WO2002074163A1 - Method and device for cardiac radiological examination - Google Patents
Method and device for cardiac radiological examination Download PDFInfo
- Publication number
- WO2002074163A1 WO2002074163A1 PCT/US2002/008104 US0208104W WO02074163A1 WO 2002074163 A1 WO2002074163 A1 WO 2002074163A1 US 0208104 W US0208104 W US 0208104W WO 02074163 A1 WO02074163 A1 WO 02074163A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- contrast medium
- images
- injection
- image plane
- introduction
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 32
- 230000000747 cardiac effect Effects 0.000 title claims abstract description 18
- 239000002872 contrast media Substances 0.000 claims abstract description 56
- 210000004351 coronary vessel Anatomy 0.000 claims abstract description 47
- 238000002347 injection Methods 0.000 claims abstract description 44
- 239000007924 injection Substances 0.000 claims abstract description 44
- 210000001765 aortic valve Anatomy 0.000 claims abstract description 13
- 230000033764 rhythmic process Effects 0.000 claims abstract description 9
- 230000001360 synchronised effect Effects 0.000 claims abstract description 9
- 210000005240 left ventricle Anatomy 0.000 claims description 14
- 210000004165 myocardium Anatomy 0.000 claims description 11
- 210000000709 aorta Anatomy 0.000 claims description 4
- 238000001514 detection method Methods 0.000 claims description 4
- 238000006073 displacement reaction Methods 0.000 abstract description 15
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 230000003287 optical effect Effects 0.000 abstract 1
- 239000012530 fluid Substances 0.000 description 21
- 210000001367 artery Anatomy 0.000 description 20
- 238000002586 coronary angiography Methods 0.000 description 7
- 238000003384 imaging method Methods 0.000 description 6
- 238000012800 visualization Methods 0.000 description 5
- 230000001133 acceleration Effects 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 238000002594 fluoroscopy Methods 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 230000003068 static effect Effects 0.000 description 3
- 210000003462 vein Anatomy 0.000 description 3
- 230000002861 ventricular Effects 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- 210000000038 chest Anatomy 0.000 description 2
- 230000000644 propagated effect Effects 0.000 description 2
- 238000002601 radiography Methods 0.000 description 2
- 230000004913 activation Effects 0.000 description 1
- 210000003484 anatomy Anatomy 0.000 description 1
- 238000002583 angiography Methods 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 210000004204 blood vessel Anatomy 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000002059 diagnostic imaging Methods 0.000 description 1
- 230000010339 dilation Effects 0.000 description 1
- 210000001105 femoral artery Anatomy 0.000 description 1
- 230000002262 irrigation Effects 0.000 description 1
- 238000003973 irrigation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000003387 muscular Effects 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 210000001147 pulmonary artery Anatomy 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 210000005241 right ventricle Anatomy 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 238000004846 x-ray emission Methods 0.000 description 1
- PICXIOQBANWBIZ-UHFFFAOYSA-N zinc;1-oxidopyridine-2-thione Chemical class [Zn+2].[O-]N1C=CC=CC1=S.[O-]N1C=CC=CC1=S PICXIOQBANWBIZ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B6/00—Apparatus or devices for radiation diagnosis; Apparatus or devices for radiation diagnosis combined with radiation therapy equipment
- A61B6/54—Control of apparatus or devices for radiation diagnosis
- A61B6/541—Control of apparatus or devices for radiation diagnosis involving acquisition triggered by a physiological signal
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B6/00—Apparatus or devices for radiation diagnosis; Apparatus or devices for radiation diagnosis combined with radiation therapy equipment
- A61B6/02—Arrangements for diagnosis sequentially in different planes; Stereoscopic radiation diagnosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B6/00—Apparatus or devices for radiation diagnosis; Apparatus or devices for radiation diagnosis combined with radiation therapy equipment
- A61B6/48—Diagnostic techniques
- A61B6/481—Diagnostic techniques involving the use of contrast agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B6/00—Apparatus or devices for radiation diagnosis; Apparatus or devices for radiation diagnosis combined with radiation therapy equipment
- A61B6/50—Apparatus or devices for radiation diagnosis; Apparatus or devices for radiation diagnosis combined with radiation therapy equipment specially adapted for specific body parts; specially adapted for specific clinical applications
- A61B6/504—Apparatus or devices for radiation diagnosis; Apparatus or devices for radiation diagnosis combined with radiation therapy equipment specially adapted for specific body parts; specially adapted for specific clinical applications for diagnosis of blood vessels, e.g. by angiography
-
- 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
- A61M31/00—Devices for introducing or retaining media, e.g. remedies, in cavities of the body
- A61M31/005—Devices for introducing or retaining media, e.g. remedies, in cavities of the body for contrast media
Definitions
- the invention concerns medical imaging in cardiology and, in particular, coronary angiography and, as the case may be, in ventriculography.
- Radiological examinations in coronary angiography and ventriculography are usually carried out by dynamic filming from different fixed image planes around the heart, which constitute reference angulations. Several sequences of images are then obtained, typically for a few seconds each, making it possible to visualize as a whole, through those different planes, the structure of the coronary arterial tree, of the aorta and of the left ventricle, each plane offering a two- dimensional point of view.
- the parts of interest are revealed by opacification by means of a contrast medium in liquid form introduced in well controlled areas.
- a contrast medium in liquid form introduced in well controlled areas.
- three different catheters are ordinarily used.
- the protocol as a whole is lengthy and labored owing to the fact that it requires successively introducing and withdrawing three different catheters, with an injection each time of contrast medium for each image plane. Furthermore, the total quantity of contrast fluid injected has to be limited because of its toxicity. The time allotted to the injections in the coronary arteries is therefore very short and may be insufficient to follow the progress of the product well.
- the protocol also has the disadvantage of requiring many repeated positionings of the source-detector tandem in order to make the different acquisitions, which also shortens the examination time, especially in the case of a cradle with manual displacement. As for costs, it is necessary to arrange, among other things, to make three different catheters available for a complete examination.
- the invention is directed to a protocol, i.e., method, of coronary angiographic imaging, possibly accompanied by ventriculographic imaging, which makes better use of the contrast medium possible and which is well suited to three- dimensional dynamic imaging.
- the invention concerns a method of cardiac radiological examination in coronary angiography, comprising: a) introducing a contrast medium simultaneously in the left coronary artery and in the right coronary artery from the root of aorta and, in parallel, b) acquiring a sequence of dynamic images of propagation of the contrast medium in the left and right coronary arteries with procession of the image plane, upon acquisition of images, on a given path.
- the invention also concerns a device for injection of contrast medium in a catheter intended for cardiac radiology, which it is guided by a signal detecting cardiac rhythms, so as to inject the contrast medium during cycles synchronized with given phases of the cardiac rhythm.
- FIG. 1 is a general view of the heart:
- Figure 2 is a view of the injection end of a catheter intended for the introduction of contrast fluid in the right coronary artery, used in the prior art;
- Figure 3 is a view of the injection end of a catheter intended for the introduction of contrast fluid in the left coronary artery, used in the prior art
- Figure 4 is a view of the injection end of a "pigtail" catheter commonly used to introduce contrast fluid in the left ventricle;
- Figure 5 is a diagram showing different angulations for radiological image acquisitions
- Figure 6 is a flow chart showing the principal stages of a standard protocol of coronary angiography and ventriculography
- Figure 7 is a general view of a radiography apparatus, with schematic representation of accessories, according to an embodiment of the invention.
- Figure 8 is a flow chart showing the principal stages of a coronary angiography and ventriculography protocol according to an embodiment of the invention.
- Figure 9 is a schematic representation of the path and reference angulations for the rotation acquisitions that can be used in the protocol of Figure 8;
- Figure 10 is a view showing the positioning of the pigtail catheter in proximity to the left and right coronary arteries upon the introduction of contrast fluid for the second rotation acquisition of Figure 8;
- Figure 1 1 is a diagram showing the opacifications on each of the four rotation acquisitions made, in the form of respective standard images designated I to IV, the figure also indicating the types of 3D and 4D images possible from different acquisitions; and
- Figure 12 is a timing diagram showing the synchronization of the cycles of introduction of contrast medium with closing of the aortic valve, with reference to the diastole peaks of a patient's electrocardiogram.
- the three different catheters are positioned respectively as shown in Figure 1 : the aperture of the left coronary artery 2, the aperture of the right coronary artery 4 and the interior of the left ventricle 6.
- Figure 1 further identifies in the heart: the right auricle 8, the left auricle 10, the right ventricle 12, the superior caval vein 14, the inferior caval vein 16, the aorta 18, the pulmonary artery 20, the anterior interventricular artery 22, the posterior interventricular artery 24 and the circumflex left artery 26.
- Figures 2, 3 and 4 respectively show the shapes that the injection ends of the three aforementioned catheters take when deployed.
- the catheter 28 intended for the right coronary artery, as shown in Figure 2 presents an appreciably straight section 28a which ends in an elbowed portion 28b in order to guide the tip 28c to approximately 90° from the straight part 28a, so that it can partially enter the coronary artery.
- the tip 28c affords a single outlet for the contrast fluid, situated at its end point.
- the catheter 30 intended for the left coronary artery as shown in Figure 3, takes appreciably the same shape, but of opposite geometry, so that tip 30c can partially enter that coronary artery.
- the catheter 32 intended for the left ventricle presents, in the extension of an appreciably straight part 32a, a spiraled end 32b.
- this type of catheter is generally known as a "pigtail”.
- the spiral shape ensures that tip 32c of the catheter does not come too close to or in contact with the walls of the left ventricle.
- catheter 32 is generally inserted "blind” and the contrast fluid is ejected there from tip 30c at a very high pressure, necessary to overcome the pressure prevailing in the ventricular cavity. The spurt of fluid could damage the wall if it were too close to the walls.
- the 32c of the pigtail catheter contains several outlets for the contrast fluid, uniformly distributed on the periphery of its wall just before its termination point.
- the contrast fluid is appreciably dispersed uniformly around the end portion and rapidly fills the cavity of the left ventricle.
- Catheters 28, 30, 32 are introduced in the body from a part distant from the heart, generally from a peripheral artery or vein.
- the catheters are guided along the arteries by a wire contained inside and which keeps the injection ends appreciably straight until approaching the point of arrival.
- the wire is then withdrawn from the end to enable the latter to recover its adapted shape.
- the opposite end of the catheter is connected either to a manually operated syringe, in the case of catheters intended for the coronary arteries, or to an electrically controlled automatic injector, in the case of a pigtail catheter intended for the ventricle.
- FIG. 5 shows schematically, the patient 36 (head and shoulders represented) is positioned stretched out in a radiology apparatus having a radiological image sensor 38 (film or electronic) and an X-radiation source 40.
- the tandem formed by the sensor 38 and the source 40 is aligned on an axis A-A' perpendicular to the head-to-toe axis (longitudinal) of the patient at chest level.
- the tandem is rotatable around the head-to-toe axis of the patient, the sensor 38 and the source 40 being normally mounted at the respective ends of a semicircular cradle in which the patient is centered. It is thus possible to take image acquisition sequences at dilierent angles in the plane of rotation of the source-detector tandem.
- FIG. 6 is a flow chart of the principal stages of the standard coronary angiography and ventriculography protocol, according to which dynamic image sequences are obtained, each sequence being taken from a respective fixed plane.
- the catheter 28 in the aperture of the left coronary artery (stage E2). Its positioning is generally made by touch on manipulation of the catheter. If necessary, a little contrast medium can be sent in during that stage to visualize the environment of the end of the catheter in fluoroscopy (real-time imaging under low dose without recording).
- a procedure of acquisitions (PA) of dynamic image sequences is undertaken, the principal stages of which are represented in the right part of Figure 6.
- This PA procedure obtains and records several dynamic image sequences showing the progress of the contrast medium in the coronary artery, each taken on a different plane constituting a reference position (or angulation).
- the reference positions are as follows (cf. Figure 5): (1) front, with the detector 38 directly facing the patient; (2) OAG 70 [LAO 70], i.e., left anterior oblique projection at 70° (the direction is always referenced in relation to the patient); (3) OAG 90 [LAO 90], i.e., left anterior oblique projection at 90°, or strict profile, and (4) OAD 20 [RAO 20], i.e., right anterior profile at 20°.
- a dosed quantity of contrast medium normally about five cubic centimeters, is manually injected throughout the filming sequence, that is, over a period of five to six seconds.
- the rate of acquisition is 25 or 30 images per second (according to European or United States standards), giving a total in the order of 150 to 200 acquired images per plane.
- the method begins by placing the source-sensor tandem 38, 40 for acquisition of the front sequence (stage E3). During the positioning, it is verified by fluoroscopy that the image plane is correctly framed and that the catheter is always well positioned (stage E4), making adjustments when necessary. Acquisition of the dynamic sequence is then controlled (stage E5) under X-rays and the contrast medium is simultaneously injected under the aforesaid conditions (stage E6). When acquisition is completed, the same procedure is undertaken for each of the following planes (OAG 70, OAG 90 and OAD 20), with the respective positioning stages (E7, E8, E9). Altogether, approximately 20 seconds of dynamic sequences of the left coronary artery are thus acquired, with a total dose in the order of 20 cubic centimeters.
- the catheter 28 is then withdrawn (stage E10) and, in its place, the catheter 30 intended for the right coronary artery is introduced in the aperture of the latter (stage El 1).
- the PA procedure of acquisitions of dynamic sequences described above is then restarted. That PA procedure can possibly be modified at the reference positions in order to better suit the configuration of the structure of the right coronary artery.
- the catheter is withdrawn (stage E10').
- the method continues with ventriculography by introduction of the pigtail catheter 32 in the cavity of the left ventricle (stage El 2), with a right anterior oblique positioning of the image plane at 30° (OAD 30) (stage El 3).
- the acquisition of a dynamic image sequence is then begun over a period in the order of three or four seconds (stage El 4).
- stage El 4 approximately 40 cubic centimeters of contrast medium is injected by means of an electromechanical injector (stage El 5). Exploration of the ventricle makes it possible to visualize its general shape and to observe the manner in which it is contracted. In some cases, views are also acquired in the OAG 60 axis, when it is a question of detecting anomalies of movement of the wall of the septum.
- the catheter 32 is withdrawn on completion of the examination protocol (stage E10").
- the apparatus 34 comprises a bearing structure comprising a flat base 36 standing on the floor, with a support wall 38 at right angles to that base. The support wall maintains at a raised level a rotary shaft 40 aligned on a horizontal axis 42.
- Shaft 40 fits laterally into the end 44a of a rotary support arm 44 of a semicircular cradle 46, to the free ends of which an X-ray source 48 and a detector 50 are respectively attached.
- the support arm 44 is L-shaped, so that the axial displacement of the cradle 46 produced by the branch of the L perpendicular to the horizontal axis 42 compensates for the laterally offset mounting of the source 48 and detector 50 on the cradle 46.
- the axis 52 connecting the source 48 to the detector 50 crosses the axis of rotation 42.
- the cradle 46 is in turn mounted sliding on the support arm 44 to afford a circum-ferential rotation.
- the sliding thus makes it possible to displace the position in space of the source-detector axis 52 around a sliding axis 54 centered on the cradle 46.
- the respective axes 42, 52 and 54 of rotation of the support arm 44, of source-detector alignment 48, 50 and of sliding are secant at a point 56 called isocenter and are mutually perpendicular (orthogonal).
- the patient is maintained in a horizontal plane on a table 59 aligned with the horizontal axis 42.
- the arrangement of axes 42, 52 and 54 permits a three-dimensional displacement in space of the source-detector tandem 48, 50 with degrees of freedom on two perpendicular planes, respectively aligned with the craniocaudal axis and with the right-left axis of the patient.
- the movements in each of these degrees of freedom are controlled independently by means of respective programmable actuators (not represented), although it is possible to form paths of the axis 52 of the source-detector tandem 48, 50 following left surfaces.
- the element of interest for that path being the sensitive surface of the detector 50, a path will be defined below in terms of displacement of the center of the image plane, comparable to the center of that sensitive surface 50.
- This central point therefore captures the radiation coming from the focal point of the source 48 after having crossed the patient at the isocenter 56.
- the entire operation of the apparatus 34 is managed by a microprocessor-based control unit 58 with an access console for the different functions 60 and a screen 62 for visualization of the different parameters and radiological images acquired.
- the control unit is connected to an electrocardiograph machine 64 in order to synchronize certain actions with the movements of the heart and to an electromechanical injector 65 of contrast fluid having an injection tube 65a intended to fit into a catheter 32.
- the functionalities managed by the control unit 58 are: (1) the respective actuators for the displacements of the source-detector tandem 48, 50 around axes 42, 54, with programming of: the path along a left (or flat) curve, the course of the rate of displacement (accelerations, decelerations) and stops on the path; (2) filming parameters: control of activation of the source and detector; and (3) operation of the injector 65, including control of an injection sequence divided into several injection cycles, with the following parameters: the start and interruption of an injection sequence synchronized with the start and stop of the image acquisition sequence, the beginning and end of each injection cycle as a function of the electrocardiogram (ECG) delivered by the electrocardiograph machine 64, the number of injection cycles and the injection delivery.
- ECG electrocardiogram
- the control unit 58 also calculates a path and/or to memorize it.
- the path can be calculated from angulations, which can be indicated either by the user via the console 60 or by manually positioning the mobile unit of the apparatus 34 according to that angulation and memorizing it. For example, by defining an angulation by three angles along the three three-dimensional marking axes 42, 52 and 54 linked to the apparatus 34, the user can, for instance, define a first angulation of coordinates (0, 0, 0), a second angulation of coordinates (0, 0, ⁇ ) and a third angulation of coordinates (0, 0, ⁇ ) with ⁇ and ⁇ not nil.
- the path can, of course, be programmed on a greater number of angulations.
- the control unit 58 determines a path to be followed by the moving parts of the apparatus, by controlling the actuators in an appropriate manner, in order to make the image plane 50 pass through the angulations programmed, while taking into account the characteristics of the apparatus, such as: (1) possible angulations prohibited, because of the risk of causing collisions with the table 59, the patient, the source 48 or the detector 50, and (2) the mechanical or electromechanical stresses of the apparatus, such as maximum angular acceleration for each axis and the travel time, which should be as short as possible in order to minimize the total dose of contrast fluid to be injected.
- the path is programmed to describe a first passage around the patient in the left-right direction, followed by a second passage in the right-left direction, or vice versa, in order to define a loop.
- the loop can be open (end point not matching the starting point) or closed (end point matching the starting point).
- the rate of displacement of the image plane on the path is further programmed to be reduced on passages at angulations corresponding to chosen reference planes and increased between those points.
- the displacement of the image plane along the path is controlled with the electrocardiograph machine, so that the arrival at a reference plane systematically occurs at the time the heart is in a same given phase of its cycle, for example, the filling phase. That control is accomplished by an analysis of the electrocardiogram (ECG) produced by the electrocardiograph machine 64, the periodicity of which makes it possible to anticipate the different phases.
- ECG electrocardiogram
- the programming starts with the location of positions of the image plane which are going to constitute reference angulations. These reference angulations are represented by large dots P1 -P5 in Figure 9, which is a spherical chart representing the different movements of the image plane.
- the center of the sphere is the isocenter 56 ( Figure 7) and its radius is equal to the distance between the isocenter and the focus of the X-ray source 48.
- the reference angulations include in part those commonly used in coronary arteriography (cf. Figure 5), to which are added others chosen for an optimization of the points of view of the areas to be explored. For that purpose, it is taken into account that those angulations are used for imaging of both the left coronary artery and the right coronary artery.
- the positions of reference angulations P1-P5 are freely chosen around the patient's craniocaudal axis 42 and right-left axis 54.
- the angulations number five and include two "standard" angula-tions (on a same plane of rotation around the craniocaudal axis), namely: left anterior oblique at 60° (OAG 60)
- point PI and "frontal,” where the axis of the X-ray beam is vertical, with the image plane positioned directly above the patient (point P2).
- a third angulation (point P3) corresponds to the OAG 30 image plane, but with a caudal deflection of 15°.
- P4 and P5 chosen, for example, to better discern the structure of the right coronary artery.
- a reference position in right anterior oblique view at 30° makes it possible to analyze the circumflex branch and a part of the left anterior descending artery.
- Another reference position on angulation of slightly caudal type i.e., with the detector 50 close to the patient's feet, while maintaining the azimuth angle of 30°, can be used to visualize another part of the left anterior descending artery and to avoid having it covered on the image by the circumflex branch of the intermediate vessels.
- a reference position in cranial-type angulation on right anterior oblique projection makes possible a good visualization of the diagonal arteries.
- the reference position in left anterior oblique angulation at 60° can be used for study of the diagonal arteries and of a part of the anterior interventricular artery (IVA).
- IVA anterior interventricular artery
- the left anterior oblique angulation at 60° can be applied to avoid shortening of a part of the IVA and provides good images of the left main trunk and diagonal branches.
- side view i.e., with the axis of the X- ray beam horizontal, particularly in left side view, another part of the IVA and the different parts of the first diagonal artery and of the marginal artery of the left edge can be optimally seen.
- a reference position in angulation of left anterior oblique type at 45° can be used associated with a caudal angle of 15°.
- the reference position in left anterior oblique angulation at 90° with caudal deflection of 15° can be used for analysis of the vertical part of the right coronary artery and collateral branches, right ventricular artery and right edge marginal artery.
- the reference position in right anterior oblique angulation at 45° with caudal deflection of 15° can be used for visualization of the posterior interventricular artery and collateral branches, right ventricular artery and right edge marginal artery.
- the control unit 58 calculates a path which passes over each of them.
- that path globally designated by T, consists of three parts which are linked together without interruption, namely: (1) a first part Tl corresponding to the left-right displacement of the image plane in a first direction (outward) and around the craniocaudal axis, beginning at angulation PI and ending at angulation P3; (2) a second part T2 corresponding to the right-left displacement of the image plane in a second direction (inward) and around the craniocaudal axis, beginning at angulation P3 and ending at angulation P5; and (3) a third part T3 which joins angulations P5 to PL
- the displacement of the image plane on that whole path will be designated by the term "rotation,” the filming and recording of images on a rotation being designated by the term “rotation acquisition.”
- the third part T3 of the path serves essentially to create a closed loop, i.e., to bring the image plane back to the starting point. In that way, it is possible to perform a succession of rotations without interruption.
- the path T is calculated to produce a fluid movement of the image plane, with phases of acceleration at the start and deceleration at the approach of each reference angulation P1-P5.
- the movement is further subject to the ECG, so that the rapid displacements between two reference angulations occur during the diastole phase (when the heart is in quasi-stationary phase) and the slow passages at the reference angulations occur during the systole phase of the heart.
- synchronization on the ECG ensures that the heart will be in the same phase on passage at each of the reference angulations P1-P5.
- the duration of the dynamic acquisition sequence on a rotation acquisition corresponds to four or five heart beats, that is, approximately five seconds.
- the source 48 and the detector 50 are activated with suitable adjustments of X-ray emission and filming.
- the acquisition sequence covers the entire duration of the first and second parts Tl, T2 of the path and possibly an initial portion of the third part T3.
- the acquisitions are made at a rate of 25 or 30 images per second.
- the portions of the path on which the images are acquired are symbolized by a series of small dots in Figure 9.
- the programming stage E20 is executed only on initialization of the apparatus 34 for the protocol; that stage is therefore omitted for the examinations on the following patients, except in case of change of parameters.
- the examination proper then begins with the patient positioned on the table 59 and the introduction of a "pigtail" catheter 32, of gauge 6, for example, from the femoral artery to the aortic root, at the starting points of the left and right coronary arteries (stage E22).
- a "pigtail" catheter 32 of gauge 6, for example, from the femoral artery to the aortic root, at the starting points of the left and right coronary arteries.
- stage E22 The positioning of the injection end of the catheter 32 is represented in Figure 10. If necessary, the proper positioning of the catheter can be controlled on a fluoroscopy screen (stage E24).
- a first rotation acquisition is executed on the path T with the characteristics of acceleration-deceleration and ECG synchronization, as described above, and without injection of contrast medium (stage E26). That sequence without opacification makes possible the acquisition of reference images for digital image subtraction. It also makes it possible to visualize the patient's anatomical structures, notably, the general positioning of the heart relative to the thorax and to the vertebral column. A representation of one of the images acquired during that first rotation acquisition is given in Figure 1 1 (image I).
- a second rotation acquisition identical to the first is then made, but with injection of contrast medium (stage E28).
- the catheter 32 is connected to the tube 65a of the injector 65, the latter being filled with contrast medium and capable of responding to the injection commands coming from the control unit 58.
- the latter is emitted with appreciably isotropic force and reaches the aperture of each of the left and right coronary arteries in order to be propagated along the coronary arterial tree.
- the injection of contrast medium is not carried out continuously, but rather in spurts synchronized with the heart rate, so that the product is introduced on closing phases of the aortic valve (concomitant phase E30). The synchronization of the injection will be more specifically described by reference to
- the aortic valve 70 is closed during the parts of the ECG cycle preceding the diastole peak 66. On periods of closing of the aortic valve, there is appreciably no backflow of blood from the ventricle. Thus, by introducing the contrast medium only during those closing phases, it will preferably enter the apertures of the left and right coronary arteries with minimum loss.
- the contrast fluid injection phases (hatched rectangles 72) occupy preferably approximately half the period tb between two diastole peaks and are situated just before passing the peak.
- the synchronization is accomplished by the control unit 58 by automatically detecting the diastole peaks 66 and by determining their periodicity t b , which makes it possible, on the one hand, to command the injector 65 to start the injection, at approximately a half-period t b after a detected peak and, on the other, to command the injector to stop the injection the moment the following peak appears.
- the injector 65 is thus commanded in pulse mode to send a succession of contrast medium flows during the cycles indicated 72.
- the total quantity of contrast fluid injected is in the order of five to seven cubic centimeters, distributed over four or five injection cycles.
- the start and stop of all the injection cycles are generally synchronized respectively with the beginning and end of the image acquisition sequence of a rotation.
- the contrast fluid is propagated along the coronary arteries and dependent arteries in order to irrigate the myocardium.
- a series of images is then obtained, such as the one referenced II in Figure 1 1, after subtraction and processing.
- the sequence of dynamic images thus acquired makes it possible to simultaneously visualize the entire coronary artery tree. After a few seconds of the second rotation acquisition, a part of the contrast medium will have started perfusing the myocardium.
- a third rotation acquisition is carried out after the second one and following the same path characteristics, but without injection of contrast medium (stage E32).
- the contrast medium injected upon the second rotation acquisition will have had enough time to diffuse properly over the entire myocardium during the period of the third rotation acquisition, without it being necessary to mark a pause time after the second rotation acquisition.
- Such pause time can, however, be envisaged, if necessary.
- the third rotation acquisition thus makes it possible to obtain, without addition of a dose of contrast medium, a three-dimensional visualization of the wall of the left ventricle ( Figure 1 1 , image III) and to detect the possible areas of the myocardium poorly irrigated because of obstructions of the blood vessels.
- the embodiment of the invention makes it possible to continue with a ventriculographic examination by pushing the pigtail catheter 32 beyond the aortic valve into the ventricle (stage E34).
- a fourth rotation acquisition is earned out with injection of contrast fluid (E36).
- the path for that acquisition can be the same as for the three preceding ones or can be different, depending on the images desired for that examination.
- approximately 40 cubic centimeters of contrast fluid are introduced at constant flow.
- the dynamic acquisitions upon that fourth rotation acquisition make it possible to visualize the course of the contrast fluid in the left ventricle ( Figure 1 1 , image IV). An evolving three-dimensional image is thus obtained, associated with the time variable, which gives a four-dimensional (4D) image.
- the pigtail catheter 32 is withdrawn (stage E38). From the set of images obtained upon the rotation acquisitions, different digital processings are possible in order to obtain static (3D) or evolving (4D) three- dimensional views.
- the disclosed embodiment of the invention thus provide that: (1 ) all of the views indicated are obtained with the use of a single catheter 32 and a single injection of contrast medium; (2) the contrast medium is introduced simultaneously in the left coronary artery and in the right coronary artery, which makes it possible to visualize in a single sequence the opacification of all of the coronary arteries; (3) it is possible to obtain, some instants after injection of the contrast fluid in the coronary arteries and by simple repetition of a rotation acquisition, a view of the opacification of the tissues of the myocardium, which enables irrigation defects to be clearly detected; (4) by simple prolongation of the advance of the catheter into the left ventricle, the protocol can be continued with a dynamic examination of the movements of that part of the heart; and (5) introducing the contrast fluid into the left and right coronary arties solely during the phases of closing of the aortic valve, according to an embodiment, alone makes it possible to reduce the dose by approximately 50% or to make acquisitions over period twice as long at equal dose.
- the contrast medium is advantageously introduced cyclically during the dynamic image acquisition, each cycle of introduction co ⁇ 'esponding to a phase of closing of the aortic valve in the cardiac rhythm.
- the dose of contrast medium is delivered in spurts and only at times during which the product is in a relatively static environment and therefore has the best chance of entering the two. coronary arteries.
- This arrangement can be obtained subject to a diastole peak detected on the electrocardiogram of the heart examined.
- each cycle of introduction of the contrast medium is begun at an instant situated roughly midway between a first and a second successive diastole peak and is interrupted approximately upon the appearance of that second peak.
- the path of the image plane advantageously defines a left curve evolving around the patient's head-to-toe axis and left-right axis.
- the path can define a loop, open or closed, with one part corresponding to a movement in a first direction around the head-to-toe axis and a second part corresponding to a movement in a second direction around the head-to-toe axis opposite to the first one.
- the path preferably embraces points of passage corresponding to reference angulations, the rate of procession of the image plane being increased outside the points of passage and reduced at the points of passage.
- the procession of the image plane is advantageously synchronized with the cardiac rhythm, so that the moment of passage on each reference angulation is situated at a same phase of the cardiac cycle, notably in the systole phase of the heart.
- An image subtraction technique may be used, in which, the method can further entail a preliminary stage consisting of acquiring a dynamic image sequence with procession of the image plane on the given path, without introduction of contrast medium.
- the method can also provide a stage, following stage b), comprising acquiring a new dynamic image sequence with procession of the image plane, without introduction of contrast medium, making it possible to visualize the opacification of the myocardium.
- the examination can be continued by ventriculography, with injection of contrast medium and parallel acquisition of dynamic images with procession of the image plane.
- Stage a) of introduction of the contrast medium is preferably carried out with the aid of a so-called "pigtail" catheter or the like.
- the acquired images are advantageously processed in order to make at least one of the following: (1) a three-dimensional reconstruction of the heart not opacified; (2) a three-dimensional reconstruction of the myocardium; (3) a three- dimensional reconstruction of the coronary artery tree evolving in time, and (4) a three-dimensional reconstruction of the left ventricle evolving in time.
- It can thus be guided to inject the contrast medium only during closing of the aortic valve.
- it can contain an electrocardiogram signal input and means of detection of diastole peaks in that signal, the injection being interrupted on detection of a diastole peak.
- the device can contain means of starting the injection of contrast medium at a predetermined time, which can be programmable, before the arrival of a diastole peak. This time can be roughly midway between two successive diastole peaks.
- the device can be further programmable to inject the contrast medium over a given number of injection cycles.
- the device can further contain means of synchronization of the overall start and stop of injection with the start and stop of a filming sequence.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Medical Informatics (AREA)
- Heart & Thoracic Surgery (AREA)
- Biomedical Technology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Radiology & Medical Imaging (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Physics & Mathematics (AREA)
- Molecular Biology (AREA)
- Surgery (AREA)
- Pathology (AREA)
- Optics & Photonics (AREA)
- High Energy & Nuclear Physics (AREA)
- Biophysics (AREA)
- Physiology (AREA)
- Vascular Medicine (AREA)
- Dentistry (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Anesthesiology (AREA)
- Hematology (AREA)
- Apparatus For Radiation Diagnosis (AREA)
Abstract
A method of cardiac radiological examination for coronarography comprises the steps of: a) introducing contrast medium simultaneously in the left coronary artery and in the right coronary artery from the aortic root and, in parallel, b) acquiring a sequence of dynamic images of the propagation of the contrast medium in the left and right coronary arteries with a displacement of the image plane, during the acquisition of said images, along a determined trajectory (E28). The contrast medium can be introduced in a cyclic manner during the acquisition of dynamic images, each cycle of introduction corresponding to a phase of closure of the aortic valve in the cardiac rhythm. 3D and 4D images with optical efficiency can be obtained in the use of contrast medium. An injection device for producing the above cycles is synchronized with the introduction of the contrast medium.
Description
METHOD AND DEVICE FOR CARDIAC RADIOLOGICAL EXAMINATION
CROSS REFERENCE TO RELATED APPLICATIONS
[0001 ] This application claims the benefit of a priority under 35 USC 1 19 to French Patent Application No. 0103699 filed March 19, 2001 , the entire contents of which are hereby incorporated by references.
BACKGROUND OF THE INVENTION
[0002] The invention concerns medical imaging in cardiology and, in particular, coronary angiography and, as the case may be, in ventriculography.
[0003] Radiological examinations in coronary angiography and ventriculography are usually carried out by dynamic filming from different fixed image planes around the heart, which constitute reference angulations. Several sequences of images are then obtained, typically for a few seconds each, making it possible to visualize as a whole, through those different planes, the structure of the coronary arterial tree, of the aorta and of the left ventricle, each plane offering a two- dimensional point of view.
[0004] The parts of interest are revealed by opacification by means of a contrast medium in liquid form introduced in well controlled areas. In order to perform those injections on a coronary angiography and venticulography examination, three different catheters are ordinarily used. A protocol according to which dynamic image sequences are obtained, each sequence being taken form a respective fixed plane.
[0005] The protocol as a whole is lengthy and labored owing to the fact that it requires successively introducing and withdrawing three different catheters, with an injection each time of contrast medium for each image plane. Furthermore, the total quantity of contrast fluid injected has to be limited because of its toxicity. The time
allotted to the injections in the coronary arteries is therefore very short and may be insufficient to follow the progress of the product well. The protocol also has the disadvantage of requiring many repeated positionings of the source-detector tandem in order to make the different acquisitions, which also shortens the examination time, especially in the case of a cradle with manual displacement. As for costs, it is necessary to arrange, among other things, to make three different catheters available for a complete examination.
BRIEF DESCRIPTION OF THE INVENTION
[0006] The invention is directed to a protocol, i.e., method, of coronary angiographic imaging, possibly accompanied by ventriculographic imaging, which makes better use of the contrast medium possible and which is well suited to three- dimensional dynamic imaging.
[0007] In particular, the invention concerns a method of cardiac radiological examination in coronary angiography, comprising: a) introducing a contrast medium simultaneously in the left coronary artery and in the right coronary artery from the root of aorta and, in parallel, b) acquiring a sequence of dynamic images of propagation of the contrast medium in the left and right coronary arteries with procession of the image plane, upon acquisition of images, on a given path.
[0008] The invention also concerns a device for injection of contrast medium in a catheter intended for cardiac radiology, which it is guided by a signal detecting cardiac rhythms, so as to inject the contrast medium during cycles synchronized with given phases of the cardiac rhythm.
BRIEF DESCRIPTION OF THE DRAWINGS
[0009] The invention will be more clearly apparent, with reference to the attached drawings, in which:
[0010] Figure 1 is a general view of the heart:
[001 1] Figure 2 is a view of the injection end of a catheter intended for the introduction of contrast fluid in the right coronary artery, used in the prior art;
[0012] Figure 3 is a view of the injection end of a catheter intended for the introduction of contrast fluid in the left coronary artery, used in the prior art;
[0013] Figure 4 is a view of the injection end of a "pigtail" catheter commonly used to introduce contrast fluid in the left ventricle;
[0014] Figure 5 is a diagram showing different angulations for radiological image acquisitions;
[0015] Figure 6 is a flow chart showing the principal stages of a standard protocol of coronary angiography and ventriculography;
[0016] Figure 7 is a general view of a radiography apparatus, with schematic representation of accessories, according to an embodiment of the invention;
[0017] Figure 8 is a flow chart showing the principal stages of a coronary angiography and ventriculography protocol according to an embodiment of the invention;
[0018] Figure 9 is a schematic representation of the path and reference angulations for the rotation acquisitions that can be used in the protocol of Figure 8;
[0019] Figure 10 is a view showing the positioning of the pigtail catheter in proximity to the left and right coronary arteries upon the introduction of contrast fluid for the second rotation acquisition of Figure 8;
[0020] Figure 1 1 is a diagram showing the opacifications on each of the four rotation acquisitions made, in the form of respective standard images designated I to IV, the figure also indicating the types of 3D and 4D images possible from different acquisitions; and
[0021] Figure 12 is a timing diagram showing the synchronization of the cycles of introduction of contrast medium with closing of the aortic valve, with reference to the diastole peaks of a patient's electrocardiogram.
DETAILED DESCRIPTION OF THE INVENTION
[0022] The three different catheters are positioned respectively as shown in Figure 1 : the aperture of the left coronary artery 2, the aperture of the right coronary artery 4 and the interior of the left ventricle 6.
[0023] Figure 1 further identifies in the heart: the right auricle 8, the left auricle 10, the right ventricle 12, the superior caval vein 14, the inferior caval vein 16, the aorta 18, the pulmonary artery 20, the anterior interventricular artery 22, the posterior interventricular artery 24 and the circumflex left artery 26.
[0024] Figures 2, 3 and 4 respectively show the shapes that the injection ends of the three aforementioned catheters take when deployed. The catheter 28 intended for the right coronary artery, as shown in Figure 2, presents an appreciably straight section 28a which ends in an elbowed portion 28b in order to guide the tip 28c to approximately 90° from the straight part 28a, so that it can partially enter the coronary artery. The tip 28c affords a single outlet for the contrast fluid, situated at its end point. The catheter 30 intended for the left coronary artery, as shown in Figure 3, takes appreciably the same shape, but of opposite geometry, so that tip 30c can partially enter that coronary artery. The catheter 32 intended for the left ventricle, as shown in Figure 4, presents, in the extension of an appreciably straight part 32a, a spiraled end 32b. By reason of that particular shape, this type of catheter is generally known as a "pigtail". The spiral shape ensures that tip 32c of the catheter does not
come too close to or in contact with the walls of the left ventricle. In fact, catheter 32 is generally inserted "blind" and the contrast fluid is ejected there from tip 30c at a very high pressure, necessary to overcome the pressure prevailing in the ventricular cavity. The spurt of fluid could damage the wall if it were too close to the walls.
[0025] In contrast to catheters 28, 30 intended for the coronary arteries, the 32c of the pigtail catheter contains several outlets for the contrast fluid, uniformly distributed on the periphery of its wall just before its termination point. Hence, the contrast fluid is appreciably dispersed uniformly around the end portion and rapidly fills the cavity of the left ventricle.
[0026] Catheters 28, 30, 32 are introduced in the body from a part distant from the heart, generally from a peripheral artery or vein. The catheters are guided along the arteries by a wire contained inside and which keeps the injection ends appreciably straight until approaching the point of arrival. The wire is then withdrawn from the end to enable the latter to recover its adapted shape. The opposite end of the catheter is connected either to a manually operated syringe, in the case of catheters intended for the coronary arteries, or to an electrically controlled automatic injector, in the case of a pigtail catheter intended for the ventricle.
[0027] Referring to Figures 5 and 6, the standard protocol of image acquisition in coronary angiographic and ventriculographic radiography will now be described with use of catheters 28, 30 and 32.
[0028] As Figure 5 shows schematically, the patient 36 (head and shoulders represented) is positioned stretched out in a radiology apparatus having a radiological image sensor 38 (film or electronic) and an X-radiation source 40. The tandem formed by the sensor 38 and the source 40 is aligned on an axis A-A' perpendicular to the head-to-toe axis (longitudinal) of the patient at chest level. The tandem is rotatable around the head-to-toe axis of the patient, the sensor 38 and the source 40 being normally mounted at the respective ends of a semicircular cradle in which the
patient is centered. It is thus possible to take image acquisition sequences at dilierent angles in the plane of rotation of the source-detector tandem.
[0029] Figure 6 is a flow chart of the principal stages of the standard coronary angiography and ventriculography protocol, according to which dynamic image sequences are obtained, each sequence being taken from a respective fixed plane. The catheter 28 in the aperture of the left coronary artery (stage E2). Its positioning is generally made by touch on manipulation of the catheter. If necessary, a little contrast medium can be sent in during that stage to visualize the environment of the end of the catheter in fluoroscopy (real-time imaging under low dose without recording). Once the catheter 28 is positioned, a procedure of acquisitions (PA) of dynamic image sequences is undertaken, the principal stages of which are represented in the right part of Figure 6. This PA procedure obtains and records several dynamic image sequences showing the progress of the contrast medium in the coronary artery, each taken on a different plane constituting a reference position (or angulation). Typically, the reference positions are as follows (cf. Figure 5): (1) front, with the detector 38 directly facing the patient; (2) OAG 70 [LAO 70], i.e., left anterior oblique projection at 70° (the direction is always referenced in relation to the patient); (3) OAG 90 [LAO 90], i.e., left anterior oblique projection at 90°, or strict profile, and (4) OAD 20 [RAO 20], i.e., right anterior profile at 20°.
[0030] For each sequence, a dosed quantity of contrast medium, normally about five cubic centimeters, is manually injected throughout the filming sequence, that is, over a period of five to six seconds. The rate of acquisition is 25 or 30 images per second (according to European or United States standards), giving a total in the order of 150 to 200 acquired images per plane.
[0031] The method begins by placing the source-sensor tandem 38, 40 for acquisition of the front sequence (stage E3). During the positioning, it is verified by fluoroscopy that the image plane is correctly framed and that the catheter is always well positioned (stage E4), making adjustments when necessary. Acquisition of the dynamic sequence is then controlled (stage E5) under X-rays and the contrast medium
is simultaneously injected under the aforesaid conditions (stage E6). When acquisition is completed, the same procedure is undertaken for each of the following planes (OAG 70, OAG 90 and OAD 20), with the respective positioning stages (E7, E8, E9). Altogether, approximately 20 seconds of dynamic sequences of the left coronary artery are thus acquired, with a total dose in the order of 20 cubic centimeters.
[0032] The catheter 28 is then withdrawn (stage E10) and, in its place, the catheter 30 intended for the right coronary artery is introduced in the aperture of the latter (stage El 1). The PA procedure of acquisitions of dynamic sequences described above is then restarted. That PA procedure can possibly be modified at the reference positions in order to better suit the configuration of the structure of the right coronary artery. After the sequence acquisitions for the right coronary artery, the catheter is withdrawn (stage E10').
[0033] The method continues with ventriculography by introduction of the pigtail catheter 32 in the cavity of the left ventricle (stage El 2), with a right anterior oblique positioning of the image plane at 30° (OAD 30) (stage El 3). The acquisition of a dynamic image sequence is then begun over a period in the order of three or four seconds (stage El 4). During that acquisition approximately 40 cubic centimeters of contrast medium is injected by means of an electromechanical injector (stage El 5). Exploration of the ventricle makes it possible to visualize its general shape and to observe the manner in which it is contracted. In some cases, views are also acquired in the OAG 60 axis, when it is a question of detecting anomalies of movement of the wall of the septum. Finally, the catheter 32 is withdrawn on completion of the examination protocol (stage E10").
[0034] Embodiments of the invention are presented within the context of a radiology apparatus which enables displacements of the source-detector tandem to be made along a so-called "left" curve (i.e., not situated on a single plane), as described in FROO 07155. However, the invention can also be used with a standard radiological imaging apparatus.
[0035] As Figure 7 shows, the apparatus 34 comprises a bearing structure comprising a flat base 36 standing on the floor, with a support wall 38 at right angles to that base. The support wall maintains at a raised level a rotary shaft 40 aligned on a horizontal axis 42. Shaft 40 fits laterally into the end 44a of a rotary support arm 44 of a semicircular cradle 46, to the free ends of which an X-ray source 48 and a detector 50 are respectively attached. The support arm 44 is L-shaped, so that the axial displacement of the cradle 46 produced by the branch of the L perpendicular to the horizontal axis 42 compensates for the laterally offset mounting of the source 48 and detector 50 on the cradle 46. Hence, the axis 52 connecting the source 48 to the detector 50 crosses the axis of rotation 42. The cradle 46 is in turn mounted sliding on the support arm 44 to afford a circum-ferential rotation. The sliding thus makes it possible to displace the position in space of the source-detector axis 52 around a sliding axis 54 centered on the cradle 46. The respective axes 42, 52 and 54 of rotation of the support arm 44, of source-detector alignment 48, 50 and of sliding are secant at a point 56 called isocenter and are mutually perpendicular (orthogonal). The patient is maintained in a horizontal plane on a table 59 aligned with the horizontal axis 42.
[0036] The arrangement of axes 42, 52 and 54 permits a three-dimensional displacement in space of the source-detector tandem 48, 50 with degrees of freedom on two perpendicular planes, respectively aligned with the craniocaudal axis and with the right-left axis of the patient. The movements in each of these degrees of freedom are controlled independently by means of respective programmable actuators (not represented), although it is possible to form paths of the axis 52 of the source-detector tandem 48, 50 following left surfaces. The element of interest for that path being the sensitive surface of the detector 50, a path will be defined below in terms of displacement of the center of the image plane, comparable to the center of that sensitive surface 50. This central point therefore captures the radiation coming from the focal point of the source 48 after having crossed the patient at the isocenter 56.
[0037] It is also possible to have programming displacements of the image plane on a path which turns around the craniocaudal axis and is displaced toward the patient's head or feet on approaching its front view.
[0038] The entire operation of the apparatus 34 is managed by a microprocessor-based control unit 58 with an access console for the different functions 60 and a screen 62 for visualization of the different parameters and radiological images acquired. In the embodiment, the control unit is connected to an electrocardiograph machine 64 in order to synchronize certain actions with the movements of the heart and to an electromechanical injector 65 of contrast fluid having an injection tube 65a intended to fit into a catheter 32.
[0039] The functionalities managed by the control unit 58 are: (1) the respective actuators for the displacements of the source-detector tandem 48, 50 around axes 42, 54, with programming of: the path along a left (or flat) curve, the course of the rate of displacement (accelerations, decelerations) and stops on the path; (2) filming parameters: control of activation of the source and detector; and (3) operation of the injector 65, including control of an injection sequence divided into several injection cycles, with the following parameters: the start and interruption of an injection sequence synchronized with the start and stop of the image acquisition sequence, the beginning and end of each injection cycle as a function of the electrocardiogram (ECG) delivered by the electrocardiograph machine 64, the number of injection cycles and the injection delivery.
[0040] The control unit 58 also calculates a path and/or to memorize it. The path can be calculated from angulations, which can be indicated either by the user via the console 60 or by manually positioning the mobile unit of the apparatus 34 according to that angulation and memorizing it. For example, by defining an angulation by three angles along the three three-dimensional marking axes 42, 52 and 54 linked to the apparatus 34, the user can, for instance, define a first angulation of coordinates (0, 0, 0), a second angulation of coordinates (0, 0, α) and a third angulation of coordinates (0, 0, β) with α and β not nil. The path can, of course, be
programmed on a greater number of angulations. The control unit 58 then determines a path to be followed by the moving parts of the apparatus, by controlling the actuators in an appropriate manner, in order to make the image plane 50 pass through the angulations programmed, while taking into account the characteristics of the apparatus, such as: (1) possible angulations prohibited, because of the risk of causing collisions with the table 59, the patient, the source 48 or the detector 50, and (2) the mechanical or electromechanical stresses of the apparatus, such as maximum angular acceleration for each axis and the travel time, which should be as short as possible in order to minimize the total dose of contrast fluid to be injected.
[0041] In the disclosed embodiment, the path is programmed to describe a first passage around the patient in the left-right direction, followed by a second passage in the right-left direction, or vice versa, in order to define a loop. The loop can be open (end point not matching the starting point) or closed (end point matching the starting point). The rate of displacement of the image plane on the path is further programmed to be reduced on passages at angulations corresponding to chosen reference planes and increased between those points. Furthermore, the displacement of the image plane along the path is controlled with the electrocardiograph machine, so that the arrival at a reference plane systematically occurs at the time the heart is in a same given phase of its cycle, for example, the filling phase. That control is accomplished by an analysis of the electrocardiogram (ECG) produced by the electrocardiograph machine 64, the periodicity of which makes it possible to anticipate the different phases.
[0042] The protocol of coronary angiographic examination according to an embodiment of the invention, made with the apparatus of Figure 7 so programmed, will be described by reference to the flow chart of Figure 8 and to Figures 9 to 12. In the disclosed embodiment, the examination is followed by a ventriculographic examination. The sequences of acquired dynamic images make it possible to obtain by reconstruction three-dimensional (3D) images which evolve in time, giving rise to so-called four-dimensional (4D) images.
[0043] An initial phase of programming of the path of the image plane (stage
E20) is provided. The programming starts with the location of positions of the image plane which are going to constitute reference angulations. These reference angulations are represented by large dots P1 -P5 in Figure 9, which is a spherical chart representing the different movements of the image plane. The center of the sphere is the isocenter 56 (Figure 7) and its radius is equal to the distance between the isocenter and the focus of the X-ray source 48. The reference angulations include in part those commonly used in coronary arteriography (cf. Figure 5), to which are added others chosen for an optimization of the points of view of the areas to be explored. For that purpose, it is taken into account that those angulations are used for imaging of both the left coronary artery and the right coronary artery. It is to be noted that the positions of reference angulations P1-P5 are freely chosen around the patient's craniocaudal axis 42 and right-left axis 54. In the disclosed embodiment, the angulations number five and include two "standard" angula-tions (on a same plane of rotation around the craniocaudal axis), namely: left anterior oblique at 60° (OAG 60)
(point PI ) and "frontal," where the axis of the X-ray beam is vertical, with the image plane positioned directly above the patient (point P2). A third angulation (point P3) corresponds to the OAG 30 image plane, but with a caudal deflection of 15°.
[0044] To those three angulations, two others are added, P4 and P5, chosen, for example, to better discern the structure of the right coronary artery.
[0045] In general, the following reference points can be considered. For a good visualization of the left coronary artery, a reference position in right anterior oblique view at 30° makes it possible to analyze the circumflex branch and a part of the left anterior descending artery. Another reference position on angulation of slightly caudal type, i.e., with the detector 50 close to the patient's feet, while maintaining the azimuth angle of 30°, can be used to visualize another part of the left anterior descending artery and to avoid having it covered on the image by the circumflex branch of the intermediate vessels. Conversely, a reference position in cranial-type angulation on right anterior oblique projection makes possible a good visualization of the diagonal arteries.
[0046] The reference position in left anterior oblique angulation at 60° can be used for study of the diagonal arteries and of a part of the anterior interventricular artery (IVA). With a cranial angulation at 20°, the left anterior oblique angulation at 60° can be applied to avoid shortening of a part of the IVA and provides good images of the left main trunk and diagonal branches. In side view, i.e., with the axis of the X- ray beam horizontal, particularly in left side view, another part of the IVA and the different parts of the first diagonal artery and of the marginal artery of the left edge can be optimally seen.
[0047] For the right anterior artery, a reference position in angulation of left anterior oblique type at 45° can be used associated with a caudal angle of 15°. The reference position in left anterior oblique angulation at 90° with caudal deflection of 15° can be used for analysis of the vertical part of the right coronary artery and collateral branches, right ventricular artery and right edge marginal artery. The reference position in right anterior oblique angulation at 45° with caudal deflection of 15° can be used for visualization of the posterior interventricular artery and collateral branches, right ventricular artery and right edge marginal artery.
[0048] When the reference angulations P1-P5 have been programmed, the control unit 58 calculates a path which passes over each of them. As shown in Figure 9, that path, globally designated by T, consists of three parts which are linked together without interruption, namely: (1) a first part Tl corresponding to the left-right displacement of the image plane in a first direction (outward) and around the craniocaudal axis, beginning at angulation PI and ending at angulation P3; (2) a second part T2 corresponding to the right-left displacement of the image plane in a second direction (inward) and around the craniocaudal axis, beginning at angulation P3 and ending at angulation P5; and (3) a third part T3 which joins angulations P5 to PL
[0049] The displacement of the image plane on that whole path will be designated by the term "rotation," the filming and recording of images on a rotation being designated by the term "rotation acquisition."
[0050] The third part T3 of the path serves essentially to create a closed loop, i.e., to bring the image plane back to the starting point. In that way, it is possible to perform a succession of rotations without interruption.
[0051] The path T is calculated to produce a fluid movement of the image plane, with phases of acceleration at the start and deceleration at the approach of each reference angulation P1-P5. The movement is further subject to the ECG, so that the rapid displacements between two reference angulations occur during the diastole phase (when the heart is in quasi-stationary phase) and the slow passages at the reference angulations occur during the systole phase of the heart. Furthermore, synchronization on the ECG ensures that the heart will be in the same phase on passage at each of the reference angulations P1-P5.
[0052] By way of indication, the duration of the dynamic acquisition sequence on a rotation acquisition corresponds to four or five heart beats, that is, approximately five seconds. During the acquisition sequence, the source 48 and the detector 50 are activated with suitable adjustments of X-ray emission and filming.
[0053] The acquisition sequence covers the entire duration of the first and second parts Tl, T2 of the path and possibly an initial portion of the third part T3. The acquisitions are made at a rate of 25 or 30 images per second. The portions of the path on which the images are acquired are symbolized by a series of small dots in Figure 9.
[0054] In general, the programming stage E20 is executed only on initialization of the apparatus 34 for the protocol; that stage is therefore omitted for the examinations on the following patients, except in case of change of parameters.
[0055] The examination proper then begins with the patient positioned on the table 59 and the introduction of a "pigtail" catheter 32, of gauge 6, for example, from the femoral artery to the aortic root, at the starting points of the left and right coronary arteries (stage E22). The positioning of the injection end of the catheter 32 is
represented in Figure 10. If necessary, the proper positioning of the catheter can be controlled on a fluoroscopy screen (stage E24).
[0056] Once the catheter 32 is positioned, a first rotation acquisition is executed on the path T with the characteristics of acceleration-deceleration and ECG synchronization, as described above, and without injection of contrast medium (stage E26). That sequence without opacification makes possible the acquisition of reference images for digital image subtraction. It also makes it possible to visualize the patient's anatomical structures, notably, the general positioning of the heart relative to the thorax and to the vertebral column. A representation of one of the images acquired during that first rotation acquisition is given in Figure 1 1 (image I).
[0057] A second rotation acquisition identical to the first is then made, but with injection of contrast medium (stage E28). For that purpose, the catheter 32 is connected to the tube 65a of the injector 65, the latter being filled with contrast medium and capable of responding to the injection commands coming from the control unit 58. Thus, on injection of contrast medium, the latter is emitted with appreciably isotropic force and reaches the aperture of each of the left and right coronary arteries in order to be propagated along the coronary arterial tree. In the disclosed embodiment, the injection of contrast medium is not carried out continuously, but rather in spurts synchronized with the heart rate, so that the product is introduced on closing phases of the aortic valve (concomitant phase E30). The synchronization of the injection will be more specifically described by reference to
Figure 12. The peaks 66 of the ECG wave 68 indicative of diastole (dilation) are identified in the electrocardiogram (ECG) supplied by the electrocardiograph machine
64 (Figure 7), those peaks corresponding to the closing phase of the aortic valve. The starting positions of opening and closing of the aortic valve are schematically represented by the referenced symbol 70 at different positions along the axis of time t.
It is to be noted that the aortic valve 70 is closed during the parts of the ECG cycle preceding the diastole peak 66. On periods of closing of the aortic valve, there is appreciably no backflow of blood from the ventricle. Thus, by introducing the
contrast medium only during those closing phases, it will preferably enter the apertures of the left and right coronary arteries with minimum loss.
[0058] As the lower part of Figure 12 shows, the contrast fluid injection phases (hatched rectangles 72) occupy preferably approximately half the period tb between two diastole peaks and are situated just before passing the peak. The synchronization is accomplished by the control unit 58 by automatically detecting the diastole peaks 66 and by determining their periodicity tb, which makes it possible, on the one hand, to command the injector 65 to start the injection, at approximately a half-period tb after a detected peak and, on the other, to command the injector to stop the injection the moment the following peak appears.
[0059] The injector 65 is thus commanded in pulse mode to send a succession of contrast medium flows during the cycles indicated 72. The total quantity of contrast fluid injected is in the order of five to seven cubic centimeters, distributed over four or five injection cycles. The start and stop of all the injection cycles are generally synchronized respectively with the beginning and end of the image acquisition sequence of a rotation.
[0060] On that second rotation acquisition, the contrast fluid is propagated along the coronary arteries and dependent arteries in order to irrigate the myocardium. A series of images is then obtained, such as the one referenced II in Figure 1 1, after subtraction and processing. In an embodiment of the invention the sequence of dynamic images thus acquired makes it possible to simultaneously visualize the entire coronary artery tree. After a few seconds of the second rotation acquisition, a part of the contrast medium will have started perfusing the myocardium.
[0061] In order to visualize that opacification of the myocardium more specifically, a third rotation acquisition is carried out after the second one and following the same path characteristics, but without injection of contrast medium (stage E32). Normally, the contrast medium injected upon the second rotation acquisition will have had enough time to diffuse properly over the entire myocardium
during the period of the third rotation acquisition, without it being necessary to mark a pause time after the second rotation acquisition. Such pause time can, however, be envisaged, if necessary. The third rotation acquisition thus makes it possible to obtain, without addition of a dose of contrast medium, a three-dimensional visualization of the wall of the left ventricle (Figure 1 1 , image III) and to detect the possible areas of the myocardium poorly irrigated because of obstructions of the blood vessels.
[0062] The embodiment of the invention makes it possible to continue with a ventriculographic examination by pushing the pigtail catheter 32 beyond the aortic valve into the ventricle (stage E34). When the catheter 32 is thus positioned, a fourth rotation acquisition is earned out with injection of contrast fluid (E36). The path for that acquisition can be the same as for the three preceding ones or can be different, depending on the images desired for that examination. During this period, approximately 40 cubic centimeters of contrast fluid are introduced at constant flow. The dynamic acquisitions upon that fourth rotation acquisition make it possible to visualize the course of the contrast fluid in the left ventricle (Figure 1 1 , image IV). An evolving three-dimensional image is thus obtained, associated with the time variable, which gives a four-dimensional (4D) image.
[0063] At the end of the protocol, the pigtail catheter 32 is withdrawn (stage E38). From the set of images obtained upon the rotation acquisitions, different digital processings are possible in order to obtain static (3D) or evolving (4D) three- dimensional views.
[0064] As shown in the lower part of Figure 11 , it is possible to extract from those acquisitions the following views: (1) the group of coronary arteries in 3D, by subtraction of the corresponding images of the first and second rotation acquisitions (images II - images I) and digital calculation from reference films (box 74); (2) the muscular tissue (myocardium) of the heart in 3D by subtraction of the corresponding images of the first and third rotation acquisitions (images III - images I) and digital calculation from reference films (box 76); (3) the interior of the left ventricle in 4D
by subtraction of the corresponding images of the first and fourth rotation acquisitions (images IV - images 1) (box 78); in that case, the first rotation acquisition will also include dynamic images synchronized with those of the fourth rotation acquisition, and (4) the group of coronary arteries in 4D by digital combination of the views of those arteries in 3D with the views in 4D of the left ventricle (box 80).
[0065] The disclosed embodiment of the invention thus provide that: (1 ) all of the views indicated are obtained with the use of a single catheter 32 and a single injection of contrast medium; (2) the contrast medium is introduced simultaneously in the left coronary artery and in the right coronary artery, which makes it possible to visualize in a single sequence the opacification of all of the coronary arteries; (3) it is possible to obtain, some instants after injection of the contrast fluid in the coronary arteries and by simple repetition of a rotation acquisition, a view of the opacification of the tissues of the myocardium, which enables irrigation defects to be clearly detected; (4) by simple prolongation of the advance of the catheter into the left ventricle, the protocol can be continued with a dynamic examination of the movements of that part of the heart; and (5) introducing the contrast fluid into the left and right coronary arties solely during the phases of closing of the aortic valve, according to an embodiment, alone makes it possible to reduce the dose by approximately 50% or to make acquisitions over period twice as long at equal dose.
[0066] Thus, a single stage of introduction of the contrast medium suffices to enable the structure of the coronary arterial tree to be visualized from the left and right coronary arteries. The fact that the image plane is made to file by upon acquisition makes possible a three-dimensional reconstruction of that structure by digital processing. It is to be noted that this possibility is hard to conceive of in the standard approach described in the introduction, where the planes are instead static.
[0067] The contrast medium is advantageously introduced cyclically during the dynamic image acquisition, each cycle of introduction coπ'esponding to a phase of closing of the aortic valve in the cardiac rhythm. Thus, the dose of contrast medium is delivered in spurts and only at times during which the product is in a relatively
static environment and therefore has the best chance of entering the two. coronary arteries. This arrangement can be obtained subject to a diastole peak detected on the electrocardiogram of the heart examined. In a embodiment, each cycle of introduction of the contrast medium is begun at an instant situated roughly midway between a first and a second successive diastole peak and is interrupted approximately upon the appearance of that second peak. The path of the image plane advantageously defines a left curve evolving around the patient's head-to-toe axis and left-right axis. The path can define a loop, open or closed, with one part corresponding to a movement in a first direction around the head-to-toe axis and a second part corresponding to a movement in a second direction around the head-to-toe axis opposite to the first one. The path preferably embraces points of passage corresponding to reference angulations, the rate of procession of the image plane being increased outside the points of passage and reduced at the points of passage.
[0068] The procession of the image plane is advantageously synchronized with the cardiac rhythm, so that the moment of passage on each reference angulation is situated at a same phase of the cardiac cycle, notably in the systole phase of the heart.
[0069] An image subtraction technique may be used, in which, the method can further entail a preliminary stage consisting of acquiring a dynamic image sequence with procession of the image plane on the given path, without introduction of contrast medium.
[0070] The method can also provide a stage, following stage b), comprising acquiring a new dynamic image sequence with procession of the image plane, without introduction of contrast medium, making it possible to visualize the opacification of the myocardium. The examination can be continued by ventriculography, with injection of contrast medium and parallel acquisition of dynamic images with procession of the image plane.
[0071] Stage a) of introduction of the contrast medium is preferably carried out with the aid of a so-called "pigtail" catheter or the like.
[0072] The acquired images are advantageously processed in order to make at least one of the following: (1) a three-dimensional reconstruction of the heart not opacified; (2) a three-dimensional reconstruction of the myocardium; (3) a three- dimensional reconstruction of the coronary artery tree evolving in time, and (4) a three-dimensional reconstruction of the left ventricle evolving in time.
[0073] It can thus be guided to inject the contrast medium only during closing of the aortic valve. For that purpose, it can contain an electrocardiogram signal input and means of detection of diastole peaks in that signal, the injection being interrupted on detection of a diastole peak.
[0074] The device can contain means of starting the injection of contrast medium at a predetermined time, which can be programmable, before the arrival of a diastole peak. This time can be roughly midway between two successive diastole peaks. The device can be further programmable to inject the contrast medium over a given number of injection cycles. The device can further contain means of synchronization of the overall start and stop of injection with the start and stop of a filming sequence.
[0075] Various modifications in structure and/or steps and/or function may be made by one skilled in the art without departing form the scope and extent of the invention as recited in the claims.
Claims
1 . A method of cardiac radiological examination comprising the steps of:
a) introducing a contrast medium simultaneously in the left coronary artery and in the right coronary artery (2, 4) from the root of aorta and, in parallel;
b) acquiring a sequence of dynamic images of propagation of the contrast medium in the left and right coronary arteries with procession of an image plane (50), upon acquisition of the images, on a given path (T) (E 28).
2. The method according to claim 1 , wherein the contrast medium is introduced cyclically during the dynamic image acquisition, each cycle of introduction (72) corresponding to a phase of closing of the aortic valve in the cardiac rhythm.
3. The method according to claim 2, wherein each cycle (72) of introduction of contrast medium is controlled subject to a diastole peak (66) detected on the electrocardiogram of the heart examined.
4. The method according to claim 3, wherein each cycle (72) of introduction of the contrast medium is begun at an instant situated roughly midway between a first and a second successive diastole peak (66) and is interrupted approximately upon the appearance of the second peak.
5. The method according to any one of claims 1 to 4, wherein the path (T) of the center of the image plane (50) defines a left curve evolving around a longitudinal axis (42) and a left-right axis (54).
6. The method according to any one of claims 1 to 5, wherein the path (T) defines a loop, open or closed, with one part (Tl) corresponding to a movement in a first direction around the longitudinal axis (42) and a second part (T2) corresponding to a movement in a second direction around the longitudinal axis opposite the first one.
7. The method according to any one of claims 1 to 6, wherein the path (T) embraces points of passage (P1-P5) corresponding to reference angulations, the rate of procession of the image plane (50) being increased outside the points of passage and reduced at the points of passage.
8. The method according to claim 7, wherein the procession of the image plane (50) is synchronized with the cardiac rhythm, so that the moment of passage on each reference angulation (P1 -P5) is situated at a same phase of the cardiac cycle.
9. The method according to claim 8, wherein the moments of passage on each reference angulation correspond to the systole phase of the heart.
10. The method according to any one of claims 1 to 8, comprising a preliminary stage comprising acquiring a dynamic image sequence with procession of the image plane (50) on the given path (T), without introduction of contrast medium.
1 1 . The method according to any one of claims 1 to 10, comprising a stage (E 32), following stage b), comprising acquiring a new dynamic image sequence with procession of the image plane (50), without introduction of contrast medium, to visualize opacification of the myocardium.
12. The method according to any one of claims 1 to 1 1, wherein the examination is continued by ventriculography, with injection of contrast medium and parallel acquisition of dynamic images (E 36) with procession of the image plane (50).
13. The method according to any one of claims 1 to 12, wherein step a) of introduction of the contrast medium is carried out with the aid of a so-called "pigtail" catheter (32) or the like.
14. The method according to any one of claims 1 to 13, wherein the acquired images are processed to make a three-dimensional reconstruction of the heart not opacified.
15. The method according to any one of claims 1 to 14, wherein the acquired images are processed in order to make a three-dimensional reconstruction of the myocardium.
16. The method according to any one of claims 1 to 15, wherein the acquired images are processed in order to make a three-dimensional reconstruction of the coronary artery tree evolving in time.
17. The method according to any one of claims 1 to 16, wherein the acquired images are processed in order to make a three-dimensional reconstruction of the left ventricle evolving in time.
18. A device for injection of contrast medium in a catheter (32) for cardiac radiology, comprising: means for guiding the catheter (58) by a signal detecting cardiac rhythms (66, 68), so as to inject the contrast medium during cycles synchronized with given phases of the cardiac rhythm.
19. The device according to claim 18, wherein the means for guiding injects the contrast medium only during closing of the aortic valve.
20. The device according to claim 19, comprising: means for providing an electro-cardiogram signal input (64); and means (58) for detection of diastole peaks (66) in that signal, the injection being interrupted on detection of a diastole peak.
21. The device according to claim 20, comprising means s) oi starang tne injection of contrast medium at a predetermined time before the arrival of a diastole peak (66).
22. The device according to claim 21 , wherein the time is programmable.
23. The device according to claim 21 or 22, wherein the time is roughly midway between two successive diastole peaks (60).
24. The device according to any one of claims 18 to 23, comprising means for programming to inject the contrast medium over a given number of injection cycles (72).
25. The device according to any one of claims 18 to 24, comprising means (58) for synchronization of the overall start and stop of injection with the start and stop of a filming sequence.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2002572878A JP4233326B2 (en) | 2001-03-19 | 2002-03-15 | Radiation cardiac examination method and apparatus |
US10/295,055 US7065395B2 (en) | 2001-03-19 | 2002-11-04 | Method and apparatus for cardiac radiological examination in coronary angiography |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR01/03699 | 2001-03-19 | ||
FR0103699A FR2822048B1 (en) | 2001-03-19 | 2001-03-19 | METHOD OF CARDIAC RADIOLOGICAL EXAMINATION IN CORONAROGRAPHY AND DEVICE FOR IMPLEMENTING SAME |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/295,055 Continuation US7065395B2 (en) | 2001-03-19 | 2002-11-04 | Method and apparatus for cardiac radiological examination in coronary angiography |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2002074163A1 true WO2002074163A1 (en) | 2002-09-26 |
WO2002074163A9 WO2002074163A9 (en) | 2002-11-28 |
Family
ID=8861290
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2002/008104 WO2002074163A1 (en) | 2001-03-19 | 2002-03-15 | Method and device for cardiac radiological examination |
Country Status (3)
Country | Link |
---|---|
JP (1) | JP4233326B2 (en) |
FR (1) | FR2822048B1 (en) |
WO (1) | WO2002074163A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2014221430A (en) * | 2004-03-03 | 2014-11-27 | 株式会社根本杏林堂 | Drug solution injection system |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1778087A1 (en) * | 2004-08-13 | 2007-05-02 | Koninklijke Philips Electronics N.V. | Alternative acquisition scheme for coronary angiography |
DE102005049603B4 (en) | 2005-10-17 | 2010-09-16 | Siemens Ag | Method and device for imaging an organ |
WO2007116840A1 (en) * | 2006-04-04 | 2007-10-18 | Nemoto Kyorindo Co., Ltd. | Drug solution injector |
JP5111901B2 (en) * | 2007-03-13 | 2013-01-09 | 株式会社東芝 | X-ray equipment |
CN102958440B (en) * | 2011-06-23 | 2015-12-02 | 株式会社东芝 | Image processing apparatus and radiographic apparatus |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5476453A (en) * | 1994-05-20 | 1995-12-19 | Mehta; Sameer | Catheter for simultaneous right and left coronary cannulization |
US6269140B1 (en) * | 1995-09-11 | 2001-07-31 | Hitachi Medical Corporation | X-ray computerized tomography apparatus control method therefor and image generating method using the apparatus |
US6337992B1 (en) * | 1997-01-29 | 2002-01-08 | Philips Medical Systems Technologies Ltd. | Predictive bolus tracking |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4006736A (en) * | 1974-11-27 | 1977-02-08 | Medrad, Inc. | Angiographic injector |
JPS59214431A (en) * | 1983-05-20 | 1984-12-04 | 株式会社東芝 | Radiation diagnostic apparatus |
JPS60190968A (en) * | 1984-01-30 | 1985-09-28 | マリンクロツド・インコ−ポレイテツド | Catheter for contrast photographing of coronary arteries |
JPH0657208B2 (en) * | 1985-12-27 | 1994-08-03 | 株式会社東芝 | Digital Fluorographer |
JPH0337631Y2 (en) * | 1986-10-30 | 1991-08-08 | ||
GB9203132D0 (en) * | 1992-02-14 | 1992-04-01 | Univ Southampton | Computer assisted dynamic digital angiography |
-
2001
- 2001-03-19 FR FR0103699A patent/FR2822048B1/en not_active Expired - Fee Related
-
2002
- 2002-03-15 JP JP2002572878A patent/JP4233326B2/en not_active Expired - Fee Related
- 2002-03-15 WO PCT/US2002/008104 patent/WO2002074163A1/en active Application Filing
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5476453A (en) * | 1994-05-20 | 1995-12-19 | Mehta; Sameer | Catheter for simultaneous right and left coronary cannulization |
US6269140B1 (en) * | 1995-09-11 | 2001-07-31 | Hitachi Medical Corporation | X-ray computerized tomography apparatus control method therefor and image generating method using the apparatus |
US6337992B1 (en) * | 1997-01-29 | 2002-01-08 | Philips Medical Systems Technologies Ltd. | Predictive bolus tracking |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2014221430A (en) * | 2004-03-03 | 2014-11-27 | 株式会社根本杏林堂 | Drug solution injection system |
Also Published As
Publication number | Publication date |
---|---|
FR2822048A1 (en) | 2002-09-20 |
WO2002074163A9 (en) | 2002-11-28 |
FR2822048B1 (en) | 2003-09-26 |
JP4233326B2 (en) | 2009-03-04 |
JP2004523318A (en) | 2004-08-05 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US7065395B2 (en) | Method and apparatus for cardiac radiological examination in coronary angiography | |
US20240260914A1 (en) | Method And Apparatus For Reconstructing Image Projections | |
CN100443050C (en) | Rotational angiography based hybrid 3D reconstruction of coronary arterial structure | |
JP5639764B2 (en) | Imaging and tools for use with moving organs | |
US9775538B2 (en) | System and method for determining the position of the tip of a medical catheter within the body of a patient | |
US9807860B2 (en) | Gated image acquisition and patient model construction | |
JP5161118B2 (en) | Arterial imaging system | |
JP5797763B2 (en) | Gated image acquisition and patient model structure | |
US6909769B2 (en) | Method and apparatus for three-dimensional imaging of a moving examination subject, particularly for heart imaging | |
US6628981B2 (en) | Adaptive heart rate prediction algorithm for computed tomography imaging | |
US7403591B2 (en) | Alternative acquisition scheme for coronary angiography | |
US20070055142A1 (en) | Method and apparatus for image guided position tracking during percutaneous procedures | |
JP4712331B2 (en) | Organ imaging method, organ imaging apparatus, and computer-readable recording medium recording a computer program | |
WO2013001635A1 (en) | X-ray diagnostic device | |
US6324254B1 (en) | Method and x-ray device for picking up x-ray images of a substantially rhythmically moving vessel or organ | |
CN102542584B (en) | Image processing apparatus and image processing method | |
WO2023070968A1 (en) | Interventional operation robot system and navigation method | |
JP2008006083A (en) | Three-dimensional image forming apparatus | |
JP2016221054A (en) | Radiographic blood vessel imaging device | |
JP2007502140A (en) | Apparatus and method for producing an image of the heart | |
JP6445593B2 (en) | Control of X-ray system operation and image acquisition for 3D / 4D aligned rendering of the targeted anatomy | |
JP4974126B2 (en) | Method and device for image acquisition with multiple viewpoints | |
WO2002074163A1 (en) | Method and device for cardiac radiological examination | |
JP2007111530A (en) | Method and device for imaging organ | |
JPS6050900A (en) | X-ray diagnostic apparatus |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): JP US |
|
WWE | Wipo information: entry into national phase |
Ref document number: 10295055 Country of ref document: US |
|
AK | Designated states |
Kind code of ref document: C2 Designated state(s): JP US |
|
COP | Corrected version of pamphlet |
Free format text: PAGE 5/9, DRAWINGS, ADDED |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2002572878 Country of ref document: JP |