Patent Application
20140100524
1. Field of the Invention
The present invention is directed to medical imaging and more particularly to a catheter discrimination and guidance system for an infrared detector and image display system to assist clinicians in performing intravenous and other vein access procedures.
2. Description of the Related Art
Intravenous (IV) catheters are used to access veins for blood draw, and for fluid delivery. There are very few techniques for assisting clinicians in verifying a positive cannulation of a vein. The standard technique for peripheral IV access involves using a tourniquet to engorge veins, followed by palpation to identify a suitable vein and finally insertion of the catheter needle. Clinicians must rely on “feel” when inserting the needle into a vein and on observing blood flashback to ascertain when the catheter has successfully cannulated the vein. Statistics indicate that this trial-and-error process requires an average of 2.4 attempts and up to 20 min for a clinician to successfully cannulate a vein. Aside from the increased pain and anxiety experienced by patients, there are real costs associated with IV care. Patient throughput, nurse time, consumables, and increased infection rates all contribute to increased medical care costs for hospitals and governments.
Systems have been developed for assisting in venous access and overcoming the disadvantages of traditional trial-and-error techniques. One such system is the VeinViewer® infrared detector and image projector manufactured and sold by Christie Medical Holdings, Inc., a division of Christie Digital Systems, Inc., which is described in U.S. Pat. No. 7,239,909, and US Publication Nos. 2010051808, 20070158569 and 20060122515, the contents of which are incorporated herein by reference.
According to the VeinViewer® system, diffuse infrared light is used to image vasculature below the surface of the skin, and the image is then projected onto the skin to reveal the location of the vasculature. The vasculature image is projected in exactly the same anatomical location as the vasculature itself, and in its three-dimensional context (skin of patient) making it very easy to see the vessels. Also, since there is no transducer to hold, the clinician's hands are free to perform venous access.
Although the VeinViewer® system has been widely adopted by hospitals, its application has been somewhat limited by the fact that it cannot detect a successful cannulation event. Ultrasound is the only current visualization technology that can show if a successful cannulation has occurred. Ultrasound is commonly used for deep vein access such as PICC lines and CVC's, but is not typically used for peripheral veins.
Prior art relevant to the invention includes literature on the theory and mathematical modeling of the opto-characteristics of different materials, such as disclosed in:
Also relevant to the present invention are prior art needle guidance systems, such as disclosed in:
It is an object of an aspect of this specification to set forth a system for improving intravenous and other vein access procedures by guiding clinicians in achieving optimal intravenous (IV) placement while minimizing infiltration and extravasations effects.
According to the present invention, a catheter discrimination and guidance system is provided that detects the catheter and its related parameters from an acquired infrared image and uses these parameters to direct a clinician during the vein access procedure.
These together with other aspects and advantages which will be subsequently apparent, reside in the details of construction and operation as more fully hereinafter described and claimed, reference being had to the accompanying drawings forming a part hereof, wherein like numerals refer to like parts throughout.
a is a schematic representation of the needle-tissue-vein interfaces and related physical parameters, and
Prior to describing the principles of the present invention, it is helpful to briefly review the theory behind optical vascular imaging. Photon scattering in soft tissue is dependent on photon wavelength and tissue composition. Projecting an incident beam of diffuse light on tissue results partly in backscattered light that is detectable at the surface of the tissue, and forward-scattered light that travels through the tissue. The forward scattered light interacts with scattering sites within the tissue and loses its intensity due to elastic and inelastic scattering phenomena. The inelastic phenomenon is also known as absorption. The intensity of the backscattered light is dependent on the type of tissue at the point of observation.
Turning to
According to the known Kubelka-Munk theory of reflectance, a relationship exists, specifically a paired differential equation, between the incident and backscattered light and the tissue thickness. Solutions to the equation exist for different boundary conditions.
In order to estimate the depth xv, under the skin, of a vein 100-3, three boundary conditions must be considered: (1) infinite tissue thickness, (2) tissue—vein boundary, and (3) needle—vein boundary.
Having regard to the first boundary condition, if the tissue is very thick (i.e. infinite tissue thickness), the incident beam 100-1 loses all of its intensity through scattering. Utilizing this condition, one can solve for all of the involved unknown parameters except for the scattering factor of the tissue.
At the tissue-vein boundary, almost all of the incident beam intensity is absorbed through elastic/inelastic scattering from blood within the vein, resulting in negligible reflectance. For a finite tissue thickness, there is no reflection at the exterior end medium (i.e. air). Using this condition, an equation can be arrived at for depth of the vein that is also irrespective of the tissue scattering parameter; however, it relies on the known thickness of the tissue where the total light absorption occurs.
Most light is absorbed within centimeters of the tissue thickness but this thickness value is unknown and its evaluation is not practical during performance of a clinical routine, due to various human tissue variants. This thickness dependency can be resolved using a predefined needle specific light reflectance over the skin and the measureable physical depth of the needle tip below the skin during the procedure. The needle depth can be measured for a standard catheter needle size through a procedure described in greater detail below.
In order to determine the needle-vein intersection (i.e. when the needle tip touches the vein surface, consecutive values of needle reflectance below the skin are registered during the catheter insertion process. It will be noted that, due to the high absorption of blood, the same needle reflectance values are expected to be detected at the needle tip (observed over the skin) while it is in the vein. Accordingly, needle-vein intersection occurs when the observed needle tip reflectance becomes equal to vein reflectance.
Turning to
The exemplary catheter system 210 depicted in
IR light 225 from IR imager/projector 200-5 illuminates the patient's soft tissue 215 with light in the range of 850+/−40 nm, which is mainly absorbed by blood (haemoglobin) in the vein 220. The unabsorbed light 230 is reflected back and is detected by the IR imager/projector 200-5. The reflected image is processed by the image processing subunit 200-3, and then re-projected on the patient's skin in real-time to show the location of vein 220 beneath the patient's skin. The IR imager/projector 200-5 preferably includes a cut-off filter and a polarizer to differentiate reflected imaging light from background IR light in the environment.
With reference to
The catheter outline is detected and the device observed catheter length is determined at step 310. The catheter length is the observed distance between the catheter tip to the catheter housing, which are discriminated accordingly. The detected length value is used to calculate the insertion angle of the needle and locate the tip of the needle as it is inserted into the skin and as it penetrates the vein. Since the system 200 captures a two dimensional view of a scene, the actual length of the catheter 210-2 is different from its device observed value but is related to it by the angle it makes with the skin surface and can be determined using perpendicular projection, as described below. The maximum observed length is the actual length of the catheter and can be estimated according to a calibration process described below. Finally, the location of the catheter start and end points are determined (i.e. the point that connects the catheter to the catheter housing is the start point and the free end of the catheter is the end point), as discussed below.
Since catheters are gauged according to their expected usage and come in various sizes, the calibration process permits calculation of the length for various catheter sizes without requiring any external predefined input from the user. The actual length of the catheter 210 is closely related to the length value as observed by the IR imager/projector 200-5 by the angle it makes with the skin surface at the point of vein access. Therefore, in use the clinician first follows a calibration process by which the catheter is positioned under the IR imager/projector 200-5 of system 200 and is rotated through small positive and negative angles relative to the skin surface, passing through zero degrees, in order to register and measure the actual catheter length, illustrated schematically in
The system 200-4 must discriminate the catheter from its environment. The catheter discrimination process is slightly different depending on whether the catheter is translucent or opaque. In either case, multi-resolution analysis is performed to expedite the catheter and needle discrimination processes, whereby captured images are first reduced to a lower resolution and an initial analysis is performed. Later the remaining analyses (e.g. frequency filtering, length and angle measurements) are performed using the original-size images.
Translucent catheters are composed of material that is permeable to infrared light and accordingly not visible to the IR imager/projector 200-5. However, by using a physical polarizer with the IR imager/projector 200-5, the catheter appears as a solid black line of measurable thickness in the captured image (
An opaque catheter has different characteristics than a translucent catheter, and is visible in the infrared wavelength region. The opaque catheter covers the metallic needle and totally absorbs the infrared light. The detection process for opaque catheters is similar to the process for translucent catheters discussed above, but the seed point is chosen as the point having maximum intensity value (rather than minimum intensity value). A small length of the needle (about 1-2 mm) is uncovered at the tip of the catheter and its length is measured using the procedure described earlier for translucent catheters.
The image is later thresholded about the intensity of the seed point, thereby allowing a range of intensities. However, as a result of catheter positioning, angle, absorption and other factors involving scattering, it is not possible through the use of simple thresholding to obtain a solid line representing the catheter. Therefore, as shown in
As an alternative to catheter discrimination based on detecting the location of the catheter start point at the catheter housing 210-1, opto-genic catheters may be used. This alternative is especially useful with non-standard catheters whose length does not fit within the field of view of the system 200. Specifically, opto-genic catheters may be provided with optical markings that can be detected using image processing algorithms and used to estimate the visible length of the catheter (i.e. from the marking to the catheter tip). Opto-genic markings can be made using an etching process on the catheter to change its optical characteristics (e.g. specular reflection). The markings do not hamper the hygienic or normal clinical functionalities of the catheters.
Where opto-genic catheters are not available, a clip-on marker 210-4 may be provided, according to an additional aspect of the invention, to assist in discriminating different catheter types that are not compatible the preferred catheter discrimination and guidance system 200 (i.e. the Vein Viewer system, discussed above). The marker 210-4 is attached to or removed from the catheter housing 210-1 by a simple clip-on arrangement. The length and end point features of the marker are identified using the image processing algorithms already set forth herein, followed by the angle measurement and calibration process set forth herein.
The marker 210-4 is designed so as not to hamper the normal functionality of the catheter 210. The markings can include security-enabled, manufacturer-specific features that can be identified using the image processing routines set forth herein.
With reference to
Although the marker set forth herein is described as being of added clip-on design, a person of skill in the art will understand that the marker can be molded in as part of the catheter housing.
Returning to
At this stage, the required catheter-related values (e.g. its length, angle and tip) have been determined and the IR imager/projector 200-5 then projects images and information onto the skin in order to assist the clinician in visualizing the catheter insertion process while the catheter is partly in the skin and out of view (step 340) and informs the user when the catheter and needle enter the vein (step 350), as discussed further below.
Finally, at step 360, the IR imager/projector 200-5 generates and projects a map (location and depth) of veins in close proximity to the vein access point, irrespective of the type and color of the skin. No tissue characteristic parameters have to be known a priori.
The critical vein depth value can be evaluated, as described previously, and the catheter positioning angle can be calculated from the catheter observed length based on perpendicular image acquisition and projection:
l′
c
=l
c.cos(θ) (1.1)
where l′c is the value observed at the IR imager/projector 200-5. At the start of the clinical procedure, the catheter tip is at the skin surface of the tissue at point a (the catheter—skin access point). When the tip penetrates the skin to the vein surface, it travels from point a to point b (the needle—vein access point) on the skin surface: Where point b can be calculated using the procedure explained earlier using the needle reflectance and its tip location.
Thus, at the vein surface:
|{right arrow over (b)}−{right arrow over (a)}|=|{right arrow over (ab)}|=x
v.tan(θ) (1.2)
Thus, according to step 360, the system 200-4 causes IR imager/projector 200-5 to project the points a and b on the skin surface (e.g. using high intensity coloured dots) so that, the clinician is guided to adjust the direction of the catheter from the insertion point a in a straight line following the vein to point b, as shown in the inset portion at the top right of
The present invention has been described with respect to the forgoing embodiments and variations. Other embodiments and variations are possible. For example, although the preferred embodiment is discussed in connection with an infrared detector and image projector system 200, such as the VeinViewer® system manufactured and sold by Christie Medical Holdings, Inc., the principles of catheter discrimination and guidance may be implemented in HUD (head's up display) or other types of vascular imaging systems.
The many features and advantages of the invention are apparent from the detailed specification and, thus, it is intended by the appended claims to cover all such features and advantages of the invention that fall within the true spirit and scope of the invention. Further, since numerous modifications and changes will readily occur to those skilled in the art, it is not desired to limit the invention to the exact construction and operation illustrated and described, and accordingly all suitable modifications and equivalents may be resorted to, falling within the scope of the claims.
