APPARATUSES AND METHODS TO GUIDE PLACEMENT OF NEEDLES WITHIN THE BODY
20190321072 ยท 2019-10-24
Inventors
- Kalpathi L. Venkatachalam (Jacksonville, FL, US)
- Vivek Gupta (Jacksonville, FL, US)
- Prasanna Vibhute (Jacksonville, FL, US)
- Alexander Bills (Atlanta, GA, US)
- Lucas Muller (Atlanta, GA, US)
- Dev Mandavia (Atlanta, GA, US)
- Cassidy Wang (Atlanta, GA, US)
- Marci Medford (Atlanta, GA, US)
Cpc classification
A61B2017/0046
HUMAN NECESSITIES
A61B17/3401
HUMAN NECESSITIES
A61B2090/064
HUMAN NECESSITIES
A61B2017/00128
HUMAN NECESSITIES
International classification
Abstract
Apparatuses and methods can be used to guide placement of needles within the body. For example, this document describes apparatuses that measure impedance and/or force as a needle is passed through tissue to inform user of which anatomical space they are in. Low-cost portable bedside electro-physical apparatuses and methods for needle guidance and confirmation of successful placement in portions of the human body such as vessels and thecal sac are described herein.
Claims
1. An apparatus for identifying a position within a human body, the apparatus comprising: a handle; a needle, releasably coupleable with the handle, the needle comprising a first conductor including a first electrically-uninsulated portion positioned along a shaft of the needle and a second conductor including a second electrically-uninsulated portion positioned at a tip of the needle; and circuitry within the handle and in electrical communication with the first and second conductors, the circuitry configured to determine a bioimpedance of tissue between the first and second electrically-uninsulated portions while the needle is inserted within the human body.
2. The apparatus of claim 1, wherein the handle comprises one or more user feedback devices configured to provide an indication of the position within the human body based on the bioimpedance.
3. The apparatus of claim 1, further comprising a force sensor positioned to detect force exerted to the needle while the needle is being inserted within the human body.
4. The apparatus of claim 3, wherein the circuitry is configured to determine the detected force, and wherein the circuitry is configured to determine the position within the human body based on both: (i) the bioimpedance of tissue between the first and second electrically-uninsulated portions while the needle is inserted within the human body, and (ii) the detected force.
5. An apparatus for identifying a position within a human body, the apparatus comprising: a handle; a needle extending from the handle; a force sensor positioned to detect force exerted to the needle while the needle is being inserted within the human body; and circuitry within the handle and in electrical communication with the force sensor; the circuitry configured to determine the detected force.
6. A method of determining a position within a human body, the method comprising inserting the needle of the apparatus of any claim of claims 1 through 5 into the human body.
Description
DESCRIPTION OF THE DRAWINGS
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[0021] Like reference numbers represent corresponding parts throughout.
DETAILED DESCRIPTION
[0022] This document describes apparatuses used to guide the placement of needles within the body. In some embodiments, the apparatuses can differentiate between tissue layers using force and/or impedance measurements, among many other potential characterization techniques. For example, this document describes apparatuses that measure impedance and/or force as a needle is passed through tissue to inform user of which anatomical space they are in. In one example implementation, the apparatuses described herein are used to guide the placement of a needle for neuraxial anesthesia during labor and delivery.
[0023] Currently, blind placement of anesthesia is dependent on tactile feedback and the Loss of Resistance (LoR) encountered upon entry into the epidural space. Proficiency is gained and maintained only by continuous practice.
[0024] The devices described herein will allow physicians to identify entry into specific anatomical spaces by using bioelectric impedance analysis and/or force sensing (or other modalities). Bioelectric impedance analysis can be performed by generating alternating current (AC) in an electronics module (capital element) at the proximal end of the device with a frequency between 50 kHz and 100 kHz and limited to a maximum current of 100 A. The epidural needle and an enclosed insulated stylet (disposable element) act as electrodes, which run current through the tissue at the tip of the needle. Tissue impedance will be measured in the electronics module. Based on results from clinical testing, tissue types can be characterized. An indicator system on the surface of the electronics module will notify the practitioner of current tissue location.
[0025] In some embodiments, the devices, systems, and methods described herein use a combination of force sensing and impedance to guide the user. Accordingly, the devices, systems, and methods described herein facilitate a way of navigating by stimulating a lower extremity and using a sensor array on the lower back to give the best location to start the access. In some embodiments, the devices described herein are configured to use any access needle in conjunction with a custom stylet attached to a syringe-like device that holds all of the electronics.
[0026] In some embodiments, force sensing is implemented by placing a force sensor such as a force-sensitive resistor (FSR) behind the needle to measure transmitted force. The signal will be processed in the electronics module and will be used to enhance the current method of identifying tissue layer.
[0027] The devices and techniques described herein provide an objective means for practitioners to identify entry into a target location (e.g., for administration of neuraxial anesthesia). As a result, the devices and techniques can improve clinician confidence, minimize complication rates, and eliminate the steep learning curve of current practice.
[0028] Referring to
[0029] Referring to
[0030] The device 200 consists of two primary components, one reusable (the electronics housing module 210) and one disposable (the needle 240). The two components can be releasably coupled together using, for example, a luer lock connection as illustrated.
[0031] In some embodiments, the device 200 generates alternating current (AC) within a frequency 50-100 kHz and passes it through the substance at the tip of the needle 240 to characterize its impedance. As the needle 240 passes through tissues and anatomical structures of different compositions it can identify them based on their impedances. An indicator system on the handle 210 of the device 200 is used to signal to the user in what space the tip of the needle 240 currently resides.
[0032] The advantages of the illustrated device compared to current techniques include: provides tissue layer and anatomical space detection, allows the physician to hold the needle with both hands to increase stability and confidence, provides visual feedback for confirmation of placement within tissue layers that is not subjective, allows for easier training of medical personnel such as Residents, and eliminates physicians from having to rely on techniques such as tactile feedback and palpation which lack consistency.
[0033] Referring also to
[0034] Referring also to
[0035] Referring to
[0036] The device 300 uses a sensor to measure the force transmitted and passes the signal through an algorithm for processing. This method enhances the current method of identifying tissue layer location by providing quantitative information on where the tip of the needle 340 is located in the body.
[0037] In some embodiments, the force sensing of the device 300 can be accomplished using a force sensing resistor (FSR). The electrical resistance of the FSR changes with changing force applied to its surface. The resistance is read by some outside device (e.g. a microcontroller) and is processed to determine the tissues in which the needle 340 is located and through which it has passed through. To measure resistance, a resistor of known value is placed in series with the FSR and a known voltage is applied to the circuit. The outside device measures the voltage across the FSR, and determines the resistance.
[0038] The needle 340 is mounted to and extends from an outside housing 330, with the FSR located behind the needle in a position such that any force pushing on the needle from the tip in the direction of the handle will be opposed by a force between the FSR and the needle. Therefore, all the force transmitted through the needle will be passed through the FSR.
[0039] Other methods could also be used to calculate force passed through the needle 340. For example, strain gauges, piezoelectric sensors, elastic devices, magneto-elastic devices, and plastic deformation devices may also be used to measure forces transmitted through the needle 340. In addition, changes may also be implemented on the algorithm or the measurement device. For example, a wheatstone bridge, rather than a voltage divider, may be used to measure the resistance of and thereby the force on the FSR.
[0040] While the device 200 (
[0041] While this specification contains many specific implementation details, these should not be construed as limitations on the scope of any invention or of what may be claimed, but rather as descriptions of features that may be specific to particular embodiments of particular inventions. Certain features that are described in this specification in the context of separate embodiments can also be implemented in combination in a single embodiment. Conversely, various features that are described in the context of a single embodiment can also be implemented in multiple embodiments separately or in any suitable subcombination. Moreover, although features may be described herein as acting in certain combinations and even initially claimed as such, one or more features from a claimed combination can in some cases be excised from the combination, and the claimed combination may be directed to a subcombination or variation of a subcombination.
[0042] Similarly, while operations are depicted in the drawings in a particular order, this should not be understood as requiring that such operations be performed in the particular order shown or in sequential order, or that all illustrated operations be performed, to achieve desirable results. In certain circumstances, multitasking and parallel processing may be advantageous. Moreover, the separation of various system modules and components in the embodiments described herein should not be understood as requiring such separation in all embodiments, and it should be understood that the described program components and systems can generally be integrated together in a single product or packaged into multiple products.
[0043] Particular embodiments of the subject matter have been described. Other embodiments are within the scope of the following claims. For example, the actions recited in the claims can be performed in a different order and still achieve desirable results. As one example, the processes depicted in the accompanying figures do not necessarily require the particular order shown, or sequential order, to achieve desirable results. In certain implementations, multitasking and parallel processing may be advantageous.