The invention relates to medical devices and, in particular to devices for measuring physiological information. Particular embodiments of the invention provide devices for assessing conditions of the prostate gland and/or associated tissues.
Prostate cancer and other prostate pathologies affect a large proportion of men. Current techniques for evaluating the condition of the prostate include digital rectal examination and blood tests for prostate specific antigen (PSA). The efficacy of digital rectal examination depends on the skill and sensitivity of the physician performing the procedure.
Near Infrared Spectroscopy (“NIRS”) is a technique which involves emitting near infrared (“NIR”) light and receiving the NIR light after it has passed through a tissue or other medium of interest. NIRS can be applied to study and monitor biochemical compounds in the body. Emitted NIR light penetrates skin and other tissues and some of it is absorbed by biochemical compounds which have an absorption spectrum in the NIR region. NIR light which is not absorbed is scattered. Each biochemical compound has a different absorption spectrum. It is possible to estimate the concentration of biochemical compounds in the tissues by measuring characteristics of NIR light that has been detected after it has passed through the tissues.
There is a need for practical and cost-effective systems that provide physicians and other medical practitioners with additional information regarding conditions that may affect the health of their patients. There is a need for practical and cost-effective systems capable of providing physicians with more information regarding the prostate and associated tissues.
Aspects of the invention and features of specific embodiments of the invention are described below
According to one aspect of the invention, an apparatus for evaluating one or more physiological conditions of a subject's tissue is provided. The apparatus has one or more sensors. Support means support the one or more sensors removably in place over a member insertable in a body cavity of the subject. A control unit is operatively connected to the one or more sensors. When a user places the support means supporting the one or more sensors over the member in the body cavity in proximity to the subject's tissue, the one or more sensors can sense and transmit to the control unit information relevant to the physiological condition of the subject's tissue.
According to another aspect of the invention, an apparatus for evaluating one or more physiological conditions of a subject's prostate and/or associated tissue is provided. The apparatus has a sleeve dimensioned to be worn on a finger of a user. The sleeve comprising a proximal end open to receive the user's finger. One or more sensors are supported by the sleeve. A control unit is operatively connected to the one or more sensors. When the user places the one or more sensors supported by the sleeve on the user's finger in proximity to the subject's prostate, the one or more sensors can sense and transmit to the control unit information relevant to the one or more physiological conditions of the subject's prostate and/or associated tissue.
According to a further aspect of the invention, an apparatus for evaluating one or more physiological conditions of a subject's prostate and/or associated tissue is provided. The apparatus has a sleeve dimensioned to be fitted over an anal ultrasound probe. The sleeve has a proximal end open to receive the anal ultrasound probe. One or more sensors are supported by the sleeve. A control unit is operatively connected to the one or more sensors. When a user places the one or more sensors supported by the sleeve fitted over the anal ultrasound probe in proximity to the subject's prostate, the one or more sensors can sense and transmit to the control unit information relevant to the one or more physiological conditions of the subject's prostate and/or associated tissue.
According to yet another aspect of the invention, an apparatus for evaluating one or more physiological conditions of a subject's prostate and/or associated tissue. The apparatus comprises an anal probe which supports a plurality of ultrasonic transducers and a plurality of near infrared (NIR) light sensors. An ultrasound control unit is operatively connected to the ultrasonic transducers, and an NIR light sensor control unit is operatively connected to the NIR light sensors. When a user places the probe in proximity to the subject's prostate, the ultrasonic transducers can obtain and transmit to the ultrasound control unit information for generating an ultrasound image of the subject's prostate and/or associated tissue, and the NIR light sensors can sense and transmit to the NIR light sensor control unit information relevant to the one or more physiological conditions of the subject's prostate and/or associated tissue corresponding to the ultrasound image.
According to another aspect of the invention, a method for evaluating one or more physiological conditions of a subject's tissue is provided. The method includes the steps of:
According to a further aspect of the invention, a method for evaluating one or more physiological conditions of a subject's prostate and/or associated tissue is provided. The method includes the steps of:
According to yet another aspect of the invention, a method for evaluating one or more physiological conditions of a subject's prostate and/or associated tissue is provided. The method includes the steps of:
According to another aspect of the invention, a method for evaluating one or more physiological conditions of a subject's prostate and/or associated tissue is provided. The method includes the steps of:
The accompanying drawings illustrate non-limiting embodiments of the invention.
Throughout the following description, specific details are set forth in order to provide a more thorough understanding of the invention. However, the invention may be practiced without these particulars. In other instances, well known elements have not been shown or described in detail to avoid unnecessarily obscuring the invention. Accordingly, the specification and drawings are to be regarded in an illustrative, rather than a restrictive, sense.
This invention provides apparatus for evaluating physiological conditions of individuals. The apparatus comprises one or more sensors that can be removably supported in place by support means over a member insertable in a body cavity of the subject. The support means may be a flexible sleeve. The insertable member may be a probe or a physician's finger. The sensors can then be placed in proximity to tissues of a subject to permit the sensors to detect one or more physiological characteristics of the tissues. Some embodiments provide an array of sensors capable of measuring information about the tissues of the subject that can be processed to generate an image of the tissues or an image of the variation of some characteristic of the tissues with position.
Sleeve 12 is dimensioned to be worn on a physician's finger. Sleeve 12 may comprise an elastic tube which fits smoothly around a physician's finger and supports sensor array 15. One end of sleeve 12 is open to receive the physician's finger. The other end of sleeve 12 may be closed, like the finger of a glove, or open.
Sensors 14 may include one or more of the following types of sensor, for example:
Sensors 14 may be arranged densely enough to provide data that can be processed to provide “images” of the properties that they detect. For example, sensors 14 may be arranged to have a spacing between adjacent sensors 14 of about 1½ mm or less. In some embodiments, sensors 14 have a spacing between nearest-neighbors of about ¾ mm or less, or ½ mm or less.
In some embodiments, sensors 14 include sensors that detect signals indicative of physiological conditions at a plurality of different distances from sensors 14. Such embodiments may permit the acquisition of data from which three-dimensional images may be generated (or for which parameters somehow indicative of one or more physiological conditions can be measured at points of a three-dimensional point-cloud).
Preferably, sleeve 12 and array 15 are flexible and adapt to the contours of Finger F such that the physician retains some “feel” for the surrounding tissues even while wearing sleeve 12. In some embodiments, as shown for example in
Light sources 25 emit radiation of two or more wavelengths (typically NIRS uses light in two or three narrow wavelength bands). In the illustrated embodiment, light sources comprise optical fibers 27 that carry light from laser diodes or other suitable sources of light in controller 16. In the illustrated embodiment there are three laser diodes 29A, 29B and 29C. The multiple wavelengths may be combined and carried in a single set of optical fibers 27, as illustrated or separate sets of optical fibers may be provided for different wavelengths.
In the illustrated embodiment, sensors 14 comprise optical fibers 32 that receive light and carry the light to photo diodes, phototransistors, or other light detectors 34 that generate electrical signals indicative of the intensity of light incident at the distal ends of optical fibers 32. In this embodiment, sensor assembly 11 does not need to include any active electronic devices.
In other embodiments, sensors 14 comprise active electronic devices mounted on or to sleeve 12 that generate signals indicative of the intensity of light incident upon them.
In some embodiments, each sensor 14 is paired with a light source 25. In some embodiments, a light source 25 is associated with a plurality of sensors 14. In some such embodiments, the plurality of sensors 14 are spaced apart from the corresponding light source by a plurality of different distances.
In some embodiments, there are two or more sets of light sources 25 that are independently controllable or differently modulated (so that light from different sets of light sources 25 can be distinguished). In such embodiments, measurements at various depths in the subject's tissues may be achieved by detecting at a sensor 14 light originating from different light sources 25 at different distances from the sensor 14.
It is desirable to prevent sensors 14 from picking up signals relating to tissues in finger F. Where sensors 14 sense light, this may be accomplished, for example, by one or more of:
It is not mandatory that light sources 25 be on assembly 11. Instead, light sources 25 may be supported on an element independent of assembly 11.
Control unit 16 may comprise a display 50 on which operational information relating to system 10 and/or data (including images in some embodiments) acquired by system 10 may be displayed. A data store 52 permits storage of data acquired from a subject (and/or information derived from that data). In the illustrated embodiment, control unit 16 comprises a microprocessor 55 executing stored instructions 56 that cause microprocessor 55 to control the operation of apparatus 10 by way of suitable interfaces 58.
Where sensors 14 are applied to detect light from suitable light sources to perform NIRS, the signals output by sensors 14 may be processed to yield values indicative of the concentrations of bio-compounds such as:
Total Haemoglobin (HbTot);
Oxygenated Haemoglobin (HbO2);
Non-oxygenated haemoglobin (Hb);
Cytochrome C Oxydase (Cyt);
Myoglobin (Mb); and,
other chromophores;
at points within the subject's tissues. In some embodiments, the signals output by sensors 14 may be processed to detect the presence of and/or measure concentrations of exogenous markers or other chemical agents that may be introduced into the tissues of subject S for the purpose of imaging or the detection of certain conditions. In some embodiments the signals output by sensors 14 are processed to provide indications of blood flow or blood volume at locations within the subject's tissues. Such measures can be useful in the diagnosis of conditions which involve increased vascularization or increased metabolic activity in the vicinity of tumors or other lesions.
Apparatus and methods as described herein may be applied to detect conditions such as cancers, tumors, increased vascularity or the like and/or to differentiate tissues affected by such conditions from normal tissues and/or to locate tumors, areas of increased vascularity or the like.
Transrectal ultrasound imaging may also be applied to study the prostate. An example system for transrectal ultrasound imaging is described in Fenster, A. et al., Three-dimensional ultrasound imaging systems for prostate cancer diagnosis and treatment Instrumentation & Measurement Magazine, IEEE Vol. 1, No. 4, December 1998, pp. 32-35. An assembly 11 as described above may be carried on an anal ultrasound probe to provide simultaneous ultrasound imaging of the prostate and surrounding tissues and NIRS studies of the prostate.
NIRS system 64 comprises a sleeve 70 which supports light sources 25 and sensors 14 as described above. Sleeve 70 slips over anal probe 65. Sleeve 70 is substantially acoustically transparent so that it does not interfere with ultrasound imaging. Water or a suitable acoustic gel 71 may be provided between sleeve 70 and anal probe 65 to facilitate clean transmission of acoustic signals between anal probe 65 and the subject's tissues. Sleeve 70 may comprise a flexible material or may be rigid or semi-rigid.
A controller 16 as described above drives light sources 25 to emit light of wavelengths suitable for detecting one or more biochemical compounds of interest by NIRS and processes signals received from sensors 14.
Sleeve 70 may be constructed to permit it to be aligned in a known way with anal ultrasound probe 65. For example:
Synergies may be obtained by providing an ultrasound probe which includes sensors 14 or both sensors 14 and light sources 25 for use in NIRS.
A pair made up of a NIRS light source and detector is most sensitive to the presence of bio-compounds at a location in the subject's tissues that is between the light source and detector and is at a depth depending on the spacing between the light source and detector. The size, shape and precise location of the location at which a light-source-sensor pair is most sensitive is determined by a range of factors including the light emission pattern of the light source 25 and any variations in sensitivity with direction for sensor 14.
In some embodiments display 90 includes elements of a graphical user interface GUI. In such embodiments, a user may be able to identify a location of interest in ultrasound image 92, for example by positioning a cursor using a pointing device, touching on a touch-sensitive part of display 90 or the like. In response to identification of a location of interest, controller 16 may identify one or more light-source-sensor pairs that yield information relevant to the identified location. Control unit 16 then computes one or more parameter values (such as estimated concentrations of one or more bio-compounds) from outputs corresponding to the identified light-source-sensor pairs. The parameter values corresponding to the selected location may be displayed on display 90. In the illustrated embodiment, a graph 96 illustrates variation in a parameter (for example, [HbTot]) with time for the currently-selected location.
As shown in
In some embodiments, controller 16 is configured to determine a parameter value for a plurality of different regions within a subject's tissues and to determine a degree of variation in the resulting set of parameter values. Controller 16 may store and/or display a graph or a value indicative of the degree of variation, non-uniformity or the like of values in the set of parameter values.
Where a component (e.g. a sensor, cable, sleeve, software module, processor, assembly, device, circuit, etc.) is referred to above, unless otherwise indicated, reference to that component (including a reference to a “means”) should be interpreted as including as equivalents of that component any component which performs the function of the described component (i.e., that is functionally equivalent), including components which are not structurally equivalent to the disclosed structure which performs the function in the illustrated exemplary embodiments of the invention.
As will be apparent to those skilled in the art in the light of the foregoing disclosure, many alterations and modifications are possible in the practice of this invention without departing from the spirit or scope thereof. For example:
Instead of a sleeve 12, other support means may be provided for supporting one or more sensors on a user's finger or an anal probe. For example, sensors 14 may be disposed on a self-adhesive patch that can be stuck onto the user's finger; sensors 14 may be held in place by one or more elastic rings or bands; sensors 14 may be disposed on one or more fingers of a glove; or the like.
apparatus as described herein may be applied to trans-vaginal probing. Catheter 40 may be a vaginal catheter in such an application.
This application claims priority from U.S. patent application No. 61/033,737 filed 4 Mar. 2008 entitled DIGITALLY-SUPPORTED PHYSIOLOGICAL SENSORS and U.S. patent application No. 60/915,399 filed 1 May 2007 entitled DIGITALLY-SUPPORTED PHYSIOLOGICAL SENSORS. For purposes of the United States of America, this application claims the benefit under 35 U.S.C. §119 of U.S. patent application No. 61/033,737 filed 4 Mar. 2008 entitled DIGITALLY-SUPPORTED PHYSIOLOGICAL SENSORS and U.S. patent application No. 60/915,399 filed 1 May 2007 entitled DIGITALLY-SUPPORTED PHYSIOLOGICAL SENSORS, both of which are hereby incorporated herein by reference.
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/CA08/00821 | 5/1/2008 | WO | 00 | 10/30/2009 |
| Number | Date | Country | |
|---|---|---|---|
| 60915399 | May 2007 | US | |
| 61033737 | Mar 2008 | US |