The following relates generally to magnetic resonance (MR) imaging. It finds particular application in conjunction with Electrocardiography (ECG) during MR imaging, and will be described with particular reference thereto. However, it will be understood that it also finds application in other usage scenarios and is not necessarily limited to the aforementioned application.
MR imaging often involves biopotential measurements such ECG monitoring during the imaging procedure. Patients can be monitored for vital signs with ECG or other monitors during MR procedures to ensure patient health. ECG monitors can be used in MR imaging as triggers or gates for image capture. For example, images can be triggered such that the heart of a subject is shown only in images in a certain phase or which compensates for heart motion artifacts in the image.
ECG monitoring uses electrodes affixed to the patient at different points on the body. The electrodes sense weak electrical signals from the body which indicate phases of the heart. The electrodes are attached to leads which transmits the sensed signals to an ECG monitor which analyses the signal and/or displays the signal visually. Each lead includes a conductive wire or trace which connects the electrode to the ECG monitor and transmits signals from the attached electrode to the ECG monitor. The number of electrodes and corresponding leads can vary which means the number of wires connecting electrodes of one patient to an ECG monitor can vary. The leads can also include leads for other biopotential measurements of the patient such as respiratory monitors and the like.
Magnetic Resonance scanners use strong magnetic fields for imaging the patient and the strong magnetic fields can induce electric currents in conductive wires such as ECG traces or wires. The magnetic fields of the scanner can induce currents on the ECG wires such that give potentially false heart rate readings or obscure ECG R-waves from waveform detection schemes. The wires are susceptible to triboelectric effects and are hyper-sensitive to patient movement. Cross-talk between wires can interfere with the transmitted signals. Looping of wires can add to the interference where one or more wires loop around in close proximity to the same or other lead wires. Discrete wires can be inconsistent and/or inaccurate with transmitting the ECG signals. Improperly selected materials of the wire, cabling and/or insulating material which emits protons can cause artifacts in images.
Care must be taken in selecting and configuring the materials of the cabling including the wires because of patient safety. Ferrous materials can become projectiles in the strong magnetic fields of scanners which can injure patients and/or healthcare workers. Induced currents on non-MR ECG cables in the magnetic field can cause heating of the wires which may subject the patient to burns.
Current approaches for MR cables typically use high resistance wires which are braided or twisted to reduce susceptibility to noise pickup from the MR scanner. The braided or twisted bundles of wire are then insulated. Some approaches then add a shielding to further minimize interference from the magnetic field. However, these approaches still contend with cross talk between the wires twisted or braided together and do not address problems caused with looping of wires. Additionally, the twisting or braiding of the wires, and adding components such as shielding adds to the cost of the cable.
The following discloses a new and improved planar magnetic resonance safe cable for biopotential measurements which addresses the above referenced issues, and others.
In accordance with one aspect, a magnetic resonance (MR) safe cable includes four or more controlled resistance electrically conductive wires disposed in a planar configuration and parallel to each other, and a stiff non-proton emitting substrate which holds the four or more controlled resistance conductive wires in the planar configuration and parallel to each other.
In accordance with another aspect, a method of using a magnetic resonance (MR) safe cable includes attaching at least four electrodes to a subject. The MR safe cable is disposed along the subject supported by the subject or a subject support, and the MR cable includes at least four controlled resistance conductive wires disposed in a parallel planar configuration. A connector attached to one of the corresponding connectors of a first end of the at least four controlled resistance conductive wires is connected to the electrodes. Connectors attached to a second end of the controlled resistance conductive wires are connected to a patient monitor. The four or more controlled resistance conductive wires in the planar and parallel configuration are held with a stiff non-proton emitting substrate of the MR safe cable which encases the controlled resistance wires in the parallel planar configuration.
In accordance with another aspect, a method of manufacturing a magnetic resonance (MR) safe cable includes stretching at least four controlled resistance electrically conductive wires parallel and in a plane, and coating the stretched at least four controlled resistance electrically conductive wires with a stiff foam jacket.
One advantage is a cable which operates in a strong magnetic field that is more reliable and repeatable for biopotential measurements.
Another advantage is in reducing variation in induction of interference currents in the electrode and resistive traces from the static and gradient magnetic fields.
Another advantage is in reducing triboelectric and microphonic effects by eliminating movement between resistive traces in the cable.
Another advantage resides in the increased likelihood of induced currents equally on each lead which can then be canceled out by a common mode filter.
Another advantage resides in patient safety in a strong magnetic field.
Another advantage resides in a stable, distributed, and high resistance trace.
Another advantage resides in a cable which does not cause artifacts in MR imaging.
Still further advantages will be appreciated to those of ordinary skill in the art upon reading and understanding the following detailed description.
The invention may take form in various components and arrangements of components, and in various steps and arrangement of steps. The drawings are only for purposes of illustrating the preferred embodiments and are not to be construed as limiting the invention.
With reference to
The cable 10 includes a stiff flat substrate 14 which holds the four or more controlled resistance conductive wires in the common plane and parallel to each other. The substrate is made of a non-proton emitting material. The stiff planar substrate can include a foam plastic jacket which surrounds and holds the conductive wires parallel and in the common plane. Holding the conductive wires parallel and in a common plane increases the likelihood that induced currents will be induced equally on equal wire and therefore can be filtered out more easily due to “common-mode”. The foam jacket thermally and electrically insulates the wires from contact with the patient. The foam in one embodiment includes at least 2.5 mm of foam 18 between each controlled resistance electrically conductive wire and an outside surface. The foam can include open or closed cell foam. The closed cell foam provides easier clean-up.
End caps 20 attached to each end of the stiff planar substrate can provide strain relief to the four or more controlled resistance electrically conductive wires and guide the wires into predetermine connections. For example, each wire can be supported with strain relief 22 between a connector and an end of the substrate or foam jacket. The end caps can provide a rigid surface for grasping the cable and fitting the connector. The end caps reduce overall wear on the cable. Connectors 24 disposed at one end of the cable connect, e.g. clip, each wire to a contact of an ECG electrode. Connectors 26 disposed at another end connect, e.g. plug, the wires to a patient monitor. The connectors can be keyed such as color coded, marked, shaped, and the like, which provide a healthcare practitioner easy identification of corresponding predetermined connections for each connector. The connectors can be individual connectors such as shown with individual leads 27 and the electrode connectors, or unitary connector such as shown with the patient monitor connectors. A unitary connector can include webbing which additionally provides strain relief, organization, and ordered connection. The leads 27 can be in a staggered configuration as shown with varying length of leads or in a straight configuration with equal length leads.
The cabling can include necking 28 in the foam jacket or substrate to facilitate storage. For example, the cable can be wound in a large coil and fastened with a temporary fastener for storage. Removing the fasteners allows the cable to extend or return to the planar position.
With reference to
Each controlled resistance electrically conductive wire can include electric shock inhibiting components 34, such as discrete resistors, RF chokes, and the like. For example, a predetermined or variable resistor is spliced into each wire to control resistance of the wire. The wires 12 can individually or collectively include one or more additional components 36 such as a notch filter, low pass filter, integrated circuit, sensor, and the like. The filters can block currents at frequencies other than the frequencies with ECG signals.
The embodiment of
With reference to
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The cable 10 holds the controlled resistance electrically conductive wires planar and parallel. The cable substrate forms a stiff jacket that resists looping and twisting. The substrate returns to the cable to a substantially straight cable run. The cable without force applied returns to a planar configuration, e.g. if placed on a flat surface will return to straight and flat.
With reference to
In a step 82, a stiff foam jacket coats the stretched at least four controlled resistance electrically conductive wires. The stiff foam jacket holds or fixes the wires parallel and in the common plane. In one embodiment, the foam jacket is pressure molded. The cable combs can be integrated into the stiff foam jacket.
Affixing end caps to each end of the foam jacket provide strain relief in a step 84. The end caps can be integrated with the foam jacket or added as a separate step.
In a step 86, the least four controller resistance electrically conductive wires are terminated at a first end with electrode connectors and at a second end with patient monitor connectors. The step can include adding keys to the connectors or leads.
With reference to
In a step 92, the MR safe cable is disposed along the subject supported by the subject or a subject support. The MR safe cable includes the at least four controlled resistance conductive wires disposed in a parallel planar configuration. The step can include releasing the MR safe cable from a storage configuration to an operation configuration.
A connector attached to one of the corresponding connectors of a first end of the at least four controlled resistance conductive wires is connected to the electrodes in a step 94. Connectors attached to a second end of the controlled resistance conductive wires are connected to a patient monitor in a step 96.
With a stiff non-proton emitting or MR inert substrate of the MR safe cable which encases the controlled resistance wires in the parallel planar configuration, the four or more controlled resistance conductive wires are held in the planar and parallel configuration in a step 98. The wires transmit the ECG signals from the electrodes to the patient monitor for biopotential measurements. The stiff substrate can include the embodiments of the cable as described in reference to
In a step 100, the subject can be imaged with a magnetic resonance scanner and the connected MR safe cable. The step includes transmitting physiological signals such as ECG signals with the MR safe cable concurrently with the imaging which are analyzed and/or displayed. The imaging can include processing of the transmitted signals such as with triggered or gated imaging.
It is to be appreciated that in connection with the particular illustrative embodiments presented herein certain structural and/or function features are described as being incorporated in defined elements and/or components. However, it is contemplated that these features may, to the same or similar benefit, also likewise be incorporated in other elements and/or components where appropriate. It is also to be appreciated that different aspects of the exemplary embodiments may be selectively employed as appropriate to achieve other alternate embodiments suited for desired applications, the other alternate embodiments thereby realizing the respective advantages of the aspects incorporated therein.
For example, the lead wires 12 can be disposed in other relationships that resist looping, twisting, or otherwise moving relative to each other. In one example, the lead wires are disposed alternately in first and second adjacent parallel planes.
It is also to be appreciated that particular elements or components described herein may have their functionality suitably implemented via hardware, software, firmware or a combination thereof. Additionally, it is to be appreciated that certain elements described herein as incorporated together may under suitable circumstances be stand-alone elements or otherwise divided. Similarly, a plurality of particular functions described as being carried out by one particular element may be carried out by a plurality of distinct elements acting independently to carry out individual functions, or certain individual functions may be split-up and carried out by a plurality of distinct elements acting in concert. Alternately, some elements or components otherwise described and/or shown herein as distinct from one another may be physically or functionally combined where appropriate.
In short, the present specification has been set forth with reference to preferred embodiments. Obviously, modifications and alterations will occur to others upon reading and understanding the present specification. It is intended that the invention be construed as including all such modifications and alterations insofar as they come within the scope of the appended claims or the equivalents thereof. That is to say, it will be appreciated that various of the above-disclosed and other features and functions, or alternatives thereof, may be desirably combined into many other different systems or applications, and also that various presently unforeseen or unanticipated alternatives, modifications, variations or improvements therein may be subsequently made by those skilled in the art which are similarly intended to be encompassed by the following claims.
Filing Document | Filing Date | Country | Kind |
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PCT/IB2014/066379 | 11/27/2014 | WO | 00 |
Number | Date | Country | |
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61914414 | Dec 2013 | US |