Patent Application
20160081585
The present apparatus relates to the field of manufacture of tissue sampling devices for obtaining specimens of tissue for pathological examination, and to the field of medical instrumentation devices.
When lumps, tumors, inhomogenicities, or other inclusions appear within human and other biological tissues, imaging is often insufficient to fully identify and type the inclusion. For example, imaging alone cannot provide genetic analysis of a tumor, such as may be useful in determining susceptibility to particular chemotherapy agents. It is therefore often desirable to obtain samples of the inclusion for analysis so as to determine a type and treatment susceptibility of the inclusion. Typing of inclusions is also desirable to assist in determining whether treatment is necessary; since some inclusions may be malignant, others benign, and others may be abscesses or cysts. Cysts and abscesses require quite different treatment from malignant inclusions.
Samples are often taken from inclusions using a sampling device having an outer tube and an inner probe or needle having a cutting cavity on a side. The device is inserted into the inclusion and the inner probe or needle is operated to capture a small piece of tissue from the inclusion in the cavity. The device is removed and the sample analyzed.
A problem when taking samples of inclusions, especially smaller inclusions, in tissues is that it can be difficult to ensure that the sample is taken of the inclusion and not of adjacent, likely healthy, tissue. When normal, nearby, tissue is sampled instead of the inclusion, pathological analysis of the sample will not give a correct diagnosis and may give sufficiently misleading information that no or inappropriate treatment is provided to patients instead of appropriate curative treatment. Similarly, even when a tumor is sampled, current sampling devices may capture small samples not representative of tumor as a whole, also potentially leading to inappropriate treatment. For example, a single sample might be taken from a necrotic core of a tumor, while omitting better-vascularized and rapidly-growing peripheral tissue.
In order to obtain samples from an inclusion instead of from normal tissue, imaging-guided biopsy techniques may be used. For example, Computed Tomography (CT)—guided biopsy techniques are often used with some organs. These techniques require taking multiple images of a patient to observe both the inclusion and a sampling device; the images are taken at intervals during the process of inserting and manipulating the sampling device into the inclusion. CT-guided biopsy techniques pose issues with high radiation dose from multiple CT images, and do not always provide good resolution of the inclusions, especially when the inclusions are in low density tissues surrounded by high density tissues. Further, CT machines are somewhat bulky and moderately expensive. Alternatively, Magnetic Resonance Imaging (MRI) may be used to image tissue immobilized in a frame, and the frame and images used to guide sampling. MRI machines, however, are even more expensive than CT machines, cannot be used on some patients due to metallic implants, and both tissue and inclusion may shift as a biopsy sampling device is inserted into the tissue.
WO/2002/085216 describes a biopsy sampling device adapted for Magnetic Resonance Imaging (MRI)-guided biopsies. This device has an outer shield and an inner probe, where the inner probe is electrically insulated from the outer shield by an insulation layer on the inner conductor. This device serves as a radio-frequency antenna to sense resonance during operation of an MRI system, requiring an expensive MRI machine during taking of a biopsy sample. Also, since it is intended for use within the intense magnetic field of an MRI system, it must be made of non-ferrous materials that are not affected by, and do not affect, the magnetic field of the MRI machine. This device is used to sample an organ while imaging the organ, so that samples may be obtained from particular suspicious inclusions within the organ.
It is desirable to find alternative ways of guiding biopsy sampling devices to obtain samples of tumors and other inclusions in organs; in particular it is desirable to find ways that do not require use of such an expensive and bulky device as an MRI imaging system while obtaining biopsy samples for pathological analysis. It is also desirable to sense the pathological state of the tissue in areas close to where the sample was collected to provide a more accurate estimate of disease extent, if any.
We have previously proposed a two-electrode electrical impedance imaging device.
In an embodiment, a biopsy sampling device has an inner trocar having a sharpened tip and a sampling opening; an outer needle having a central cavity, the outer needle formed of a material selected from the group consisting of insulators and metal coated with an insulator; at least a first, a second, a third, and a fourth electrical conductor formed on an insulating layer on the outer needle, the conductors forming a first, a second, a third, and a fourth electrode; an insulating coating formed over at least a central portion of the electrical conductors, an impedance measuring apparatus coupled to drive current through a first and a second selected electrode of the electrodes, and measure voltages through a third and fourth selected electrode of the electrodes to measure an impedance of tissue adjacent to the electrodes; wherein the inner trocar is adapted to be removed from the outer needle after positioning it with tip and sampling opening protruding from the end of the outer needle and thereby capture a sample in the sampling opening; and wherein the impedance measurement apparatus for measuring an alternating current impedance at at least one frequency between one hundred and ten million hertz.
In an embodiment, a method of forming an outer needle of a biopsy sampling device includes spiral-winding four conductive metal strips along an insulating tubular layer, the insulating tubular layer selected from the group consisting of an insulating catheter and an insulating tube disposed on a hollow needle. A coating is then applied to at least a portion of the metal conductive metal strips and insulating tubular layer with an insulating polymer coating, a window in the coating exposing a portion of the strips at a distal end of the tubular layer; and finished by attaching leads to a proximal end of the metal conductive strips.
Another method of forming an outer needle of a biopsy sampling device includes forming an insulating tubular layer on a hollow needle; depositing four or more parallel lines of conductive ink extending from a proximal to a distal end of the hollow needle; and curing the conductive ink. An insulating layer is then formed over the parallel lines of conductive ink in at least a central portion of the hollow needle; and conductive leads are attached to a proximal portion of the parallel lines of conductive ink.
In a study of radical prostatectomy specimens (Halter R J, Schned A R, Heaney J A, et al. Electrical impedance spectroscopy of benign and malignant prostatic tissues. Journal of Urology, 179(4):1580-1586, 2008) from fourteen men, it was found that some tumors of the prostrate have an electrical impedance (inverse of admittance) that differs from the electrical properties of surrounding, normal, tissues. In particular, at least some adenocarcinoma (malignant) tumors of the prostate were found to have electrical conductivity and permittivity (components of electrical impedance) that differed from tissues associated with benign prostate hypertrophy or normal prostate stroma at frequencies of greater than 92 KHz. Particular samples of adenocarcinoma of the prostate were found to have significantly lower conductivity (higher resistance) than normal prostate stroma.
A more recent study (Halter R J, Schned A R, Heaney J A, et al. Electrical properties of prostatic tissues: I. Single frequency admittivity properties. Journal of Urology, 182:1600-1607, 2009) has also been done. In this study of tissue samples of adenocarcinoma, benign prostatic hyperplasia, non-hyperplastic glandular tissue, and stroma samples taken from radical prostatectomy specimens from 50 men, it was shown that, in addition to significant conductivity differences between malignant and benign prostate tissue, there are significant permittivity differences. The direction and magnitude of these differences changes depending on the frequency at which the electrical properties were gauged. In particular, the permittivity of prostate cancer at 100 kHz is twice that of benign prostatic hyperplasia, non-hyperplastic glandular tissue, and normal prostatic stroma. When permittivity at 100 kHz was used to discriminate cancer from benign tissues it provided a specificity of 77% at a sensitivity level of 70%.
The electrical properties of tissue are a function of the AC frequency at which they are sampled. This frequency dependence is also a function of tissue morphology and this spectral dependence has the potential to provide enhanced clinical utility. In this same cohort of 50 men, the electrical properties were sampled at 31 logarithmically spaced frequencies ranging from 100 Hz to 100 kHz. Four multi-frequency based spectral parameters defining the recorded spectrum (σ∞, Δσ, fc, and α) using a Cole-type model were extracted from each of the electrical property spectra. The Cole-type model is similar to that described in Cole K S and Cole R H, Dispersion and absorption in dielectrics: I. Alternating current characteristics J Chem Phys, 9: 341-351, 1941. These spectral parameters are typically thought to represent:
The results of the spectral decomposition are presented in Halter R J, Schned A R, Heaney J A, et al. Electrical properties of prostatic tissues: II. Spectral admittivity properties Journal of Urology, 182:1608-1613, 2009. Significant differences between malignant and benign prostate were noted for σ∞, Δσ, and fc. Of the spectral parameters, fc provided the best cancer discrimination with a specificity of 81.5% at a sensitivity level of 70%. Spectral representations other than the Cole-model can be employed to parameterize the frequency-dependent electrical properties. These spectral parameters provide more contrast than the discrete frequency parameters (conductivity and permittivity), but require a longer acquisition time since the electrical properties at multiple frequencies must be sampled. Depending on the clinical situation either spectral or discrete frequency electrical properties could be gauged.
Finally, in Halter R J, Schned A R, Heaney J A, Hartov A. Passive bioelectrical properties for assessing high- and low-grade prostate adenocarcinoma. The Prostate, 71:1759-1767, 2011 it is shown that these electrical properties (both discrete frequency and spectral) provide enhanced discriminatory power when just high-grade prostate cancers were compared to all benign tissues. Specifically, of the 546 prostate tissue samples explored in the study, 71 were identified as cancer and 465 as benign. ∈ (at 100 kHz), Δσ, σ∞, and fc provided the most discriminatory power with area under the curves (AUCs) ranging from 0.77-0.82 for detecting any cancer, 0.72-0.8 for low-grade cancer, and increasing to 0.87-0.9 for detecting high-grade cancer. Further, ∈ (at 100 kHz), Δσ, and σ∞, provided AUCs ranging from 0.74 to 0.75 for discriminating between low- and high-grade cancers.
Similar electrical property differences have been noted between malignant and benign tissues in a number of other organs including breast, liver, kidney, and others. The sampling device herein described, including the improved multiple-electrode sampling device of
It is believed that electrical conductivity and permittivity measurements, and the Cole-Cole spectral parameters derived from them, made using a biopsy sampling device as an electrode will provide information about tissue near the sampling device at the time a sample is taken, and may be able to provide some guidance to a physician so that samples may be taken of malignant inclusions as well as surrounding tissues. The physician may insert the device into tissue while observing impedance, and take samples when the sampling device has penetrated an inclusion having impedance differing from that of most surrounding tissue.
These conductivity and permittivity measurements may also provide some additional diagnostic information regarding the extent of disease since many biopsy samples only show a small foci of cancer. These measurements may indicate if the tissue surrounding the biopsy site is diseased or not.
Our earlier biopsy sampling device 100 (
The central sampling needle trocar 102 and its coating 104 is slideably engaged within an outer hollow needle 106. In an embodiment, outer hollow needle 106 is an 18-gauge needle. Similarly, all but a tip portion of outer hollow needle 106 is coated with an outer-needle insulating, biocompatible, coating 108 adherent thereto; in an embodiment this is formed of the same polyimide or Epoxylite 6000 M material used for the coating on the sampling needle trocar 102. In an embodiment, the uninsulated tip portion of the outer needle has length about two millimeters.
In an embodiment, insulating coating 104 is less than fifty microns thick so that the central sampling needle trocar 102 of about ninety-nine hundredths inch diameter can freely slide within the outer hollow needle 106.
Since the sampling device 100 need not be used in a magnetic resonance imaging environment, in an embodiment the central sampling needle trocar 102 and outer hollow needle 106 are made of ferrous metal, such as stainless steel as known in the surgical instrument art.
Central sampling needle trocar 102 has a sample slot 110 cut into it. When the device is inserted into tissue with the sampling needle trocar fully extended, tissue —possibly including a portion of an inclusion—enters the sample slot 110. The sampling needle trocar 102 may then be withdrawn through the outer needle 106 and a cutting edge 112 separates a sample of the tissue from the tissue. The sample may be placed in a pathology sample container (not shown) and the sampling needle trocar 102 reinserted into the outer needle 106 to obtain additional samples.
Outer hollow needle 106 is fitted with a manipulation handle 120, which is adapted with mechanical keying apparatus such that, in embodiments like that of
The manipulation handle 120 is also fitted with an impedance test button 126 to trigger measurement and acquisition of electrical impedance data.
For some inclusions and tissues, the sampling device of
An improved sampling device having four electrodes is illustrated in
Formed over the outer surface of needle 204 if needle 204 is nonconductive, or over the first insulating coating if needle 204 is conductive, are four or more conductors 206, 208, 210, 212. Formed over the conductors 206, 208, 210, 212, is an outer electrically insulating, biocompatible, coating 214. A portion of needle 204 for a first distance 216 back from a first end of needle 204 is bare of outer coating 214, exposed portions of the conductors forming electrodes for contacting tissue. The electrode portions of the conductors may be plated with a biocompatible conductive material such as gold. Also bare of outer coating is a portion of needle 204 for a second distance 218 from a second end of needle 204; such that the outer insulating coating covers only a central portion of the needle.
Second end of needle 204 has an orientation key 220 that prevents rotation of the needle in a contactor ring 222, key 220 may take the form of either a notch in needle 204, or a tab formed on needle 204, or may have some other form. Contactor ring 222 has multiple electrical contacts 224, each electrical contact 224 disposed such that it makes contact with a conductor 206, 208, 210, 212 and its associated electrode. Each contact 224 is attached to a wire of a wire bundle or cable 226 for coupling to an impedance measurement apparatus 250.
Impedance measurement apparatus 250 has at least one high frequency alternating-current driver 254 that couple through cable 226 of at least one pair of the electrodes 206, 208, 210, 212, and at least one measurement unit 256 that couples through cable 226 to at least one different pair of the conductors and associated electrodes 206, 208, 210, 212. In a particular embodiment, both current driver 254 and measurement unit 256 couple to cable 226 through an electronic crossbar switching unit 252 that permits coupling of the driver to any pair of the electrodes, and of the measurement unit to any other pair of the electrodes. Both current driver 254 and measurement unit 256 operate under control of a microprocessor 258 executing firmware including machine readable instructions stored in memory 260; microprocessor 258 also drives a display 262 with information derived from impedance measurements. In some embodiments, there is also an additional “subject-ground” or external electrode 264 coupled to the measurement unit, the external electrode 264 coupled through a conductive gel to a common point on the subject's skin. In an embodiment, the impedance measurements are derived by driving a pair of electrodes, such as electrodes 206, 208, while measuring voltages at a different pair of electrodes, such as electrodes 210, 212.
Particular embodiments may have other numbers of electrodes than four, for example an eight-electrode embodiment of the needle is illustrated in cross-section
In an eight-electrode embodiment, electrodes are scanned, by altering a configuration of switching unit 252 under control of processor 258 according to the following table, where electrodes are indicated by reference number in the figures, a “D” indicates electrodes driven, an “M” indicates electrodes measured, the near-field table portion being used to determine tissue impedance of tissue adjacent to the biopsy sampling device, and the distant-field table portion being used in conjunction with near-field results to determine tissue impedance of tissue a little bit further from the biopsy sampling device:
In an embodiment having an eight-electrode tube and near versus far impedance discrimination, tissue impedance determined by processor 258 are displayed in a sectored display, with eight near and eight far segments, as illustrated in
A system estimates the electrical property distribution around the needle tip using electrical impedance tomography-based algorithms. These algorithms couple together the impedance measurements recorded from all electrode configurations to estimate the spatial distribution of conductivity and permittivity around the needle tip. A map of the electrical properties is provided, which may be displayed as a pie-diagram as illustrated in
In an alternative embodiment having six or more electrodes, a first pair of electrodes is coupled to a current-driven stimulus source, while voltage measurements are made at more than two other electrodes to estimate electrical properties both as near-probe impedances, and as far-from-probe impedances simultaneously, as illustrated in
Far-from-probe properties are displayed to the clinician as outer regions 504 on the pie-diagram as illustrated in
In a first method of operation, as illustrated in
In embodiments using multiple frequencies, four multi-frequency based spectral parameters defining the recorded spectrum (σ∞, Δσ, fc, and α) using the Cole-type model are then extracted from the recorded impedance measurements. Other spectral decompositions methods can also be used including Warbug model, discrete component model, constant-phase element models, or general polynomial-based curve fitting models. The sampling needle trocar 202 is then withdrawn 306 to excise and remove a sample from the organ for pathological analysis. Since the stimulus current flows through a radius of about 2½ millimeters around the tip of sampling device 102 several cubic millimeters of the organ are sampled. The measured conductivity, permittivity, and spectral impedance properties give information not just of the sample, but of a region near the sample that may or may not contain possible tumors. If 310 all desired samples have not yet been taken, the trocar 202 is reinserted 308 and the sampling device tip advanced further or otherwise repositioned to obtain additional samples; as an example additional samples might be collected following a predetermined, 12-point, pattern as is often used for prostate biopsy.
Once 310 all desired samples have been taken, the measured pattern of conductivity, permittivity, and spectral parameters, measured within the organ is compared 312 to patterns of conductivity, permittivity, and spectral parameters of both normal and diseased organs. Pathological examination of samples is also performed 314. Both information from the pattern of impedance and spectral parameters, and from the pathological examinations are used to establish 316 a diagnosis and treatment plan. In this method, the impedance and spectral parameter measurements give additional information about tissue characteristics surrounding an analyzed sample that is useful for diagnosis 316, and in particular useful for estimating tumor size and aggressiveness.
The estimated tumor size and aggressiveness is critical to tumor staging; tumor staging in turn is of great interest in devising a treatment plan. In particular, large rapidly growing tumors may require radical prostatectomy, while smaller tumors are more likely to be treated by less invasive techniques such as transurethral resection or active surveillance.
In an alternative method of operation, as illustrated in
Monitored 404 measurements are averaged and filtered over a short period of time to avoid artifacts, in embodiments using multiple frequencies the spectral parameters are extracted, and selected impedance measurements and/or spectral parameters for near and far impedance in each direction around the sampling device are displayed to an operator. The measurements are repeated for additional combinations of electrodes according to table 1 and the display, illustrated in
Once the sampling device is positioned within the area of suspect impedance, impedance is measured 409 and recorded, and the center trocar 202 of the sampling device is then withdrawn 410 to obtain a biopsy sample of the suspected inclusion. Once the sample is placed in a sample container, the center trocar 202 is reinserted 412 into the sampling device and advancement of the sampling device is then continued towards other locations, such as predetermined locations or locations guided by other imaging methods, within the organ from which samples are to be taken.
In embodiments, both samples according to predetermined locations in the organ and samples according to impedance changes may be taken and submitted for pathological analysis for diagnostic purposes. Information from pathological analysis of the samples, and information from comparing a measured pattern of impedance and spectral parameters at the sampling points to known impedance patterns and spectral parameters of normal and diseased organs, are used in establishing 316, 418 a diagnosis and treatment plan.
In an alternative embodiment of the method, after positioning the sampling slot of the trocar 202 of the device 200 by advancing it into an area of interest in the organ, the outer needle 204 is advanced to excise a sample since cutting by trocar 202 occurs by relative motion of needle and trocar. The trocar 202 is then removed to transfer the sample to a pathology sample container and reinserted into the outer needle 204 before advancing the device to any additional sampling points.
In some embodiments, should impedance measurements indicate a high likelihood of malignancy, treatment may be offered 416 immediately post-biopsy to prevent tissue dislodged by device 200 from forming metastases. Whether or not immediate treatment was offered, the biopsy samples are analyzed and, if necessary, a treatment plan is established 418.
It is expected that multiple-electrode (defined as those having more than two electrodes all located on the sampling device) biopsy sampling devices may have configurations of electrodes other than the multiple electrodes spaced radially around a circumference of the outer needle as illustrated in
In another alternative embodiment, as illustrated in
Yet another alternative outer needle 700 is illustrated in
An outer needle as herein described may be fabricated in several ways. In an embodiment, outer needle 600, 200, 650, is fabricated by forming a printed circuit having electrodes on a thin, insulating, substrate, the substrate is then wrapped about a stainless-steel needle and cemented in place, the substrate becoming the first insulating coating over the conductive needle core previously described with reference to
It is expected that the electrical impedance measurement and monitoring described herein can be added to other biopsy sampling devices that may be known in the art of Medicine.
In a particular embodiment, outer needle of the biopsy sampling device is more than five centimeter long, yet less than two millimeters in outer diameter. We have devised two ways to make the device: 1) using a stylet to print a thin trace of conductive ink along the length of the needle followed by optional electroplating and insulation with a polymer coating and 2) embedding a set of 4 or more coiled conductors within a catheter that is then positioned over the needle shaft with a window cut into the catheter to enable the inner conductors to communicate with tissue surrounding the needle/catheter assembly.
Conductive Ink Fabrication
In order to lay traces down along the shaft of a longer than five centimeters 18 gauge (approximately 0.05 inch diameter) hypodermic needle of under two millimeters in diameter we use the following process 800 (
a. The needle is clamped 802 in a single axis stage.
b. An insulating layer is placed or formed 804 on the needle. In an embodiment, the needle is insulated by either placing a 0.05+ inch inner diameter formed of polyimide or other insulating polymer, thin-walled, in an embodiment with wall thickness about 0.001 inch, is placed over the needle. In alternative embodiments, the needle is coated with a nonconductive polymer such as parylene.
c. A conductive line is drawn 806 on the needle by using a stylus or “pen tip” to deposit a silver-based conductive ink such as DuPont 5000 Silver Conductor, or LOCTITE M 4100 E&C. In forming the lines, the pen tip is placed in contact with the polyimide and the needle is translated while the stylus remains fixed in placed (or the stylus is translated with the needle fixed in place) while conductive ink flows onto the polyimide tubing
d. The needle is rotated 808 and additional ink traces are applied.
e. Once 4 or more traces are applied on the insulating layer, the ink is cured 810 with an appropriate curing technique for the ink used (i.e. IR, UV, thermal, or similar), and an optional copper plating is applied 812 to the conductive ink by electroplating.
f. The traces are insulated 814 with either a second polyimide tube or a coating of parylene or other polymer deposited over the middle section of the traces—leaving both the proximal and distal ends exposed.
g. A distal end of the needle is optionally then gold-plated to decrease tissue/electrode impedance, or other surface finish can be applied if needed.
h. Conducting wires are then attached 816 by soldering, or electrically connected, using conductive epoxy or silver paste, to the exposed traces on the proximal ends; these wires interface to the electrical hardware.
In an alternative embodiment requiring the ink has a low viscosity and tends to “run,” a mask with a cutout running the length of the needle is positioned above the needle—the ink is then run along the mask with only the ink passing through the cutout actually interacting with the needle and forming a line, the needle is then rotated for each additional line.
Conductor-Embedded Catheter Fabrication
In order to produce 850 (
While the forgoing has been particularly shown and described with reference to particular embodiments thereof, it will be understood by those skilled in the art that various other changes in the form and details may be made without departing from the spirit hereof. It is to be understood that various changes may be made in adapting the description to different embodiments without departing from the broader concepts disclosed herein and comprehended by the claims that follow.
This application is a continuation-in-part of U.S. patent application Ser. No. 13/958,121 filed 2 Aug. 2013. The contents of the aforementioned patent application are incorporated herein by reference.
The present invention was made with government support under grant W81XH-07-1-0104 awarded by the US Department of Defense Congressionally Directed Medical Research Program. The present invention was made with government support under Grant Number 1R41CA192502-01A1 awarded by the National Institutes of Health. The United States Government has certain rights in the herein described invention.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 13958121 | Aug 2013 | US |
| Child | 14955016 | US |
