The invention relates to a catheter for administering a substance into a body tissue, in particular into brain structures.
To place a catheter in a patient, a physician ordinarily predetermines or plans a trajectory for the catheter. To assist the physician in adhering to the planned trajectory, the catheter can be made of a relatively rigid material, or the catheter can be used with a stylet made of a rigid material (e.g., stainless steel).
During the placement of the catheter, the physician may encounter obstacles in the form of resistance properties of the anatomical structures in the treatment vicinity or along the planned trajectory. In such circumstances, the placement of some catheters can deviate from the planned trajectory. The deviation can occur due to surfaces present (for example, sulci) or due to heterogeneous properties of the brain tissue (for example, different elasticities). To plan for a reliable and predictable dispersion of a substance in the treatment vicinity, the dispersion may be simulated in advance with computer assistance.
In convection-enhanced delivery, a positive pressure gradient is used to aid in the dispersion of the substance. U.S. Pat. Nos. 5,987,995 and 6,120,457 disclose the use of catheters to measure the pressure at a particular point in the tissue or in the body.
A catheter in accordance with the invention is configured for administering a substance into a body tissue (e.g., brain structures), such that the dispersion of the substance introduced through the catheter is reliable and predictable. To this end, the catheter may be configured to change shape while the catheter is being introduced into the tissue and the changes to the shape of the catheter may be detected using pressure sensors integrated into the catheter design. The pressure sensors may also be used to determine the presence and extent of any backflow along an exterior surface of the catheter. The information related to changes in the shape of the catheter or related to the presence of a backflow along the exterior of the catheter may be provided to a computer for simulation and/or adaptation of a treatment plan.
In accordance with one aspect of the invention, a catheter may be provided that includes an elongated catheter body surrounding a lumen (through which a substance can flow) and a pressure sensor array provided on the catheter exterior surface or in the catheter body, wherein the pressure sensor array is used to detect a pressure distribution along a length or portion of the catheter.
In accordance with another aspect of the invention, an end of the catheter that penetrates into the body tissue (the distal end) may include a number of pressure sensors or a pressure sensor system that detects the pressure status of the catheter itself, namely the pressure exerted on the surface material of the catheter or the pressure in the catheter material. In other words, the catheter status is detected by ascertaining a pressure status along the surface of the catheter or within the catheter.
A method in accordance with the invention may include ascertaining the surface or material pressure status of the catheter with the aid of a pressure sensor system, and using the ascertained pressure status to determine the presence or direction of any bends in the catheter or the presence and/or length of any backflow along the exterior of the catheter.
When a pressure distribution over a portion or length of a catheter is detected, it is possible to determine a deformation or change in shape of the catheter. For example, if the catheter is bent or compressed towards one side, a higher pressure in the catheter body material can be measured on an inner side of the catheter (the concave side), and a lower pressure in the catheter body material can be measured on an outer side of the catheter (the convex side). Using information obtained from a catheter equipped with a pressure sensor array, it is possible to ascertain directional information related to the bending of the catheter. From this directional information, the user can obtain real-time feedback related to any deviation from the catheter's planned trajectory. Relying on this feedback, the physician may chose to remove and replace the catheter or adapt an administration plan to accommodate the actual position at which the catheter is administering the substance. The administration plan may be simulated again (with computer assistance) using a new administration point or region, and/or a new administration plan may be developed or simulated with adaptations to the original plan. Such adaptations can be changes to the substance flow rate or changes to the catheter position, such as repositioning the catheter slightly forward or slightly retracted to ensure that the substance is dispersed in the desired manner.
In one embodiment of the invention, the pressure sensor array measures a pressure profile in a catheter body, and is introduced at least partially into the material of the catheter body, e.g., in a catheter wall. Alternatively, the pressure sensor array can be used to measure an ambient pressure profile exerted on the catheter, e.g., the array can be arranged at least partially on a surface of the catheter. The pressure sensor array can be arranged on the surface of the catheter in the form of a coating or covering.
A length or portion of the catheter over which the pressure distribution is detected can be designed in several ways. The length can include an area around a single pressure sensor or an area around a number of pressure sensors.
In accordance with another embodiment of the invention, a number of pressure sensors can be arranged along a substantially longitudinal portion of the catheter. The pressure sensors can be arranged at predetermined locations along the catheter or arranged along the catheter in a uniform or otherwise predetermined spacing. Alternatively or additionally, a number of pressure sensors can be arranged in a substantially cross-sectional plane of the catheter. For example, the sensors can be distributed circumferentially on or in the catheter body. A number of pressure sensors also can be arranged at a distal end of the catheter or over a length at the distal end of the catheter.
The pressure sensors can have various configurations suited to individual treatment cases, and can include piezoelectric elements, resistive wire strain elements (e.g., strain gages), or electrical resistance elements that respond to changes in pressure or length. Interfaces or signal taps and/or signal relaying devices can be provided to relay the data ascertained by the pressure sensors to a computer (for determination of a pressure profile along the catheter's length or for simulating a dispersion in a patient). For example, an embodiment in accordance with the invention can include thin conductive paths that are printed, vapor-deposited or embedded in the catheter material and are arranged with the number of pressure sensors.
If piezoelectric pressure sensors are used, these sensors may be provided as a catheter covering, coating, or as integrated components. In such an arrangement, a measured pressure can be derived from a measured voltage, as the measured voltage at each piezoelectric pressure sensor can be directly or indirectly related to the sensor's degree of bending and/or change in pressure. The measured voltage thus enables the pressure intensity or degree of bending to be quantified.
In accordance with another embodiment of the invention, the catheter configuration can provide continuous feedback concerning a pressure profile along a surface of the catheter body. The pressure profile data obtained can be used as an input variable to deduce the pressure profile in the vicinity of a catheter tip. The pressure profile at the catheter tip may allow the determination of fluid backflow length, as can occur during infusions. The pressure profile data obtained may allow precise simulation of the actual substance dispersion, even while administering the substance. Additionally, pressure profiles observed during the infusion can be used as valuable input variables for further infusion simulations. Treatment after the catheter has been placed may be optimized by altering administering parameters and/or treatment parameters such as the flow rate, administration duration, etc. The observed results of an infusion and the results of any simulations performed may be used in the treatment optimization process.
The forgoing and other features of the invention are hereinafter discussed with reference to the figures.
A schematic representation of an exemplary catheter in accordance with the invention is shown in
In this embodiment, a plurality of pressure sensors 14A through 140 are introduced in the walls W of the catheter body 13, and the pressure sensors 14A and 14C can be seen in the representation in
In
The measurements of the pressures PA, PB, PC (or pressure profile) can be voltage or current values, for example, provided or tapped at each respective pressure sensor 14A, 148, 14C (e.g., piezoelectric pressure measuring device) 15 and provided to the computer to qualitatively determine that the catheter has been bent in the direction of the arrow (1), and quantitatively determine the extent of the bending.
When such a catheter 40 is used to administer a liquid drug into a portion of a patient's body (e.g., into a brain tissue), a so-called backflow is generated (e.g., the drug returns along the exterior of the catheter). When a backflow is generated, the drug can exert a pressure on a catheter wall 55, and this pressure decreases with the distance from a catheter tip 56, such that the pressures P41 to P44 decrease from the sensor 41 to the sensor 44. Such a pressure distribution can be measured using the sensors 41 to 44, and the distribution can provide the user information concerning the actual backflow status, in particular how far along the catheter 40 (from the catheter tip 56 towards the proximal end) the backflow to region extends. This information can be used in a new simulation of the dispersion of the drug or to adapt and/or improve an already existing simulation. Should the simulation reveal that treatment adaptations or adjustments are desired due to the actual backflow (e.g., adaptations to the flow rate and/or duration of infusion), such adaptations can be made to ensure a positive treatment result.
Various embodiments of pressure sensors have been shown in the figures (pressure sensors in the catheter wall in
Moving now to
A processor 65, such as an AMD Athlon 64® processor or an Intel Pentium lv® processor, combined with a memory 66 execute programs to perform various functions, such as data entry, numerical calculations, screen display, system setup, etc. The memory 66 may comprise several devices, including volatile and non-volatile memory components. Accordingly, the memory 66 may include, for example, random access memory (RAM), read-only memory (ROM), hard disks, floppy disks, optical disks (e.g., COs and DVDs), tapes, flash devices and/or other memory components, plus associated drives, players and/or readers for the memory devices. The processor 65 and the memory 66 are coupled using a local interface (not shown). The local interface may be, for example, a data bus with accompanying control bus, a network, or other subsystem.
The memory may form part of a storage medium for storing information, such as application data, screen information, programs, etc., part of which may be in the form of a database. The storage medium may be a hard drive, for example, or any other storage means that can retain data, including other magnetic and/or optical storage devices. A network interface card (NIC) 67 allows the computer 60 to communicate with other devices such as the plurality of electrical conductive paths 15 (e.g., printed conductive paths or thin metal fibres) or the measuring device 16.
A person having ordinary skill in the art of computer programming and applications of programming for computer systems would be able in view of the description provided herein to program a computer system 60 to operate and to carry out the functions described herein. Accordingly, details as to the specific programming code have been omitted for the sake of brevity. Also, while software in the memory 66 or in some other memory of the computer and/or server may be used to allow the system to carry out the functions and features described herein in accordance with the preferred embodiment of the invention, such functions and features also could be carried out via dedicated hardware, firmware, software, or combinations thereof, without departing from the scope of the invention.
Computer program elements of the invention may be embodied in hardware and/or in software (including firmware, resident software, micro-code, etc.). The invention may take the form of a computer program product, which can be embodied by a computer-usable or computer-readable storage medium having computer-usable or computer-readable program instructions, “code” or a “computer program” embodied in the medium for use by or in connection with the instruction execution system. In the context of this document, a computer-usable or computer-readable medium may be any medium that can contain, store, communicate, propagate, or transport the program for use by or in connection with the instruction execution system, apparatus, or device. The computer-usable or computer-readable medium may be, for example but not limited to, an electronic, magnetic, optical, electromagnetic, infrared, or semiconductor system, apparatus, device, or propagation medium such as the Internet. Note that the computer-usable or computer-readable medium could even be paper or another suitable medium upon which the program is printed, as the program can be electronically captured, via, for instance, optical scanning of the paper or other medium, then compiled, interpreted, or otherwise processed in a suitable manner. The computer program product and any software and hardware described herein form the various means for carrying out the functions of the invention in the example embodiments.
Although the invention has been shown and described with respect to a certain preferred embodiment or embodiments, it is obvious that equivalent alterations and modifications will occur to others skilled in the art upon the reading and understanding of this specification and the annexed Figures. In particular regard to the various functions performed by the above described elements (components, assemblies, devices, software, computer programs, etc.), the terms (including a reference to a “means”) used to describe such elements are intended to correspond, unless otherwise indicated, to any element which performs the specified function of the described element (i.e., that is functionally equivalent), even though not structurally equivalent to the disclosed structure which performs the function in the herein illustrated exemplary embodiment or embodiments of the invention. In addition, while a particular feature of the invention may have been described above with respect to only one or more of several illustrated embodiments, such feature may be combined with one or more other features of the other embodiments, as may be desired and advantageous for any given or particular application.
Number | Date | Country | Kind |
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07005469.7 | Mar 2007 | EP | regional |
This application claims priority of U.S. Provisional Application No. 60/908,216 filed on Mar. 27, 2007, and EP07005469 filed on Mar. 16, 2007, which are incorporated herein by reference in their entirety.
Number | Date | Country | |
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Parent | 12048647 | Mar 2008 | US |
Child | 14164667 | US |