Catheters are commonly used for a variety of infusion therapies. For example, catheters may be used for infusing therapeutic agents or fluids into a patient. Catheters may also be used for withdrawing blood from the patient. There are a variety of catheters commonly used in a medical setting, including, for example, peripherally-inserted central catheters, midline catheters, central venous catheters, dialysis catheters, and arterial catheters. A common type of catheter device includes a catheter that is over-the-needle. As its name implies, the catheter that is over-the-needle may be mounted over an introducer needle having a sharp distal tip.
The catheter and the introducer needle may be assembled so that the distal tip of the introducer needle extends beyond the distal tip of the catheter with the bevel of the needle facing up away from skin of the patient. The catheter and introducer needle are generally inserted at a shallow angle through the skin into vasculature of the patient. To verify proper placement of the introducer needle and/or the catheter in the blood vessel, a clinician generally confirms that there is “flashback” of blood in a flashback chamber of the catheter assembly. Once placement of the needle has been confirmed, the catheter may be left in place for future blood withdrawal or fluid infusion.
Although catheter indwell performance (i.e., how long the catheter can be safely left in the vasculature) has improved in recent years, there remains a significant number of complications that may develop throughout the intended dwell time of a vascular access device. These complications may include dislodgement, infiltration, extravasation, phlebitis, catheter-related infection, and loss of patency, among others.
The subject matter claimed herein is not limited to embodiments that solve any disadvantages or that operate only in environments such as those described above. Rather, this background is only provided to illustrate one example technology area where some implementations described herein may be practiced.
The present disclosure relates generally to vascular access devices, systems, and methods. In particular, the present disclosure relates to vascular access systems and methods for continuous ultrasound monitoring and integrated sensor array. A vascular access system can include a vascular access device, an ultrasound assembly, a securement dressing, a base unit, and one or more monitoring devices. The ultrasound assembly can include an ultrasound probe that can be positioned overtop a catheter that is inserted into a patient's vasculature and can be configured to allow one or more sensors to be integrated. Images from the ultrasound probe and readings from the one or more sensors can be processed to generate parameters representing status, events, or other information about the catheter. Display content including the images and the parameters can be provided to the monitoring devices.
In some embodiments, a vascular access system may include a vascular access device comprising a catheter, an ultrasound assembly comprising an ultrasound probe and a sensor array, the ultrasound probe being configured to be positioned overtop the catheter when the catheter is inserted into a patient's vasculature, and a base unit that is configured to receive images from the ultrasound probe.
In some embodiments, the ultrasound assembly may include a cable that connects the ultrasound probe and the sensor array to the base unit.
In some embodiments, the ultrasound assembly may include a wireless adapter that wirelessly connects the ultrasound probe and the sensor array to the base unit.
In some embodiments, the vascular access system may include a securement dressing that is configured to secure the ultrasound probe and the sensor array overtop the catheter.
In some embodiments, the base unit may be configured to generate display content from the images and the readings and transmit the display content to one or more monitoring devices.
In some embodiments, the base unit may be configured to generate one or more parameters from the images and the readings and to include the one or more parameters in the display content.
In some embodiments, the parameters may include catheter geometry or position information.
In some embodiments, the parameters may include one or more of catheter movement or displacement, catheter kinking, dislodgment events, extravasation, infiltration detection, thrombus development, phlebitis, patency indicators, blood flow characteristics, fluid administration flow characteristics, procedural events, or line draw tubing, probe or sensor position.
In some embodiments, a method for using a vascular access system includes inserting a catheter of a vascular access device into a patient's vasculature, positioning an ultrasound assembly that includes an ultrasound probe and a sensor array on the patient's skin overtop a portion of the catheter that is inserted into the patient's vasculature, and establishing a connection between the ultrasound assembly and a base unit to thereby enable the base unit to receive ultrasound images from the ultrasound probe and readings from the sensor array, the ultrasound images capturing the portion of the catheter that is inserted into the patient's vasculature.
In some embodiments, the connection is wired or wireless.
In some embodiments, the method may also include placing a securement dressing overtop the ultrasound probe, the sensor array, and a catheter adapter from which the catheter extends.
In some embodiments, a method for monitoring a catheter may include receiving, from an ultrasound probe that is positioned overtop a catheter that is inserted into a patient's vasculature, images that capture the catheter, receiving readings from a sensor array that is integrated with the ultrasound probe, processing the images and the readings to determine one or more parameters, and generating display content that includes the one or more parameters.
In some embodiments, processing the images and the readings to determine one or more parameters may include determining geometry or position information or the catheter, line draw tubing, a probe or a sensor.
In some embodiments, processing the images and the readings to determine one or more parameters may include detecting catheter movement or displacement.
In some embodiments, processing the images and the readings to determine one or more parameters may include detecting extravasation or infiltration.
In some embodiments, processing the images and the readings to determine one or more parameters may include detecting thrombus or phlebitis.
In some embodiments, processing the images and the readings to determine one or more parameters may include determining blood or fluid administration flow characteristics.
In some embodiments, processing the images and the readings to determine one or more parameters may include detecting a procedural event.
In some embodiments, the display content may also include at least some of the images.
In some embodiments, the one or more parameters may be determined using artificial intelligence.
It is to be understood that both the foregoing general description and the following detailed description are examples and explanatory and are not restrictive of the invention, as claimed. It should be understood that the various embodiments are not limited to the arrangements and instrumentality illustrated in the drawings. It should also be understood that the embodiments may be combined, or that other embodiments may be utilized and that structural changes, unless so claimed, may be made without departing from the scope of the various embodiments of the present invention. The following detailed description is, therefore, not to be taken in a limiting sense.
Example embodiments will be described and explained with additional specificity and detail through the use of the accompanying drawings in which:
Referring now to
Ultrasound assembly 200 may include an ultrasound probe 201, a securing mechanism 202 for securing ultrasound probe 201 to the skin and/or to catheter 102, an electrical adapter 203 by which a cable 204 is connected to ultrasound probe 201, a sensor array that includes one or more sensors 207, and a base unit 205 to which cable 204 may be connected to enable base unit 205, ultrasound probe 201, and each sensor 207 in the sensor array to communicate. In some embodiments, securing mechanism 202 may be an adhesive film on the underside of ultrasound probe 201 that may be used to adhere ultrasound probe 201 directly to a patient's skin overtop catheter 102. In some embodiments, securing mechanism 202 can be a mechanical connection between ultrasound probe 201 and catheter adapter 101 and/or catheter 102. In some embodiments, electrical adapter 203 may be separable from ultrasound probe 201, while in other embodiments, electrical adapter 203 may be integrated with ultrasound probe 201. In some embodiments, electrical adapter 203 can include one or more connectors by which sensors 207 may be selectively connected to form the sensor array. In some embodiments, one or more sensors 207 may be integrated into electrical adapter 203.
Base unit 205 can be any device that includes circuitry for communicating with ultrasound probe 201 and each sensor 207 in the sensor array. In some embodiments, base unit 205 may provide power to ultrasound probe 201 and each sensor 207. In some embodiments, base unit 205 may directly process images received from ultrasound probe 201 and readings from sensor(s) 207, while in other embodiments, base unit 205 may receive images from ultrasound probe 201 and readings from sensor(s) 207 and forward the images and/or readings to another device for processing. In some embodiments, base unit 205 may include user input elements to allow a user (e.g., a clinician and/or the patient) to control ultrasound probe 201 and/or sensor(s) 207. In some embodiments, base unit 205 may be connected to one or more other devices to allow users of the one or more other devices to control ultrasound probe 201 and/or sensor(s) 207.
Securement dressing 300 may be sized and shaped to cover and secure ultrasound probe 201, sensor(s) 207, and catheter adapter 101 against the patient's skin. For example, in some embodiments, securement dressing 300 may fully cover catheter adapter 101 and may include an opening through which extension tubing 106 extends. The underside of securement dressing 300 may be adhesive to prevent securement dressing 300 from moving once placed on the skin. In some embodiments, a transparent window 301 may be formed in securement dressing 300 to facilitate viewing catheter 102 and ultrasound probe 201.
In some embodiments, ultrasound probe 201 may be integrated into securement dressing 300. In other embodiments, ultrasound probe 201 may be separate from securement dressing 300. In such embodiments, ultrasound probe 201 may be placed overtop catheter 102 and then securement dressing 300 may be placed overtop ultrasound probe 201, sensor(s) 207, and catheter adapter 101. In any case, ultrasound probe 201 can be positioned on the patient's skin so that it is overtop the distal tip of catheter 102 when catheter 102 is inserted into the patient's vasculature. Sensor(s) 207 may also be placed overtop or near the distal tip of catheter 102.
Monitoring device(s) 400 can represent any device having a display on which images generated by ultrasound probe 201 may be displayed and/or on which information obtained from such images and/or readings from sensor(s) 207 may be displayed. As examples, monitoring device(s) 400 could include a smart phone, a tablet, a laptop, a desktop, a thin client, a television, a dedicated display device, an infusion pump, a patient vital sign monitor, an arterial monitor, an ultrasound system visual display, etc. In some embodiments, a monitoring device 400 could function as base unit 205. A monitoring device 400 could also be configured to interface with one or more separate computing systems such as a system for storing patient data.
The display also includes indicators 602a, 602b, 602c, and 602d for different parameters. In some embodiments, these parameters could be selectable. For example, in
The display further includes indicators 603a and 603b that provide information about the portion of catheter 102 that is inside vasculature 501. Indicator 603a defines the catheter to vein ratio (i.e., the ratio of the catheter's diameter to the vein's diameter at a particular location). Indicator 603b defines the purchase of catheter 102 (i.e., the length of catheter 102 that is inside vasculature 501). The display additionally includes an indicator 604 defining a patency status of catheter 102 (i.e., whether catheter 102 can safely remain within vasculature 501). Base unit 205 (or a monitoring device 400) could calculate the patency status using the images provided by ultrasound probe 201 (e.g., to detect the extent to which catheter 102 and/or vasculature 501 around catheter 102 may be blocked).
As suggested above, vascular access system 50 can be configured to monitor and/or display information relating to the status of catheter 102, vasculature 501, or the surrounding tissue and a variety of associated physiological or procedural parameters by leveraging images that are provided by ultrasound probe 201 and/or readings from sensor(s) 207 in the integrated sensor array. This information includes catheter geometry information (e.g., the catheter to vein ratio, the purchase of the catheter, flow restrictions around the catheter), catheter position information (axial position of the catheter within the vein, the position or angle of the distal tip of the catheter relative a vein wall, valve, branch or other physiological feature), catheter movement or displacement, catheter kinking, dislodgment events, extravasation, infiltration detection (e.g., by monitoring tissue surrounding vasculature 501), thrombus development, phlebitis (visual or correlated cumulative movement), patency indicators, blood flow characteristics (e.g., by using doppler to detect velocity and/or volume of blood flowing into catheter 102), fluid administration flow characteristics (e.g., by using doppler to detect velocity, volume, direction, and/or duration of fluid flow), procedural events (e.g., flush, draw, fluid administration), and/or line draw tubing, probe or sensor position in the vein or relative to the distal tip of the catheter or physiological feature (e.g., thrombus, valve, wall, branch, etc.).
Vascular access system 50 may provide a display including indicators of any of the above-mentioned information and may provide corresponding alerts. For example, base unit 205 or a monitoring device 400 may be configured to output a visual, audible, tactile, or digital alert when a condition or event is detected from the ultrasound images or sensor readings. In some embodiments, ultrasound probe 201, electrical adapter 203, cable 204, wireless adapter 206, and/or sensor(s) 207 could include one or more alerting mechanisms (e.g., LEDs, speakers, haptic units, etc.) to provide an alert.
Base unit 205 may be configured to receive ultrasound images from ultrasound probe 201 and readings from sensor(s) 207 continuously, periodically, on demand, etc. Base unit 205 may include an image processor 205a that is configured to process the ultrasound images to generate processing image data. This processed image data can be input to an artificial intelligence engine 205b that may be configured to detect and/or generate parameters from the processed image data. The parameters along with the ultrasound images can be provided to a display module 205c that can generate the display content that includes the images and the parameters. Sensor readings may also be provided to display module 205c for inclusion in the display content. In some embodiments, the sensor readings may be input to artificial intelligence engine 205b to be used, whether alone or in conjunction with the processed image data, to generate parameters.
In some embodiments, image processor 205a can be configured to determine from an image or sequence of images various status information such as catheter geometry or position information or the presence of a thrombus, kink, or other blockage. In some embodiments, artificial intelligence engine 205b can be trained to detect when parameters are present in a stream of ultrasound images and/or sensor readings. For example, artificial intelligence engine 205b could detect when a sequence of ultrasound images is indicative of a flush event, a draw event, the occurrence of extravasation, a dislodgement or movement event, etc.
All examples and conditional language recited herein are intended for pedagogical objects to aid the reader in understanding the invention and the concepts contributed by the inventor to furthering the art and are to be construed as being without limitation to such specifically recited examples and conditions. Although embodiments of the present inventions have been described in detail, it should be understood that the various changes, substitutions, and alterations could be made hereto without departing from the spirit and scope of the invention.
This application claims the benefit of U.S. Provisional Patent Application No. 63/419,969, which was filed on Oct. 27, 2022, which is incorporated herein in its entirety.
Number | Date | Country | |
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63419969 | Oct 2022 | US |