The present technology generally relates to a deployable radio-frequency (RF) ablation needle or probe affording a relatively small insertion size to facilitate insertion thereof into hard and/or soft tissues, and, after insertion, affording reconfiguration from an undeployed configuration to a deployed configuration that expands an end portion thereof to correspondingly increase the size of an ablation zone.
Nerve pain and spinal metastases can be common causes of severe pain among patients with back pain. RF ablation can be used to treat these common causes of severe back pain. Standard RF ablation techniques (without cooling) and cooled RF ablation techniques are options to facilitate such ablation. Needles/probes used for standard RF ablation are generally smaller than needles/probes used for cooled RF ablation. However, ablation zones created using standard RF ablation techniques typically are smaller than ablation zones created using cooled RF ablation techniques. As such, standard RF ablation techniques can require precise placement of the electrodes thereof to be effective. Previously, larger needles/probes and longer ablation times have been employed to increase the size of ablation zones using standard RF ablation techniques and correspondingly mitigate the need for such precise placement. Nevertheless, there remains a need to minimize the size of the needles/probes used for standard RF ablation techniques, while simultaneously affording the creation of larger ablation zones. As discussed below, a deployable RF ablation needle according to the present disclosure is reconfigurable between an undeployed configuration that affords a relatively small insertion size to facilitate insertion into hard and/or soft tissues, and a deployed configuration that expands an end portion of the deployable RF needle to correspondingly increase the size of the ablation zone.
The techniques of this disclosure generally relate to a deployable RF ablation needle.
In one aspect, the present disclosure provides a deployable radio-frequency (RF) ablation needle for penetrating into hard and/or soft tissues of a patient, and ablating portions of the hard and/or soft tissues, the deployable RF ablation needle including a proximal end, an opposite distal end, a length between the proximal end and the distal end, and a mid-longitudinal axis extending through the proximal end and the distal end, and along the length of the deployable RF ablation needle; an outer portion extending from at least adjacent the proximal end toward the distal end, the outer portion including an interior cavity defined by an interior first surface; an intermediate portion extending from at least adjacent the proximal end toward the distal end, the intermediate including an exterior second surface and an interior cavity defined by an interior third surface, the intermediate portion terminating at an expandable end portion adjacent the distal end, the expandable end portion including at least two tines moveable between an undeployed configuration and a partially or completely deployed configuration; and an inner portion including a body portion and a head portion, the body portion extending from at least adjacent the proximal end to the head portion, and the head portion extending from the body portion to the distal end, the body portion including an exterior fourth surface; where portions of the intermediate portion are received within the interior cavity of the outer portion, and portions of the body portion of the inner portion are received within the interior cavity of the intermediate portion; where each of the at least two tines includes a first inner surface portion formed as a portion of the interior third surface, and the head portion includes a rearward-facing inclined surface contactable to the first inner surface portions of the at least two tines; and where the head portion is moveable between a first position and a second position, with the second position being closer to the proximal end than the first position, and movement of the head portion from the first position toward the second position contacts the rearward-facing inclined surface with the first inner surface portions, and interaction of the rearward-facing inclined surface and the first inner surface portions expands the expandable end portion by forcing the at least two tines apart from another from the undeployed configuration toward the partially or completely deployed configuration.
In another aspect, the present disclosure provides a deployable radio-frequency (RF) ablation needle for penetrating into hard and/or soft tissues of a patient, and ablating portions of the hard and/or soft tissues, the deployable RF ablation needle including a proximal end, an opposite distal end, a length between the proximal end and the distal end, and a mid-longitudinal axis extending through the proximal end and the distal end, and along the length of the deployable RF ablation needle; an outer portion extending from at least adjacent the proximal end toward the distal end; an intermediate portion extending from at least adjacent the proximal end toward the distal end, a portion of the intermediate portion being received in the outer portion, the intermediate portion terminating at an expandable end portion adjacent the distal end, the expandable end portion including at least four tines moveable between an undeployed configuration and a partially or completely deployed configuration, each of the at least four tines including a first inner surface; and an inner portion including a body portion and a head portion, the body portion extending from at least adjacent the proximal end to the head portion, and the head portion extending from the body portion to the distal end, a portion of the body portion of the inner portion being received in the intermediate portion, and the head portion including a rearward-facing inclined surface; where the head portion is moveable between a first position and a second position, with the second position being closer to the proximal end than the first position, and movement of the head portion from the first position toward the second position contacts the rearward-facing inclined surface with the first inner surface portions, and interaction of the rearward-facing inclined surface and the first inner surface portions expands the expandable end portion by forcing the at least four tines apart from another from the undeployed configuration toward the partially or completely deployed configuration; and where, when the at least four tines are in the undeployed configuration, the distal ends of a first one and a second one of at least four tines are opposite from and spaced apart from one another a first distance in a direction perpendicular to the mid-longitudinal axis, and, when the at least four tines are in the partially or completely deployed configuration, the distal ends of the first one and the second one of the at least four tines are opposite from and spaced apart from one another a second distance in the direction perpendicular to the mid-longitudinal axis, the second distance being greater than the first distance.
In yet another aspect, the present disclosure provides a deployable radio-frequency (RF) ablation needle for penetrating into hard and/or soft tissues of a patient, and ablating portions of the hard and/or soft tissues, the deployable RF ablation needle including a proximal end, an opposite distal end, a length between the proximal end and the distal end, and a mid-longitudinal axis extending through the proximal end and the distal end, and along the length of the deployable RF ablation needle; an outer portion extending from at least adjacent the proximal end toward the distal end; an intermediate portion extending from at least adjacent the proximal end toward the distal end, a portion of the intermediate portion being received in the outer portion, the intermediate portion terminating at an expandable end portion adjacent the distal end, the expandable end portion including at least four tines moveable between an undeployed configuration and a partially or completely deployed configuration, each of the at least four tines including a first inner surface portion; and an inner portion including a body portion and a head portion, the body portion extending from at least adjacent the proximal end to the head portion, and the head portion extending from the body portion to the distal end, a portion of the body portion of the inner portion being received in the intermediate portion, and the head portion including a rearward-facing inclined surface; where the head portion is moveable between a first position and a second position with the second position being closer to the proximal end than the first position, and movement of the head portion from the first position toward the second position contacts the rearward-facing inclined surface with the first inner surface portions, and interaction of the rearward-facing inclined surface and the first inner surface portions expands the at least four tines of the expandable end portion; and where expansion of the at least four tines of the expandable end portion correspondingly increases an ablation zone in the hard and/or soft tissues surrounding the at least four tines with the ablation zone having a first size when the expandable end portion is in the undeployed configuration, and the ablation zone having a second size when the expandable end portion is in the partially or completely deployed configuration, the second size being larger than the first size.
The details of one or more aspects of the disclosure are set forth in the accompanying drawings and the description below. Other features, objects, and advantages of the techniques described in this disclosure will be apparent from the description and drawings, and from the claims.
A deployable RF ablation needle in accordance with a preferred embodiment of the present disclosure is generally indicated by the numeral 10 in
The undeployed configuration of these portions of the deployable RF ablation needle 10 affords a relatively small insertion size to facilitate insertion thereof into the hard and/or soft tissues, and the expansion of these portions from the undeployed configuration to the partially or completely deployed configuration correspondingly increases the application area of the RF energy to correspondingly increase the ablation zone afforded by use thereof. Once these portions of the deployable RF ablation needle 10 are positioned adjacent the hard and/or soft issues requiring ablation, these portions can be expanded from the undeployed configuration to the partially or completely deployed configuration via actuation by the user, and thereafter, the user can activate ablation of the hard and/or soft tissues via application of the RF energy thereto through these portions.
As depicted in
As discussed below, the outer portion 20 can be configured as a collar, and can surround portions of the intermediate portion 22 and the inner portion 24; the intermediate portion 22 can include or be formed as one or more tines, and the intermediate portion 22 can surround portions of the inner portion 24; and the inner portion 24 can be configured as a trocar. As such, portions of the inner portion 24 extend within portions of the intermediate portion 22, and portions of the intermediate portion 22 extend within portions of the outer portion 20. As discussed below, portions of the inner portion 24 (and/or the outer portion 20) can be moved with respect to the intermediate portion 22.
As depicted in
As depicted in
The expandable end portion 60 can be formed from multiple tines 64, and all or portions the tines 64 can each serve as an electrode of the deployable RF ablation needle 10. As depicted in
The tines 64 can be moveable between an undeployed configuration (
Each of the tines 64 can include a proximal end 70, a distal end 72, a first surface portion 74 (that is part of the interior fourth surface 54), and a second surface portion 76 (that is also part of the interior fourth surface 54), with the proximal ends 70 being located adjacent a corresponding one of the areas 66, and the distal ends 72 being collocated with the distal end 62. The scorings at the areas 66 can be formed by indentations formed in the exterior third surface 52 of the body portion 50 that form pivot points affording each of the tines 64 to bend outwardly when pressure is applied thereto. In the undeployed configuration (
A second aperture 78 (
As depicted in
The rearward-facing inclined surface(s) 96 can have frusto-conical shape(s) for contacting the tines 64. Furthermore, the forward-facing surface(s) 102, as depicted in
As depicted in
As discussed above, the tines 64 serve as electrodes, and the size of the ablation zone of the deployable RF ablation needle 10 is dependent on the amount of expansion of the tines 64 of the expandable end portion 60. The expansion of the expandable end portion 60 relative to the mid-longitudinal axis MPA increases the application area of the RF energy to correspondingly increase the ablation zone afforded by use of the deployable RF ablation needle 10. In other words, the larger the expansion of the tines 64 due to movement of the head portion 82 from the first position P1 toward the second position P2, the larger the ablation zone. As such, the user can control the size of the ablation zone by selecting the amount of expansion of the tines 64 of the expandable end portion 60.
Once the tines 64 are expanded to a selected amount, electrical current can be applied to the ablation zone via the tines 64. The application of the electrical current, for example, can be controlled by the user with or without use of the handle. To illustrate, as discussed above, the intermediate portion 22 (including the tins 64) can be formed from a conductive material. The intermediate portion 22 (including the tines 64) can be electrically connected to an electrical-current generator (not shown) using one or more wires (not shown), and operation of the electrical-current generator can be controlled by the user at the handle. The amount of electrical current applied through the tines 64 to the hard and/or soft tissues can be adjusted via adjustment by the user of the electrical-current generator, for example, at the generator itself and/or at the handle. Thus, via adjustment and activation/deactivation thereof, the user can control amount(s) and/or duration(s) of the electrical current applied to the hard and/or soft tissues via the tines 64. Thus, the size of the ablation zone can be controlled via the amount of expansion of the tines 64 of the expandable end portion 60, and the amount(s) and/or the duration(s) of the electrical current applied to the hard and/or soft tissues through the tines 64. The ablation zone can be sized to encompass all or portions of the hard and/or soft tissues requiring ablation.
While the shapes of the body portion 30, the body portion 50, and the body portion 80 are depicted in
In addition to the inner portion 22 being moveable relative to the intermediate portion 22, the outer portion 20 can be moveable relative to the intermediate portion 22 to facilitate covering, then uncovering and exposing the tines 64. To illustrate, the body portion 30 of the outer portion 20 can be moveable to position the distal end 42 of the end portion 40 at or adjacent the distal ends 72 of the tines 64. In doing so, the distal end portion 40 can cover all or portions of the tines 64 to aid ease of penetration of the deployable RF ablation needle 10 into the hard and/or soft tissues. Thereafter, the distal end portion 40 can be moved to uncover and expose the tines 64.
In addition to bending outwardly due to force applied by the head portion 82 against the tines 64, the tines 64, rather than being unbiased or biased toward the undeployed configuration, can be biased to toward the deployed configuration to bend outwardly relative to the mid-longitudinal axis MLA. Thus, after movement of the outer portion 20 away from the distal ends 72 that uncovers the tines 64 (after being formerly covered by the distal end portion 40), the tines 64 can bend outwardly due to such bias. The head portion 82 of the inner portion 24 can then be moved, as described above, from the first position P1 toward the second position P2 to further expand the expandable end portion 60.
During use thereof, the deployable RF ablation needle 10 is inserted by the user into a patient to ultimately position the expandable end portion 60 (and the tines 64) adjacent the hard and/or soft tissues requiring ablation. The user can manipulate the placement of the end portion 60 with or without use of the handle. Once the tines 64 are positioned adjacent the hard and/or soft tissues requiring ablation, the user can manipulate the deployable RF ablation needle 10 move the head portion 82 of the inner portion 24 from the first position P1 toward the second position P2. In doing so, the tines 64 are expanded to expand the distal ends 72 thereof from the minimum undeployed dimension D1 toward the maximum deployed dimension D2. If the outer portion 20 is moveable relative to the intermediate portion 22 to facilitate covering then exposure of the tines 64, the outer portion 20 first would need to be moved to uncover and expose all or portions of the tines 64 to allow expansion thereof.
The user can select the amount of expansion of the tines 64 to control the size of the ablation zone via the amount of movement of the head portion 82 from the first position P1 toward the second position P2. Furthermore, the user can also control the size of the ablation zone 60 by adjusting the amount(s) and/or activating/deactivating the duration(s) of the electrical current applied to the hard and/or soft tissues through the tines 64. After ablation of the hard and/or soft tissues, the insertion process can be repeated in reverse to facilitate removal of the deployable RF ablation needle 10 from the patient.
As discussed above, the undeployed configuration of the tines 64 affords a relatively small insertion size to facilitate insertion thereof into the hard and/or soft tissues, and the expansion of the tines 64 from the undeployed configuration to a partially or completely deployed configuration correspondingly increases the application area of the RF energy to correspondingly increase the ablation zone afforded by use thereof.
It should be understood that various aspects disclosed herein may be combined in different combinations than the combinations specifically presented in the description and the accompanying drawings. It should also be understood that, depending on the example, certain acts or events of any of the processes of methods described herein may be performed in a different sequence, may be added, merged, or left out altogether (e.g., all described acts or events may not be necessary to carry out the techniques). In addition, while certain aspect of this disclosure are described as being performed by a single module or unit for purposes of clarity, it should be understood that the techniques of this disclosure may be performed by a combination of units or modules associated with, for example, a medical device.