The present invention relates generally to medical devices used during medical procedures and may be particularly suitable for MRI-guided interventional procedures.
Some medical and surgical procedures use interventional or monitoring devices with relatively long lengths of various “loose” cables to connect to different electronic power and control systems during the procedures.
Embodiments of the invention may reduce lengths of loose cables and/or tubes conventionally used in medical procedures.
Some embodiments are directed to medical mats that include: (a) a mat body; (b) a plurality of discrete electrical paths in or on the mat body extending between at least one inlet location and a plurality of different outlet locations spaced apart about the mat body; (c) at least one inlet connector held by the mat body residing at the at least one inlet location in communication with one or more of the electrical paths; and (d) a plurality of outlet connectors held by the mat body at the different outlet locations, a respective outlet connector in communication with one or more of the electrical paths.
The mat body has a perimeter and the at least one inlet location may reside at a first perimeter edge portion and the plurality of different outlet locations may reside at different perimeter edge portions. In some embodiments, the inlet and outlet connectors can all reside on edge portions of the mat body. For example, at least one of the inlet and outlet connectors can reside on a primary upper surface of the mat body and other connectors can reside at outer edge portions of the mat body.
In some particular embodiments, the mat includes an electrical ground pad and/or external defibrillator pads. In some embodiments, the mat may optionally include at least one surface coil and/or at least one gradient receive coil.
Some embodiments are directed to systems. The systems include: (a) at least one medical mat having a plurality of discrete electrical paths that extend from at least one electrical input connector to a plurality of spaced apart electrical outlet connectors; (b) a first diagnostic or therapeutic medical tool with a first lead that connects to the at least one input connector and a second lead that connects to one of the outlet connectors; and (c) a second diagnostic or therapeutic medical tool with a first lead that connects to the at least one input connector and a second lead that connects to a different one of the outlet connectors.
The first tool can be an external ECG monitor and the second tool can be a cryogenic or electrode ablation catheter.
Still other embodiments are directed to methods of connecting medical instruments for a medical procedure. The methods can include: (a) placing at least one medical mat on a patient support surface, the at least one medical mat having defined electrical paths from at least one electrical input connector to spaced apart electrical output connectors; (b) having a patient lay on the at least one medical mat; (c) attaching at least one electrical input lead to the at least one input connector; and (d) connecting electrical output leads in communication with different medical tools to the output connectors.
A medical procedure can be carried out after the attaching and connecting steps using the medical tools. The placing step can be carried out by placing the at least one mat on a gantry of an MRI Scanner system.
Embodiments of the invention provide medical mats which define electrical paths that may reduce problems associated with conventional loose cables and/or tubes used during a medical procedure. The mats can help control the orientation and routing of electrical leads and/or cables used during a medical procedure to reduce “kinking” and/or electrical shorts from same, fluid in connectors and tangling of loose cables, and/or improve patient transportability.
Further features, advantages and details of the present invention will be appreciated by those of ordinary skill in the art from a reading of the figures and the detailed description of the preferred embodiments that follow, such description being merely illustrative of the present invention. Features described with respect with one embodiment can be incorporated with other embodiments although not specifically discussed therewith. That is, it is noted that aspects of the invention described with respect to one embodiment, may be incorporated in a different embodiment although not specifically described relative thereto. That is, all embodiments and/or features of any embodiment can be combined in any way and/or combination. Applicant reserves the right to change any originally filed claim or file any new claim accordingly, including the right to be able to amend any originally filed claim to depend from and/or incorporate any feature of any other claim although not originally claimed in that manner. The foregoing and other aspects of the present invention are explained in detail in the specification set forth below.
The present invention now is described more fully hereinafter with reference to the accompanying drawings, in which some embodiments of the invention are shown. This invention may, however, be embodied in many different forms and should not be construed as limited to the embodiments set forth herein; rather, these embodiments are provided so that this disclosure will be thorough and complete, and will fully convey the scope of the invention to those skilled in the art.
Like numbers refer to like elements throughout. In the figures, the thickness of certain lines, layers, components, elements or features may be exaggerated for clarity.
The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting of the invention. As used herein, the singular forms “a”, “an” and “the” are intended to include the plural forms as well, unless the context clearly indicates otherwise. It will be further understood that the terms “comprises” and/or “comprising,” when used in this specification, specify the presence of stated features, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, steps, operations, elements, components, and/or groups thereof. As used herein, the term “and/or” includes any and all combinations of one or more of the associated listed items.
Unless otherwise defined, all terms (including technical and scientific terms) used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. It will be further understood that terms, such as those defined in commonly used dictionaries, should be interpreted as having a meaning that is consistent with their meaning in the context of the specification and relevant art and should not be interpreted in an idealized or overly formal sense unless expressly so defined herein. Well-known functions or constructions may not be described in detail for brevity and/or clarity.
It will be understood that when an element is referred to as being “on”, “attached” to, “connected” to, “coupled” with, “contacting”, etc., another element, it can be directly on, attached to, connected to, coupled with or contacting the other element or intervening elements may also be present. In contrast, when an element is referred to as being, for example, “directly on”, “directly attached” to, “directly connected” to, “directly coupled” with or “directly contacting” another element, there are no intervening elements present. It will also be appreciated by those of skill in the art that references to a structure or feature that is disposed “adjacent” another feature may have portions that overlap or underlie the adjacent feature.
Spatially relative terms, such as “under”, “below”, “lower”, “over”, “upper” and the like, may be used herein for ease of description to describe one element or feature's relationship to another element(s) or feature(s) as illustrated in the figures. It will be understood that the spatially relative terms are intended to encompass different orientations of the device in use or operation in addition to the orientation depicted in the figures. For example, if the device in the figures is inverted, elements described as “under” or “beneath” other elements or features would then be oriented “over” the other elements or features. Thus, the exemplary term “under” can encompass both an orientation of “over” and “under”. The device may be otherwise oriented (rotated 90 degrees or at other orientations) and the spatially relative descriptors used herein interpreted accordingly. Similarly, the terms “upwardly”, “downwardly”, “vertical”, “horizontal” and the like are used herein for the purpose of explanation only unless specifically indicated otherwise.
The term “mat” refers to a substantially flat device such as a pad, cover or other device with electrical paths extending through portions thereof and that is typically resilient or flexible but has sufficient rigidity and/or thickness to hold the electrical paths and/or leads in a manner that does not cause discomfort to a user or patient. The mat can comprise an elastomeric and/or fabric body. The electrical paths held by the mat can be formed as internal wires, filars, metallic traces or cables. For MRI procedures, the conductive material used to form the electrical paths in the mat (e.g., the leads held by the mat) can be non-ferromagnetic. The term “lead” means an electrical path created by one or more wires. The wires are typically insulated wires, particularly where exposed. The term “cable” is used interchangeably with the term lead.
The term “MRI-compatible” means that a device is safe for use in an MRI environment and/or that a device that can operate as intended in an MRI environment and not introduce artifacts into MRI signal data. As such, if residing within the high-field strength region of the magnetic field of an MRI suite, the MRI-compatible device is typically made of a non-ferromagnetic MRI-compatible material(s) suitable to reside and/or operate in a high magnetic field environment. The term “high magnetic field” refers to magnetic fields above 0.5 T, typically between 1.5 T to 10 T. Although described as particularly suitable for MRI procedures or suites, the medical mats can also be used with CT or other imaging modalities, such as for example, for CT-guided cardiac EP procedures or robotic surgical procedures.
Referring now to the figures,
The medical mats 10 contemplated by embodiments of the present invention may be used with respect to any medical or surgical procedure including diagnostic, interventional or exploratory procedures. For example, the mats 10 can be used with ultrasound, X-ray, CT or other imaging modalities. The mats 10 may be particularly suitable for use with MRI-guided surgical procedures, such as cardiac procedures, including but not limited to cardiac EP procedures where heat or cryogenic ablation is used and where the procedure is carried out in an MRI scanner or MRI interventional suite.
One or more of the electrical paths 25 can extend from a primary “input” end to branch out to other edge portions, e.g., side or end perimeter portions of the mat 10. As shown, for example, in
As shown in
The mats 10 can be used to control the orientation and/or reduce the lengths of loose cables associated with conventional procedures (see, e.g.,
The mat 10 can be sterile (meaning that it meets clinical cleanliness standards for medical procedures) and may optionally be single-use disposable. Alternatively, or additionally, a sterile cover or case can be used as appropriate. The mat 10 can be a “universal” mat configured for multiple different procedures or may be procedure-specific, e.g., a cardiac mat and/or a cardiac EP (electrophysiology) mat.
The mat 10 may directly or indirectly contact the patient. The mat 10 can be releasably attached to the support surface 100 using adhesives, straps or the like. The mat 10 may be configured to be used without such an affirmative attachment feature, and may optionally include an anti-slide or textured surface or a contact surface with an increased friction material or coating that inhibits sliding.
The mat 10 may cover all or substantially all of the patient support surface 100 as shown in
The electrical connectors 20 or 30 can be standard connectors such as BNC connectors, coaxial connectors and the like or the connectors 20, 30 may be customized connectors. The input connector(s) 20 can be provided as a main cable connection hub 20h of closely spaced electrical connectors. As shown in
Some or all of the connectors 30 and 20 can reside within the bounds of the mat body 10b as shown in
The different systems can be positioned at one common end of the patient support surface or placed where suitable. As will be discussed further below, one of the tools 40 can be an ECG monitor and the monitor can be at the input end and connect through the input connector 20 with one or more cardiac cycle sensors (e.g., 10 or more electrodes) connecting through a connector 35e to a respective connector 30 and path 25 to provide the output to the monitor. Each sensor may connect to separate connectors 30 or grouped to connect otherwise.
The connectors 30 may be color-coded to the external lead to Facilitate set-up and proper connection. The connectors 30 may have different shapes to inhibit improper connection of external leads. As shown in
EP clinical procedures involve recording and displaying in real-time numerous external and internal ECG signals. A coronary sinus catheter simultaneously measures as many as fourteen different ECG signals from inside the patient's heart (and may measure less or more than fourteen). In such an embodiment, these signals come down fourteen different wires down the catheter and the output connector has at least fourteen pins to transfer these measurements to the subsystems that process these measurements. Similarly, the output connector of the lasso catheter has eight ECG signal pins while the ablation catheter has between about two to four ECG signal pins and two tip temperature pins. The external ECG can be recorded separately, typically using twelve (12) patch electrodes. Besides recording ECG, some of the same connector pins are used for externally pacing and/or defibrillating the patient's heart. In the ECG monitor subsystem fractionated ECG signals are displayed on a monitor and these signals guide the physician to specific target sites. A physician refers back to this monitor to confirm success of ablation procedure. Further, these ECG signals are one of the inputs used to generate the electro-anatomical map by the workstation subsystem.
The mat 10 can be formed of one or more materials. The outer surfaces can be formed of a material(s) that is substantially impermeable to fluids. According to some embodiments, the mat 10 can include a biocompatible polymeric material, such as those suitable for use in MRI systems. Exemplary polymeric materials may include polyvinyl, PET, silicone, polyethylene, polyurethane, and/or polyamide. Where the mat 10 contacts the patient, the mat 10 may be configured to provide heating or cooling as desired for patient comfort or treatment. Where the patient lies on the mat 10, the mat 10 may be configured to provide cushioning using an air pocket, flexible soft material such as memory foam and/or gel material for patient comfort. Where the mat lies on the patient, the mat can be configured to be light weight and substantially conformable to the patient.
The mats 10 can be fabricated in any suitable manner. In some embodiments, it is contemplated that the mat can be molded and the electrical paths can be molded internal to the exterior surface of the mat. In some embodiments, a first layer of the mat can be molded with mold forms defining open cavities or channels that will hold the wires in the desired locations and orientations and route them to the outlet locations. The mold forms can be removed and wires placed into those cavities or channels, and a second layer can be molded over the wires (or tubes for fluid channels where used) to encase them and hold them in position (when fabricating the internal wire path configuration). Alternatively, the mat can be molded in one step with the mold form channels left in position and the wires threaded through the channels (either before or after the molding step). However, the mat is not required to be molded. In some alternate embodiments, fabric can be used to form the mat and the mat electrical paths can be formed by threading cables or wires through sewn or adhesively formed channels. The mats 10 can also be fabricated in yet other manners. The mats 10 and electrical paths 25 can be sterilized and packaged in a sterile package for medical use during a medical procedure.
The foregoing is illustrative of the present invention and is not to be construed as limiting thereof. Although a few exemplary embodiments of this invention have been described, those skilled in the art will readily appreciate that many modifications are possible in the exemplary embodiments without materially departing from the teachings and advantages of this invention. Accordingly, all such modifications are intended to be included within the scope of this invention as defined in the claims. The invention is defined by the following claims, with equivalents of the claims to be included therein.
This application claims the benefit of priority of and priority to U.S. Provisional Application Ser. No. 61/119,149, filed Dec. 2, 2008, the contents of which are hereby incorporated by reference as if recited in full herein.
Number | Date | Country | |
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61119149 | Dec 2008 | US |