This invention relates to invasive medical devices and more particularly, the present invention relates to anatomical-positioning medical devices for controlled advancement thorough multiple tissues of various types and cavities disposed there between, until reaching a target position. For example, an Epidural anesthesia device to provide controlled access to the Epidural space, while preventing puncturing the Dura mater.
In medical procedures, needle insertion and localization are issues of great importance. Misplacement of a needle tip or a trocar can harm essential tissues such as blood vessels, nerves or internal organs and lead to major complications. For example, during a procedure of Epidural anesthesia the needle tip should be placed inside the Epidural space (ES), to thereby facilitate administration of anesthetic agents. This has become a common and effective procedure for controlling pain during childbirth, major surgery, and chronic back pain.
Reference is made to
Overshooting of the tip of the needle beyond the ES may puncture the Dura mater 80 causing a leak of the cerebral-spinal fluid (CSF) from spinal cord 85 into the ES, leading to severe headaches (post dural puncture headaches syndrome).
The majority of current injection techniques are “blind” techniques, mainly tactile based. For example, the main technique of Epidural block is based on the “loss of resistance technique” (LORT). In LORT, a fluid or air filled syringe is attached to a needle. While the needle is advanced through different layers in the insertion site, the physician taps on the syringe. Inside dense Ligament layers, the physician fills a strong resistance, but when crossing the LF 60 and entering the ES 70, there is a substantial loss of resistance so that the fluid or air from the syringe can be easily pushed into the low-pressured ES 70, thus signaling the physician to stop advancing needle 92.
In practice, the LORT holds some major disadvantages. Because of the elastic properties of the LF 60, the elastic fibers are pushed by the needle and are stretched into the ES 70. For this reason, the rupture of these fibers takes place deep inside the ES 70 increasing the risk of an overshooting of the needle tip into the Dura mater 80. Moreover, the resolution of the non-controlled advancement-increments of the needle-tip is very limited and differs extensively from one physician to another. Another disadvantage of LORT is the relatively high risk of a false loss of resistance, taking place for instance inside the LF 60 due to a small space between adjacent fibers.
a-2d illustrate cross sectional views of the stages of a typical Epidural anesthesia procedure, including the penetration of Ligamentum Flavum 60 and including entering into Epidural space 70. When needle 95 is advanced through Ligamentum
Flavum 60, the elastic fibers of Ligamentum Flavum 60 are stretched by pushing pressure exerted by needle 95 deep into Epidural space 70, before entering Epidural space 70 (see
U.S. Pat. No. 5,188,594, given to Michael Zilberstein, provides a device and method for administering medicine into the Epidural space by first supplying air through a valve connected to a needle and provided with an inflatable element so that before the needle reaches the Epidural space the inflatable element is inflated. The needle is advanced and when the needle reaches the Epidural space 70 the inflatable element is deflated, which deflation is, typically, observed by the physician (or his/her stuff); medication is then administered through the valve and through the needle into the Epidural space.
There is a need for and it would be advantageous to have an injection device that can overcome the disadvantages mentioned hereabove, including the disadvantages of the LORT, and is relatively a low cost solution.
The terms “Epidural anesthesia procedure” and “Epidural block procedure” are used herein interchangeably.
By way of introduction, the principal intentions of the present invention include providing an anatomical-positioning apparatus, such as an injection device, that facilitates acquiring mechanical data from a mammalian tissue by an expandable device, while the expandable device exerts pressure onto portions of said mammalian tissue. Thereby facilitating to determine the type of a mammalian tissue, as well as determining transition between different mammalian tissues and cavities. An aspect of the present invention is to provide safe methods for advancing an introducer, typically a sharp introducer, from an elastic tissue to a soft tissue, such as from the Ligamentum Flavum to the Epidural space.
According to the teachings of the present invention there is provided an anatomical-positioning apparatus for acquiring mechanical data from a mammalian tissue to facilitate determining type of the tissue and transition between different tissues and cavities. The anatomical-positioning apparatus includes a cannula, having a tip at the distal section of the cannula, an expandable device having a contracted form size, when in a contracted state, and an expanded form size, when in an expanded state, wherein the expanded form size is substantially larger than the contracted form size. The anatomical-positioning apparatus further includes an introducer, having a longitudinal axis and a distal end, facilitating the introduction of the expandable device into the mammalian tissue, the expandable device being in the contracted state, an expanding-mechanism for expanding and contracting the expandable device, and a sensor for measuring physical parameters associated with the expandable device, to thereby provide sensed data.
The sensed data is acquired while the expandable device exerts pressure onto portions of the mammalian tissue, to thereby facilitating determining the type of tissue that is in contact with the expandable device and to determine a transition between different tissues and cavities. The sensor includes one or more sensing devices selected from the group of devices consisting of a pressure sensor, strain gauge, force sensor, tactile sensor, displacement sensor, volume sensor, flow sensor and a piezoelectric transducer. Optionally, the sensing device includes an array of sensors disposed on the expandable device.
Typically, the sensed data is indicated by one or more indication devices selected from the group of devices consisting of a display, a gage, a light indicator, an audio indicator and a tactile indicator.
Optionally, the sensed data includes a measurement of the advancement of the cannula against the mammalian tissue, and wherein the displacement of the expandable device, along the longitudinal axis, is inferred from the sensed data.
Optionally, the sensed data includes a one-dimensional measurement of the displacement of the expandable device, during the expanding against the mammalian tissue or contracting away from the mammalian tissue.
Optionally, the sensed data includes one or more measurements selected from a group of measurements consisting of the pressure inside the expandable device, the volume of gas or fluid inside the expandable device, an external force applied on the expandable device by the mammalian tissue and the spatial pressure or spatial force applied on the expandable device by the mammalian tissue, while the expandable device exerts pressure onto portions of the mammalian tissue.
Optionally, the sensed data facilitates determining one or more measurements selected from a group of measurements consisting of the volume-pressure work performed by the expandable device, a volume-pressure profile of the expandable device, the work being done by the expandable device and the force-displacement profile of the expandable device, while the expandable device exerts pressure onto portions of the mammalian tissue.
The expandable device is securely attached to the tip of the cannula or on the external circumference of the cannula, proximal to the tip of the cannula and when the expandable device expands from the contracted state to the expanded form size, the expandable device is disposed outside the introducer, and a blunt contact surface is formed at the external surface of the expanded expandable device.
The expandable device protects the mammalian tissue or an anatomical structure ahead of the mammalian tissue, from being punctured by the introducer of the expandable device. The cannula protects the expandable device from being punctured by the introducer. Typically, the expandable device expands and contracts under fluid or gas pressure provided by the expanding-mechanism through the cannula.
In variations of the present invention, the introducer is an openable introducer, having an openable sharp tip, wherein the openable sharp tip of the openable introducer has a closed state and an open state, and wherein the expandable device is trapped inside the openable sharp tip, the openable sharp tip being in a closed state. Preferably, the expandable device facilitates the openable sharp tip to remain in the closed state, when the expandable device is loaded by a preconfigured expanding force and the sharp tip is situated in a high density tissue. The expandable device facilitates the opening of the openable sharp tip, when the expandable device is loaded be a preconfigured expanding force and the openable sharp tip enters a low density tissue or cavity. The closed state facilitates advancement of the openable introducer through the mammalian tissue, while the open state prevents advancement of the openable introducer through the mammalian tissue. It should be noted that the expandable device also protects soft tissues ahead of expandable device.
Optionally, the introducer is selected from the group consisting of a veress needle, an epidural needle, a biopsy needle, a trocar, a cannula, a catheter, a Tuohy type needle and a surgical instrument.
Optionally, the expandable device is selected from a group of devices consisting of a balloon, a membrane, a diaphragm, a spring and a flexible device. Optionally, the expandable device includes one or more mechanical devices selected from a group of devices consisting of a spring and a balloon enclosed in a conical element, wherein the conical element protects the balloon from being punctured.
Optionally, the cannula and the expandable device is introduced on-demand and can be withdrawn during a procedure in order to enable utilization of other tools inside the mammalian tissue.
Optionally, the cannula includes a double lumen, wherein a first lumen facilitates a pathway for the fluid or gas into the expandable device, and wherein a second lumen facilitates a pathway for one or more devices selected from a group of devices consisting of a thin needle, a catheter, an optical fiber, an electrode and a surgical instrument.
Optionally, the cannula includes a single lumen facilitating a pathway for the fluid or gas into the expandable device, and wherein the single lumen facilitating a pathway for an optical fiber or a miniature camera, to thereby facilitate visualization of the mammalian tissue through the expandable device, the expandable device being in contact with the mammalian tissue.
Preferably, the anatomical-positioning apparatus further includes an advancement mechanism for incrementally advancing, in a controlled manner, one or more devices selected from the group consisting of the introducer, the cannula and the expandable device. Optionally, the advancement mechanism is selected from the group of devices consisting of a motor based device, hydraulic device, gear based device and a screw based device. Optionally, the introducer can be advanced incrementally together with the cannula and the expandable device. Optionally, the introducer can be advanced incrementally with respect to the cannula and the expandable device.
Preferably, the anatomical-positioning apparatus further includes a processor facilitated to record and analyze the sensed data, to thereby determine the type of tissue that is in contact with the expandable device and to determine the transition between tissues and cavities, wherein the sensed data is acquired while the expandable device is expanding, contracting or in a steady expansion level.
It is an aspect of the present invention to provide a method for acquiring mechanical data from a mammalian tissue by an expandable device, while the expandable device exerts pressure onto portions of the mammalian tissue. The method includes the steps of:
Preferably, the method further includes the step of analyzing the sensed data, using a processor, thereby determining the type of the mammalian tissue being in contact with the expandable device, and determining a transition between different mammalian tissues and cavities.
Optionally, in the method, the sensed data includes one or more measurements selected from a group of measurements consisting of the displacement of the expandable device and cannula, the pressure inside the expandable device, the volume of gas or fluid inside the expandable device, the external force applied on the expandable device by the mammalian tissue and the spatial pressure or spatial force applied on the expandable device by the mammalian tissue, while the expandable device exerts pressure onto portions of the mammalian tissue.
Optionally, in the method, the sensed data facilitates determining one or more measurements selected from a group of measurements consisting of the volume-pressure work performed by the expandable device, the volume-pressure profile of the expandable device, the work being done by the expandable device and the force-displacement profile of the expandable device, while the expandable device exerts pressure onto portions of the mammalian tissue.
Optionally, in the method, the measuring of the sensed data is performed during states selected from a group of states consisting of an expansion of the expandable device, a contraction of the expandable device and a displacement of the cannula and the expandable device, while the expandable device is expanded.
It is another aspect of the present invention to provide a spring-back method for a controlled insertion of an introducer into and through an elastic mammalian tissue. The spring-back method includes the steps of:
Optionally, in the spring-back method, the incremental advancing of the introducer is performed while also incrementally advancing the expandable device, wherein the expandable device is expanded.
Optionally, in the spring-back method, the incremental advancing of the introducer is performed, while the expandable device is expanded and in steady position, wherein the introducer is incrementally displaced beyond the undistorted position of the mammalian tissue, and wherein the introducer tip is kept at a shorter distance from the mammalian tissue, with respect to steady position of the front end of the expandable device.
It is another aspect of the present invention to provide a method for a controlled insertion of a cannula, using an inner needle, into and through an elastic mammalian tissue, the method including the steps of:
Optionally, the insertion method further includes the step of expanding the expandable device by the expanding-mechanism, thereby anchoring the cannula in position, upon transition of the expandable device from the elastic tissue into a different tissue or cavity.
It is yet another aspect of the present invention to provide a method for a controlled insertion of an openable introducer into and through a mammalian tissue, the method including the steps of:
Optionally, in the method with the openable introducer, the device further includes an advancement mechanism for incrementally advancing, in a controlled manner, devices selected from the group consisting of the openable introducer, the cannula and the expandable device.
The present invention will become fully understood from the detailed description given herein below and the accompanying drawings, which are given by way of illustration and example only and thus not limitative of the present invention, and wherein:
a-2d (prior art) illustrate cross sectional views of the stages of a typical Epidural anesthesia procedure, including penetration of the Ligamentum Flavum and including entering into the Epidural space;
a-4e illustrate cross sectional views of the distal portion of an anatomical-positioning apparatus as shown in
a-10e illustrate cross sectional views of the distal portion of an anatomical-positioning apparatus, as shown in
a-12d illustrate side views of the distal portion of an anatomical-positioning apparatus, according to variations of the present invention, having a thin-needle being introduced through a cannula for facilitating a spring-back method.
a-13g illustrate cross sectional views of the distal portion of an anatomical-positioning apparatus, as shown in
a illustrates a cross sectional view of the distal portion of the anatomical-positioning apparatus shown in
b illustrates a cross sectional view of the distal portion of the anatomical-positioning apparatus shown in
a-18b illustrate side views of an anatomical-positioning apparatus, according to variations of the present invention, having a guide-wire attached to the expandable device for measuring the displacement of the expandable device.
The present invention now will be described more fully hereinafter with reference to the accompanying drawings, in which preferred embodiments of the invention are shown. This invention may, however, be embodied in many different forms and should not be construed as limited to the embodiments set forth herein; rather, these embodiments are provided, so that this disclosure will be thorough and complete, and will fully convey the scope of the invention to those skilled in the art.
Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. The methods and examples provided herein are illustrative only and not intended to be limiting.
Referring back to
Referring is also to
In variations of the present invention, cannula 120 has an elongated hollow body (single lumen) facilitating the insertion and evacuation of gas or fluid into expandable device 130, wherein expandable device 130 is securely attached to distal end 124 (tip) of cannula 120. The elongated hollow body of cannula 120 can also provide a pathway for an optical fiber or a miniature camera, to thereby facilitate visualization of a mammalian tissue or cavity through expandable device 130, when expandable device 130 is expanded.
In embodiments, introducer 110 can be a Veress needle, an Epidural needle, a biopsy needle, a trocar, a cannula, a catheter, a Tuohy type needle, a surgical instrument or any other sharp object facilitated to be inserted into at least one mammalian tissue.
It should be noted that the present invention will be described mostly in terms of an anatomical-positioning apparatus for performing a procedure of Epidural anesthesia, including determining the type of one or all tissues the introducer is advancing through, including Interspinous Ligament 52, Ligamentum Flavum 60 and inside Epidural space 70, as well as indicating transition between tissues and cavities. But the present invention is not limited to anatomical-positioning apparatus for performing a procedure of Epidural anesthesia, including determining the type of one or all tissues the introducer is advancing through and indicating transition between tissues and cavities. The present invention includes all anatomical-positioning apparatuses for determining the type of one or more tissues, the introducer is advancing through, as well as indicating transition between different tissues and cavities.
Distal end 112 of introducer 110 is typically, with no limitation, a sharp end. Cannula 120 can be made of any biocompatible material, preferably hard plastic or stainless still. Expandable device 130 can be expanded to a preconfigured volume or shape and have a preconfigured displacement along longitudinal axis 115 of introducer 110 using air or fluid passing through first lumen 125 of cannula 120 and into expandable device 130.
Alternatively, the expandable device can be made of a shape memory alloy, such as NiTi alloy, so that under certain conditions (for instance, heat) it expands. Optionally, the expandable device can be expanded using a mechanical mechanism that is based on springs or any other mechanical element. In one preferred embodiment of the present invention, without limiting the scope of this invention, expandable device 130 is an inflatable balloon that can be made of any elastic material known in the art, such as polyurethane, flexible PVC, PET, nylon, nylon elastomers and thermoplastic elastomers.
Reference is now made to
In the contracted state, balloon 130 is completely deflated, and is protectively disposed inside introducer 110. Balloon 130 is kept deflated by mechanical biasing force or by maintaining partial vacuum-pressure inside balloon 130.
In the expanded state or in a partially expanded state, balloon 130 is popped out of introducer 110, such that introducer 110 does not damage balloon 130. Balloon 130 is kept inflated by providing controlled gas or fluid pressure into balloon 130. When balloon 130 is inflated, distal end 132 of expandable device 130 forms a blunt surface.
Referring back to
Anatomical-positioning apparatus 100 further includes a sensor 170 for measuring physical parameters associated with expandable device 130, while expandable device 130 exerts pressure onto portions of the mammalian tissue being operationally pressed by expandable device 130. The measuring of the physical parameters, associated with expandable device 130, facilitates determining the type of tissue that is in contact with a blunt external surface, typically distal surface 132 of balloon 130, as well as determining transition between tissues and cavities.
The measuring of the physical parameters, associated with expandable device 130, may take place when expandable device 130 expands, when expandable device 130 contracts, or when expandable device 130 is already expanded and in a steady state.
Reference is now made to
As shown in
Proximal end 238 of proximal section 232 of balloon 230 is securely attached to proximal end 248 of spring 240, both of which are securely attached to distal end 124 (tip) of cannula 120. The proximal end of distal end section 234 of balloon 230 is disposed at proximal end 252 of conical element 250, wherein conical element 250 has a proximal end 252 and a distal end 254, and wherein proximal end 252 of conical element 250 is securely attached to distal end 246 of spring 240. Proximal end 252 of conical element 250 has a substantially constant diameter that fits inside the internal diameter of introducer 110. In the collapsed state of expandable device 230, distal end 254 of conical element 250 has a smaller or equal diameter to the diameter of proximal end 252 of conical element 250. When expandable device 230 is expanded, distal end 254 of conical element 250 has a larger diameter than the internal diameter of introducer 110.
As depicted in an exemplary embodiment in
Preferably, gas (preferably air) or fluid is injected through cannula 120 and into balloon 230, thereby inflating balloon 230. Hence, proximal section 232 of balloon 230 stretches spring 240 distally, towards distal end 112 of introducer 110, and outside of distal end 112 of introducer 110. As fluid pressure continues to build up, balloon further inflates to an extent that forces flaps 256 of conical element 250 to open, thus facilitating distal section 234 of balloon 230 to reach the preconfigured volume and surface area. Flaps 256 of conical element 250 protect distal section 234 of balloon 230 from being punctured by tip 112 of introducer 110.
Upon deflation of balloon 230, elastic flaps 256 apply the force, stored while being inflated, against distal section 234 of balloon 230, thus collapsing distal section 234 of balloon 230 back into the smaller diameter of the contracted state. As the gas or fluid pressure inside balloon 230 continues to drop, balloon 230 further deflates and spring 240 returns to the unbiased position. Thereby, expandable device 230 is back inside introducer 110, proximal to distal end 112, as depicted in
When the expandable device is expandable device 230, the expanding-mechanism, typically, includes a pump (not shown) for controllably pump gas (air) or fluid into and out of balloon 230, wherein the operation of the pump is synchronized with biasing element 240 and flaps 256.
An aspect of the present invention is to facilitate determining the tissue type, as well as transition between tissues and cavities. The following describes a method describes the steps of an Epidural anesthesia procedure, by way of example, without limiting the scope of this invention. During Epidural anesthesia procedure, a physician performs procedural steps, in order to differentiate between Ligamentum Flavum 60 and Epidural space 70, wherein a principle intention of the Epidural block procedure is to be able to stop the advancement of introducer 110 upon entering Epidural space 70.
In an embodiment of the present invention, during the inflation of balloon 130, a measurement that reflects the mechanical resistance of the tissue to the inflation of balloon 130, is taken, using selected sensors 170 (see
The measured physical parameters, associated with expandable device 130, may include the pressure inside balloon 130, the instantaneous volume of balloon 130, the displacement of expandable device 130, the external force applied on the expandable device by the mammalian tissue, spatial force or spatial pressure applied on expandable device 130 or any other measurement known in the art. Other data can be concluded by processing the sensed data using a processor 160, such as the volume-pressure work performed by expandable device 130, volume-pressure profile of expandable device 130, work performed by expandable device 130 and force-displacement profile of expandable device 130, while expandable device exerts pressure onto portions of a mammalian tissue, For example, a pressure sensor can measure the pressure that builds up inside balloon 130 for a given volume. According to the measurement, the type of tissue being pushed by balloon 130 is determined and a decision is made whether to advance introducer 110 by another increment or whether to stop introducer 110 from further advancing, due to entrance into Epidural space 70.
The measurement may be continuous during the expansion, the contraction or the steady expanded state of expandable device 130, thus providing a unique set of measurements for a specific tissue. For instance, a measurement of the external force applied by a mammalian tissue against an expanded expandable device 130 as a function of the displacement of expandable device 130, may provide a curve that is typical for a certain type of tissue, for example an elastic tissue, and is substantially different from a non-elastic tissue.
The measurement can be of spatial force or spatial pressure applied on expandable device 130 by a mammalian tissue. In one embodiment, tactile sensors 175 disposed on expandable device 130 provide spatial data reflecting the mechanical resistance of the tissue being pressed by expandable device 130 in various locations along the circumference of expandable device 130. Such measurements can facilitate determining the direction of the fibers of the mammalian tissue being pressed by the expandable device 130. In addition, such measurements can facilitate determining the existence and direction of a hard tissue (such as a spinal process) that is in the vicinity of the mammalian tissue being pressed by the expandable device 130.
a-18b illustrate an embodiment of the present invention, wherein a distal tip 174 of a guide-wire 172 is attached to distal end 234 of balloon 230, and proximal tip 176 of guide-wire 172 is located near a displacement sensor 170. Upon expansion of balloon 230, distal end 234 of balloon 230 advances forward along longitudinal axis 115, thereby facilitating the advancement of guide-wire 172 along longitudinal axis 115. Displacement sensor 170, for example a photoelectric sensor, measures the displacement of proximal end 176 of guide-wire 172, thereby facilitating determining the displacement of balloon 230 while exerting pressure on portions of a mammalian tissue.
The main advantage of the method for determining tissue type and transition between tissues and cavities by an expandable device is in actively acquiring data regarding a mammalian tissue, by deforming the tissue, in order to determine mechanical properties, such as elasticity, that can otherwise be hard to discover by a passive measurement. Moreover, the larger surface area of distal end 132 of balloon 130, compared the to the tip surface area of tip 112 of introducer 110, finds an expression in that the mechanical resistance of elastic tissues is being amplified by the larger surface area of distal end 132, whereas the mechanical resistance of loose tissues does not change significantly. Thus, it is possible to differentiate between tissues types, although there are variations in population.
In addition, when measuring forces that develop against an introducer 110, friction forces operating on the body of introducer 110 have major influence on the measurement. However, when measuring forces against an expandable device 130, the friction forces operating on the body of introducer 110 have no effect on the measurement. Therefore, a measurement of mechanical resistance against an expandable device is less biased than a measurement against introducer 110.
One more advantage is in the ability to perform multiple measurement by expandable device 130 whether in a specific anatomical location or in a series of locations along the path of tip 112 of introducer 110.
Indicator 180 indicates the type of tissue being in contact with expandable device 130, as well as possible transition between different tissues and cavities. Such an indication can be visual, for example using a display showing a curve of force versus displacement of expandable device, light indication, acoustic indication, for instance when expandable device reaches Epidural space, a gage and a tactile indication, for example a vibration that is indicative to the extent of tissue elasticity.
Referring back to
As the operator does not see and thereby does not know that introducer 110 has penetrated Ligamentum Flavum 60, the operator activates expanding mechanism 150 to thereby expand balloon 130. The elasticity of Ligamentum Flavum 60 responds to expanded balloon 130, disposed inside Ligamentum Flavum 60, to set a pressure level P1 inside balloon 130. Knowing, for example the quantity of gas/fluid inserted by expanding mechanism 150, processor 160 analyzes measured pressure P1, to thereby provide the type of tissue balloon 130 is disposed in. In the described example, processor 160 activates indicator 180 to indicate to the operator that balloon 130 is disposed inside Ligamentum Flavum 60.
Typically, the operator of anatomical-positioning apparatus 100 activates expanding mechanism 150 to bring back expand balloon 130 to contracted state. Alternatively, balloon 130 automatically contracts back to a contracted state. Then, the operator activates an incremental mechanism for controllably advancing both introducer 110 and cannula 120 further towards Epidural space 70. The operator may activate an introducer-incremental-advancing-mechanism 190 (see
Since the anatomical-positioning apparatus 100 is held by the operator's hands and is inserted into a living body, movements of both the operator and the patient may interfere with positioning of tip 112 of introducer 110 inside a mammalian tissue. Therefore, when using the incremental advancing mechanism, the anatomical-positioning apparatus 100 may be stabilized by securing housing 140 of apparatus 100 against the entrance site of introducer 110, for instance, the back of a patient.
When the operator activates expanding mechanism 150 to thereby expand balloon 130, the fat tissue inside Epidural space 70 responds to expanded balloon 130 to set a pressure level P2 (see
In
Therefore, it is clear that displacing an elastic tissue increases its mechanical resistance, thereby increasing the pressure measured inside a balloon 130, while the resistance of a non elastic and low density tissue remains substantially unchanged under similar displacement. Hence, active measurement of the resistance of a tissue, while expanding or contracting balloon 130 provides data that facilitate determining the type of tissue balloon 130 is situated in.
In variation of the present invention, a ratio between the previous measurement and current measurement is calculated. If the ratio is smaller than a preconfigured threshold value, it is determined that balloon 130 is still inside the Ligamentum Flavum 60, and introducer 110 is incrementally advanced. If the ratio is bigger than the preconfigured value, it means that introducer 110 is inside Epidural space 70. Balloon 130 is deflated and cannula 120 is removed from anatomical-positioning apparatus 100 to enable threading of a catheter through introducer 110 to administrate anesthetics.
Reference is now made to
An aspect of the present invention is to provide a method of advancing introducer 110 accurately to a preconfigured in-vivo location, for example, into Epidural space 70, in an Epidural anesthesia (block) procedure. Since, Overshooting of tip 112 of introducer 110 beyond Epidural space 70 may puncture Dura mater 80, it would be advantageous to have a procedure that substantially reduce the risk of tip 112 of introducer 110 puncturing Dura mater 80. It is the intention of the present invention to provide a spring-back method of erupting Ligamentum Flavum 60, such that introducer 110 is inside Epidural space 70 at a distance d2 (see
The principle idea behind the various spring-back methods is to bring tip 112 of introducer 110 to a special position beyond virtual line 65, denoting the undistorted position of the wall of Ligamentum Flavum 60 that is the internal wall of Epidural space 70; keep introducer 110 spatially stationary; use expandable device 130 of anatomical-positioning apparatus 100 to further push elastic Ligamentum Flavum 60 by a preconfigured distance; contract expandable device 130 at once and return expandable device 130 back inside introducer 110. Thereby, the elasticity of Ligamentum Flavum 60 moves Ligamentum Flavum 60 towards the undistorted position 65, rapidly. Thereby, spearingly meeting tip 112 of introducer 110, on the way back, which cause Ligamentum Flavum 60 to rupture after one or more spring-back iterations.
In
Reference is now made to
In
a-13g illustrate cross sectional views of the distal portion of anatomical-positioning apparatus 500, showing the stages of a spring-back method of safe penetration of an elastic tissue, for example, Ligamentum Flavum 60 using, for example, expandable device 530 of anatomical-positioning apparatus 500, is illustrated.
In this spring-back method, when the elasticity of Ligamentum Flavum 60 rapidly moves Ligamentum Flavum 60 back towards the undistorted position 65, Ligamentum Flavum 60 is spearingly meeting the tip of thin-needle 510, rather than tip 112 of introducer 110. Eventually, thin-needle 510 causes Ligamentum Flavum 60 to rupture after one or more spring-back iterations.
Reference is now made to
Epidural space 70, during an Epidural block procedure, according to embodiments of the present invention. Method 600 begins by administrating introducer 110 of anatomical-positioning apparatus 500 into a mammalian tissue (See
The operator activates expandable mechanism 150 and thereby, balloon 530 is expanded (see
Locking cannula 520 and inner needle 510 in position, using inner needle-incremental-advancing-mechanism and cannula-incremental-advancing-mechanism 192.
An aspect of the present invention is to provide an anatomical-positioning apparatus and method of use thereof, having an introducer with an openable tip.
The principle idea behind an introducer with an openable tip is to have a balloon trapped inside the openable tip. The openable tip of the introducer has a closed state and an opened state, wherein in the closed state the openable tip forms a sharp tip facilitating penetration in and through a tissue, and wherein in the opened state the openable tip expands to forms a blunt surface, anchoring the introducer in position.
A preconfigured pressure is maintained inside the balloon trapped inside the openable tip. As long as introducer with a openable tip is situated inside a tissue, such as
Ligamentum Flavum 60, wherein the pressure applied on the openable tip by the tissue exceeds the preconfigured pressure inside the balloon, the openable tip stays in a closed state. Once the openable tip of the introducer moves into a softer tissue, such as in Epidural space 70, wherein the surrounding pressure, due to tissue properties, is significantly lower than the internal pressure inside the balloon, the balloon expands rapidly. Thereby, the expanding balloon causes the openable tip of the introducer to open and anchor the openable tip of the introducer inside Epidural space 70, wherein the balloon protects tissues and anatomical structures ahead of it.
Anatomical positioning apparatus 700 further includes cannula 720 having an expandable device 730, typically a balloon, wherein proximal end 732 of balloon 730 is securely attached to the external circumference of cannula 720, proximal to distal end 724 of cannula 720. Openable tip 750 includes a preconfigured number of elastic flaps 756 that are separated by a slot cut into the distal section of flexible tip 750. Typically, flaps 756 have a pointing tip and can operatively hingedly bend or deflect outwards as a result of a preconfigured pressure being built inside balloon 732, when the pressure external to flaps 756 is lower than the pressure inside balloon 732. Otherwise, balloon 730 stays trapped inside openable tip 750 of introducer 710 and thereby, openable tip 750 can be advanced through tissue.
Reference is now made to
The invention being thus described in terms of several embodiments and examples, it will be obvious that the same may be varied in many ways. Such variations are not to be regarded as a departure from the spirit and scope of the invention, and all such modifications as would be obvious to one skilled in the art.
This application claims the benefit under 35 USC 119(e) from U.S. provisional application 61/354,225, filed on Jun. 13, 2010, the disclosure of which is incorporated by reference for all purposes as if fully set forth herein.
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/IL11/00465 | 6/13/2011 | WO | 00 | 12/11/2012 |
| Number | Date | Country | |
|---|---|---|---|
| 61354225 | Jun 2010 | US |