
catheterization theatre and in this case the introduction into the right
ventricle is carried out through a small hole formed in a peripheral vein;
the introduction into the left ventricle is effected through a peripheral
artery. During surgery, the introduction into the right ventricle is
effected through a hole formed in the superior vena cava or in the right
auricle. The introduction into the left ventricle is effected through a
pulmonary vein or the left auricle or possibly the aorta. During the
operation, the catheter is introduced with the thorax open but the heart
closed before the initiation of extracorporeal circulation. In the example
described above, the end portion 1 of the catheter is obviously introduced
in the uninflated condition and is inflated after the introduction by the
immission of oil or a physiological solution. After the start of
tachycardia, which as already mentioned may be caused by the known method
of programmed cardiac stimulation, should tachycardia not be present
naturally at the time of the operation, the instrument connected by the
electrical conductor wires 4 to the sensor electrodes 2 records a series
of maps relative to the cardiac beat. These maps constantly show a minimum
potential located at the point on the surface of the end portion 1 of the
catheter which faces the zone of origin of the tachycardia. Thus the
endocardial region from which arrhythmia starts is easily identifiable.
One example of a map which can be obtained by means of a catheter of the
type described above is illustrated in FIG. 4.
This map shows a series of equi-potential lines P distinguished by a series
of negative potential values. The zone corresponding to the minimum
potential, that is the negative potential having the highest absolute
value, is that which faces the seat or focus of the tachycardia.
The reason for this phenomenon is explained with reference to FIGS. 1 and
2. In these Figures, reference C indicates the wall of the cardiac chamber
while reference S indicates the blood which fills the cardiac chamber.
After tachycardia has started, an excitation wave-front propagates within
the thickness of the cardiac wall starting from the focus F in accordance
with the wave lines 5, with a velocity of the order of 1 m/sec. If at any
given instant the wave-front which is propagated covers the surface
portion indicated 6 in FIG. 2, the sensor electrode 2 which "views" the
surface portion 6 with the maximum viewing angle (the central electrode in
FIG. 2) is that which registers the highest absolute value of negative
potential. In the majority of cases, the focus F (FIG. 1) is located on
the endocardial surface (portion 6 of FIG. 2).
In rarer cases the focus F is located within the thickness of the
ventricular wall. In these cases, the situation described in FIG. 2 is
reproduced immediately the excitation wave-front reaches the ventricular
cavity. Again in these cases the maps show a potential minimum located at
the point of the surface of the end portion 1 of the catheter which faces
the zone of origin of the tachycardia.
As already stated, the blood S acts as a conductive medium and allows the
sensor electrodes 2 to detect the potential field generated by the
excitation wave-front which is propagated through the cardiac wall. After
a single cardiac beat it is possible to obtain immediately a map of the
type illustrated in FIG. 4 so that the focus of the tachycardia can be
identified promptly. It is thus possible to identify this in a very short
time without disturbing the normal cardiac function. By virtue of this
rapidity, the method of the invention may be used even with tachycardia of
very short duration. The method also lends itself to the study of other
rhythm and conduction disturbances, for example extrasystoles,
Wolff-Parkinson White disease, and fascicular blocks.
In one variant, the distal end portion 1 of the catheter is in the form of
a rigid body.
* * * * *
|
|
|
|
|
Description  |
|