Threaded cannula depth limiter
A surgical access device assembly. The assembly includes a cannula having a working channel and a helical tissue engagement feature disposed along an outer surface of the cannula and configured to stabilize the cannula relative to a body cavity wall of a patient. The assembly also includes a depth limiter movably coupled with the cannula. The depth limiter includes a body portion extending about a central axis of the depth limiter and including a protrusion extending radially inwardly relative to the central axis. The body portion is movable angularly relative to the cannula between a fine adjustment configuration and a coarse adjustment configuration. In the fine adjustment configuration the protrusion is configured to selectively threadably engage the helical tissue engagement feature. In the coarse adjustment configuration the protrusion is configured to selectively threadably disengage the helical tissue engagement feature such that the depth limiter is translatable axially along the cannula.
1. A surgical access device assembly comprising:
(a) a cannula including:
(i) a working channel configured to guide a surgical instrument along a central axis of the cannula,
(ii) at least one helical tissue engagement feature disposed along an outer surface of the cannula, wherein the helical tissue engagement feature is configured to stabilize the cannula relative to a body cavity wall of a patient when the cannula is inserted distally through the body cavity wall, and
(iii) at least one longitudinal track disposed along the outer surface of the cannula; and
(b) a depth limiter movably coupled with the cannula, wherein the depth limiter comprises:
(i) a first body portion,
(ii) a second body portion, wherein each of the first and second body portions extends about a central axis of the depth limiter, and
(iii) at least one protrusion extending radially inwardly relative to the central axis of the depth limiter,
wherein the first and second body portions are rotatable relative to one another and relative to the cannula about the central axis between a fine adjustment configuration and a coarse adjustment configuration, wherein in the fine adjustment configuration the at least one protrusion is configured to selectively threadably engage the at least one helical tissue engagement feature, wherein in the coarse adjustment configuration the at least one protrusion is configured to selectively threadably disengage the at least one helical tissue engagement feature and selectively slidably engage the at least one longitudinal track such that the depth limiter is translatable axially along the cannula.
2. The surgical access device assembly of claim 1 , wherein the at least one protrusion includes a plurality of circumferentially arranged protrusions.
3. The surgical access device assembly of claim 1 , wherein the at least one protrusion includes a first protrusion presented by the first body portion and a second protrusion presented by the second body portion.
4. The surgical access device assembly of claim 3 , wherein the first and second body portions are rotatable relative to each other about the central axis of the depth limiter between a clocked configuration in which the first and second protrusions are radially aligned with each other and at least one unclocked configuration in which the first and second protrusions are radially misaligned from each other.
5. The surgical access device assembly of claim 4 , wherein at least one of the first or second protrusions is configured to selectively threadably engage the at least one helical tissue engagement feature in response to the first and second body portions being in the unclocked configuration.
6. The surgical access device assembly of claim 5 , wherein the at least one longitudinal track has a width, and wherein the first and second protrusions collectively occupy an envelope having an effective width greater than the width of the at least one longitudinal track when the first and second body portions are in the unclocked configuration.
7. The surgical access device assembly of claim 4 , wherein the first and second protrusions are configured to selectively slidably engage the at least one longitudinal track when the first and second body portions are in the clocked configuration.
8. The surgical access device assembly of claim 7 , wherein the at least one longitudinal track has a width, and wherein the first and second protrusions collectively occupy an envelope having an effective width less than the width of the at least one longitudinal track when the first and second body portions are in the clocked configuration.
9. The surgical access device assembly of claim 4 , wherein the first and second body portions are biased toward the unclocked configuration.
10. The surgical access device assembly of claim 1 , wherein the at least one body portion includes first and second body portions pivotably coupled together by a hinge such that the first and second body portions are pivotable relative to each other about the hinge between the fine adjustment configuration and the coarse adjustment configuration, wherein the at least one protrusion includes a first protrusion presented by the first body portion and a second protrusion presented by the second body portion.
11. The surgical access device assembly of claim 10 , wherein the first and second protrusions are configured to be pivoted radially outwardly from the at least one helical tissue engagement feature when in the coarse adjustment configuration.
12. The surgical access device assembly of claim 10 , wherein the hinge includes a living hinge.
13. The surgical access device assembly of claim 12 , wherein the first and second body portions and the living hinge are integrally formed together as a unitary piece.
14. The surgical access device assembly of claim 10 , wherein the first and second body portions are biased toward the fine adjustment configuration.
15. A depth limiter configured to couple with a cannula tube of a trocar having at least one helical tissue engagement feature disposed along an outer surface of the cannula tube, the depth limiter comprising:
(a) a first body portion;
(b) a second body portion movably coupled to the first body portion such that the first and second body portions are movable relative to each other between a fine adjustment configuration and a coarse adjustment configuration;
(c) a first protrusion presented by the first body portion and extending radially inwardly relative to a central axis of the depth limiter; and
(d) a second protrusion presented by the second body portion and extending radially inwardly relative to the central axis of the depth limiter,
wherein in the fine adjustment configuration at least one of the first or second protrusions is configured to selectively threadably engage the at least one helical tissue engagement feature of the cannula tube, wherein in the coarse adjustment configuration the first and second protrusions are configured to selectively threadably disengage the at least one helical tissue engagement feature of the cannula tube,
wherein the first and second body portions are rotatable relative to each other about the central axis of the depth limiter between a clocked configuration in which the first and second protrusions are radially aligned with each other and an unclocked configuration in which the first and second protrusions are radially misaligned from each other, wherein the clocked configuration at least partially defines the coarse adjustment configuration and the unclocked configuration at least partially defines the fine adjustment configuration.
16. The depth limiter of claim 15 , wherein the first and second body portions are pivotable relative to each other about a hinge axis perpendicular to the central axis of the depth limiter between the fine adjustment configuration and the coarse adjustment configuration.
17. A surgical access device assembly comprising:
(a) a cannula including:
(i) a working channel configured to guide a surgical instrument along a central axis of the cannula, and
(ii) a helical tissue engagement protrusion disposed along an outer surface of the cannula, wherein the helical tissue engagement protrusion is configured to stabilize the cannula relative to a body cavity wall of a patient when the cannula is inserted distally through the body cavity wall; and
(b) a depth limiter movably coupled with the cannula and configured to limit a depth of the cannula relative to the body cavity wall, wherein the depth limiter comprises:
(i) a first body portion that extends about a central axis of the depth limiter, and
(ii) a second body portion that extends about the central axis,
wherein the first and second body portions are rotatable relative to each other about the central axis and relative to the cannula between a fine adjustment configuration and a coarse adjustment configuration,
wherein in the fine adjustment configuration at least one of the first or second body portions is threadably engaged with helical tissue engagement protrusion,
wherein in the coarse adjustment configuration each of the first and second body portions is threadably disengaged from the helical tissue engagement protrusion such that the depth limiter is axially translatable relative to the cannula.
18. The surgical access device of claim 17 , wherein the first body portion includes a first protrusion and the second body portion includes a second protrusion, wherein in the fine adjustment configuration at least one of the first or second protrusions is threadably engaged with the helical tissue engagement protrusion, and wherein in the coarse adjustment configuration each of the first and second protrusions is threadably disengaged from the helical tissue engagement protrusion such that the depth limiter is translatable axially along the cannula.
19. The surgical access device of claim 18 , wherein first and second protrusions are of equal radial height.
20. The surgical access device of claim 18 , wherein the depth limiter includes a biasing spring positioned between the first body portion and second body portion, wherein the biasing spring is configured to bias the first and second body portions relative to one another such that first and second protrusions are radially unaligned with each other.